Thomas Liehr (2023)
web-presence: https://cs-tl.de/Start.html
Created by Dr. Thomas Liehr (PhD),
affiliation: Institute of Human Genetics, 07740 Jena, Germany;
e-mail: Thomas.Liehr@med.uni-jena.de or LiehrT@web.de
Articles
List of species studies with colleagues - HERE.
|
Abbreviations
for Research Topics CG =
Clinical genetics; EVO = evolution; HET
= heterochromatin; INT =
interphase and chromosome structure; M
= method / probeset development; PRE =
prenatal; sSMC = small supernumerary
marker chromosomes; TCG =
tumorcytogenetics; UPD = uniparental
disomy |
2024
2023
| Number |
Authors/
Title/ Where Contribution was Published |
Impact
Factor |
Topic |
| 850 |
V
Sales‑Oliveira, M Altmanova, V Gvozdik, R
Kretschmer, T Ezaz, T Liehr,
N Padutsch, G Badjedjea, R Utsunomia, A
Tanomtong, M Cioffi.
Cross-species chromosome painting and repetitive DNA mapping illuminate the karyotype evolution in true crocodiles (Crocodylidae). Chromosoma 2023, 132:289-303.. |
1.600 | EVO |
| 849 |
D
Dedukh, A Maslova, A Al-Rikabi, N Padutsch,
T Liehr, A Krasikova.
Karyotypes of water frogs from the Pelophylax esculentus complex: results of cross-species chromosomal painting. Chromosoma 2023, 132:329-342.. |
1.600 | EVO |
| 848 |
T
Liehr, M Ziegler, L Person, S Kankel, N
Padutsch, A Weise, JP Weimer, H Williams, S
Ferreira, JB Melo, IM Carreira.
Small supernumerary marker chromosomes derived from human chromosome 11. Front Genet 2023, 14:1293652. |
4.200 | sSMC |
| 847 |
E
Angelopoulou, A Theodosiou, I Papaevripidou,
A Alexandrou, T Liehr, Y
Gyftodimou, EG Stefanou, C Sismani.
CHD2 pathogenic nonsense variant in a three-generation family with variable phenotype and a paracentric inversion 16: Case report. Heliyon 2023, 9:e22987. |
4.000 | CG |
| 846 |
T
Liehr.
Perspective: Is there any reason to stay in human genetic societies as cytogeneticists? Qeios 2023, VY79EZ. |
n.a. | other |
| 845 |
F
dMC Sassi, A Sember, GA Deon, T Liehr,
N Padutsch, OT Oyakawa, MR Vicari, LAC
Bertollo, O Moreira‑Filho, MdB Cioffi.
Homeology of sex chromosomes in Amazonian Harttia armored catfishes supports the X‑fission hypothesis for the X1X2Y sex chromosome system origin. Sci Reports 2023, 13:15756. |
4.600 | EVO |
| 844 | n.a. | other |
|
| 843 |
E
Behluli, T Liehr, R
Hadziselimovic, G Temaj.
Epigenetics and treatment of systemic lupus erythematosus. Pharmacia 2023, 70:1005-1013. |
1.100 | CG |
| 842 |
RLR
de Moraes, FdMC Sassi, JAD Vidal ,CAG Goes,
RZ dos Santos, JHF Stornioli, F
Porto-Foresti, T Liehr, R
Utsunomia, MdB Cioffi.
Chromosomal rearrangements and satellite DNAs: Extensive chromosome reshuffling and the evolution of neo-sex chromosomes in the genus Pyrrhulina (Teleostei; Characiformes). Int J Mol Sci 2023, 24:13654. |
5.600 | EVO |
| 841 |
G
Hovhannisyan, T Harutyunyan, R Aroutiounian,
T Liehr.
The diagnostic, prognostic and therapeutic potential of cell-free DNA with a special focus on COVID-19 and other viral infections. Int J Mol Sci 2023, 24:14163. |
5.600 | CG |
| 840 |
S
Khensuwan, W Supiwong, C Suwannapoom, P
Buasriyot, S Jantarat, W Thongnetr, N
Muanglen, P Kaewmad, P Saenjundaeng, K
Seetapan, T Liehr, A
Tanomtong.
A comparative cytogenetic study of Hypsibarbus malcolmi and H. wetmorei (Cyprinidae: Tribe Poropuntiini). Comp Cytogenet 2023, 17: 181-194. |
n.a. | EVO |
| 838 |
PS
Ambulkar, T Liehr, M Jain, J
Waghmare, N Gangane, P Narang, AK Pal.
Molecular characterization of de novo ring chromosome 21 in a child with seizures, growth retardation, and multiple congenital anomalies. J Genet 2023, 102:44. |
1.500 | CG |
| 838 |
MP
Barcellos de Oliveira, R Kretschmer, GA
Deon, GA Toma, T Ezaz, CA Gomes Goes, F
Porto-Foresti, T Liehr, R
Utsunomia, MdB Cioffi.
Following the pathway of W chromosome differentiation in Triportheus (Teleostei: Characiformes). Biology 2023, 12: 1114. |
4.200 | EVO |
| 837 |
FdMC
Sassi, GA Deon, A Sember, T Liehr, OT
Oyakawa, O Moreira-Filho, LAC Bertollo, MR
Vicari, MdB Cioffi.
Turnover of multiple sex chromosomes in Harttia catfish (Siluriformes, Loricariidae): a glimpse from whole chromosome painting. Front Genet 2023, 14:1226222. |
4.700 | EVO |
| 836 |
E
Jamali, A Safarzadeh, BM Hussen, T
Liehr, S Ghafouri-Fard, M
Taheri.
Single cell RNA-seq analysis with a systems biology approach to recognize important differentially expressed genes in pancreatic ductal adenocarcinoma compared to adjacent non-cancerous samples by targeting pancreatic endothelial cells. Pathol Res Pract 2023, 248: 154614 |
2.800 | TCG |
| 835 |
L
Spahiu, JA Sayera, E Behluli, T Liehr,
G Temaj.
Identification of likely recurrent CEP290 mutation in a child with Joubert syndrome and cerebello-retinal-renal features. F1000Res 2023, 11:388 |
n.a. | CG |
| 834 |
GA
Toma, N Dos Santos, RZ Dos Santos, P Rab, R
Kretschmer, T Ezaz, LAC Bertollo, T
Liehr, F Porto-Foresti, T
Hatanaka, A Tanomtong, R Utsunomia, MB
Cioffi.
Cytogenetics meets genomics: Cytotaxonomy and genomic relationships among color variants of the Asian arowana Scleropages formosus. Int J Mol Sci 2023, 24:9005 |
5.600 | EVO |
| 833 |
EH
Steffensen, A Skakkebæk, K Gadsbøll, OB
Petersen, T Westover, H Strange, The
NIPT-SCA-map Study Group (including among
many other T Liehr), I Vogel.
Inclusion of sex chromosomes in noninvasive prenatal testing in Asia, Australia, Europe and the USA: A survey study. Prenat Diagn 2023, 43:144-155. |
3.000 | CG |
| 832 |
JAD
Vidal, FdeMC Sassi, RLR de Moraes, RF
Artoni, T Liehr, MB Cioffi,
MC de Almeida.
Giant sex chromosomes in omophoita species (Coleoptera, Chrysomelidae): Structural and evolutionary relationships revealed by Zoo-FISH and comparative genomic hybridization (CGH). Insects 2023, 14:440. |
3.000 | EVO |
| 831 |
S
Khensuwan, FdMC Sassi, RLR Moraes, S
Jantarat, K Seetapan, K Phintong, W
Thongnetr, S Kaewsri, S Jumrusthanasan , W
Supiwong, P Rab, A Tanomtong, T Liehr,
MB Cioffi.
Chromosomes of Asian cyprinid fishes: Genomic differences in conserved karyotypes of ‘Poropuntiinae’ (Teleostei, Cyprinidae). Animals 2023, 13: 1415. |
3.000 | EVO |
| 830 |
B
Mingkwan, FdMC Sassi, N Muanglenm, S
Pinmongkhonkul, K Pinthong, S Tongnunui, P
Yeesin, A Tanomtong, T Liehr,
MdB Cioffi, W Supiwong.
Evolutionary tracks of chromosomal diversification in Trichopsis (Anabantiformes, Osphronemidae) fishes: New insights from a molecular cytogenetic perspective. Biodiversitas 2023, 24: 1551-1559. |
n.a. | EVO |
| 829 |
D
Heydeck, C Ufer, KR Kakularam, M Rothe, T
Liehr, P Poulain, H Kuhn.
Functional characterization of transgenic mice overexpressing human 15-lipoxygenase-1 (ALOX15) under the control of the aP2 promoter. Int J Mol Sci 2023, 24:4815. |
5.600 | CG |
| 828 |
V
Graiqevci-Uka, E Behluli, L Spahiu, T
Liehr, G Temaj.
A new case of childhood acute lymphoblastic B-cell leukemia from Pristina. Acta Med Bulg 2023, 50:59-62. |
n.a. | TCG |
| 827 |
L
Spahiu, E Behluli, V Graiqevci-Uka, T
Liehr, G Temaj.
Joubert syndrome: molecular basis and treatment. J Mother Child / Medycyna Wieku Rozwojowego 2023, 26:118-123. |
n.a. | CG |
| 826 |
L
Spahiu, E Behluli, R Hadziselimovic, T
Liehr, G Temaj.
Mucopolysaccharidosis type III (subtype IIIB) diagnosis as a spectrum disorder: A case report from Kosovo. Fol Med 2023, 65: 161-165. |
n.a. | CG |
| 825 |
V
Graiqevci-Uka, E Behluli, L Spahiu, T
Liehr, G Temaj.
Targeted treatment and immunotherapy in high-risk and relapsed/ refractory pediatric acute lymphoblastic leukemia. Curr Ped Rev 2023, 19: 150-156. |
n.a. | TCG |
| 25% of publications of
Institute of Human Genetics Jena in the actual
year |
|||
2022
| Number |
Authors/
Title/ Where Contribution was Published |
Impact
Factor |
Topic |
| 824 |
G
Loof, D Szabo, V Garg, A Kukalev, LZ
Redondo, R Kempfer, TM Sparks, Y Zhang, CJ
Thieme, S Carvalho, A Weise, M Balachandran,
T Liehr, LR Welch, A-K Hadjantonakis, A
Pombo.
3D genome topologies distinguish pluripotent epiblast and primitive endoderm cells in the blastocyst. bioRxiv 2022, 10.19.512781. |
n.a. | INT |
| 823 |
E
Behluli, N Nuhii, T Liehr, G Temaj.
Suspicions regarding the genetic inheritance of acute lymphoblastic leukemia in patients with Down syndrome. J Mother Child / Medycyna Wieku Rozwojowego 2022, 26:104-110 |
n.a. | TCG |
| 822 |
S
Azawi, S Kankel, T Liehr, M
Rincic.
First cytogenomic characterization of murine testis tumor cell line MLTC-1. MEBM 2022, 4: 10-14. |
n.a. | TCG |
| 821 |
T
Liehr, T Harutyunyan, H
Williams, A Weise.
Restrictions and advantages of non-invasive prenatal testing (NIPT). Encylopedia, 2022, 38834. |
n.a. | CG |
| 820 |
Y
Khalifa, HY Hassan, A Weise, T Liehr,
H Alkhayyat.
Molecular cytogenetic and phenotypic characterization of Phelan McDermid and 22q13 duplication syndrome: a case report. Mol Cytogenet 2022, 15: 52. |
1.300 | CG |
| 819 |
LA
Méndez-Rosado, N de León-Ojeda, A García, F
Sheth, A Gaadi, AA Bousfiha, M Lehlimi, A
Natiq, OS Kurinnaia, SG Vorsanova, I Iourov,
D Huhle, T Liehr.
Clinical characterization of 72 patients with del(22)(q11.2q11.2) from different ethnic background. Egypt J Med Hum Genet 2022, 23:158. |
1.300 | CG |
| 818 |
T Liehr.
Was man zu Grenzen und Möglichkeiten des Noninvasive prenatal testing (NIPT) unbedingt wissen sollte. pädiatrische praxis 2022, 99: 7-14. |
n.a. | CG |
| 817 |
L
Spahiu, E Behluli, R Hadziselimovic, T
Liehr, G Temaj.
Pathogenesis and therapy in polycystic kidney disease. Acta Medica Mediter 2022, 38: 3001-3009. |
0.300 |
CG |
| 816 |
V
Graiqevci-Uka, E Behluli, LSpahiu, T
Liehr, G Temaj.
Targeted treatment and immunotherapy in high-risk and relapsed/ refractory pediatric acute lymphoblastic leukemia. Curr Ped Rev 2023, 19: 150-156. |
n.a. |
TCG |
| 815 |
Y
Wang, KR Kumar, T Liehr.
Molecular combing and its application in clinical settings. Mol Cytogenet 2022, 15: 50. |
1.300 |
CG |
| 814 |
T
Liehr, T Harutyunyan, H
Williams, A Weise.
Non-invasive prenatal testing in Germany. Diagnostics 2022, 12: 2816. |
3.600 |
CG |
| 813 |
P
Mohanty, D Shetty, T Liehr,
K Mrasek, N Khattry.
Intrachromosomal amplification of BCR expressed as homogenously staining region (hsr) in a case of acute myeloid leukemia with myelodysplasia-related changes. Int J Lab Hematol 2022, 44: 993-994. |
3.000 |
TCG |
| 812 |
G
Alves, MH Ornellas, T Liehr.
The role of Calmodulin Binding Transcription Activator 1 (CAMTA1) gene and its putative genetic partners in the human nervous system. Psychogeriatrics 2022, 22: 869-878. |
2.000 |
CG |
| 811 |
S
Classen, E Rahlf, J Jungwirth, N Albers,
LP Hebestreit, A Zielinski, L Poole, M
Groth, P Koch,
T Liehr, S Kankel, N Cordes, C Petersen, K Rothkamm, H Pospiech, K Borgmann. Partial reduction in BRCA1 gene dose modulates DNA replication stress level and thereby contributes to sensitivity or resistance. Int J Mol Sci 2022, 23:13363. |
5.600 |
TCG |
| 810 |
T
Liehr.
Chromosomal heteromorphisms and cancer susceptibility revisited. Cells 2022, 11: 3239. |
6.000 |
TCG |
| 809 |
Z
El Amrani, SC Elalaoui, W Jdioui, A Sbiti,
I Ratbi, T Liehr, A
Sefiani, A Natiq.
Complex translocation leading to13q interstitial deletion in a Moroccan child with retinoblastoma and intellectual disability. Ophthalmic Genetics 2022; 43:689-692. |
1.200 |
CG TCG |
| 808 |
P
Li, B Dupont, Q Hu, M Crimi, Y Shen, I
Lebedev, T Liehr.
The past, present, and future for constitutional ring chromosomes: A report of the International Consortium for Human Ring Chromosomes (ICHRC). HGG Adv 2022, 3: 100139. |
4.400 |
CG |
| 807 |
V
Nilius-Eliliwi, M Tembrink, WM Gerding, KP
Lubieniecki, JM Lubieniecka, S Kankel, T
Liehr, T Mika, F Dimopoulos, K
Döhner, R Schroers, HHP Nguyen, DB
Vangala.
Broad genomic workup including optical genome mapping uncovers a DDX3X::MLLT10 gene fusion in acute myeloid leukemia. Front Oncol 2022, 12: 959243 |
4.700 |
TCG |
| 806 |
E
Souche, S Beltran, E Brosens, JW Belmont,
M Fossum, O Riess, C Gilissen, A
Ardeshirdavani, G Houge, M van Gijn, J
Clayton-Smith, M Synofzik, N de Leeuw, ZC
Deans, Y Dincer, SH Eck, S van der
Crabben, M Balasubramanian, H Graessner, M
Sturm, H Firth, A Ferlini, R Nabbout, F De
Baere, T Liehr, M Macek, G
Matthijs, H Scheffer, P Bauer, HG Yntema,
MM Weiss.
Recommendations for whole genome sequencing in diagnostics for rare diseases. Europ J Hum Genet 2022, 30:1017-1021. |
5.200 |
CG |
| 805 |
T
Liehr.
False-positives and false-negatives in non-invasive prenatal testing (NIPT): what can we learn from a meta-analyses on > 750,000 tests? Mol Cytogenet 2022, 15: 36. |
1.300 |
CG |
| 804 |
TD
de Oliveira, NA Bertocchi, R Kretschmer,
EHC de Oliveira, MB de Cioffi, T
Liehr, TR Ochotorena de
Freitas.
Genomic organization of microsatellites and LINE-1-like etrotransposons: evolutionary implications for Ctenomys minutus (Rodentia: Ctenomyidae) cytotypes. Animals 2022, 12: 2091. |
3.000 |
EVO |
| 803 |
T
Harutyunyan, T Liehr.
Can age related mosaic loss of Y chromosome really cause cardiac damage in men? eletter (1) for Sano, et al. Science 2022, 377:292-297 |
n.a. (as just a comment) |
CG |
| 802 |
V
Barbaro, A Orvieto, G Alvisi, M Bertolin,
F Bonelli, T Liehr, T
Harutyunyan, S Kankel, G Joksic, S
Ferrari, E Daniele, D Ponzin, D Bettio, L
Salviati, E Di Iorio.
Analysis and pharmacological modulation of senescence in human epithelial stem cells. J Cell Mol Med 2022, 26: 3977-3994. |
5.300 | CG |
| 801 |
S
Azawi, L-M Barf, T Liehr, S
Kankel, M Rincic.
First cytogenomic characterization of murine testicular tumor cell line I-10. OBM Genetics 2022, 6: 159. |
n.a. | TCG |
| 800 |
M
Paneque, T Liehr, C
Serra-Juhe, U Moog, B Melegh, I Carreira.
The need for recognition of core professional groups in genetics healthcare services in Europe. Europ J Hum Genet 2022; 30: 639-640. |
5.200 | other |
| 799 |
GA
Deon, L Glugoski, T Hatanaka, FdMC Sassi, V
Nogaroto, LAC Bertollo, T Liehr,
A Al-Rikabi, O Moreira-Filho, MdB Cioffi, MR
Vicari.
Evolutionary breakpoint regions and chromosomal remodeling in Harttia (Siluriformes: Loricariidae) species diversification. Genet Mol Biol 2022, 45: e20210170. |
2.100 | EVO |
| 798 |
T Liehr.
Was man zu Grenzen und Möglichkeiten des Noninvasive prenatal testing (NIPT) unbedingt wissen sollte. gynäkologische praxis 2022, 49: 425-432. |
n.a. | CG |
| 797 |
N
Baba, A Lengyel, E Pinti, E Yapici, I
Schreyer, T Liehr, G Fekete,
T Eggermann.
Microdeletions in 1q21 and 8q12.1 depict two additional molecular subgroups of Silver-Russell syndrome like phenotypes. Mol Cytogenet 2022, 15:19. |
1.300 | UPD |
| 796 |
A
Weber, T Liehr,
A Al-Rikabi, S Bilgen, U Heinrich, J
Schiller, M Stumm.
The first neocentric, discontinous, and complex small supernumerary marker chromosome composed of 7 euchromatic blocks derived from 5 different chromosomes. Biomedicines 2022, 10: 1102. |
4.700 | sSMC |
| 795 |
M
Paneque, C Serra Juhé, B Melegh, I Carreira,
U Moog, T Liehr.
Über die Notwendigkeit der Anerkennung von sog. Kernberufsgruppen innerhalb der genetischen Gesundheitsversorgung in Europa. Med Gen 2022, 34:81-83, correction under 34:189-191. |
1.100 | other |
| 794 |
PHN
Ferreira, FHS de Souza, RLR de Moraes, M
Perez, F de MC Sassi, PF Viana, E Feldberg,
T Ezaz, T Liehr, LAC
Bertollo, M de B Cioffi.
The genetic differentiation of Pyrrhulina (Teleostei, Characiformes) species is likely influenced by both geographical distribution and chromosomal rearrangements. Front Genet 2022, 13: 869073 |
3.700 | EVO |
| 793 |
W
Kasiroek, S Phimphan, K Pinthong, C
Suwannapoom, S Aiumsumang, T Liehr,
W Supiwong, A Tanomtong.
Comparative cytogenomic analysis of cardinalfishes (Perciformes, Apogonidae) from Thailand. The Nucleus 2022, 65: 57-66. |
4.700 | EVO |
| 792 |
RRC
de Matos, GM Ferreira, C Meyer, R
Marschalek, P Larghero, RC Ribeiro, T Liehr,
M Othman, MTdeSM Bizarro, E Sobral da Costa,
MGP Land, E Abdelhay, R Binato, MLM Silva.
KMT2A-MLLT1 and the novel SEC16A-KMT2A in a cryptic three-way translocation t(9;11;19) present in an infant with acute lymphoblastic leukemia. J Pediatr Hematol Oncol 2022, 44: e719. |
1.200 | TCG |
| 791 |
GA
Deon, L Glugoski, FdMC Sassi, T Hatanaka, V
Nogaroto, LAC Bertollo, T Liehr,
A Al-Rikabi, OdB Moreira-Filho, MdB Cioffi,
MR Vicari.
Chromosomal rearrangements and origin of the multiple XX/XY1Y2 sex chromosome system in Harttia species (Siluriformes: Loricariidae). Front Genet 2022, 13: 877522. |
3.700 | EVO |
| 790 |
X
Fan, K Pinthong, EHC de Oliveira, A
Tanomtong, H Chen, A Weise, T Liehr.
First comprehensive characterization of Phayre’s leaf-monkey (Trachypithecus phayrei) karyotype. Front Genet 2022, 13: 841681. |
3.700 | EVO |
| 789 |
T
Liehr, A Weise, L Person, N
Padutsch, S Kankel.
How to obtain high quality metaphase spreads for molecular cytogenetics. Current Protocols 2022, 2:e392. |
n.a. | M |
| 788 |
T
Liehr.
Uniparental disomy is a chromosomic disorder in the first place. Mol Cytogenet 2022, 15: 5. |
1.300 | UPD |
| 787 |
FHS
de Souza, FdMC Sassi, PHN Ferreira, LAC
Bertollo, T Ezaz, T Liehr, MF
Perez, MB Cioffi.
Integrating cytogenetics and population genomics: Allopatry and neo-sex chromosomes shaped the genetic divergence in the Erythrinus erythrinus species complex (Teleostei, Characiformes). Biology 2022, 11: 315. |
4.200 | EVO |
| 786 |
A
Wafa, B Ali, F Moassass, M Kheder, A
Aljapawe, B AL-Halabi, K Mrasek, T
Liehr, W Al-Achkar.
Acute myeloid leukemia due to germline CEBPA mutation in a Syrian family. Mol Genet Genomic Med 2022, 10: e1854. |
2.000 | TCG |
| 785 |
S
Eck, B Fritz, C Haferlach, J Kunz, T
Liehr, S Matos-Meder, H Rieder,
D Schäfer, I Schanze.
Web-based external quality assessment (EQA) for genetic diagnostics provided by the German Association of Professionals for Human Genetics (BVDH). ECA newsletter 2022, 49: 2-4. |
n.a. | other |
| 784 | n.a. | sSMC |
|
| 783 |
S
Azawi, M Balachandran, F Kramer, S Kankel, M
Rincic, T Liehr.
Molecular cytogenetic characterization of urethane induced murine lung cell line LA-4 as model for human squamous cell lung cancer. Mol Clin Oncol 2022, 16:9. |
1.200 | TCG |
| 782 |
RR
Capela de Matos, M Othman, GM Ferreira, K
Monteso, MT de Souza, M Rouxinol, JB Melo,
IM Carreira, E Abdelhay, T Liehr,
RC Ribeiro, M Silva.
Somatic homozygous loss of SH2B3, and a non-Robertsonian translocation t(15;21)(q25.3;q22.1) with NTRK3 rearrangement, in an adolescent with progenitor B-cell acute lymphoblastic leukemia with the iAMP21. Cancer Genet 2022, 262-263:16-22. |
1.900 | TCG |
| 29% of publications of
Institute of Human Genetics Jena in the actual
year |
|||
2021
| Number |
Authors/
Title/ Where Contribution was Published |
Impact
Factor |
Topic |
| 781 |
CF
Yano, A Sember, R Kretschmer, LAC Bertollo,
T Ezaz, T Hatanaka, T Liehr,
P Ráb, A Al-Rikabi, P Ferreira Viana, E
Feldberg, EA de Oliveira, GA Toma, MdB
Cioffi.
Against the mainstream: exceptional evolutionary stability of l ZW sex chromosomes across fish families Triportheidae and Gasteropelecidae (Teleostei: Characiformes). Chromosome Res 2021, 29:391-416. |
4.620 | EVO |
| 780 |
M
Volleth, S Müller, K-G Heller, V Trifonovo,
T Liehr, H-S Yong, RJ Baker, FA
Aanwarali Khan, CG Sotero-Caio.
Cytogenetic analyses detect cryptic diversity in Megaderma spasma from Malaysia. Acta Chiropt 2021, 23: 271-284. |
1.145 | EVO |
| 779 |
AS
Koltsova, OA Efimova, OV Malysheva, NS
Osinovskaya, T Liehr, A
Al-Rikabi, NY Shved, IY Sultanov, OG
Chiryaeva, MI Yarmolinskaya, NI Polenov, VV
Kunitsa, MI Kakhiani, TG Tral, G K Tolibova,
ON Bespalova, IY Kogan, AS Glotov, VS
Baranov, AA Pendina.
Cytogenomic profile of uterine leiomyoma: in vivo vs in vitro comparison. Biomedicines 2021, 9: 1777. |
4.757 | TCG |
| 778 |
B
Imarazene, K Du, S Beille, E Jouanno, R
Feron, Q Pan, J Torres-Paz, C Lopez-Roques,
A Castinel, L Gil, C Kuchly, C Donnadieu, H
Parrinello, L Journot, C Cabau, M Zham, C
Klopp, T Pavlica, A Al-Rikabi, T
Liehr, S Simanovsky, J Bohlen, A
Sember, J Perez, F Veyrunes, T Mueller, J
Postlethwait, M Schartl, A Herpin, S Rétaux,
Y Guiguen.
A supernumerary “B-sex” chromosome drives male sex determination in the Pachón cavefish, Astyanax mexicanus. Curr Biol 2021, 31: 4800-4809.e9. |
10.900 | EVO |
| 777 |
L
Spahiu, E Behluli, R Hadziselimovic, T
Liehr, G Temaj.
Mucopolysaccharidosis III: Molecular basis and treatment. Pediatr Endocrinol Diab Metabol 2021, 27: 201-208. |
n.a. | CG |
| 776 |
T Liehr.
Molecular cytogenetics in the era of chromosomics and cytogenomic approaches. Front Genet 2021, 12: 720507 |
4.772 | M |
| 775 |
RLR de Moraes, F de
MC Sassi, LAC Bertollo, MM Koh, PF Viana, E
Feldberg, VCS Oliveira, GA Deon, ABH
Al-Rikabi, T Liehr, M de Bello
Cioffi.
Tracking the evolutionary trends among small-sized fishes of the genus Pyrrhulina (Characiformes, Lebiasinidae): New insights from a molecular cytogenetic perspective. Front Genet 2021, 12: 769984. |
4.772 | EVO |
| 774 |
O
Kadioglu, MEM Saeed, N Mahmoud, S Azawi, K
Mrasek, T Liehr, T Efferth.
Identification of novel drug resistance mechanisms by genomic and transcriptomic profiling of glioblastoma cells with mutation-activated EGFR. Life Sciences 2021, 284: 119601. |
6.780 | TCG |
| 773 |
F
Santiago, R Tavares Silvestre, U Barros
Otero, M Medeiros Tabalipa, M de Moura
Ribeiro-Carvalho, L Rios Scherrer, ABH
Al-Rikabi, T Liehr, G Alves,
MH Ornellas.
The association of three DNA repair genes polymorphisms on the frequency of chromosomal alterations detected by fluorescence in situ hybridization. Int Arch Occup Environ Health 2021, 94: 1567-1577. |
2.851 | TCG |
| 772 |
F de MC Sassi, O
Moreira-Filho, GA Deon, A Sember, LAC
Bertollo, T Liehr, VCS
Oliveira, PF Viana, E Feldberg, MR Vicari, M
de B Cioffi.
Adding new pieces to the puzzle of karyotype evolution in Harttia (Siluriformes, Loricariidae): Investigation of Amazonian species. Biology 2021, 10:922. |
5.168 | EVO |
| 771 |
M
Abdulazeez, S Kankel, T Liehr.
About the origin of the acrocentric part of non-acrocentric satellited chromosomes in humans. Research Results Biomedicine 2021, 7:215-219. |
n.a. | HET |
| 770 |
T
Liehr.
International System for Human Cytogenetic or Cytogenomic Nomenclature (ISCN) – some thoughts. Cytogenet Genome Res 2021;161(5):223-224. |
1.941 | other |
| 769 |
T Liehr,
N Fleischer, A Al-Rikabi.
Next-generation phenotyping in cat- eye syndrome based on computer-aided facial dysmorphology analysis of normal photographs. Mol Genet Genomic Med. 2021; 9:e1785. |
2.473. | sSMC |
| 768 |
S
Tsan, S Kankel, N Padutsch, L Person, M
Ziegler, A Al-Rikabi, A Weise, K Mrasek, T
Liehr.
About cryptic acrocentric pericentromeric abnormalities in infertile. OBM Genetics 2021, 5:11. |
n.a. | CG |
| 766 |
S
Azawi, T Liehr, M Rincic.
First molecular cytogenetic characterisation of tracheal squamous cell carcinoma cell line KLN 205. J Cancer Metast Treatm 2021, 7:38. |
n.a. | TCG |
| 765 |
S
Fuchs, J Lisfeld, S Kankel, L Person, T
Liehr.
The acrocentric part of der(Y)t(Y;acro)(q12;p1?2) contains D15Z1 sequences in the majority of cases. Hum Genome Var 2021, 8:32. |
n.a. | HET |
| 764 |
M Volleth, FAA Khan, S Müller, RJ Baker, D
Arenas-Viveros, RD Stevens, V Trifonov, T
Liehr, K-G Heller, CG
Sotero-Caio.
Cytogenetic investigations in Bornean rhinolophoidea revealed cryptic diversity in Rhinolophus sedulus entailing classification of peninsular Malaysia specimens as a new species. Acta Chiropt 2021, 23: 1-20. |
1.145 | EVO |
| 763 | n.a. | sSMC |
|
| 762 |
T Liehr.
Noninvasive prenatal testing (NIPT), what patients do not learn, may be due to lack of specialist genetic training by gynecologists and obstetricians? Front Genet 2021, 12: 682980. |
4.772 | CG |
| 761 |
VCS Oliveira, M
Altmanová, PF Viana, T Ezaz, LAC Bertollo, P
Ráb, T Liehr, A Al-Rikabi, E
Fedberg, T Hatanaka, S Scholz, A Meurer, M
Cioffi.
Revisiting the karyotypes of alligators and caimans (Crocodylia, Alligatoridae) after a half-century delay: Bridging the gap in chromosomal evolution of reptiles. Cells 2021, 10: 1397. |
7.294 | EVO |
| 760 |
K
Piaszinski, M Rincic, T Liehr,
S Azawi.
Molecular cytogenetic characterization of the murine melanoma cell lines S91 clone M3 and B16-F1 with variant B16-4A5. Cytogenet Genome Res 2021, 161: 82-92. |
1.941 | TCG |
| 759 | 1.941 | other |
|
| 758 |
S
Ditcharoen, S Khensuwan, K Seetapan, P
Soonthornvipat, C Suwannapoom, K Pinthong, S
Tongnunui, MdB Cioffi, T Liehr,
A Tanomtong, W Supiwong.
First classical and molecular cytogenetic analyses of Sperata acicularis (Siluriformes, Bagridae). Taiwania 2021, 66: 203-213. |
0.816 | EVO |
| 757 |
P Yeesin, P
Buasriyot, S Ditcharoen, P Chaiyasan, C
Suwannapoom, S Juntaree, S Jantarat, S
Talumphai, MdB Cioffi, T Liehr,
A Tanomtong, W Supiwong.
Comparative study of four Mystus species (Bagridae, Siluriformes) from Thailand: insights into their karyotypic diversity. Comp Cytogenet 2021, 15: 119-136. |
1.182 | EVO |
| 756 |
ÁS Roco, T
Liehr, A Ruiz-García, K Guzmán,
M Bullejos.
Comparative distribution of repetitive sequences in the karyotypes of Xenopus tropicalis and Xenopus laevis (Anura, Pipidae). Genes 2021, 12:617. |
4.141 | EVO |
| 755 |
R
Hochstenbach, T Liehr, RJ
Hastings.
Chromosomes in the genomic age. Preserving cytogenomic competence of diagnostic genome laboratories. Europ J Hum Genet 2021, 29:541-552. |
5.351 | CG |
| 754 |
KCDA
Monteso , MAK Othman, RR Capela de Matos, DR
Ney Garcia, MM da Rocha, MT de Souza,
LF Albagli, T Liehr, MGP
Land, MLM Silva, ES Costa.
An original complex rearrangement involving chromosomes 9, 11, and 14, harboring a complex KMT2A gene rearrangement in an infant with mixed-phenotype acute leukemia. J Pediatr Hematol Oncol 2021, 43:e371-e374. |
n.a. | TCG |
| 753 |
A
Grigoryan, J Pospiech, S Krämer, D Lipka, T
Liehr, H Geiger, H Kimura, MA
Mulaw, MC Florian.
Attrition of X chromosome inactivation in aged hematopoietic stem cells. Stem Cell Reports. 2021 Apr 13;16(4):708-716. |
7.294 | TCG |
| 752 |
S
Azawi , L-M Barf , T Liehr.
First molecular cytogenetic characterization of the MMT 060562 murine breast cancer cell line. Research Results Biomedicine 2021, 7: 4-14. |
n.a. | TCG |
| 751 |
EG
Coci, U Koehler, T Liehr, A
Stelzner, C Fink, H Langen, J Riedel.
Correction to: CANPMR syndrome and chromosome 1p32-p31 deletion syndrome coexist in two related individuals affected by simultaneous haplo-insufficiency of CAMTA1 and NFIA genes. Mol Cytogenet 2021;14:17. Erratum for: Mol Cytogenet 2016; 9:10. |
1.904 | CG |
| 750 |
T Liehr.
About classical molecular genetics, cytogenetic and molecular cytogenetic data not considered by Genome Reference Consortium and thus not included in genome browsers like UCSC, Ensembl or NCBI Mol Cytogenet 2021, 14:20. |
1.904 | CG |
| 749 |
I Miura, F Shams, S-M
Lin, M de Bello Cioffi, T Liehr,
A Al-Rikabi, C Kuwana, K Srikulnath, Y
Higaki, T Ezaz.
Evolution of a multiple sex-chromosome system by three-sided translocations among potential sex-chromosomes in the Taiwanese frog, Odorrana swinhoana. Cells 2021, 10:661 |
7.666 | EVO |
| 748 | n.a. | HET | |
| 747 |
V
Spangenberg, M Arakelyan, E Galoyan, I
Martirosyan, A Bogomazova, E Martynova, M de
Bello Cioffi, T Liehr, A
Al-Rikabi, F Osipov, V Petrosyan, O
Kolomiets.
Meiotic synapsis of homeologous chromosomes and mismatch repair protein detection in the parthenogenetic rock lizard Darevskia unisexualis. Mol Reprod Dev 2021;88:119-127. |
2.812 | EVO |
| 746 |
P
Chaiyasan, B Mingkwan, S Jantarat, C
Suwannapoom, MdB Cioffi, T Liehr,
S Talumphai, A Tanomtong, W Supiwong.
Classical and molecular cytogenetics of Belontia hasselti (Perciformes: Osphronemidae): Insights into the ZZ/ZW sex chromosome system. Biodiversitas 2021, 22:546-554. |
n.a. | EVO |
| 745 |
T
Liehr, HE Williams, M Ziegler, S
Kankel, N Padutsch, Ahmed Al-Rikabi.
Small supernumerary marker chromosomes derived from chromosome 14 and/or 22. Mol Cytogenet 2021, 14:13. |
1.904 | sSMC |
| 744 |
O
Kadioglu, M Saeed, N Mahmoud, S Azawi, K
Mrasek, T Liehr, T Efferth.
Identification of potential novel drug resistance mechanisms by genomic and transcriptomic profiling of colon cancer cells with p53 deletion. Arch Toxicol 2021, 95:959-974. |
6.168 | TCG |
| 743 |
S
Lutz-Bonengel, H Niederstätter, J Naue, R
Koziel, F Yang, T Sänger, G Huber, C Berger,
R Pflugradt, C Strobl, C Xavier, M Volleth,
SC Weiß, JA Irwin, EL Romsos, PM Vallone, G
Ratzinger, M Schmuth, P Jansen-Dürr, T
Liehr, P Lichter, TJ Parsons, S
Pollak, W Parson.
Evidence for multi-copy MEGA-NUMTs in the Human Genome. Nucleic Acids Res 2021, 49:1517-1531. |
19.160 | HET |
| 742 | 5.923 | HET | |
| 741 |
F Sassi, M Perez, V
Oliveira, GA Deon, F Souza, P Ferreira, E
Oliveira, T Hatanaka, T Liehr,
LAC Bertollo, M de Bello Cioffi.
High genetic diversity despite conserved karyotype organization in the giant trahiras from genus Hoplias (Characiformes, Erythrinidae). Genes 2021; 12:252. |
4.141 | EVO |
| 740 |
ME Rodríguez, I
Cross, A Arias-Pérez, S Portela-Bens, MA
Merlo, T Liehr, L Rebordinos.
Cytogenomics unveil the transposable elements driving rearrangements in chromosomes 2 and 4 of Solea senegalensis. Int J Mol Sci 2021, 22:1614. |
6.261 | EVO |
| 739 |
M Rincic, M Rados, J
Kopic, Z Krsnik, T Liehr.
7p21.3 together with a 12p13.32 deletion in a patient with microcephaly - does 12p13.32 locus possible comprises a candidate gene region for microcephaly? Front Mol Neuroscience 2021; 14: 613091 |
6.261 | CG |
| 738 |
S
Azawi, M Rincic, T Liehr.
Cytogenomic characteristics of murine breast cancer cell line JC. Mol Cytogenet 2021, 14:7. |
1.904 | TCG |
| 737 |
S
Azawi, K Piaszinski, M Balachandran, T
Liehr, M Rincic.
Molecular cytogenomic characterization of two murine liver cancer cell lines: MH-22A and Hepa 1-6. J Genet Genomes 2021, 5:1 |
n.a. | TCG |
| 736 |
IF
Alarbeed, A Wafa, F Moassass, B Al-Halabi, W
Al-Achkar, T Liehr, I
Aboukhamis.
De novo adult acute myeloid leukemia with two new mutations in juxtatransmembrane domain of the FLT3 gene: a case report. J Med Case Reports 2021, 15:22. |
n.a. | TCG |
| 735 | n.a. | sSMC | |
| 734 |
O
Kadioglua, MEM Saeed, N Mahmoud, SSH Azawi,
M Rincic, T Liehr, T Efferth.
Identification of metastasis-related genes by genomic and transcriptomic studies in murine melanoma. Life Sciences 2021, 267:11892 |
6.780 | TCG |
| 733 |
M Weber, A Weise, F
Vasheghani, C Göhner, JS Fitzgerald, T
Liehr, UR Markert.
Cytogenomics of six human trophoblastic cell lines. Placenta 2021, 103:72-75. |
3.287 | TCG |
| 75% of publications of
Institute of Human Genetics Jena in the actual
year |
|||
2020
| Number |
Authors/
Title/ Where Contribution was Published |
Impact
Factor |
Topic |
| 732 |
V Velissariou, F
Sachinidi, S Christopoulou, L Florentin, T
Liehr, A Efthymiadou, E
Angelopoulou, D Chrysis, EG Stefanou.
Low-level trisomy 14 mosaicism: A carrier of an isochromosome 14 and a supernumerary marker chromosome 14. Cytogenet Genome Res 2020, 160:664-670. |
1.636 | sSMC |
| 731 |
M Manferrari, M
Rincic, T Liehr, S Azawi.
Cytogenomics of murine melanoma cell lines C57/B1 and B16-F0. Mol Exp Biol Med 2020, 3: 39-44. |
n.a. | TCG |
| 730 |
GA Deon, L Glugoski,
MR Vicari, V Nogaroto, F de Menezes C Sassi,
M de Bello Cioffi, T Liehr,
LAC Bertollo, OM Filho.
Highly rearranged karyotypes and multiple sex chromosome systems in armored catfishes from the genus Harttia (Teleostei, Siluriformes). Genes 2020, 11:1366. |
4.096 | EVO |
| 729 |
V Spangenberg, O
Kolomiets, I Stepanyan, E Galoyan, MdB
Cioffi, E Martynova, I Martirosyan, T
Grishaeva, F Danielyan, A Al-Rikabi, T
Liehr, M Arakelyan.
Evolution of the parthenogenetic rock lizard hybrid karyotype: Robertsonian translocation between two maternal chromosomes in Darevskia rostombekowi. Chromosoma 2020, 129:275-283. |
4.316 | EVO |
| 728 |
M
Chaplin, JJ Kirkham, K Dwan, DJ Sloan, G
Davies, AL Jorgensen (T Liehr was Delphi
participant)
STrengthening the Reporting Of Pharmacogenetic Studies: Development of the STROPS guideline. PLoS Med 2020, 17:e1003344. |
n.a. | other |
| 727 |
S
Ditcharoen, FMC Sassi, LAC Bertollo, WF
Molina, T Liehr, P Saenjundaeng, A
Tanomtong, W Supiwong, C Suwannapoom, MB
Cioffi.
Comparative chromosomal mapping of microsatellite repeats reveals divergent patterns of accumulation in 12 Siluridae (Teleostei: Siluriformes) species. Genet Mol Biol 2020, 43: e20200091. |
1.771 | EVO |
| 726 |
T Harutyunyan, A
Al-Rikabi, A Sargsyan, G Hovhannisyan, R
Aroutiounian, T Liehr.
Doxorubicin-induced translocation of mtDNA into the nuclear genome of human lymphocytes detected using a molecular-cytogenetic approach. Int J Mol Sci 2020; 21:7690. |
5.923 | TCG |
| 725 |
I
Joksic, T Liehr, M Toljic, N
Karadzov-Orlic, Z Milovanovic, Z Mikovic, A
Egic.
Prenatal ultrasonographic manifestations of partial trisomy 12q (12q24.2→qter) and partial monosomy 2q (2q37.3→2qter). Vojnosanit Pregl 2020, 77:754-757. |
0.430 | CG |
| 724 |
FdMC Sassi, GA Deon,
O Moreira-Filho, MR Vicari, LAC Bertollo, T
Liehr, EAd Oliveira, MB Cioffi.
Multiple sex chromosomes and evolutionary relationships in amazonian catfishes: The outstanding model of the genus harttia (Siluriformes: Loricariidae). Genes 2020, 11:1179.476. |
4.096 | EVO |
| 723 |
PF Viana, T Ezaz, MdB
Cioffi, T Liehr, A Al‐Rikabi,
R Tavares‐Pinheiro, LAC Bertollo, E
Feldberg.
Revisiting the karyotype evolution of neotropical boid snakes: A puzzle mediated by chromosomal fissions. Cells 2020, 9:2268. |
6.600 | EVO |
| 722 |
N Ziller, R
Kotolloshi, M Esmaeili, M Liebisch, R
Mrowka, A Baniahmad, T Liehr,
G Wolf, I Loeffler.
Sex differences in diabetes- and TGF-β1-induced renal damage. Cells 2020, 9:2236. |
6.600 | CG |
| 721 |
H Sheth, S Trivedi, T
Liehr, K Patel, D Jain, J Sheth,
F Sheth.
Mosaic chromosome 18 anomaly delineated in a child with dysmorphism using a three-pronged cytogenetic techniques approach: a case report. BMC Medical Genomics 2020, 13:141. |
3.063 | CG |
| 720 |
VI Romero, JC Pozo, S
Saenz, A Llamos-Paneque, T Liehr,
K Hosomichi, A Tajima.
A toddler with phylloid-type pigmentary mosaicism and ambiguous genitalia resulting from trisomy 14 induced by a der(Y)t(Y;14). Hum Genome Var 2020, 7:28. |
n.a. | CG |
| 719 |
A Wafa, RA Jarjour, D
Alolabi, T Liehr, O Hamdan,
JB Melo, IM Carreira, MAK Othman, W
Al‑Achkar.
A new childhood ALL case with an extremely complex karyotype and acute spontaneous tumor lysis syndrome. Mol Cytogenet 2020, 13:44 |
2.009 | TCG |
| 718 |
E Wahlbul, T
Liehr, M Rincic, S Azawi.
Cytogenomic characterization of three murine malignant mesothelioma tumor cell lines. Mol Cytogenet 2020, 13:43. |
2.009 | TCG |
| 717 |
PF Viana, E
Feldberg, MB Cioffi , VT de Carvalho, S
Menezes, RC Vogt, T Liehr, T
Ezaz.
The amazonian red side-necked turtle Rhinemys rufipes (Spix, 1824) (Testudines, Chelidae) has a GSD sex-determining mechanism with an ancient XY sex microchromosome system. Cells 2020, 9:2088. |
6.600 | EVO |
| 716 |
M
Pissaparn, S Phimphan, P Chaiyasan, A
Tanoamting, T Liehr, C
Suwannapoom, M Reungsing, W Supiwong.
First chromosome analysis of Thai pufferfish Pao cochinchinensis (Steindachner, 1866). Biodiversitas 2020, 21:4309-4316. |
n.a. | EVO |
| 715 |
A
Al-Rikabi, L-B Liehr, T Liehr.
Glass-needle based chromosome microdissection – how to set up probes for molecular cytogenetics? Video J Clin Res 2020;2:100004VAM08AR2020. |
n.a. | M |
| 714 |
T
Liehr.
Is molecular cytogenetic diagnostics of rare diseases in Europe close to extinction. J Genet Genom 2020, 4:2. |
n.a. | other |
| 713 |
C
Sismani, S-M Rapti, P Iliopoulou, A Spring,
R Neroutsou, M Lagou, M Robola, E
Tsitsopoulos, L Kousoulidou, A Alexandrou, I
Papaevripidou, A Theodosiou, M Syrrou, S
Fuchs, M Hempel, D Huhle, T Liehr,
M Ziegler, M Duesberg, V Velissariou.
Novel pericentric inversion inv(9)(p23q22.3) in unrelated individualswith fertility problems in the Southeast European population. J Hum Genet 2020, 65:783-795. |
3.172 | CG |
| 712 |
W
Slimani, A Jelloul, A Al-Rikabi, A Sallem, Y
Hasni, S Chachia, A Ernez, A Chaieb, M Bibi,
T Liehr, A Saad, S
Mougou-Zerelli.
Small supernumerary marker chromosomes (sSMC) and male infertility: characterization of five new cases, review of the literature, and perspectives. J Assist Reprod Genet 2020, 37:1729-1736. |
3.412 | sSMC |
| 711 |
M
Zamariolli, A Di-Battista, M
Moyses-Oliveira, CB de Mello, MA Ramos, T
Liehr, MI Melaragno.
Disruption of PCDH10 and TNRC18 genes due to a balanced translocation. Cytogenet Genome Res 2020, 160:321-328. |
1.636 | CG |
| 710 |
H Hamdaoui, A Natiq,
O Benlarroubia, T Liehr, H
Dehbi, L Loukhmas, F Chegdani.
Near tetrapoloid karyotype with translocation t(11;14) in a Moroccan patient with amyloid light-chain amyloidosis and multiple myeloma. Leuk Res Rep 2020, 14:100217. |
n.a. | TCG |
| 709 |
P
Viana, T Ezaz, M Cioffi, T Liehr,
A Al-Rikabi, L Goll, A Rocha, E Feldberg.
Landscape of snake’ sex chromosomes evolution spanning 85MYR: Ancestry or co-opted sequences acquisition along their evolution? Scient Rep 2020, 10:12499. |
4.379 | EVO |
| 708 |
A
Wafa, F Moassass, S Almedani, T Liehr,
K Wilhelm, M As'sad, S Knippenberg, R
Glaubitz, RA Jarjour, W Al Achkar.
A novel heterozygous variant in exon 32 of the CHD7 gene (c.6923C>T) in a Syrian family with Kallmann syndrome. Res Results Biomed 2020, 6:154-159. |
n.a. | CG |
| 707 |
A
Wafa, RA Jarjour, A Aljapawe, S ALmedania, T
Liehr, JB Melo, IM Carreira, MAK
Othman, W Al-Achkar.
An acquired stable variant of a dicentric dic(9;20) and complex karyotype in a Syrian childhood B-acute lymphoblastic leukemia case. Mol Cytogenet 2020, 13:29. |
2.009 | TCG |
| 706 |
A Garcia-Angulo, MA
Merlo, R Itiga, ME Rodriguez, S
Portella-Bens, A Al-Rikabi, T
Liehr, L. Rebordinos.
Gene clusters related to metamorphosis in Solea senegalensis are highly conserved. Comp Biochem Physiol D 2020, 35:100706. |
2.674 | EVO |
| 705 |
A Azawi, T Liehr,
M Rincic, M Manferrari.
Molecular cytogenomic characterization of the murine breast cancer cell lines C-127I, EMT6/P and TA3 Hauschka. Int J Mol Sci 2020,
21:4716.
|
5.923 | TCG |
| 704 |
AF
de Figueiredo, MGP Land, GM Ferreira, A
Mencalha, R Binato, RR Capela de Matos, T
Liehr, MLM Silva, E Abdelhay. Clinical and biological correlates of the expression of select Polycomb complex genes in Brazilian children with acute promyelocytic leukaemia. Br J Haematol 2020, 189:e222-e265. |
5.923 | TCG |
| 703 |
K Gadsbøll, OB
Petersen, V Gatinois, H Strange, B Jacobsson,
R Wapner, JR Vermeesch; NIPT-map Study Group
(including T Liehr), I Vogel. Current use of noninvasive prenatal testing in Europe, Australia and the USA: A graphical presentation. Acta Obstet Gynecol Scand 2020; 99:722-730. |
3.636 | CG |
| 702 |
BP Potlapalli, V
Schubert, J Metje-Sprink, T Liehr,
A Houben. Application of Tris-HCl allows the specific labelling of regularly prepared chromosomes by CRISPR-FISH. Cytogenet Genome Res 2020;160:156-165 |
1.636 | M |
| 701 |
V
Spangenberg, M Arakelyan, M Cioffi, T
Liehr, A Al-Rikabi, E Martynova, I
Stepanyan, F Danielyan, E Galoyan, O
Kolomiets. Cytogenetic mechanisms of unisexuality in rock lizards. Scient Rep 2020, 10:8697. |
4.379 | EVO |
| 700 |
M
Volleth, M Zenker, I Joksic, T
Liehr. Long-term culture of EBV-induced human lymphoblastoid cell lines reveals chromosomal instability. J Histochem Cytochem 2020, 68:239-251 |
2.479 | CG M |
| 699 |
RA Pilz,
K Schwefel, A Weise, T Liehr,
P Demmer, A Spuler, S Spiegler, E Gilberg,
CA Hübner, U Felbor, M Rath. First interchromosomal insertion in a patient with cerebral and spinal cavernous malformations. Sci Rep 2020, 10:6306. |
4.379 | CG |
| 698 |
WF
Molina, GWWF Costa, IMC Cunha, LAC
Bertollo, T Ezaz, T Liehr,
MB Cioffi. Molecular cytogenetic analysis in freshwater prawns of the genus Macrobrachium (Crustacea: Decapoda: Palaemonidae). Int J Mol Sci 2020, 21: E2599 |
5.923 | EVO |
| 697 |
FMC
Sassi, T Hatanaka, RLR Moraes, GA Toma, EA
Oliveira, T Liehr, P Rab,
LAC Bertollo, PF Viana, E Feldberg, M
Nirchio, MMF Marinho, JFSE Souza, MB
Cioffi. An insight into the chromosomal evolution of Lebiasinidae (Teleostei, Characiformes). Genes (Basel) 2020, 11: E365 |
4.096 | EVO |
| 696 |
MAK
Othman,
M Đurišić, G Samardzija, D Vujić, N Lakic,
Z Zecevic, F Al-Shaheri, R Aroutiounian,
JB Melo, IM Carreira, B Meyer, T
Liehr. Complex karyotype with cryptic FUS gene rearrangement and deletion of NR3C1 and VPREB1 genes in childhood B-cell acute lymphoblastic leukemia: A case report. Oncol Lett 2020, 19:2957-2962 |
2.967 | TCG |
| 695 |
A Zlotina, A Maslova, O
Pavlova, N Kosyakova, A Al-Rikabi, T
Liehr, A Krasikova. New insights into chromomere organization provided by lampbrush chromosome microdissection and high-throughput sequencing. Frontiers in Genetics 2020, 11:57 |
4.599 | EVO INT |
| 694 |
RT
Silvestre, M
Bravo, F Santiago, L Delmonico, L
Scherrer, U Barros Otero, T Liehr,
G Alves, M Chantre-Justino, MH Ornellas. Hypermethylation in gene promoters are induced by chronic exposure to benzene, toluene, ethylbenzene and xylenes. Pak J Biol Sci 2020, 23:518-525 |
n.a. | TCG |
| 693 |
LA Mendez Rosado, D García,
O Molina, A García, N de León, A
Lantigua-Cruz, T
Liehr. Diagnostico citogenetico molecular en pacientes con trastornos del neurodesarrollo. Arch Argentin Pediat 2020, 118:52-55. |
0.635 | CG |
| 692 |
T
Liehr. PWG: Marker chromosomes. ECA newsletter 2020, 45: 6-7. |
n.a. | sSMC |
| 691 |
IP Ribeiro, IM Carreira,
L Esteves, F Caramelo, T Liehr,
JB Melo. Chromosomal breakpoints in a cohort of head and neck squamous cell carcinoma patients. Genomics 2020, 112: 297-303. |
5.736 | TCG |
| 690 |
J Thielker, A Weise, MAK
Othman, IM Carreria, JB Melo, F von Eggeling, O
Guntinas-Lichius, M Ziegler, T Liehr.
Molecular cytogenetic pilot study on pleomorphic adenoma of salivary gland. Oncol Lett 2020, 19:1125-1130. |
2.967 | TCG |
| 63% of publications of
Institute of Human Genetics Jena in the actual
year |
|||
2019
| Number |
Authors/
Title/ Where Contribution was Published |
Impact
Factor |
Topic |
| 689 |
P Brown, RELISH
Consortium (including T Liehr),
Y Zhou. Large expert-curated database for benchmarking document similarity detection in biomedical literature search. Database 2019, baz085 |
2.593 | M |
| 688 |
GA Toma, RLR de Moraes,
FMC Sassi, LAC Bertollo, EA de Oliveira, P
Rab, A Sember, T Liehr, T
Hatanaka, PF Viana, MMF Marinho, E Feldberg,
MB Cioffi. Cytogenetics of the small-sized fish, Copeina guttata (Characiformes, Lebiasinidae): Novel insights into the karyotype differentiation of the family. PLoS One 2019, 14:e0226746. |
2.740 |
EVO |
| 687 |
A Al-Rikabi, MdB
Cioffi, T Liehr. Chromosome microdissection on semi-archived material. Cytometry A 2019, 95:1285-1288. |
3.124 | M EVO |
| 686 |
A
LLamos-Paneque, MA Recalde-Baez, M
Garzón-Castro, S Montúfar, C Rivas-Iglesias,
E Lamar-Segura, M Román-Naranjo, N Tambaco-
Jijón, P Hernández-Iñiguez, K Mrasek,
T Liehr, R Odales-Ibarra.
Supernumerary marker of chromosome 15 associated with paternal uniparental disomy in a case with Angelman syndrome. J
Mol Genet Med 2019, 13: 1000439
|
n.a. | sSMC |
| 685 |
T Liehr,
A Weise, K Mrasek, M Ziegler, N Padutsch, K
Wilhelm, A Al-Rikabi. Recombinant chromosomes resulting from parental pericentric inversions - Two new cases and a review of the literature. Front Genet 2019, 10:1165 |
3.258 | CG |
| 684 |
T Liehr,
A Al-Rikabi. Mosaicism: Reason for normal phenotypes in carriers of small supernumerary marker chromosomes with known adverse outcome. A Systematic Review. Front Genet 2019, 10:1131 |
3.258 |
sSMC |
| 683 |
E García, I Cross, S
Portela-Bens, ME Rodríguez, A García-Angulo, B
Molina, A Cuadrado, T Liehr, L
Rebordinos. Integrative genetic map of repetitive DNA in the sole Solea senegalensis genome shows a Rex transposon located in a proto-sex chromosome. Sci Rep 2019, 9:17146 |
3.998 |
EVO |
| 682 |
VE Gokhman, MB Cioffi,
C König, M Pollmann, C Gantert, L Krogmann,
JML Steidle, N Kosyakova, T Liehr,
A Al-Rikabi. Microdissection and whole chromosome painting confirm karyotype transformation in cryptic species of the Lariophagus distinguendus (Förster, 1841) complex (Hymenoptera: Pteromalidae). PLoS One 2019, 14:e0225257 |
2.740 |
EVO |
| 681 |
T
Liehr, IM Carreira. PWG: Marker chromosomes. ECA newsletter 2019, 43: 14-15 |
n.a. |
sSMC |
| 680 |
T
Liehr. Report from the European Board of Medical Genetics. ESHG Newsletter 2019, 34: 11-12 |
n.a. | other |
| 679 |
T
Liehr. Non-invasive prenatal testing – safer or simply more profitable? https://atlasofscience.org/non-invasive-prenatal-testing-safer-or-simply-more-profitable/ |
n.a. | PRE M |
| 678 |
ME Rodríguez, B Molina,
MA Merlo, A Arias-Pérez, S Portela-Bens, A
García-Angulo, I Cross, T Liehr,
L Rebordinos. Evolution of the proto sex-chromosome in Solea senegalensis. Int J Mol Sci 2019, 20: 5011 |
4.556 |
EVO |
| 677 |
IP Ribeiro, JM
Rodrigues, A Mascarenhas, V Marques, F
Caramelo, MJ Julião, T Liehr, JB
Melo, IM Carreira. (Cyto)genomic and epigenetic characterization of BICR 10 cell line and three new established primary human head and neck squamous cell carcinoma cultures. Genes Genomics 2019, 41: 1207-1221 |
1.188 | TCG |
| 676 |
A Zlotina, A Maslova, N
Kosyakova, AB Hamid Al-Rikabi, T Liehr,
A Krasikova. Heterochromatic regions in Japanese quail chromosomes: comprehensive molecular-cytogenetic characterization and 3D mapping in interphase nucleus. Chromosome Res 2019, 27: 253-270 |
3.413 | EVO INT |
| 675 |
IY
Iourov, T Liehr, SG Vorsanova,
LA Mendez-Rosado, YB Yurov. The applicability of interphase chromosome-specific multicolor banding (ICS-MCB) for studying neurodevelopmental and neurodegenerative disorders. Res Results Biomed 2019, 5: 4-9. |
n.a. | INT |
| 674 |
G Hovhannisyan, T
Harutyunyan, R Aroutiounian, T Liehr.
DNA copy number variations as markers of mutagenic impact. Int J Mol Sci 2019, 20: 4723 |
4.556 | TCG |
| 673 |
FHS Souza, MF Perez,
LAC Bertollo, EA Oliveira, S Lavoué, C
Gestich, P Ráb, T Ezaz, T Liehr,
PF Viana, E Feldberg, MB Cioffi. Interspecific genetic differences and historical demography in South American arowanas (Osteoglossiformes, Osteoglossidae, Osteoglossum). Genes 2019, 10: 693 |
3.759 | EVO |
| 672 |
MdB Cioffi, P Ráb, T
Ezaz, LAC Bertollo, S Lavoué, EA de Oliveira,
A Sember, WF Molina, FHS de Souza, Z
Majtánová, T Liehr, ABH
Al-Rikabi, CF Yano, P Viana, E Feldberg, P
Unmack, T Hatanaka, A Tanomtong, MF Perez. Deciphering the evolutionary history of Arowana fishes (Teleostei, Osteoglossiformes, Osteoglossidae): Insight from comparative cytogenomics. Int J Mol Sci 2019, 20: 4296 |
4.556 | EVO |
| 671 |
GWWF da Costa, MdB
Cioffi, T Liehr, E Feldberg,
LAC Bertollo, WF Molina. Extensive chromosomal reorganization in Apistogramma fishes (Cichlidae, Cichlinae) fits the complex evolutionary diversification of the genus. Int J Mol Sci 2019, 20: 4077 |
4.556 | EVO |
| 670 |
RLR de Moraes, A
Sember, LAC Bertollo, EA De Oliveira, P Rab, T
Hatanaka, MMF Marinho, T Liehr,
ABH Al-Rikabi, E Feldberg, PF Viana, M De
Bello Cioffi. Comparative cytogenetics and neo-Y formation in small-sized fish species of the genus Pyrrhulina (Characiformes, Lebiasinidae). Front Genet 2019, 10: 678 |
3.258 | EVO |
| 696 |
H
Merhni, M Zerkaoui, A Natiq, A Sbiti, T
Liehr, A Sefiani. Constitutional partial proximal trisomy 14q11.2 to 14q21: two new Moroccan cases and review of the literature. OBM Genetics 2019, 3: 1903085 |
n.a. | CG |
| 695 |
D Xu, A Sember, Q Zhu,
EA de Oliveira, T Liehr, ABH
Al-Rikabi, Z Xiao, H Song, M Cioffi. Deciphering the origin and evolution of a unique X1X2Y system in two closely related Oplegnathus species (Oplegnathidae, Centrarchiformes). Int J Mol Sci 2019, 20: 3570 |
4.556 | EVO |
| 694 |
S Ditcharoen, LAC
Bertollo, P Rab, E Hnátková, WF Molina, T
Liehr, A Tanomtong, C
Triantaphyllidis, C Ozouf-Costaz, S Tongnunui,
P Pengseng, W Supiwong, R Aroutiounian, M
Cioffi. Genomic organization of repetitive DNA elements and extensive karyotype diversity of Silurid catfishes (Teleostei: Siluriformes): A comparative cytogenetic approach. Int J Mol Sci 2019, 20: 3545 |
4.556 | EVO |
| 693 |
T Liehr,
IM Carreira, Z Balogh, ED Garrido, I
Verdorfer, DA Coviello, L Florentin, H
Scheffer, M Rincic, HE Williams. Regarding the rights and duties of Clinical Laboratory Geneticists in genetic healthcare systems; results of a survey in over 50 countries. Eur J Hum Genet 2019, 27: 1168-1174 |
3.657 | other |
| 692 |
R De Matos, D Ney
Garcia, M Othman, G Ferreira, J Melo, I
Carreira, C Meyer, R Marschalek, E Costa, M
Land, T Liehr, R Ribeiro, M
Macedo Silva. A new complex karyotype involving a KMT2A-r variant three-way translocation, in a rare clinical presentation of a pediatric patient with acute myeloid leukemia. Cytogenet Genome Res 2019, 157: 213-219 |
1.114 | TCG |
| 691 |
A Garcia-Angulo, MA
Merlo, ME Rodriguez, S Portela-Bens, T
Liehr, L Rebordinos. Genome and phylogenetic analysis of genes involved in the immune system of Solea senegalensis - potential applications in aquaculture. Front Genet 2019, 10: 529 |
3.258 | EVO |
| 690 |
T
Liehr, LB Liehr. An update on small supernumerary marker chromosomes (sSMC). Res Results Biomed 2019, 5: 4-6 |
n.a. | sSMC |
| 689 |
W
Al-Achkar, M As’sad, T Liehr, A
Ikhtiar, A Wafa. A de novo childhood case of T-cell lymphoblastic leukemia with high hyperdiploid karyotype carrying an unreported balanced translocation t(X;5)(q26;q31.3~32) in a male patient. OBM Genetics 2019, 3:1902081 |
n.a. | CG |
| 688 |
FMC Sassi, EA de
Oliveira, LAC Bertollo, M Nirchio, T Hatanaka,
MMF Marinho, O Moreira-Filho, R Aroutiounian,
T Liehr, ABH Al-Rikabi, MB
Cioffi. Chromosomal evolution and evolutionary relationships of Lebiasina species (Characiformes, Lebiasinidae). Int J Mol Sci 2019, 20: E2944 |
4.556 | EVO |
| 687 |
IA Pessôa, CK Amorim,
WAS Ferreira, F Sagica, JR Brito, M Othman, B
Meyer, T Liehr, EHC de
Oliveira. Detection and correlation of single and concomitant TP53, PTEN and CDKN2A alterations in gliomas. Int J Mol Sci 2019, 20: 2658 |
4.556 | TCG |
| 686 |
T Harutyunyan, G
Hovhannisyan, A Sargsyan, B Grigoryan, AH
Al-Rikabi, A Weise, T Liehr, R
Aroutiounian. Analysis of copy number variations induced by ultrashort electron beam radiation in human leukocytes in vitro. Mol Cytogenet 2019, 12: 18 |
1.233 | TCG |
| 685 |
M Moysés-Oliveira, A
Di-Battista, M Zamariolli, VA Meloni, S
Bragagnolo, DM Christofolini, CE Steiner, N
Kosyakova, T Liehr, A Reymond,
MI Melaragno. Breakpoint mapping at nucleotide resolution in X-autosome balanced translocations associated with clinical phenotypes. Eur J Hum Genet 2019, 27: 760-771 |
3.657 | CG |
| 684 |
N
Padutsch, T Liehr. First report on a 20qh+ heteromorphism characterized by molecular cytogenetics as amplification of D20Z1 sequences. Res Results Biomed 2019, 5: 22-24 |
n.a. | HET |
| 683 |
R
Steinacker, T Liehr, N
Kosyakova, M Rincic, SS Hussein Azawi. Molecular cytogenetic characterization of two murine cancer cell lines derived from salivary gland. Biol Commun 2019, 63: 243-255 |
n.a. | TCG |
| 682 |
EA de Oliveira, LAC
Bertollo, P Rab, T Ezaz, CF Yano, T Hatanaka,
OI Jegede, A Tanomtong, T Liehr,
A Sember, SR Maruyama, E Feldberg, PF Viana. Cytogenetics, genomics and biodiversity of the South American and African Arapaimidae fish family (Teleostei, Osteoglossiformes). PLoS One 2019, 14: e0214225 |
2.740 | EVO |
| 681 |
W Supiwong, K Pinthong,
K Seetapan, P Sanjundaeng, LAC Bertollo, E
Aguiar de Oliveira, CF Yano, T Liehr,
S Phimphan, A Tanomtong, M de Bello Cioffi. Karyotype diversity and evolutionary trends in the Asian swamp eel Monopterus albus (Synbranchiformes, Synbranchidae). A case of chromosomal speciation? BMC Evolutionary Biology 2019, 19: 73 |
3.058 | EVO |
| 680 |
JP Chaudhuri, S
Karamanov, L Scott, T Liehr, JU
Walther. Leukocyte nucleus reveals a linear order of chromosomes separated in two parental genomes that favors the process of gene activation. J Histochem Cytochem 2019, 67: 151-158 |
2.187 | INT |
| 679 |
NE Kurtas, L Xumerle, U
Giussani, A Pansa, L Cardarelli, V Bertini, A
Valetto, T Liehr, C Bonaglia, E
Errichiello, M Delledonne, O Zuffardi. Insertional translocation involving an additional non-chromothriptic chromosome in constitutional chromothripsis: rule or exception? Mol Genet Genomic Med 2019, 7: e496 |
1.995 | CG INT |
| 678 |
MLRDR Borges, EM
Soares-Ventura, T Liehr, TJ
Marques-Salles. Minimally differentiated acute myeloid leukemia wth ring/marker derived chromosome 7 in a child with Down syndrome. Hematol Transfus Cell Ther 2019, 41: 84-88 |
n.a. | TCG |
| 677 |
A
Weise, K Mrasek, C Pentzold, T Liehr.
Chromosomes in the DNA era: Perspectives in diagnostics and research. Med Genetik 2019, 31: 8-19 |
0.964 | M |
| 676 |
T Liehr.
From human cytogenetics to human chromosomics. Int J Mol Sci 2019, 20: 826 |
4.556 | M |
| 675 |
FF Barby, LAC Bertollo,
EA de Oliveira, CF Yano, T Hatanaka, P Ráb, A
Sember, T Ezaz, R Ferreira Artoni, T
Liehr, ABH Al-Rikabi, V Trifonov,
EHC de Oliveira, WF Molina, OI Jegede, A
Tanomtong, M de Bello Cioffi. Emerging patterns of genome organization in Notopteridae species (Teleostei, Osteoglossiformes) as revealed by Zoo-FISH and Comparative Genomic Hybridization (CGH). Scient Rep 2019, 9: 1112 |
3.998 | EVO |
| 674 |
A Krumbholz, J Roempke,
T Liehr, M Groth, A Meerbach, M
Schacke, G Maschkowitz, H Fickenscher, W
Klapper, A Sauerbrei, P Wutzler, R Zell. Macaca arctoides gammaherpesvirus 1 (strain herpesvirus Macaca arctoides): virus sequence, phylogeny and characterisation of virus-transformed macaque and rabbit cell lines. Medic Microbiol Immunol 2019, 208: 109-129 |
1.961 | TCG |
| 673 |
NE Kurtas, L Xumerle,
L Leonardelli, M Delledonne, A Brusco, K
Chrzanowska, A Schinzel, D Larizza, S
Guerneri, F Natacci, MC Bonaglia, P Reho, E
Manolakos, T Mattina, F Soli, A Provenzano, AH
Al-Rikabi, E Errichiello, L Nazaryan-Petersen,
S Giglio, N Tommerup, T Liehr,
O Zuffardi. Small supernumerary marker chromosomes: a legacy of trisomy rescue. Hum Mutat 2019, 40: 193-200 |
4.124 | sSMC |
| 80% of publications of Institute of Human Genetics Jena in the actual year | |||
2018
| Number |
Authors/
Title/ Where Contribution was Published |
Impact
Factor |
Topic |
| 672 |
T
Liehr, IM Carreira. PWG: Marker chromosomes. ECA newsletter 2018, 41: 17 |
n.a. |
sSMC |
| 671 |
Deutsche Gesellschaft für Humangenetik e.V.
(GfH), Berufsverband Deutscher Humangenetiker
e.V (T Liehr and A Weise
included in commission). S2k-Leitlinie Humangenetische Diagnostik und Genetische Beratung. Med Genetik 2018, 30: 469-522 |
0.104 | other |
| 670 |
L Castiglia, R Husain,
I Marquardt, C Fink, T Liehr, D
Serino, Melia, E Coci. 7q11.23 micro-duplication syndrome: neuro-physiological and neuro-radiological insights into a rare chromosomal disorder. J Intellect Disab Res 2018, 62: 359-370 |
1.941 | CG |
| 669 |
MH Ornellas, MC Maioli, S
Lucena, E Bastos, TS Chaves, K Vieira de
Melo, M Carvalho, T Liehr.
Complex karyotype including ring 11 chromosome
in woman with acute myeloid leukemia. São Paulo Medical Journal 2018, 136: 361-367 |
1.423 | TCG |
| 668 |
V Čulić, R Lasan-Trcić,
T Liehr, IN Lebedev, M Pivić, J
Pavelic, R Vulić. A familial small supernumerary marker chromosome 15 associated with cryptic mosaicism with two different additional marker chromosomes derived de novo from chromosome 9: Detailed case study and implications for recurrent pregnancy loss. Cytogenet Genome Res 2018, 156: 179-184 |
1.423 | sSMC |
| 667 |
T Araújo, A Khayat, L
Quintana, D Calcagno, R Mourão, A Modesto, J
Paiva, A Lima, F Moreira, E Oliveira, M Souza,
M Othman, T Liehr, E Abdelhay,
R Gomes, S Santos, P Assumpção. Piwi like RNA-mediated gene silencing 1 gene as a possible major player in gastric cancer. World J Gastroenterol 2018, 24: 5338-5350 |
3.411 | TCG |
| 666 |
T
Liehr. Importance of databases for human genetic diagnostics. J Genet Genom 2018, 2: e105 |
4.650 | CG |
| 665 |
T
Liehr, I Schreyer, K Mrasek, A
Weise. Neue Entwicklungen in der humangenetischen pränatalen Diagnostik. Ärzteblatt Thüringen 2018, 12: 689-691 |
n.a. | CG PRE |
| 664 |
T Liehr,
AB Hamid Al-Rikabi. Impaired spermatogenesis due to small supernumerary marker chromosomes: The reason for infertility is only reliably ascertainable by cytogenetics. Sex Dev 2018, 12: 281-287 |
2.250 | sSMC |
| 663 |
I Cross, S
Portela-Bens, A García-Angulo, MA Merlo, ME
Rodríguez, T Liehr, L
Rebordinos. A preliminary integrated genetic map distinguishes every chromosome pair and locates essential genes related to abiotic adaptation of Crassostrea angulata/gigas. BMC Genet 2018, 19: 104 |
2.547 | EVO |
| 662 |
A García-Angulo, MA
Merlo, S Portela-Bens, ME Rodríguez, E García,
A Al-Rikabi, T Liehr, L
Rebordinos. Evidence for a Robertsonian fusion in Solea senegalensis (Kaup, 1858) revealed by zoo-FISH and comparative genome analysis. BMC Genomics 2018, 19: 818 |
3.501 | EVO |
| 661 |
A Grigoryan, N Guidi, K
Senger, T Liehr, K Soller, G
Marka, A Vollmer, Y Markaki, H Leonhardt, C
Buske, D Lipka, C Plass, Y Zheng, MA Mulaw, H
Geiger, MC Florian. LaminA/C regulates epigenetic and chromatin architecture changes upon aging of hematopoietic stem cells. Genome Biology 2018, 19: 189 |
14.028 | INT TCG |
| 660 |
A
Arias-Pérez, D Ramírez-Torres, ME Rodríguez, S
Portela-Bens, E García-Suarez, MA Merlo, A
García-Angulo, I Cross, T Liehr,
L Rebordinos. In silico detection and FISH location of miRNAs in Solea senegalensis chromosomes using BACs. OBM Genet 2018, 2: 1804044 |
n.a. | EVO |
| 659 |
F Sheth, T Liehr,
V Shah, H Sheth, S Tewari, D Solanki, S
Trivedi, J Sheth. A child with intellectual disability and dysmorphism due to complex ring chromosome 6: Identification of molecular mechanism with review of literature. Ital J Pediatr 2018, 44: 114 |
1.726 | CG |
| 658 |
MAK
Othman, B Grygalewicz, A Kołkowska-Leśniak, JB
Melo, IM Carreira, T Liehr. Cryptic NUP214-ABL1 fusion with complex karyotype, episomes and intra-tumor genetic heterogeneity in a T-cell lymphoblastic lymphoma. J Cancer Metastasis Treat 2018, 4: 50 |
n.a. | TCG |
| 657 |
H
Rhode, T Liehr, N Kosyakova, M
Rinčic, SSH Azawi. Molecular cytogenetic characterization of two murine colorectal cancer cell lines. OBM Genetics 2018, 2: 1803037 |
n.a. | TCG |
| 656 |
A Wafa, S ALmedania, A
Aljapawe, T Liehr, SE
Soulaiman, R Mouna, MAK Othman, W ALachkar. A new adult AML case with an extremely complex karyotype, remission and relapse combined with high hyperdiploidy of a normal chromosome set in secondary AML. BMC Hematology 2018, 18: 21 |
n.a. | TCG |
| 655 |
P Saenjundaeng, M de
Bello Cioffi, E Aguiar de Oliveira, A
Tanomtong, W Supiwong, S Phimphan, MJ
Collares-Pereira, A Sember, LAC Bertollo, T
Liehr, CF Yano, T Hatanaka, P Rab.
Chromosomes of Asian cyprinid fishes: Cytogenetic analysis of two representatives of small paleotetraploid tribe Probarbini. Mol Cytogenet 2018, 11:51 |
1.331 | EVO |
| 654 |
F
Sheth, T Liehr, K Mrasek, J
Andrieux, S Tewari, N Lubna, J Sheth. sSMC characterization in a male with Turner syndrome stigmata. OBM Genetics 2018, 2: 1803033 |
n.a. | sSMC |
| 653 |
T
Hatanaka, EA de Oliveira, P Ráb, CF Yano, LAC
Bertollo, T Ezaz, OOI Jegede, T Liehr,
VF Olaleye, M de Bello Cioffi. First chromosomal analysis in Gymnarchus niloticus (Gymnarchidae, Osteoglossiformes): Insights into the karyotype evolution of this ancient fish order. Biol J Linn Soc 2018, 125: 83-92 |
2.203 | EVO |
| 652 |
PG Maass, A Weise, K
Rittscher, J Lichtenwald, AR Barutcu, T
Liehr, A Aydin, Y
Wefeld‐Neuenfeld, L Pölsler, S Tinschert, JL
Rinn, FC Luft, S Bähring. Reorganization of inter‐chromosomal interactions in the 2q37‐deletion syndrome. EMBO J 2018, 37: e96257 |
11.227 | INT CG |
| 651 |
FF Barby, P Ráb, S
Lavoué, T Ezaz, LAC Bertollo, A Kilian, SR
Maruyama, EA de Oliveira, RF Artoni, MH
Santos, OI Jegede, T Hatanaka, A Tanomtong, T
Liehr, M de Bello Cioffi. From chromosomes to genome: Insights into the evolutionary relationships and biogeography of old world knifefishes (Notopteridae; Osteoglossiformes). Genes 2018, 9: 306 |
3.331 | EVO |
| 650 |
S Akbaroghli, SH
Tonekaboni, R Kariminejad, T Liehr,
EG Coci. De novo interstitial 2.33 Mb deletion in 8q24.3: New insights on a very rare partial monosomy syndrome. Clin Dysmorphol 2018, 27: 97-100 |
0.760 | CG |
| 649 |
PK Priya, VV Mishra ,
T Liehr, M Ziegler, S Tiwari, A
Patel, SS Chettiar, H Patel. Characterization of a complex chromosomal rearrangement involving chromosomes 1, 3 and 4 in a slightly affected male partner with unsuccessful obstetric history. J Assist Reprod Genet 2018, 35: 721-725 |
2.820 | CG |
| 648 |
T
Liehr, ABH Al-Rikabi, N Kosyakova,
M Ziegler. User-friendly approach to gain isolation of interphase cells for fluorescence in situ hybridization. OBM Genetics 2018, 2: 021 |
n.a. | M |
| 647 |
MB Cioffi, A Sánchez,
JA Marchal, N Kosyakova, T Liehr,
V Trifonov, LAC Bertollo. Correction to: Whole chromosome painting reveals independent origin of sex chromosomes in closely related forms of a fish species. Genetica 2018, 146: 123 |
1.229 | EVO |
| 646 |
IP Ribeiro, JM
Rodrigues, A Mascarenhas, N Kosyakova, F
Caramelo, T Liehr, JB Melo, IM
Carreira. Cytogenetic, genomic, and epigenetic characterization of the HSC-3 tongue cell line with lymph node metastasis. J Oral Sci 2018, 60: 70-81 |
1.104 | TCG |
| 645 |
E Aguiar de Oliveira, A
Sember, LAC Bertollo, CF Yano, T Ezaz, O
Moreira-Filho, T Hatanaka, V Trifonov, T
Liehr, AB Hamid Al-Rikabi, P Ráb,
H Pains, M de Bello Cioffi. Tracking the evolutionary pathway of sex chromosomes among fishes: characterizing the unique XX/XY1Y2 system in Hoplias malabaricus (Teleostei, Characiformes). Chromosoma 2018, 127: 115-128 |
3.530 | EVO |
| 644 |
F Moassass, A Wafa, T
Liehr, A Al-Ablog, W Al-Achkar. Down syndrome associated childhood myeloid leukemia with yet unreported acquired chromosomal abnormalities and a new potential adverse marker: dup(1)(q25q44). Mol Cytogenet 2018, 11: 22 |
1.331 | TCG |
| 643 |
T Liehr,
I Schreyer, A Kuechler, E Manolakos, S Singer,
A Dufke, K Wilhelm, T Jančušková, R Čmejla,
MAK Othman, AH Al-Rikabi, K Mrasek, M Ziegler,
S Kankel, K Kreskowski, A Weise. Parental origin of deletions and duplications – about the necessity to check for cryptic inversions. Mol Cytogenet 2018, 11: 20 |
1.331 | CG |
| 642 |
I Papoulidis, A Vetro,
V Paspaliaris, M Ziegler, K Kreskowski, G
Daskalakis, V Papadopoulos, T Dagklis, T
Liehr, L Thomaidis, E Manolakos. A girl with 10 Mb distal Xp deletion arising from maternal pericentric inversion: Clinical data and molecular characterization. Curr Genomics 2018, 19: 240-246 |
2.174 | CG |
| 641 |
W Sangpakdee, A
Tanomtong, A Chaveerach, K Pinthong, V
Trifonov, K Loth, C Hensel, T Liehr,
A Weise, X Fan. Molecular cytogenetic analysis of one African and five Asian macaque species reveals identical karyotypes as in mandrill. Curr Genomics 2018, 19: 207-215 |
2.174 | EVO |
| 640 |
ABH Al-Rikabi, S
Pekova, X Fan, T Jančušková, T Liehr.
Small supernumerary marker chromosome may provide information on dosage-insensitive pericentric regions in human. Curr Genomics 2018, 19: 192-199 |
2.174 | sSMC |
| 639 |
T Liehr,
N Acquarola, K Pyle, S St-Pierre, M Rinholm, O
Bar, K Wilhelm, I Schreyer. Next generation phenotyping in Emanuel and Pallister Killian Syndrome using computer-aided facial dysmorphology analysis of 2D photos. Clin Genet 2018, 93: 378-381 |
4.104 | sSMC |
| 638 |
M Moysés-Oliveira, G
Giannuzzi, RJ Fish, JA Rosenfeld, F Petit, M
de Fatima Soares, L Domenici Kulikowski, A Di
Battista, M Zamariolli, F Xia, T Liehr,
N Kosyakova, G Carvalheira, M Parker, EG
Seaby, S Ennis, RD Gilbert, T Hagelstrom, DG
Basel, J Andrieux, T Stumpp, F Antunes, GJ
Pereira, M Neerman-Arbez, VA Meloni, M
Drummond-Borg, MI Melaragno, A Reymond. Inactivation of AMMECR1 is associated with growth, bone and heart alterations. Hum Mut 2018, 39: 281-291 |
4.453 | CG |
| 637 |
RR Capela de Matos, MAK
Othman, GM Ferreira, ES Costa, JB Melo, IM
Carreira, MT de Souza, BA Lopes, M
Emerenciano, MGP Land, T Liehr,
RC Ribeiro, MLM Silva. Molecular approaches identify a cryptic MECOM rearrangement in a child with a rapidly progressive myeloid neoplasm. Cancer Genet 2018, 221: 25-30 |
2.183 | TCG |
| 636 |
A
Wafa, B Ali, A Aljapawe, T Liehr,
S ALmedani, W Al Achkar. Unreported combination of rearrangements in a childhood B-cell acute lymphoblastic leukemia case: Coexistence of translocation t(8;14) and monoallelic loss of tumor suppressor gene TP53. Gene Reports 2018, 10: 66-70 |
n.a. | TCG |
| 635 |
MT De Souza, G
Vera-Lozada, M Othman, TJ Marques-Salles, LW
Pinto, MM da Rocha, S Rouxinol, T Liehr,
RC Ribeiro, R Hassan, MLM Silva. Molecular and cytogenetic studies in a child with Burkitt lymphoma and ataxia-telangiectasia syndrome harboring MYC overexpression and partial trisomy 8. Ann Lab Med 2018, 38: 63-66 |
2.635 | TCG |
| 70% of publications of Institute of Human Genetics Jena in the actual year | |||
2017
| Number |
Authors/
Title/ Where Contribution was Published |
Impact
Factor |
Topic |
| 634 |
T
Liehr. What about the real costs of next generation sequencing (NGS) in human genetic diagnostics? http://atlasofscience.org/what-about-the-real-costs-of-next-generation-sequencing-ngs-in-human-genetic-diagnostics/ |
n.a. |
M |
| 633 |
T
Liehr, IM Carreira. PWG: Marker chromosomes. ECA newsletter 2017, 40: 9 |
n.a. | sSMC |
| 632 |
T
Liehr. What about noninvasive prenatal testing (NIPT) from ‘cell-free fetal DNA’ (cffDNA)? http://atlasofscience.org/what-about-noninvasive-prenatal-testing-nipt-from-cell-free-fetal-dna-cffdna/ |
n.a. | PRE M |
| 631 |
T
Liehr. Human cells can count their chromosomes – but how do they do? http://atlasofscience.org/human-cells-can-count-their-chromosomes-but-how-do-they-do/#more-19201 |
n.a. | INT |
| 630 |
T
Liehr, IM Carreira. PWG: Marker chromosomes. ECA newsletter 2017, 39: 27 |
n.a. | sSMC |
| 629 |
T
Liehr. How to characterize best the genetic content of small supernumerary marker chromosomes. http://atlasofscience.org/how-to-characterize-best-the-genetic-content-of-small-supernumerary-marker-chromosomes/ |
n.a. | sSMC |
| 628 |
T
Liehr. Chronic lymphocytic leukemia (CLL) diagnostics better to do in cultivated than native cells. http://atlasofscience.org/chronic-lymphocytic-leukemia-cll-diagnostics-better-to-do-in-cultivated-than-native-cells/ |
n.a. | TCG |
| 627 |
A
Wafa, S ALmedani, T Liehr, F
Moassass, W Al-Achkar. Successful management of three pregnancies under Imatinib treatment in a chronic myeloid leukemia patient: a case report and review of the literature. J Genetics Genomes 2017, 1: 111 |
n.a. | TCG |
| 626 |
IR
Tkach, NL Huleyuk, DV Zastavna, A Weise, T
Liehr, E Ciszkowicz, M Tyrka. Chromosomal aberrations in spontaneously aborted products of conception from Ukraine. Biopolymers Cell 2017, 33: 424-433 |
n.a. | PRE CG |
| 625 |
T Liehr.
Expert knowledge on human genetic counselling and chromosomics are necessary for sound genetic laboratory diagnostics. Mol Exp Biol Med 2017, 1: 1-3 |
n.a. | M |
| 624 |
A
Kurtovic-Kozaric, L Mehinovic, H Komic, M
Kozaric, A Husic-Selimovic, M Ziegler, T
Liehr. Human cytogenetics case report: Yet unreported heteromorphic variant in chromosome 17. J Genetics Genomes 2017; 1: 101 |
4.066 | HET |
| 623 |
T
Liehr, K Mrasek, E Klein, A Weise.
Modern high throughput approaches are not meant to replace ‘old fashioned’ but robust techniques. J Genetics Genomes 2017, 1 :e101 |
4.066 | M |
| 622 |
H
Sheth, S Tewari, K Shah, T Liehr,
J Trivedi, M Pandya, JJ Sheth, F Sheth. Prenatal detection of cryptic genomic rearrangement: role of detailed family history, pedigree analysis and advanced genomic technologies. Int J Preg Child Birth 2017, 3: 00071 |
n.a. | CG |
| 621 |
DR Ney Garcia, MT de
Souza, AF de Figueiredo, MGP Land, MAK Othman,
K Rittscher, E Abdelhay, RR Capela de Matos, C
Meyer, R Marschalek, T Liehr,
RC Ribeiro, MLM Silva. Molecular characterization of KMT2A-fusion partner genes in 13 cases of pediatric leukemia with a complex or cryptic karyotype. Hem Oncol 2017, 35: 760-768 |
3.193 | TCG |
| 620 |
Z Papadopoulou, I
Papoulidis, S Sifaki, G Markopoulos, A Vetro,
A-M Vlaikou, M Ziegler, T Liehr,
L Thomaidis, O Zuffardi, M Syrrou, K George, E
Manolakos. Partial monosomy 8p and trisomy 16q in two children with developmental delay detected with aCGH. Mol Med Rep 2017, 16: 8808-8818. |
1.922 | CG |
| 619 |
PC Carvalho, E Aguiar
de Oliveira, LAC Bertollo, CF Yano, C
Oliveira, E Decru, OI Jegede, T Hatanaka, T
Liehr, ABH Al-Rikabi, M de Bello
Cioffi. Insights into relationship between African and Neotropical fish groups: First chromosomal analysis in Hepsetidae (Actinopterygii, Characiformes). Frontiers in Genetics, section Evolutionary and Population Genetics 2017, 8: 203 |
4.151 | EVO |
| 618 |
T Liehr,
O Buleu, T Karamysheva, A Bugrov, N Rubtsov. New insights into Phasmatodea chromosomes. Genes (Basel) 2017, 8: E327 |
3.191 | EVO |
| 617 |
K Guja, T Liehr,
M Rincic, N Kosyakova, SS Hussein Azawi. Molecular cytogenetic characterization identified the murine B-Cell lymphoma cell line A-20 as a model for sporadic Burkitt's lymphoma. J Histochem Cytochem 2017, 65: 669-677 |
2.816 | TCG |
| 616 |
T
Liehr. The first internet page on chromosomal heteromorphisms (HMs). ECA newsletter 2017, 40: 32-33. |
n.a. | HET |
| 615 |
TV Karamysheva, AA
Torgasheva, YR Yefremov, AG Bogomolov, T
Liehr, PM Borodin, NB Rubtsov. Spatial organization of fibroblast and spermatocyte nuclei with different B chromosome content in Korean field mouse Apodemus peninsulae (Rodentia, Muridae). Genome 2017, 60: 815-824 |
1.892 | EVO |
| 614 |
J Karimzad Hagh, T
Liehr, H Ghaedi, MM Mossalaeie, S
Alimohammadi , F Inanloo Hajiloo , Z Moeini ,
S Sarabi , D Zare-Abdollahi. Prenatal diagnosis of mosaic tetrasomy 18p in a case without sonographic abnormalities. Int J Mol Cell Med (IJMCM) 2017, 6: 61-65 |
n.a. | sSMC |
| 613 |
M Donat, A Louis, K
Kreskowski, M Ziegler, A Weise, I Schreyer, T
Liehr. X-autosome and X-Y translocations in female carriers: X-chromosome inactivation easily detectable by 5-ethynyl-2-deoxyuridine (EdU). Balk J Med Genet 2017, 20: 87-90 |
0.306 | M |
| 612 |
DC de Souza, AF de
Figueiredo, DR Ney Garcia, ES da Costa, MAK
Othman, T Liehr, E Abdelhay,
MLM Silva, T de Souza Fernandez. A unique set of complex chromosomal abnormalities in an infant with myeloid leukemia associated with Down syndrome. Mol Cytogenet 2017, 10: 35 |
1.167 | TCG |
| 611 |
R Capela de Matos, D
Ney Garcia, E Batista, M Othman, M de Souza, E
Carboni, G Ferreira, T Liehr, R
Ribeiro, MLM Silva. GAS6 oncogene and reverse MLLT3-KMT2A duplications in an infant with acute myeloid leukemia and a novel complex hyperdiploid karyotype: detailed high-resolution molecular cytogenetic studies. Cytogenet Genome Res 2017, 152: 33-37 |
1.587 | TCG |
| 610 |
LA Mendez-Rosado, A
Lantigua, J Galarza, ABH Al-Rikabi, M Ziegler,
T Liehr. Unusual de novo partial trisomy 17p12p11.2 due to unbalanced insertion into 5p13.1 in a severely affected boy. J Pediatr Genet 2017, 6: 165-168 |
n.a. | CG |
| 609 |
EG Coci, A Auhuber, A
Langenbach, K Mrasek, J Riedel, A Leenen, T
Lücke, T Liehr. Novel unbalanced translocations affecting the long arms of chromosome 10 and 22 causes complex syndromes with very severe neuro-developmental delay, speech impairment, autistic behavior and epilepsy. Cytogenet Genome Res 2017, 151: 171-178 |
1.587 | CG |
| 608 |
T
Liehr. Thorough discussion of cancer research – thoughts against the main stream. Europ J Hum Genet 2017, 25: 902-903 |
3.636 | TCG |
| 607 |
A
Wafa, S Almedani, T Liehr, M
Ziegler, A Aljapawe, W Al Achkar. Complex karyotype involving six chromosomes, with one dicentric and three yet unreported acquired chromosomal aberrations in a case of splenic marginal zone lymphoma. Gene Rep 2017, 8: 79-83 |
n.a. | TCG |
| 606 |
T Liehr,
A Weise, I Schreyer. Humangenetische Diagnostik – muss es immer NGS sein? BIOspektrum 2017, 03/17: 350-351 |
n.a. | M |
| 605 |
MA Merlo, R Iziga, S
Portela, I Cross, N Kosyakova, T Liehr,
M Manchado, L Rebordinos. Analysis of the histone cluster in Senegalese sole (Solea senegalensis): evidence for a divergent evolution of two canonical histone clusters. Genome 2017, 60: 441-453 |
1.892 | EVO |
| 604 |
W
Al-Achkar, F Moassass, R Aroutiounian, T
Harutyunyan, T Liehr, A Wafa. Effect of Glutathione S-transferase mu 1 (GSTM1) gene polymorphism on chronic myeloid leukemia risk and Imatinib treatment response. Metagene 2017, 12: 113-117 |
n.a. | TCG |
| 603 |
CF Yano, LA Bertollo, L
Rebordinos, MA Merlo, T Liehr,
S Portela-Bens, MB Cioffi. Evolutionary dynamics of rDNAs and U2 small nuclear DNAs in Triportheus (Characiformes, Triportheidae): High variability and particular syntenic organization. Zebrafish 2017, 14: 146-154 |
1.733 | EVO |
| 602 |
T Liehr,
IM Carreira, D Aktas, E Bakker, M Rodríguez de
Alba, DA Coviello, L Florentin, H Scheffer, M
Rincic; the Clinical Laboratory Geneticists
Professional Branch Board, European Board of
Medical Genetics, Vienna, Austria. European registration process for Clinical Laboratory Geneticists in genetic healthcare. Europ J Hum Genet 2017, 25: 515-519 |
3.636 | other |
| 601 |
A Wafa, M As’sad, T
Liehr, A Aljapawe, W Al-Achkar. Childhood pre-B-acute lymphoblastic leukemia with translocation t(1;19)(q21.1;p13.3) and two additional chromosomal aberrations involving chromosomes 1, 6 and 13. J Med Case Rep 2017, 11: 94 |
n.a. | TCG |
| 600 |
S Portela-Bens, MA
Merlo, ME Rodríguez, I Cross, M Manchado, N
Kosyakova, T Liehr, L
Rebordinos. Integrated gene mapping and synteny studies give insights into the evolution of a sex proto-chromosome in Solea senegalensis. Chromosoma 2017; 126: 261-277 |
4.021 | EVO |
| 599 |
M
Volleth, N Truong Son, Y Wu, Y Li, W Yu, L-K
Lin, S Arai, V Trifonov, T Liehr,
M Harada. Comparative chromosomal studies in Rhinolophus formosae and R. luctus from China and Vietnam: elevation of R. l. lanosus to species rank. Acta Chiropt 2017, 19: 41-50 |
1.097 | EVO |
| 598 |
T Liehr,
A Lauten, U Schneider, E Schleussner, A Weise.
Noninvasive prenatal testing (NIPT) – when is it advantageous to apply? Biomed Hub 2017, 2: 458432 |
n.a. | M PRE |
| 597 |
T
Thooptianrat, A Chaveerach, R Sudmoon, T
Tanee, T Liehr, N Babayan. Screening of phytochemicals and toxicity of medicinal plants, Dillenia species, reveals potential natural product resources. J Food Biochem 2017, e12363 |
1.552 | EVO |
| 596 |
ML Borges, RR Capela
de Matos, BD Amaral, EM Soares-Ventura, EP
Leite, MO Silva, MT Cornélio, ML Silva, T
Liehr, T Marques-Salles. Molecular cytogenetic approach to characterize novel and cryptic chromosome abnormalities in childhood myeloid malignances of Fanconi anemia. J Ped Hematol Oncol 2017, 39: e85-e91 |
1.060 | TCG |
| 595 |
T Liehr.
“Classical cytogenetics” is not equal to “banding cytogenetics”. Mol Cytogenet 2017, 10: 3 |
1.167 | M |
| 594 |
R Hochstenbach, M Poot,
T Liehr. Mechanisms of origin and clinical effects of multiple small supernumerary marker chromosomes, each derived from a different chromosome. OBM Genetics 2017, 1: 002 |
n.a. | sSMC |
| 593 |
CF Yano, LAC Bertollo,
T Ezaz, V Trifonov, A Sember, T Liehr,
MB Cioffi. Highly conserved Z and molecularly diverged W chromosomes in the fish genus Triportheus (Characiformes, Triportheidae). Heredity 2017, 118: 276-283 |
3.872 | EVO |
| 592 |
M Fischer, N Kosyakova,
T Liehr, P Dobrowolski. Large deletion on the Y-chromosome long arm (Yq) of C57BL/6JBomTac inbred mice. Mamm Genome 2017, 28: 31-37 |
2.687 | EVO |
| 591 |
F Santiago, S Lima, T
Pinheiro, RT Silvestre, UB Otero, MM Tabalipa,
N Kosyakova, MH Ornellas, T Liehr,
G Alves. Benzene poisoning, clinical and blood abnormalities in two Brazilian female gas station attendants: two case reports. BMC Res Notes 2017, 10: 52 |
n.a. | TCG |
| 590 |
E Kubicova, V Trifonov, F Borovecki, T
Liehr, M Rincic, N Kosyakova, SS
Hussein. First molecular cytogenetic characterization of murine malignant mesothelioma cell line AE17 and in silico translation to the human genome. Curr Bioinform 2017, 12: 11-18 |
0.540 | TCG |
| 63% of publications of Institute of Human Genetics Jena in the actual year | |||
2016
| Number |
Authors/
Title/ Where Contribution was Published |
Impact
Factor |
Topic |
| 589 |
AC Malinverni, ME
Colovati, AB Perez, TP Caneloi, HR Oliveira
Jr, N Kosyakova, T Liehr, AB
Hamid, MI Melaragno. Unusual duplication in the pericentric region of chromosome 9 in a patient with phenotypic alterations. Cytogenet Genome Res 2016, 150: 100-105 |
1.354 | CG HET |
| 588 |
A Wafa, F Moassass, T
Liehr, S Bhatt, A Aljapawe, W Al
Achkar. A high complex karyotype involving eleven chromosomes including three novel chromosomal aberrations and monoallelic loss of TP53 in case of follicular lymphoma transformed into B-cell lymphoblastic leukemia. Mol Cytogenet 2016, 9: 91 |
1.455 | TCG |
| 587 |
FJ
Sheth, L Naznin, T Liehr, JJ
Sheth. FISH – The best technique in characterization of prenatally detected small supernumerary marker chromosomes (sSMC). Int J Pregn & Chi Birth 2016, 1: 00005 |
n.a. | sSMC |
| 586 |
A
Wafa, F Moassass, T Liehr, A
Aljapawe, W Al Achkar. Partial trisomy 1q21-qter and partial monosomy 7q21-qter due to a derivative chromosome 7 in myelodysplastic syndrome associated with squamous cell carcinoma: Case report. Case Rep Clin Med 2016, 5: 518-527 |
n.a. | TCG |
| 585 |
O Kadioglu, J Cao, N
Kosyakova, K Mrasek, T Liehr, T
Efferth. Genomic and transcriptomic profiling of resistant CEM/ADR-5000 and sensitive CCRF-CEM leukaemia cells for unraveling the full complexity of multifactorial multidrug resistance. Sci Rep 2016, 6: 36754 |
4.259 | TCG |
| 584 |
T
Liehr. Editorial: BIRC3 as a yet underestimated prognostic marker of malignancies? Translat Cancer Res 2016 doi: 10.21037/tcr.2016.09.29 |
1.167 | TCG |
| 583 |
J Filipović, G Joksić,
D Vujić, I Joksić, K Mrasek, A Weise, T
Liehr. First molecular-cytogenetic characterization of Fanconi anemia fragile sites in primary lymphocytes of FA-D2 patients in different stages of the disease. Mol Cytogenet 2016, 9: 70 |
1.455 | TCG |
| 582 |
R Joshi, P Garg, N
Zaitlen, T Lappalainen, CT Watson, N Azam, D
Ho, SE Antonarakis, HG Brunner, K Buiting, SW
Cheung, B Coffee, T Eggermann, D Francis, JP
Geraedts, G Gimelli, SG Jacobson, C Le
Caignec, N de Leeuw, T Liehr,
DJ Mackay, SB Montgomery, AT Pagnamenta, P
Papenhausen, DO Robinson, C Ruivenkamp, C
Schwartz, B Steiner, DA Stevenson, U Surti, T
Wassink, AJ Sharp. DNA methylation profiling of uniparental disomy subjects provides a map of parental epigenetic bias in the human genome. Am J Hum Genet 2016, 99: 555-566 |
9.025 | UPD |
| 581 |
V Bugarski Stanojević,
G Stamenković, J Blagojević, T Liehr,
N Kosyakova, M Rajičić, M Vujošević. Exploring supernumeraries - a new marker for screening of B-chromosomes presence in the yellow necked mouse Apodemus flavicollis. PLoS One 2016, 11: e0160946 |
2.806 | EVO |
| 580 |
H Fryssira, E Tsoutsou,
S Psoni, S Amenta, T Liehr, E
Anastasakis, C Skentou, A Ntouflia, I
Papoulidis, E Manolakos, N Chaliasos. Partial monosomy14q involving FOXG1 and NOVA1 in an infant with microcephaly, seizures and severe developmental delay. Mol Cytogenet 2016, 9: 55 |
1.455 | CG |
| 579 |
M Rinčić, IY Iourov, T
Liehr. Thoughts about SLC16A2, TSIX and XIST gene like sites in the human genome and a potential role in cellular chromosome counting. Mol Cytogenet 2016, 9: 56 |
1.455 | INT |
| 578 |
W
Sangpakdee, S Phimphan, T Liehr,
X Fan, K Pinthong, I Patawang, A Tanomtong. Characterization of chromosomal rearrangements in pileated gibbon (Hylobates pileatus) using multiplex-FISH technique. The Nucleus 2016; 59: 131-135 |
n.a. | EVO |
| 577 |
A Wafa, F Moassass, T
Liehr, A Al-Ablog, W Al-Achkar. Acute promyelocytic leukemia with the translocation t(15;17)(q22;q21) associated with t(1;2)(q42~43;q11.2~12): a case report. J Med Case Rep 2016, 10: 203 |
n.a. | TCG |
| 576 |
MH Ornellas, MdF Silva,
C Solza, SBSdL Goncalves, L Silva de Almeida,
JdP Ayres-Silva, TL Seixa, EF Bastos, T
Liehr, G Alves. Myelodysplastic syndrome without ring sideroblasts and with Janus kinase 2 gene mutation: An unusual case report. Mol Clin Oncol 2016, 5: 227-230 |
n.a. | TCG |
| 575 |
E Alhourani, R
Aroutiounian, T Harutyunyan, A Glaser, C
Schlie, B Pohle, T Liehr. Interphase molecular cytogenetic detection rates of chronic lymphocytic leukemia specific aberrations are higher in cultivated cells than in blood or bone marrow smears. J Histochem Cytochem 2016, 64: 495-501 |
2.511 | TCG |
| 574 |
A
Wafa, M Assad, T Liehr, A
Aljapawe, W Al Achkar. A new complex karyotype in a unique de novo myelodysplastic syndrome case involving ten chromosomes and monoallelic loss of TP53. Gene Rep 2016, 4: 208-212 |
n.a. | TCG |
| 573 |
G Hovhannisyan, R
Aroutiounian, N Babayan, T Harutyunyan, T
Liehr. Comparative analysis of individual chromosome involvement in micronuclei induced by mitomycin C and bleomycin in human leukocytes. Mol Cytogenet 2016, 9: 49 |
1.455 | TCG |
| 572 |
B Wannenmacher, D
Mitter, F Kießling, T Liehr, A
Weise, M Siekmeyer, W Kiess. A 33-year-old male patient with paternal derived duplication of 14q11.2-14q22.1~22.3: clinical course, phenotypic and genotypic findings. J Pediatr Endocrinol Metab 2016, 29: 611-616 |
1.233 | CG |
| 571 |
S Amasdl, A Natiq, SC
Elalaoui, A Sbiti, T Liehr, A
Sefiani. Insulin-like growth factor type 1 deficiency in a Moroccan patient with de novo inverted duplication 9p24p12 and developmental delay: a case report. J Med Case Rep 2016, 10: 122 |
n.a. | CG |
| 570 |
CF Yano, LA Bertollo, T
Liehr, WP Troy, MB Cioffi. W chromosome dynamics in Triportheus species (Characiformes, Triportheidae) - an ongoing process narrated by repetitive sequences. J Hered 2016, 2016: 342-348 |
2.432 | EVO |
| 569 |
T Liehr.
Benign and pathological gain or loss of genetic material - about microscopic and submicroscopic copy number variations (CNVs) in human genetics. Tsitologiya 2016, 58: 476-477 |
n.a. | HET |
| 568 |
A Weise, S Bhatt, K
Piaszinski, N Kosyakova, X Fan, A
Altendorf-Hofmann, A Tanomtong, A Chaveerach,
M Bello de Cioffi, E de Oliveira, J-U Walther,
T Liehr, JP Chaudhuri. Chromosomes in a genome-wise order: evidence for metaphase architecture. Mol Cytogenet 2016, 9: 36 |
1.455 | INT |
| 567 |
E Alhourani, MAK
Othman, JB Melo, IM Carreira, B Grygalewicz, D
Vujić, Z Zecević, G Joksić, A Glaser, B Pohle,
C Schlie, S Hauke, T Liehr. BIRC3 alterations in chronic and B-cell acute lymphocytic leukemia patients. Oncol Lett 2016, 11: 3240-3246 |
1.390 | TCG |
| 566 |
M Rincic, M Rados, Z
Krsnik, K Gotovac, F Borovecki, T Liehr,
L Brecevic. Complex intrachromosomal rearrangement in 1q leading to 1q32.2 microdeletion: a potential role of SRGAP2 in the gyrification of cerebral cortex. Mol Cytogenet 2016, 9: 19 |
1.455 | CG |
| 565 |
A Zlotina, T Kulikova,
N Kosyakova, T Liehr, A
Krasikova. Microdissection of lampbrush chromosomes as an approach for generation of locus-specific FISH-probes and samples for high-throughput sequencing. BMC Genomics 2016, 17: 126 |
3.729 | INT M EVO |
| 564 |
W Sangpakdee, A
Tanomtong, X Fan, K Pinthong, A Weise, T
Liehr. Application of multicolor banding combined with heterochromatic and locus-specific probes identify evolutionary conserved breakpoints in Hylobates pileatus. Mol Cytogenet 2016, 9:17 |
1.455 | EVO |
| 563 |
MAK Othman, B
Grygalewicz, B Pienkowska-Grela, J Rygier, A
Ejduk, M Rincic, JB Melo, IM Carreira, B
Meyer, T Liehr. A new IGH@ gene rearrangement associated with CDKN2A/B deletion in a young adult B-cell acute lymphoblastic leukemia (B-ALL). Oncol Lett 2016, 11: 2117-2122 |
1.390 | TCG |
| 562 |
T
Liehr, H Heng, Y Yurov, A
Meloni-Ehrig, I Iourov. Reviewer acknowledgement 2016. Mol Cytogenet 2016, 9: 24 |
1.455 | other |
| 561 |
EG Coci, U Koehler, T
Liehr, A Stelzner, C Fink, H
Langen, J Riedel. CANPMR syndrome and chromosome 1p32-p31 deletion syndrome coexist in two related individuals affected by simultaneous haplo-insufficiency of CAMTA1 and NIFA genes. Mol Cytogenet 2016, 9: 10 |
1.455 | CG |
| 560 |
T Liehr.
Cytogenetically visible copy number variations (CG-CNVs) in banding and molecular cytogenetics of human; about heteromorphisms and euchromatic variants. Mol Cytogenet 2016, 9: 5 |
1.455 | HET |
| 559 |
S Amasdl, A Natiq, A
Sbiti, M Zerkaoui, J Lyahyai, T Liehr,
S Amzazi, A Sefiani. 20p12.3 deletion is rare cause of syndromic cleft palate: case report and review of literature. BMC Research Notes 2016, 9: 5 |
n.a. | CG |
| 58% of publications of Institute of Human Genetics Jena in the actual year | |||
| Number |
Authors/
Title/ Where Contribution was Published |
Impact Factor | Topic |
| 558 |
T
Liehr, IM Carreira. PWG: Marker chromosomes. ECA newsletter 2015, 36: 5-6 |
n.a. | sSMC |
| 557 |
T
Liehr. PWG: Marker chromosomes. ECA newsletter 2015; 35: 31 |
n.a. | sSMC |
| 556 |
IE
Gooma, S Bhatt, T Liehr, M
Glei, TA El-Tayeb. Comparative study of Ag and Co / Ag nanoparticles mediated by photothermal therapy of cancer. Egypt J Zool 2015, 63: 99-117 |
n.a. | TCG |
| 555 |
M Kontodiou, G
Daskalakis, A Vetro, V Paspaliaris, G
Papaioannou, T Dagklis, I Tsakiridis, M
Ziegler, T Liehr, L Thomaidis,
I Papoulidis, E Manolakos. Complex rearrangement involving three chromosomes, four breakpoints and a 2.7 Mb deletion on 18q segment observed in a girl with mild learning difficulties. Cytogenet Genome Res 2015, 147: 118-123 |
1.638 | CG |
| 554 |
AA Darouich, T
Liehr, A Weise, D Schlembach, E
Schleußner, M Kiehntopf, I Schreyer. Alpha-fetoprotein and its value for predicting pregnancy outcomes – a re-evaluation. J Prenat Med 2015, 9: 18-23 |
n.a. | PRE |
| 553 |
R Hochstenbach, B
Nowakowska, M Volleth, A Ummels, A
Kutkowska-Kamierczak, E Obersztyn, K
Ziemkiewicz, C Gerloff, D Schanze, M Zenker, P
Muschke, I Schanze, M Poot, T Liehr.
Multiple small supernumerary marker chromosomes resulting from maternal meiosis I or II errors. Mol Syndromol 2015, 6: 210-221 |
n.a. | sSMC |
| 552 |
A Wafa, S Almedani, T
Liehr, W Al-Achkar. Masked inv dup(22)(q11.23), tetrasomy 8 and trisomy 19 in a blast crisis-chronic myeloid leukemia after interrupted Imatinib-treatment. Mol Cytogenet 2015, 8: 98 |
1.506 | TCG |
| 551 |
M Manvelyan, I
Simonyan, G Hovhannisyan, R Aroutiounian, AB
Hamid, T Liehr. A new case of a complex small supernumerary marker chromosome, a der(9)t(7;9)(p22;q22) due to a maternal balanced rearrangement. J Ped Genet 2015, 4: 199-200 |
n.a. | sSMC |
| 550 |
E Alhourani, M Rincic,
JB Melo, IM Carreira, A Glaser, B Pohle, C
Schlie, T Liehr. Isochromosome 17q in chronic lymphocytic leukemia. Leuk Res Treatment 2015, 2015: 489592 |
n.a. | TCG |
| 549 |
K Reichwald, A Petzold,
P Koch, BR Downie, N Hartmann, S Pietsch, M
Baumgart, D Chalopin, M Felder, M Bens, A
Sahm, K Szafranski, S Taudien, M Groth, I
Arisi, A Weise, SS Bhatt, V Sharma, JM Kraus,
F Schmid, S Priebe, T Liehr, M
Görlach, ME Than, M Hiller, HA Kestler, J-N
Volff, M Schartl, A Cellerino, C Englert, M
Platzer. Insights into sex chromosome evolution and aging from the genome of a short-lived fish. Cell 2015, 163: 1527-1538 |
28.710 | EVO |
| 548 |
X Fan, W Supiwong, A
Weise, K Mrasek, N Kosyakova, A Tanomtong, K
Pinthong, VA Trifonov, M de Bello Cioffi, P
Grothmann, T Liehr, EHC de
Oliveira. Comprehensive characterization of evolutionary conserved breakpoints in four New World Monkey karyotypes compared to Chlorocebus aethiops and Homo sapiens. Helyion 2015, 1: e00042 |
n.a. | EVO |
| 547 |
M Moysés-Oliveira, RS
Guilherme, VA Meloni, A Di Battista, CB de
Mello, S Bragagnolo, D Moretti-Ferreira, N
Kosyakova, T Liehr, GM
Carvalheira, MI Melaragno MI. X-linked intellectual disability related genes disrupted by balanced X-autosome translocations. Am J Med Genet B Neuropsychiatr Genet 2015, 168: 669-677 |
3.391 | CG |
| 546 |
M Rath, J Najm, H Sirb,
K Kentouche, A Dufke, S Pauli, K Hackmann, T
Liehr, CA Hübner, U Felbor,
Kompetenznetzwerk Hämorrhagische Diathesen Ost
(KHDO). Large deletions play a minor but essential role in congenital coagulation factor VII and X deficiencies. Hämostaseologie 2015, 35: S36-42 |
1.547 | CG |
| 545 |
MAM
Abo-Zeid, T Liehr, M Glei, AM
Gamal-Eldeen, M Zawrah, M Ali. Detection of cyto- and genotoxicity of rod-shaped gold nanoparticles in human blood lymphocytes using comet-FISH. Cytologia 2015, 80: 173-181 |
0.227 | TCG |
| 544 |
N Armanet, L Tosca, S
Brisset, T Liehr, G Tachdjian.
Small supernumerary marker chromosomes in human infertility. Cytogenet Genome Res 2015, 146: 100-108 |
1.638 | sSMC |
| 543 |
S Winkler, M Hempel, S
Brückner, F Mallek, A Weise, T Liehr,
HM Tautenhahn, M Bartels, B Christ. Mouse white adipose tissue-derived mesenchymal stem cells gain pericentral and periportal hepatocyte features after differentiation in vitro, which are preserved in vivo after hepatic transplantation. Acta Physiol 2015, 215: 89-104 |
4.066 | CG |
| 542 |
H Jafari-Ghahfarokhi, M
Moradi-Chaleshtori, T Liehr, M
Hashemzadeh-Chaleshtori, H Teimori, P
Ghasemi-Dehkordi. Small supernumerary marker chromosomes and their correlation with specific syndromes. Adv Biomed Res 2015, 4: 140 |
n.a. | sSMC |
| 541 |
AF de Figueiredo, RR
Capela de Matos, MA Othman, T Liehr,
ES da Costa, MG Land, RC Ribeiro, E Abdelhay,
ML Silva. Molecular cytogenetic studies characterizing a novel complex karyotype with an uncommon 5q22 deletion in childhood acute myeloid leukemia. Mol Cytogenet 2015, 8: 62 |
1.506 | TCG |
| 540 |
A Wafa, M Asa‘ad,
A Ikhtiar, T Liehr, W
Al-Achkar. Deletion 9p23 to 9p11.1 as sole additional abnormality in a Philadelphia positive chronic myeloid leukemia in blast crisis: a rare event. Mol Cytogenet 2015, 8: 59 |
1.506 | TCG |
| 539 |
E Aguiar de Oliveira,
LAC Bertollo, CF Yano, T Liehr,
M de Bello Cioffi. Comparative cytogenetics in the genus Hoplias (Characiformes, Erythrinidae) highlights contrasting karyotype evolution among congeneric species. Mol Cytogenet 2015, 8: 56 |
1.506 | EVO |
| 538 |
F Sheth, T Liehr,
K Shah, J Sheth. Prader-Willi syndrome - type 1 deletion, a consequence of an unbalanced translocation of chromosomes 13 and 15, easily to be mixed up with a Robertsonian translocation. Mol Cytogenet 2015, 8: 52 |
1.506 | CG |
| 537 |
MAK Othman, JB Melo, IM
Carreira, M Rincic, A Glaser, B Grygalewicz, B
Gruhn, K Wilhelm, K Rittscher, B Meyer, MLM
Silva, T de Jesus Marques Salles, T
Liehr. High rates of submicroscopic aberrations in karyotypically normal acute lymphoblastic leukemia. Mol Cytogenet 2015, 8: 45 |
1.506 | TCG |
| 536 |
RR Capela de Matos, AF
De Figueiredo, T Liehr, E
Alhourani, MT De Souza, E Abdelhay, RC
Ribeiro, MLM Silva. A novel three-way variant t(8;13;21)(q22;q33;q22) in a child with acute myeloid leukemia FAB AML-M2: contribution of molecular approaches to reveal t(8;21) variants. Acta Hematol 2015, 134: 243-245 |
1.506 | TCG |
| 535 |
MAM Abo-Zeid, T
Liehr, AM Gamal-Eldeen, M Zawrah,
M Ali, MAK Othman. Potential of rod, sphere and semi-cube shaped gold nanoparticles to induce cytotoxicity and genotoxicity in human blood lymphocytes in vitro. Eur J Nanomed 2015, 7: 63-75 |
n.a. | TCG |
| 534 |
A Weise, N Kosyakova, M
Voigt, N Aust, K Mrasek, S Löhmer, N Rubtsov,
T Karamysheva, V Trifonov, D Hardekopf, T
Jancuková, S Pekova, K Wilhelm, T Liehr,
X Fan. Comprehensive analyses of white handed gibbon chromosomes enables access to 92 evolutionary conserved breakpoints compared to the human genome. Cytogenet Genome Res 2015, 145: 42-49 |
1.638 | EVO |
| 533 |
DR Ney Garcia, T
Liehr, M Emerenciano, C Meyer, R
Marschalek, M do Socorro Pombo de Oliveira, RC
Ribeiro, MGP Land, ML Macedo Silva. Molecular studies reveal MLL-MLLT3 gene fusion displaced in a case of childhood acute lymphoblastic leukemia with complex karyotype. Cancer Genet 2015, 208: 143-147 |
2.333 | TCG |
| 532 |
PG Maass, A Aydin, FC
Luft, C Schächterle, A Weise, S Stricker, C
Lindschau, M Vaegler, F Qadri, HR Toka, H
Schulz, PM Krawitz, J Hecht, I Hollfinger, Y
Wefeld-Neuenfeld, E Bartels-Klein, A Mühl, M
Kann, H Schuster, D Chitayat, MG Bialer, TF
Wienker, J Ott, K Rittscher, T Liehr,
J Jordan, G Plessis, J Tank, K Mai, R Naraghi,
R Hodge, M Hopp, LO Hattenbach, A Busjahn, A
Rauch, F Vandeput, M Gong, F Rüschendorf, N
Hübner, H Haller, S Mundlos, N Bilginturan, MA
Movsesian, E Klussmann, O Toka, S Bähring. PDE3A mutations cause autosomal-dominant hypertension with brachydactyly. Nat Genet 2015, 46: 647-653 |
31.616 | CG |
| 531 |
SA Romanenko, PL
Perelman, VA Trifonov, NA Serdyukova, T Li, B
Fu, PC O'Brien, BL Ng, W Nie, T Liehr,
R Stanyon, AS Graphodatsky, F Yang. A first generation comparative chromosome map between guinea pig (Cavia porcellus) and humans. PLoS One 2015, 10: e0127937 |
3.057 | EVO |
| 530 |
S Ledig, S
Preisler-Adams, S Morlot, T Liehr,
P Wieacker. Premature ovarian failure caused by a heterozygous missense mutation in POF1B and a reciprocal translocation 46,X,t(X;3)(q21.1;q21.3). Sex Dev 2015, 9: 86-90 |
2.164 | CG |
| 529 |
G Kirkpatrick, H Ren, T
Liehr, V Chow, S Ma. Meiotic and sperm aneuploidy studies in three carriers of Robertsonian translocations and small supernumerary marker chromosomes. Fertil Steril 2015, 103: 1162-1169.e7 |
4.426 | sSMC |
| 528 |
M Moysés-Oliveira, RD
Guilherme, AG Dantas, R Ueta, AB Perez, M
Haidar, R Canonaco, VA Meloni, N Kosyakova, T
Liehr, GM Carvalheira, MI
Melaragno. Genetic mechanisms leading to primary amenorrhea in balanced X-autosome translocations. Fertil Steril 2015, 103: 1289-1296.e2 |
4.426 | CG |
| 527 |
W Al-Achkar, F
Moassass, A Al-Ablog, T Liehr,
X Fan, A Wafa. A Syrian couple with chromosomal aberration and MTHFR polymorphism leads to recurrent pregnancy loss and partial trisomy of 5p12-15.3 in the offspring: Case report and review to the literature. Zhonghua Nan Ke Xue = Nat J Androl 2015, 21: 219-224 |
n.a. | CG |
| 526 |
MAK Othman, B
Grygalewicz, B Pienkowska-Grela, M Rincic, K
Rittscher, JB Melo, IM Carreira, B Meyer, W
Marzena, T Liehr. Novel cryptic rearrangements in adult B cell precursor acute lymphoblastic leukemia involving MLL gene. J Histochem Cytochem 2015, 63: 384-390 |
1.953 | TCG |
| 525 |
F Sheth, M Rahman, T
Liehr, M Desai, B Patel, C Modi, S
Trivedi, J Sheth. Prenatal screening of cytogenetic anomalies – a Western Indian experience. BMC Preg Childbirth 2015, 15: 90 |
2.180 | PRE CG |
| 524 |
T Harutyunyan, G
Hovhannisyan, N Babayan, M Othman, T
Liehr, R Aroutiounian. Influence of aflatoxin B1 on copy number variants in human leukocytes in vitro. Mol Cytogenet 2015, 8: 25 |
1.506 | TCG |
| 523 |
MAK Othman, D Vujić, Z
Zecević, M Đurišić, B Slavković, B Meyer, T
Liehr. A cryptic three-way translocation t(10;19;11)(p12.31;q13.31;q23.3) with a derivative Y-chromosome in an infant with acute myeloblastic leukemia (M5b). Gene 2015, 563: 115-119 |
2.319 | TCG |
| 522 |
IR
Tkach, KO Sosnina, NL Huleyuk, OI Terpylyak,
DV Zastavna, A Weise, N Kosyakova, T
Liehr. Contribution of chromosomal abnormalities and genes of the major histocompatibility complex to early pregnancy losses. Biopolymers and Cell 2015, 31: 38-45 |
n.a. | PRE CG |
| 521 |
T Liehr,
MA Othman, K Rittscher, E Alhourani. The current state of molecular cytogenetics in cancer diagnosis. Expert Rev Mol Diagn 2015, 15: 517-526 |
3.333 | TCG |
| 520 |
T
Liehr, H Heng, Y Yurov, A
Meloni-Ehrig, I Iourov. Reviewer acknowledgement 2015. Mol Cytogenet 2015, 8: 23 |
1.506 | other |
| 519 |
L Brečević, M Rinčić, Ž
Krsnik, G Sedmak, AB Hamid, N Kosyakova, I
Galić, T Liehr, F Borovečki. Association of new deletion/duplication region at chromosome 1p21 with intellectual disability, severe speech deficit and autism spectrum disorder-like behavior: an all-in approach to solving the DPYD enigma. Translat Neuroscience 2015, 6: 59-86 |
1.012 | CG |
| 518 |
IE Gomaa, SA Abdel
Gaber, S Bhatt, T Liehr, M
Glei, TA El-Tayeb, MH Abdel-Kader. In vitro cytotoxicity and genotoxicity studies of gold nanoparticles-mediated photo-thermal therapy versus 5-fluorouracil. J Nanopart Res 2015, 17: 102 |
2.101 | TCG |
| 517 |
M Kehrer, T
Liehr, T Benkert, S Singer, U
Grasshoff, K Schaeferhoff, M Bonin, A
Weichselbaum. Interstitial duplication of chromosome region 1q25.1q25.3: Report of a patient with mild cognitive deficits, tall stature and facial dysmorphisms. Am J Med Genet 2015, 167: 653-656 |
2.082 | CG |
| 516 |
T Karamysheva, N
Kosyakova, N Guediche, T Liehr.
Small supernumerary marker chromosomes and the nuclear architecture of sperm – a study in a fertile and an infertile brother. Syst Biol Reprod Med 2015, 61: 32-36 |
1.204 | sSMC INT |
| 515 |
VS Baranov, TE
Ivaschenko, T Liehr, MI
Yarmolinskaya. Systems genetics view of endometriosis – a common complex disorder. Eur J Obstet Gynecol Reprod Biol 2015, 185: 59-65 |
1.662 | CG TCG |
| 514 |
MAK Othman, JB Melo,
IM Carreira, M Rincic, E Alhourani, K Wilhelm,
B Gruhn, A Glaser, T Liehr. MLLT10 and IL3 rearrangement together with a complex four-way-translocation and trisomy 4 in a patient with early T-cell precursor acute lymphoblastic leukemia. Oncol Rep 2015, 33: 625-630 |
2.486 | TCG |
| 513 |
T Sahoo, J-C Wang, MM
Elnaggar, P Sanchez-Lara, LP Ross, LW Mahon, K
Hafezi, A Deming, L Hinman, Y Bruno, JA
Bartley, T Liehr, A Anguiano, M
Jones. Concurrent triplication and uniparental isodisomy: evidence for microhomology-mediated break-induced replication model for genomic rearrangements. Europ J Hum Genet 2015, 23: 61-66 |
4.580 | UPD |
| 66% of publications of Institute of Human Genetics Jena in the actual year | |||
2014
| Number |
Authors/
Title/ Where Contribution was Published |
Impact Factor | Topic |
| 512 |
T Liehr. Updates on „EBMG Professional Board for Clinical Laboratory Geneticists“ – Open for applications. ESHG newsletter 2014, 25: 1-2 |
n.a. |
other |
| 511 |
T
Liehr. PWG: Marker chromosomes. ECA newsletter 2014, 33: 19 |
n.a. | sSMC |
| 510 |
T
Liehr. PWG: Marker chromosomes. ECA newsletter 2014, 34: 26 |
n.a. | sSMC |
| 509 |
A Sanubol, A
Chaveerach, R Sudmoon, T Tanee, T Liehr.
Verification of selected piper species (Piperaceae) using morphological characters, molecular data, and chemical constituents. Malay Nat J 2014, 66: 60-81 |
n.a. | EVO |
| 508 |
X
Fan, A Tanomtong, A Chaveerach, K Pinthong, S
Pornnarong, W Supiwong, T Liehr,
A Weise. High resolution karyotype of Thai crab-eating macaque (Macaca fascicularis). Genetika 2014, 46: 877-882 |
0.347 | EVO |
| 507 |
W Al-Achkar, F
Moassass, A Ikhtiar, T Liehr,
MAK Othman, A Wafa. Hyperdiploidy associated with T315I mutation in BCR-ABL kinase domain in an accelerated phase-chronic myeloid leukemia case. Mol Cytogenet 2014, 7: 89 |
2.140 | TCG |
| 506 |
A
Weise, K Mrasek, T Liehr. Zytogenetische und molekularzytogenetische Methoden in der Pränataldiagnostik. Med Genetik 2014, 26: 391-397 |
0.131 | PRE M |
| 505 |
W Supiwong, T
Liehr, MB Cioffi, A Chaveerach, N
Kosyakova, X Fan, T Tanee, A Tanomtong. Comparative cytogenetic mapping of rRNA genes among naked catfishes: Implications for genomic evolution in the Bagridae family. Genet Mol Res 2014, 13: 9533-9542 |
0.775 | EVO |
| 504 |
A Natiq, S Amsdel, T
Liehr, K Kreskowski, B Meyer, I
Ratbi, S Amzazi, A Sefiani. 11p13 deletion syndrome: first case in Morocco detected by FISH. J Pediatr Neonatal Care 2014, 1: 00048 |
n.a. | CG |
| 503 |
A Wafa, A Aljapawe, MAK
Othman, T Liehr, E Alhourani, W
Al Achkar. Do novo del(9)(p13) in a childhood T-cell prolymphocytic leukemia as sole abnormality. Exp Hematol Oncol 2014, 3: 28 |
n.a. | TCG |
| 502 |
E Alhourani, M Rincic,
MAK Othman, B Pohle, C Schlie, A Glaser, T
Liehr. Comprehensive chronic lymphocytic leukemia diagnostics by combined multiplex ligation dependent probe amplification (MLPA) and interphase fluorescence in situ hybridization (iFISH). Mol Cytogenet 2014, 7: 79 |
2.140 | TCG |
| 501 |
IY
Iourov, SG Vorsanova, T Liehr,
YB Yurov. Mosaike im Gehirn des Menschen. Med Genetik 2014, 26: 242-345 |
0.131 | INT |
| 500 |
T
Liehr. Entstehungsmechanismen von Zellmosaiken in der genetischen Diagnostik. Med Genetik 2014, 26: 298-301 |
0.131 | CG |
| 499 |
T
Liehr. Bedeutung von Zellmosaiken in der genetischen Diagnostik. Med Genetik 2014, 26: 297 |
0.131 | CG |
| 498 |
T Liehr.
Small supernumerary marker chromosomes detected in connection with infertility. Zhonghua Nan Ke Xue = Nat J Androl 2014, 20: 771-780 |
n.a. | sSMC |
| 497 |
AV Bispo, P
Burégio-Frota, L Oliveira dos Santos, GF Leal,
AR Duarte, J Araújo, V Cavalcante da Silva, MT
Cartaxo Muniz, T Liehr, N
Santos. Y-chromosome in Turner syndrome: detection of hidden mosaicism and the report of a rare X;Y translocation case. Reprod Fert Develop 2014, 26: 1176-1182 |
2.400 | CG |
| 496 |
MAK Othman, M Rincic,
JB Melo, IM Carreira, E Alhourani, F Hunstig,
A Glaser, T Liehr. A novel cryptic three-way translocation t(2;9;18)(p23.2;p21.3;q21.33) with deletion of tumor suppressor genes in 9p21.3 and 13q14 in a T-cell acute lymphoblastic leukemia. Leuk Res Treatment 2014, 2014: 357123 |
n.a. | TCG |
| 495 |
L Nazaryan, EG
Stefanou, C Hansen, N Kosyakova, M Bak, FH
Sharkey, T Mantziou, AD Papanastasiou, V
Velissariou, T Liehr, M Syrrou,
N Tommerup. The strength of combined cytogenetic and mate-pair sequencing techniques illustrated by a germline chromothripsis rearrangement involving FOXP2. Europ J Hum Genet 2014, 22: 338-343. |
4.349 | CG |
| 494 |
SS Hussein, K
Kreskowski, M Ziegler, E Klein, AB Hamid, N
Kosyakova, M Volleth, T Liehr,
X Fan, K Piaszinski. Mitotic stability of small supernumerary marker chromosomes depends on their shape and telomeres - a long term in vitro study. Gene 2014, 552: 246-248 |
2.138 | sSMC |
| 493 |
W Al-Achkar, A Wafa,
MAK Othman, F Moassass, A Aljapawe, T
Liehr. An adult B-cell precursor acute lymphoblastic leukemia with multiple secondary cytogenetic aberrations. Mol Cytogenet 2014, 7: 60 |
2.140 | TCG |
| 492 |
J Roediger, W
Hessenkemper, S Bartsch, M Manvelyan, SS
Huettner, T Liehr, M Esmaeili,
S Foller, I Petersen, M-O Grimm, A Baniahmad.
Supraphysiological androgen levels induce cellular senescence in human prostate cancer cells through the Src-Akt pathway. Mol Cancer 2014, 13: 214 |
4.257 | TCG |
| 491 |
Y Sahin, PÖ Kiper, Y
Alanay, T Liehr, GE Utine, K
Boduroğlu. Partial monosomy 3q26.33-q27.3 presenting with intellectual disability, facial dysmorphism, and diaphragm eventration: a case report. Clin Dysmorphol 2014, 23: 147-151 |
0.416 | CG |
| 490 |
SG Vorsanova, IY Iourov, IA
Demidova, AD Kolotii, T Liehr, YB
Yurov. Microdeletion 1p36 syndrome: diagnostic problems and the use of molecular cytogenetics for the solution. Yakut Medical Journal 2014, 2: 47-48 (in Russian) |
n.a. | CG |
| 489 |
DC de Souza, AF de
Figueiredo, H Mkrtchyan, MA Othman, T
Liehr, J Dobbin, ML Silva, E
Abdelhay, T de S Fernandez. A yet unreported der(11)t(6;11)(p21;q21) included in a complex karyotype of a refractory anemia with ring sideroblasts and poor prognosis. Blood Cells Mol Dis 2014, 53: 91-93 |
2.646 | TCG |
| 488 |
M de Souza, R Hassan, T
Liehr, T Marques-Salles, AM
Boulhosa, E Abdelhay, R Ribeiro, MLM Silva. Conventional and molecular cytogenetic characterization of Burkitt lymphoma with bone marrow involvement in Brazilian children and adolescents. Ped Blood Cancer 2014, 61: 1422-1426 |
2.386 | TCG |
| 487 |
CF Yano, LAC Bertollo,
WF Molina, T Liehr, M de Bello
Cioffi. Genomic organization of repetitive DNAs and its implications for male karyotype and the neo-Y chromosome differentiation in Erythrinus erythrinus (Characiformes, Erythrinidae). Comp Cytogen 2014, 8: 139-151 |
1.210 | EVO |
| 486 |
DR Ney Garcia, TP
Vieira, T Liehr, E Abdelhay, R
Binato, F Neves, MT de Souza, RC Ribeiro, MLM
Silva. Cryptic t(19;19)(p13.3;q13.2), involving the TCF3/E2A gene, detected and described by molecular cytogenetics in a patient with childhood B-cell progenitor acute lymphoblastic leukemia. Atlas Genet Cytogenet Oncol Haematol 2014, 18: 217-221 |
n.a. | TCG |
| 485 |
K Varvagiannis, I
Papoulidis, T Koromila, K Kefalas, M Ziegler,
T Liehr, MB Petersen, Y
Gyftodimou, E Manolakos. De novo 393kb microdeletion of 7p11.2 characterized by aCGH in a boy with psychomotor retardation and dysmorphic features. Meta Gene 2014, 2: 274-282 |
n.a. | CG |
| 484 |
AM Vlaikou, E
Manolakos, D Noutsopoulos, G Markopoulos, T
Liehr, A Vetro, M Ziegler, A
Weise, K Kreskowski, I Papoulidis, L
Thomaidis, M Syrrou. An interstitial 4q31.21q31.22 microdeletion associated with developmental delay: Case report and literature review. Cytogenet Genome Res 2014, 142: 227-238 |
1.561 | CG |
| 483 |
A Natiq, SC Elalauoi, T
Liehr, S Amzazi, A Sefiani. Characterization of a rare short arm heteromorphism of chromosome 22 in a girl with down-syndrome like facies. Ind J Hum Genet 2014, 20: 89-91 |
n.a. | HET |
| 482 |
S Sifakis, M
Eleftheriades, D Kappou, R Murru, A
Konstantinidou, S Orru, M Ziegler, T
Liehr, E Manolakos, I Papoulidis.
Prenatal diagnosis of proximal partial trisomy 1q confirmed by comparative genomic hybridization array: molecular cytogenetic analysis, fetal pathology and review of the literature. Birth Defects Research Part A: Clinical and Molecular Teratology 2014, 100: 284-293 |
2.089 | CG |
| 481 |
H Spittel, F Kubek, K
Kreskowski, M Ziegler, E Klein, AB Hamid, N
Kosyakova, G Radhakrishnan, A Junge, P
Kozlowski, B Schulze, T Martin, D Huhle, K
Mehnert, L Rodríguez, MA Ergun, C Sarri, M
Militaru, F Stipoljev, H Tittelbach, X Fan, F
Vasheghani, SS Hussein, M Volleth, T
Liehr. Mitotic stability of small supernumerary marker chromosomes – a study based on 93 immortalized cell lines. Cytogenet Genome Res 2014, 142: 151-160 |
1.561 | sSMC |
| 480 |
W Supiwong, T
Liehr, MB Cioffi, A Chaveerach, N
Kosyakova, K Pinthong, T Tanee, A Tanomtong. Chromosomal evolution in naked catfishes (Bagridae, Siluriformes): A comparative chromosome mapping study. Zool Anzeiger 2014, 253: 316-320 |
1.483 | EVO |
| 479 |
X
Fan, W Sangpakdee, A Tanomtong, A Chaveerach,
K Pinthong, S Pornnarong, W Supiwong, V
Trifonov, G Hovhannisyan, K Loth, C Hensel, T
Liehr, A Weise. Comprehensive molecular cytogenetic analysis of Barbary macaque (Macaca sylvanus). Biol J Arm 2014, 66: 98-102 |
n.a. | EVO |
| 478 |
X Fan, W Sangpakdee, A
Tanomtong, A Chaveerach, K Pinthong, S
Pornnarong, W Supiwong, VA Trifonov, GG
Hovhannisyan, RM Aroutouinian, T
Liehr, A Weise. Molecular cytogenetic analysis of Thai southern pig-tailed macaque (Macaca nemestrina) by multicolor banding. Proceedings of Yerevan State University 2014, 2014: 46-50 |
n.a. | EVO |
| 477 |
CF Yano, J Poltronieri,
LAC Bertollo, R Ferreira Artoni, T
Liehr, M de Bello Cioffi. Chromosomal mapping of repetitive DNAs in Triportheus trifurcatus (Characidae, Characiformes): Insights into the differentiation of the Z and W chromosomes. PLOS One 2014, 9: e90946 |
3.234 | EVO |
| 476 |
YB Yurov, SG Vorsanova,
T Liehr, AD Kolotii, IY Iourov.
X chromosome aneuploidy in the Alzheimer's disease brain. Mol Cytogenet 2014, 7: 20 |
2.140 | INT |
| 475 |
F Santiago, G Alves, UB
Otero, MM Tabalipa, LR Scherrer, N Kosyakova,
MH Ornellas, T Liehr. Monitoring of gas station attendants exposure to benzene, toluene, xylene (BTX) using three-color chromosome painting. Mol Cytogenet 2014, 7: 15 |
2.140 | TCG |
| 474 |
E Manolakos, A Vetro, A
Garas, L Thomaidis, K Kefalas, G Kitsos, M
Ziegler, T Liehr, O Zuffardi, I
Papoulidis. A new case of proximal 10q duplication in a child with severe central hypotonia characterized by array CGH and review. Exp Therap Med 2014, 7: 953-957 |
1.269 | CG |
| 473 |
T
Liehr, H Heng, Y Yurov. Reviewer acknowledgement 2014. Mol Cytogenet 7: 11 |
2.140 | other |
| 472 |
SS Bhatt, M
Manvelyan, K Moradkhani, F Hunstig, K
Mrasek, J Puechberty, G Lefort, P Sarda, A
Weise, T Liehr, F Pellestor. Inverted segment size and the presence of recombination hot spot clusters matter in sperm segregation analysis. Cytogenet Genome Res 2014,142:145-149 |
1.561 | CG INT |
| 471 |
I Pappoulidis, E
Papageorgiou, E Siomou, E Oikonomidou, L
Thomaidou, A Vetro, O Zuffardi, T Liehr,
E Manolakos. A patient with partial trisomy 21 and 7p deletion expresses mild Down syndrome phenotype. Gene 2014, 536: 441-443 |
2.138 | CG |
| 470 |
W Al Achkar A Aljapawe,
T Liehr, A Wafa. De novo acute myeloid leukemia subtype-M4 with initial trisomy 8 and later acquired t(3;12)(q26;p12) leading to ETV6/MDS1/EVI1 fusion transcript expression: A case report. Onc Lett 2014, 7: 787-790 |
0.987 | TCG |
| 469 |
I Iourov, Y Yurov, H
Heng, T Liehr. In memoriam of Anna D Polityko (17.12.1959 - 20.04.2013). Mol Cytogenet 2014, 7: 2 |
2.140 | other |
| 468 |
L Rodríguez, SS Bhatt,
M García-Castro, A Plasencia, J
Fernández-Toral, E Abarca, M de Bello Cioffi,
T Liehr. A unique case of a discontinuous duplication 3q26.1-3q28 resulting from a segregation error of a maternal complex chromosomal rearrangement involving an insertion and an inversion. Gene 2014, 535: 165-169 |
2.138 | CG |
| 467 |
J Poltronieri, V
Marquioni, LAC Bertollo, E Kejnovsky, WF
Molina, T Liehr, MB Cioffi. Comparative chromosomal mapping of microsatellites in Leporinus species (Characiformes, Anostomidae): Unequal accumulation on the W chromosomes. Cytogenet Genome Res 2014, 142: 40-45 |
1.561 | EVO |
| 466 |
T Schmidt, T Bierhals,
F Kortüm, I Bartels, T Liehr, P
Burfeind, M Shoukier, V Frank, C Bergmann, K
Kutsche. Branchio-Otic syndrome caused by a genomic rearrangement: clinical findings and molecular cytogenetic studies in a patient with a pericentric inversion of chromosome 8. Cytogenet Genome Res 2014; 142: 1-6 |
1.561 | CG |
| 68% of publications of Institute of Human Genetics Jena in the actual year | |||
2013
| Number |
Authors/
Title/ Where Contribution was Published |
Impact Factor | Topic |
| 465 |
T
Liehr. Anna D. Polityko (1959-2013). ECA newsletter 2013, 32: 37 |
n.a. |
other |
| 464 |
T
Liehr. PWG: Marker chromosomes. ECA newsletter 2013, 32: 6-7 |
n.a. | sSMC |
| 463 |
T
Jančušková, R Plachý, J Štika, L Krutílková,
DW Hardekopf, T Liehr, N
Kosyakova, R Čmejla, L Žejšková, T Kozák, P
Žák, M Karas, S Peková. Identifikace novych molekularnich “marker pro sledovani minimalni rezidualni nemoci u akutnich leumkemii. Transfuze a Hematologie Dnes 2013, 19: 8-21 |
n.a. | TCG M |
| 462 |
T Liehr.
Copy number variations - is there a biological difference between submicroscopic and microscopically visible ones? OA Genetics 2013, 1: 2 |
n.a. | HET |
| 461 |
W Al-Achkar, Wafa A,
Al-Ablog A, Moassas F, T Liehr.
Molecular cytogenetic characterization on an inv(Y)(p11.2q11.221q11.222) in a Syrian family. Balk J Med Genet 2013, 16 :73-76 |
0.167 | CG |
| 460 |
FY AbdElmontalab, IE
Fadl, HM Abushama, K Kreskowski, T
Liehr. Molecular cytogenetic study of the NF2 gene deletion in meningioma in Sudanese patients. Balk J Med Genet 2013, 16: 29-32 |
0.167 | TCG |
| 459 |
FJ Sheth, T
Liehr, P Kumari, R Akinde, HJ
Sheth, JJ Sheth. Chromosomal abnormalities in couples with repeated fetal loss: an Indian retrospective study. Indian J Hum Genet 2013, 19: 415-422 |
n.a. | CG |
| 458 |
RS Guilherme, MC
Cernach, TE Sfakianakis, SS Takeno, LM
Nardozza, C Rossi, SS Bhatt, T Liehr,
MI Melaragno. A complex chromosome rearrangement involving four chromosomes, nine breakpoints and a cryptic 0.6-Mb deletion in a boy with cerebellar hypoplasia and defects in skull ossification. Cytogenet Genome Res 2013, 141: 317-323 |
1.905 | CG |
| 457 |
N
Karadeniz, T Liehr, K Mrasek, I
Aşık, Z Aşık, N Kosyakova, H Mkrtchyan. C-type lectins and human epithelial membrane protein1: Are they new proteins in keratin disorders? Open J Genet 2013, 3: 262-269 |
n.a. | CG |
| 456 |
X Fan, K Pinthong, H
Mkrtchyan, P Siripiyasing, N Kosyakova, W
Supiwong, A Tanomtong, A Chaveerach, T
Liehr, M de Bello Cioffi, A Weise. First detailed reconstruction of the karyotype of Trachypithecus cristatus (Mammalia: Cercopithecidae). Mol Cytogenet 2013, 6: 58 |
2.660 | EVO |
| 455 |
W Al
Achkar, A Wafa, A Aljapawe, MAK Othman, T
Liehr. A novel cytogenetic abnormality r(7)(::p11.2->q36.3::) in a Philadelphia-positive chronic myeloid leukemia case. Case Rep Clin Med 2013, 2: 517-520 |
n.a. | TCG |
| 454 |
W Supiwong, T
Liehr, MB Cioffi, A Chaveerach, N
Kosyakova, K Pinthong, T Tanee, A Tanomtong. Karyotype and cytogenetic mapping of 9 classes of repetitive DNAs in the genome of the naked catfish Mystus bocourti (Siluriformes, Bagridae). Mol Cytogenet 2013, 6: 51 |
2.660 | EVO |
| 453 |
MB Cioffi, T
Liehr, V Trifonov, WF Molina, LAC
Bertollo. Independent sex chromosome evolution in lower vertebrates: A molecular cytogenetic overview in the Erythrinidae fish family. Cytogenet Genome Res 2013, 141: 186-194 |
1.905 | EVO |
| 452 |
T Liehr,
S Cirkovic, T Lalic, M Guc-Scekic, C de
Almeida, J Weimer, I Iourov, MI Melaragno, RS
Guilherme, E-GG Stefanou, D Aktas, K
Kreskowski, E Klein, M Ziegler, N Kosyakova, M
Volleth, AB Hamid. Complex small supernumerary marker chromosomes – an update. Mol Cytogenet 2013, 6: 46 |
2.660 | sSMC |
| 451 |
AD Bhatt, T
Liehr, SR Bakshi. Phenotypic spectrum in uniparental disomy: low incidence or lack of study? Indian J Hum Genet 2013, 19: 311-314 |
n.a. | UPD |
| 450 |
N Aust, S Schüle, AK
Altendorf-Hofmann, Y Chen, T Knösel, O Dirsch,
U Settmacher, A Weise, K Mrasek, T
Liehr. Loss of chromosome 4 correlates with better long-term survival and lower relapse rate after R0-resection of colorectal liver metastases. J Cancer Res Clin Oncol 2013, 139: 1861-1867 |
3.009 | TCG |
| 449 |
A Vičić, D Zudenigo, P
Korać, T Liehr, F Stipoljev. Prenatally detected interstitial deletion 13q12.3-q22 in a fetus with a cystic hygroma. Gene 2013, 531: 90-91 |
2.082 | CG |
| 448 |
DS Vasconcelos, FPE da
Silva, LG Quintana, NP Anselmo, MAK Othman, T
Liehr, EHC de Oliveira. Numerical aberrations of chromosome 17 and TP53 in brain metastases derived from breast cancer. Genet Mol Res 2013, 12: 2594-2600 |
0.850 | TCG |
| 447 |
W Al Achkar, F
Moassass, A Ikhtiar, MAK Othman, T
Liehr, A Wafa. Cytogenetic evolution in a patient with chronic developing a secondary acute myelogenous leukemia subtype M5 resistant to Imatinib mesylate therapy. J Leuk 2013, 1: 118 |
n.a. | TCG |
| 446 |
T Jancuskova, R Plachy,
J Stika, L Zemankova, DW Hardekopf, T
Liehr, N Kosyakova, R Cmejla, L
Zejskova, T Kozak, P Zak, A Zavrelova, P
Havlikova, M Karas, A Junge, C Ramel, S
Pekova. A method to identify new molecular markers for assessing minimal residual disease in acute leukemia patients. Leuk Res 2013, 37: 1363-1373 |
2.692 | TCG M |
| 445 |
RS Guilherme, E Klein,
AB Hamid, S Bhatt, M Volleth, A Polityko, A
Kulpanovich, A Dufke, B Albrecht, S Morlot, L
Brecevic, MB Petersen, E Manolakos, N
Kosyakova, T Liehr. Human ring chromosomes – new insights for their clinical significance. Balk J Med Genet 2013, 16: 13-19 |
0.167 | CG |
| 444 |
W Al Achkar, A Wafa, A
Aljapawe, T Liehr. A de novo del(9)(p22.3) in a primary plasma cell leukemia case. Mol Cytogenet 2013, 6: 33 |
2.660 | TCG |
| 443 |
T Liehr,
H Heng, Y Yurov, A Meloni-Ehrig, I Iourov. Molecular Cytogenetics: the first impact factor (2.36). Mol Cytogenet 2013, 6: 28 |
2.660 | other |
| 442 |
MAM Abo-Zeid, T
Liehr , SM El-Daly, AM
Gamal-Eldeen, M Glei, A Shabaka, S Bhatt, A
Hamid. Molecular cytogenetic evaluation of the efficacy of photodynamic therapy by Indocyanine Green in breast adenocarcinoma MCF-7 cells. Photodiagn Photodynam Therapy 2013, 10: 194-202 |
2.524 | TCG |
| 441 |
RS Guilherme, ARN
Dutra, ABA Perez, SS Takeno, MM Oliveira, LD
Kulikowski, E Klein, AB Hamid, T Liehr,
MI Melaragno. First report of a small supernumerary der(8;14) marker chromosome. Cytogenet Genome Res 2013, 139: 284-288 |
1.905 | sSMC |
| 440 |
E Manolakos, A Vetro, E
Papadopoulou, K Kefalas, M Lagou, L Thomaidis,
P Peitsidis, S Sifakis, A Divane, M Ziegler, T
Liehr, O Zuffardi, I Papoulidis. Partial trisomy 2p and partial monosomy 2q arising from a paternal intrachromosomal 2q-into-2p between-arm insertion and paracentric inversion: molecular cytogenetic characterization of a four break rearrangement. Cytogenet Genome Res 2013, 140: 12-20 |
1.905 | CG |
| 439 |
T Liehr,
E Klein, K Mrasek, N Kosyakova, RS Guilherme,
N Aust, C Venner, A Weise, AB Hamid. Clinical impact of somatic mosaicism in cases with small supernumerary marker chromosomes. Cytogenet Genome Res 2013, 139: 158-163 |
1.905 | sSMC |
| 438 |
T
Liehr, H Heng, Y Yurov. Reviewer acknowledgement 2013. Mol Cytogenet 2013, 6: 9 |
2.660 | other |
| 437 |
T Liehr,
A Weise, AB Hamid, X Fan, E Klein, N Aust, MAK
Othman, K Mrasek, N Kosyakova. Multicolor FISH methods in current clinical diagnostics. Exp Rev Mol Diag 2013, 13: 251-255 |
4.270 | M |
| 436 |
W Al-Achkar, A Wafa, M
Assaad, C Ehlers, T Liehr. A unique case of female pseudohermaphroditism with 21-hydroxylase deficiency and small supernumerary marker chromosome 7. Mol Med Rep 2013, 7: 1545-1548 |
1.484 | sSMC |
| 435 |
W Al-Achkar, A Wafa, A
Ikhtiar, T Liehr. T Three-way Philadelphia translocation t(9;10;22)(q34;p11.2;q11.2) as a secondary abnormality in an imatinib mesylate-resistant chronic myeloid leukemia patient. Oncol Lett 2013, 5: 1656-1658 |
0.987 | TCG |
| 434 |
W Al-Achkar, A Wafa, F
Moassass, E Klein, T Liehr. Multiple copies of BCR-ABL fusion gene on two isodicentric Philadelphia chromosomes in an imatinib mesylate-resistant chronic myeloid leukemia patient. Oncol Lett 2013, 5: 1579-1582 |
0.987 | TCG |
| 433 |
N Kosyakova, A
Grigorian, T Liehr, M
Manvelyan, I Simonyan, H Mkrtchyan, R
Aroutiounian, AD Polityko, AI Kulpanovich, T
Egorova, E Jaroshevich, A Frolova, N Shorokh,
IV Naumchik, M Volleth, I Schreyer, H Nelle, M
Stumm, R-D Wegner, G Reising-Ackermann, M
Merkas, L Brecevic, T Martin, L Rodríguez, S
Bhatt, M Ziegler, K Kreskowski, A Weise, A
Sazci, S Vorsanova, M de Bello Cioffi, E
Ergul. Heteromorphic variants of chromosome 9. Mol Cytogenet 2013, 6: 14 |
2.660 | HET |
| 432 |
T Liehr,
N Kosyakova. Small supernumerary marker chromosomes (sSMC) – what about the genotype-phenotype correlation? Tsitologiya 2013, 55: 165-166 |
n.a. | sSMC |
| 431 |
N Kosyakova, V
Trifonov, S Romanenko, H Mkrtchyan, A
Graphodatsky, T Liehr. Murine multicolor banding. Tsitologiya 2013, 55:259-260 |
n.a. | M |
| 430 |
C Leibiger, N
Kosyakova, H Mkrtchyan, M Glei, V Trifonov, T
Liehr. First molecular cytogenetic high resolution characterization of the NIH 3T3 cell line by murine multicolor banding. J Histochem Cytochem 2013, 61:306-312 |
2.403 | TCG |
| 429 |
RRC Matos, H Mkrchyan,
BA Amaral, T Liehr, MT de
Souza, DR Ney-Garcia, N Santos, TJ
Marques-Salles, RC Ribeiro, AF Figueiredo, MLM
Silva. An unusual cytogenetic rearrangement originating from two different abnormalities in chromosome 6 in a child with acute promyelocytic leukemia. Acta Hematologica 2013, 130:23-26 |
0.850 | TCG |
| 428 |
TV
Karamysheva, МА Prokhorovich, MA Lagarkova, SL
Kiselev, T Liehr, NB Rubtsov. Chromosome rearrangements in sublines of human embryonic stem cell lines hESM01 and hESM03. BioDiscovery 2013, 7:1 |
n.a. | CG |
| 427 |
B Cavdarli, G Ozgen,
AO Kaymak, B Göker, T Liehr, MA
Ergun, EF Percin. A case with double translocation and Sjögren syndrome. Turkiye J Med Sci 2013, 33: 233-236 |
0.841 | CG |
| 426 |
JC Barber, V Hall, VK
Maloney, S Huang, AM Roberts, AF Brady, N
Foulds, B Bewes, M Volleth, T Liehr,
K Mehnert, M Bateman, H White. 16p11.2-p12.2 duplication syndrome; a genomic condition differentiated from euchromatic variation of 16p11.2. Eur J Hum Genet 2013, 21: 182-189 |
4.225 | CG |
| 425 |
DR Ney-Garcia, TP
Vieira, T Liehr, S Bhatt, MT de
Souza, AF de Figueiredo, RC Ribeiro, MLM
Silva. A case of childhood T cell acute lymphoblastic leukemia with a complex t(9;9) and homozygous deletion of CDKN2A gene associated with a Philadelphia-positive minor subclone. Blood Cells Mol Dis 2013, 50: 131-133 |
2.331 | TCG |
| 424 |
T Schmidt, I Bartels,
T Liehr, P Burfeind, B Zoll, M
Shoukiera. A family with an inverted tandem duplication 5q22.1q23.2. Cytogenet Genome Res 2013,139: 65-70 |
1.905 | CG |
| 423 |
J Ou, W Wang, T
Liehr, E Klein, AB Hamid, F Wang,
C Duan, H Li. Characterization of three small supernumerary marker chromosomes (sSMC) in humans. J Matern Fetal Neonatal Med 2013, 26: 106-108 |
1.208 | sSMC |
| 422 |
W Al-Achkar, A Wafa, T
Liehr. A new t(9;11;20;22)(q34;p11.2;q11.21;q11) in a Philadelphia-positive chronic myeloid leukemia case. Oncol Lett 2013, 5: 605-608 |
0.987 | TCG |
| 421 |
W Al-Achkar, A
Aljapawe, S Almedani, T Liehr,
A Wafa. A novel cytogenetic abnormality t(7;8)(p11.2;q11.2) and a four-way Philadelphia translocation in an imatinib mesylate-resistant chronic myeloid leukemia patient. Oncol Lett 2013, 5: 617-620 |
0.237 | TCG |
| 52% of publications of Institute of Human Genetics Jena in the actual year | |||
2012
| Number |
Authors/
Title/ Where Contribution was Published |
Impact Factor | Topic |
| 420 |
T
Liehr. PWG: Marker chromosomes ECA newsletter 2012, 31: 26 |
n.a. |
sSMC |
| 419 |
T
Liehr. PWG: Marker chromosomes. ECA newsletter 2012, 30: 23-24 |
n.a. | sSMC |
| 418 |
AB Hamid, A Weise, M
Voigt, M Bucksch, N Kosyakova, T Liehr,
E Klein. Clinical impact of proximal autosomal imbalances. Balk J Med Genet 2012, 15: 15-21 |
0.077 | sSMC |
| 417 |
F Sheth, N Gohel, T
Liehr, O Akinde, M Desai, O
Adeteye, J Sheth. Gain of chromosome 4qter and loss of 5pter – an unusual case with features of Cri du chat syndrome (CdCS). Case Reports Genet 2012, 153405 |
n.a. | CG |
| 416 |
RS Guilherme, E Klein,
C Venner, AB Hamid, S Bhatt, MI Melaragno, M
Volleth, A Polityko, A Kulpanovich, N
Kosyakova, T Liehr. Human ring chromosomes and small supernumerary marker chromosomes – do they have telomeres? Chromosome Res 2012; 20: 825-835 |
2.847 | sSMC |
| 415 |
NLL Corrales, K Mrasek,
M Voigt, T Liehr, N Kosyakova.
Comprehensive characterization of genomic instability in pluripotent stem cells and their derived neuroprogenitor cell lines. Applied & Translational Genomics 2012, 1: 21-24 |
n.a. | CG |
| 414 |
MAK
Othman, A Lier, S Junker, P Kempf, F Dorka, E
Gebhart, FJ Sheth, B Grygalewicz, S Bhatt, A
Weise, K Mrasek, T Liehr, M
Manvelyan. Does positioning of chromosomes 8 and 21 in interphase drive t(8;21) in acute myelogenous leukemia? BioDiscovery 2012, 4: 4 |
n.a. | INT TCG |
| 413 |
K Ma, L Qiu, K Mrasek,
J Zhang, T Liehr, LG Quintana,
Z Li. Common fragile sites: genomic hotspots of DNA damage and carcinogenesis. Int J Mol Sci 2012, 13: 11974-11999 |
2.464 | TCG INT |
| 412 |
A Serra, K Eirich, AK
Winkler, K Mrasek, G Göhring, G Barbi, H
Cario, B Schlegelberger, B Royer-Pokora, T
Liehr, C Leriche, D Henne-Bruns,
TF Barth, D Schindler. Shared copy number variation in simultaneous nephroblastoma and neuroblastoma due to Fanconi anemia. Mol Syndromol 2012, 3: 120-130 |
n.a. | TCG |
| 411 |
NLL Corrales, K Mrasek,
M Voigt, T Liehr, N Kosyakova. Copy number variations (CNVs) in human pluripotent cell-derived neuroprogenitors. Gene 2012, 506: 377-379 |
2.196 | CG |
| 410 |
AB Hamid, K Kreskowski,
A Weise, N Kosayakova, K Mrasek, M Voigt, RS
Guilherme, R Wagner, D Hardekopf, S Pekova, T
Karamysheva, T Liehr, E Klein.
How to narrow down chromosomal breakpoints in small and large derivative chromosomes – a new probe set. J Appl Genet 2012, 53: 259-269 |
1.847 | M sSMC |
| 409 |
M Bucksch, M Ziegler, N
Kosayakova, MV Mulhatino, JC Llerena Jr., S
Morlot, W Fischer, AD Polityko, AI
Kulpanovich, MB Petersen, B Belitz, V
Trifonov, A Weise, T Liehr, AB
Hamid. A new multicolor-fluorescence in situ hybridization probe set directed against human heterochromatin: HCM-FISH. J Histochem Cytochem 2012, 60: 530-536 |
2.255 | M HET |
| 408 |
MV Mulatinho, C Luiz de
Carvalho Serao, F Scalco, D Hardekopf, S
Pekova, K Mrasek, T Liehr, A
Weise, N Rao, JC Llerena Jr. Severe intellectual disability, omphalocele, hypospadia and high blood pressure associated to a deletion at 2q22.1q22.3: Case report. Mol Cytogenet 2012, 5: 30 |
2.360 | CG |
| 407 |
W Al-Achkar, A Wafa, T
Liehr, E Klein, F Moassass. Detailed analysis of an idic(Y)(q11.21) in a mosaic karyotype. Mol Med Report 2012, 6: 293-296 |
1.170 | CG |
| 406 |
W Al-Achkar, A Wafa, F
Moassass, T Liehr. A unique cytogenetic abnormality, t(2;7)(p13.1;p21.3), in a Philadelphia-positive chronic myeloid leukemia. Onc Letters 2012, 4: 209-212 |
0.237 | TCG |
| 405 |
I Papoulidis, E
Manolakos, AB Hamid, E Klein, N Kosyakova, U
Kordaß, J Kunz, E Siomou, M Kontodiou, M
Tzimina, P Nicolaides, T Liehr,
MB Petersen. Tetrasomy 9p mosaicism associated with a normal phenotype in two cases. Cytogenet Genome Res 2012, 136:237-241 |
1.839 | sSMC |
| 404 |
A Faria de Figueiredo,
TP Vieira, T Liehr, S Bhatt, R
Binato, T de Jesus Marques Salles, E Carboni,
RC Ribeiro, ML Macedo Silva, E Abdelhay. A rare cryptic and complex rearrangement leading to MLL-MLLT10 gene fusion masked by del(10)(p12) in a child with acute monoblastic leukemia (AML-M5). Leuk Res 2012, 36: e74-e77 |
2.764 | TCG |
| 403 |
A Weise, K Mrasek, E
Klein, M Mulatinho, JC Llerena Jr., D
Hardekopf, S Pekova, S Bhatt, N Kosyakova, T
Liehr. Microdeletion and microduplication syndromes. J Histochem Cytochem 2012, 60:346-358. |
2.255 |
CG |
| 402 |
E Klein, M Rocchi, A
Ovens-Raeder, N Kosyakova, A Weise, M Ziegler,
M Meins, S Morlot, W Fischer, M Volleth, A
Polityko, C Mackie Ogilvie, C Kraus, T
Liehr. Five novel locations of neocentromeres in human: 18q22.1, Xq27.1~27.2, acro p13, acro p12, and heterochromatin of unknown origin. Cytogenet Genome Res 2012, 136:163-166 |
1.839 | CG sSMC |
| 401 |
MA Fonzar Hernandes, T
de Jesus Marques-Salles, H Mkrtchyan, EM
Soares-Ventura, E Pereira Leite, MT Cartaxo
Muniz, MT Marquim Nogueira Cornélio, T
Liehr, N Santos, ML Macedo Silva.
Extra copies of der(21)t(12;21) plus deletion of ETV6 gene due to dic(12;18) in B-cell precursor ALL with poor outcome. Case Reports Genet 2012, 2012:186532 |
n.a. | TCG |
| 400 |
A Vetro, E Manolakos,
MB Petersen, L Thomaidis, T Liehr
G Croci, F Franchi, M Marinelli, E Meneghelli,
B Dal Bello, S Cesari, A Iasci, G Arrigo, O
Zuffardi. Unexpected results in the constitution of small supernumerary marker chromosomes. Europ J Med Genet 2012, 55:185–190 |
1.685 | sSMC |
| 399 |
G Hovhannisyan, R
Aroutiounian, T Liehr. Chromosomal composition of micronuclei in human leukocytes exposed to mitomycin C. J Histochem Cytochem 2012, 60:316-322 |
2.255 | TCG |
| 398 |
E Klein, M Manvelyan, I
Simonyan, AB Hamid, R Santos Guilherme, T
Liehr, T Karamysheva. Centromeric association of small supernumerary marker chromosomes with their sister-chromosomes detected by three dimensional molecular cytogenetics. Mol Cytogenet 2012, 5:15 |
2.410 | sSMC INT |
| 397 |
W Al-Achkar, A Wafa, F
Moassass, T Liehr. A chronic myeloid leukemia case with a unique variant Philadelphia translocation: t(9;22;21)(q34;q11;p12). Oncol Lett 2012, 3: 1027-1029 |
0.237 | TCG |
| 396 |
E Manolakos, S Sifakis,
S Sotiriou, P Peitsidis, M Eleftheriades, V
Mersinias, T Liehr, L
Thomaidis, G Kitsos, I Papoulidis, MB
Petersen, S Orru S. Prenatal detection of an inverted duplication deletion in the long arm of chromosome 1 in a fetus with increased nuchal translucency. Molecular cytogenetic analysis and review of the literature. Clin Dysmorphol 2012, 21:101-105 |
0.608 | CG |
| 395 |
DR Ney-Garcia, T
Liehr, S Bhatt, MT de Souza, RR de
Matos, G Pimenta, W Pulcheri, RC Ribeiro, E
Abdelhay, MLM Silva. Childhood B-cell progenitor acute lymphoblastic leukemia presenting a three-way t(11;12;21)(q14;p13;q22) with a RUNX1 gene signal on chromosome 11. Int J Hematol 2012, 95:112-114 |
1.681 | TCG |
| 394 |
DR Ney-Garcia, T
Liehr, S Bhatt, MT de Souza, RR
Capela de Matos, R Binato, FC Jordy, E
Abdelhay, RC Ribeiro, MLM Silva. Molecular cytogenetic studies reveal an unexpected chromosomal inversion as a variant of t(12;21)(p13;q22) in a child with B-cell precursor acute lymphoblastic leukemia. Leuk Lymphoma 2012, 53:342-344 |
2.301 | TCG |
| 393 |
C Eckmann-Scholz, H
Tönnies, T Liehr, S Gesk, W
Jonat, A Caliebe. Normal prenatal ultrasound findings in a case with de novo mosaic small supernumerary marker chromosome 18 – how to counsel? J Mat-Fet Neonat Med 2012, 25:200-202 |
1.518 | sSMC |
| 48% of publications of Institute of Human Genetics Jena in the actual year | |||
2011
| Number |
Authors/
Title/ Where Contribution was Published |
Impact Factor | Topic |
| 392 |
T
Liehr. PWG: Marker chromosomes. ECA newsletter 2011, 27: 6 |
n.a. |
sSMC |
| 391 |
C Backsch, B Pauly, M
Liesenfeld, C Scheungraber, M Gajda, K Mrasek,
T Liehr, A Clad, E Schröck, IB
Runnebaum, M Dürst. Two novel unbalanced whole arm translocations are frequently detected in cervical squamous cell carcinoma. Cancer Genetics 2011, 204: 646-653 |
n.a. | TCG |
| 390 |
C Woelfel, T
Liehr, A Weise, J Langrehr, W Amin
Kotb, M Pacyna-Gengelbach, D Katenkamp, I
Petersen. Molecular cytogenetic characterization of epithelioid hemangioendothelioma. Cancer Genetics 2011, 204:671-676 |
n.a. | TCG |
| 389 |
T Milenkovic, M
Guc-Scekic, D Zdravkovic, V Topic, T
Liehr, G Joksic, D Radivojevic, N
Lakic. Molecular analysis of ring Y chromosome in a 10-year-old boy with mixed gonadal dysgenesis and growth hormone deficiency. Balk J Med Genet 2011, 14:71-75 |
0.225 | CG |
| 388 |
T Liehr,
N Kosayakova, J Schröder, M Ziegler, K
Kreskowski, B Pohle, S Bhatt, L Theuss, K
Wilhelm, A Weise, K Mrasek. Evidence for correlation of fragile sites and chromosomal breakpoints in carriers of constitutional balanced chromosomal rearrangements. Balk J Med Genet 2011, 14:13-16 |
0.225 | CG INT |
| 387 |
V
Westrich, T Liehr. Molecular cytogenetic approaches and array-diagnostics in prenatal medicine. Med Genetik 2011, 22:463-468 |
0.059 | PRE M |
| 386 |
G Dobbernack, W Meinl,
N Schade, S Florian, K Wend, I Voigt, H
Himmelbauer, M Gross, T Liehr,
H Glatt. Altered tissue distribution of 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine-DNA adducts in mice transgenic for human sulfotransferases 1A1 and 1A2. Carcinogenesis 2011, 32:1734-1740 |
5.702 | TCG |
| 385 |
M de Bello Cioffi, A
Sánchez, JA Marchal, N Kosyakova, T
Liehr, V Trifonov, LA Bertollo. Whole chromosome painting reveals independent origin of sex chromosomes in closely related forms of a fish species. Genetica 2011, 139:1065-1072 |
2.148 | EVO |
| 384 |
F Braulke, J Schanz, R
Steffens, T Liehr, M Manvelyan,
I Chudoba, D Haase. Two different del(5q) clones in a patient with myelodysplastic syndrome. Leuk Lymph 2011, 52:1811-1844 |
2.580 | TCG |
| 383 |
O Villa, M Mallo, N
Kosyakova, M Salido, T Liehr, L
Martínez-Avilés, C Pedro, M García-Aragonés, B
Espinet, L Florensa, L Arenillas, I Cuscó, LA
Pérez Jurado, F Solé. Deletion of TET2 gene in an acute myeloid leukemia case with a t(4;15)(q24;q26) characterized by glass needle based chromosome microdissection and oligonucleotide array. Leuk Res 2011, 35: e161– e163 |
2.923 | TCG |
| 382 |
T Liehr,
E Ewers, AB Hamid, N Kosyakova, M Voigt, A
Weise, M Manvelyan. Small supernumerary marker chromosomes and uniparental disomy have a story to tell. J Histochem Cytochem 2011, 59:842-848 |
2.725 | sSMC UPD |
| 381 |
L Kraoua, M Chaabouni,
E Ewers, I Chelly, I Ouertani, LB Jemaa, F
Maazoul, T Liehr, H Chaabouni.
Hexasomy of the Prader-Willi/Angelman critical region, including the OCA2 gene in a patient with pigmentary dysplasia: case report. Europ J Med Genet 2011, 54:e446-450 |
2.178 | CG |
| 380 |
A Faria de Figueiredo,
T Liehr, S Bhatt, R Binato, M
Tavares de Souza, R Rodrigues Capela de Matos,
T de Jesus Marques Salles, FC Jordy, RC
Ribeiro, E Abdelhay, ML Macedo Silva. A complex karyotype masked a cryptic variant t(8;21)(q22;q22) in a child with acute myeloid leukemia. Leuk Lymph 2011, 52:1593-1596 |
2.580 | TCG |
| 379 |
MB Cioffi, A Sánchez,
JA Marchal, N Kosyakova, T Liehr,
V Trifonov, LAC Bertollo. Cross-species chromosome painting tracks the independent origin of multiple sex chromosomes in two cofamiliar Erythrinidae fishes. BMC Evolutionary Biology 2011, 11:186 |
3.521 | EVO |
| 378 |
M
Stuhrmann-Spangenberg, H Engels, B Fritz, H
Gabriel, D Gläser, W Henn, T Liehr,
K Miller, H Rieder. S2-Leitlinie Humangenetische Diagnostik. Med Genetik 2011, 23:281-323 |
0.059 | other |
| 377 |
F Pellestor, T Anahory,
G Lefort, J Puechberty, T Liehr,
B Hédon, P Sarda. Complex chromosomal rearrangements: origin and meiotic behavior. Hum Reprod Update 2011, 17:476-494 |
9.234 | CG |
| 376 |
F Pellestor, J
Puechberty, A Weise, G Lefort, T Anahory, T
Liehr, P Sarda. Meiotic segregation of complex reciprocal translocations: direct analysis of the spermatozoa of a t(5;13;14) carrier. Fertil Steril 2011, 95:2433.e17-2433.e22 |
3.564 | CG |
| 375 |
E Manolakos, A Vetro, K
Kefalas, L Thomaidis, G Aperis, S Sotiriou, G
Kitsos, M Merkas, S Sifakis, I Papoulidis, T
Liehr, O Zuffardi, MB Petersen. Deletion 2q31.2-q31.3 in a 4-year-old girl with microcephaly and severe mental retardation. Am J Med Genet A 2011, 155:1476-1482 |
2.391 | CG |
| 374 |
JB Melo, L Backx, JR
Vermeesch, HG Santos, AC Duarte, N Kosyakova,
A Weise, F von Eggeling, T Liehr,
IM Carreira. Chromosome 5 derived small supernumerary marker: towards a genotype/phenotype correlation of proximal chromosome 5 imbalances. J Appl Genet 2011, 52:193-200 |
1.664 | sSMC |
| 373 |
FJ Sheth, J Andrieux, E
Ewers, N Kosyakova, A Weise, H Sheth, S-P
Romana, M LeLorc’h, B Deloben, O Theisen, T
Liehr, S Numpoothiri, J Sheth. Characterization of sSMC by FISH and molecular techniques. Europ J Med Genet 2011, 54:247-255 |
2.178 | sSMC |
| 372 |
EM Soares-Ventura, H
Mkrtchyan, T de Jesus Marques-Salles, M Silva,
N Santos, B de Araujo Silva Amaral, T
Liehr, E Abdelhay, ML Macedo
Silva, MT Cartaxo Muniz. Molecular cytogenetics reveals complex karyotype in apparent t(8;13) therapy-related acute myeloid leukemia M2 after fibrosarcoma. Leuk Res 2011, 35:e27–e29 |
2.923 | TCG |
| 371 |
B Horsthemke, M
Wawrzik, S Groß, C Lich, B Sauer, I Rost, E
Krasemann, N Kosyakova, T Liehr,
A Weise, JN Dybowski, D Hoffmann, D Wieczorek.
Parental origin and functional relevance of a de novo UBE3A variant. Europ J Med Genet 2011, 54:19-24 |
2.178 | UPD CG |
| 370 |
M Tavares de Souza, H
Mkrtchyan, R Hassan, D Ribeiro Ney Garcia, AM
Boulhosa de Azevedo, E Sobral da Costa, A
Faria de Figueiredo, T Liehr, E
Abdelhay, ML Macedo Silva. Secondary abnormalities involving 1q or 13q and poor outcome in high stage Burkitt leukemia/lymphoma cases with 8q24 rearrangement at diagnosis. Int J Hematol 2011; 93:232-236 |
1.268 | TCG |
| 369 |
W Al-Achkar, A Wafa, T
Liehr. Complex translocation involving four chromosomes in a novel Philadelphia-positive chronic myeloid leukemia case. Onc Lett 2011, 2: 273-276 |
0.108 | TCG |
| 368 |
T Liehr. What is uniparental disomy (UPD)? [online] Oxford Gene Technology. originally available at: http://www.ogt.co.uk/cytosure_whatisUPD.html |
n.a. | UPD |
| 367 |
M Manvelyan, FW Cremer,
J Lancé, R Kläs, C Kelbova, C Ramel, H
Reichenbach, C Schmidt, E Ewers, K Kreskowski,
M Ziegler, N Kosyakova, T Liehr.
New cytogenetically visible copy number variant in region 8q21.2. Mol Cytogenet 2011, 4:1 |
2.410 | HET |
| 366 |
T Liehr,
I Bartels, B Zoll, E Ewers, K Mrasek, N
Kosyakova, M Merkas, AB Hamid, F von Eggeling,
N Posorski, A Weise. Is there a yet unreported unbalanced chromosomal abnormalities without phenotypic consequences in proximal 4p? Cytogenet Genome Res 2011, 132: 121-123 |
1.533 | HET |
| 46% of publications of Institute of Human Genetics Jena in the actual year | |||
2010
| Number |
Authors/
Title/ Where Contribution was Published |
Impact Factor | Topic |
| 365 |
K Karaer, MA Ergun, A
Weise, E Ewers, T Liehr, N
Kosyakova, H Mkrtchyan. The case of an infertile male with an uncommon reciprocal X-autosomal translocation: how does this affect male fertility? Genet Couns 2010, 21:397-404 |
0.395 | CG |
| 364 |
O Egritas, B Cavdarli,
B Dalgic, MA Ergun, F Percin, M Ziegler, B
Pohle, T Liehr. Duplication 4q associated with chronic cholestatic changes in liver biopsy. Eur J Med Genet 2010, 53:411-414 |
2.335 | CG |
| 363 |
E Manolakos, A Vetro, K
Kefalas, SM Rapti, E Louizou, A Garas, G
Kitsos, L Vasileiadis, P Tsoplou, M
Eleftheriades, P Peitsidis, S Orru, T
Liehr, MB Petersen, L Thomaidis. The use of array-CGH in a cohort of Greek children with developmental delay. Mol Cytogenet 2010, 3:22 |
n.a. | CG |
| 362 |
W Al-Achkar, A Wafa, M
Manvelyan, A Ikhtiar, T Liehr.
De novo translocation involving two chromosomes in adult prolymphocytic leukemia - A rare case. Leuk Res 2010, 34:e345-347 |
2.555 | TCG |
| 361 |
W Al Achkar, A Wafa, F
Moassass, T Liehr. Partial trisomy 9p22 to 9p24.2 in combination with partial monosomy 9pter in a Syrian girl. Mol Cytogenet 2010, 3:18. |
n.a. | CG |
| 360 |
K Gersak, K Writzl, A
Veble, T Liehr. Primary amenorrhoea in a patient with mosaicism for monosomy X and a derivative X-chromosome. Genet Couns 2010, 21:335-342 |
0.395 | CG |
| 359 |
T Liehr,
T Karamysheva, M Merkas, L Brecevic, AB Hamid,
E Ewers, K Mrasek, N Kosyakova, A Weise. Somatic mosaicism in cases with small supernumerary marker chromosomes. Curr Genomics 2010, 11:432-439 |
2.487 | sSMC |
| 358 |
H Mkrtchyan, M Gross, S
Hinreiner, A Polytiko, M Manvelyan, K Mrasek,
N Kosyakova, E Ewers, H Nelle, T Liehr,
S Bhatt, K Thoma, E Gebhart, S Wilhelm, R
Fahsold, M Volleth, A Weise. The human genome puzzle – the role of copy number variation in somatic mosaicism. Curr Genomics 2010, 11:426-431 |
2.487 | INT HET |
| 357 |
A Faria de Figueiredo,
T Liehr, S Bhatt, R Binato, EM
Soares Ventura, M Tavares de Souza, R
Rodrigues Capela de Matos, R Correa Ribeiro, E
Abdelhay, ML Macedo Silva. A new cryptic ins(11;1)(q23;q21q31) detected in a t(1;8;11)(q21;p21;q23) in a baby with acute myeloid leukemia FAB AML-M5. Blood Cells Mol Dis 2010, 45:197-198 |
2.716 | TCG |
| 356 |
E Manolakos, K Kefalas,
R Neroutsou, M Lagou, N Kosyakova, E Ewers, M
Ziegler, A Weise, P Tsoplou, S-M Rapti, I
Papoulidis, E Anastasakis, A Garas, S
Sotiriou, M Eleftheriades, P Peitsidis, D
Μalathrakis, L Thomaidis, G Kitsos, S Orru, T
Liehr, MB Petersen, S
Kitsiou-Tzeli. Characterization of 23 small supernumerary marker chromosomes detected at pre-natal diagnosis: The value of fluorescence in situ hybridization. Mol Med Rep 2010, 3:1015-1022 |
0.307 | sSMC |
| 355 |
W Al-Achkar, T
Liehr, A Wafa. Insertion of the 3' ABL region into the long arm of chromosome 1 in a Philadelphia chromosome-negativechronic myeloid leukemia case. Oncol Lett 2010, 1:951-954 |
n.a. | TCG |
| 354 |
M Santos, K Mrasek, I
Madrigal, MR Martorell, A González-Meneses, G
Rodríguez-Criado, M Milà, T Liehr,
C Fuster. Characterization of a complex cryptic mosaicism for an sSMC derived from the X chromosome present in a boy with congenital malformations. Am J Med Genet 2010, 152A: 2161-2163 |
2.505 | sSMC |
| 353 |
S Balci, B Yuksel
Konuk, F Atik, AK Oguz, MA Ergun, V Baltaci, N
Kosyakova, T Liehr. Partial deletion of the long arm of chromosome 13 (q32q33.2) associated with mental retardation, choanal atresia and fish mouth. Genet Couns 2010, 21:317-324 |
0.395 | CG |
| 352 |
J Fernández-Toral, L
Rodríguez, A Plasencia, ML Martínez-Frías, E
Ewers, AB Hamid, M Ziegler, T Liehr.
Four small supernumerary marker chromosomes derived from chromosomes 6, 8, 11 and 12 in a patient with minimal clinical abnormalities – a case report. J Med Case Reports 2010, 4:239 |
n.a. | sSMC |
| 351 |
W Al Achkar, A Wafa, H
Mkrtchyan, F Moassass, T Liehr.
A unique complex translocation involving six different chromosomes in a case of childhood acute lymphoblastic leukemia with the Philadelphia chromosome and adverse prognosis. Oncol Lett 2010, 1:801-804 |
n.a. | TCG |
| 350 |
W Al Achkar, A Wafa, BY
Ali, M Manvelyan, T Liehr. A rare chronic myeloid leukemia case with Philadelphia chromosome, BCR-ABL e13a3 transcript and complex translocation involving four different chromosomes. Oncol Lett 2010, 1:797-800 |
n.a. | TCG |
| 349 |
W Al Achkar, A Wafa, H
Mkrtchyan, F Moassass, T Liehr.
A rare case of Philadelphia chromosome-positive chronic myelogenous leukemia with inversion in chromosome 9 and t(10;17). Oncol Lett 2010, 1:793-795. |
n.a. | TCG |
| 348 |
T
Liehr. A new internet page on uniparental disomy. ECA-newsletter 2010, 26:22-24. |
n.a. | UPD |
| 347 |
SI Ferreira, E Matoso,
M Pinto, J Almeida, T Liehr, JB
Melo, IM Carreira. X-chromosome terminal deletion in a female with premature ovarian failure: Haploinsufficiency of X-linked genes as a possible explanation. Mol Cytogenet 2010, 3:14 |
n.a. | CG |
| 346 |
E Ewers, K Yoda, AB
Hamid, A Weise, M Manvelyan, T Liehr.
Centromere activity in dicentric small supernumerary marker chromosomes. Chromosome Res 2010; 18:555-562 |
3.130 | sSMC |
| 345 |
SB
Niksic, VI Deretic, GR Pilic, E Ewers, M
Merkas, M Ziegler, T Liehr. Trisomy 21 with a small supernumerary marker chromosome derived from chromosomes 13/21 and 18. Balk J Med Genet 2010, 13:55-58 |
0.075 | sSMC |
| 344 |
T de Jesus
Marques-Salles, H Mkrtchyan, E Pereira Leite,
EM Soares-Ventura, MT Cartaxo-Muniz, E
Ferreira, T Liehr, ML Macedo
Silva, N Santos. Complex karyotype defined by molecular cytogenetic FISH and M-FISH in an infant with acute megakaryoblastic leukemia and neurofibromatosis. Cancer Genet Cytogenet 2010, 200: 167-169 |
1.551 | TCG |
| 343 |
T de Jesus
Marques-Salles, JEX da Silva Barros, EM
Soares-Ventura, MT Cartaxo-Muniz, N Santos, E
Ferreira, ML Macedo Silva, T Liehr,
H Mkrtchyan. Unusual childhood biphenotypic acute leukemia with a yet unreported t(3;13)(p25.1;q13). Leuk Res 2010, 34: e206-e207 |
2.555 | TCG |
| 342 |
H Nelle, I Schreyer, E
Ewers, K Mrasek, N Kosyakova, M Merkas, AB
Hamid, A Weise, T Liehr. Presence of harmless small supernumerary marker chromosomes hampers molecular genetic diagnosis: a case report. Mol Med Rep 2010, 3:571-574 |
0.307 | sSMC |
| 341 |
D Aktas, EG Utine, K
Mrasek, A Weise, F von Eggeling, K Yalaz, N
Posorski, N Akarsu, M Alikasifoglu, T
Liehr, E Tuncbilek. Derivative chromosome 1 and GLUT1 deficiency syndrome in a sibling pair. Mol Cytogenet 2010, 3:10 |
n.a. | CG |
| 340 |
I Papoulidis, E
Manolakos, E Siomou, K Kefalas, L Thomaidis, T
Liehr, A Vetro, A Athanasiadis, O
Zuffardi, MB Petersen. A fetus with ring chromosome 21 characterized by aCGH shows no clinical findings after birth. Prenat Diag 2010, 30:586-588 |
2.152 | CG |
| 339 |
B Auber, P Burfeind, C
Thiels, EA Alsat, M Shoukier, T Liehr,
H Nelle, I Bartels, G Salinas-Riester, F
Laccone. An unbalanced translocation resulting in a duplication of Xq28 causes a Rett syndrome-like phenotype in a female patient. Clin Genet 2010, 77:593-597 |
2.942 | CG |
| 338 |
E Ktistaki, A
Garefalaki, A Williams, SR Andrews, DM Bell,
KE Foster, CG Spilianakis, RA Flavell, N
Kosyakova, V Trifonov, T Liehr,
D Kioussis. CD8 locus nuclear dynamics during thymocyte development. J Immunol 2010, 184:5686-5695 |
5.745 | CG |
| 337 |
E Uz, Y Alanay, D
Aktas, I Vargel, S Gucer, G Tuncbilek, F von
Eggeling, E Yilmaz, O Deren, N Posorski, H
Ozdag, T Liehr, S Balci, M
Alikasifoglu, B Wollnik, NA Akarsu. Disruption of ALX1 causes extreme microphthalmia and severe facial clefting: expanding the spectrum of autosomal-recessive ALX-related frontonasal dysplasia. Am J Hum Genet 2010, 86:789-796 |
11.680 | CG |
| 336 |
T Liehr,
R-D Wegner, M Stumm, T Martin, G
Gillessen-Kaesbach, N Kosyakova, E Ewers, AB
Hamid, F von Eggeling, J Hentschel, M Ziegler,
A Weise. Three new cases with small supernumerary marker chromosomes 1 and normal phenotype. J Chin Med Assoc 2010, 73: 205-207 |
0.678 | sSMC |
| 335 |
Z Li, Q Zhang, J-H Mao,
A Weise, K Mrasek, X Fan, X Zhang, T
Liehr, KH Lu, A Balmain, W-W Cai.
A HDAC1-binding domain within FATS bridges p21 turnover to radiation-induced tumorigenesis. Oncogene 2010, 29:2659-2671 |
7.414 | TCG |
| 334 |
T Liehr,
N Kosyakova, A Weise, M Ziegler, G
Raabe-Meyer. First case of a neocentromere formation in an otherwise normal chromosome 7. Cytogenet Genome Res 2010, 218: 189-191 |
1.783 | CG |
| 333 |
P Burégio-Frota, L
Valença, GF Leal, AR Duarte, AV Bispo-Brito,
EM Soares-Ventura, TJ Marques-Salles, MT
Nogueira, MT Muniz, ML Silva, F Hunstig, T
Liehr, N Santos. Identification of a de novo inv dup(X)(pter->q22) by multicolor banding in a girl with Turner syndrome. Genet Mol Res 2010, 9:780-784 |
1.013 | CG |
| 332 |
E Manolakis, P
Peitsidis, M Elefteriades, E Dedoulis, M
Ziegler, S Orru, T Liehr, MB
Petersen. Prenatal detection of full monosomy 21 in a fetus with an increased nuchal translucency. Molecular cytogenetic analysis and review of the literature. J Obstet Gynaecol Res 2010, 36: 435–440 |
0.440 | CG |
| 331 |
T Liehr.
Cytogenetic contribution to uniparental disomy (UPD). Mol Cytogenet 2010, 3:8 |
n.a. | UPD |
| 330 |
VA Trifonov, N
Kosyakova, SA Romanenko, AS Graphodatsky, T
Liehr. New insights into the karyotypic evolution in muroid rodents revealed by multicolor banding applying murine probes. Chr Res 2010, 18:265–275 |
3.130 | EVO |
| 329 |
A Weise, B Timmermann,
M Grabherr, M Werber, P Heyn, N Kosyakova, T
Liehr, H Neitzel, K Konrat, C
Bommer, C Dietrich, A Rajab, R Reinhardt, S
Mundlos, TH Lindner, K Hoffmann. High-throughput sequencing of microdissected chromosomal regions. Eur J Hum Genet 2010, 18:457–462 |
4.380 | M |
| 328 |
W Al Achkar, A Wafa, H
Mkrtchyan, F Moassas, T Liehr.
A rare case of chronic myeloid leukemia with secondary chromosomal changes including partial trisomy 17q21 to 17qter and partial monosomy of 16p13.3. Mol Cytogenet 2010, 3:6 |
4.380 | TCG |
| 327 |
H Mkrtchyan, M Gross, S
Hinreiner, A Polytiko, M Manvelyan, K Mrasek,
N Kosyakova, E Ewers, H Nelle, T Liehr,
M Volleth, A Weise. Early embryonic chromosome instability results in stable mosaic pattern in human tissues. PLoS ONE 2010, 5: e9591 |
4.411 | CG |
| 326 |
A Polityko, O Khurs, N
Rumyantseva, I Naumchik, N Kosyakova, H
Tönnies, K Sperling, H Neitzel, A Weise, T
Liehr. Two siblings with immunodeficiency, facial abnormalities and chromosomal instability without mutation in DNMT3B gene but liability towards malignancy; a new chromatin disorder delineation? Mol Cytogenet 2010, 3:5 |
n.a. | CG |
| 325 |
K Mrasek, C Schoder, AC
Teichmann, K Behr, B Franze, K Wilhelm, N
Blaurock, U Claussen, T Liehr,
A Weise. Global screening and extended nomenclature for 230 aphidicolin-inducible fragile sites, including 61 yet unreported ones. Int J Oncol 2010, 36:929-940 |
2.571 | INT CG |
| 324 |
JC Barber, D Bunyan, M
Curtis, D Robinson, S Morlot, A Dermitzel, T
Liehr, C Alves, J Trindade, AI
Paramos, C Cooper, K Ocraft, E Taylor, VK
Maloney. 8p23.1 duplication syndrome differentiated from copy number variation of the defensin cluster at prenatal diagnosis in four new families. Mol Cytogenet 2010, 3:3 |
n.a. | CG |
| 323 |
H Mkrtchyan, DR Garcia
Ney, ES de Ventura, T Liehr, GR
Felix, T de Jesus Marques-Salles, E Abdelhay,
ML Macedo Silva. Molecular cytogenetic studies characterize near-triploid complex karyotype in a child with acute lymphoblastic leukemia. Cancer Genet Cytogenet 2010, 197:71-74 |
1.551 | TCG |
| 322 |
C Schoder, T
Liehr, E Velleuer, K Wilhelm, N
Blaurock, A Weise, K Mrasek. New aspects on chromosomal instability: Chromosomal break-points in Fanconi anemia patients co-localize on the molecular level with fragile sites. Int J Oncol 2010;36:307-312 |
2.571 | INT |
| 321 |
FE da Silva, AB
Cordeiro, CY Nagamachi, JC Pieczarka, W Rens,
A Weise, T Liehr, H Mkrtchyan,
NP Anselmo, EHC de Oliveira. A case of aggressive medulloblastoma with multiple recurrent chromosomal alterations. Cancer Genet Cytogenet 2010; 196:198-200 2.571 |
2.571 | TCG |
| 78% of publications of Institute of Human Genetics Jena in the actual year | |||
| Number |
Authors/
Title/ Where Contribution was Published |
Impact Factor | Topic |
| 320 |
T
Liehr. PWG: Marker chromosomes. ECA newsletter 2009, 25: 23 |
n.a. | sSMC |
| 319 |
A
Weise, T Liehr, B Fritz, K
Schubert, S Neubauer. Überarbeitung der Leitlinie Molekularzytogenetische Labordiagnostik. Med Genetik 2009, 21: 539-542 |
n.a. | other |
| 318 |
T
Liehr. PWG: Marker chromosomes; Permanent working groups (PWGs) report of ECA meeting 2009. ECA newsletter 2009, 24: 9-10 |
n.a. | sSMC |
| 317 |
J
Barber, T Liehr. Molecular Cytogenetics; a new open access journal. ECA-Newsletter, 24: 41 |
n.a. | others |
| 316 |
T
Liehr. In memoriam Prof. Dr. med. Uwe Claussen (* 30.04.1945 † 20.07.2008). ECA-Newsletter 2009, 23: 33 |
n.a. | others |
| 315 |
T
Liehr, J Crolla. Announcement of the permanent working group (PWG) Marker chromosomes meeting. ECA-Newsletter 2009, 23; 31 |
n.a. | sSMC |
| 314 |
H Mkrtchyan, S Scheler,
I Klein, A Fahr, P-O Couraud, IA Romero, B
Weksler, T Liehr. Molecular cytogenetic characterization of the human cerebral microvessel endothelial cell line hCMEC/D3. Cytogenet Genome Res 2009; 126:313-317 |
1.729 | CG |
| 313 |
A Polityko, O Khurs, T
Liehr. Human genomic disorders. Analysis of 22q11. Proceedings of the Institute of Genetics and Cytology of National Academy of Sciences Belarus, Minsk, Special issue „Molecular and applied genetics“ 2009; 10:80-88 (in Russian) |
n.a. | CG |
| 312 |
Y Soysal, S Balci, K
Hekimler, T Liehr, E Ewers, J
Schoumans, TH Bui, FM Içduygu, N Kosyakova, N
Imirzalıoğlu. Characterization of double ring chromosome 4 mosaicism associated with bilateral hip dislocation, cortical dysgenesis, and epilepsy. Am J Med Gen A 2009;149A:2782-2787 |
2.404 | CG |
| 311 |
F Sheth, E Ewers, N
Kosyakova, A Weise, J Sheth, M Desai, J
Andrieux, J Vermeesch, AB Hamid, M Ziegler, T
Liehr. A small supernumerary marker chromosome present in a Turner syndrome patient not derived from X- or Y-chromosome. Mol Cytogenet 2009; 2:22 |
n.a. | sSMC |
| 310 |
W Al Achkar, A Wafa, H
Mkrtchyan, F Moassass, T Liehr.
Novel complex translocation involving 5 different chromosomes in a chronic myeloid leukemia with Philadelphia chromosome: a case report. Mol Cytogenet 2009; 2:21 |
n.a. | TCG |
| 309 |
T Liehr.
Small supernumerary marker chromosomes (sSMC) – a spotlight on some nomenclature problems. J Histochem Cytochem 2009; 57:991-993 |
2.372 | sSMC |
| 308 |
JB Melo, E Matoso, A
Polityko, J Saraiva, L Backx, JR Vermeesch, N
Kosyakova, E Ewers, T Liehr, IM
Carreira. Molecular cytogenetic characterization of two cases with a small supernumerary marker chromosome derived from chromosome 16: Towards a genotype/phenotype correlation. Cytogenet Genome Res 2009; 125:109-114 |
1.729 | sSMC |
| 307 |
F Sheth, E Ewers, N
Kosyakova, A Weise, J Sheth, S Patil, M
Ziegler, T Liehr. A neocentric isochromosome Yp present as additional small supernumerary marker chromosome – evidence against U-type exchange mechanism? Cytogenet Genome Res 2009; 125:115-116 |
1.729 | sSMC |
| 306 |
E Manolakis, A Vetro, S
Kitmirides, I Papoulidis, N Kosyakova, K
Mrasek, A Weise, E Agapitos, S Orru, P
Peitsidis, T Liehr, MB
Petersen. Prenatal diagnosis, of a fetus with ring chromosome 15 characterized by array-CGH. Prenat Diag 2009; 29:884-888 |
1.707 | CG |
| 305 |
A Faria de Figueiredo,
H Mkrtchyan, T Liehr, EM Soares
Ventura, T de Jesus Marques-Salles, N Santos,
R Corrêa Ribeiro, E Abdelhay, ML Macedo Silva.
A case of childhood acute myeloid leukemia AML (M5) with a neocentric chromosome neo(1)(qter->q23~24::q23~24->qter) and tetrasomy 8 and 21. Cancer Genet Cytogenet 2009; 193:123-126 |
1.537 | TCG |
| 304 |
M Manvelyan, P Kempf, A
Weise, K Mrasek, A Heller, A Lier, K Höffken,
H-J Fricke, HG Sayer, T Liehr,
H Mkrtchyan. Preferred co-localization of chromosome 8 and 21 in myeloid bone marrow cells detected by three dimensional molecular cytogenetics. Int J Mol Med 2009; 24:335-341 |
1.980 | TCG INT |
| 303 |
AD Polityko, OM Khurs,
AI Kulpanovich, KA Mosse, AV Solntsava, NV
Rumyantseva, IV Naumchik, T Liehr,
A Weise, H Mkrtchyan. Paternally derived der(7)t(Y;7)(p11.1~11.2;p22.3)dn in a mosaic case with Turner syndrome. Europ J Med Gen 2009; 52:207–210 |
1.568 | CG |
| 302 |
E Ergul, T Liehr,
K Mrasek, A Sazci. A de novo complex chromosome rearrangement involving three chromosomes (2, 13, and 18) in an oligospermic male. Fertil Steril 2009; 92:391.e9-391.e12 |
3.970 | CG |
| 301 |
L Uroz, T Liehr,
K Mrasek, C Templado. Centromere-specific multicolour fluorescence in situ hybridization on human spermatocyte I and II metaphases. Hum Reprod 2009; 24:2029-2033. |
3.859 | CG |
| 300 |
D Aktas, A Weise, E
Utine, D Alehan, K Mrasek, F v Eggeling, H
Thieme, E Tuncbilek, T Liehr. Clinically abnormal case with paternally derived partial trisomy 8p23.3 to 8p12 including maternal isodisomy of 8p23.3: a case report. Mol Cytogenet 2009; 2:14 |
3.705 | CG UPD |
| 299 |
A Weise, K Mrasek, E
Ewers, H Mkrtchyan, N Kosyakova, T
Liehr. Diagnostic applications of fluorescence in situ hybridization. Expert Opin Med Diagn 2009, 3: 453-460 |
3.705 | M |
| 298 |
IY Iourov, SG
Vorsanova, T Liehr, AD Kolotii,
YB Yurov. Increased chromosome instability dramatically disrupts neural genome integrity and mediates cerebellar degeneration in the ataxia-telangiectasia brain. Hum Mol Genet 2009 18(14):2656-2669 |
7.386 | INT CG |
| 297 |
A Tzschach, C Ramel, A
Kron, B Seipel, C Wüster, U Cordes, T
Liehr, M Hoeltzenbein, C Menzel,
HH Ropers, R Ullmann, V Kalscheuer, J Decker,
D Steinberger. Hypergonadotropic hypogonadism in a patient with inv ins (2;4). Int J Androl 2009; 32:226-230 |
3.705 | CG |
| 296 |
J Erlecke, I Hartmann,
M Hoffmann, T Kroll, H Starke, A Heller, A
Gloria, HG Sayer, T Johannes, U Claussen, T
Liehr, IF Loncarevic. Automated detection of residual cells after sex-mismatched stem-cell transplantation - evidence for presence of disease-marker negative residual cells. Mol Cytogenet 2009; 2:12 |
n.a. | CG M |
| 295 |
T Liehr,
E Ewers, N Kosyakova, V Klaschka, F Rietz, R
Wagner, A Weise. Handling small supernumerary marker chromosomes in prenatal diagnostics. Expert Rev Mol Diagn 2009; 9:317-324 |
3.693 | sSMC |
| 294 |
IY Iourov, SG
Vorsanova, T Liehr, YB Yurov. Aneuploidy in the normal, Alzheimer's disease and ataxia-telangiectasia brain: differential expression and pathological meaning. Neurobiol Dis 2009; 34:212–220 |
4.518 | CG |
| 293 |
T Liehr,
M Stumm, R-D Wegner, S Bhatt, P Hickmann, PC
Patsalis, M Meins, S Morlot, V Klaschka, E
Ewers, S Hinreiner, K Mrasek, N Kosyakova, WW
Cai, SW Cheung, A Weise. 10p11.2 to 10q11.2 is a yet unreported region leading to unbalanced chromosomal abnormalities without phenotypic consequences. Cytogenet Genome Res 2009;24:102-105 |
1.729 | HET |
| 292 |
AP Cordeiro, FPE da
Silva, JC Pieczarka, CY Nagamachi, NP Anselmo,
JR Brito, DS Vasconcelos, T Liehr,
A Weise, EHC de Oliveira. Comparative analysis of proliferative and genetic alterations in a primary chordoid meningioma and its recurrent case using locus-specific probes and AgNOR. Mol Med Rep 2009; 2:449-454 |
0.220 | TCG |
| 291 |
H Aurich, M Sgodda, P
Kaltwaßer, M Vetter, A Weise, T Liehr,
M Brulport, JG Hengstler, MM Dollinger, WE
Fleig, B Christ. Hepatocyte differentiation of mesenchymal stem cells from human adipose tissue in vitro promotes hepatic integration in vivo. Gut 2009; 58:570-5811 |
9.357 | CG |
| 290 |
B Auber, V Bruemmer, B
Zoll, P Burfeind, D Boehm, T Liehr,
K Brockmann, E Willichowski, L Argyriou, I
Bartels. Identification of subtelomeric genomic imbalances and breakpoint mapping with quantitative PCR in 296 individuals with congenital defects and/or mental retardation. Mol Cytogenet. 2009; 2:10 |
n.a. | CG M |
| 289 |
ML Macedo Silva, M do
Socorro Pombo-de-Oliveira, SC Raimondi, T
Liehr, E Abdelhay, A Faria de
Figueiredo, M Tavares de Souza, D Ribeiro Ney
Garcia, E Maria Soares de Ventura, A Martins
de Sousa, H Mkrtchyan. Unbalanced chromosome 1 abnormalities in four infants with Down syndrome and acute megakaryocytic leukemia. Mol Cytogenet 2009; 2:7 |
n.a. | TCG |
| 288 |
T de Jesus
Marques-Salles, T Liehr, H
Mkrtchyan, SC Raimondi, M Tavares de Souza, A
Faria de Figueiredo, S Rouxinol, FC Jordy
Macedo, E Abdelhay, N Santos, ML Macedo Silva.
A new chromosomal three-way rearrangement involving MLL masked by a t(9;19)(p11;p13) in an infant with acute myeloid leukemia FAB-M5. Cancer Genet Cytogenet 2009, 189:59-62 |
1.537 | TCG |
| 287 |
N Kosyakova, A Weise, K
Mrasek, U Claussen, T Liehr, H
Nelle. The hierarchically organized splitting of chromosomal bands for all human chromosomes. Mol Cytogenet 2009, 2:4 |
n.a. | INT |
| 286 |
M Gross, H Mkrtchyan, M
Glaser, HJ Fricke, K Höffken, A Heller, A
Weise, T Liehr. Delineation of yet unknown cryptic subtelomere aberrations in 50% of acute myeloid leukemia with normal GTG-banding karyotype. Int J Oncol 2009, 34:417-423 |
2.447 | TCG |
| 285 |
S Kitsiou-Tzeli, E
Manolakos, M Lagou, K Anagnostopoulou, M
Kontodiou, N Kosyakova, E Ewers, A Weise, A
Garas, S Orru, T Liehr, A
Metaxotou. Characterization of a prenatally assessed de novo supernumerary minute ring chromosome 20 in a phenotypically normal male. Mol Cytogenet 2009, 2:8 |
n.a. | sSMC |
| 284 |
T
Liehr. The internet page on small supernumerary marker chromosomes (sSMC). ECA Newsletter 2009, 23:10-14 |
n.a. | sSMC |
| 283 |
S Bhatt, K Moradkhani,
K Mrasek, J Puechberty, M Manvelyan, F
Hunstig, G Lefort, A Weise, J Lespinasse, P
Sarda, T Liehr, S Hamamah, F
Pellestor. Breakpoint mapping and complete analysis of meiotic segregation patterns in three men heterozygous for paracentric inversions. Eur J Hum Genet 2009, 17:44–50 |
3.564 | CG |
| 62% of publications of Institute of Human Genetics Jena in the actual year | |||
2008
| Number |
Authors/
Title/ Where Contribution was Published |
Impact
Factor |
Topic |
| 282 |
T
Liehr, F v Eggeling. In memoriam Professor Dr. Uwe Claussen (*30.04.1945, † 20.07.2008). Ärtzeblatt Thüringen 2008, 9: 494-495 |
n.a. |
other |
| 281 |
T Liehr, R-D Wegner, M Stumm, G
Joksi, A Polityko, N Kosyakova, E Ewers, D
Reich, R Wagner, A Weise. Pallister-Killian syndrome. Rare phenotypic features and variable karyotypes. Balk J Med Gen 2008; 11:65-67 |
n.a. |
sSMC |
| 280 |
GG Hovhannisyan, H Mkrtchyan, T Liehr,
R Aroutiounian. Distribution of the chromosomes X, 7 and 18 in mitomycin C induced micronuclei. Balk J Med Gen 2008; 11:45-49 |
n.a. |
CG |
| 279 |
T Liehr. Multicolor-fluorescence in situ hybridization - Molecular cytogenetics in nowadays diagnostics and research. Med Gen 2008, 20:374-378 (German) |
n.a. |
M |
| 278 |
M Manvelyan, F
Hunstig, S Bhatt, K Mrasek, F Pellestor, A
Weise, I Simonyan, R Aroutiounian, T
Liehr. Chromosome distribution in human sperm - a 3D multicolor banding-study. Mol Cytogent 2008, 1:25 |
n.a. |
INT |
| 277 |
E Manolakos, N
Kosyakova, L Thomaidis, R Neroutsou, A Weise,
M Mihalatos, S Orru, H Kokotas, G Kitsos, T
Liehr, MB Petersen. Complex chromosome rearrangement in a child with microcephaly, dysmorphic facial features and mosaicism for a terminal deletion del(18)(q21.32-qter) investigated by FISH and array-CGH: Case report. Mol Cytogenet 2008, 1:24 |
n.a. |
CG |
| 276 |
T
Liehr. The multicolor fluorescence in situ hybridization (mFISH) homepage. Balk J Med Gen 2008; 11:27-31 |
n.a. |
M |
| 275 |
K Mrasek, G Krüger, I
Bauer, J Müller-Navia, T Liehr, A Weise. A new unbalanced chromosomal abnormality in 1q31.1 to 1q32 without phenotypic consequences. Cytogenet Genome Res 2008, 121:286-287 |
1.965 |
HET |
| 274 |
IY Iourov, SG
Vorsanova, T Liehr, VV
Monakhov, IV Soloviev, YB Yurov. Dynamic mosaicism manifesting as loss, gain and rearrangement of an isodicentric Y chromosome in a male child with growth retardation and abnormal external genitalia. Cytogenet Genome Res 2008, 121:302-306 |
1.965 |
CG |
| 273 |
J Lian, Y Yin, M
Oliver-Bonet, T Liehr, E Ko, P
Turek, F Sun, R H Martin. Variation in crossover interference levels on individual chromosomes from human males. Hum Mol Gen 2008, 17:2583-2594 |
7.249 |
CG |
| 272 |
AD Polityko, GI Lazjuk, T Liehr.
High resolution molecular cytogenetic approaches and study of marker chromsomes. Medica Genetics 2008, 7:34-40. |
n.a. |
sSMC |
| 271 |
A Weise, T
Liehr. Fluorescence in situ hybridization for prenatal screening of chromosomal aneuploidies. Expert Rev Mol Diagn 2008, 8:355-357 |
3.472 |
PRE CG |
| 270 |
SG Vorsanova, IY
Iourov, VY Voinova-Ulas, A Weise, VV Monakhov,
AD Kolotii, IV Soloviev, PV Novikov, T
Liehr, YB Yurov. Partial monosomy 7q34-qter and 21pter-q22.13 due to cryptic unbalanced translocation t(7;21) but not monosomy of the whole chromosome 21: a case report plus review of the literature. Mol Cytogenet 2008, 1:13 |
n.a. |
CG |
| 269 |
T Pramparo, M de
Gregori, S Gimelli, R Ciccone, D Frondizi, T
Liehr, S Pellacani, G Masi, P
Brovedani, O Zuffardi, R Guerrini. A 7 Mb duplication at 22q13 in a girl with bipolar disorder and hippocampal malformation. Am J Med Genet A. 2008, 146A:1754-1760. |
2.555 |
CG |
| 268 |
H Mkrtchyan, S
Ghazaryan, G Avetisyan, A Hovhannisyan, L
Muradyan, S Daghbashyan, C Karst, M Gross, S
Hinreiner, R Aroutiounian, T Liehr.
Novel complex t(V;9;22) rearrangements in three cases with chronic myeloid leukemia and a rare translocation in a case with classical Philadelphia chromosome. Oncol Reports 2008, 20:99-104 |
1.524 |
TCG |
| 267 |
T Liehr,
K Mrasek, N Kosyakova, C Mackie Ogilvie, J
Vermeesch, V Trifonov, N Rubtsov. Small supernumerary marker chromosomes (sSMC) in humans. Are there B chromosomes hidden among them? Mol Cytogenet 2008; 1:12 |
n.a. |
sSMC |
| 266 |
M Manvelyan, M Riegel,
M Santos, C Fuster, F Pellestor, M-L Mazauric,
B Schulze, A Polityko, H Tittelbach, G
Reising-Ackermann, B Belitz, U Hehr, C
Kelbova, M Volleth, E Gödde, J Anderson, P
Küpferling, S Köhler, H-C Duba, A Dufke, D
Aktas, T Martin, I Schreyer, E Ewers, D Reich,
K Mrasek, A Weise, T Liehr. 32 new cases with small supernumerary marker chromosomes (sSMC) detected in connection with fertility problems – detailed molecular cytogenetic characterization and review of the literature. Int J Mol Med 2008, 21:705-714 |
1.880 |
sSMC |
| 265 |
M Manvelyan, F
Hunstig, K Mrasek, S Bhatt, F Pellestor, A
Weise, T Liehr. Position of chromosomes 18, 19, 21 and 22 in 3D-preserved interphase nuclei of human and gorilla and white hand gibbon. Mol Cytogenet 2008, 1:9 |
n.a. |
EVO |
| 264 |
A Koç, D Kan, K
Karaer, MA Ergün, K Gücüyener, S Hinreiner, T
Liehr, EF Perçin. An unexpected finding in a child with neurological problems: Mosaic Ring Chromosome 18. Europ J Pediatrics 2008, 167:655–659 |
1.416 |
CG |
| 263 |
A Weise, K Mrasek, I
Fickelscher, U Claussen, SW Cheung, WW Cai, T
Liehr, N Kosyakova. Molecular definition of high resolution multicolor banding (MCB) probes – first within the human DNA-sequence anchored FISH-banding probe set. J Histochem Cytochem 2008, 56:487-493 |
2.823 |
M |
| 262 |
V Trifonov, S Fluri, F
Binkert, A Nandini, J Andersen, L Rodriguez, M
Gross, N Kosyakova, H Mkrtchyan, E Ewers, D
Reich, A Weise, T Liehr. Three new cases of complex rearranged small supernumerary marker chromosomes. Evidence for an underestimated entity? Mol Cytogenet 2008, 1:6 |
n.a. |
sSMC |
| 261 |
L Rodriguez, T
Liehr, ML Martinez-Fernandez, A
Lara, A Torres, ML Martinez-Frias. A new small supernumerary marker chromosome, generating mosaic pure trisomy 16q11.1-q12.1 in a healthy man. Mol Cytogenet 2008, 1:4 |
n.a. |
sSMC |
| 260 |
YB Yurov, T
Liehr, LG Shaffer, IY Iourov, SG
Vorsanova. A new open access journal for a rapidly evolving biomedical field: introducing Molecular Cytogenetics. Mol Cytogenet 2008, 1:1 |
n.a. |
other |
| 259 |
MLM Silva, SC
Raimondi, E Abdelhay, M Gross, H Mkrtchyan, A
F de Figueiredo, RC Ribeiro, TdJ
Marques-Salles, ES Sobral, MPG Land, T
Liehr. Banding and molecular cytogenetic studies detected a CBFß-MYH11 fusion gene that appeared as abnormal chromosomes 1 and 16 in a baby with acute myeloid leukemia FAB M4-Eo. Cancer Genet Cytogenet 2008, 182:56-60 |
1.482 |
TCG |
| 258 |
A Weise, M Gross, K
Mrasek, H Mkrtchyan, B Horsthemke, C Jonsrud,
F von Eggeling, S Hinreiner, V Witthuhn, U
Claussen, T Liehr. Parental-origin-determination fluorescence in situ hybridization distinguishes homologous human chromosomes on a single-cell level. Int J Mol Med 2008, 21:189-200 |
1.880 |
M UPD |
| 257 |
I Balikova, K Martens,
C Melotte, M Amyere, S Van Vooren, Y Moreau, D
Vetrie, H Fiegler, NP Carter, T Liehr,
M Vikkula, G Matthijs, JP Fryns, I Casteels, K
Devriendt, JR Vermeesch. Autosomal-dominant microtia linked to five tandem copies of a copy-number-variable region at chromosome 4p16. Am J Hum Genet 2008, 82:181-187. |
10.153 |
CG |
| 256 |
YB Yurov, IY Iourov,
SG Vorsanova, IA Demidova, VS Kravetz, AK
Beresheva, AD Kolotii, VV Monakhov, NA
Uranova, VM Vostrikov, IV Soloviev, T
Liehr. The schizophrenia brain exhibits low-level mosaic aneuploidy involving chromosome 1. Schizophr Res 2008, 98:139-147 |
4.174 |
CG INT |
| 56% of publications of Institute of Human Genetics Jena in the actual year | |||
2007
| Number |
Authors/
Title/ Where Contribution was Published |
Impact Factor | Topic |
| 255 |
T
Liehr, A Weise. Neuer Ansatz zum Studium epigenetischer Veränderungen bei der akuten myeloischen Leukämie. Leukämie Rundbrief 2007 Vol 11, pp 8-9. |
n.a. | TCG |
| 254 |
T
Liehr. PWG: Marker chromosomes; Permanent working groups (PWGs) report of ECA meeting 2007. ECA newsletter 2007 Vol 20, pp 8-9. |
n.a. | sSMC |
| 253 |
T
Liehr, H Tönnies, L Rodriguez, M
Hulten. Supernumerary Ring 1. Leaflet published in 2007 by UNIQUE, Rare Chromosome Disorder Support Group |
n.a. | sSMC |
| 252 |
T
Liehr. Small supernumerary marker chromosomes. Leaflet published in 2007 by UNIQUE, Rare Chromosome Disorder Support Group |
n.a. | sSMC |
| 251 |
T
Liehr, J Crolla. Announcement of the new permanent working group (PWG) Marker chromosomes. ECA newsletter 2007, 19: 31 |
n.a. | sSMC |
| 250 |
T Liehr,
K Mrasek, S Hinreiner, D Reich, E Ewers, I
Bartels, J Seidel, E Manolakos, M Petersen, A
Polityko, A Dufke, I Iourov, V Trifonov, J
Vermeesch, A Weise. Small supernumerary marker chromosomes (sSMC) in patients with a karyotype 45,X/46,X,+mar – 17 new cases and a review of the literature. Sex Dev 2007, 1:353-362 |
n.a. | sSMC |
| 249 |
F Sun, M Oliver-Bonet,
T Liehr, H Starke, E Ko, A
Rademaker, RH Martin. Discontinuities and unsynapsed regions in meiotic chromosomes have a trans effect on meiotic recombination of some chromosomes in human males. Cytogenet Genome Res 2007, 119:27-32 |
2.402 | CG |
| 248 |
T Felka, J Lemke, C
Lemke, S Michel, T Liehr, U
Claussen. DNA degradation during maturation of erythrocytes—molecular cytogenetic characterization of Howell–Jolly bodies. Cytogenet Genome Res 2007, 119:2-8 |
2.402 | CG |
| 247 |
NP Bochkov, ES
Voronina, NV Kosyakova, T Liehr,
AA Rzhaninova, LD Katosova, VI Platonova, DV
Goldshtein. Chromosome variability of human multipotent mesenchymal stromal cells. Bull Exp Biol Med 2007, Vol 143, pp 122-126. – also in Kletochnye Tehnologii v Biologii i Medicine 2007, 1:11-15 (in Russian) |
n.a. | CG |
| 246 |
M Santos, K Mrasek, MA
Rigola, H Starke, T Liehr, C
Fuster. Identification of a “cryptic mosaicism” involving at least 4 different small supernumerary markers, derived from chromosome 9, in a woman without reproductive success. Fertil Steril 2007, 88:969.e11-7 |
3.168 | sSMC |
| 245 |
I Carreira, A
Mascarenhas, E Matoso, A Couceiro, L Ramos, A
Dufke, M Mazauric, R Stressig, N Kosyakova, J
Melo, T Liehr. Three unusual but cytogenetically similar cases with up to five different cell lines involving structural and numerical abnormalities of chromosome 18. J Histochem Cytochem 2007, 55:1123-1128 |
2.335 | CG |
| 244 |
L Rodríguez, T
Liehr, K Mrasek, E Mansilla, ML
Martínez-Fernández, G Ángel, ML
Martínez-Frías. First inherited small supernumerary chromosome marker generating complete trisomy 18p, characterized by molecular cytogenetic techniques and review. Am J Med Gen A 2007, 143:2727-2732 |
2.440 | sSMC |
| 243 |
S Bhatt, K Moradkhani,
K Mrasek, J Puechberty, G Lefort, J
Lespinasse, P Sarda, T Liehr, S
Hamamah, F Pellestor. Breakpoint characterization: a new approach for segregation analysis of paracentric inversion in human sperm. Mol Hum Reprod 2007, 13:751-756 |
2.871 | CG |
| 242 |
T Liehr,
GE Utine, U Trautmann, A Rauch, A Kuechler, J
Pietrzak, E Bocian, N Kosyakova, K Mrasek, K
Boduroglu, A Weise, D Aktas. Neocentric small supernumerary marker chromosomes (sSMC) - three more cases plus review of the literature. Cytogenet Genome Res 2007, 118:31-37 |
2.402 | sSMC |
| 241 |
IY Iourov, T
Liehr, SG Vorsanova, YB Yurov. Interphase chromosome-specific multicolor banding (ICS-MCB): a new tool for analysis of interphase chromosomes in their integrity. Biomolecul Engineer 2007, 24:415-417 |
4.246 | INT M |
| 240 |
I Fickelscher, T
Liehr, K Watts, V Bryant, JCK
Barber, R Siebert, S Heidemann, JM Hertz, Z
Tümer, NS Thomas. The variant inv(2)(p11.2q13) is a genuinely recurrent rearrangement but displays some breakpoint heterogeneity. Am J Hum Gen 2007, 81:847-856 |
11.092 | HET |
| 239 |
GE Utine, D Aktas, Y
Alanay, S Gücer, E Tuncbilek, K Mrasek, T
Liehr. Distal partial trisomy 1q: report of two cases and a review of the literature. Prenat Diagn 2007, 27:865-871 |
1.319 | CG |
| 238 |
J Mattes, B Whitehead,
T Liehr, I Wilkinson, J Bear, K
Fagan, P Craven, B Bennett, M Edwards. Paternal uniparental isodisomy for chromosome 14 with a mosaicism for a supernumerary marker chromosome 14. Am J Med Gen A 2007, 143A:2165-2171 |
2.440 | sSMC |
| 237 |
I Fickelscher, H
Starke, E Schulze, G Ernst, N Kosyakova, H
Mkrtchyan, K MacDermont, N Sebire, T
Liehr. A further case with a small supernumerary marker chromosome (sSMC) derived from chromosome 1 – evidence for high variability in mosaicism in different tissues of sSMC-carriers. Prenat Diagn 2007, 27:783-785 |
1.319 | sSMC |
| 236 |
T
Liehr, V Trifonov, A Polityko, L
Brecevic, K Mrasek, A Weise, E Ewers, D Reich,
I Iourov, H Mkrtchyan, M Manvelyan, N
Kosyakova. Characterization of small supernumerary marker chromosomes (sSMC) by a simple molecular and molecular cytogenetics approach. Balk J Med Gen 2007, 10:33-37 |
n.a. | sSMC |
| 235 |
A Serra, HK Schackert,
B Mohr, A Weise, T Liehr, G
Fitze. t(11;19)(q21;p12 ~ p13.11) and MECT1-MAML2 fusion transcript expression as a prognostic marker in infantile lung mucoepidermoid carcinoma. J Pediatr Surg 2007, 42:e23-29 |
1.227 | TCG |
| 234 |
YB Yurov, IY Iourov, SG
Vorsanova, T Liehr, AD Kolotii,
SI Kutsev, F Pellestor, AK Beresheva, IA
Demidova, VS Kravets, VV Monakhov, IV
Soloviev. Aneuploidy and confined chromosomal mosaicism in the developing human brain. PLoS ONE 2007, 2:e558 |
n.a. | INT |
| 233 |
J Rosenhahn, A Weise, S
Michel, K Hennig, I Hartmann, J Schiefner, K
Schubert, T Liehr, F v
Eggeling, IF Loncarevic. Cytogenetic characterisation and proteomic profiling of the Imatinib-resistant cell line KCL22-R. Int J Onc 2007, 31:121-128 |
2.295 | TCG |
| 232 |
H Tönnies, J Pietrzak,
E Bocian, K MacDermont, A Kuechler, B Belitz,
U Trautmann, A Schmidt, B Schulze, L
Rodríguez, F Binkert, C Yardin, N Kosyakova, M
Volleth, H Mkrtchyan, I Schreyer, F von
Eggeling, A Weise, K Mrasek, T Liehr.
16 new immortalized cell lines of patients with small supernumerary marker chromosome (sSMC) – towards the establishment of a cell bank. J Histochem Cytochem 2007, 55:651-660 |
2.335 | sSMC |
| 231 |
J Pietrzak, K Mrasek, E
Obersztyn, P Stankiewicz, N Kosyakova, A
Weise, SW Cheung, WW Cai, F von Eggeling, T
Mazurczak, E Bocian, T Liehr. Molecular cytogenetic characterization of eight supernumerary marker chromosomes (sSMC) originating from chromosomes 2, 4, 8, 18, and 21 in three patients. J Appl Genet 2007, 48:167-175 |
0.967 | sSMC |
| 230 |
M Manvelyan, I
Schreyer, I Höls-Herpertz, S Köhler, R
Niemann, U Hehr, B Belitz, I Bartels, J Götz,
D Huhle, M Kossakiewicz, H Tittelbach, S
Neubauer, A Polityko, M-L Mazauric, R Wegner,
M Stumm, P Küpferling, F Süss, H Kunze, A
Weise, T Liehr, K Mrasek. 48 new cases with infertility due to balanced chromosomal rearrangements – detailed molecular cytogenetic analysis of the 90 involved breakpoints. Int J Mol Med 2007, 19:855-864 |
1.847 | CG |
| 219 |
SM Sauter, D Böhm, I
Bartels, P Burfeind, FA Laccone, J Neesen, B
Wilken, T Liehr, B Zoll. Partial trisomy of distal 19q detected by quantitative real-time PCR and FISH in a girl with mild facial dysmorphism, hypotonia and developmental delay. Am J Med Genet A 2007, 143A:1091-1099 |
2.440 | CG |
| 218 |
B Zoll, D Böhm, SM Sauter, T
Liehr, R Funke, B Auber, I Bartels,
P Burfeind. Subtelomere Rerrangements. Eine Ursache für geistige Behinderung? Kinder und Jugendarzt 2007, 38:236-243 |
n.a. | CG |
| 217 |
T Liehr,
A Weise. Frequency of small supernumerary marker chromosomes in prenatal, newborn, developmentally retarded and infertility diagnostics. Int J Mol Med 2007, 19:719-731 |
1.847 | sSMC |
| 216 |
I Bartels, H Starke, L
Argyriou, SM Sauter, B Zoll, T Liehr.
An exceptional complex chromosomal rearrangement (CCR) with 8 breakpoints involving four chromosomes (1;3;9;14) in an azoospermic male with normal phenotype. Europ J Med Gen 2007, 50:133-138 |
1.857 | CG |
| 215 |
M Glei, A
Schaeferhenrich, U Claussen, A Kuechler, T
Liehr, A Weise, B Marian, W Sendt,
BL Pool-Zobel. Comet fluorescence in situ hybridization analysis for oxidative stress-induced DNA damage in colon cancer relevant genes. Toxicol Sci 2007, 96:279-284 |
3.814 | TCG |
| 214 |
L Backx, H Van Esch, C
Melotte, N Kosyakova, H Starke, JP Frijns, T
Liehr, JR Vermeesch. Array painting using microdissected chromosomes to map chromosomal breakpoints. Cytogenet Genome Res 2007, 116:158-166 |
2.402 | sSMC M |
| 213 |
S Balci, A Ünal, D
Aktaş, Ö Engiz, T Liehr, M
Gross, K Mrasek, S Saygi. Bilateral periventricular nodular heterotopia (PNH), severe mental retardation and epilepsy in a male patient with 46,XY,der(19)t(X;19)(q11.1-11.2;p13.3) due to maternal balanced translocation. Develop Med Child Neurol 2007, 49:219-224 |
2.433 | CG |
| 212 |
J
Seidel, A Hübler, D Schlenvoigt, P Hilliges, M
Harbich, A Küchler, T Liehr, U
Claussen, E Kauf. Schwere Wachstumsretardierung bei Deletion des IGF1-Rezeptor-Gens. Praktische Pädiatrie 2007, 13:1-5 |
n.a. | CG |
| 211 |
A Weise, M Gross, S
Schmidt, U Claussen, T Liehr. New aspects of chromosomal evolution in gorilla and orangutan. Int J Mol Med 2007, 19:437-443 |
1.847 | EVO |
| 41% of publications of Institute of Human Genetics Jena in the actual year | |||
2006
| Number |
Authors/
Title/ Where Contribution was Published |
Impact Factor | Topic |
| 210 |
J Seidel, H Hübler, A
Küchler, M Harbich, P Hilliges, E Kauf, U
Claussen, T Liehr. Genetisch bedingte Wachstumsstörungen: Syndromatischer Kleinwuchs am Beispiel von Falldemonstrationen. Medreport 2006, 4: 9 |
n.a. |
CG |
| 209 |
E Papadopoulou, S
Sifakis, C Sarri, J Gyftodimou, T Liehr,
K Mrasek, M Kalmanti, MB Petersen. A case report of pure 7p duplication syndrome and review of the literature. Am J Med Gen A 2006, 140A:2802-2806 |
2.063 | CG |
| 208 |
F Sun, M Oliver-Bonet,
T Liehr, H Starke, P Turek, E
Ko, A Rademaker, RH Martin. Analysis of non-crossover bivalents in pachytene cells from 10 normal male. Hum Reprod 2006, 21:2335-2339. |
3.769 | CG |
| 207 |
D Mitter, K Buiting, F
von Eggeling, A Kuechler, T Liehr,
UA Mau-Holzmann, EC Prott, D Wieczorek, G
Gillessen-Kaesbach. Is there a higher incidence of maternal uniparental disomy 14 [upd(14)mat]? Detection of 10 new patients by methylation-specific PCR. Am J Med Genet A 2006, 140A:2039-2049 |
2.063 | CG UPD |
| 206 |
L Brecevic, S Michel, H
Starke, K Müller, N Kosyakova, K Mrasek, A
Weise, T Liehr. Multicolor FISH used for the characterization of small supernumerary marker chromosomes (sSMC) in commercially available immortalized cell lines. Cytogenet Genome Res 2006, 114:319-324 |
1.993 | sSMC |
| 205 |
H Mkrtchyan, M Glaser,
M Gross, U Wedding, K Höffken, T Liehr,
C Karst, R Aroutiounian. Multicolor-FISH applied to resolve complex chromosomal changes in a case of T-ALL (FAB L2). Cytogenet Genome Res 2006, 114:270-273 |
1.993 | TCG |
| 204 |
T Liehr,
H Starke H, A Heller, N Kosyakova, K Mrasek, M
Gross, C Karst, U Steinhaeuser, F Hunstig, I
Fickelscher, A Kuechler, V Trifonov, SA
Romanenko, A Weise. Multicolor fluorescence in situ hybridization (FISH) applied for FISH-banding. Cytogenet Genome Res 2006, 114:240-244 |
1.993 | M |
| 203 |
T
Liehr. Preface to the special issue Multicolor FISH in Human Cytogenetics. Cytogenet Genome Res 2006, 114:187-188 |
1.993 | M |
| 202 |
T Liehr.
Familial small supernumerary marker chromosomes are predominantly inherited via the maternal line. Genet Med 2006, 8:459-462 |
3.427 | sSMC |
| 201 |
F Sun, M Oliver-Bonet,
T Liehr, H Starke, P Turek, E
Ko, A Rademaker, RH Martin. Variation in MLH1 distribution in recombination maps for individual chromosomes from human males. Hum Mol Genet 2006, 15:2376-2391 |
8.099 | CG |
| 200 |
IY Iourov, T
Liehr, SG Vorsanova, AD Kolotii,
YB Yurov. Visualization of interphase chromosomes in postmitotic cells of the human brain by multicolour banding (MCB). Chromosome Res 2006, 14:223-229 |
3.057 | CG INT |
| 199 |
C Karst, M Gross, D
Haase, U Wedding, K Höffken, T Liehr,
H Mkrtchyan. Novel cryptic chromosomal rearrangements detected in acute lymphoblastic leukemia (ALL) detected by application of new multicolor fluorescent in situ hybridization approaches. Int J Onc 2006, 28:891-897 |
2.556 | TCG |
| 198 |
C Rudolph, T
Liehr, D Steinemann, M Emura, M
Daibata, Y Matsuo, N Emi, M Abe, R Lai, K
Mrasek, U Claussen, B Schlegelberger. Different breakage-prone regions on chromosome 1 detected in t(11;14)-positive mantle cell lymphoma cell lines and multiple myeloma cell lines are associated with different tumor progression-related mechanisms. Cytogenet Genome Res 2006, 112:213-221 |
1.993 | TCG |
| 197 |
S Balci, Ö Engiz, D
Aktaş, I Vargel, MS Beksaç, K Mrasek, T
Liehr. Ring chromosome 4 and Wolf-Hirschhorn syndrome (WHS) in a child with multiple malformations. Am J Med Gen 2006, 140A:628-632 |
2.063 | CG |
| 196 |
P Stankiewicz, A
Kuechler, CD Eller, T Sahoo, C Baldermann, U
Lieser, M Hesse, C Gläser, M Hagemann, SA
Yatsenko, T Liehr, B
Horsthemke, U Claussen, Y Marahrens, JR
Lupski, I Hansmann. Minimal phenotype in a girl with trisomy 15q due to t(X;15)(q22.3;q11.2) translocation - do LINE-1 elements facilitate spreading of X inactivation? Am J Med Gen 2006, 140A:442-452 |
2.063 | CG |
| 195 |
C Karst, V Trifonov, SA
Romanenko, U Claussen, K Mrasek, S Michel, P
Avner, T Liehr Molecular cytogenetic characterization of the mouse cell line WMP2 by spectral karyotyping (SKY) and multicolor banding (mcb) applying murine probes. Int J Mol Med 2006, 17:209-213 |
1.854 | TCG |
| 194 |
T Liehr,
M Gross, C Karst, M Glaser, H Mkrtchyan, K
Mrasek, H Starke, A Kuechler, A Weise. FISH-banding in tumor cytogenetics. Cancer Genet Cytogenet 2006, 164:88-89 |
1.544 | TCG |
| 193 |
T Liehr,
K Mrasek, A Weise, A Dufke, L Rodríguez, N
Martínez Guardia, A Sanchís, JR Vermeesch, C
Ramel, A Polityko, O Haas, J Anderson, U
Claussen, F von Eggeling, H Starke. Small supernumerary marker chromosomes - progress towards a genotype-phenotype correlation. Cytogenet Genome Res 2006, 112:23-34 |
1.993 | sSMC |
| 192 |
T Liehr,
H Starke, G Senger, C Melotte, A Weise, JR
Vermeesch. Overrepresentation of small supernumerary marker chromosomes (sSMC) from chromosome 6 origin in cases with multiple sSMC. Am J Med Gen 2006, 140A:46-51 |
2.063 | sSMC |
| 191 |
M Gross, H Starke, V
Trifonov, U Claussen, T Liehr,
A Weise. A molecular cytogenetic study of chromosome evolution in chimpanzee. Cytogenet Genome Res 2006, 112:67-75 |
1.993 | EVO |
| 40% of publications of Institute of Human Genetics Jena in the actual year | |||
2005
| Number |
Authors/
Title/ Where Contribution was Published |
Impact Factor | Topic |
| 190 |
T Liehr. Eine erste Genotyp-Phänotyp-Korrelation bei kleinen überzähligen Marker-Chromosomen (small supernumerary marker chromosomes = sSMC) des Menschen. Medgen 2005, 17:454-456 |
n.a. | sSMC |
| 189 |
M
Glaser, C Karst, M Gross, H Mkrtchyan, T
Liehr. Chromosome torsions in cytogenetic preparations of bone-marrow – artifacts or leukemia-specific? Balk J Med Gen 2005, 8:27-31 |
n.a. | TCG |
| 188 |
F Sun, M Oliver-Bonet,
T Liehr, H Starke, K Trpkov, E
Ko, A Rademaker, R H Martin. Discontinuities and unsynapsed regions in meiotic chromosomes have a cis effect on meiotic recombination patterns in normal human males. Human Molecular Genetics 2005, 14:3013-3018 |
7.764 | CG |
| 187 |
T Kautenburger, G
Beyer-Sehlmeyer, G Festag, N Haag, S Kuhler, A
Kuchler, A Weise, B Marian, WH Peters, T
Liehr, U Claussen, BL Pool-Zobel.
The gut fermentation product butyrate, a chemopreventive agent, suppresses glutathione S-transferase theta (hGSTT1) and cell growth more in human colon adenoma (LT97) than tumor (HT29) cells. J Cancer Res Clin Oncol 2005, 131:692-700 |
2.503 | TCG |
| 186 |
C Gutiérrez-Mateo, J
Benet, H Starke, M Oliver-Bonet, S Munné, T
Liehr, J Navarro. Karyotyping of human oocytes by cenM-FISH, a new 24-colour centromere-specific technique. Hum Reprod 2005, 20:3395-3401 |
3.669 | CG |
| 185 |
A Weise, T Liehr,
U Claussen, K-J Halbhuber. Increased efficiency of fluorescence in situ hybridization (FISH) using the microwave. J Histochem Cytochem 2005, 53:1301-1303 |
2.208 | M |
| 184 |
JC Barber, V Maloney,
EJ Hollox, A Stuke-Sontheimer, G du Bois, E
Daumiller, U Klein-Vogler, A Dufke, JA Armour,
T Liehr. Duplications and copy number variants of 8p23.1 are cytogenetically indistinguishable but distinct at the molecular level. Eur J Hum Genet 2005, 13:1131-1136 |
3.251 | CG |
| 183 |
JR Vermeesch, C
Melotte, I Salden, M Riegel, V Trifnov, A
Polityko, N Rumyantseva, I Naumchik, H Starke,
G Matthijs, A Schinzel, JP Fryns, T
Liehr. Tetrasomy 12pter-12p13.31 in a girl with partial Pallister-Killian syndrome phenotype. Eur J Med Genet 2005, 48:319-327 |
0.625 | sSMC |
| 182 |
T Pramparo, T Mattina,
S Gimelli, T Liehr, O Zuffardi.
Narrowing the deleted region associated with the 15q21 syndrome. Europ J Med Gen 2005, 48:346-352 |
0.625 | CG |
| 181 |
L Rodriguez, H Starke,
NM Guardia, H Tönnies, H Neitzel, P Kozlowski,
ML Mazauric, A Heller, FL Grondona, E
Mansilla, MJ Santos Munoz, T Liehr,
ML Martinez-Frias. Three new cases with a supernumerary ring chromosome 1. Clin Dysmorphol 2005, 14:169-175 |
0.667 | sSMC |
| 180 |
T Liehr,
K Mrasek, H Starke, U Claussen, G Schreiber. Unusual small supernumerary marker chromosome (sSMC) 9 in a Klinefelter patient. Cytogenet Genome Res 2005, 111:179-181 |
2.076 | sSMC |
| 179 |
A Polityko, H Starke, N
Rumyantseva, U Claussen, T Liehr,
S Raskin. Three cases with rare interstitial rearrangements of chromosome 1 characterized by multicolor banding. Cytogenet Genome Res 2005, 111:171-174 |
2.076 | CG |
| 178 |
ML Macedo Silva, M
Land, A Heller, E Abdelhay, M do Socorro
Pombo-de-Oliveira, K Ribeiro, G Alves, D
Lerner, T Liehr. New rearrangement t(3;17)(q26.3;q12) in an AML patient with a poor outcome. Oncol Rep 2005, 14:663-666 |
1.572 | TCG |
| 177 |
G von Beust, SM Sauter,
T Liehr, P Burfeind, I Bartels,
H Starke, F von Eggeling, B Zoll. Molecular cytogenetic characterization of a de novo supernumerary ring chromosome 7 resulting in partial trisomy, tetrasomy, and hexasomy in a child with dysmorphic signs, congenital heart defect, and developmental delay. Am J Med Gen 2005, 137:59-64 |
1.913 | sSMC |
| 176 |
C Karst, A Heller, U
Claussen, E Gebhart, T Liehr. Detection of cryptic chromosomal aberrations in the in vitro non-proliferating cells of acute myeloid leukemia. Int J Oncol 2005, 27:355-359 |
2.681 | TCG |
| 175 |
S Schmidt, U Claussen,
T Liehr, A Weise. Evolution versus constitution: Differences in chromosomal inversion. Hum Genet 2005, 117:213-219 |
4.331 | EVO |
| 174 |
V Trifonov, C Karst, U
Claussen, K Mrasek, S Michel, P Avner, T
Liehr. Microdissection derived murine mcb probes from somatic cell hybrids. J Histochem Cytochem 2005, 53:791-792 |
2.208 | M |
| 173 |
T Liehr,
E Brude, G Gillessen-Kaesbach, R König, K
Mrasek, F von Eggeling, H Starke. Prader-Willi syndrome with a karyotype 47,XY,+min(15)(pter->q11.1:) and maternal UPD 15 - case report plus review of similar cases. Europ J Med Genet 2005, 48:175-181 |
1.614 | sSMC UPD |
| 172 |
A Kuechler, M Ziegler,
C Blank, B Rommel, J Bullerdiek, J Ahrens, U
Claussen, T Liehr. A highly complex chromosomal rearrangement between five chromosomes in a healthy female diagnosed in preparation for ICSI. J Histochem Cytochem 2005, 53:355-357 |
2.208 | CG |
| 171 |
T Liehr,
M Ziegler. Rapid prenatal diagnostics in the interphase nucleus – procedure and cut-off rates. J Histochem Cytochem 2005, 53:289-291 |
2.208 | PRE CG |
| 170 |
M Trimborn, T
Liehr, B Belitz, L Pfeiffer, R
Varon, H Neitzel, H Tönnies. Prenatal diagnosis and molecular cytogenetic characterisation of a complex structural rearrangement in a pregnancy following intracytoplasmic sperm injection (ICSI). J Histochem Cytochem 2005, 53:351-354 |
2.208 | CG |
| 169 |
H Starke, K Mrasek, T
Liehr. 3 cases with enlarged acrocentric p-arms – 2 cases with cryptic partial trisomies. J Histochem Cytochem 2005, 53:359-360 |
2.208 | CG HET |
| 168 |
I Schreyer, A Neumann,
V Beensen, K-H Eichhorn, A Heller, U Claussen,
T Liehr. dup(13)(q14.2-q14.3) - yet another new differential diagnostic aspect for short stature like phenotype. J Histochem Cytochem 2005, 53:365-366 |
2.208 | CG |
| 167 |
K Mrasek, H Starke, T
Liehr. Another small supernumerary marker chromosome (sSMC) derived from chromosome 2 – towards a genotype/ phenotype correlation. J Histochem Cytochem 2005, 53:367-370 |
2.208 | sSMC |
| 166 |
T Liehr,
H-UG Weier. 14th Workshop on Fetal Cells and Fetal DNA. J Histochem. Cytochem 2005, 53:253-254 |
2.208 | CG |
| 165 |
JCK Barber, NS Thomas,
MN Collinson, NR Dennis, T Liehr,
A Weise, B Belitz, L Pfeiffer, M Kirchhoff, B
Krag-Olsen, C Lundsteen. Segmental haplosufficiency: transmitted deletions of 2p12 include a pancreatic regeneration gene cluster and have no apparent phenotypic consequences. Europ J Hum Gen 2005, 13:283-291 |
3.251 | CG |
| 164 |
M Oliver-Bonet, J
Benet, F Sun, J Navarro, C Abad, T
Liehr, H Starke, C Greene, E Ko,
RH Martin. Meiotic studies in two human reciprocal translocations and their association with spermatogenic failure. Human Reproduction 2005, 20:683-688 |
3.669 | CG |
| 163 |
A Weise, H Starke, K
Mrasek, U Claussen, T Liehr. New insights into the evolution of chromosome 1. Cytogenet Genome Res 2005, 108:217-222 |
2.076 | EVO |
| 56% of publications of Institute of Human Genetics Jena in the actual year | |||
2004
| Number |
Authors/
Title/ Where Contribution was Published |
Impact Factor | Topic |
| 162 |
T Liehr. 14. Fetal Cell Workshop. Down’s Screening News 2004, 11: 42 |
n.a. |
PRE |
| 161 |
T Liehr. 14. Workshop on fetal Cells and fetal DNA. ECA-newsletter 2004, 14: 16 |
n.a. | PRE |
| 160 |
T Liehr.
Pränataldiagnostik – Zwischen Gen-check und Ultraschall – Tagungsbericht. Uni-Journal Jena 2004, 07/04: 28 |
n.a. | PRE |
| 159 |
T Liehr. 14 Workshop on Fetal Cells and Fetal DNA – Tagungsbericht; Med Genetik 2004, 16: p132 |
n.a. | PRE |
| 158 |
T Liehr,
A Heller, KH Eichhorn, V Beensen, E Schulze, H
Starke, U Claussen, I Schreyer. Inherited cryptic chromosomal aberrations may be more easily detected in their balanced forms: a case report with hidden der(1)t(1;17)(q44;p13.2). Prenat Diagn 2004, 24:1022-1024 |
1.612 | CG |
| 157 |
E Gebhart, J Ries, J
Wiltfang, T Liehr, T Efferth. Genomic gain of the epidermal growth factor receptor harboring band 7p12 is part of a complex pattern of genomic imbalances in oral squamous cell carcinomas. Arch Med Res 2004, 35:385-394 |
1.286 | TCG |
| 156 |
A Polityko, O Maltseva,
N Rumyantseva, O Khurs, J Seidel, U Claussen,
A Weise, T Liehr, H Starke. Two further AHO-like syndrome patients with deletion of glypican 1 gene region in 2q37.2-q37.3. Int J Mol Med 2004, 14:977-979 |
3.190 | CG |
| 155 |
C Rudolph, D
Steinemann, N Von Neuhoff, D Gadzicki, T
Ripperger, HG Drexler, K Mrasek, T
Liehr, U Claussen, M Emura, E
Schröck, B Schlegelberger. Molecular cytogenetic characterization of the mantle cell lymphoma cell line GRANTA-519. Cancer Genet Cytogenet 2004, 153:144-150 |
1.577 | TCG |
| 154 |
W Zumkeller, M Volleth,
P Muschke, H Tönnies, A Heller, T Liehr,
P Wieacker, M Stumm. Genotype/phenotype analysis in a patient with pure and complete trisomy 12p. Am J Med Genet A 2004, 129A:261-264 |
0.815 | CG |
| 153 |
T Liehr,
U Claussen, H Starke. Small supernumerary marker chromosomes (sSMC) in humans. Cytogenet Genome Res 2004, 107:55-67 |
1.341 | sSMC |
| 152 |
H Lehrer, A Weise, S
Michel, H Starke, K Mrasek, A Heller, A
Kuechler, U Claussen, T Liehr.
The hierarchically organized splitting of chromosomal bands into sub-bands analyzed by multicolor banding (MCB). Cytogenet Genome Res 2004, 105:25-28 |
1.341 | INT |
| 151 |
M Codina-Pascual, M
Oliver-Bonet, J Navarro, H Starke, T
Liehr, C Gutierrez-Mateo, JF
Sanchez-Garcia, O Arango, J Egozcue, J Benet.
FISH characterization of a dicentric Yq (p11.32) isochromosome in an azoospermic male. Am J Med Genet A 2004, 127:302-306 |
0.815 | CG |
| 150 |
J Camps, K Mrasek, E
Prat, A Weise, H Starke, J Egozcue, R Miró, T
Liehr. Molecular cytogenetic characterisation of the colorectal cancer cell line SW480. Oncol Rep 2004, 11:1215-1218 |
1.356 | TCG |
| 149 |
U Keller, A Kuechler, T
Liehr, E Müller, G Grabenbauer, R
Sauer, L Distel. Impact of various parameters in detecting chromosomal aberrations by FISH to describe radiosensitivity. Strahlenther Onkol 2004, 180:289-296 |
3.121 | TCG |
| 148 |
T Liehr, K Mrasek, A Weise, A
Kuechler, F von Eggeling, U Claussen, H
Starke. Characterization of small supernumerary marker chromosomes (sSMC) in human. Current Genomics 2004, 5:279-286 |
n.a. | sSMC |
| 147 |
T Liehr,
G Hickmann, P Kozlowski, U Claussen, H Starke.
Molecular-cytogenetic characterization of the origin and presence of pericentromeric euchromatin on minute supernumerary marker chromosomes (SMCs). Chromosome Res 2004, 12:239-244 |
2.346 | sSMC |
| 146 |
D Boehm, S Herold, A
Kuechler, T Liehr, F Laccone. Rapid detection of subtelomeric deletion/duplication by novel real-time quantitative PCR using SYBR-green dye. Hum Mutat 2004, 23:368-378 |
6.845 | CG M |
| 145 |
F Sun, M Oliver-Bonet,
T Liehr, H Starke, E Ko, A
Rademaker, J Navarro, J Benet, RH Martin. Human male recombination maps for individual chromosomes. Am J Hum Genet 2004, 74:521-531 |
12.340 | CG |
| 144 |
T Liehr,
H Starke, A Weise, H Lehrer, U Claussen. Multicolor FISH probe sets and their applications. Histol Histopathol 2004, 19:229-237 |
1.931 | M |
| 143 |
A Heller, HJ Fricke, H
Starke, IF Loncarevic, U Claussen, T
Liehr. Characterization of a highly aberrant plasma cell leukemia karyotype: A case report. Oncol Rep. 2004, 11:89-92 |
1.356 | TCG |
| 142 |
A Heller, IF
Loncarevic, M Glaser, E Gebhart, U Trautmann,
U Claussen, T Liehr. Breakpoint differentiation in chromosomal aberrations of hematological malignancies: Identification of 33 previously unrecorded breakpoints. Int J Onc 2004, 24:127-136 |
3.056 | TCG |
| 66% of publications of Institute of Human Genetics Jena in the actual year | |||
2003
| Number |
Authors/
Title/ Where Contribution was Published |
Impact Factor | Topic |
| 141 |
U Grasshoff, S Singer,
T Liehr, H Starke, B Fode, M
Schoning, A Dufke. A complex chromosomal rearrangement with a translocation 4;10;14 in a fertile male carrier: ascertainment through an offspring with partial trisomy 14q24-->1q22 and partial monosomy 4q27-->q28. Cytogenet Genome Res 2003, 103:17-23 |
0.497 | CG |
| 140 |
T
Liehr, A Nietzel, A Weise, K
Mrasek, F von Eggeling, U Claussen, H Starke.
A strategy for the characterization of small supernumerary marker chromosomes (SMC). Balk J Med Gen 2003, 6:69-72 |
n.a. | sSMC |
| 139 |
A Weise, A Heller, H
Starke, K Mrasek, A Kuechler, BL Pool-Zobel, U
Claussen, T Liehr. Multitude multicolor chromosome banding (mMCB)- a comprehensive one-step multicolor FISH banding method. Cytogenet Genome Res 2003, 103:34-39. |
0.497 | M |
| 138 |
A Weise, O Rittinger, H
Starke, M Ziegler, U Claussen, T Liehr.
De novo 9-break-event in one chromosome 21 combined with a microdeletion in 21q22.11 in a mentally retarded boy with short stature. Cytogenet Genome Res 2003, 103:14-16 |
0.497 | CG |
| 137 |
H Starke, A Nietzel, A
Weise, A Heller, K Mrasek, B Belitz, C
Kelbova, M Volleth, B Albrecht, B Mitulla, R
Trappe, I Bartels, S Adolph, A Dufke, S
Singer, M Stumm, R-D Wegner, J Seidel, A
Schmidt, A Kuechler, I Schreyer, U Claussen, F
von Eggeling, T Liehr. Small supernumerary marker chromosomes (SMC): genotype-phenotype correlation and classification. Hum Genet 2003, 114:51-67 |
4.022 | sSMC |
| 136 |
E Gebhart, T
Liehr, E Wolff, J Wiltfang, S
Koscielny, J Ries. Loss of 9p21 is embedded in a complex but consistent pattern of genomic imbalances in oral squamous cell carcinomas. Cytogenet Genome Res 2003, 101:106-112 |
0.497 | TCG |
| 135 |
I Bartels, G Schlueter,
T Liehr, F von Eggeling, H
Starke, R Glaubitz, P Burfeind. Supernumerary small marker chromosome (SMC) and uniparental disomy 22 in a child with confined placental mosaicism of trisomy 22: Trisomy rescue due to marker chromosome formation. Cytogenet Genome Res 2003, 101:103-105 |
0.497 | CG |
| 134 |
M
Volleth, M Stumm, VM Kalscheuer, K Reschke, T
Liehr, P Wieacker. Prämature Ovarialinsuffizienz bei einer Patientin mit einem ungewöhnlichen pseudoisodizentrischen X-Chromosom. Geburtshilfe Frauenheilkd 2003, 63:1054-1057 |
n.a. | CG |
| 133 |
M Oliver-Bonet, T
Liehr, A Nietzel, A Heller, H
Starke, U Claussen, M Codina-Pascual, A Pujol,
C Abad, J Egozcue, J Navarro, J Benet. Karyotyping of human synaptonemal complexes by cenM-FISH. Europ J Hum Genet 2003, 11:879-883 |
3.669 | INT |
| 132 |
A Heller, V Trifonov, N
Rubtsov, A Sauerbrey, H Starke, IF Loncarevic,
U Claussen, T Liehr. Complex chromosomal rearrangements in a secondary acute myeloblastic leukemia after chemotherapy in TRAPS. Oncol Rep 2003, 10: 1789-1792 |
1.256 | TCG |
| 131 |
H Starke, B Mitulla, V
Beensen, V Trifonov, N Rubtsov, A Heller, M
Ziegler, A Neumann, U Claussen, T Liehr.
First postnatal case of mosaic del(22)/r(22). Prenat Diagn 2003, 23:765-767 |
1.475 | CG |
| 130 |
A Heller, L Brecevic, M
Glaser, I Loncarevic, E Gebhart, U Claussen, T
Liehr. Trisomy 8 as the sole chromosomal aberration in myelocytic malignacies: a comprehensive molecular cytogenetic analysis reveals no cryptic aberrations. Cancer Genet Cytogenet 2003, 146:81-83 |
1.542 | TCG |
| 129 |
F von Eggeling, S
Langer, C Hoppe, T Liehr, A
Weise, G Lederer, D Kotzot. Presumed mutation in a microsatellite marker mimicking segmental uniparental disomy in a case of a small supernumerary marker chromosome detected at prenatal diagnosis. Clin Genet 2003, 64:168-171 |
2.025 | sSMC UPD |
| 128 |
S Sauter, G von Beust,
P Burfeind, A Weise, H Starke, T Liehr,
B Zoll. Autistic disorder and chromosomal mosaicism 46,XY[123]/46,XY,del(20)(pter->p12.2)[10]. Am J Med Genet 2003, 120A:533-536 |
2.603 | CG |
| 127 |
RW Kinne, W Kunisch, V
Beensen, T Zimmermann, F Emmrich, P Petrow, W
Lungershausen, G Hein, RK Braun, M Foerster, C
Kroegel, R Winter, E Liesaus, RA Fuhrmann, A
Roth, U Claussen, T Liehr. Synovial fibroblasts and synovial macrophages from patients with rheumatoid arthritis and other inflammatory joint diseases show chromosomal aberrations. Genes Chromosomes Cancer 2003, 38:53-67 |
4.192 | CG |
| 126 |
T Liehr,
M Ziegler, H Starke, A Heller, A Kuechler, G
Kittner, V Beensen, J Seidel, H Häßler, J
Müsebeck, U Claussen. Conspicuous GTG banding results of the centromere near region can be caused by alphoid DNA heteromorphism. Clin Genet 2003, 64:166-167 |
2.025 | HET |
| 125 |
K Mrasek, A Heller, N
Rubtsov, V Trifonov, H Starke, U Claussen, T
Liehr. Detailed Hylobates lar karyotype defined by 25-color FISH and multicolor banding. Int J Mol Med 2003, 12:139-146 |
1.940 | EVO |
| 124 |
J Seidel J, A Heller,
G Senger, H Starke, I Chudoba, C Kelbova, H
Tonnies, H Neitzel, C Haase, V Beensen, F
Zintl, U Claussen, T Liehr. A multiple translocation event in a patient with hexadactyly, facial dysmorphism, mental retardation and behaviour disorder characterized comprehensively by molecular cytogenetics. Case report and review of the literature. Eur J Pediatr 2003, 162:582-588 |
1.157 | CG |
| 123 |
A Kuechler, M Dreidax,
SU Piegorsch, T Liehr, U
Claussen, TG Wendt, J Dunst. Residual chromosomal damage after radiochemotherapy with and without amifostine detected by 24-color FISH. Strahlenther Onkol 2003, 179:493-498 |
2.634 | TCG |
| 122 |
A Heller, N Rubtsov, S
Kytölä, TV Karamysheva, OV Sablina, MM
Degtyareva, H Starke, H Metzke, U Claussen, T
Liehr. Highly complex karyotypic changes in acute myelogenous leukemia: a case report. Int J Onc 2003, 23:139-143 |
2.536 | TCG |
| 121 |
V Trifonov, J Seidel, H
Starke, M Prechtel, V Beensen, M Ziegler, I
Hartmann, A Heller, A Nietzel, U Claussen, T
Liehr. Enlarged chromosome 13 p-arm hiding a cryptic partial trisomy 6p22.2-pter. Prenat Diagn 2003, 23:427-430 |
1.475 | CG |
| 120 |
A Schaeferhenrich, G
Beyer-Sehlmeyer, G Festag, A Kuechler, N Haag,
A Weise, T Liehr, U Claussen,
Marian, W Sendt, J Scheele, BL Pool-Zobel. Human adenoma cells are highly susceptible to the genotoxic action of 4-hydroxy-2-nonenal. Mutat Res 2003, 526:19-32 |
1.748 | TCG |
| 119 |
T Liehr,
H Starke, A Heller, A Weise, V Beensen, G
Senger, G Kittner, M Prechtel, U Claussen, J
Seidel. Evidence for a new microdeletion syndrome in 15q21. Int J Mol Med, 11:575-578 |
1.940 | CG |
| 118 |
G Houge, T Liehr,
J Schoumans, GO Ness, K Solland, H Starke, U
Claussen, P Strømme, B Åkre, S Vermeulen. Ten years follow up of a boy with a complex chromosomal rearrangement: Going from a > 5 to 15-breakpoint CCR. Am J Med Genet 2003, 118A:235-240 |
2.603 | CG |
| 117 |
A Schaeferhenrich, W
Sendt, J Scheele, A Kuechler, T Liehr,
U Claussen, A Rapp, KO Greulich, BL
Pool-Zobel. Putative colon cancer risk factors damage global DNA and TP53 in primary human colon cells isolated from surgical samples. Food Chem Toxicol 2003, 41:655-664 |
1.898 | TCG |
| 116 |
A Weise, P Harbarth, U
Claussen, T Liehr. Fluorescence in situ hybridization (FISH) on human chromosomes using PHOTOPROBE(R) biotin labeled probes. J Histochem Cytochem 2003, 51:549-551 |
2.408 | M |
| 115 |
A Nietzel, B Albrecht,
H Starke, A Heller, G Gillessen-Kaesbach, U
Claussen, T Liehr. Partial hexasomy 15pter->15q13 including SNRPN and D15S10: first molecular cytogenetically proven case report. J Med Genet 2003, 40:E28,1-4 |
6.368 | CG |
| 114 |
T Liehr,
A Nietzel, H Starke, A Heller, A Weise, A
Kuechler, G Senger, S Ebner, T Martin, M
Stumm, R Wegner, H Tönnies, C Hoppe, U
Claussen, F von Eggeling. Characterization of small marker chromosomes (SMC) by recently developed molecular cytogenetic approaches. J Ass Genet Techn 2003, 29:5-10 |
n.a. | sSMC |
| 113 |
A Kuechler, A Weise, S
Michel, A Schaeferhenrich, BL Pool-Zobel, U
Claussen, T Liehr. Precise breakpoint characterization of the colon adenocarcinoma cell line HT-29 clone 19A by means of 24-color fluorescence in situ hybridization and multicolor banding. Genes Chromosomes Cancer 2003, 36:207-210 |
4.192 | TCG |
| 112 |
H Starke, B Mitulla, A
Nietzel, A Heller, V Beensen, G Grosswendt, U
Claussen, F von Eggeling, T Liehr. First case of trisomy 21 accompanied by an additional der(4)(:p11->q11:) plus partial uniparental disomy 4p15-16. Am J Med Genet 2003, 116A:26-30 |
2.603 | sSMC |
| 62% of publications of Institute of Human Genetics Jena in the actual year | |||
2002
| Number |
Authors/
Title/ Where Contribution was Published |
Impact Factor | Topic |
| 111 |
U Claussen, S Michel, P
Mühlig, M Westermann, UW Grummt, K
Kromeyer-Hauschild, T Liehr. Demystifying chromosome preparation and the implications for the concept of chromosome condensation during mitosis. Cytogenet Genome Res 2002, 98:136-146 |
1.114 | CG M |
| 110 |
A Weise, T Liehr,
T Efferth, A Kuechler, E Gebhart. Comparative M-FISH and CGH analyses in sensitive and drug-resistant human T-cell acute leukemia cell lines. Cytogenet Genome Res 2002, 98:118-125 |
1.114 | TCG |
| 109 |
R Trappe, D Böhm, J
Kohlhase, A Weise, T Liehr, G
Essers, M Meins, B Zoll, I Bartels, P
Burfeind. A novel family-specific translocation t(2;20)(p24.1;q13.1) associated with recurrent abortions: molecular characterization and segregation analysis in male meiosis. Cytogenet Genome Res 2002, 98:1-8 |
1.114 | CG |
| 108 |
U Steinhaeuser, H
Starke, A Nietzel, J Lindenau, P Ullmann, U
Claussen, T Liehr. Suspension S-FISH a new technique for interphase. J Histochem Cytochem, 2002 50:1697-1698 |
2.283 | M INT |
| 107 |
H Starke, J Seidel, W
Henn, S Reichardt, M Volleth, M Stumm, C
Behrend, KR Sandig, C Kelbova, G Senger, B
Albrecht, I Hansmann, A Heller, U Claussen, T
Liehr. Homologous sequences at human chromosome 9 bands p12 and q13-21.1 are involved in different patterns of pericentric rearrangements. Eur J Hum Genet 2002, 10:790-800 |
3.136 | HET |
| 106 |
J Lemke, J Claussen, S
Michel, I Chudoba, P Mühlig, M Westermann, K
Sperling, N Rubtsov, UW Grummt, P Ullmann, K
Kromeyer-Hauschild, T Liehr, U
Claussen. The DNA-based structure of human chromosome 5 in interphase. Am J Hum Genet 2002, 71:1051-1059 |
10.649 | INT |
| 105 |
T Liehr,
A Weise, A Heller, H Starke, K Mrasek, A
Kuechler, H-UG Weier, U Claussen. Multicolor chromosome banding (MCB) with YAC/BAC-based probes and region-specific microdissection DNA libraries. Cytogenet Genome Res 2002, 97:43-47 |
1.114 | M |
| 104 |
T Liehr, A
Nietzel, H Starke, A Heller, A Weise, K Mrasek,
U Claussen. Characterization of small human marker chromosomes by centromere-specific multicolor-FISH (cenM-FISH) and high resolution multicolor banding (MCB). ECA-newsletter 2002, 10:3-8 |
n.a. | sSMC |
| 103 |
F v Eggeling, C Hoppe,
U Bartz, H Starke, G Houge, U Claussen, G
Ernst, D Kotzot, T Liehr. Maternal uniparental disomy 12 in a healthy girl with a 47,XX,+der(12)(:p11->q11:)/46,XX karyotype. J Med Gen 2002, 39:519-521 |
7.774 | sSMC UPD |
| 102 |
T Liehr,
I Schreyer, A Neumann, V Beensen, M Ziegler, I
Hartmann, H Starke, A Heller, A Nietzel,
Claussen. Two more possible pitfalls of rapid prenatal diagnosis using interphase nuclei. Prenat Diagn 2002, 22:497-499 |
1.802 | CG PRE |
| 101 |
A Weise, H Starke, A
Heller, H Tönnies, M Volleth, M Stumm, G
Senger, A Nietzel, U Claussen, T Liehr.
Chromosome 2 aberrations in clinical cases characterized by high resolution multicolor banding (MCB) and region specific FISH probes. J Med Genet 2002, 39:434-439 |
7.774 | CG |
| 100 |
T Liehr,
U Claussen. Current developments in human molecular cytogenetic techniques. Curr Mol Med 2002, 2:283-297 |
n.a. | M |
| 99 |
T Liehr, U Claussen. Multicolor-FISH approaches for the characterization of human chromosomes in clinical genetics and tumor cytogenetics. Current Genomics 2002, 3:213-235 |
n.a. | CG TCG |
| 98 |
T Liehr,
A Heller, H Starke, U Claussen. FISH banding methods: applications in research and diagnostics. Expert Review Mol Diagn 2002, 2:217-225. |
n.a. | M |
| 97 |
A Heller, H Starke, V
Trifonov, N Rubtsov, U Wedding, I Loncarevic,
C Bleck, U Claussen, T Liehr. A complex translocation event between the two homologues of chromosomes 5 leading to a del(5)(q21q33) as a sole aberration in a case clinically diagnosed as CML – characterization of the aberration by multicolor banding (MCB). Int J Onc 2002, 20:1179-1181 |
2.931 | TCG |
| 96 |
IF Loncarevic, J Römer,
H Starke, A Heller, C Bleck, M Ziegler, W
Fiedler, T Liehr, JH Clement, U
Claussen. Heterogenic molecular basis for loss of ABL1-BCR transcription: Deletions in der(9)t(9;22) and variants of standard t(9;22) in BCR-ABL1-positive chronic myeloid leukemia. Genes Chr Cancer 2002, 34:193-200 |
4.199 | TCG |
| 95 |
A Kuechler, S Neubauer,
GG Grabenbauer, U Claussen, T Liehr,
R Sauer, TG Wendt. Is 24-color-FISH-detection of in vitro radiation-induced chromosomal aberrations suited to determine individual intrinsic radiosensitivity? Radiother Oncol 2002, 178:209-215 |
2.838 | TCG |
| 94 |
T Liehr,
M Schmidt, H Starke, M Ziegler, G Kittner, A
Heller, N Rubtsov, V Trifonov, U Claussen. First case of trisomy 13 plus mosaic trisomy 1q. Fetal Diag Ther 2002, 17:133-136 |
1.053 | CG |
| 93 |
T Liehr,
A Heller, H Starke, N Rubtsov, V Trifonov, K
Mrasek, A Weise, A Kuechler, U Claussen. Microdissection based high resolution multicolor banding (MCB) for all 24 human chromosomes. Int J Mol Med 2002, 9:335-339 |
2.063 | M |
| 92 |
A Weise, H Starke, A
Heller, U Claussen, T Liehr. Evidence for interphase DNA decondensation transverse to the chromosome axis – a multicolor banding (MCB) analysis. Int J Mol Med 2002, 9:359-361 |
2.063 | INT |
| 91 |
T Liehr, A
Heller, H Starke, U Claussen. High quality CGH slides irrespective of used lymphocyte suspension. Technical Tips Online Internet: (http://www.elsevier.com/locate/tto) TTO 2002, 1:138, T02436 no longer available |
13.216 | M |
| 61% of publications of Institute of Human Genetics Jena in the actual year | |||
2001
| Number |
Authors/
Title/ Where Contribution was Published |
Impact
Factor |
Topic |
| 90 |
A Kuechler, CR Mueller,
T Liehr, U Claussen. Detection of microdeletions in the short arm of the X chromosome by chromosome stretching. Cytogenet Cell Genet. 2001, 95:12-16 |
1.271 | CG |
| 89 |
H Starke, G Senger, M
Kossakiewicz, H Tittelbach, D Rau, N Rubtsov,
V Trifonov, A Heller, I Hartmann, U Claussen,
T Liehr. Maternal insertion of 18q11.2-q12.2 in 18p11.3 of the same chromosome analysed by microdissection and multicolour banding (MCB). Prenat Diag 2001, 21:1049-1052 |
1.792 | CG |
| 88 |
S Scheil, S Brüderlein,
T Liehr, H Starke, J Herms, M
Schulte, P Möller. Genome-wide analysis of sixteen chordomas by comparative genomic hybridization and cytogenetics of the first human chordoma cell line, U-CH1. Genes Chr Cancer 2001, 32:203-211 |
4.416 | TCG |
| 87 |
K Mrasek, A Heller, N
Rubtsov, V Trifonov, H Starke, M Rocchi, U
Claussen, T Liehr. Reconstruction of the female Gorilla gorilla karyotype by Zoo-FISH using 25-color FISH and multicolor banding (MCB). Cytogenet Cell Genet 2001, 93:242-248 |
1.271 | EVO |
| 86 |
RW Kinne, T
Liehr, V Beensen, E Kunisch, T
Zimmermann, H Holland, R Pfeiffer, H-D Stahl,
W Lungershausen, G Hein, A Roth, F Emmrich, U
Claussen, UG Froster. Mosaic chromosomal aberrations in synovial fibroblasts of patients with rheumatoid arthritis, osteoarthritis, and other inflammatory joint diseases. Arthritis Res, 2001, 3:319-330 |
3.436 | CG |
| 85 |
A Dufke, C Walczak, T
Liehr, H Starke, V Trifonov, N
Rubtsov, M Schöning, H Enders, T Eggermann. Partial tetrasomy 12pter-12p12.3 in a girl with Pallister-Killian syndrome: extraordinary finding of an analphoid, inverted duplicated marker. Europ J Hum Genet 2001, 9:572-576 |
3.173 | sSMC |
| 84 |
T Liehr,
V Beensen, H Starke, R Hauschild, E Hempel, V
Fritsche, C Hoppe, G Großwendt, M Prechtel, M
Ziegler, U Claussen, F von Eggeling. Tetrasomy 21 due to a de novo Robertsonian translocation t(14;21) and an additional free trisomy 21. Clin Genet 2001, 60:83-86 |
2.395 | CG |
| 83 |
H Starke, M Raida, V
Trifonov , J H Clement, IF Loncarevic, A
Heller, C Bleck, A Nietzel, N Rubtsov, U
Claussen, T Liehr. Molecular cytogenetic characterization of an acquired supernumerary minute marker chromosome as sole abnormality in a case clinically diagnosed as Philadelphia negative chronic myelogenous leukaemia. Br J Haematol 2001, 113:435-438 |
2.815 | TCG |
| 82 |
T Liehr, V Beensen, R
Hauschild, M Ziegler, I Hartmann, H Starke, A
Heller, C Kähler, M Schmidt, W Reiber, M
Hesse, U Claussen. Pitfalls of rapid prenatal diagnosis using the interphase nucleus. Prenat Diagn 2001, 21:419-421 |
1.792 | PRE CG |
| 81 |
A Bleichert, W Fiedler,
U Claussen, G Ernst, IF Loncarevic, A Heller,
T Liehr, C Kunert, F von
Eggeling. A long distance-PCR derived FISH probe detects a deletion between p15 and p16 in CML and T-ALL patients. Int J Mol Med 2001, 7:591-595 |
1.689 | TCG |
| 80 |
A Rump, G Kasper, C
Hayes, G Wen, H Starke, T Liehr,
R Lehmann, D Lagemann, A Rosenthal. Complex arrangement of genes within a 220-kb region of double-duplicated DNA on human 2q37.1. Genomics 2001, 73:50-55 |
3.418 | CG |
| 79 |
YX Yu, A Heller, T
Liehr, L Aurelian. Expression analysis and chromosome location of a novel gene (H11) associated with the growth of human melanoma cells. Int J Onc 2001, 18:905-911 |
2.330 | TCG |
| 78 |
G Alves, A Heller, W
Fiedler, M Mendes Campos, U Claussen, AA
Ornellas, T Liehr. Genetic imbalances in 26 penile SCC cases. Genes Chr Cancer 2001, 31:48-53 |
4.416 | TCG |
| 77 |
T Liehr,
LT Reiter, JR Lupski, T Murakami, U Claussen,
B Rautenstrauss. Regional localization of 10 mariner transposon like ESTs by means of FISH – evidence for a correlation with fragile sites. Mamm Genome 2001, 12:326-328. |
2.318 | INT |
| 76 |
A Nietzel, M Rocchi, A
Heller, H Starke, I Wlodarska, V Beensen, U
Claussen, T Liehr. A new multicolor-FISH approach for the characterization of marker chromosomes: Centromere-specific multicolor-FISH (cenM-FISH). Hum Genet 2001, 108:199-204 |
3.209 | sSMC M |
| 75 |
S Stein, T Liehr,
K Eschrich. Characterization of the mouse liver fructose-1,6-bisphosphatase gene. Gene 2001, 264:215-224 |
3.041 | CG |
| 74 |
V Bureau, S Marionneau,
A Cailleau-Thomas, B Le Moullac-Vaidye, T
Liehr, J Le Pendu. Comparison of the three rat GDP-L-fucose:beta-D-galactoside 2-alpha-L-fucosyltransferases FTA, FTB and FTC. Eur J Biochem 2001, 268:1006-1019 |
2.849 | CG |
| 33% of publications of Institute of Human Genetics Jena in the actual year | |||
2000
| Number |
Authors/
Title/ Where Contribution was
Published |
Impact Factor | Topic |
| 73 |
A
Dufke, J Seidel, M Schöning, M
Döbler-Neumann, C Kelbova, T
Liehr, V Beensen, C
Backsch, U Klein-Vogler, H Enders. Microdeletion 4p16.3 in three unrelated patients with Wolf-Hirschhorn-syndrome. Cytogenet Cell Genet 2000, 91:81-84 |
1.409 | CG |
| 72 |
NB
Rubtsov, TV Karamisheva, NM
Astakhova, T Liehr, U
Claussen, NS Zhdanova. Zoo-FISH with region-specific paints for the mink chromosome 5q: delineation of inter- and intrachromosomal rearrangements in human, pig, fox, and Iberian shrew. Cytogenet Cell Genet 2000, 90:268-270 |
1.409 | EVO |
| 71 |
C
Kebelmann-Betzing, K Seeger, A
Kulozik, G Henze, T Liehr,
A Heller, A Teigler-Schlegel. Secondary acute myeloid leukemia after treatment of acute monoblastic leukemia. N Engl J Med 2000, 343:1897-1898 |
29.512 | TCG |
| 70 |
S
Jakubiczka, B Mitulla, T
Liehr, J Arnemann, H
Lehrach, R Sudbrak, M Stumm, PF
Wieacker, T Bettecken. Incidental prenatal detection of an Xp deletion using an anonymous primer pair for fetal sexing. Prenat Diagn 2000, 20:842-846 |
1.647 | CG |
| 69 |
C
Helmken, A Wetter, S
Rudnik-Schöneborn, T Liehr,
K Zerres, B Wirth. An essential SMN interacting protein (SIP1) is not involved in the phenotypic variability of spinal muscular atrophy (SMA). Europ J Hum Genet 2000, 8:493-499 |
3.175 | CG |
| 68 |
A
Heller, J Seidel, A Hübler, H
Starke, V Beensen, G Senger, M
Rocchi, J Wirth, I Chudoba, U
Claussen, T Liehr. Molecular cytogenetic characterisation of partial trisomy 9q in a case with pyloric stenosis and a review. J Med Genet 2000, 37:529-532 |
3.290 | CG |
| 67 |
H
Tillmann, S Stein, T Liehr,
K Eschrich. Structure and chromosomal localization of the human and mouse muscle fructose-1,6-bisphosphatase genes. Gene 2000, 247:241-253 |
2.461 | CG |
| 66 |
A
Hübler, J Seidel, E Kauf, D Schramm,
V Beensen, A Heller, T Liehr,
F Zintl.
Insulin-like growth factor serum concentrations reflect insufficient growth in a hypoplastic infant with partial trisomy 9q in the 12th week of life. J Pediatr Endocrinol Metab 2000, 13:445-450 |
0.638 | CG |
| 65 |
K
Bayerlein, T Rith, I Verdörfer, T
Liehr, E Wolff, S Girod,
E Gebhart. I-FISH control of CGH-detected gain of DNA sequence copy number in oral squamous cell carcinomas. Anticancer Res 2000, 20:427-432 |
1.331 | TCG |
| 64 |
K
König, A Göhlert, T Liehr,
I F Loncarevic, I Riemann. Two-Photon Multicolor FISH: a versatile technique to detect specific sequences with in single DNA molecules in cells and tissues. Single Molecules 2000, Vol 1:41-51 |
n.a. | M |
| 63 |
A
Heller, I Chudoba, C Bleck, G
Senger, U Claussen, T Liehr. Microdissection based comparative genomic hybridization (micro-CGH) analysis of secondary acute myelogenous leukemias. Int J Onc 2000, 16:461-468 |
2.142 | TCG |
| 62 |
E
Gebhart, T Liehr.
Patterns of genomic imbalances in human solid tumors (Review). Int J Onc 2000, 16:383-399. |
2.142 | TCG |
| 44% of publications of Institute of Human Genetics Jena in the actual year | |||
1999
| Number |
Authors/
Title/ Where Contribution was Published |
Impact Factor | Topic |
| 61 |
H Starke, I Schreyer, C
Kähler, W Fiedler, V Beensen, A Heller, A
Nietzel, U Claussen, T Liehr. Molecular cytogenetic characterization of a prenatally detected supernumerary minute marker chromosome 8. Prenatal Diagn 1999, 19:1169-1174 |
1.885 | sSMC |
| 60 |
D Carbonnelle, T
Liehrr, C Jacquot, D Masson, P
Lustenberger, MG Denis, C Roussakis. Assignment of the serologically defined colon cancer antigen 1 gene (SDCCAG1) to human chromosome band 14q22 by in situ hybridization. Cytogenet Cell Genet 1999, 86:248-249 |
1.604 | CG |
| 59 |
K Hühne, O Park, T
Liehr, B Rautenstrauss. Expression analysis of the PMP22 gene in glioma and osteogenic sarcome cell lines. J Neurosci Res 1999, 58:624-631 |
3.126 | TCG |
| 58 |
LT Reiter, T
Liehr, B Rautenstrauss, HM
Robertson, JR Lupski. Localization of mariner DNA Transposons in the Human Genome by PRINS. Genome Res 1999, 9:839-843 |
7.062 | CG |
| 57 |
E Gebhart, T
Liehr. Clonality determined by fluorescence in situ hybridization of single-cell aberrations in hematopoietic neoplasias. Cancer Genet Cytogenet 1999, 113:193-194 |
1.756 | TCG |
| 56 |
F von Deimling, JM
Scharf, T Liehr, M Rothe, AR
Kelter, P Albers, WF Dietrich, LM Kunkel, N
Wernert, B Wirth. Human and mouse RAD17 genes: identification, localization, genomic structure and histological expression pattern in normal testis and seminoma. Hum Genet 1999, 105:17-27 |
3.145 | TCG |
| 55 |
T Liehr,
G Kuhlenbäumer, P Wulf, V Taylor, U Suter, C
Van Broeckhoven, J R Lupski, U Claussen, B
Rautenstrauss. Regional localization of the human epithelial membrane protein genes 1, 2, and 3 (EMP1, EMP2, EMP3) to 12p12.3, 16p13.2, and 19q13.3. Genomics, 1999, 58:106-108 |
3.386 | CG |
| 54 |
T Liehr,
U Claussen, E Gebhart. Nucleus extraction from single mounted tissue section. Genetic Analysis (Biomolecular Engeneering), 1999, 15:65-69 |
0.778 | M |
| 53 |
M Döbler, J Schuh, F
Kiesewetter, H Schell, T Liehr,
E Gebhart. Deletion monitoring in skin tumors by interphase-FISH using band-specific DNA probes. Int J Oncol 1999, 14:571-576 |
1.381 | TCG |
| 52 |
T Liehr,
H Starke, V Beensen, C Kähler, M Harbich, E
Bude, M Ziegler, U Claussen. Translocation trisomy dup(21q) and free trisomy 21 can be distinguished by interphase-FISH. Int J Mol Med 1999, 3:11-14 |
1.058 | CG |
| 8% of publications of
Institute of Human Genetics Jena in the actual
year coauthor or author in 25% of publications of Institute of Human Genetics Erlangen in the actual year |
|||
1998
| Number |
Authors/
Title/ Where Contribution was Published |
Impact Factor | Topic |
| 51 |
C Fuchs, T Liehr,
S Özbey, A Ekici, B Rautenstrauss. Charcot-Marie-Tooth disease type 1A and hereditary neuropathy with liability to pressure palsies: a SacI polymorphism in the proximal CMT1A-REP elements may lead to genetic misdiagnosis. Neurogenetics 1998, 2:43-46 |
2.094 | CG |
| 50 |
S Neubauer, T
Liehr, S Birkenhake, E Gebhart, R
Fietkau, R Sauer. Estimation of DNA single strand breaks by single cell gel electrophoresis in tumor cells. Genetic Analysis (Biomolecular Engineering) 1998, 14:121-124 |
0.778 | TCG M |
| 49 |
A Taubald, T
Liehr, E Haßfurther, J Ries, S
Girod, E Gebhart. CGH-detected DNA sequence copy number amplifications can be confirmed by interphase-FISH: new possiblities for prognostic approaches in oral squamous cell carcinomas. Int J Mol Med 1998, 2:555-560 |
1.058 | TCG |
| 48 |
T Liehr,
M Kirsch, U Trautmann, E Gebhart. Fluorescence in situ hybridization on G-banded chromosome preparations mounted with Eukitt in a retrospective study and in routine diagnostics. Cancer Genet Cytogenet 1998, 107:85-86 |
1.756 | TCG |
| 47 |
C Lange, T Liehr,
M Goen, E Gebhart, B Fleckenstein, A Ensser. New eukaryotic semaphorins with close homology to semaphorins of DNA-viruses. Genomics 1998, 51:340-350 |
3.386 | CG |
| 46 |
T Liehr,
J Ries, E Wolff, W Fiedler, R Dahse, G Ernst,
H Steininger, S Koscielny, S Girod, E Gebhart.
Gain of DNA copy number on chromosomes 3q26-qter and 5p14-pter is a frequent finding in head and neck squamous cell carcinomas. Int J Mol Med 1998, 2:173-179 |
1.058 | TCG |
| 45 |
E Wolff, S Girod, T
Liehr, U Vorderwülbecke, J Ries, H
Steininger, E Gebhart. Oral squamous cell carcinomas are characterized by a rather uniform pattern of genomic imbalances detected by comparative genomic hybridization. Europ J Cancer 1998, 34:186-190 |
2.537 | TCG |
| 44 |
T Liehr,
RA Pfeiffer, U Trautmann, E Gebhart. Centromeric alphoid DNA heteromorphisms of chromosome 22 revealed by FISH-technique. Clin Genet 1998, 53:231-232 |
1.391 | HET |
| 43 |
E Gebhart, T
Liehr, E Wolff, J Ries, W Fiedler,
H Steininger, S Koscielny, S Girod. Pattern of genomic imbalances in oral squamous cell carcinomas with and without an increased copy number of 11q13. Int J Onc 1998, 12:1151-1155 |
1.381 | TCG |
| 42 |
B Rautenstrauss, C
Fuchs, A Ekici, E Nelis, C Van Broeckhoven, T
Liehr. Assay of transfection rate in insect cells on a single cell level. Genetic Analysis (Biomolecular Engineering) 1998, 14:103-104 |
0.778 | M |
| 41 |
B Rautenstrauss, U
Zechner, H Hameister, H Grehl, T Liehr.
Expression pattern of the peripheral myelin protein 22kDa (PMP22) in neural and non-neural tissue types of adult wildtype and trembler mice - a comparative study. J Periph Nerv Syst 1998, 3:117-124 |
n.a. | CG |
| 40 |
B Rautenstrauss, T
Liehr, C Fuchs, A Bevot, A
Bornemann, E Postler, R Meyermann, S Uhlhaas,
W Friedl, R Michaelis. Mosaicism for Charcot-Marie-Tooth disease type 1A: Onset in childhood suggests somatic reversion in early developmental stages. Int J Mol Med 1998, 1:333-337 |
1.058 | CG |
| 39 |
KG
Michels-Rautenstrauss, CY Mardin, W M Budde, T
Liehr, J Polansky, T Nguyen, V
Timmerman, C Van Broeckhoven, GOH Naumann, RA
Pfeiffer, BW Rautenstrauss. Juvenile open angle glaucoma: fine mapping of the TIGR gene to 1q24.3-25.2 and mutation analysis. Hum Genet 1998, 102:103-106 |
3.145 | CG |
| 38 |
F Pröls, T Liehr, B Loser, B
Rautenstrauss. Regional localization of rat Flic1, a calcyclin/S100A6-like gene to rat chromosome 7q22-31 by means of FISH. Mamm Genome 1998, 9:94-95 |
1.890 | CG |
| 18% of publications of
Institute of Human Genetics Jena in the actual
year coauthor or author in ~40% of publications of Institute of Human Genetics Erlangen in the actual year |
|||
1997
| Number |
Authors/
Title/ Where Contribution was Published |
Impact Factor | Topic |
| 37 |
F Pröls, T Liehr,
R Rinka, B Rautenstrauss. Assignement of microvascular endothelial differentiation gene 1 (MDG1) to human chromosome band 14q24.2->q24.3 by fluorescence in situ hybridization. Cytogenet. Cell Genet 1997, 79:149-150 |
1.604 | CG |
| 36 |
T Liehr. Two-color or one-color FISH? - Comment to: A rapid method for the diagnosis of Charcot Marie Tooth disease type 1A by FISH. Trends in Genetics 1997, 13:p?? |
16.342 | CG M |
| 35 |
T Liehr,
H Grehl, B Rautenstrauss. Accumulation of periperal myelin protein 22 (PMP22) in onion bulbs of nerves biopsied from patients with different subtypes of Charcot-Marie-Tooth (CMT) disease type 1. Acta Neuropathol 1997, 94:514-516 |
2.402 | CG |
| 34 |
B Rautenstrauss, C
Fuchs, T Liehr, H Grehl, T
Murakami, J R Lupski. Visualization of the CMT1A duplication and HNPP deletion by FISH on streched chromosome fibers. J Periph Nervous Syst 1997, 2,319-322 |
n.a. | CG |
| 33 |
B Rautenstrauss, T
Liehr, UMH Schrell, H Grehl. Use of FISH analyzis for prostate tumors and other tissue types. Am J Pathol 1997, 151:1171-1172 |
6.436 | TCG |
| 32 |
B Rautenstrauss, T
Liehr, K D Bathke, H Lauffer, A
Ekici A, C Fuchs, E Nelis, C Van Broeckhoven, H
Grehl. Fortschritte in der molekulargenetischen Diagnostik der Charcot-Marie-Tooth’schen Erkrankung (CMT) sowie der tomakulösen Neuropathie (engl.: hereditary neuropathy with liability to pressure palsies, HNPP). Med Genetik 1997, 9:501-504 |
n.a. | CG |
| 31 |
T Liehr,
H Grehl, B Rautenstrauss. Molecular diagnosis of PMP22-associated neuropathies using fluorescence in situ hybridization (FISH) on archival peripheral nerve tissue preparations. Acta Neuropathol 1997, 94:266-271 |
2.402 | CG |
| 30 |
E Wolff, T Liehr,
U Vorderwülbecke, A H Tulusan, E M Husslein, E
Gebhart. Frequent gains and losses of specific chromosome segments in human ovarian carcinomas shown by comparative genomic hybridization. Int J Onc 1997, 11:19-23 |
1.381 | TCG |
| 29 |
C Fuchs, T Liehr,
B Rautenstrauss. High-resolution FISH of streched chromosome fibers. Trends in Genetics 1997, 13:287 |
16.342 | CG M |
| 28 |
T Liehr,
O Park, B G Feuerstein, E Gebhart, B
Rautenstrauss. The peripheral myelin protein 22kDa (PMP22) gene is amplified in cell lines derived from glioma and osteogenic sarcoma: a new candidate for an oncogene? Int J Onc 1997, 10:915-919 |
1.381 | TCG |
| 27 |
T Liehr,
F Hallouin, B Rautenstrauss, J LePendu, M G
Denis. Mapping of two different alpha-1,2-fucosyltransferase genes to rat chromosome 1q22-31. Mamm Genome 1997, 8:297-298 |
1.890 | CG |
| 26 |
C Chadéneau, T
Liehr, B Rautenstrauss, M G Denis.
The Tage4 gene maps to rat chromosome 1q22. Mamm Genome 1997, 8:157-158 |
1.890 | CG |
| 25 |
H Grehl, B
Rautenstrauss, T Liehr, A
Ekici, A Bickel, K Bathke, B Neundörfer. Clinical and morphological phenotype of HMSN 1A mosaicism. Neuromusc Disord 1997, 7:27-31 |
2.749 | CG |
| 24 |
J Draeger, H Schell, F
Kiesewetter, T Liehr, E
Gebhart. Chromosome gain and loss in paraffin sections from malignant melanomas of the skin. Int J Onc 1997, 10:89-92 |
1.381 | TCG |
| 23 |
A Dimmler, F
Kiesewetter, T Liehr, S
Neubauer, H Schell, E Gebhart. Interphase-FISH examinations in paraffin sections from benign, precancerous, and cancerous lesions of the skin and oral mucosa. Int J Onc 1997, 10:83-88 |
1.381 | TCG |
| 22 |
V Timmerman, B
Rautenstrauss, L T Reiter, T Koeuth, A
Löfgren, T Liehr, E Nelis, K D
Bathke, P De Jonghe, H Grehl, J-J Martin, J R
Lupski, C Van Broeckhoven. Detection of the CMT1A/HNPP recombination hotspot in unrelated patients of European descent. J Med Genet 1997, 34:43-49 |
2.986 | CG |
|
coauthor
or author in ~40% of publications of Institute
of Human Genetics Erlangen in the actual year
|
|||
1996
| Number |
Authors/
Title/ Where Contribution was Published |
Impact Factor | Topic |
| 21 |
F Pröls, T Liehr,
M Marx, B Rautenstrauss. Regional localization of rat microvascular endothelial differentiation gene 1 (Mdg1) to chromosome 6q16-23 by means of FISH. Mamm Genome 1996, 7:867-868 |
1.890 |
CG |
| 20 |
E Gebhart, P Hofbeck, Y
Hofmann, R Lerch, G Schmitt, T Liehr.
Recovering of archival tumor cytogenetic slides for two-color-interphase FISH. Appl Cytogenet 1996, 22:146-148 |
n.a. | M |
| 19 |
T Liehr,
B Rautenstrauss, H Grehl, K D Bathke, A Ekici,
A Rauch, H D Rott. Mosaicism for the Charcot-Marie-Tooth disease type 1A duplication suggests somatic reversion. Human Genet 1996, 98:22-28 |
3.145 | CG |
| 18 |
T Liehr. PMP22-expression in Nervus suralis biopsies of CMT1A- and HNPP-patients studied by means of immunohistochemistry. Futura 1996, 2:158-160 |
n.a. | CG M |
| 17 |
T Liehr,
H Grehl, B Rautenstrauss. A rapid method for FISH analysis on interphase nuclei extracted from cryofixed tissue. Trends in Genetics 1996, 12:505-506 |
16.342 | M |
| coauthor or author in ~18% of publications of Institute of Human Genetics Erlangen in the actual year | |||
1995
| Number |
Authors/
Title/ Where Contribution was Published |
Impact Factor | Topic |
| 16 |
T Liehr, K
Thoma, K Kammler, C Gehring, A Ekici, K D
Bathke, H Grehl, B Rautenstrauss. Direct preparation of uncultured EDTA-treated or heparinized blood for interphase FISH analysis. Appl Cytogenet 1995, 21:185-188 |
n.a. | M |
| 15 |
T Liehr,
A Ekici, R Hillenbrand, B Rautenstrauss. Regional localization of rat myelin protein zero Mpz gene to chromosome 13q24-25 by means of FISH. Mamm Genome 1995, 6:824-825 |
1.890 | CG |
| 14 |
T Liehr,
H Grehl, B Rautenstrauss. FISH analysis of interphase nuclei extracted from paraffin-embedded tissue. Trends in Genetics 1995, 11:377-378 |
16.342 | M |
| 13 |
D Bächner, T
Liehr, H Hameister, H Altenberger,
H Grehl, U Suter, B Rautenstrauss. Widespread expression of the peripheral myelin protein-22 gene (pmp22) in neural and non-neural tissues during murine development. J Neuroscience Res 1995, 42:733-741 |
3.126 | CG |
| 12 |
T Liehr,
B Rautenstrauss. Regional localization of rat peripheral myelin protein 22 (Pmp22) gene to chromosome 10q22 by FISH. Mamm Genome 1995, 6:489 |
1.890 | CG |
| 11 |
E Gebhart, T
Liehr, P Harrer, S Reichardt, G
Schmitt, K Thoma, M Gramatzki, U Trautmann. Determination by interphase FISH of the clonality of aberrant karyotypes in human hematopoietic neoplasias. Leukemia and Lymphoma 1995, 17:295-302 |
1.140 | TCG |
| 10 |
T Liehr,
H Altenberger, B Rautenstrauss. Rapid fluorescence in situ detection of heterologous expression in E. coli and counterstaining with diaminophenylindol. Trends in Genetics 1995, 11:129 |
16.342 | M |
| coauthor or author in 35% of publications of Institute of Human Genetics Erlangen in the actual year | |||
1994
| Number |
Authors/
Title/ Where Contribution was
Published |
Impact Factor | Topic |
| 9 |
C
Kraus, T Liehr, J
Hülsken, J Behrens, W Birchmeier, KH
Greschick, WG Ballhausen. Localization of the human ß-catenin gene (CTNNB1) to 3p21: a region implicated in tumor development. Genomics 1994, 23:272-274 |
3.386 |
TCG |
| 8 |
U
Trautmann, M Gramatzki, M Krauß, A
Fritz, T Liehr, E
Gebhart. Tetrasomy 8 as a clonal anomaly in myeloic neoplasias. Cancer Genet Cytogent 1994, 72:101-104 |
1.756 | TCG |
| 7 |
T
Liehr, A Stübinger, K
Thoma, H A Tulusan, E Gebhart. Comparative interphase cytogenetics using FISH on human ovarian carcinomas. Anticancer Research 1994, 14:183-218 |
1.375 | TCG |
| 6 |
S Neubauer, T
Liehr, H A Tulusan, E
Gebhart. Interphase cytogenetics by FISH on archival paraffin material and cultured cells of human ovarian tumors. Int J Onc 1994, 4:317-321 |
1.381 | TCG |
| coauthor or author in ~20% of publications of Institute of Human Genetics Erlangen in the actual year | |||
1993
| Number |
Authors/
Title/ Where Contribution was
Published |
Impact
Factor |
Topic |
| 5 |
E Gebhart, U
Trautmann, S Reichardt, T
Liehr. Chromosomal heterogenety of aneuploid leukemic cell populations detected by conventional karyotyping and by fluorescence in situ hybridization (FISH). Anticancer Res 1993, 13:1857-1862 |
1.375 | TCG |
| 4 |
E
Gebhart, U Trautmann, S Reichardt, T
Liehr. Use of fluorescence in situ hybridization (FISH) for the estimation of the aberrant cell clone in leukemias with trisomy 8 or monosomy 7 detected by karyotyping. Int J Onc 1993, 3:191-195 |
1.381 | TCG |
| 3 |
T Liehr,
N Atanasov, A H Tulusan, E
Gebhart. Amplification of proto-oncogenes in human ovarian carcinomas.
Int J Onc 1993, 2:155-160
|
1.381 | TCG |
| coauthor or author in ~15% of publications of Institute of Human Genetics Erlangen in the actual year | |||
|
Number |
Authors/
Title/ Where Contribution was
Published |
Impact
Factor |
Topic |
| 2 |
A Rauch, R A
Pfeiffer, U Trautmann, T Liehr, H D Rott,
R Ulmer. A study of ten small supernumerary (marker) chromosomes identified by fluorescence in situ hybridization (FISH). Clin Genet 1992, 4:84-90 |
1.391 | sSMC |
| 1 |
T
Liehr, RA Pfeiffer, U Trautmann. Typical and partial cat eye syndrome: identification of the marker chromosome by FISH. Clin Genet 1992, 42:91-96 |
1.391 |
sSMC |
| coauthor or author in ~8% of publications of Institute of Human Genetics Erlangen in the actual year | |||
