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 |
2023
| Number |
Authors/
Title/ Where Contribution was Published |
Impact
Factor |
Topic |
| 844 | n.a. | other |
|
| 843 |
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 |
| 842 |
E
Behluli, T Liehr, R
Hadziselimovic, G Temaj.
Epigenetics and treatment of systemic lupus erythematosus. Pharmacia 2023, 70:1005-1013. |
1.100 | CG |
| 841 |
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 |
| 840 |
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 |
| 839 |
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 |
| 837 |
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 |
| 836 |
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 |
| 835 |
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 |
| 834 |
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 |
| 833 |
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 |
| 832 |
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 |
| 831 |
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 |
| 830 |
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 |
| 829 |
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 |
| 828 |
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 |
| 827 |
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 |
| 826 |
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 |
| 825 |
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 |
| 824 |
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 |
2022
| Number |
Authors/
Title/ Where Contribution was Published |
Impact
Factor |
Topic |
| 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 |