Thomas Liehr (2019)
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
Abstracts (published in Journals)
|
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 |
Poster (p) or oral (o) |
Topic |
| 570 |
T Liehr. Applications, challenges and ethical issues of non-invasive prenatal testing (NIPT). Azerb J Lab Med. 2023; Congress Edition: 131 (recorded talk). |
(o) |
CG |
2022
| Number |
Authors/ Title/ Where Contribution was
Published |
Poster (p) or oral (o) |
Topic |
| 569 |
MM
Rocha, RRC Matos, AF Figueiredo, AH Melgaco, LB
Lima, TJ Marques-Salles, T
Liehr, E Abdelhay, GM
Ferreira, MLM Silva. Flexibility of FISH probes in monitoring iAMP21 acute lymphoblastic leukemia: Study of four Brazilian children. HEMA 2022, October 26-29, Sao Paulo, Brazil. Hematol Transfus Cell Ther. 2022; 44(S2):S343-344 |
(o) |
TCG |
2021
| Number |
Authors/
Title/ Where Contribution was Published |
Poster (p)
or oral (o) |
Topic |
| 568 |
GM Ferreira, RRC Matos, KC
Monteso, MM Rocha, MT Bizarro, C Meyer, T
Liehr, E Abdelhay, R Binato, MLM
Silva. Quantitative real-time PCR (RT-QPCR) comparing the relative expression levels of gene transcripts involved in a cryptic three-way translocation t(9;11;19): an original case of an infant with dismal prognosis acute lymphoblastic leukemia. Hematol Transfus Cell Ther 2021, 43(S1): S300. |
(p) | TCG |
| 567 |
RRC Matos, KC Monteso, MT
Bizarro, MM Rocha, T Liehr, M
Rouxinol, E Abdelhay, R Binato, RC Ribeiro. Cytogenetic and clinical data of variant three-way translocation t(8;V,21) in childhood acute myeloid leukemia. Hematol Transfus Cell Ther 2021, 43(S1): S279-280. |
(p) |
TCG |
2020
| Corona Pandemia - None |
|||
2019
| Number |
Authors/
Title/ Where Contribution was Published |
Poster (p)
or oral (o) |
Topic |
| 566 |
T
Liehr. (Moleklulare) Zytogenetik in Zeiten von NGS. MedGen 2019, 31: 430. |
o |
CG |
| 565 |
A Garcia-Angulo, MA Merlo, ME
Rodriguez, S Portela-Bens, E Garcia, A
Arias-Perez, I Cross, T
Liehr,
L Rebordinos. Genome and phylogenetic analysis of genes belonging to the immune system of the flatfish Solea senegalensis. Hematol Transfus Cell Therap 2019; 41: S271 (Abstract 704) (Sao Paulo, Brazil) II Congresso de Jovenes Investigadoros des Mar. 2019 |
(p) |
EVO |
| 564 |
A Al-Rikabi, T Liehr.
Are there B-chromosomes in human? BMC Proceedings 2019; 13; S11 (Abstract S4-01) (Botucatu, Brazil) |
(o) |
sSMC |
| 563 |
A Zlotina, A Maslova, O
Pavlova, N Kosyakova, T Liehr, A
Krasikova. New insights into chromomere organization provided by lampbrush chromosome microdissection and high throughput sequencing. Mol Cytogenet 2019; 12: S61 (Abstract 4.P4) (Salzburg, Austria) |
(p) |
EVO |
| 562 |
S Singer, W Habhab, K
Schaeferhoff, M Kehrer, U Grasshoff, A Dufke, KO
Kagan, T Liehr, UA Mau-Holzmann.
Multiple structural chromosomal aberrations in a fetus with holoprosencephaly median cleft lip palate nasal agenesy and hypotelorism. Mol Cytogenet 2019; 12: S58 (Abstract 3.P16) (Salzburg, Austria) |
(p) |
CG |
| 561 |
W Habhab, S Singer, A Rieß,
KO Kagan, T Liehr, K Schäferhoff,
A Dufke, U Mau-Holzmann, M Kehrer. Pre and postnatal findings in a patient with a rec(8)(qter->q21.11::p23.3->qter) due to a paternal inv(8)(p23.3q21.11). Mol Cytogenet 2019; 12: S57 (Abstractn 3.P12) (Salzburg, Austria) |
(p) |
CG |
| 560 |
AS Koltsova, AA Pendina, OA
Efimova, OV Malysheva, NY Shved, T Liehr,
MAK Othman, MI Kakhiani, VS Baranov. Cytogenetic abnormalities in uterine leiomyoma cells in vivo and in vitro. Mol Cytogenet 2019; 12: S45 and 51-52 (Abstract 2.P15/ 2.P35) |
(p) |
TCG |
| 559 |
W Slimani, M Kammoun, A Atig,
S Meddeb, J Mathlouthi, D Sanlaville, T
Liehr, A Saad, S Mougou-Zerelli. Array CGH and FISH characterization of six new cases of small supernumerary marker chromosomes encompassing the 15q11q13 region. Mol Cytogenet 2019; 12: S32 (Abstract 1.P45) |
(p) |
sSMC |
| 558 |
B Pfütze, V Langhof, S
Anders, P Lorenz, T Liehr, M
Klaus, A Junge. Two unbalanced recombinant cases in a family with an intrachromosomal insertion in 1q. Mol Cytogenet 2019; 12: S27 (Abstract 1.P27) (Salzburg, Austria) |
(p) |
CG |
| 557 |
IY Iourov, SG Vorsanova, T
Liehr. In memoriam: Professor Yuri B. Yurov — Molecular Cytogenetics (BMC-Springer/Nature) and beyond. Mol Cytogenet 2019; 12: S12 (Abstract S2) (Salzburg, Austria) |
(o) |
other |
| 556 |
T Liehr, A
Al-Rikabi. Molecular cytogenetics – indispensability of the approach highlighted by sSMC characterization. Mol Cytogenet 2019; 12: S11 (Abstract S1) (Salzburg, Austria) |
o |
sSMC |
| 555 |
T Liehr. European certification and continuous education of clinical laboratory geneticists working in cytogenetics. Mol Cytogenet 2019; 12: S10 (Abstract L22) (Salzburg, Austria) |
o |
other |
| 554 |
HI Petermann, T Liehr.
The influence of natural sciences on the development of human genetics as a medical field in the federal republic of Germany. Poster on the ESHG Meeting, 15.-18.06.2019; P19.19B (Gothenburg, Sweden) |
(p) |
other |
| 553 |
T Liehr. From human cytogenetics to human chromosomics. Eposter on the ESHG Meeting, 15.-18.06.2019; E-P13.01 (Gothenburg, Sweden) |
p |
M |
| 552 |
M Ziegler, ABH Al-Rikabi, T
Liehr. Interphase cells for fluorescence in situ hybridization from human skin. Med Genetik 2019; 31: 170 (Abstract P-Techno-207) (Weimar, Germany) |
(p) |
M |
| 551 |
T Liehr. From human cytogenetics to human chromosomics. Med Genetik 2019; 31: 149 (Abstract P-CytoG-144) (Weimar, Germany) |
(p) |
M |
| 550 |
N Ziller, A Ziegfeld, L
Lipfert, C Scheunengraber, C Greinke, L Jansen,
K Beer, T Liehr, M Gajda, IB
Runnebaum, M Dürst, C Backsch. Epigenetic and genetic alterations of ITIH5 during cervical carcinogenesis. Med Genetik 2019; 31: 115 (Abstract P-CancG-042) (Weimar, Germany) |
(p) |
TCG |
| 549 |
MAK Othman, B Grygalewicz, JB
Melo, IM Carreira, A Glaser, T Liehr.
KMT2A gene rearrangements displaying an important molecular marker in the diagnostic and prognostic of acute leukemia. Med Genetik 2019; 31: 110 (Abstract P-CancG-030) (Weimar, Germany) |
(p) |
TCG |
2018
| Number |
Authors/
Title/ Where Contribution was Published |
Poster (p)
or oral (o) |
Topic |
| 548 |
MT Souza, IA Pereira, M
Othman, GV Lozada, K Monteso, RC Ribeiro, T
Liehr, TJM Salles, R Hassan, MLM
Silva. Molecular cytogenetic characterization of partial trisomies: secondary chromosome abnormalities in childhood Burkitt lymphoma/ leukemia. Hematol Transfus Cell Therap 2018; 40: S303-S304 (Abstract 792) (Sao Paulo, Brazil) |
(p) |
TCG |
| 547 |
RRC Matos, K Monteso, MAK
Othman, MT Souza, DR Ney-Garcia, GM Ferreira,
MGP Land, T Liehr, RC Ribeiro,
MLM Silva. Molecular approaches to reveal a new three-way variant t(8;19;219 in a pediatric case of acute myeloid leukemia with RUNX-RUNX1T1. Hematol Transfus Cell Therap 2018; 40: S292 (Abstract 764) (Sao Paulo, Brazil) |
(p) |
TCG |
| 546 |
RRC Matos, DRN Garcia, MAK
Othman, GM Ferreira, K Monteso, JB Melo, C
Meyer, MGP Land, T Liehr, MLM
Silva. New complex KMT2A-R involving chromosomes 11, 16 and 19 in a child with acute myeloid leukemia/ myeloid sarcoma associated with overexpression of MLLT1 and ELL. Hematol Transfus Cell Therap 2018; 40: S292 (Abstract 763) (Sao Paulo, Brazil) |
(p) |
TCG |
| 545 |
DR Ney-Garcia, RRC Matos, MA
Othman, GM Ferreira, MT Souza, K Monteso, M
Land, RC Ribeiro, T Liehr, MLM
Silva. Molecular approaches reveal RUNX1 amplification and a rearrangement of NTRK3, a new leukemia putative gene, in a pediatric case of B-ALL: Discussing the intrachromosomal amplification of chromosome 21 (iAMP21). Hematol Transfus Cell Therap 2018; 40: S291 (Abstract 761) (Sao Paulo, Brazil) |
(p) |
TCG |
| 544 |
AM Zlotina, AV Maslova, NV
Kosyakova, T Liehr, AV Krasikova.
3D architecture of japanese quail DNA repeats in interphase nucleus. In Galkina S, Vishnevskaya M (2018) 23rd International Colloquium on Animal Cytogenetics and Genomics (23 ICACG) June 9–12, 2018, Saint-Petersburg, Russia. Comparative Cytogenetics 2018; 12: 299-360 (Abstract P33) |
(p) |
EVO |
| 543 |
TV Kulikova, LV Kazakova, AV
Maslova, DV Dedukh, IL Trofimova, T Liehr,
AV Krasikova. Loci-specific RNP-rich nuclear domains on lampbrush chromosomes: data pointing at RNA editing. In Galkina S, Vishnevskaya M (2018) 23rd International Colloquium on Animal Cytogenetics and Genomics (23 ICACG) June 9–12, 2018, Saint-Petersburg, Russia. Comparative Cytogenetics 2018; 12: 299-360 (Abstract P12) |
(p) |
EVO |
| 542 |
T Liehr. Molecular cytogenetics in Zoo-FISH-studies – still urgently needed. In Galkina S, Vishnevskaya M (2018) 23rd International Colloquium on Animal Cytogenetics and Genomics (23 ICACG) June 9–12, 2018, Saint-Petersburg, Russia. Comparative Cytogenetics 2018; 12: 299-360 (Abstract L6) |
o |
EVO |
20 17
| Number |
Authors/
Title/ Where Contribution was Published |
Poster (p)
or oral (o) |
Topic |
| 541 |
T Liehr. What about benign chromosomal imbalances in cancer genetics. Mol Cytogenet 2017; 10: S85 (Abstract A11) (Berkely, USA) |
o |
HET TCG |
| 540 |
EG Coci, A Auhuber, A
Langenbach, K Mrasek, J Riedel, A Leenen, T
Lücke, T Liehr. Unbalanced translocation affecting the long arms of chromosome 10 and 22 causes complex syndromes with very severe neurodevelopmental delay, speech impairment, autistic behavior, and epilepsy. Neuropediatrics 2017; 48: S1-S45(?) |
(p) |
CG |
| 539 |
M Volleth, M Zenker, T
Liehr. Destroying a myth LCLs are neither immortal nor karyotypically stable but acquire trisomy 12 as an early recurrent aberration. Mol Cytogenet 2017; 10: S72 (Abstract 8.P4) (Florence, Italy) |
(p) |
M |
| 538 |
A Zlotina, N Kosyakova, A
Maslova, T Liehr, A Krasikova. Lampbrush chromosome microdissection as an approach to comprehensive investigation of heterochromatic chromosome regions. Mol Cytogenet 2017; 10: 62 (Abstract 4.P10) |
(p) |
EVO |
| 537 |
S Singer, K Schaeferhoff, M
Kehrer, A Rieß, A Dufke, M Schoening, T
Liehr, UA Mau-Holzmann. Interstitial deletion 4q21.21q21.23 in a boy with severe developmental delay hypotonia macrocephaly and dysmorphic features due to a cryptic paracentric inversion inv(4)(q21.21q21.23)in the mother. Mol Cytogenet 2017; 10: S28-S29 (Abstract 1.P49) (Florence, Italy) |
(p) |
CG |
| 536 |
M Kehrer, A Dufke, S Singer,
T Liehr, U Grasshoff, K Buechner,
K Schaeferhoff. Terminal duplication of chromosome region 19q13.31q13.43 report of an infant with VACTERL association biliary atresia and global developmental delay. Mol Cytogenet 2017; 10: S25 (Abstract 1.P39) (Florence, Italy) |
(p) |
CG |
| 535 |
W Slimani, M Kammoun, H
Hannachi, A Jalloul, HB Hmida, Z Chioukh, A
Mlika, M Bibi, T Liehr, A Saad, S
Mougou-Zerelli. Strategy of identification and characterization of supernumerary marker chromosomes (SMC) a study about 29 cases. Mol Cytogenet 2017; 10: S19-S20 (Abstract 1.P20) (Florence, Italy) |
(p) |
sSMC |
| 534 |
M Moyses-Oliveira, R Fish, G
Giannuzzi, E Karaca, Z Akdemir, F Petit, V
Meloni, M Soares, L Kulikowski, A Di Battista, M
Zamariolli, T Liehr, N Kosyakova,
G Carvalheira, J Andrieux, M Neerman-Arbez, J
Lupski, MI Melaragno, A Reymond. Balanced X autosome translocation suggests association of AMMECR1 disruption with hearing loss short stature bone and heart alterations. Mol Cytogenet 2017; 10: S9-S10 (Abstract O5) (Florence, Italy) |
(p) |
CG |
| 533 |
I Iourov, S Vorsanova, T
Liehr, M Zelenova, O Kurinnaia, K
Vasin, Y Yurov. Chromothripsis as a mechanism driving genomic instability mediating brain diseases. Mol Cytogenet 2017; 10: S8-S9 (Abstract O2) (Florence, Italy) |
(p) |
CG |
2016
| Number |
Authors/
Title/ Where Contribution was Published |
Poster (p)
or oral (o) |
Topic |
| 532 |
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. Neuropediatrics 2016; 47 - P07-20 |
(p) |
CG |
| 531 |
M Weber, F Vasheghani, C
Göhner, T Liehr, E Schleussner,
JS Fitzgerald, UR Markert, A Weise. Karyotypes of trophoblastic cell lines. Placenta 2016; 45, 108 (Abstract P2.16) |
(p) |
CG |
| 530 |
S Winkler, S Brückner, M
Hempel, L Tietze, A Weise, N Kosyakova, S
Löhmer, T Liehr, B Christ. Verbesserung der Leberfunktion durch mesenchymale Stammzellen im Mausmodell des Alpha-1-Antitrypsinmangels. Zeitschrift für Gastroenterologie 2016; 54: 1343-1404 |
(p) |
CG |
| 529 |
A Faria de Figueiredo, A
Mencalha, R Rodrigues Capela de Matos, T
Liehr, B de Araujo Amaral, R Correa
Ribeiro, ML Macedo Silva, E Abdelhay. Clinical and biological correlates of selected polycomb complex genes expression in Brazilian children with acute promyelocytic leukemia. SIOP Congress 2016; no page# |
(p) |
TCG |
| 528 |
T Liehr. Cytogenetically visible copy number variations (CG-CNVs) in banding and molecular cytogenetics of human: About heteromorphisms and euchromatic variants. Cytogenet Genome Res 2016; 148: 145 (Abstract VI.12) (Foz de Iguazu, Brazil) |
o |
HET |
| 527 |
A Weise, K Wilhelm, LG
Quintana, B Franze, C Schider, AC Teichmann, K
Behr, T Liehr, K Mrasek. The fragile secret of 28 new molecularly mapped aphidicolon induced fragile sites shed light on gene and genome evolution. Med Genetik 2016; 28: 188 (Abstract P-CytoG-189) (Lübeck, Germany) |
(p) |
INT |
| 526 |
K Mrasek, K Wilhelm, C
Graetz, T Liehr, A Weise. Fanconi anemia as a model for the characterization of low frequency common fragile sites on human chromosome 1. Med Genetik 2016; 28: 186-187 (Abstract P-CytoG-185) (Lübeck, Germany) |
(p) |
INT |
| 525 |
PM Kroisel, S Verheyen, K
Wagner, MR Speicher, A Schwerin-Nagel, T
Liehr. Constitutional inverted insertion in a healthy parent as a pathogenetic cause for recurrent duplications in offspring. Med Genetik 2016; 28: 184 (Abstract P-CytoG-179) (Lübeck, Germany) |
(p) |
CG |
| Number |
Authors/
Title/ Where Contribution was Published |
Poster (p)
or oral (o) |
Topic |
| 524 |
AF Figueiredo, RRC Matos, M
Othman, T Liehr, EC Batista, ES
Costa, M Land, R Ribeiro, E Aabdelhay, MLM
Silva. Molecular cytogenetic studies characterizing a novel complex karyotype with an uncommon 5q22 deletion in childhood acute myeloid leukemia. Braz J Hematol Hemother 2015; 37: 214. (Abstract 604) (Sao Paulo, Brazil) |
(p) |
TCG |
| 523 |
EB Cifoni, RRC Matos, DR
Ney-Garcia, TF Borges, MT Souza, K Rittscher, T
Liehr, AF Figueiredo, MLM Silva. MLL/MLLT4 and MLL/MLLT10 fusion genes within complex karyotypes: Molecular cytogenetics and LDI-PCR characterization of 2 childhood cases with acute myeloid leukemia. Braz J Hematol Hemother 2015; 37: 213 (Abstract 602) (Sao Paulo, Brazil) |
(p) |
TCG |
| 522 |
RRC Matos, EC Batista, T
Liehr, M Othman, M Emerenciano, B
Lopes, MT Souza, AF Figueiredo, R Ribeiro, MLM
Silva. Conventional and molecular cytogenetic studies revealing an original karyotype, 46,XX,der(3)t(3;7)(q26;q21.1̃21.2),del(7)(q21.1̃21.2), associated with a dismal outcome in a pediatric acute myeloid leukemia patient. Braz J Hematol Hemother 2015; 37: 212 (Abstract 600) (Sao Paulo, Brazil) |
(p) |
TCG |
| 521 |
A Weise, N Kosyakova, M
Voigt, N Aust, K Mrasek, S Löhmer, N Rubtsov, T
Karamysheva, V Trifonov, D Hardekopf, 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. Russ Bull Perinat Pediatr 2015; 4: 180 (Moscow, Russia) |
(p) |
EVO |
| 520 |
A Wafa, M Asa’ad, A Ikhtiar,
T Liehr, W Al Achkar. Interstitial deletion 9p23 to 9p11.1 as sole additional abnormality in a Philadelphia positive chronic myeloid leukemia in blast crisis: A rare event. Russ Bull Perinat Pediatr 2015; 4: 179-180 (Moscow, Russia) |
(p) | TCG |
| 519 |
A Wafa, S Almedani, F
Moassass, T Liehr, MAK Othman, 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. Russ Bull Perinat Pediatr 2015; 4: 179 (Moscow, Russia) |
(p) | TCG |
| 518 |
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. Russ Bull Perinat Pediatr 2015; 4: 179 (Moscow, Russia) |
(p) | CG |
| 517 |
F Santiago, S Lima, T
Pinheiro, R Tavares Silvestre, U Barros Otero, M
Medeiros Tabalipa, N Kosyakova, MH Ornellas, T
Liehr, G Alves. Complex chromosomal rearrangements in peripheral blood and decreased amount of natural killer cells in two female gas station attendants of Rio de Janeiro. Russ Bull Perinat Pediatr 2015; 4: 178-179 (Moscow, Russia) |
(p) | TCG |
| 516 |
K Rittscher, 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). Russ Bull Perinat Pediatr 2015; 4: p178 (Moscow, Russia) |
(p) | TCG |
| 515 |
S Portela-Bens, MA Merlo, ME
Rodriguez, I Cross, M Manchado, N Kosyakova, T
Liehr, L Rebordinos. Integrated gene mapping and synteny studies give insights into the evolution of a sexual proto-chromosome in Solea senegalensis. Russ Bull Perinat Pediatr 2015; 4: 178 (Moscow, Russia) |
(p) | EVO |
| 514 |
MAK Othman, JB Melo, IM
Carreira, M Rincic, A Glaser, B Grygalewicz, B
Gruhn, K Wilhelm, K Rittscher, B Meyer, ML
Macedo Silva, T de Jesus Marques Salles, T
Liehr. High rates of submicroscopic aberrations in karyotypically normal acute lymphoblastic leukemia. Russ Bull Perinat Pediatr 2015; 4: 177-178 (Moscow, Russia) |
(p) | TCG |
| 513 |
MAK Othman, B Grygalewicz, B
Pienkowska-Grela, A Ejduk, M Rincic, J Melo, IM
Carreira, B Meyer, W Marzena, T Liehr.
A new IGH@ gene rearrangement associated with CDKN2A/B deletion in a young adult B-cell acute lymphoblastic leukemia (B-ALL). Russ Bull Perinat Pediatr 2015; 4: 177 (Moscow, Russia) |
(p) | TCG |
| 512 |
M Moysés-Oliveira, R Santos
Guilherme, V Ayres Meloni, A Di Battista, C
Berlim de Melo, S Bragagnolo, D
Moretti-Ferreira, N Kosyakova, T Liehr,
GM Carvalheira, MI Melaragno. X-linked intellectual disability-related genes disrupted by balanced X-autosome translocations. Russ Bull Perinat Pediatr 2015; 4: 176-177 (Moscow, Russia) |
(p) | CG |
| 511 |
O Kadioglu, J Cao, N
Kosyakova, K Mrasek, T Liehr, T
Efferth. Gene expression profiling of multidrug resistant CEM/ADR-5000 and sensitive CCRF-CEM leukemia cells to shed light on drug resistance mechanisms of tumors. Russ Bull Perinat Pediatr 2015; 4: 176 (Moscow, Russia) |
(p) | TCG |
| 510 |
R Hochstenbach, B Nowakowska,
M Volleth, A Ummels, A Kutkowska-Kaźmierczak, E
Obersztyn, K Ziemkiewicz, D Schanze, M Zenker, P
Muschk, I Schanze, C Gerloff, M Poot, T
Liehr. Parental origin of multiple small supernumerary marker chromosomes: evidence from a rare prenatal and postnatal case. Russ Bull Perinat Pediatr 2015; 4: 175-176 (Moscow, Russia) |
(p) | sSMC |
| 509 |
A Babameto-Laku, V Mokini, D
Roko, A Angioni, R Mingarelli, T Liehr,
B Dallapiccola. Clinical and molecular characterization of a patient with a 2q22.3 to 2q24.1 deletion. Russ Bull Perinat Pediatr 2015; 4: 175 (Moscow, Russia) |
(p) | CG |
| 508 |
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. Russ Bull Perinat Pediatr 2015; 4: 175 (Moscow, Russia) |
(p) | TCG |
| 507 |
W Al Achkar, F Moassass, R
Aroutiounian, T Harutyunyan, T Liehr,
A Wafa. Influence of Glutathione S-transferase (GSTT1 and GSTM1) gene polymorphism on imatinib failure in chronic myeloid leukemia patients. Russ Bull Perinat Pediatr 2015; 4: 174 (Moscow, Russia) |
(p) | TCG |
| 506 |
W Al Achkar, F Moassass, S
Almedani, T Liehr, A Wafa. Molecular cytogenetic characteristics of 24 variant Philadelphia translocations in Syrian chronic myeloid leukemia patients: a closer look on the derivative chromosomes 9. Russ Bull Perinat Pediatr 2015; 4: 173-174 (Moscow, Russia) |
(p) | TCG |
| 505 |
A Zlotina, N Kosyakova, T
Kulikova, T Liehr, A Krasikova. Microdissection of chicken lampbruch chromosome regions for FISH-probes generation and high-throughput sequencing. Chromosome Res 2015; 23: S77-S78 (Abstract 2.P7) (Strassburg, France) |
(p) |
EVO M |
| 504 |
T Jancuskova, R Plachy, J
Stika, L Zejskova, I Praulich, K-A Kreuzer, N
Kosyakova, T Liehr, S Pekova. Identification of two novel fusion partners of the MECOM gene in acute myeloid leukemia. Chromosome Res 2015; 23: S77-S78 (Abstract 2.P9) (Strassburg, France) |
(p) |
TCG |
| 503 |
T Liehr. European standards for clinical laboratory geneticist. Chromosome Res 2015; 23: S21 (Abstract L24) (Strassburg, France) |
o |
other |
| 502 |
T Liehr, S
Bhatt, K Piaszinski, N Kosyakova, F Xiaobo, E
Alhourani, JP Chaudhuri, A Weise. Chromosomes in a genome-wise order change the landscape of genetics. Europ J Hum Genet 2015; 23: S269 (Abstract PM13.10) (Glasgow, UK) |
p |
CG INT |
| 501 |
J Vukajlovic, S Cirkovic, D
Radivojevic, T Liehr, B Dobric, N
Ilic, M Miskovic, T Lalic, M Djurisic. Ring chromosome 22 in patients with multiple congenital anomalies. Europ J Hum Genet 2015; 23: S230 (Abstract PS11.111) (Glasgow, UK) |
(p) |
CG |
| 500 |
G Kayhan, MA Ergun, T
Liehr, M Yirmibes Karaoguz, EF
Percin. Primary amenorrhea, visual impairment and intellectual disability in a girl with a complex rearrangement involving 5q33.3 and 9q21.2 microdeletions. Europ J Hum Genet 2015; 23: S228-S229 (Abstract PM11.106) (Glasgow, UK) |
(p) |
CG |
| 499 |
YB Yurov, IY Iourov, SG
Vorsanova, T Liehr. Genome organization and instability in the schizophrenia brain. Europ J Hum Genet 2015; 23: S192-S193 (Abstract PM09.120) (Glasgow, UK) |
(p) |
INT |
| 498 |
I Tkach, K Sosnina, N
Huleyuk, O Terpylyak, D Zastavna, H Akopyan, A
Weise, N Kosyakova, T Liehr. Contribution of chromosomal abnormalities and genes of the major histocompatibility complex to early pregnancy losses. Europ J Hum Genet 2015; 23: S66 (Abstract PS01.65) (Glasgow, UK) |
(p) |
CG |
| 497 |
TV Karamysheva, T
Liehr, NB Rubtsov. Spatial organization of the intephase nucleus of human cells and positioning of small supernumerary chromosome in them. Meditsinskaya genetika [Medical genetics] 2015; 14: 9 (St. Petersburg, Russia) |
(p) |
INT sSMC |
| 496 |
Y Hellenbroich, J Weichert, G
Gillessen-Kaesbach, J Ribbat-Idel, T
Liehr. Prenatal diagnosis of a complex deletion and duplication of chromosome 2q due to a maternal paracentric double inversion. Med Genentik 2015; 1: 176 (Abstract P-Prenat-182) (Graz, Austria) |
(p) |
CG |
| 495 |
K Mrasek, X Fan, K Pinthong,
H Mkrtchyan, P Siripiyasing, N Kosyakova, W
Supiwong, A Tanomtong, A Chavareech, T
Liehr, M de Bello Cioffi, A Weise. First detailed reconstruction of the male Trachypithecus cristatus karyotype 44,XY1Y2. Med Genentik 2015; 1: 175 (Abstract P-NormV-178) (Graz, Austria) |
(p) |
EVO |
| 494 |
M Kehrer, T Liehr,
T Benkert, S. Singer, U Grasshoff, K
Schaferhoff, M Bonin, A Weicheslbaum, A
Tzschach. Interstitial duplication of chromosome region 1q25.1q25.3: report of a patient with mild congnitive deficits, tall structure and facial dysmorphisms. Med Genentik 2015; 1: 156-157 (Abstract P-ClinG-128) (Graz, Austria) |
(p) |
CG |
| 493 |
D Korinth, D Horn, A von
Moers, U Remmels, W Heinritz, P Küpferling, T
Liehr, NC Oien, H Neitzel, C Bommer,
E Klopocki, R Henze-Kersten, S Picht, S Mundlos.
Two patients with proximal deletion 20q syndrome. Med Genentik 2015; 1: 135 (Abstract P-ClinG-068) (Graz, Austria) |
(p) |
CG |
2014
| Number |
Authors/
Title/ Where Contribution was Published |
Poster (p)
or oral (o) |
Topic |
| 492 |
LT Cabral, DRN Garcia, TF
Borges, S Rouxinol, F Neves, TJ Marques-Salles,
T Liehr, MLM Silva. Utilização diferenciada da ETV6/RUNX1 auxilia a detecção de diferentes anormalidades citogenéticas em pacientes com LLA pediátrica. Revista Brasileira de Hematologia e Hemoterapia São Paulo - ABHH 2014; 36: 210 (Forianopolis, Brazil) |
(p) |
TCG |
| 491 |
RR Capela de Matos, AF De
Figueiredo, T Liehr, MAK Othman,
E Alhourani, TF Borges, R Binato, E
Abdelhay, RC Ribeiro, MLM Silva. Novel variant three-way t(8;13;21)(q22;q33;q22) revealed in a child with Acute Myeloid Leukemia FAB AML-M2: A contribution by molecular approaches. Revista Brasileira de Hematologia e Hemoterapia São Paulo - ABHH 2014; 36: 207 (Forianopolis, Brazil) |
(p) |
TCG |
| 490 |
DRN Garcia, T Liehr,
E Abdelhay, R Binato, F Neves, MT De Souza, TF
Borges, MAK Othman, 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. Revista Brasileira de Hematologia e Hemoterapia São Paulo - ABHH 2014; 36: 206-207 (Forianopolis, Brazil) |
(p) |
TCG |
| 489 |
RRC Matos, AF De Figueiredo,
BAS Amaral, TF Borges, T Liehr, F Neves, K
Carriço, TJ Marques-Salles, RC Ribeiro, MLM
Silva. Molecular characterization of 14 complex karyotypes in a cohort of 115 pediatric patients with acute myeloid leukemia. Revista Brasileira de Hematologia e Hemoterapia São Paulo - ABHH 2014; 36: 204 (Forianopolis, Brazil) |
(p) |
TCG |
| 488 |
DRN Garcia, T Liehr,
M Emerenciano, MSP Oliveira, E Alhourani, MT De
Souza, TF Borges, RC Ribeiro, M Land, MLM Silva.
A cryptic translocation fusing the MLL and MLLT3 genes in a case of childhood Acute Lymphoblastic Leukemia with complex karyotype. Revista Brasileira de Hematologia e Hemoterapia São Paulo - ABHH 2014; 36: 203-204 (Forianopolis, Brazil) |
(p) |
TCG |
| 487 |
DRN Garcia, AF De Figueiredo,
MT De Souza, TF Borges, TJ Marques-Salles, MAK
Othman, T Liehr, RC Ribeiro, M
Land, MLM Silva. Cytogenetics and molecular
characterization of mixed lineage leukemia gene
rearrangements in childhood acute leukemia with
complex karyotypes. Revista Brasileira de Hematologia e Hemoterapia São Paulo - ABHH 2014; 36: 203 (Forianopolis, Brazil) |
(p) |
TCG |
| 486 |
AM Zlotina, N Kosyakova, TV
Kulikova, T Liehr, AV Krasikova.
Microdissection of giant chromosomes from growing chicken oocytes as a method to obtain highly specific DNA probes. Abstracts of the XVII Russian Symposium on the Structure and Function of Cell Nucleus. Tsitologiia 2014; 56: 657-658 (in Russian) |
(p) |
EVO |
| 485 |
MM Oliveira, RS Guilherme, SS
Takeno, MA Haidar, GM Carvalehira, N Kosyakova,
K Mrasek, E Klein, T Liehr, MI
Melaragno. Gonadal dysgenesis in a women with an unusual t(X;9) and partial trisomy of chromosome 9 centromeric region. Europ J Hum Genet 2014; 21: S464 (Abstractnr. P20.61) (Milan, Italy) |
(p) |
CG |
| 484 |
RS Guilherme, S Bragagnolo,
ARN Dutra, ABA Perez, SS Takeno, MM Oliveira, LD
Kulikowski, E Klein, AB Hamid, T Liehr,
MI Melaragno. First report of a small supernumerary marker chromosome derivative from chromosomes 8 and 14. Europ J Hum Genet 2014; 21: S461 (Abstract P20.52) (Milan, Italy) |
(p) |
sSMC |
| 483 |
RS Guilherme, MCP Cenarch, TE
Sfakianakis, SS Takeno, LMM 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 hypoplasia cerebellar and defects in skull ossification. Europ J Hum Genet 2014; 21: S425-S426 (Abstract P20.15) (Milan, Italy) |
(p) |
CG |
| 482 |
YB Yurov, SG Vorsanova, AD
Kolotii, IA Demidova, T Liehr, IY
Iourov. Paradoxical somatic genetics of neurodegeneration: spotlight on postzygotic chromosome instability in the ataxia telangiectasia brain and implications for neurodegenerative diseases. Europ J Hum Genet 2014; 21: S232 (Abstract P08.82) (Milan, Italy) |
(p) |
INT |
| 481 |
IY Iourov, SG Vorsanova, IA
Demidova, OS Kurinnaia, AD Kolotii, VS Kravets,
MA Zelenova, T Liehr, YB Yurov. Mosaic copy number variation in the autism and schizophrenia brain: providing a basis for a new (mitotic) theory of neuropsychiatric diseases. Europ J Hum Genet 2014; 21: S194 (Abstract P06.13) (Milan, Italy) |
(p) |
INT |
| 480 |
L Rodríguez, M
García-Castro, A Plasencia, J Fernández-Toral, S
Bhatt, T Liehr, E Abarca. A characterization of a new complex chromosome rearrangement (CCR) between chromosome 3 and chromosome 8. Europ J Hum Genet 2014; 21: S90 (Abstract P02.020) (Milan, Italy) |
(p) |
CG |
| 479 |
K Writzl, A Veble, L
Lovrečić, T Liehr, B Peterlin. Microduplication of 17q22q23.2 due to a supernumerary marker chromosome in a girl with macrocephaly and global developmental delay. Europ J Hum Genet 2014; 21: S89 (Abstract P02.017) (Glasgow, UK) |
(p) |
sSMC |
| 478 |
K Mrasek, SS Bhatt, M
Manvelyan, K Moradkhani, F Hunstig, 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. Med Genetik 2014; 26: 169 (Abstract P-CytoG-180) (Essen, Germany) |
(p) |
CG |
| 477 |
UA Mau-Holzmann, S Singer, M
Bonin, K Schaeferhoff, K-O Kagan, S Haen, T
Liehr. 46,XX,der(6)(pter->q27::q27->q24::q27->qter) in a fetus with mutiple malformations and complex mosaic in the placenta: unexpected cytogenetic findings, limitations in array-anaylsis and clinical findings. Med Genetik 2014; 26: 169 (Abstract P-CytoG-179) (Essen, Germany) |
(p) |
CG |
| 476 |
E Klein, AB Hamid, M Volleth,
T Liehr. Human dicentric chromosomes and their centromere activity. Med Genetik 2014; 26: 168 (Abstract P-CytoG-177) (Essen, Germany) |
(p) |
sSMC |
| 475 |
JP Chauduri, K Piazinski, JU
Walter, N Kosyakova, X Fan, E Alhourani, T
Liehr, A Weise. Chromosomes in a genome-wise order change the landscape of genetics in form and function. Med Genetik 2014; 26: 166 (Abstract P-CytoG-170) (Essen, Germany) |
(p) |
CG INT |
| 474 |
B Patel, T Liehr,
M Desai, B Parikh, J Sheth, F Sheth. Characterization of prenatally detected small Supernumerary Marker Chromosomes (sSMC) by molecular cytogenetic technique: FISH. Mol Cytogenet 2014; 7: SP55 (Ahmedabad, India) |
(p) |
sSMC |
| 473 |
T Liehr. Uniparental disomy - clinical consequences due to imprinting and activation of recessive genes. Mol Cytogenet 2014; 7: SI21 (Ahmedabad, India) |
o |
UPD |
| 472 |
T Liehr. Small supernumerary marker chromosomes – an update. Mol Cytogenet 2014; 7: SI11 (Ahmedabad, India) |
o |
sSMC |
2013
| Number |
Authors/
Title/ Where Contribution was Published |
Poster (p)
or oral (o) |
Topic |
| 471 |
T Liehr. Benign and pathological chromosomal imbalances – microscopic and submicroscopic copy number variations (CNVs) in human genetics. Biol J Arm 2013: 65: S17-S18 |
o |
HET |
| 470 |
I Iourov, S Vorsanove, T
Liehr, Y Yurov. Aneuploidy-driven non-heritable genomic variations demonstrate area-specific distribution in the Alzheimer’s disease brain. Mol Neuodegen 2013; 8: S30-S31 (Abstract P52) (Cannes, France) |
(p) |
INT |
| 469 |
Y Yurov, S Vorsanova, T
Liehr, I Yurov. Ataxia-teleangiectasia paradoxes: spotlight on post-zygotic chromosome instability in the brain and its contribution to neurodegenerationpathways. Mol Neuodegen 2013; 8: S30 (Abstract P51) (Cannes, France) |
(p) |
INT |
| 468 |
S Singer, A Rieß, T
Liehr, UA Mau-Holzmann. Male infertility and short stature due to a complex mosaicism of the Y-chromosome. Chromosome Res 2013; 21: S59 (Abstract 1P56) (Dublin, Ireland) |
(p) |
CG |
| 467 |
I Škrlec, J Wagner, M Merkaš,
S Pušeljić, M Heffer, L Brečević, T Liehr.
De novo case of 3p deletion syndrome. Chromosome Res 2013; 21: S47 (Abstract 1P31) (Dublin, Ireland) |
(p) |
CG |
| 466 |
S Custódio, R
Silveira-Santos, S Serafim, M Ávila, A Sousa, AB
Sousa, E Klein, AB Hamid, T Liehr,
I Cordeiro. Neocentromere formation on an 8q-derived ring chromosome. Chromosome Res 2013; 21: S46 (Abstract 1P29) (Dublin, Ireland) |
(p) |
CG |
| 465 |
M Vešić, M Jelisavčić, S
Nikšić, G Čuturilo, VI Deretić, T Liehr.
A case of a patient with multiple sSMC without phenotypic effect. Chromosome Res 2013; 21: S16 (Abstract 1P1) (Dublin, Ireland) |
(p) |
sSMC |
| 464 |
T Liehr. Small supernumerary marker chromosomes (sSMC) – what about the genotype-phenotype correlation? Chromosome Res 2013; 21: S16 (Abstract L17) (Dublin, Ireland) |
o |
sSMC |
| 463 |
MM Oliveira, RS Guilherme, SS
Takeno, MA Haidar, GM Carvalehira, N Kosyakova,
K Mrasek, E Klein, T Liehr, MI
Melaragno. Gonadal dysgenesis in a woman with an unusual t(X;9) and partial trisomy of chromosome 9 centromeric region. Europ J Hum Genet 2013; 21: S464 (Abstract P20.61) (Paris, France) |
(p) |
CG |
| 462 |
RS Guilherme, S Bragagnolo,
ARN Dutra, ABA Perez, SS Takeno, MM Oliveira, LD
Kulikowski, E Klein, AB Hamid, T Liehr,
MI Melaragno. First report of a small supernumerary marker chromosome derivative from chromosome 8 and 14. Europ J Hum Genet 2013; 21: S461 (Abstract P20.52) (Paris, France) |
(p) |
sSMC |
| 461 |
RS Guilherme, MCP Cenarch, TE
Sfakianakis, SS Takeno, LMM 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 hypoplasia cerebellar and defects in skull ossification. Europ J Hum Genet 2013; 21: S452-453 (Abstract P20.15) (Paris, France) |
(p) |
CG |
| 460 |
YB Yurov, SG Vorsanova, AD
Kolotii, IA Demidova, T Liehr, IY
Iourov. Paradoxical somatic genetics of neurodegeneration: spotlight on postzygotic chromosome instability in the ataxia telangiectasia brain and implications for neurodegenerative diseases. Europ J Hum Genet 2013, Vol 21 Suppl 2, p 232 (Abstractnr P08.82) (Paris, France) |
(p) |
INT |
| 459 |
IY Iourov, SG Vorsanova, IA
Demidova, OS Kurinnaia, AD Kolotii, VS Kravets,
MA Zelenova, T Liehr, YB Yurov. Mosaic copy number variation in the autism and schizophrenia brain: providing a basis for a new (mitotic) theory of neuropsychiatric diseases. Europ J Hum Genet 2013; 21: S194 (Abstract P06.1) (Paris, France) |
(p) |
INT |
| 458 |
L Rodríguez, M García-Castro,
A Plasencia, J Fernández-Toral, S Bhatt, T
Liehr, E Abarca. Characterization of a new complex chromosome rearrangement. Europ J Hum Genet 2013; 21: S90 (Abstract P02.020) (Paris, France) |
(p) |
CG |
| 457 |
K Writzl, A Veble, L
Lovrečić, T Liehr, B Peterlin. Microduplication of 17q22q23.2 due to a supernumerary marker chromosome in a girl with macrocephaly and global developmental delay. Europ J Hum Genet 2013; 21: S89 (Abstract P02.17) (Paris, France) |
(p) |
CG |
| 456 |
A Weise, S Bhatt, JU Walther,
T Liehr, A Altendorf-Hofmann, JP
Chaudhuri. The long shadow of parental genomes - organizing the next generation nuclei. Med Genetik 2013; 25:155 (Abstractn P-CytoG-177) (Dresden, Germany) |
(p) |
CG INT |
| 455 |
M Voigt, 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. Med Genetik 2013; 25: 155 (Abstract P-CytoG-176) (Dresden, Germany) |
(p) |
TCG |
| 454 |
H Nelle, R Santos Guilherme,
E Klein, C Venner, M Volleth, AD Polityko, T
Liehr. Human ring chromosomes and small supernumerary marker chromosomes - do they have telomeres? Med Genetik 2013; 25:152 (Abstract P-CytoG-168) (Dresden, Germany) |
(p) |
sSMC |
| 453 |
T Liehr, A
Grigorian, M Manvelyan, I Simonyan, H Mkrtchyan,
R Aroutiounian, AD Polityko, AI Kulpanovich, M
Volleth, M Ziegler, K Kreskowski, A Weise, N
Kosyakova. Heteromorphic variants of chromosome 9. Med Genetik 2013; 25:152 (Abstract P-CytoG-167) (Dresden, Germany) |
(p) |
HET |
| 452 |
JP Chaudhuri, S Bhatt, T
Liehr, JU Walther, A Weise. Spatial organisation of the two parental genomes of a blood/bone marrow cell as tested by pod-FISH and its promotion of granulocytic function. Med Genetik 2013; 25: 148-149 (Abstract P-CytoG-157) (Dresden, Germany) |
(p) |
INT |
| 451 |
D Prütz, S Krüger, B Belitz,
T Liehr, W Heinritz. Syndromal mental retardation in a boy with a maternally inherited interstitial duplication Xp21.3p22.12. Med Genetik 2013; 25: 133 (Abstract P-ClinG-111) (Dresden, Germany) |
(p) |
CG |
| 450 |
K Mrasek, A Weise, T Knösel,
T Liehr, U Settmacher, A
Altendorf-Hofmann, N Aust. The loss of chromosome 4 - a correlation with the long-term survival and the recurrence rate after R0 resection of colorectal liver metastasis. Med Genetik 2013; 25: 107 (Abstract P-CancG-032) (Dresden, Germany) |
(p) |
CG |
| 449 |
T Liehr. The Clinical Laboratory Geneticists Section of the European Board of Medical Genetics (EBMG). Med Genetik 2013; 25: 66 (Abstract Talk nach 12) (Dresden, Germany) |
o |
other |
2012
| Number |
Authors/
Title/ Where Contribution was Published |
Poster (p)
or oral (o) |
Topic |
| 448 |
AF Figueiredo, TAP Vieira, T
Liehr, E Carboni, F Watanabe, MT
Souza, TJM Salles, E Abdelhay, MLM Silva. A rare t(8;17)(q21;q12) with the loss of P53 gene in a child with myeloid sarcoma that present involvement of bone marrow. Rev Bras Hematol Hemoter 2012; 34: S352 (Abstract 0697) (Rio de Janeiro, Brazil) |
(p) |
TCG |
| 447 |
TP Vieira, DR Ney-Garcia, MT
Souza, LT Cabral, AMA Boulhosas, ES Costa, T
Liehr, E Abdelhay, RC Ribeiro, ML
Macedo-Silva. Cytogenetic and CDKN2A deletion analysis in 18 cases of childhood T-cell acute lymphoblastic leukemia. Rev Bras Hematol Hemoter 2012; 34: S351-S352 (Abstract 0689) (Rio de Janeiro, Brazil) |
(p) |
TCG |
| 446 |
AF Figueiredo, T Liehr,
GR Oberlaender, TJM Salles, MT Souza, TF Borges,
MM Campos, RC Ribeiro, E Abdelhay, MLM Silva. Different MLL rearrangements at diagnosis of AML-M5 and relapse detected in a child : ins(11;1)(q23;q21q31) and t(11;19)(q23;p13). Rev Bras Hematol Hemoter 2012; 34: S351-352 (Abstract 0687) (Rio de Janeiro, Brazil) |
(p) |
TCG |
| 445 |
DRN Garcia, TP Vieira, T
Liehr, MT Souza, RRC Matos, AF
Figueiredo, J Dobbin, E Abdelhay, RC Ribeiro,
MLM Silva. A T-ALL childhood case with a complex t(9;9) and homozygous deletion of CDKN2A gene associated to a Philadelphia-positive minor subclone. Rev Bras Hematol Hemoter 2012; 34: S343-S344 (Abstract 0678) (Rio de Janeiro, Brazil) |
(p) |
TCG |
| 444 |
LT Cabral, DR Ney-Garcia, MT
Souza, AP Bueno, AM Boulhosas, T Liehr,
E Abdelhay, RC Ribeiro, MLM Silva, TP Vieira. Estudio citogenetico molecular em leukemia linfoblastica aguda da infancia com fusao ETV/RUNX1. comparacao das alteracoes adicionais entre casos de diagnostico e recaida. Rev Bras Hematol Hemoter 2012; 34: S354 (Abstract 0702) (Rio de Janeiro, Brazil) |
(p) |
TCG |
| 443 |
DS Cetra, AF Figueiredo, MT
Souza, RR Matos, BA Amaral, T Liehr,
E Abdelhay, TJ Salles, MLM Silva. Análise citogenetica de casos de leucemia promielocitica aguda da infancia no Brasil através do emprego de multicolor FISH. Rev Bras Hematol Hemoter 2012; 34: S341 (Abstract 0672) (Rio de Janeiro, Brazil) |
(p) |
TCG |
| 442 |
MT Souza, TP Vieira, T
Liehr, TF Borges, S Bhatt, TJM
Salles, BA Amaral, AMB Azevedo, Raul, MLM Silva.
Classic and molecular cytogenetic studies of
Brazilian childhood and adolescent Burkitt
lymphoma/leukemia. Rev Bras Hematol Hemoter 2012; 34: S338 (Abstract 0665) (Rio de Janeiro, Brazil) |
(p) |
TCG |
| 441 |
RRC Matos, T Liehr,
S Bhatt, H Mkrtchyan, AF Figueiredo, TJM Salles,
BA Amaral, MT Souza, E Abdelhay, MLM Silva. Cytogenetic and molecular studies in karyotypes presenting cryptical abnormalities in childhood acute myeloid leukemia. Rev Bras Hematol Hemoter 2012; 34: S344 (Abstract 0679) (Rio de Janeiro, Brazil) |
(p) |
TCG |
| 440 |
X Fan, T Liehr,
M Voigt, N Kosyakova, K Mrasek, V Trifonov, T
Karamysheva, N Rubtsov, A Weise. Array painting in Hylobates lar characterizes in detail 44 evolutionary conserved breakpoints. Chromosome Res 2012; 20: 807 (Abstract PIV-34) (?) |
(p) |
EVO |
| 439 |
AF Figueiredo, BA Amaral, T
Liehr, TP Vieira, DS Cintras, RR
Capela de Matos, TJ Marques-Salles, EM Soares
Ventura, RC Ribeiro, E Abdelhay, MLM Silva. Improved childhood acute myeloid leukemia chromosomic profile with the application of multicolor banding chromosome. Rev Bras Hematol Hemoter 2012; 34: S29 (Abstract PO0015) (São José do Rio Preto, Brazil) |
(p) |
TCG |
| 438 |
MT de Souza, TP Vieira, AF de
Figueiredo, TJ Marques-Salles, BA Amaral, E
Abdelhay, TF Borges, AMB Azevedo, J Dobbin, T
Liehr, RC Ribeiro, MLM Silva. Estudo citogenetico e molecular revelou anormalidades cromossomicas cripticas e heterogeneidade da fusao IGH/MYC em caso de linfoma de Burkitt da infancia. Rev Bras Hematol Hemoter 2012; 34: S27-S28 (Abstract PO011) (São José do Rio Preto, Brazil) |
(p) |
TCG |
| 437 |
RCC de Matos, AF Figueiredo,
BA Amaral, TP Vieira, MT de Souza, E Abdelhay,
IC Machado, J Dobbin, RC Riebeiro, T
Liehr, H Mktrchyan. Cytogenetic and multicolor FISH studies revealed an cryptic rearrangement of the chromosome in addition to a t(15;17)(q22;q21) in a child with acute promyelocytic leukemia. Rev Bras Hematol Hemoter 2012; 34: S26-S27 (Abstract PO009) (São José do Rio Preto, Brazil) |
(p) |
TCG |
| 436 |
ML Macedo-Silva, DR
Ney-Garcia, MT Souza, T Liehr, E
Abdelhay, RCC Matos, TJ Marques-Salles, TF
Borges, J Dobbin, RC Ribeiro, TP Vieira. Clinical, G banding and molecular cytogenetic studies uncover a rare case of childhood T-cell acute lymphoblastic leukemia presenting a t(9;9)(p12;q12) and homozygous deletion of CDKN2A with a subpopulation. Rev Bras Hematol Hemoter 2012; 34: S25-S26 (Abstract PO006) (São José do Rio Preto, Brazil) |
(p) |
TCG |
| 435 |
ML Macedo-Silva, DR
Ney-Garcia, T Liehr, S Bhatt, E
Sobral, E Abdelhay, AF de Figueiredo, MT de
Souza, J Dobbin, RC Ribeiro, TP Vieira. Caraterizacao citigenetica molecular de rearranjos ou raros de gene MLL em leucemias agudas da infancia. Rev Bras Hematol Hemoter 2012; 34: S25 (Abstract PO005) (São José do Rio Preto, Brazil) |
(p) |
TCG |
| 434 |
MV Mulatinho, CLC Serao, K
Mrasek, A Weise, T Liehr, JC
Llerena Jr. Derivative chromosome 13 defined by molecular cytogenetic as direct tandem duplication [46,XY,dup(13)(pter->q31.3:q14.3- >qter)] associated to intellectual disability, Kallman syndrome and overgrowth. Resumos do 58o Congresso Brasileiro de Genética 2012; ISBN 978-85-89109-06-2. (Foz do Iguaçu, Paraná, Brasil.) |
(p) |
CG |
| 433 |
A Weise, M Voigt, K Mrasek, N
Rubtsov, T Karamysheva, V Trifonov, N Kosyakova,
X Fan, T Liehr. Array painting of Gibbon chromosomes enables access to 44 evolutionary breakpoints compared to the human genome. Europ J Hum Genet 2012; 20: S250 (Abstract P10.08) (Nürnberg, Germany) |
(p) |
EVO |
| 432 |
M Volleth, T Liehr,
D Schanze, M Zenker, P Muschke, I Schanze. Prenatal diagnosis of multiple small supernumerary marker chromosomes (sSMCs) of different centromeric origin. Europ J Hum Genet 2012; 20: S 149 (Abstract P05.32) (Nürnberg, Germany) |
(p) |
sSMC |
| 431 |
K Mrasek, E Klein, D
Hardekopf, S Pekova, S Bhatt, N Kosyakova, T
Liehr, A Weise. Microdeletion and microduplication syndromes. Europ J Hum Genet 2012; 20: S122 (Abstract P03.091) (Nürnberg, Germany) |
(p) |
CG |
| 430 |
H Nelle, M Buksch, M
Ziegler, N Kosyakova, S Morlot, W Fischer, B
Belitz, V Trifonov, A Weise, A Hamid, T
Liehr. A new multicolor-fluorescence in situ hybridization probe set directed against human heterochromatin: HCM-FISH. Europ J Hum Genet 2012; 20: S116-S117 (Abstract P03.063) (Nürnberg, Germany) |
(p) |
HET M |
| 429 |
A Hovhanissyan, S Midyan, A
Gasparyan, T Liehr, H Mkrtchyan.
A de novo interstitial duplication 14q32.11-q32.32. Europ J Hum Genet 2012; 20: S115 (Abstract P03.057) (Nürnberg, Germany) |
(p) |
CG |
| 428 |
H Mkrtchyan, S Midyan, A
Gasparyan, T Liehr, A
Hovhannisyan. A new case with de novo proximal duplication of 10q11.2q21.3. Europ J Hum Genet 2012; 20: S115 (Abstract P03.055) (Nürnberg, Germany) |
(p) |
CG |
| 427 |
S Midyan, A Hovhannisyan, A
Gasparyan, E Klein, T Liehr, H
Mkrtchyan. Trisomy 8p11.23 as a result of a dicentric chromosome 8. Europ J Hum Genet 2012; 20: S114 (Abstract P03.052) (Nürnberg, Germany) |
(p) |
CG |
| 426 |
YB Yurov, SG Vorsanova, AD
Kolotii, T Liehr, IY Iourov. Brain-specific X chromosome aneuploidy is likely to contribute to the pathogenesis of autism and can explain the unsolved paradox of male susceptibility. Europ J Hum Genet 2012; 20: S109 (Abstract P03.022) (Nürnberg, Germany) |
(p) |
INT |
| 425 |
IY Iourov, SG Vorsanova, T
Liehr, AD Kolotii, IA Demidova, AK
Beresheva, IV Soloviev, YB Yurov. Genomic instability in the Alzheimer’s disease brain: cancer-like cellular behavior mediates neurodegeneration via non-malignant aneuploidization. Europ J Hum Genet 2012; 20: S107 (Abstract P03.014) (Nürnberg, Germany) |
(p) |
INT |
| 424 |
DT Babikyan, H Mkrtchyan, S
Midyan, M Nõukas, K Männik, A Hovhannesyan, A
Gasparyan, T Liehr, A Kurg, TF
Sarkisian. Molecular cytogenetic characterization of a family with 3p deletion and 3p duplication cases. Europ J Hum Genet 2012; 20: S52 (Abstract P02.009) (Nürnberg, Germany) |
(p) |
CG |
| 423 |
C Wölfel, T Knösel, T
Liehr, S Hauke, A Altendorf Hofmann,
D Katenkamp, I Petersen. c-Met in undifferentiated pleomorphic sarcomas and fibroblastic/myofibroblastic tumors. Der Pathologe 2012; 33: S139 (Abstract FR-P-175) (Berlin, Germany) |
(p) |
TCG |
| 422 |
AF Figueiredo, BA Amaral, T
Liehr, TP Vieira, DS Cintra, RR
Capela de Matos, TJ Marques Salles, EM Soares
Ventura, RC Ribeiro, E Abdelhay, MLM Silva. Improved childhood acute myeloid leukemia chromosomic profile with the application of multicolor banding. Rev Bras Hematol Hemoterap 2012; 34: S29 (Abstract PO015) (Natal, Brazil) |
(p) |
TCG |
| 421 |
MT de Souza, TP Vieira, AF de
Figueiredo, TJ Marques-Salles, BA Amaral, E
Abdehay, TF Borges, AMB Azevedo, J Dobbin, T
Liehr, RC Ribeiro, MLM Silva. Estudio citogenetico e molecular revelou anormalidades cromossomicas cripticas e heterogeneidade da fusao IGH/MYC em casos de linfomo de Burkitt da infancia. Rev Bras Hematol Hemoterap 2012; 34: S27-S28 (Abstract PO011) (Natal, Brazil) |
(p) |
TCG |
| 420 |
RRC de Matos, AF Figueiredo,
BA Amaral, TP Vieira, MT de Souza, E Abdelhay,
IC Machado, J Dobbin, RC Ribeiro, MLM Silva, T
Liehr, H Mkrtchyan. Cytogenetic and multicolor FISH studies revealed an cryptic rearrangement of the chromosome 6 in addition to a t(15;17)(q22;q21) in a child with acute promyelocytic leukemia. Rev Bras Hematol Hemoterap 2012; 34: S26-S27 (Abstract PO009) (Natal, Brazil) |
(p) |
TCG |
| 419 |
ML Macedo-Silva, DR
Ney-Garcia, MT de Souza, T Liehr,
E Abdelhay, RRC Matos, TL Marques-Salles, TF
Borges, J Dobbin, RC Ribeiro, TP Vieira. Clinical, G banding and molecular cytogenetic studies uncover a rare case of childhood T cell acute lymphoblastic leukemia presenting a t(9;9)(p12;q12) and homocygous deletion of CDKN2A with a subpopulation. Rev Bras Hematol Hemoterap 2012; 34: S25-S26 (Abstract PO006) (Natal, Brazil) |
(p) |
TCG |
| 418 |
ML Macedo-Silva, DR
Ney-Garcia, T Liehr, S Bhatt, E
Sobral, E Abdelhay, AF de Figueiredo, MT de
Souza, J Dobbin, RC Ribeiro, TP Vieira. Caractericao citogenetica molecular de rearranjos complexos ou raros do gene MLL em leucemias agudas da infancia. Rev Bras Hematol Hemoterap 2012; 34: S25 (Abstract PO005) (Natal, Brazil) |
(p) |
TCG |
2011
| Number |
Authors/
Title/ Where Contribution was Published |
Poster (p)
or oral (o) |
Topic |
| 417 |
M Weber, A Weise, K Mrasek, L
Khachaturyan, DM Morales Prieto, T Liehr,
UR Markert, JS Fitzgerald. Cytogenetic and STAT3 expression analysis of HTR8/SVneo. Am J Reprod Immunol 2011; 65: S15 (?) (?) |
(p) |
TCG |
| 416 |
A Weise, M Weber, T
Liehr, UR Markert, JS Fitzgerald. Fusion between HTR8/SVneo and HUVEC. J Reprod Immunol 2011; 90: 183 (Abstract P37) (Copenhagen, Denmark) |
(p) |
TCG |
| 415 |
TJ Marques-Salles, EM
Soares-Ventura, MTC Muniz, EF Silva, EP Leite,
JEXS barros, H Mkrtchyan, T Liehr,
MLM Silva, N Santos. Estudos citogenéticos nas leucemias do lactente. Rev Bras Hematol Hemoterap 2011; 33: S319 (Abstract 0758) (Sao Paulo, Brazil) |
(p) |
TCG |
| 414 |
TJ Marques-Salles, N Santos,
EM Soares-Ventura, BAS Amaral, TC Munic, EF
Silva, T Marquim, S Bhatt, T Liehr,
MLM Silva. Down syndrome AML-M0 with ring chromosome 7 defined by molecular cytogenetics studies. Rev Bras Hematol Hemoterap 2011; 33: S320 (Abstract 0759) (Sao Paulo, Brazil) |
(p) |
TCG |
| 413 |
EM Soares-Ventura, H
Mkrtchyan, TJ Marques-Salles, JEXS Barros, MTMN
Cornelio, BAS Amaral, MAF Hernandes, T
Liehr, MLM Silva, MTC Muniz. Estudo citogenético e molecular em cariótipos complexos ne leukemia aguda de infância. Rev Bras Hematol Hemoterap 2011; 33: S179 (Abstract 0422) (Sao Paulo, Brazil) |
(p) |
TCG |
| 412 |
YB Yurov, SG Vorsanova, A
Kolotii, T Liehr, IY Iourov. Aneuploidy in the autistic brain. The first molecular cytogenetic study. Balk J Med Genet 2011; 14: S73 (Abstract P59) (Timisoara, Romania) |
(p) |
INT CG |
| 411 |
IY Iourov, SG Vorsanova, AD
Kolotii, T Liehr, IA Demidova, AK
Beresheva, VS Kravets, OS Kurinnaia, IV
Soloviev, YB Yurov. Non-malignanat aneuploidization of the human brain is a susceptibility factor complex for neuropsychiatric diseases. Balk J Med Genet 2011, Vol 14 (Suppl), pp 9-10 (Abstractnr. L 05) (Timisoara, Romania) |
(o) |
INT CG |
| 410 |
A Weise, M Weber, T
Liehr, UR Markert, JS Fitzgerald. Fusion between HTR/8SVneo and HUVEC. J Reproduct Immunol 2011; 90: 183 (Abstract P37) (Copenhagen. Denmark) |
(p) |
TCG |
| 409 |
M Weber, A Weise, K Mrasek, M
P San Roman, l Khachaturyan, DM Morlaes, T
Liehr, UR Markert, JS Fitzgerald. Cytogenetic and Stat3 expression analysis of HTR8/SVneo. Placenta 2011; 32: A36 (Abstract P1.48) (Brescia, Italy) |
(p) |
TCG |
| 408 |
UA Mau-Holzmann, N Wagner, S
Mackensen-Haen, A Dufke, AB Hamid, E Ewers, M
Voigt, T Liehr. Prenatal suspicion of trisomy 13: cytogenetic analysis reveals an unusual karyotype with multiple sSMC. Chromosome Res 2011; 19: S216 (Abstract 10.P29) (Porto, Portugal) |
(p) |
sSMC |
| 407 |
J Wagner, F Stipoljev, S
Puselijc, I Skrlec, M Heffer, T Liehr.
Characterization of a familial case with complex rearrangement involving chromosomes 1, 10, 11, 13 and 18. Chromosome Res 2011; 19: S87-S88 (Abstract 1.P92) (Porto, Portugal) |
(p) |
CG |
| 406 |
J Melo, N Lavoura, H Santos,
J Vermeesch, N Kosyakova, T Liehr,
I Carreira. Small supernumerary marker chromosome derived from chromosome 5 – genotype/ phenotype correlation of proximal chromosome 5 imbalances. Chromosome Res 2011; 19: S78-S79 (Abstract 1.P76) (Porto, Portugal) |
(p) |
sSMC |
| 405 |
E-G Stefanou, M Syrrou, T
Liehr, N Kosyakova, T Mantziou, S
Mantagos, F Sharkey. Molecular cytogenetic characterization of a CCR in a boy with severe global developmental delay. Chromosome Res 2011; 19: S66 (Abstract 1.P54) (Porto, Portugal) |
(p) |
CG |
| 404 |
M Guc-Scekic, T Milenkovic,
D Zdravkovic, V Topic, T Liehr, G
Joksic, D Radivojevic, N Lakic. Classic and molecular cytogenetic findings in a 10-year-old boy with ring Y chromosome mosaicism: a case report. Chromosome Res 2011; 19: S38-S39 (Abstract 1.P3) (Porto, Portugal) |
(p) |
CG |
| 403 |
T Liehr. Cytogenetic contribution to uniparental disomy (UPD). Chromosome Res 2011; 19: S37 (Abstract 1.P1) (Porto, Portugal) |
(p) |
CG UPD |
| 402 |
A Polityko, S Bhatt, O Khurs,
A Kulpanovich, L Isakovich, N Yakutina, A
Frolova, N Kvasnikova, I Naumchik, T
Liehr. Williams-Beuren syndrome (WBS) atypical phenotype due to rare familial inversion inv(7)(p10q11.23) in mother and her child: fluorescence in situ hybridization (FISH) analysis of rearrangement breakpoints. Europ J Hum Genet 2011; 19: S153-S154 (Abstract P03.096) (Amsterdam, Netherlands) |
(p) |
CG |
| 401 |
JB Melo, A Jardim, N Lavoura,
M Pires, E Matoso, JR Vermeesch, N Kosyakova, T
Liehr, IM Carreira. Refined molecular cytogenetic characterization of the breakpoints of small supernumerary marker chromosomes derived from chromosome 15. Europ J Hum Genet 2011; 19: S150 (Abstract P03.084) (Amsterdam, Netherlands) |
(p) |
sSMC |
| 400 |
YB Yurov, SG Vorsanova, T
Liehr, MK Tagirova, IY Iourov. Genetic instabilities in the ataxia-telangiectasia brain: evidence for a neuroprotective effect of non-malignant genome/ chromosome instability. Europ J Hum Genet 2011; 19: S138-S139 (Abstract P03.037) (Amsterdam, Netherlands) |
(p) |
CG INT |
| 399 |
M Weber, A Weise, K Mrasek, L
Khachaturyan, DM Morales Prieto, T Liehr,
UR Markert, JS Fitzgerald. Cytogenetic and STAT3 expression analysis of HTR8/SVneo. Am J Rep Imm 2011; 65: S15 (Abstract T14) (Salt Lake City, USA) |
(p) |
TCG |
| 398 |
Y Yurov, S Vorsanova, T
Liehr, M Tagirova, I Iourov. Somatic genome instability in the ataxia telangiectasia brain: evidence for age-dependant increase in aneuploidy and chromosome breaks in degenerating cerebellum. HUGO J 2011; 5: 242-243 (Abstract P218) (Sydney, Australia) |
(p) |
CG INT |
| 397 |
K Mrasek, H Nelle, I
Schreyer, E Ewers, M Merkas, N Kosyakova, AB
Hamid, R Fahsold, A Ujfalusi, j Anderson, N
Rubtsov, A Küchler, F von Eggeling, J Hentschel,
A Weise, T Liehr. Presence of harmless small supernumerary marker chromosomes hampers molecular genetic diagnosis: a case report. Med Genetik 2011; 23: 165 (Abstract P-CytoG-187) (Regensburg, Germany) |
(p) |
sSMC |
| 396 |
A Weise, H Mkrtchyan, M
Gross, S Hinreiner, A Polityko, M Manvelyan, K
Mrasek, N Kosyakova, E Ewers, H Nelle, S Bhatt,
K Thoma, E Gebhart, S Wilhelm, R Fahsold, M
Volleth, T Liehr. The human genome puzzle – the role of copy number variation in somatic mosaicism. Med Genetik 2011; 23: 169 (Abstract P-CytoG-199) (Regensburg, Germany) |
(p) |
INT CG |
| 395 |
C Backsch, A Scheider, J
Herrmann, N Shabai, C Richter, K Kreskowski, T
Liehr, M Linsenfeld. Validation of two novel unbalanced whole arm-translocations in cervical cancer. Med Genetik 2011; 23: 170 (Abstract P-CancG-203) (Regensburg, Germany) |
(p) |
TCG |
2010
| Number |
Authors/
Title/ Where Contribution was Published |
Poster (p)
or oral (o) |
Topic |
| 394 |
IY Iourov, SG Vorsanova, T
Liehr, IV Soloviev, YB Yurov. A new integrated interphase molecular cytogenetic approach for detection of chromosome abnormalities in human embryonic tissues. Reproductive BioMedicine Online 2010; 20: S24 (Abstract P4) (Moscow, Russia) |
(p) |
CG M |
| 393 |
IY Iourov, SG Vorsanova, T
Liehr, AD Kolotii, IA Demidova, AK
Beresheva, VS Kravets, OS Kurinnaia, MK
Tagirova, EA Saprina, IV Soloviev, YB Yurov. Molecular neurocytogenetic, in silico and proteome (interactome/reactome) evaluations of brain-specific somatic genome variations in neurodegenerative diseases. Europ J Hum Genet 2010; 18: S287-S288 (Abstract P11.085) (Gothenburg, Sweden) |
(p) |
INT |
| 392 |
EO Onat, S Balci, O Engiz, T
Liehr, T Ozcelik. X-inactivation silencing is not maintained on the autosomal segment of an inherited unbalanced X;19 translocation in a male. Europ J Hum Genet 2010; 18: S130-S131 (Abstract P03.127) (Gothenburg, Sweden) |
(p) |
CG |
| 391 |
A Polityko, N Kosyakova, H
Tönnies, K Sperling, O Khurs, N Rumyantseva, I
Naumchik, H Neitzel, A Weise, T Liehr.
A liability to malignancy, immunodeficiency, facialabnormalities and chromosomal instability without mutation in DNMT3B gene in two siblings: new chromatin disorder delineation? Europ J Hum Genet 2010; 18: S116-S117 (Abstract P03.061) (Gothenburg, Sweden) |
(p) |
CG |
| 390 |
E Manolakos, L Thomaidis, M
Lagou, R Neroutsou, K Kefalas, E Louizou, M
Rapti, M Kontodiou, N Triga, P Tsoplou, T
Liehr, MB Petersen, A Metaxotou. Supernumerary minute chromosome 17 in a boy with severe developmental delay: molecular breakpoint in the unstable proximal 17p region. Europ J Hum Genet 2010; 18: S113 (Abstract P03.047) (Gothenburg, Sweden) |
(p) |
sSMC |
| 389 |
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. Another gene for autosomal recessive ALX-related frontonasal dysplasias: disruption in ALX1 (CART1) causes anophthalmia and severe facial clefting. Europ J Hum Genet 2010; 18: S38-S39 (Abstract C14.5) (Gothenburg, Sweden) |
(o) |
CG |
| 388 |
T Liehr, VA
Trifonov, SA Romanenko, C Leibiger, H Mkrtchyan,
A Weise, R Stanyon, AS Graphodatsky, N
Kosyakova. Murine FISH-banding – mcb probe development and application. Book of abstracts of 19th international colloquium on animal cytogenetics and gene mapping. P40. and Chromosome Res 2010; 18: 723-724 (Abstract O10) (Balice/Krakow, Poland) |
o |
M |
| 387 |
IY Iourov, SG Vorsanova, T
Liehr, IV Soloviei, YB Yurov. A new integrated interphase molecular cytogenetic approach for detection of chromosome abnromalities in human embryonic tissues. Reprod BioMed Online 2010, 20: S24 (Abstract P4) (Montpellier, France) |
(p) |
CG |
| 386 |
C Wölfel, T Liehr,
A Weise, I Petersen. Characterisation of epitheloid haemangioendothelioma with a new interphase-FISH-test. Der Pathologe 2010; 31: 45-46 (Abstract Fr-086) (Berlin, Germany) |
(p) |
TCG |
| 385 |
M Ziegler, R-D Wegner, M
Stumm, T Martin, G Gillessen-Kaesbach, N
Kosyakova, E Ewers, AB Hamid, F von Eggeling, J
Hentschel, A Weise, T Liehr. Three new cases with small supernumerary marker chromosomes 1 and normal phenotype. Med Genetik 2010; 22: 141-142 (Abstract P-CytoG-157) (Hamburg, Germany) |
(p) |
sSMC |
| 384 |
A Weise, N Kosyakova, K
Mrasek, E Ewers, S Hinreiner, C Bacino, A Patel,
SW Cheung, WW Cai, G Senger, JB Melo, IM
Carreira, A Dufke, K Mehnert, C Yardin, R-D
Wegner, M Stumm, G Kistner, M Leipoldt, G Thiel,
MB Petersen, A Junge, B Fritz, G Joksić, H
Heilbronner, A Ujfalusi, L Brecevic, AB Hamid, T
Liehr. Detailed characterization of small supernumerary marker chromosomes reveals breakpoint hot spots and narrows down the critical regions of clinical impact. Med Genetik 2010; 22: 141 (Abstract P-CytoG-154) (Hamburg, Germany) |
(p) |
sSMC |
| 383 |
K Mrasek, N Blaurock, K
Wilhelm, K Behr, A-C Teichmann, T Liehr,
A Weise, C Schoder. Fanconi anemia (FA) as a model for the mapping of rarely observable FS. Med Genetik 2010; 22: 138 (Abstract P-CytoG-145) (Hamburg, Germany) |
(p) |
INT |
| 382 |
M Merkas 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 multiple hyperpigmented skin nevi and almost no other clinical signs. Med Genetik 2010; 22: 138 (Abstract P-CytoG-144) (Hamburg, Germany) |
(p) |
sSMC |
| 381 |
M Manvelyan, T de Jesus
Marques-Salles, E Pereira Leite, EM
Soares-Ventura, MT Cartaxo-Muniz, E Ferreira, T
Liehr, ML Macedo Silva, N Santos, S
Junker, H Mkrtchyan. Complex karyotype defined by FISH and M-FISH studies in an infant with acute megakarioblastic leukemia and neurofibromatosis. Med Genetik 2010; 22: 137 (Abstract P-CytoG-143) (Hamburg, Germany) |
(p) |
CG |
| 380 |
T Liehr, N
Kosyakova, M Ziegler, G Raabe-Meyer, H Wagner, W
Stibbe, A Weise. Centromere repositioning can be easily mixed up with a pericentric inversion. Med Genetik 2010; 22: 137 (Abstract P-CytoG-141) (Hamburg, Germany) |
(p) |
CG |
| 379 |
N Kosyakova, M Santos, K
Mrasek, A Plaja, T Vendrell, C Fuster, T
Liehr. Accurate characterization of an sSMC derived from chromosome 2 in a child with multiple congenital malformations confirms the adverse clinical effects of partial trisomies distal from 2q11.2. Med Genetik 2010; 22: 136 (Abstract P-CytoG-139) (Hamburg, Germany) |
(p) |
sSMC |
| 378 |
B Horsthemke, M Wawrik, S
Groß, C Lich, K Buiting, E Krasemann, N
Kosyakova, T Liehr, A Weise, JN
Dybowski, D Hoffmann, D Wiczorek. Parental origin and functional relevance of a de novo UBE3A variant. Med Genetik 2010; 22: 136 (Abstract P-CytoG-138) (Hamburg, Germany) |
(p) |
CG |
| 377 |
AB Hamid, S Brankovic Nisic,
V Ivanovic Deretic, R Radivojevic Pilic, E
Ewers, M Merkas, M Ziegler, T Liehr.
A unique case of free trisomy 21 combined with a complex rearranged small supernumerary marker chromosome derived from chromosome 13/21 and 18. Med Genetik 2010; 22: 135 (Abstract P-CytoG-135) (Hamburg, Germany) |
(p) |
sSMC |
| 376 |
E Ewers, F Sheth, 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 – evidence for an underestimated entity? Med Genetik 2010; 22: 134 (Abstract P-CytoG-131) (Hamburg, Germany) |
(p) |
sSSMC |
| 375 |
A Caliebe, JI Martin Subero,
S Gesk, S Von Spiczak, K Bruhn, C
Eckmann-Scholz, M Kautza, J Weimer, T
Liehr, R Siebert, H Tönnies. Identification and characterization of small supernumerary marker chromosomes by molecular karyotyping. Med Genetik 2010; 22: 133-134 (Abstract P-CytoG-130) (Hamburg, Germany) |
(p) |
sSMC |
| Number |
Authors/
Title/ Where Contribution was Published |
Poster (p)
or oral (o) |
Topic |
| 374 |
A Küchler, A Rauch, J
Doernbrack, A Dost, P Sitte-Zoellner, U
Trautmann, U Claussen, O Zuffardi, T
Liehr. Neocentric case report: a patient with mosaic tetrasomy (15)(q24->qter) due to an analphoid supernumerary marker chromosome. ECA-Newsletter 2009; 24: 12 |
(p) |
sSMC |
| 373 |
U Mau-Holzmann, S Singer, H
Enders, S Haen, I Tekesin, T Liehr.
Pitfall: False-negative 46,XX finding in CVS: chromosome mosaicism involving a de novo autosomal structural abnormality and unexpected diagnosis of a third cell line in a fetus. Chromosome Res 2009; 17: S236 (Abstract 13.68-P) (Honolulu, USA) |
(p) |
CG |
| 372 |
E Manolakos, R Neroutsou, M
Lagou, K Kefalas, N Trigka, P Tsoplou, H Kontos,
P Michael, M Aikaterini, T Liehr.
Prenatal detection and characterization of 21 small supernumerary marker chromosomes out of 25,000 prenatal cases in Greece. Chromosome Res 2009; 17: S211-S212 (Abstract 13.19-P) (Honolulu, USA) |
(p) |
sSMC |
| 371 |
J Melo, N Kosyakova, T
Liehr, L Backx, J Vermeesch, I
Carreira. Multicolour FISH versus array CGH techniques. Which to choose for the characterization of small supernumerary marker chromosomes? Chromosome Res 2009; 17: S190-S191 (Abstract 12-15-P) |
(p) |
sSMC |
| 370 |
A Polityko, E Goncharova, J
Jaroshevich, O Khurs, L Isakovich, K Mrasek, T
Liehr. Molecular cytogenetic characterization of rare mosaic karyotype associated with chromosome 21 monosomy clone and cell line with ring chromosomes 21: three new cases. Chromosome Res 2009; 17: S179-S180 (Abstract 11.6-P) (Honolulu, USA) |
(p) |
CG |
| 369 |
I Iourov, S Vorsanova, A
Kolotii, M Tagirova, T Liehr, Y
Yurov. Mosaic expression of chromosome instability in the ataxia telangiectasia brain. Chromosome Res 2009; 17: S177-S178 (Abstract 11.2-P) (Honolulu, USA) |
(p) |
CG |
| 368 |
J Wagner, S Dorner, F
Stipoljev, I Skrlec, G Lauc, A Weise, K Mrasek,
T Liehr, L Brecevic. Partial monosomy 4q and partial trisomy 13q: phenotype and molecular mapping of the breakpoints. Chromosome Res 2009; 17: S32 (Abstract 1.3-P) (Honolulu, USA) |
(p) |
CG |
| 367 |
C Sarri, S Douzgou, Y
Gyftodimou, A Dinopoulus, E Pandelia, K Merou, N
Kosyakova, T Liehr, A Weise, K
Mrasek, M Petersen. Mulitcolor FISH approaches reveal partial trisomy 3q27->qter in combination with partial monosomy 21q22.2->qter in a boy with neurodevelopmental delay and facial dysmorphism. Chromosome Res 2009; 17: S55 (Abstract 1.54-P) (Honolulu, USA) |
(p) |
CG |
| 366 |
T Liehr, E
Ewers, K Mrasek, H Mkrtchyan, N Kosyakova, L
Brecevic, J Wagner, A Weise. Low grade mosaicism in marker chromosomes. Chromosome Res 2009; 17: S25-S26 (Abstract 32-L) (Honolulu, USA) |
o |
sSMC |
| 365 |
LG Shaffer, LJ Campbell, ML
Slovak, M Chabouni, Y Fukushima, C Harrison, T
Liehr, P Mandon, N Mandahl, KW Rao,
C Rosenberg, A Schinzel, H Tönnies, JC Barber. ISCN(2009): Important revisions and new additions to molecular methods for copy number detection for cytogenetic analysis. Chromosome Res 2009; 17: S10 (Abstract 4-L) (Honolulu, USA) |
(o) |
other |
| 364 |
YB Yurov, IY Iourov, SG
Vorsanova, AD Kolotii, T Liehr. Mosaic expression of aneuploidy involving chromosomes 21 in the Alzheimers’s disease brain: evidence for the causal association between aneuploidy and neurodegeneration. Paed Croatia 2009; 53: S35-S36 (Abstract 79-CGN) (Zagreb, Croatia) |
(p) |
CG |
| 363 |
IY Iourov, SG Vorsanova, AD
Kolotii, AK Beresheva, IA Demidova, VS Kravets,
OS Kurinnaya, MK Tagirova, T Liehr,
YB Yurov. Chromosome instability at the subtissue level mediates neurodegeneration: a molecular neuocytogenetic study of the ataxia telangiectasia brain. Paed Croatia 2009; 53: S29 (Abstract 73-CGN) (Zagreb, Croatia) |
(p) | CG |
| 362 |
A Weise, M Werber, P Heyn, N
Kosyakova, T Liehr, H Neitzel, K
Konrat, C Bommer, R Reinhardt, S Mundlos, TH
Lindner, B Timmermann, K Hoffmann. High-throughput sequencing of microdissected chromosomal regions. Med Genetik 2009; 21: 166 (Abstract P301) (Aachen, Germany) |
(p) |
M |
| 361 |
H Nelle, C Schoder, N
Blaurock, A-C Teichmann, K Behr, T Liehr,
A Weise, K Mrasek. Chromosome fragility as part of the normal chromosome structure compared to Fanconi anemia patients. MedGen 2009, Vol 21, p 111 (Abstract P115) (Aachen, Germany) |
(p) |
INT |
| 360 |
C Baksch, J Hermann, N
Shabani, M Liesenfeld, L Jansen, T Liehr,
IB Runnebaum, M Dürst. Validation of two novel unbalanced whole arm translocations in cervical smears. Med Genetik 2009; 21: 110-111 (Abstract P113) (Aachen, Germany) |
(p) |
TCG |
| 359 |
H Mkrtchyan, M Manvelyan, P
Kempf, A Lier, A Heller, K Mrasek, F Hunstig, A
Weise, T Liehr. 3D-interphase studies of chromosomes 8 and 21 in AML patients with trisomy 8. Med Genetik 2009; 21: 110 (Abstract P112) (Aachen, Germany) |
(p) |
TCG |
| 358 |
H Fink, C Kelbova, C Heine, B
Prager, T Liehr, A Junge. Mosaicism for an unbalanced structural rearrangement and a normal cell line associated with infertility – a case report. Med Genetik 2009; 21: 104 (Abstract P098) (Aachen, Germany) |
(p) |
CG |
| 357 |
AD Polityko, IV Naumchick, T
Liehr. Pallister-Killian syndrome (PKS): 4 cases of pre- and postnatal cytogenetic diagnostics. Med Genetik 2009; 21: 103 (Abstract P086) (Aachen, Germany) |
(p) |
sSMC |
| 356 |
A Weise, C Schoder, A-C
Teichmann, K Behr, B Franze, U Claussen, T
Liehr, K Mrasek. Global screening and extended nomenclature for 230 aphidicolin-inducible fragile sites – including 61 yet unreported ones. Med Genetik 2009; 21: 100 (Abstract P076) (Aachen, Germany) |
(p) |
INT |
| 355 |
K Mrasek, C Schoder, A-C
Teichmann, K Behr, B Franze, U Claussen, T
Liehr, A Weise. The ‘fragile secret’ of 32 new molecular mapped aphidicolin induced fragile sites. Med Genetik 2009; 21: 100 (Abstract P075) (Aachen, Germany) |
(p) |
INT |
| 354 |
M Ziegler, JB Melo, IM
Carreira, A Polityko, A Junge, C Kelbova, H
Heilbronner, L Backx, JR Vermeesch, N Kosyakova,
E Ewers, T Liehr, A Weise. Molecular cytogenetic characterization of four new cases with a small supernumerary marker chromosome derived from chromosome 16. Med Genetik 2009; 21: 100 (Abstract P074) (Aachen, Germany) |
(p) |
sSMC |
| 353 |
N Kosyakova, V Trifonov, S
Romanenko, R Wagner, H Mkrtchyan, A Weise, T
Liehr. Generation of murine whole and partial chromosome painting probes based on FISH-microdissection. Med Genetik 2009; 21: 99 (Abstract P072) (Aachen, Germany) |
(p) |
M |
| 352 |
E Ewers, M Stumm, R-D Wegner,
S Bhatt, P Hickmann, PC Patsalis, M Meins, S
Morlot, V Klaschka, S Hinreiner, K Mrasek, N
Kosyakova, WW Cai, SW Cheung, A Weise, T
Liehr. A yet unreported region leading to unbalanced chromosomal abnormalities without phenotypic consequences in 10p11.2 to 10q11.2. Med Genetik 2009; 21: 81 (Abstract P011) (Aachen, Germany) |
(p) |
CG |
| 351 |
D Wieczorek, S Fischer, D
Böhm, J Kohlhase, T Liehr, C
Roll, G Gillessen-Kaesbach, H-J Lüdecke, B
Horsthemke. Chromosome 4p aberrations in microtia/ oculo-auriculo-vertebral spectrum (OAVS)/ Goldenhar syndrome. Med Genetik 2009; 21: 62-63 (Abstract W1_03) (Aachen, Germany) |
(o) |
CG |
| 350 |
T Liehr, F
Hunstig, S Bhatt, F Pellestor, K Mrasek, A
Weise, I Simonyan, R Aroutiounian, M Manvelyan.
3-dimensional multicolor banding (3D-MCB) reveals the distribution of chromosomes in human sperm. Med Genetik 2009; 21: 76 (Abstract W8_04) (Aachen, Germany) |
o |
INT |
| 349 |
H Tönnies, LJ Campbell, ML
Slovak, M Chabouni, Y Fukushima, CJ Harrison, T
Liehr, P Mandon, N Mandahl, KW Rao,
C Rosenberg, A Schinzel, JC Barber, LG Shaffer.
ISCN(2009): Important revisions and new additions to molecular methods for copy number detection for cytogenetic analysis. Med Genetik 2009; 21: 76 (Abstract W8_06) (Aachen, Germany) |
(o) |
other |
2008
| Number |
Authors/
Title/ Where Contribution was Published |
Poster (p)
or oral (o) |
Topic |
| 348 |
YB Yurov, IY Iourov, SG
Vorsanova, T Liehr, AD Kolotii,
AK Beresheva, IA Demidova, VS Kravets, MK
Tagirova, OS Kurinnaya, VV Monakhov, IV
Soloviev. Somatic genome instability closely associates with cerebellar neurodegeneration in the ataxia teleangiectasia. Genomic Med 2008, 2: 379 (Abstract: 457) (Hyderabad, India) |
(p) |
CG |
| 347 |
IY Iourov, SG Vorsanova, T
Liehr, YB Yurov. Intercellular genomic variations manifesting as aneuploidy in the normal, Alzheimer’s disease and ataxia-telangiectasia brain. Genomic Med 2008; 2: 362 (Abstract: 409) (Hyderabad, India) |
(p) |
CG |
| 346 |
YB Yurov, IY Iourov, SG
Vorsanova, IA Demidova, AK Beresheva, VS
Kravets, VV Monakhov, AD Kolotii, IV Soloviev,
VM Vostrikov, NA Uranova, T Liehr.
Genomic instability in the schizophrenia brain: Highlighting new intracellular mechanism for pathopsychophysiology of brain diseases. Int J Psychophys 2008; 69: 24 (St. Petersburg, Russia) |
(o) |
CG |
| 345 |
IY Iourov, SG Vorsanova, T
Liehr, AD Kolotii, IV Soloviev, VM
Vostrikov, NA Uranova, YB Yurov. Association of genome instability and neurodegeneration in the cerebral cortex and hippocampus in Alzheimer's disease brain: Evidences for a new pathogenetic mechanism of the disease. Int J Psychophys 2008; 69: 288 (St. Petersburg, Russia) |
(o) |
CG |
| 344 |
ID Papoulidis, AP
Athanasiadis, MB Petersen, E Drosopoulou, I
Simou, C Malamaki, T Liehr, ZG
Scouras. A case of de novo 16 rearrangement diagnosed prenatally. Europ J Hum Gen 2008; 16: S231 (Abstract P03.58) (Barcelona, Spain) |
(p) |
CG |
| 343 |
M Miskovic, T Liehr, M
Gic-Scekic, A Weise, K Mrasek, T Liehr,
N Lakic. Characterization of small supernumerary marker chromosomes using cytogenetic and molecular cytogenetic methods (two case reports). Europ J Hum Gen 2008; 16: S164 (Abstract P02.199) (Barcelona, Spain) |
(p) |
sSMC |
| 342 |
JB Melo, E Matoso, MR Lima, L
Backx, JR Vermeesch, N Kosyakova, T Liehr,
IM Carreira. Molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 11 in a mother and child with distinct phenotypes. Europ J Hum Gen 2008; 16: S164 (Abstract P02.197) (Barcelona, Spain) |
(p) |
sSMC |
| 341 |
AD Polityko, I Naumchick, N
Rumyantseva, O Khurs, E Jaroshevich, K Mrasek, T
Liehr. Characterization of rare karyotype anomaly 45,XX,-21/46,XX,r(21) by comprehensive FISH: mosaic status and constitution of ring chromosome 21. Europ J Hum Gen 2008; 16: S158 (Abstract P02.169) (Barcelona, Spain) |
(p) |
CG |
| 340 |
N Ploumis, E Manolakos, MB
Petersen, H Kontos, P Malligians, A Boll, T
Liehr, R Neroutsou. Characterization of nine small supernumerary marker chromosomes detected in 7000 fetal karyotypes. Europ J Hum Gen 2008; 16: S156 (Abstract P02.160) (Barcelona, Spain) |
(p) |
sSMC |
| 339 |
J Puechberty, G Lefort, A
Schneider, A Chaze, A Weise, T Liehr,
H Starke, F Pellestor, P Sarda. Pure 20q11.2 duplication: a specific behavioural phenotype? Europ J Hum Gen 2008; 16: S151-S152 (Abstract P02.141) (Barcelona, Spain) |
(p) |
CG |
| 338 |
M Martinez-Fernandez, L
Rodriguez, T Liehr, K Mrasek, M
Martinez-Frias. Chaotic banding pattern of chromosome 3 in a patient with mental retardation. Europ J Hum Gen 2008; 16: S148 (Abstract P02.124) (Barcelona, Spain) |
(p) |
CG |
| 337 |
IY Iourov, SG Vorsanova, T
Liehr, AD Kolotii, YB Yurov. Chromosome instability in the ataxia telangiectasia cerebellum. Europ J Hum Gen 2008; 16: S144 (Abstract P02.109) (Barcelona, Spain) |
(p) |
CG |
| 336 |
YB Yurov, IY Iourov, SG
Vorsanova, T Liehr. Aneuploidy of chromosome 21 in the Alzheimer’s disease brain. Europ J Hum Gen 2008; 16: S144 (Abstract P02.106) (Barcelona, Spain) |
(p) |
CG |
| 335 |
O Villa, N Kosyakova, I
Cusco, M Aragones, D Garcia-Cruz, F Sole, A
Plaja, T Liehr, LA Perez-Jurado.
Characterization of balanced chromosome translocation breakpoints associated to phenotype by microdissection and aCGH. Europ J Hum Gen 2008; 16: S126 (Abstract P02.026) (Barcelona, Spain) |
(p) |
M CG |
| 334 |
F Pellestor, S Bhatt, J
Puechberry, G Lefort, T Liehr, P
Sarda, S Hamamah. The meiotic segregartion of paracentric inversions: how breakpoint mapping can make the difference. Reprod Biomed Online 2008; 16: S-25 |
(o) |
CG |
| 333 |
V Trifonov, K Mrasek, N
Kosyakova, C Mackie Ogilvie, J Vermeesch, N
Rubtsov, T Liehr. Small supernumerary marker chromosomes (sSMC) in humans – are there B chromosomes hidden among them? Med Genetik 2008; 20: 156 (Abstract P266) (Hannover, Germany) |
(p) |
sSMC |
| 332 |
N Kosyakova, 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 B-lymphocytes interphase nuclei of human, gorilla and white hand gibbon compared to human sperm. Med Genetik 2008; 20:156 (Abstract P265) (Hannover, Germany) |
(p) |
INT EVO |
| 331 |
H Mkrtchyan, ML Macedo Silva,
SC Raimondi, E Abdelhay, M Gross, A Faria de
Figueiredo, RC Ribeiro, T de Jesus
Marques-Salles, ES Sobral, M Poirot Gerardin
Land, T Liehr. Banding and molecular cytogenetic studies detected a CBFß-MYH11 fusion gene in a baby with acute myeloid leukemia FAB M4-Eo. Med Genetik 2008; 20: 108 (Abstract P093) (Hannover, Germany) |
(p) |
TCG |
| 330 |
A Polityko, N Shorokh, N
Rumyantseva, I Naumchik, K Mrasek, T
Liehr. Rare pericentric inversion of chromosome 4 in parent and rec(4) in child with Wolf-Hirschhorn syndrome: diagnostics by multicolor banding FISH. Med Genetik 2008; 20: 104 (Abstractnr. P079) (Hannover, Germany) |
(p) |
CG |
| 329 |
V Schmiemann, J Bruch, W
Trawicki , T Liehr, A Weise, R
Glaubitz, B Eiben. Case report of a partial trisomy 21 without phenotypic relevance. Med Genetik 2008; 20: 103 (Abstract P075) (Hannover, Germany) |
(p) |
CG |
| 328 |
K Marsek, M Manvelyan, T
Liehr, K Behr, C Schoder, A Weise. Prove of molecular co-localization of fragile sites and evolutionary conserved breakpoints. Med Genetik 2008; 20: 102 (Abstract P073) (Hannover, Germany) |
(p) |
INT EVO |
| 327 |
C Schoder, H Tönnies, K
Marsek, K Behr, M Manvelyan, T Liehr,
A Weise. Analysis of fragile sites and breakpoints in Fanconi anemia patients. Med Genetik 2008; 20: 102 (Abstract P072) (Hannover, Germany) |
(p) |
INT |
| 326 |
M Ziegler, K Mrasek, D Reich,
E Ewers, A Weise, T Liehr. Small supernumerary marker chromosomes (sSMC) in patients with a karyotype 45,X/46,X,+mar – 17 new cases and a review of the literature. Med Genetik 2008; 20: 102 (Abstract P071) (Hannover, Germany) |
(p) |
sSMC |
| 325 |
A Weise, K Mrasek, 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. Med Genetik 2008; 20: 102 (Abstract P070) (Hannover, Germany) |
(p) |
M |
| 324 |
D Reich, N Rubtsov, M Gross,
C Mackie Ogilvie, V Trifonov, N Kosyakova, A
Weise, T Liehr. Another case of a small supernumerary marker chromosome only stainable by DNA derived from itself. Med Genetik 2008; 20: 101 (Abstract P069) (Hannover, Germany) |
(p) |
sSMC |
| 323 |
H Nelle, N Kosyakova, A
Weise, K Mrasek, U Claussen, T Liehr.
The hierarchically organized splitting of chromosomal bands for all human chromosomes. Med Genetik 2008; 20: 101 (Abstract P068) (Hannover, Germany) |
(p) |
INT |
| 322 |
V Klaschka, K Mrasek, T
Liehr, H Mkrtchyan, A Weise. A new probe set for the characterization of centromere-near rearrangements. Med Genetik 2008; 20: 101 (Abstract. P067) (Hannover, Germany) |
(p) |
sSMC M |
| 321 |
E Ewers, H M, A Weise, K
Mrasek, T Liehr. Centromere activity in dicentric small supernumerary marker chromosomes. Med Genetik 2008; 20: 101 (Abstract P066) (Hannover, Germany) |
(p) |
sSMC |
| 320 |
T Liehr, V
Trifonov, S Fluri, F Binkert, A Nandini, J
Anderson, L Rodriguez, M Gross, N Kosyakova, H
Mkrtchyan, E Ewers, D Reich, A Weise. Three new cases of complex rearranged small supernumerary marker chromosomes. Evidence for an underestimated entity? Med Genetik 2008; 20: 83 (Abstract P001) (Hannover, Germany) |
p |
sSMC |
| Number |
Authors/
Title/ Where Contribution was Published |
Poster (p)
or oral (o) |
Topic |
| 319 |
S Bhatt, K Mordkhani, K
Mrasek, J Puechberty, G Lefort, P Sarda, S
Hamamah, T Liehr, F Pellestor. The direct characterization of breakpoints: a new approach for the segregation analysis of paracentric inversions in human sperm. Chromosome Res 2007; 15: S147 (Abstract 4.1-P) (Istanbul, Turkey) |
(p) |
CG |
| 318 |
Y Yurov, I Iourov, S
Vorsanova, T Liehr, A Kolotii, A
Beresheva, I Demidova, F Pellestor, S Kutsev, I
Soloviev. Developmental chromosome instability leads to low-grade mosaicism of the normal embryonic and fetal human brain. Chromosome Res 2007; 15: S139-S140 (Abstract 3.9-P) (Istanbul, Turkey) |
(p) |
INT CG |
| 317 |
I Demidova, I Iourov, S
Vorsanova, A Kolotii, V Kravetz, V Monakchov, I
Soloviev, T Liehr, Y Yurov. Evidence for increased level of mosaic aneuploidy involving chromosome 1 in the schizophrenia brain. Chromosome Res 2007; 15: S139 (Abstract 3-8-P) (Istanbul, Turkey) |
(p) |
CG |
| 316 |
P Kieback, C Hennig, A Jauch,
T Liehr. Prenatal diagnosis of a direct intrachromosomal duplication 11p12->11q11.1~2.1. Chromosome Res 2007; 15: S125 (Abstract 1-237-P) (Istanbul, Turkey) |
(p) |
CG |
| 315 |
D Aktas, E Utine, Y Alanay,
S Gücer, E Tuncbilek, K Mrasek, T Liehr.
Two patients with distal partial trisomy 1q. Chromosome Res 2007; 15: S70-S71 (Abstract 1.111-P) (Istanbul, Turkey) |
(p) |
CG |
| 314 |
A Polityko, O Khurs, N
Rumyantseva, K Mrasek, T Liehr. Rare familial paracentric inversion of chromosome 9: prenatal and postnatal characterization of aberrations by FISH multicolor banding. Chromosome Res 2007; 15: S69 (Abstract 1.108-P) |
(p) |
HET |
| 313 |
JB Melo, E Matoso, N Lavoura,
C Pais, F Ramos, N Kosyakova, K Mrasek, T
Liehr, IM Carreira. Prenatal identification of a small supernumerary marker chromosome by molecular cytogenetics. Chromosome Res 2007; 15: S63 (Abstract 1-94-P) (Istanbul, Turkey) |
(p) |
sSMC |
| 312 |
S Balci, E Uz, O Engiz, T
Liehr, T Ozcelik. Extremely skewed X-chromosome inactivation in a male patient with 46,XY,der(19)t(X;19)(q11.1~11.2;p13.3). Chromosome Res 2007; 15: S61 (Abstract 1.89P) (Istanbul, Turkey) |
(p) |
CG |
| 311 |
L Miguez Alvarez, M Santos, T
Liehr, C Fuster. Characterization of two sSMC present in two unrelated patients. Chromosome Res 2007; 15: S39-S40 (Abstract 1.38P) (Istanbul, Turkey) |
(p) |
sSMC |
| 310 |
I Iourov, T Liehr,
S Vorsanova, I Demidova, Y Yurov. Interphase chromosome-specific multicolor banding (MCB): a new opportunity for molecular neurocytogenetics. Chromosome Res 2007; 15: S28-S29 (Abstract 1.13P) (Istanbul, Turkey) |
(p) |
CG M |
| 309 |
T Liehr. Small supernumerary marker chromosomes (sSMC) detected in connection with infertility – new surprising results. Chromosome Res 2007; 15: S24 (Abstract 1.2-P) (Istanbul, Turkey) |
p |
sSMC |
| 308 |
L Backx, H van Esch, C
Melotte, N Kosyakova, JP Frijns, H Starke, T
Liehr, JR Vermeesch. Array painting using microdissected chromosomes to map chromosomal breakpoints. Chromosome Res 2007; 15: S21-S22 (Abstract 1.2-O) (Istanbul, Turkey) |
(o) |
M |
| 307 |
SG Vorsanova, IY Iourov, T
Liehr, VV Manakhov, OS Kurinnaya, YB
Yurov. Refinement of unbalanced aberrations of chromosome 7 in two severly affected children by multicolor banding (MCB). Europ J Hum Gen 2007; 15: S127 (Abstract P0421) (Nice, France) |
(p) |
CG |
| 306 |
IY Iourov, SG Vorsanova, T
Liehr, IA Demidova, AK Beresheva, AD
Kolotii, VS Kravets, VM Vostrikov, VV Monakhov,
NA Uranova, IV Soloviev, F Pellestor, YB Yurov.
Molecular neurocytogenetic survey of intracellular genomic variations manifesting as aneuploidy in human brain. Europ J Hum Gen 2007; 15: S116 (Abstract P0370) (Nice, France) |
(p) |
CG |
| 305 |
IG Balikova, K Martens, C
Melotte, S van Vooren, Y Moreau, H Starke, D
Vetrie, H Fiegler, N Carter, T Liehr,
G Matthijs, J Fryns, I Casteels, K Devriendt, JR
Vermeesch. Familial inherited microtia caused by a benign CNV amplification at chromosome 4pter. Europ J Hum Gen 2007; 15: S23 (Abstract C32) (Nice, France) |
(p) |
CG |
| 304 |
H Mkrtchyan, S Ghazaryan, G
Avetisyan, A Hovhannisyan, S Daghbashyan, L,
Muradyan, 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 PH-chromosome. Hematologica 2007; 92: S355-S356 (Abstract 0955) (Vienna, Austria) |
(p) |
TCG |
| 303 |
M Gross, H Mkrtchyan, H
Thieme, F von Eggeling, B Horsthemke, C Jonsrud,
U Claussen, T Liehr, A Weise.
Parental origin determination I FISH. A new
method to characterizes the parental origin of
human chromosomes on a single cell level. Hematologica 2007; 92: S47 (Abstract 0129) (Vienna, Austria) |
(p) |
M |
| 302 |
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. Med Genetik 2007; 19: 78 (Abstract P060) (Bonn, Germany) |
(p) |
CG |
| 301 |
P Kieback, C Hennig, A Jauch,
T Liehr. Prenatal diagnosis of a direct intrachromosomal duplication 11p12->11q11.2~12.1, a one year follow up. Med Genetik 2007; 19: 83 (Abstract P080) (Bonn, Germany) |
(p) |
CG |
| 300 |
S Singer, H Enders, T
Liehr, JCK Barber, UA Mau-Holzmann.
Cyto-Quiz: Test and train your abilities to recognize variant chromosomes. Med Genetik 2007; 19: 85 (Abstract P087) (Bonn, Germany) |
(p) |
other |
| 299 |
A Kron, J Trübenbach, T
Liehr, J Decker, D Steinberger. Characterization of a prenatally diagnosed de novo small supernumerary marker harbouring material of chromosome 16. Med Genetik 2007; 19: 85-86 (Abstract P089) (Bonn, Germany) |
(p) |
sSMC |
| 298 |
A Weise, M Gross, H
Mkrtchyan, H Thieme, F von Eggeling, B
Horsthemke, C Jonsrud, U Claussen, T
Liehr. Advances in parental origin determination (pod) FISH – evaluation and applications. Med Genetik 2007; 19: 79 (Abstract P063) (Bonn, Germany) |
(p) |
M |
| 297 |
D Reich, K Mrasek, A Weise,
H Nelle, T Liehr. Familial small supernumerary marker chromosomes are predominantly inherited via the maternal line. Med Genetik 2007; 19: 82-83 (Abstract P077) (Bonn, Germany) |
(p) |
sSMC |
| 296 |
H Nelle, M Santos, K Mrasek,
MA Rigola, C Fuster, T Liehr. Identification of a “cryptic mosaicism” involving at least 4 different small supernumerary marker chromosomes, derived from chromosome 9, in a potential infertile woman. Med Genetik 2007; 19: 71 (Abstract P033) (Bonn, Germany) |
(p) |
sSMC |
| 295 |
K Mrasek, B Franze, U
Claussen, T Liehr, A Weise. A molecular basis for the cytogenetic co-localization of fragile sites, evolutionary conserved breakpoints and tumor breakpoints. Med Genetik 2007; 19: 80-81 (Abstract P066) (Bonn, Germany) |
(p) |
TCG INT EVO |
| 294 |
T Liehr, A
Weise. Frequency of small supernumerary marker chromosomes in prenatal, newborn, developmentally retarded and infertility diagnostics. Med Genetik 2007; 19: 56 (Abstract W8 01) (Bonn, Germany) |
o |
sSMC |
| 293 |
N Kosyakova, V Trifonov, A
Polityko, L Brecevic, K Mrasek, A Weise, I
Iourov, M Manvelyan, F von Eggeling, T
Liehr. Scheme for straightforward characterization for small supernumerary marker chromosomes (sSMC) by simple molecular and molecular cytogenetics approaches. Med Genetik 2007; 19: 85 (Abstract P086) (Bonn, Germany) |
(p) |
sSMC |
| 292 |
F Hunstig, M Manvelyan, F
Pellestor, S Bhatt, R Aroutiounian, T
Liehr. 3-D multicolor banding reveals the orientation of chromosomes in human sperm – a pilot study. Med Genetik 2007; 19: 57 (Abstract W8 04) (Bonn, Germany) |
(o) |
INT |
| 291 |
S Hinreiner, L Rodríguez, K
Mrasek, E Mansilla, ML Martínez-Fernández, G
Ángel, ML Martínez-Frías, T Liehr.
First inherited small supernumerary chromosome marker generating complete trisomy 18p. Med Genetik 2007; 19: 86 (Abstract P091) (Bonn, Germany) |
(p) |
sSMC |
| 290 |
H Mkrtchyan, S Ghazaryan, G
Avetisyan, L Muradyan, S Daghbashyan, C Karst, M
Gross, R Aroutiounian, T Liehr. A new complex translocation event described in a case with chronic myelogenous leukemia involving BCR/ABL: t(6;9;22)(q11;q34;q11). Med Genetik 2007; 19: 107 (Abstract P163) (Bonn, Germany) |
(p) |
TCG |
| 289 |
B Franze, K Mrasek, U
Claussen, T Liehr, A Weise. Molecular and molecular cytogenetic characterization of four fragile sites of chromosome 1. Med Genetik 2007; 19: 81 (Abstract P071) (Bonn, Germany) |
(p) |
INT |
| 288 |
I Fickelscher, D Aktas, A
Weise, E Utine , D Alehan, K Mrasek, F von
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. Med Genetik 2007; 19: 83 (Abstract P078) (Bonn, Germany) |
(p) |
UPD CG |
| 287 |
K Behr, SG Vorsanova, IY
Iourov, VY Voinova-Ulas, A Weise, VV Monakhov,
AD Kolotii, IV Soloviev, PV Novikov, YB Yurov, T
Liehr. Partial monosomy 7q34-qter and 21pter-q22.13 due to a de novo cryptic unbalanced translocation in a patient with multiple congenital malformations. Med Genetik 2007; 19: 86-87 (Abstract P093) (Bonn, Germany) |
(p) |
CG |
2006
| Number |
Authors/
Title/ Where Contribution was Published |
Poster (p)
or oral (o) |
Topic |
| 286 |
Kron A, Trübenbach J, Vogt P,
Liehr T, Decker J, Steinberger D. Prenatal diagnosis of a de novo small supernumerary marker chromosome 16 Geburtshilfe Frauenheilkd 2006; 66 - PO_G_04_01 |
(p) |
CG |
| 285 |
MLM Silva, M Gross, S
Raimondi, G Pimenta, GP Guasti, ES da Costa, A
de Sousa, RC Ribeiro, E Abdelhay, T Liehr.
Cytogenetic and multicolor banding studies revealed chromosome 1 abnormalities in four infants with Down syndrome with myelodysplastic disorder that evolved to acute megakaryocytic leukemia. RRevisita Brasileira de Hematologia e Hemoterapia 2006; 28 S228 (Abstract 618) (Recife, Brazil) |
(p) |
TCG |
| 284 |
MLM Silva, S Raimondi, AF de
Figueiredo, ES da Costa, G Alves, TJ
Marques-Salles, M Land, R Ribeiro, E Abdelhay, T
Liehr. Conventional cytogenetic and molecular studies (FISH and multicolor banding) detected a rearrangement of CBFß-MYH11 fusion in an original cryptical chromosomal abnormality involved chromosomes 1 and 16 in one infant with acute myeloid leukemia. Revisita Brasileira de Hematologia e Hemoterapia 2006; 28 S228 (Abstract 617) (Recife, Brazil) |
(p) |
TCG |
| 283 |
YB Yurov, IY Iourov, AD
Kolotii, AK Beresheva, T Liehr,
SG Vorsanova. Interphase FISH study of aneupolidy rate in the brain tissues of patients with ataxia-telangiectasia. Balkan J Med Genet 2006; 9: 61 (Abstract PP33) (?) |
(p) |
INT |
| 282 |
V Hall, VK Maloney, H White,
T Liehr, M Volleth, JCK Barber. The use of pyrosequencing to identify copy number variation of 16p11.2 in euchromatic variant carriers and the normal population. J Med Genet 2006; 43: S98 (Abstract 3.26) |
(o) |
HET M |
| 281 |
I Iourov, S Vorsanova, T
Liehr, Y Yurov. The schizophrenia brain demonstrates dicrepant somatic chromosome pairing. Am J Med Genet B - Neuropsychiatric Genetics 2006; 141B: 770 (Cagliari, Italy) |
(p) |
CG |
| 280 |
Y Yurov, I Iourov, S
Vorsanova, T Liehr, I Demidova, V
Vostrikov, N Uranova. First case of mosaic trisomy of chromosome 1 identified in the schizophrenic brain. Am J Med Genet B - Neuropsychiatric Genetics 2006; 141B: 770 (Cagliari, Italy) |
(p) |
CG |
| 279 |
IY Iourov, SG Vorsanova, T
Liehr, F Pellestor, YB Yurov. Detection du mosaicisme chromosomique spontane dans le cerveau human foetal par les techniques de FISH, PRINS et MCB. Medecine Science 2006; 22: 57. (in French) (Montpellier, France) |
(p) |
CG |
| 278 |
E Papadopoulou, S Sifakis, C
Sarri, J Gyftodimou, T Liehr, K
Mrasek, M Kalmanti, M Petersen. A new case of 7p duplication syndrome. Eur J Hum Gen 2006; 14: S101 (Abstract P0007) (Amsterdam, Netherlands) |
(p) |
CG |
| 277 |
M Gross, B Horsthemke, C
Karst, H Mkrtchyan, U Claussen, T Liehr,
A Weise. Parental-origin-determination (pod-FISH): a new approach to distinguish homologues chromosomes. Eur J Hum Gen 2006; 14: S178 (Abstract P365) (Amsterdam, Netherlands) |
(p) |
M |
| 276 |
AD Polityko, E Abranchik, O
Khurs, E Jaroshevich, K Mrasek, T Liehr.
Complex mosaic imbalance karyotype in prenatal diagnosis: identification of small supernumerary marker chromosomes using high resolution multicolor FISH approaches. Eur J Hum Gen 2006; 14: S186 (Abstract P0402) (Amsterdam, Netherlands) |
(p) |
sSMC |
| 275 |
IY Iourov, SG Vorsanova, T
Liehr, F Pellestor, YB Yurov. Détection du mosaicisme chromosomique spontané dans les cerveau humain foetal par les techniques de FISH, PRINS et MCB. M/S 2006; 22: 57 (Abstract P97/44) (Montpellier, France) |
(p) |
M CG |
| 274 |
M Gross, H Mkrtchyan, M
Glaser, C Karst, U Claussen, U Wedding, K
Höffken, T Liehr. Cryptic rearrangements are detectable in ~40% of AML-cases with normal routine banding karyotype – a molecular cytogenetic pilot study on 40 cases. Med Genetik 2006; 18: 46 (Abstract P005) (Heidelberg, Germany) |
(p) |
TCG |
| 273 |
K Pittasch, H Mkrtchyan, M
Glaser, M Gross, U Wedding, K Höffken, C Karst,
T Liehr. Multicolor-FISH applied to resolve complex chromosomal changes in a case of T-ALL (FAB L2). Med Genetik 2006; 18: 46 (Abstract P006) (Heidelberg, Germany) |
(p) |
TCG |
| 272 |
N Knoll, A Weise, A Kuechler,
T Liehr, BL Pool-Zobel, U
Claussen. Application of fluorescence in-situ hybridisation (24-color-FISH) in testing mutagenicity of ethylmethanesulphonate in preneoplastic human colon cells using the OECD guideline 473. Med Genetik 2006; 18: 46-47 (Abstract P008) (Heidelberg, Germany) |
(p) |
TCG M |
| 271 |
M Ziegler, K Mrasek, G
Hickmann, P Kozlowski, M Mazauric, C Fuster, M
Santos Verdaguer, T Liehr. Three more cases with small supernumerary marker chromosome (sSMC) derived from chromosome 2 further confirm the suggested genotype/ phenotype correlation. Med Genetik 2006; 18: 58 (Abstract P056) (Heidelberg, Germany) |
(p) |
sSMC |
| 270 |
A Kuechler, A Rauch, J
Doernbrack, A dost, P Sitte-Zoellner, U
Traustmann, U Claussen, T Liehr.
A patient with a mosaic tertasomy (15)(q24-qter) due to a supernumerary marker chromosome. Med Genetik 2006; 18: 65 (Abstract P086) (Heidelberg, Germany) |
(p) |
sSMC |
| 269 |
K Mrasek, F Reichelt, U
Claussen, T Liehr, A Weise. Towards the molecular basis of the cytogenetic co-localization of fragile sites, evolutionary conserved breakpoints and cancer associated breakpoints. Med Genetik 2006; 18: 74 (Abstract P123) (Heidelberg, Germany) |
(p) |
TCG INT EVO |
| 268 |
C Karst, V Trifonov, SA
Romanenko, U Claussen, K Mrasek, S Michel, T
Liehr. Molecular cytogenetic characterization of the mouse cell line WMP2 by spectral karyotyping (SKY) and multicolor banding applying murine probes (mcb). Med Genetik 2006; 18: 74 (Abstract P122) (Heidelberg, Germany) |
(p) |
M |
| 267 |
I Fickelscher, S Schmidt, U
Claussen, T Liehr, H Starke, A
Weise. Molecular variability within cytogenetic similar inversions of chromosome 2 and 9. Med Genetik 2006; 18: 74 (Abstract P121) (Heidelberg, Germany) |
(p) |
HET |
| 266 |
A Polityko, N Rumayantseva, E
Jaroshevich, I Naumchik, K Mrasek, T
Liehr. Small supernumerary ring chromosome 20 in dysmorphic child: identification of mosaic extra marker chromosome by centromere-specific multicolor FISH. Med Genetik 2006; 18: 74-75 (Abstract P125) (Heidelberg, Germany) |
(p) |
sSMC |
| 265 |
J Lemke, T Felka, S Michel, C
Lemke, B Gruhn, T Liehr, U
Claussen. Molecular cytogenetic characterisation of the DNA-degradation process in erytrocytes indicates to similarities in the marker chromosome formation. Med Genetik 2006; 18: 77-78 (Abstract P138) (Heidelberg, Germany) |
(p) |
sSMC |
| 264 |
L-E Wehner, T Liehr,
F von Eggeling, R Osmers, B Zoll, I Bartels. Prenatal detection of a de novo small supernumerary marker chromosome 4. Med Genetik 2006; 18: 78 (Abstract P142) (Heidelberg, Germany) |
(p) |
sSMC |
| 263 |
F Hunstig, F Pellestor, U
Steinhaeuser, H Starke, M Ziegler, U Claussen, T
Liehr. Multicolor banding studies on the ‘Barr-body’ in 3D-preserved human lymphocyes and on chromosomal orientation in human sperm interphase nuclei. Med Genetik 2006; 18: 83 (Abstract P161) (Heidelberg, Germany) |
(p) |
INT |
| 262 |
D Mitter, K Buiting, F
Eggeling, A Kuechler, T Liehr, UA
Mau-Holzmann, E-C Prott, D Wieczorek, G
Gillessen-Kaesbach. Is there a higher incidence of maternal uniparental disomy 14 [upd(14)mat)]? Rapid testing by DNA methylation assay. Med Genetik 2006; 18: 28 (Abstract W2 02) (Heidelberg, Germany) |
(o) |
UPD |
| 261 |
A Weise, M Gross, B
Horsthemke, U Claussen, T Liehr.
Parental-origin-determination-FISH (pod-FISH) can distinguish homologues chromosomes. Med Genetik 2006; 18: 35 (Abstract W7 01) (Heidelberg, Germany) |
(o) |
M |
| 260 |
T Liehr, K
Mrasek, N Kosyakova, P Stankiewicz, SW Cheung,
WW Cai, A Weise. Towards a molecular genotype-phenotype correlation of small supernumerary marker chromosomes (sSMC) by applying microdissected sSMC probes on a 21.5k BAC array-CGH. Med Genetik 2006; 18: 36 (Abstract W7 05) (Heidelberg, Germany) |
o |
sSMC |
2005
| Number |
Authors/
Title/ Where Contribution was Published |
Poster (p)
or oral (o) |
Topic |
| 259 |
A Diaz de Bustamente, MT
Darnaude, T Liehr, H Starke. Small supernumerary chromosome identified by cenM-FISH and subcenM-FISH as a cen 22 derived from a breakage in ther centromere of one 22. Chromosome Res 2005; 13: S130 (Abstract 7-22-P) (Madrid, Spain) |
(p) |
sSMC |
| 258 |
H Tönnies, A Gerlach, H
Starke, T Liehr, B Heineking, LM
Neumann, H Neitzel. Straightforward molecular cytogenetic identification and characterization of a de novo supernumerary neocentric derivative chromosome 13. Chromosome Res 2005; 13: S64 (Abstract 1.116-P) (Madrid, Spain) |
(p) |
sSMC |
| 257 |
AD Polityko, NV Rumyantseva,
H Starke, T Liehr. Inverted duplication of chromosome 16 characterized by high resolution multicolor banding (MCB) FISH technique in a child with congenital abnormalities. Chromosome Res 2005; 13: S36 (Abstract 1.47-P) (Madrid, Spain) |
(p) |
CG |
| 256 |
U Claussen, H Lehrer, R
Hliscs, A Kuechler, A Weise, T Liehr.
The splitting of human chromosome bands into sub-bands. Europ J Hum Genet 2005; 13: S62 (Abstract C01) (Prague, Czech) |
(o) |
INT |
| 255 |
S Balci, O Engiz, D Aktas, I
Vargel, MS Beksac, K Mrasek, T Liehr.
Ring chromosome 4 proven by FISH studiy in a child with cleft lip and palate, iris coloboma, mid-gut malrotation, hypospadias and corpus callosum hypoplasia. Europ J Hum Genet 2005; 13: S140-S141 (Abstract P0284) (Prague, Czech) |
(p) |
CG |
| 254 |
AD Polityko, NV Rumyantseva,
H Starke, T Liehr. Small supernumerary marker chromosomes characterized by multicolor FISH techniques: database of Belarusian National Registry of Chromosomal Abnormalities. Europ J Hum Genet 2005; 13: S141-S142 (Abstract P0289) (Prague, Czech) |
(p) |
sSMC |
| 253 |
T Liehr, U
Claussen, H Tönnies, H Starke. The different heteromorphic patterns in chromosome 9 pericentric region - towards a better understanding. Europ J Hum Genet 2005; 13: S142 (Abstract P0290) (Prague, Czech) |
p |
HET |
| 252 |
H Starke, C Karst, V
Trifonov, 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. Europ J Hum Genet 2005; 13: S154 (Abstract P0349) |
(p) |
M |
| 251 |
M Volleth, D Rostalski, M
Stumm, H Tönnies, T Liehr, P
Wieacker. Sensoneural hearing loss in a girl with a de novo terminal 10q26.1 deletion. Med Genetik 2005; 17: 94 (Abstract P153) (Halle, Germany) |
(p) |
CG |
| 250 |
U Claussen, H Nelle, R
Hliscs, A Küchler, A Weise, T Liehr.
The hierarchically organized splitting of chromosomes into sub-bands analysed by multicolour-banding (MCB) and chromosome stretching. Med Genetik 2005; 17: 93 (Abstract P149) (Halle, Germany) |
(p) | INT |
| 249 |
U Steinhaeuser, H Starke, M
Ziegler, U Claussen, T Liehr. Multicolorbanding applied in 3D-preserved interphase and metaphase nuclei. Med Genetik 2005; 17: 91-92 (Abstract P144) (Halle, Germany) |
(p) | INT |
| 248 |
K Mrasek, S Schmidt, H
Starke, U Claussen, T Liehr, A
Weise. Are there different ways to build chromosomal inversions during evolution and in so-called heteromorphisms in human? Med Genetik 2005; 17: 91 (Abstract P141) (Halle, Germany) |
(p) | EVO |
| 247 |
H Starke, U Claussen, H
Tönnies, T Liehr. Towards a better understanding of the heteromorphic patterns in chromosome 9. Med Genetik 2005; 17: 91 (Abstract P140) (Halle, Germany) |
(p) | HET |
| 246 |
A Heller, V Hahnemann, E
Möller, T Liehr, U Claussen, I
Loncarevic. Microarray-based comparative genomic hybridization with microdissection derived DNA-probes. Med Genetik 2005; 17: 76-77 (Abstract P081) (Halle, Germany) |
(p) | M |
| 245 |
B Zoll, A Polityko, K Mrasek,
T Liehr, J Kohlhase, I Bartels, H
Starke. Ring chromosome 4 with complex karyotypes in two patients. Med Genetik 2005; 17: 64 (Abstract P028) (Halle, Germany) |
(p) | EVO |
| 244 |
C Rudolph, L Wingen, M Emura,
R Schlegelberger, M Daibata, Y Matsuo, N Emi, M
Abe, R Lai, K Mrasek, U Claussen, T Liehr.
Molecular cytogenetic investigation of t(11;14)(q13;q32)-positive B-cell NHL cell lines increases the suspicion of tumor-associated genes on chromosome 1. Med Genetik 2005; 17: 60 (Abstract P009) (Halle, Germany) |
(p) | TCG |
| 243 |
M Glaser, A Roth, C Karst, M
Gross, U Claussen, T Liehr. Chromosome-torsions detected in cytogenetic preparations of bone-marrow – preparation induced artifacts or something leukemia-specific? Med Genetik 2005; 17: 58 (Abstract P004) (Halle, Germany) |
(p) | TCG |
| 242 |
C Karst, H Mkrtchyan, U
Claussen, A Weise, L Kearney, T Liehr.
Detection of cryptic chromosomal aberrations in acute lymphoblastic leukaemia (ALL). Med Genetik 2005; 17: 58 (Abstract P003) (Halle, Germany) |
(p) | TCG |
| 241 |
I Hansmann, CD Eller, A
Kuechler, T Sahoo, C Baldermann, U Lieser, M
Hesse, H Thiele, M Hagemann, E Fiedler, SA
Yatsenko, T Liehr, B Horsthemke,
U Claussen, Y Marahrens, JR Lupski, P
Stankiewicz. L1 elements facilitate X-inactivation spreading onto trisomic chromosome 15q in an unbalanced translocation t(X;15)(q22.3;q11.2) stimulated by low-copy repeats. Med Genetik 2005; 17: 48 (Abstract W06 04) (Halle, Germany) |
(p) | CG |
| 240 |
T Liehr, K
Mrasek, U Claussen, H Starke. Towards a first genotype-phenotype correlation of small supernumerary marker chromosomes (sSMC). Med Genetik 2005; Vol 17: 42 (Abstract W02 04) (Halle, Germany) |
o |
sSMC |
| 239 |
M Gross, T Liehr,
U Claussen, V Trifonov, A Weise. High resolution molecular cytogenetic study of chimpanzee chromosomes. Med Genetik 2005; 17: 91 (Abstract P142) (Halle, Germany) |
(p) | EVO |
| 238 |
A Weise, H Starke, U
Claussen, T Liehr. New centromere-near and subtelomeric rearrangements detected in Pongo pygmaeus supspec. Med Genetik 2005; 17: 91 (Abstract P143) (Halle, Germany) |
(p) | EVO |
2004
| Number |
Authors/
Title/ Where Contribution was Published |
Poster (p)
or oral (o) |
Topic |
| 237 |
J Barber, V Maloney, NS
Thomas, B Van Zyl, D Bunyan, A McCormick, A
Kumar, T Liehr. Imbalances of distal 8p; extent, parental origin, predisposition and clinical significance. J Med Gen 2004; 1: S21 (Abstract SP33) (York, UK) |
(o) |
CG |
| 236 |
T Liehr, K
Mrasek, H Starke. The genetic content of mosaic and non-mosaic small supernumerary marker chromosomes (sSMC). J Med Gen 2004; 1: S30 (Abstract SP61) (York, UK) |
o |
sSMC |
| 235 |
JCK Barber, NS Thomas, MN
Collinson, NR Dennis, T Liehr, A
Weise, B Belitz, L Pfeiffer, M Kirchhoff, B
Krag-Olsen, C Lundsteen. Segmental haploinsufficiency; transmitted deletions of 2p12 have no apparent phenotypic consequences. J Med Gen 2004; S60 (Abstract 2.37) (York, UK) |
(o) |
CG |
| 234 |
C Ramel, U Cordes, X Schmitt,
T Liehr, M Hoeltzenbein, J Decker,
D Steinberger. Interstitial non-reciprocal translocation with an inveretd inserton 46,XY,ins(2;4)(p23;q281q31.1) associated with primary hypogonadism. Europ J Hum Genet 2004; 12: S143 (Abstract P0281) (Munich, Germany) |
(p) | CG |
| 233 |
G von Beust. S Sauter, A
Wessel, B Zoll, T Liehr. Identification of the origin of a marker chromosome 7 in a child with dysmorphic signs and congenital heart defect. Europ J Hum Genet 2004; 12: S119 (Abstract P0172) (Munich, Germany) |
(p) | sSMC |
| 232 |
A Weise, H Starke, U
Claussen, T Liehr. New centromere-near and subtelomeric rearrangements detected in Pongo pygmaeus supspec. Europ J Hum Genet 2004; 12: S318 (Abstract P1074) (Munich, Germany) |
(p) | EVO |
| 231 |
U Steinhaeuser, H Starke, U
Claussen, T Liehr. Multicolor chromosome banding (MCB) in the interphase nucleus. Europ J Hum Genet 2004; 12: S126 (Abstract P0203) (Munich, Germany) |
(p) | INT |
| 230 |
H Starke, O Rittinger, A
Weise, 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. Europ J Hum Genet 2004; 12: S125 (Abstract P0199) (Munich, Germany) |
(p) | CG |
| 229 |
AD Polityko, H Starke, N
Rumyantseva, I Naumchik, O Khurs, I Pisarik, E
Goncharova, L Shamgina, N Drozdovskaja, L
Podleschuk, E Abramchik, E Jaroshevich, U
Claussen, T Liehr. Two cases of de novo partial duplication of 1p: molecular cytogenetic charcaterization by high resolution multicolor banding (MCB) FISH and clinical aspects. Europ J Hum Genet 2004; 12: S120 (Abstract P0178) (Munich, Germany) |
(p) | CG |
| 228 |
A Weise, H Starke, K Mrasek,
C Karst, A Kuechler, U Claussen, T Liehr.
Multicolor-banding (MCB) for all human chromosomes in one hybridization step with a resolution of 450 bands or more. Med Genetik 2004; 16: 108 (Abstract P06-017) (Munich, Germany) |
(p) | M |
| 227 |
U Steinhaeuser, H Starke, U
Claussen, T Liehr. Suspension fluorescence in situ hybridization (S-FISH) – a handy technique for interphase analyses. Med Genetik 2004; 16: 107 (Abstract P06-011) (Munich, Germany) |
(p) |
M INT |
| 226 |
H Starke, T Liehr,
A Weise, A Heller, K Mrasek, A Kuechler, U
Claussen, F von Eggeling. Small supernumerary marker chromosomes (SMC) and new FISH methods for their characterization. Med Genetik 2004; 16: 106-107 (Abstract P06-010) (Munich, Germany) |
(p) | sSMC M |
| 225 |
T Liehr. Rapid prenatal diagnostics in the interphase nucleus and possible pitfalls. Med Genetik 2004; 16: 106 (Abstract P06-007) (Munich, Germany) |
(p) |
INT CG |
| 224 |
C Karst, H Starke, V
Trifonov, J Seidel, U Claussen, T Liehr.
Enlarged chromosome 13 p-arm hiding a cryptic partial trisomy 6p22.20pter. Med Genetik 2004; 16: 105-106 (Abstract P06-005) (Munich, Germany) |
(p) | CG |
| 223 |
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). Med Genetik 2004; 16: 97 (Abstract P01-009) (Munich, Germany) |
(p) | CG |
| 222 |
I Schreyer, V Beensen, KH
Eichhorn, A Heller, T Liehr, U
Claussen. Dup(13)(q14.2q21.1) 0 yet another differential diagnostic aspect for short stature like phenotype. Med Genetik 2004; 16: 96-97 (Abstract P01-006) (Munich, Germany) |
(p) | CG |
| 221 |
K Mrasek, A Kuechler, H
Starke, M Ziegler, P Kuepferling, U Claussen, T
Liehr. Prenatal diagnosis of a duplication in 22q11.21 led to the identification of a trisomy 22q11.21 in three generations without clinical findings. Med Genetik 2004; 16: 96 (Abstract P01-004) (Munich, Germany) |
(p) | CG HET |
| 220 |
A Kuechler, M Ziegler, C
Blank, B Rommel, J Bullerdiek, J Ahrens, U
Claussen, T Liehr. Highly complex rearrangement between chromosomes 3, 4, 7, 9 and 17 in a healthy female characterized by M-FISH and multi-color banding (MCB). Med Genetik 2004; 16: 95-96 (Abstract P01-002) (Munich, Germany) |
(p) | CG |
| 219 |
M Hesse, M Hagemann, H
Thiele, I Hansmann, T Liehr, U
Claussen, A Kuechler. An unbalanced translocation t(X;15)(q22;q12) in one fetus of a dizygotic twin pregnancy diagnosed after pathologic ultrasound findings: a case report. Med Genetik 2004; 16: 95 (Abstract P01-001) (Munich, Germany) |
(p) | CG |
2003
| Number |
Authors/
Title/ Where Contribution was Published |
Poster (p)
or oral (o) |
Topic |
| 218 |
F Sun, M Oliver-Bonet, T
Liehr, K Trpkov, E Ko, J Navarro, J
Benet, RH Martin. Bivalent chiamsa frequencies in individual chromosomes using cenM-FISH analysis of human pachytene cells. Am J Hum Genet 2003; 73: 308 (Abstract 808) (Los Angeles, USA) |
(p) |
INT |
| 217 |
G Lefort, AM Chaze, A Weise,
T Liehr, H Starke, F Pellestor, M
Claustre, P Sarda. Partial trisomy 20q11.2 characterized by FISH in a child with dysmorphic features and developmental delay. Annales de Génétique 2003; Vol 46: 245-246 (Abstract 7.53.) (Bologna, Italy) |
(p) |
CG |
| 216 |
J Benet, M Codina-Pascual, M
Oliver-Bonet, H Starke, T Liehr,
C Guitiérrez, J Sánches, O Arango, J Egozccue, J
Navarro. Multiprobe FISH characterisation of a dicentric Yq (p11.32) isochromosome in an azoospermic male. Annales de Génétique 2003; 46: 181 (Abstract 4.8.) (Bologna, Italy) |
(p) |
CG |
| 215 |
HJH Decker, D Reutzel, T
Liehr, E Lausch, H Brauch, M Holl, S
Naylor, B Zabel. Characterisation of a complex chromosome 3 rearrangement in a new case of hereditary renal cell carcinoma. Annales de Genetique 2003; 46: 153 (Abstract 3.3.) (Bologna, Italy) |
(p) |
CG |
| 214 |
D Böhm, S Herold, T
Liehr, F Laccone. Rapid detection of subtelomeric deletion/duplication by novel real-time quantitative PCR using SYBR-green dye. Med Genetik 2003; 15: 274 (Abstract W2 03) (Marburg, Germany) |
(o) |
CG |
| 213 |
H Lehrer, A Weise, S Michel,
H Starke, K Mrasek, A Heller, A Kuechler, U
Claussen, T Liehr. Giemsa-dark bands split into dark and light subbands as demonstrated by multicolor banding (MCB). Med Genetik 2003; 15: 274 (Abstract W2 04) (Marburg, Germany) |
o |
INT |
| 212 |
A Weise, H Starke, K Mrasek,
A Heller, A Kuechler, U Claussen, T Liehr.
Multicolor-banding (MCB) for all human chromosomes in one hybridization step with a resolution of 450 bands or more. Med Genetik 2003; 15: 273 (Abstract W2 01) (Marburg, Germany) |
(o) |
M |
| 211 |
D Reutzel, T Liehr,
E Lausch, M Holl, S Düsterhöft, C Spangenberg, D
Prawitt, S Naylor, H Brauch, HJ Decker, B Zabel.
Characterisation of a complex chromosome 3 rearrangement in familial renal cell carcinoma. Med Genetik 2003; 15: 338-339 (Abstract P-198) (Marburg, Germany) |
(p) |
TCG |
| 210 |
C Karst, A Heller, IF
Loncarevic, OA Haas, U Claussen, T Liehr.
Cryptic chromosomal changes in the non-proliferating cells of acute myeloid leukemia with monosomy 7. Med Genetik 2003; 15: 334-335 (Abstract P-182) (Marburg, Germany) |
(p) | TCG |
| 209 |
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. Med Genetik 2003; 15: 334 (Abstract P-181) (Marburg, Germany) |
(p) | TCG |
| 208 |
E Gebhart, J Ries, T
Liehr. CGH-detected losses of 9p21 are embedded in highly complex but consistent patterns of genomic imbalances in head and neck squamous cell carcinomas (HNSCC). Med Genetik 2003; 15: 334 (Abstract P-178) (Marburg, Germany) |
(p) | TCG |
| 207 |
H Starke, A Weise, A Nietzel,
A Kuechler, A Heller, U Claussen, T Liehr.
SubcenM-FISH defines up to present hardly characterizable centromere-near rearrangements. Med Genetik 2003; 15: 315 (Abstract P-099) (Marburg, Germany) |
(p) | sSMC M |
| 206 |
K Mrasek, A Weise, H Starke,
U Claussen, T Liehr. A repetitive sequence present in human chromosome 1q21, 1p12 and 1p36.1 lead to new insights into the evolution of chromosome 1 and its homologues in human and 4 ape species. Med Genetik 2003; 15: 315 (Abstract P-098) (Marburg, Germany) |
(p) | EVO |
| 205 |
J Lemke, T Felka, S Michel, C
Lemke, B Gruhn, T Liehr, U
Claussen. Molecular cytogenetic characterization of Howel-Jolly bodies. Med Genetik 2003; 15: 313 (Abstract P-089) (Marburg, Germany) |
(p) | CG |
| 204 |
M Volleth, M Stumm, T
Liehr, A Heller, VM Kalscheuer, C
Korb, P Wieacker. Heart malformation in a boy with a 6 Mb interstitial deletion in 8p23.1. Med Genetik 2003; 15: 312 (Abstract P-085) (Marburg, Germany) |
(p) | CG |
| 203 |
G Beust, S Sauter, A Wessel,
T Liehr, B Zoll. Identification of the origin of a marker chromosome 7 in a child with dysmorphic signs and congenital heart defect. Med Genetik 2003; 15: 304 (Abstract P-045) (Marburg, Germany) |
(p) | sSMC |
| 202 |
B Zoll, A Kuechler, D Boehm,
T Liehr, K Diepold, P Burfeind. Minor anomalies in a patient with a karyotype 46,XY,der(3)t(3;4)(p26;p16). Med Genetik 2003; 15: 304 (Abstract P-044) (Marburg, Germany) |
(p) | CG |
| 201 |
M Ziegler, C Blank, B Rommel,
J Bullerdiek, J Ahrens, U Claussen, T
Liehr, A Kuechler. Highly complex rearrangement between chromosomes 3, 4, 7, 9 and 17 in a healthy female characterized by M-FISH and multicolor banding (MCB). Med Genetik 2003; 15: 302 (Abstract P-037) (Marburg, Germany) |
(p) | CG |
| 200 |
U Steinhaeuser, H Starke,V
Trifonov, J Seidel, V Beensen, A Heller, U
Claussen, T Liehr. Enlarged chromosome 13 p-arm hiding a cryptic partial trisomy 6p22.2-pter. Med Genetik 2003; 15: 302 (Abstract P-036) (Marburg, Germany) |
(p) | CG |
| 199 |
T Liehr, H
Starke, A Nietzel, A Weise, A Heller, K Mrasek,
A Kuechler, U Claussen, F von Eggeling. Small supernumerary marker chromosomes (SMC): genotype-phenotype correlation and classification. Med Genetik 2003; 15: 301-302 (Abstract P-035) (Marburg, Germany) |
(p) | sSMC |
| 198 |
A Kuechler, H Starke, K
Mrasek, M Ziegler, C Kelbova, P Kuepferling, U
Claussen, T Liehr. Prenatal diagnosis of a duplication in 22q11.21 led to the identification of a trisomy 22q11.21 in three generations without clinical findings. Med Genetik 2003; 15: 301 (Abstract P-034) (Marburg, Germany) |
(p) | CG HET |
| 197 |
M Stefanove, H Starke, T
Krastev, D Seeger, A Petrov, T Liehr,
D Marichkov. De novo complex chromosomal rearrangement with six breakpoints in a rhizomelic mentally retarded child: molecular cytogenetic study. Europ J Hum Genet 2003; 11: S123-S124 (Abstract P289) (Brimingham, UK) |
(p) |
CG |
| 196 |
H Starke, V Trifonov, J
Seidel, V Beensen, A Heller, U Claussen, T
Liehr. Enlarged chromosome 13 p-arm hiding a cryptic partial trisomy 6p22.2-pter. Europ J Hum Genet 2003; 11: S297 (Abstract P297) (Brimingham, UK) |
(p) |
CG |
| 195 |
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 characterized by 24 color-FISH and multicolor banding (MCB). Europ J Hum Genet 2003; 11: S134-135 (Abstract P341) (Brimingham, UK) |
(p) |
CG |
| 194 |
A Weise, H Starke, K Mrasek,
U Claussen, T Liehr. Studies on a repetitive sequence present in human chromosome 1q21, 1p12 and 1p36.1 lead to new insights into the evolution of chromosome 1 and its homologues in human and 4 ape species. Europ J Hum Genet 2003; 11: S135 (Abstract P342) (Brimingham, UK) |
(p) |
EVO |
2002
| Number |
Authors/
Title/ Where Contribution was Published |
Poster (p)
or oral (o) |
Topic |
| 193 |
J Erlecke, I Hartmann, H
Starke, T Liehr, U Claussen, HG
Sayer, IF Loncarevic. Molecular cytogenetic discrimination between tumor and non tumor recipient cells below 5% after sex-mismatched allogenic stem cell transplantation. Annals of Hematology 2002; 81: S56 (Abstract 3) |
(p) |
TCG |
| 192 |
I Hansmann, C Baldermann, U
Lieser, M Hesse, A Kuechler, T Liehr,
H Thiele, M Hagermann, E Fiedler, B Horsthemke,
JR Lupski, P Stankiewicz. 15q11.2-qter resulting from unbalanced translocation t(X;15)(q22.3;q11.2) in a phenotypically normal girl. Am J Hum Genet 2002; 71: 309 (Abstract 807) (Baltimore, USA) |
(p) |
CG |
| 191 |
T Liehr, A
Nietzel, M Oliver Bonet, H Starke, A Heller, A
Weise, F v Eggeling, U Claussen. Characterization of human small marker-chromosomes by centromere-specific multicolor-FISH (cenM-FISH) and high resolution multicolor banding (MCB). Med Genetik 2002; 14: 253 (no Abstract#) (Leipzig, Germany) |
o |
sSMC |
| 190 |
A Kuechler, M Hesse, M
Hagemann, H Thiele, I Hansmann, T Liehr,
U Claussen. An unbalanced translocation t(X;15)(q22;q12) in one fetus of a dizygotic twin pregnancy diagnosed after pathologic ultrasound findings: a case report. Med Genetik 2002; 14: 261 (no Abstract#) (Leipzig, Germany) |
(o) |
CG |
| 189 |
H Starke, A Heller, A Weise,
A Nietzel, U Claussen, T Liehr. A new subcentromeric probe set for the characterization of centromere-near rearrangements. Med Genetik 2002; 14: 262 (no Abstract#) (Leipzig, Germany) |
(o) |
sSMC M |
| 188 |
U Claussen, J Lemke, J
Claussen, I Chudoba, T Liehr, P
Muehlig, K Sperling. Chromosomes are chromosomes throughout the cell cycle. Med Genetik 2002; 14: 263 (no Abstract#) (Leipzig, Germany) |
(o) |
INT |
| 187 |
C Walter, D Wieczorek, A
Weise, T Liehr, G
Gillessen-Kaesbach. Deletion of 16q23: a recognizable facial phenotype. Med Genetik 2002; 14: 283 (Abstract P1-0406) (Leipzig, Germany) |
(p) | CG |
| 186 |
R Trappe, J Kohlhase, D Böhm,
A Weise, T Liehr, G Esser, M
Meins, I Bartels, P Burfeind. Partial monosomy 20q13.1-qter and 2p24.1-pter is associated with multiple abortions: molecular characterization and segregation analysis in a family bearing a t(2;20) translocation. Med Genetik 2002; 14: 283 (Abstract P1-0405) (Leipzig, Germany) |
(p) | CG |
| 185 |
A Weise, B Belitz, L
Pfeiffer, U Claussen, T Liehr. Deletion 2p12-2p11.2 without abnormal clinical findings detected over three generations. Med Genetik 2002; 14: 284 (Abstract P1-0412) (Leipzig, Germany) |
(p) | HET CG |
| 184 |
A Dufke, M Stötter, H Starke,
T Liehr. Pure trisomy 12pter-12p11.21 in a girl with X-autosomal translocation: minor congenital anomalies and moderate developmental delay. Med Genetik 2002; 14: 285 (Abstract P1-0416) (Leipzig, Germany) |
(p) | CG |
| 183 |
I Schreyer, V Beensen, K H
Eichhorn, A Heller, T Liehr, U
Claussen. Dup(13)(q14.2q21.1) - yet another differential diagnostic aspect for short stature like phenotype. Med Genetik 2002; 14: 286 (Abstract P1-0419) (Leipzig, Germany) |
(p) | CG |
| 182 |
V Beensen, T Liehr,
A Heller, H Starke. Confocal laser scanning microscopy on the cytosceleton and human chromosomes after immunostaining, multicolor FISH and Feulgen reaction. Med Genetik 2002; 14: 292 (Abstractn P1-0708) (Leipzig, Germany) |
(p) | M |
| 181 |
M Volleth, P Muschke, T
Liehr, H Starke, J Gedschold, B
Brett, M Stumm, P Wieacker. Dysmorphic stigmata and psychomotor retardation in a boy with a rare deletion del(9)(q32q34). Med Genetik 2002; 14: 293 (Abstract P1-0715) (Leipzig, Germany) |
(p) | CG |
| 180 |
A Heller, B Albrecht, A
Nietzel, H Starke, F v Eggeling, U Claussen, T
Liehr. Characterization of two small supernumerary marker chromosomes by acro/cenM-FISH – first case with partial hexasomy 15pter->15q13. Med Genetik 2002; 14: 334 (Abstract P2-1903) (Leipzig, Germany) |
(p) | sSMC |
| 179 |
U Steinhaeuser, H Starke, A
Nietzel, J Lindenau, P Ullmann, U Claussen, T
Liehr. Suspension fluorescence in situ hybridization (S-FISH) – a versatile technique for interphase analyses. Med Genetik 2002; 14: 334 (Abstract P2-1902) (Leipzig, Germany) |
(p) |
INT M |
| 178 |
I Hartmann, H Starke, B
Mitulla, V Beensen, A Heller, U Claussen, T
Liehr. Mosaic del(22)/r(22): characterization of the derivative chromosomes by multicolor banding (MCB) and region specific probes. Med Genetik 2002; 14: 335 (Abstract P2-1908) (Leipzig, Germany) |
(p) |
CG M |
| 177 |
C Hoppe, D Kotzot, S Langer,
H Starke, T Liehr, M Ziegler, A
Weise, G Ernst, F v Eggeling. Pitfalls in prenatal diagnosis of a supernumerary marker chromosome and exclusion of uniparental disomy. Med Genetik 2002; 14: 356 (Abstract P2-2703) (Leipzig, Germany) |
(p) |
sSMC UPD |
| 176 |
T Liehr, A
Nietzel, H Starke, A Heller, A Weise, K Mrasek,
U Claussen. Straight-forward characterization of small human marker-chromosomes by centromere-specific multicolor-FISH (cenM-FISH), high resolution multicolor banding (MCB) and analysis for uniparental disomy (UPD). The Scand J Clin and Lab Investig 2002, 62 (S236): 19-20 (Reykjavik, Iceland) |
o |
sSMC |
| 175 |
M Stumm, M Volleth, G
Bollmann, A Küchler, T Liehr, J
Wulf, M Flentje, U Oppitz. The analysis of chromosomal instability in 25 tumor patients with average or strong acute and/or late side effects by G2-aberration assay and/or chromosome painting. Mol Rad Biol Oncol 2002; 3: 58 (Abstract PI.26) (Wolfsberg, Germany) |
(p) |
TCG |
| 174 |
A Kuechler, M Dreidax, SU
Pigorsch, J Dunst, U Claussen, T Liehr,
TG Wendt. Residual chromosomal damage after radiochemotherapy with and without use of additional amifostine analyzed by 24-color-FISH. Mol Rad Biol Oncol 2002; 3: 38 (Abstract PI.6) (Wolfsberg, Germany) |
(p) |
TCG |
| 173 |
A Kuechler, A Weise, S
Michel, B Pool-Zobel, A Schaeferhenrich, A
Heller, H Starke, TG Wendt, U Claussen, T
Liehr. Precise characterization of chromosomal rearrangements of the colon cancer cell line HT29 clone 19A by multicolor banding (MCB). Europ J Hum Genet 2002; 10: S87 (Abstract P006) (Strassburg, France) |
(p) |
TCG |
| 172 |
A Weise, H Starke, A Heller,
U Claussen, T Liehr. Reexamination of chromosome 2 rearrangements characterized by multicolor banding (MCB) by region-specific FISH probes. Europ J Hum Genet 2002; 10: S94 (Abstract P0097) (Strassburg, France) |
(p) |
CG M |
| 171 |
A Heller, B Albrecht, A
Nietzel, H Starke, F von Eggeling, U Claussen, T
Liehr. Characterization of two small supernumerary marker chromosomes (SMC) by acro/cenM-FISH – first case with partial hexasomy 15pter->15q13. Europ J Hum Genet 2002; 10: S146 (Abstract P034) (Strassburg, France) |
(p) |
sSMC |
| 170 |
H Starke, A Weise, A Nietzel,
A Heller, U Claussen, T Liehr. A new probe set for the characterization of centromere-near rearrangements. Europ J Hum Genet 2002; 10: S147 (Abstract P0346) (Strassburg, France) |
(p) |
sSMC M |
| 169 |
U Claussen, J Lemke, J
Claussen, I Chudoba, T Liehr, P
Muehlig, K Sperling. The shape, lenght and banding pattern of human interphase chromosomes. Europ J Hum Genet 2002; 10: S151-S152 (Abstract P0369) (Strassburg, France) |
(p) |
INT |
2001
| Number |
Authors/
Title/ Where Contribution was Published |
Poster (p)
or oral (o) |
Topic |
| 168 |
IF Loncarevic, J Römer, C
Bleck, JH Clement, T Liehr, A
Heller, H Starke, M Ziegler, U Claussen. Lack of ABL-BCR transcript is an indicator for structural deviations in standard t(9;22) in BCR-ABL positive CML. Blood 2001; 98: 4460 (Abstract 4460) (?) |
(p) |
TCG |
| 167 |
U Oppitz, M Volleth, J Wulf,
G Bollmann, T Liehr, M Flentje, M
Stumm. The analysis of chromosomal instability in 18 tumor patients with strong acute and/or late side effects by G2-aberration assay and/or whole chromosome painting. Int J Radiat Oncol Biol Phys 2001; 51: S187-S188 (?) |
(p) |
TCG |
| 166 |
U Claussen, J Lemke, J
Claussen, I Chudoba, V Trifonov, N Rubtsov, A
Heller, H Starke, K Sperling, T Liehr.
The shape and DNA mediated banding pattern of chromosomes in interphase are similar to metaphase chromosomes. Am J Hum Genet 2001; 69/S1: 314 (Abstract 766) (San Diego, USA) |
(p) | INT |
| 165 |
A Heller, K Mrasek, M Rocchi,
V Trifonov, N Rubtsov, H Starke, U Claussen, T
Liehr. Human multicolor banding (MCB) probes applied for ZOO-FISH in Gorilla gorilla and Hylobates lar. Am J Hum Genet 2001; 69/S1: 323 (Abstract 821) (San Diego, USA) |
(p) | EVO |
| 164 |
T Liehr, A
Heller, H Starke, A Weise, K Mrasek, V Trifonov,
N Rubtsov, U Claussen. Application of the complete human multicolor banding (MCB) set in cancer and clinical cytogenetics. Am J Hum Genet 2001; 69/S1: 335 (Abstract 895) (San Diego, USA) |
(p) | TCG CG |
| 163 |
H Starke, F. v. Eggeling, A
Nietzel, A Heller, M Rocchi, B Mitulla, V
Beensen, U Claussen, T Liehr. Centromere specific multicolor FISH (cenM-FISH) is a versatile method for the characterization of small SMC – case report. Am J Hum Genet 2001; 69/S1: 323 (Abstract 821) (San Diego, USA) |
(p) |
sSMC M |
| 162 |
A Küchler, T Wendt, M.
Dreidax, U Claussen, T Liehr, S
Pigorsch, J Dunst. 24-Farben-FISH-Nachweis von mitotischem Non-disjunction bei der untersuchung chromosomaler Residualschäden nach kombinierter Radiochemotherapie. Strahlenther Onkol 2001; 177/S1: 104 (Abstract P10.3) (Hamburg, Germany) |
(p) | TCG M |
| 161 |
A Küchler, M Dreidax, SU
Pigorsch, J Dunst, U Claussen, T Liehr,
T Wendt. Mitotic non-disjunction as residual chromosomal damage in human lymphocytes after radiochemotherapy detected by 24-colour FISH. Chromosome Research 2001; 9/S1: 152 (Abstract P178) (Würzburg, Germany) |
(p) | TCG M |
| 160 |
A Heller, K Mrasek, N
Rubtsov, V Trivonof, H Starke, M Rocchi, U
Claussen, T Liehr. Reconstruction of the female Gorilla gorilla karyotype by ZOO-FISH using 25-colour FISH and multicolour banding (MCB). Chromosome Research 2001; 9/S1: 68 (Abstract P16) (Würzburg, Germany) |
(p) | EVO |
| 159 |
U Claussen, J Lemke, J
Claussen, S Michel, A Heller, H Starke, V
Trifonov, N Rubtsov, K Sperling, T Liehr.
Chromosomal bands in interphase nuclei. Chromosome Research 2001; 9/S1: 1 (Abstract L8) (Würzburg, Germany) |
(o) | INT |
| 158 |
A Weise, H Starke, M Rocchi,
A Heller, U Claussen, T Liehr. Chromosome 2 rearrangements characterized by MCB combined with region specific probes. Ann Genet 2001; 44/S1: 69 (Abstract 1-178) (Würzburg, Germany) |
(p) | CG M |
| 157 |
T Liehr, A
Heller, H Starke, A Weise, K Mrasek, V Trifonov,
N Rubtsov, U Claussen. Multicolor banding (MCB) of all human chromosomes using region specific midi-libraries. Ann Genet 2001; 44/S1: 161 (Abstract 3-601) (Paris, France) |
(p) |
M |
| 156 |
H Starke, A Nietzel, F von
Eggeling, A Heller, M Rocchi, V Beensen, U
Claussen, T Liehr. Characterization of a small SMC by centromere specific multicolor FISH (cenM-FISH). Ann Genet 2001; 44/S1: 161 (Abstract 3-600) (Paris, France) |
(p) |
sSMC |
| 155 |
A Heller, N Rubtsov, V
Trifonov, H Starke, IF Loncarevic, U Claussen, T
Liehr. Characterization of complex aberrant leukemias by means of multicolor banding (MCB). Ann Genet 2001; 44/S1: 112 (Abstract 2-384) (Paris, France) |
(p) |
TCG |
| 154 |
K Mrasek, A Heller, H Starke,
M Rocchi, V Trifonov, N Rubtsov, U Claussen, T
Liehr. Human multicolor banding (MCB) probes applied for ZOO-FISH in Gorilla gorilla. Ann Genet 2001; 44/S1: 33 (Abstract 1-035) (Paris, France) |
(p) |
EVO |
| 153 |
U Claussen, J Lemke, J
Claussen, A Heller, H Starke, V Trifonov, N
Rubtsov, K Sperling, T Liehr. Chromosome dynamics in vivo. Ann Genet 2001; 44/S1: 17 (Paris, France) |
(o) |
INT |
| 152 |
A Küchler, S Neubauer, R
Aroutiounian, G Grabenbauer, U Claussen, T
Liehr, T Wendt. Distribution of radiation-induced chromosomal aberrations in a NBS-family – a M-FISH study. Ann Genet 2001; 44/S1: 27 (Abstract 1-13) (Paris, France) |
(p) |
TCG |
| 151 |
R Hauschild, V Beensen, A
Heller, H Starke, T Liehr. Suspicion on triple - X - syndrome in rapid prenatal FISH diagnosis on uncultivated amniotic fluid cells: Problems and pitfalls for genetic counselling. Europ J Hum Genet 2001; 9/S1: 255-256 (Abstract P0800) (Vienna, Austria) |
(p) | sSMC |
| 150 |
H Starke, G Senger, M
Kossakiewicz, H Tittelbach, N Rubtsov, V
Trifonov, A Heller, U Claussen, T Liehr.
Maternal insertion of 18q11.2-q12.2 in 18p11.3 leading to recurrent unbalanced translocations in the offspring detected by microdissection and multicolor banding (MCB). Europ J Hum Genet 2001; 9/S1: 152 (Abstract P0265) (Vienna, Austria) |
(p) | CG |
| 149 |
U Claussen, J Lemke, J
Claussen, I Chudoba, V Trifonov, N Rubtsov, H
Starke, A Heller, K Sperling, T Liehr.
Chromosomes in interphase are similar to
metaphase chromosomes. Europ J Hum Genet 2001; 9/S1: 144 (Abstract P0221) (Vienna, Austria) |
(p) | INT |
| 148 |
A Göhlert, I Riemann, A
Nietzel, N Rubtsov, V Trifonov, U Claussen, T
Liehr, K König. A new versatile technique to detect specific sequences within single DNA molecules: Multiphoton multicolor FISH (MM-FISH). Europ J Hum Genet 2001; 9/S1: 142-143 (Abstract P0214) (Vienna, Austria) |
(p) | M |
| 147 |
A Weise, H Starke, M Volleth,
M Stumm, A Heller, N Rubtsov, V Trifonov, M
Rocchi, K Mrasek, U Claussen, T Liehr.
Chromosome 2 rearrangements precisely characterized by multicolor banding (MCB) and simultaneously with region specific probes. Europ J Hum Genet 2001; 9/S1: 142 ( Abstract P0212) (Vienna, Austria) |
(p) | CG M |
| 146 |
I Hartmann, H Starke, A
Nietzel, F Von Eggeling, A Heller, M Rocchi, V
Beensen, B Mitulla, U Claussen, T Liehr.
Characterization of a small supernumerary marker chromosome by centromere specific multicolor-color FISH (cenM-FISH): case report. Europ J Hum Genet 2001; 9/S1: 142 ( Abstract P0210) (Vienna, Austria) |
(p) | sSMC |
| 145 |
V Beensen, T Liehr,
A Heller, H Starke, M Wiederhold, P Mühlig, P
Ullmann. Ultrastructure analyses on human chromosomes in the interphase and mitosis of the cell cycle with the laser scanning microscop LSM 510. Europ J Hum Genet 2001; 9/S1: 141-142 (Abstract P0209) (Vienna, Austria) |
(p) | M |
| 144 |
T Liehr, A
Heller, H Starke, A Weise, K Mrasek, V Trifonov,
N Rubtsov, U Claussen. Multicolor banding (MCB) of all human chromosomes based on region specific microdissection libraries. Europ J Hum Genet 2001; 9/S1: 138 (Abstract P0207) (Vienna, Austria) |
p | CG M |
| 143 |
A Küchler, S Michel, B
Pool-Zobel, A Schäferhenrich, A Heller, H
Starke, V Trifonov, N Rubtsov, U Claussen, T
Liehr. Characterization of the colon cell line HT29 clone 19A by means of GTG-banding, 24-color FISH and multicolor banding (MCB). Europ J Hum Genet 2001; 9/S1: 138 ( Abstract P0193) (Vienna, Austria) |
(p) | TCG |
| 142 |
A Heller, N Rubtsov, V
Trifonov, H Starke, IF Loncarevic, U Claussen, T
Liehr. Characterization of complex aberrant leukemia cases by means of multicolor banding (MCB). Europ J Hum Genet 2001; 9/S1: 133-134 ( Abstract P0171) (Vienna, Austria) |
(p) | TCG M |
| 141 |
K Mrasek, A Heller, H Starke,
V Trifonov, N Rubtsov, U Wedding, I Loncarevic,
C Bleck, U Claussen, T Liehr. Complex translocation between the two homologue chromosomes 5 in CML - characterization of the aberration by multicolor banding (MCB). Europ J Hum Genet 2001; 9/S1: 132 (Abstract P0164) (Vienna, Austria) |
(p) |
TCG |
2000
| Number |
Authors/
Title/ Where Contribution was
Published |
Poster
(p) or oral (o) |
Topic |
| 140 |
A Küchler, S Neubauer, GG
Grabenbauer, U Claussen, T Liehr,
T Wendt. Untersuchungen zur Verteiluing und Charakterisierung von in vitro strahleninduzierten Chromosomenaberrationen bei einer NBS-Familie mittels 24-Farben-FISH. Strahlenther Onkol 2000; 176/S1: 108, (Abstract V13.0/07) (Munich, Germany) |
(p) |
TCG |
| 139 |
IF Loncarevic , H Starke, A
Heller, C Bleck, M Ziegler, W Fiedler, T
Liehr, HJ Clement, C Kelbova,
U Claussen. BCR-ABL positive but ABL-BCR negative chronic myeloid leukemia (CML) result from a deletiojn in chromosome der(9)t(9;22) and from BCR-ABL formation by gene insertion. Onkologie 2000; 23/S7: 134 (Abstract 0508) (Graz, Austria) |
(p) |
TCG |
| 138 |
U Claussen, A Heller, H
Starke, A Küchler, IF Loncarevic, M
Ziegler, I Hartmann, T Liehr.
Practical course: FISH. Cell Mol Biol 2000; 46 (Abstract 282) (?) |
(o) |
M |
| 137 |
F von Eggeling, T
Liehr, E Birch-Hirschfeld. Are the new fluorescent dyes DY630 and DY780 an alternative for Cy5 and IRD800 in molecular assays? Cell Mol Biol 2000; 46 (Abstract 260) (?) |
(p) |
M |
| 136 |
N Rubtsov, I Riemann, V
Trifonov, T Karamysheva, T Liehr,
U Claussen, K König. Chromosome microdissection using NIR femtosecond laserpulses and generation of band sepcific DNA-libraries with DOP-PCR. Cell Mol Biol 2000; 46 (Abstract 200) (?) |
(p) |
M |
| 135 |
A Heller, A Nietzel, M
Rocchi, H Starke, W Fiedler, U Claussen, T
Liehr. The identification of marker chromosomes with a new multi-color FISH technique specific for centromeres. Cell Mol Biol 2000; 46 (Abstract 90) (?) |
(p) |
sSMC M |
| 134 |
A Göhlert, I Riemann, T
Liehr, IF Loncarevic, U
Claussen, K-H Halbhuber, K König. Multiphoton multicolor FISH (MM-FISH): A versatile technique to detect specific sequences within single DNA molecules. Cell Mol Biol 2000; 46 (Abstract 69) (?) |
(p) |
M |
| 133 |
V Beensen, T Liehr,
A Heller, H Starke, M Wiedehold, P Mühlig,
P Ullmann. Three dimensional analysis of cell constituents. micro info 40-529 e/8.00; Carl Zeiss Microscopy Division (http://www.zeiss.de/micro). |
(o) |
M |
| 132 |
A Küchler, S Neubauer, GG
Grabenbauer, U Claussen, T Wendt, T
Liehr. 24-colour-FISH analysis - a new test system for the characterisation of individual radiosensitivity. Mol Rad Biol Oncol 2000; 1: 28 (Ermatingen, Switzerland) |
(p) |
TCG |
| 131 |
A Küchler, CR
Müller-Reible, T Liehr, U
Claussen. Detection of microdeletions by chromosome streching. Europ J Hum Genet 2000; 8: S81 (Abstract P-265) (Amsterdam, Netherlands) |
(p) |
CG |
| 130 |
H Starke, M Rocchi, H-U
Weier, A Heller, R Niemann, RA Pfeiffer, U
Claussen, T Liehr. Multicolor banding (MCB) of human chromosome 22 - application of the probe mix for the characterization of "cat eye chromosome" inv dup(22)(q11). Europ J Hum Genet 2000; 8: S87 (Abstract P-295) (Amsterdam, Netherlands) |
(p) |
sSMC M |
| 129 |
A Heller, A Nietzel, M
Rocchi, W Fiedler, H Starke, U Claussen, T
Liehr. Centromere specific multi-color FISH (cenM-FISH) - a new and rapid method for the identification of marker chromosomes. Europ J Hum Genet 2000; 8: S87 (Abstract P-294) (Amsterdam, Netherlands) |
(p) |
sSMC M |
| 128 |
U Claussen, K Sperling, J
Claussen, J Lemke, I Chudoba, T
Liehr. The multicolor banding (MCB) pattern of human chromosomes in interphase nuclei. Europ J Hum Genet 2000; 8: S89 (Abstract P-304) (Amsterdam, Netherlands) |
(o) |
INT |
| 127 |
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). Med Genetik 2000; 12: 55 (Abstract W4-6) (Lübeck, Germany) |
(p) |
CG |
| 126 |
C Fuchs, E Nelis, T
Liehr, A Ekici, M Schachner, C
Van Broeckhoven, B Rautenstrauss. FISH and fibre-FISH applied on YAC-DNA to visualize the presence of promotor and coding region of Myelin Protein Zero (MPZ). Med Genetik 2000; 12: 57 (Abstract W6-5) (Lübeck, Germany) |
(p) |
CG |
| 125 |
A Nietzel, I Wlodarska, A
Heller, H Starke, E Gebhart, B
Rautenstrauss, M Rocchi, A Hagemeijer, U
Claussen, T Liehr. Amplification of centromeric satellite DNA in marker chromosomes with homogeneously staining regions (HSR) identified by centromere-specific 24-color FISH. Med Genetik 2000; 12: 61 (Abstract W9-5) |
(p) |
TCG |
| 124 |
N Rubtsov, T Karamysheva, T
Babochkina, N Zhdanova, V Trifonov, H
Starke, A Heller, K Junker, T Liehr,
U Claussen. A new simple version of chromosome microdissection tested by probe generation for 24-multi-color FISH, multi-color banding (MCB), ZOO-FISH and in clinical diagnostics. Med Genetik 2000; 12: 65 (Abstract W12-4) (Lübeck, Germany) |
(p) |
M |
| 123 |
A Küchler, CR
Müller-Reible, T Liehr, U
Claussen. Detection of microdeletions in the short arm of chromosome X by chromosome stretching – determination of the resolution limits of this method. Med Genetik 2000; 12: 66 (Abstract W12-6) (Lübeck, Germany) |
(p) |
CG M |
| 122 |
A Heller, H Starke, V
Trifonov, N Rubtsov, J Lemke, J Wirth, G
Senger, I Chudoba, M Rocchi, U Claussen, T
Liehr. Multicolor banding (MCB) of human chromosomes based on region specific YAC clones and/or microdissection libraries. Med Genetik 2000; 12: 92 (Abstract P-I-2.3) (Lübeck, Germany) |
(p) |
M |
| 121 |
H Starke, W Henn, S
Reichardt, M Stumm, C Behrend, G Senger, W
Fiedler, U Claussen, T Liehrr.
Two different types of human chromosome 9 pericentric inversions – detected by a microdissection probe specific for 9p12 and 9q13. Med Genetik 2000; 12: 93 (Abstract P-I-2.7) |
(p) |
CG HET |
| 120 |
V Trifonov, VG Mateeva, TV
Karamisheva, T Liehr, U
Claussen, N Rubtsov. Molecular cytogenetic characterization of a derivative human chromosome 3. Med Genetik 2000; 12: 93 (Abstract P-I-2.9) (Lübeck, Germany) |
(p) |
CG |
| 119 |
S Jakubiczka, B Mitulla, T
Liehr, J Arnemann, R Sudbrak,
M Stumm, P Wieacker, T Bettecken. Incidental prenatal detection of a Xp deletion using an anonymous primer pair for fetal sexing. Med Genetik 2000; 12: 101 (Abstract P-I-4.11) (Lübeck, Germany) |
(p) |
CG |
| 118 |
I Schreyer, V Beensen, KH
Eichhorn, A Heller, T Liehr,
E Schulze, H Starke, U Claussen. Detection of a small unbalanced 1/17 translocation in a mentally retarded and dysmorphic child via chromosome analysis of the parents. Med Genetik 2000; 12: 101-102 (Abstract P-I-4.13) (Lübeck, Germany) |
(p) |
CG |
| 117 |
M Ziegler, A Schmidt, A
Nietzel, H Starke, A Heller, G Senger, U
Claussen, T Liehr. Identification and molecular characterization of a prenatally detected maternally inherited supernumerary small ring chromosome 8p. Med Genetik 2000; 12: 100 (Abstract P-I-4.6) (Lübeck, Germany) |
(p) |
sSMC |
| 116 |
T Liehr, V
Beensen, H Holland, G Großwendt, T
Zimmermann, E Kunisch, U Claussen, UG
Froster, RW Kinne. Parallel occurrence of chromosomal aberrations in synovial fibroblasts and synovial macrophages from patients with rheumatoid arthritis (RA) and osteoarthritis (OA). Med Genetik 2000; 12: 107 (Abstract P-II-5.15) (Lübeck, Germany) |
(p) |
CG |
| 115 |
K Huehne, T Liehr,
O Park, B Rautenstrauss. A rare transcript C of the peripheral myelin protein 22 (PMP-22) is expressed in tumor cell lines carrying an amplification of the CMT1A unit. Med Genetik 2000; 12: 123 (Abstract P-II-6.10) (Lübeck, Germany) |
(p) |
CG |
| 114 |
A Bleichert, W Fiedler, R
Dahse, U Claussen, G Ernst, IF Loncarevic,
T Liehr, F von Eggeling. A new FISH probe for the chromosomal region 9p21 derived from long distance (LD)-PCR. Med Genetik 2000; 12: 132 (Abstract P-II-7.10) (Lübeck, Germany) |
(p) |
TCG |
| 113 |
IF Loncarevic, H Starke, C
Bleck, M Ziegler, W Fiedler, T
Liehr, HJ Clement, C Kelbova,
U Claussen. Detection of 3’-BCR gene sequences on chromosome der(22)t(9;22) but not on der(9)t(9;22) by FISH in 4 patients with a conventional CML. Med Genetik 2000; 12: 132 (Abstract P-II-7.12) (Lübeck, Germany) |
(p) |
TCG |
| 112 |
E
Gebhart, T Liehr. CGH-detected patterns of Genomic imbalances in human solid tumors may reflect environmental influences on tumor development. Med Genetik 2000; 12: 130 (Abstract P-II-7.2) (Lübeck, Germany) |
(p) |
TCG |
1999
| Number |
Authors/
Title/ Where Contribution was Published |
Poster (p)
or oral (o) |
Topic |
| 111 |
IF Loncarevic , H Starke, M
Ziegler, C Bleck, T Liehr, HJ
Clement, C Kelbova, U Claussen. The lack of abl and bcr target sequences on chromosome der(9)t(9;22) in CML is a recurrent anomlay that is detected by FISH. Blood 1999; 94: 208b (Abstract 4126) (?) |
(p) |
TCG |
| 110 |
S Neubauer, T Liehr,
I Chudoba, U Claussen, R Sauer. Vergleich 24-Farben- u. Drei-Farben-FISH bei der Detektion strahleninduzierter Chromosomen-Aberrationen. Strahlenther Onkol 1999; 175: S62 (Abstract BI-P42) (?) |
(p) |
TCG |
| 109 |
S Stein, T Liehr,
K Escherich. cDNAs and genes of the mouse liver- and muscle-fructose-1,6-bisphosphatase. Biological Chemistry 1999; 380: S199 (Mosbach, Germany) |
(p) |
CG |
| 108 |
H Tillmann, T Liehr,
K Eschrich. Structure and chromosomal localization of the human muscle fructose-1,6-bisphosphatase gene (FbP2). Biological Chemistry 1999; 380: S201 (Mosbach, Germany) |
(p) |
CG |
| 107 |
T Liehr, A
Heller, H Starke, J Lemke, J Wirth, G Senger, I
Chudoba, M Rocchi, U Claussen. Multicolor banding (MCB) of human chromosomes 1, 5 and 13 based on region specific YAC clones and microdissection libraries. Am J Hum Genet 1999; 65: A9 (Abstract 39) (San Francsico, USA) |
p |
CG |
| 106 |
A Heller, H Starke, IF
Loncarevic, G Senger, I Chudoba, U Claussen, T
Liehr. Molecular cytogenetic characterization of a highly aberrant plasmocytoma case with 24-color FISH, CGH, multicolor banding (MCB) and region specific FISH probes. Am J Hum Genet 1999; 65: A130 (Abstract 695) (San Francsico, USA) |
(p) |
CG |
| 105 |
H Starke, A Rump, J Seidel, V
Beensen, M Stumm, J Wirth, A Heller, U Claussen,
T Liehr. Molecular cytogenetic characterization of the chromosomal region 2q37 in patients suffering from brachydactyly E including probes for the putative candidate gene LOBO1. Am J Hum Genet 1999; 65: A358 (Abstract 2023) (San Francsico, USA) |
(p) |
CG |
| 104 |
AR Kelter, J Herchenbach, F v
Deimling, T Liehr, JM Scharf, LM
Kunkel, WF Dietrich, B Wirth. C loning and genomic structure of a 9.5-kb transcriptional factor-like nuclear regulator (TFNR), closely localized to survival motor neuron gene. Am J Hum Genet 1999; 65: A189 (Abstract 1039) (San Francsico, USA) |
(p) |
CG |
| 103 |
B Wirth, C Helmken, A Wetter,
F Schoenen, T Liehr, S
Rudnik-Schöneborn, K Zerres. Genomic characterization of the SMN interacting protein (SIP1) and molecular genetic analysis of patients with spinal muscular atrophy. Am J Hum Genet 1999; 65: A383 (Abstract 2166) (San Francsico, USA) |
(p) |
CG |
| 102 |
E Gebhart, T Liehr.
Do patterns of genomic imbalances in human solid tumors reflect environmental influences on tumor formation? Int J Mol Med 1999; 4: S13 (Abstract 133) (Vouliagmeni, Athens, Greece) |
o |
TCG |
| 101 |
T Liehr, S
Girod, U Claussen, E Gebhart. Nucleus extraction from one paraffin-embedded section mounted on a slide for two-color FISH. Cancer Genet Cytogenet 1999; 112: 85 (Saarbrücken, Germany) |
p |
TCG |
| 100 |
E Gebhart, T Liehr,
W Fiedler, J Ries, S Girod. CGH-detected amplification of DNA copy number in head and neck squamous cell carcinomas (HNSCC). Cancer Genet Cytogenet 1999; 112: 78 (Saarbrücken, Germany) |
(p) |
TCG |
| 99 |
H Starke, A Heller, J Seidel,
V Beensen, G Senger, M Stumm, J Wirth, L
Kearney, U Claussen, T Liehr. Molecular cytogenetic characterization of the region 2q37 in patients suffering from brachydactyly E. Cytogenet Cell Genet 1999; Vol 85: 166 (Abstract P 704) (Vienna, Austria) |
(p) |
CG |
| 98 |
I Verdorfer, A Taubald, T
Rith, K Bayerlein, T Liehr, S
Girod, E Gebhart. I-FISH detected DNA-sequence copy number amplifications in oral squamous cell carcinomas. Cytogenet Cell Genet 1999; Vol 85: 109 (Abstract P 442) (Vienna, Austria) |
(p) |
TCG |
| 97 |
A Heller, H Starke, I F
Loncarevic, G Senger, I Chudoba, U Claussen, T
Liehr. Characterization of a highly aberrant plasmocytoma case with 24-color FISH, CGH, multicolor banding (MCB) and region specific FISH probes. Cytogenet Cell Genet 1999; Vol 85: 72 (Abstract P 280) (Vienna, Austria) |
(p) |
TCG |
| 96 |
A Nietzel, H Starke, A
Heller, W Fiedler, G Senger, E Gebhart, M
Rocchi, U Claussen, T Liehr. Characterization of small marker chromosomes by centromere specific 24-color FISH. Cytogenet Cell Genet 1999; 85: 40 (Abstract P 142) (Vienna, Austria) |
(p) |
M sSMC |
| 95 |
T Liehr, H
Starke, A Heller, J Wirth, G Senger, I Chudoba,
M Rocchi, U Claussen. Multicolor banding (MCB) of human chromosome 13 based on region specific YAC clones and microdissection libraries. Cytogenet Cell Genet 1999; 85: 30 (Abstract O 099) (Vienna, Austria) |
o |
M |
| 94 |
F v Deimling, J Scharf, T
Liehr, M Rothe, A Albers, W
Dietrich, L Kunkel, N Wernert, B Wirth. Identification, localization and genome structure of the human and mouse homologues to rad17 (S.pombe) and RAD24 (S.cervisiae) checkpoint genes. Putative involvement in testicular tumorigenesis. Med Genetik 1999; 11: 119 (Abstract W2-2) (Nürnberg, Germany) |
(p) |
TCG |
| 93 |
A-R Kelter, S Moskau, J
Scharf, T Liehr, L Kunkel, W
Dietrich, B Wirth. Cloning of a candidate gene for atypical SMA forms within the spinal muscular atrophy region (5q11.2-q13.3). Med Genetik 1999; 11: 136 (Abstract W12-11) (Nürnberg, Germany) |
(p) | CG |
| 92 |
A Taubald, T Liehr,
J Ries, S Girod, E Gebhart. Definition by I-FISH in archival paraffin material of human solid tumors of the cell population carrying CGH-detected DNA sequence copy number amplifications. Med Genetik 1999; 11: 161 (Abstract P3-21) (Nürnberg, Germany) |
(p) | TCG |
| 91 |
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. Med Genetik 1999; 11: 157 (Abstract P3-4) (Nürnberg, Germany) |
(p) | TCG |
| 90 |
W Fiedler, T Liehr,
C Hoppe, Z Bereczki, B Schimmel, R Dahse, F v
Eggeling, S Koscielny, E Beleites, E Gebhart, G
Ernst, U Claussen. Telomerase (in)activation in head and neck cancers is not caused by genomic alterations of genes encoding the telomerase complex or the putative telomerase suppresor gene. Med Genetik 1999; Vol 11: 152 (Abstract P2-13) |
(p) | TCG |
| 89 |
A Heller, H Starke, J Seidel,
V Beensen, G Senger, M Rocchi, J Wirth, I
Chudoba, U Claussen, T Liehr. Molecular cytogenetic characterization of a partial trisomy 9q to narrow down a putative critical region of a gene responsible for pyloric stenosis. Med Genetik 1999; 11: 166 (Abstract P4-19) (Nürnberg, Germany) |
(p) | CG |
| 88 |
J Seidel, V Beensen, S
Platzer, I Chudoba, T Liehr, U
Claussen. Paracentric inversion of chromosome 9 with probable involvement of the c-abl gene - case report. Med Genetik 1999; 11: 173 (Abstract P4-53) (Nürnberg, Germany) |
(p) | TCG |
| 87 |
H Starke, I Schreyer, W
Fiedler, V Beensen, A Heller, I Chudoba, U
Claussen, T Liehr. Alternative strategy for the molecular characterization of small marker chromosomes in prenatal cases. Med Genetik 1999; 11: 174 (Abstract P4-56) (Nürnberg, Germany) |
(p) | sSMC |
| 86 |
K Hühne, O Park, T
Liehr, W Fiedler, B Rautenstrauss. Expression analysis of the PMP22 gene in tumor cell lines with a chromosome 17p11.2 amplification. Med Genetik 1999; 11: 193 (Abstract P7-46) (Nürnberg, Germany) |
(p) | TCG |
| 85 |
T Liehr, A
Heller, H Starke, J Wirth, G Senger, I Chudoba,
M Rocchi, H-U Weier, U Claussen. High resolution mulitcolor banding (hrM-FISH) for human chromosome 13 using YAC libraries as probes. Med Genetik 1999; 11: 132 (Abstract W11-4) (Nürnberg, Germany) |
o |
M |
| 84 |
A Nietzel, H Starke, A
Heller, G Senger, U Claussen, T Liehr.
Centromere specific 24-color-FISH - a new approach for the characterization of marker chromosomes. Med Genetik 1999; 11: 132-133 (Abstract W11-6) (Nürnberg, Germany) |
o |
sSMC M |
| 83 |
S Neubauer, T Liehr,
I Chudoba, U Claussen, E Gebhart, R Sauer. Comparison of multi-color- and three-color-FISH for the detection of chromosome aberrations induced by ionizing irradiation. Med Genetik 1999; 11: 139 (Abstract W13-1) (Nürnberg, Germany) |
(p) |
TCG |
1998
| Number |
Authors/
Title/ Where Contribution was Published |
Poster (p)
or oral (o) |
Topic |
| 82 |
T Liehr, C
Fuchs, U Suter, S Sancho, H Grehl, B
Rautenstrauss. Two-color interphase FISH for CMT1A- and HNPP-diagnostics on archival nerve biopsies. J Periph Nervous Syst 1998; 3: 296 (Antwerp, Belgium) |
o |
CG |
| 81 |
C Fuchs, T Liehr,
A Ekici, S Özbey, B Rautenstrauss. CMT1A and HNPP disease: a SacI polymorphism in the proximal CMT1A-REP element may lead to genetic misdiagnosis of HNPP. J Periph Nervous Syst 1998; 3: 292-293 (Antwerp, Belgium) |
(o) |
CG |
| 80 |
F v. Deimling, J Scharf, T
Liehr, M Rothe, P Albers, W
Dietrich, L Kunkel, N Wernert, B Wirth. Cloning of the human and mouse homologues to the yeast RAD24 and rad17 genes. Putative involvement in tumorigenesis of testicular cancer. Am J Hum Genet 1998; 63: S A66 (Abstract 351) (Denver, USA) |
(p) |
TCG |
| 79 |
LT Reiter, T Liehr,
B Rautenstrauss, JR Lupski. Localization of mariner transposons in the human genome by primed in situ (PRINS). Am J Hum Genet 1998; 63: S A22 (Abstract 109) (Denver, USA) |
(p) |
CG |
| 78 |
B Stoyanov, T Liehr,
U Claussen, R Wetzker. Localization of the gene for phosphoinositide 3 kinase gamma on human chromosome 7. Biol Chem 1998; 379: S133 (Mosbach, Germany) |
(p) |
CG |
| 77 |
T Liehr, E
Gebhart. Comparative genomic hybridization (CGH) - a good tool to study genomic changes in cancer. Biol Chem 1998; 379: S97 (Mosbach, Germany) |
(o) |
TCG |
| 76 |
E Wolff, H Steininger, S
Girod, T Liehr, J Ries, T
Kirchner, E Gebhart. A rather uniform pattern of genomic imbalances in oral squamous cell carcinomas detected by comparative genomic hybridization. Pathol Res Pract 1998; 194: 251 (Abstract 151) (Kassel, Germany) |
(p) |
TCG |
| 75 |
T Liehr, E
Wolff, S Girod, J Ries, H Steininger, E Gebhart. Detection of genomic imbalances in primary oral squamous cell carcinomas and cell lines by CGH. J Cancer Res Clin Oncol 1998; 124: SR125 (Abstract P1.11.03) (Berlin, Germany) |
p |
TCG |
| 74 |
K Michels-Rautenstrauss, CY
Mardin, W M Budde, S Özbey, J Gräßer, T
Liehr, GOH Naumann, RA Pfeiffer, B
Rautenstrauss. Mutation analysis in primary open angel glaucoma patients. Europ J Hum Genet 1998; 6: S143 (Abstract P4.152) (Lisbon, Portugal) |
(p) |
CG |
| 73 |
T Liehr, W
Fiedler, S Girod, J Ries, E Wolff, E Gebhart. Genomic imbalances in primary squamous cell carcinomas of different origin. Europ J Hum Genet 1998, 6: S80 (Abstract P2.023) (Lisbon, Portugal) |
p |
TCG |
| 72 |
M Volleth, T Liehr,
H Hameister, E Gebhart, R A Pfeiffer. Chromosome painting with human specific probes reveals chromosomal changes in chiropteran evolution. Med Genetik 1998; 10: 150 (Abstract P4B-13) (Jena, Germany) |
(p) |
CG |
| 71 |
A Ekici, B Köster, B
Landwehrmeyer, UP Ketelsen, R Korinthenberg, T
Liehr, B Rautenstrauss. Dejerine Sottas Syndrome: multiple mutations of serine 72 to leucine, tryptophane and proline in PMP22 suggests a crucial role of this amino acid for the protein. Med Genetik 1998; 10: 157 (Abstract P6A-12) (Jena, Germany) |
(p) |
CG |
| 70 |
C Fuchs, M Höltzenbein, FH
Hermann, C Kraus, T Liehr, C
Opelz, RA Pfeiffer, B Rautenstrauss. The PMP22 gene and parts of the Smith-Magenis region in 17p11.2 are duplicated in patients with Charcot-Marie-Tooth disease type 1A and mental retardation. Med Genetik 1998; 10: 175-176 (Abstract P6D-6) (Jena, Germany) |
(p) |
CG |
| 69 |
K Michels-Rautenstrauss, CY
Mardin, WM Budde, S Ötzbey, J Gräßer, T
Liehr, GOH Naumann, RA Pfeiffer, B
Rautenstrauss. Mutation analysis in primary open angle glaukoma patients. Med Genetik 1998; 10:162 (Abstract P6A-36) (Jena, Germany) |
(p) |
CG |
| 68 |
O Park, T Liehr,
C-R Frick, W Fiedler, B Rautenstrauss. Which role plays the PMP22 gene in cell growth regulation. Med Genetik 1998; 10: 180 (Abstract P6D-29) (Jena, Germany) |
(p) |
CG |
| 67 |
T Liehr, A
Taubald, E Wolff, S Girod, J Ries, E Gebhart. Genomic imbalances in primary oral squamous cell carcinomas and cell lines with gain of 11q13. Med Genetik 1998; 10:127 (Abstract P2A-10) (Jena, Germany) |
p |
TCG |
1997
| Number |
Authors/
Title/ Where Contribution was Published |
Poster (p)
or oral (o) |
Topic |
| 66 |
E Nelis, J Del-Favero, T
Liehr,
LE Warner, B Rautenstrauss, JR Lupski, C Van
Broeckhoven. Development of yeast artificial chromosome constructs containing specific mutations in the myelin protein zero gene. Soc for Neurosci 1997; Vol 23: 549 (Abstract 214.2) (New Orleans, USA) |
(o) |
CG |
| 65 |
E Gebhart, E Wolff, S Girod,
T
Liehr,
AH Tulusan, F Kiesewetter, H Schell. CGH and interphase FISH studies in human ovarian and oral carcinomas. Int J Onc 1997; 11: 883 (Abstract 111) (Crete, Greece) |
(o) |
TCG |
| 64 |
C Fuchs, T
Liehr,
H Grehl, C Opelz, M Murakami, JR Lupski, K
Thoma, K Kammler, B Rautenstrauss. Visualization of the Charcot-Marie-Tooth (CMT) type 1A duplication and the hereditary neuropathy with liability to pressure palsies (HNPP) deletion in Chr. 17p11.2 by means of high resolution FISH. J Periph Nervous Syst 1997; 2: 393 (Abstract n.a.) (?) |
(p) |
CG |
| 63 |
K Michels-Rautenstrauss, CY
Mardin, WM Budde, T
Liehr,
V Timmerman, C Van Broeckhoven, GO H Naumann, RA
Pfeiffer, B Rautenstrauss. Autosomal dominant juvenile open angle glaucoma (GLC1A): fine mapping of the TIGR gene to 1q24.3-25.2 and identification of a novel mutation in a German family. Am J Hum Genet 1997; 61: A340 (Abstract 1992) (Baltimore, USA) |
(p) |
CG |
| 62 |
O Park, T
Liehr,
B Rautenstrauss. Which role plays the PMP22 gene in cell growth regulation? Am J Hum Genet 1997; 61: A179 (Abstract 1033) (Baltimore, USA) |
(p) |
CG |
| 61 |
JR Lupski, T
Liehr,
L T Reiter, B Rautenstrauss. Are mariner transposons responsible for some chromosomal deletions and duplications in humans? Am J Hum Genet 1997; 61: A133 (Abstract 753) (Baltimore, USA) |
(o) |
CG |
| 60 |
C Fuchs, T
Liehr,
M Murakami, H Grehl, JR Lupski, B Rautenstrauss.
Visualization of the normal, duplicated and deleted CMT1A region by means of high resolution fiber FISH. Am J Hum Genet 1997; 61: A125 (Abstract 708) (Baltimore, USA) |
(p) |
CG |
| 59 |
T
Liehr,
B Rautenstrauss. The peripheral myelin protein 22kDa (PMP22) gene is expressed in non-neuronal epithelial tissues of mouse, rat, cattle and human. Am J Hum Genet 1997; 61: A176 (Abstract 1015) (Baltimore, USA) |
p |
CG |
| 58 |
B Rautenstrauss, T
Liehr,
U May-Wehof, P Möller, J Sertic, M Sostarko, H
Grehl. Association of Charcot-Marie-Tooth disease type 1A (CMT1A) and Multiple Sclerosis (MS): PMP22 is an exclusive candidate for peripheral neuropathies. Am J Hum Genet 1997; 61: A319 (Abstract 1863) (Baltimore, USA) |
(o) |
CG |
| 57 |
KD Bathke, B Rautenstrauss, T
Liehr,
A Ekici, H Grehl, B Neundörfer. Mutationssuche in drei kandidatengenen der hereditären sensomotorischen Neuropathie (HMSN, CMT) bei Patienten ohne CMT1A-Duplikation. Aktuelle Neurologie 1997; 24: S41 (Abstract P145) (Dresden, Germany) |
(p) |
CG |
| 56 |
H Grehl, T
Liehr,
B Neundörfer, B Rautenstrauss. Expression der peripheral myelin protein22 (PMP22)-mRNA bei heriditärer motorisch und sensibler Neuropathie Typ 1A (HMSN 1A). Aktuelle Neurologie 1997; 24:S7 (Abstract KV25) (Dresden, Germany) |
(o) |
CG |
| 55 |
H Grehl, T
Liehr,
B Neundörfer, B Rautenstrauss. Expression of peripheral myelin protein-22 (PMP22)-mRNA in hereditary motor and sensory neuropathy type 1 (HMSN1). Neuromusc Disord 1997; 7: 470-471 (Abstract NAP10) (Tunis, Tunesia) |
(p) |
CG |
| 54 |
KD Bathke, B Rautenstrauss, T
Liehr,
A Ekici, H Grehl, B Neundörfer. Molekulargenetische Diagnostik von Mutationen in Kandidatengenen der Hereditären sensomotorischen Neuropathie (HMSN, CMT). Med Gent 1997; 9: 450 (Abstract V26) (?) |
(p) |
CG |
| 53 |
H Grehl, T
Liehr,
B Neundörfer, B Rautenstrauss. Klinik und Neurophysiologie der hereditären motorisch und sensiblen Neuropathie (HMSN 1). Med Gent 1997; 9: 450 (Abstract V25) (?) |
(p) |
CG |
| 52 |
KD Bathke, T
Liehr,
A Ekici, H Grehl, B Rautenstrauss. Breakpoint analysis and screening for recombinations in Charcot-Marie-Tooth (CMT) and HNPP patients. Med Gent 1997; 9: 354-355 (Abstract P4.258) (?) |
(p) |
CG |
| 51 |
W Fiedler, T
Liehr,
F von Eggeling, R Dahse, G Ernst, B
Rautenstrauss, U Claussen. Precise mapping of the RNA component of the human telomerase to chromosome band 3q26.2 by fluorescence in situ hybridization. Med Gent 1997; 9: 294 (Abstract P3.020) (?) |
(p) |
CG |
| 50 |
BW Rautenstrauss, KD Bathke,
T
Liehr,
A Ekici, H Grehl, R A Pfeiffer. Breakpoint analysis and screening for recombinations in Charcot-Marie-Tooth (CMT) and HNPP patients. Med Genetik 1997; 9: 113 (Abstract P10-66) (Innsbruck, Austria) |
(p) |
CG |
| 49 |
AB Ekici, C Fuchs, T
Liehr,
H Grehl, B Rautenstrauss. FISH is an appropriate technique to confirm the presence of the plasmid DNA as well as the cloned human or rat cDNA after transfection of S2 insect cells. Med Genetik 1997; 9: 103 (Abstract P10-16) (Innsbruck, Austria) |
(p) |
CG M |
| 48 |
C Fuchs, T
Liehr,
H Grehl, C Opelz, K Thoma, K Kammler, B
Rautenstrauss. Visualization of the Charcot-Marie-Tooth (CMT) type 1A duplication and the hereditary neuropathy with liability to pressure palsies (HNPP) deletion in Chr. 17p11.2 by means of high resolution FISH. Med Genetik 1997; 9: 63 (Abstract P3-12) (Innsbruck, Austria) |
(p) |
CG |
| 47 |
T
Liehr,
K Thoma, O Park, BG Feuerstein,T Murakami, JR
Lupski, E Gebhart, B Rautenstrauss. The PMP22 gene is amplified in cell lines derived from glioma and osteogenic sarcoma: a new candidate for an oncogene? Med Genetik 1997; 9: 49 (Abstract P1-27) (Innsbruck, Austria) |
p |
TCG |
1996
| Number |
Authors/
Title/ Where Contribution was Published |
Poster (p)
or oral (o) |
Topic |
| 46 |
KD Bathke, T
Liehr,
A Ekici, H Grehl, B Neundörfer, B Rautenstrauss.
Molecular genetic diagnosis of Charcot-Marie-Tooth disease (CMT/HMSN) and tomaculous neuropathy (HNPP) using three generations of chromosome 17p11.2-12 specific probes. Med Genetik 1996; 8: 291 (Abstract 10) (Ulm, Germany) |
(p) |
CG |
| 45 |
B Rautenstrauss, V Timmerman,
T
Liehr,
L Reiter, KD Bathke, T Koeuth, A Löfgren, E
Nelis, A Ekici, H Grehl, P De Jonghe, C Van
Broeckhoven, JR Lupski. The CMT1A/HNPP recombination "hotspot": meiotic recombination and somatic reversion based on CMT1A-REP elements? Med Genetik 1996; 8: 290 (Abstract 9) (Ulm, Germany) |
(o) | CG |
| 44 |
B Rautenstrauss, A Heiland, A
Ekici, T
Liehr.
Hereditary neuropathy with liability to pressure palsies (HNPP): Exclusion of PMP22 point mutations in Chr. 17p11.2 deletion carriers. Am J Hum Genet 1996; 59: SA280 (Abstract 1624) (San Francisco, USA) |
(p) | CG |
| 43 |
KD Bathke, A Ekici, T
Liehr,
H Grehl, JR Lupski, B Neundörfer, B
Rautenstrauss. The hemizygous Thr118Met amino acid exchange in Peripheral Myelin Protein 22: recessive Charcot-Marie-Tooth (CMT) disease type 1 mutation or polymorphism? Am J Hum Genet 1996; 59: SA248 (Abstract 1429) (San Francisco, USA) |
(p) | CG |
| 42 |
T
Liehr,
H Grehl, B Rautenstrauss. CMT1A/HNPP-diagnostics by means of interphase FISH is possible on various kinds of tissue. Am J Hum Genet 1996; 59: SA123 (Abstract 686) (San Francisco, USA) |
(p) |
CG |
| 41 |
B Rautenstrauss, T
Liehr,
KD Bathke, A Ekici, H Grehl, K Rautenstrauss, T
Koeuth, T Murakami, L Reiter, B Neundörfer, R A
Pfeiffer, J R Lupski. Charcot-Marie-Tooth disease and tomaculous neuropathy: identification of a recombination "hot spot" in a German study. Braz J Genet 1996; 19: S162 (Abstract 299) (Rio de Janeiro, Brazil) |
(o) | CG |
| 40 |
KD Bathke, T
Liehr,
A Ekici, L Reiter, JR Lupski, H Grehl, B
Neundörfer, B Rautenstrauss. A recessive point
mutation in the PMP22 gene determines the
Charcot-Marie-Tooth disease phenotype in
presence of a deletion in the homologous
chromosome 17. 9. Braz J Genet 1996; 19: S162 (Abstract 300) (Rio de Janeiro, Brazil) |
(p) | CG |
| 39 |
B Rautenstrauss, T
Liehr,
K D Bathke, H Grehl, K Rautenstrauss, T Koeuth,
T Murakami, L Reiter, B Neundörfer, RA Pfeiffer,
JR Lupski. Charcot-Marie-Tooth disease and tomacolous neuropathy: identification of a recombination "hot spot" in a German study. J Neurol 1996; 243: S19 (Abstract 96) (The Hague, Netherlands) |
(p) | CG |
| 38 |
WG Ballhausen, C Kraus, B
Wolff, T
Liehr.
Human chromosome 5q13 harbours a novel conserved heavy metal transporter gene with a somatostatin receptor domain (SHMT1). Europ J Hum Genet 1996; 4/1: 111 (Abstract 7.008) (London, UK) (see also here) |
(p) | CG |
| 37 |
KD Bathke, T Liehr, A Ekici, H Grehl, D Claus, B Neundörfer, R A Pfeiffer, B Rautenstrauss. Evaluation of chromosome 17p11.2 specific probes for duplication and deletion analysis in hereditary peripheral neuropathies. Europ J Hum Genet 1996; 4/1: 75-76 (Abstract 5.100) | (p) | CG |
| 36 |
K Rautenstrauss, T Koeuth, T
Murakami, L Reiter, T
Liehr,
H Grehl, V Timmerman, K D Bathke, A Ekici, L
Shaffer, C Van Broeckhoven, J R Lupski, B
Rautenstrauss. A 1.5 Mb deletion in 17p11.2
causing tomaculous neuropathy due to a mutation
besides the recombination "hot spot" in
CMT1A-REP elements. Europ J Hum Genet 1996; 4/1: 74-75 (Abstract 5.095) (London, UK) |
(p) | CG |
| 35 |
V Timmerman, L Reiter, T
Koeuth, A Löfgren, T
Liehr,
E Nelis, K D Bathke, P De Jonghe, H Grehl, C Van
Broeckhoven, J R Lupski, B Rautenstrauss. A recombination "hot spot" mutation in 17p11.2 is frequently found in European CMT1A and HNPP patients. Europ J Hum Genet 1996; 4/1: 75 (Abstract 5.097) (London, UK) |
(o) | CG |
| 34 |
O Park, T
Liehr,
H Altenberger, S Reiprich, K Rautenstrauss, F
Pröls, B Rautenstrauss. Dramatically prolonged cell cycles for the yeast Saccharomyces cervisiae and growth arrest for E. coli bacteria: induced by high dose of human peripheral myelin protein 22 (PMP22). Europ J Hum Genet 1996; 4/1: 76 (Abstract 5.102) (London, UK) |
(p) | CG |
| 33 |
T
Liehr,
A Ekici, K D Bathke, H Grehl, B Rautenstrauss. Detection of a female Charcot-Marie-Tooth type 1A (CMT1A) patient with different mosaicism patterns in different tissues concerning the duplication in 17p11.2: a casereport. Europ J Hum Genet 1996; 4/1: 129 (Abstract 9.041) (London, UK) |
p |
CG |
| 32 |
B Rautenstrauss, H Grehl, T
Liehr,
K D Bathke, D Lorek, E Nelis, V Timmerman, C Van
Broeckhoven, J R Lupski, L Reiter, A Ekici, K
Rautenstrauss, A Götz, O Park, A Heiland, D
Claus, H Schuch, A Paulini, E Gebhart, H D Rott,
B Neundörfer, R A Pfeiffer. Charcot-Marie-Tooth (CMT) disease and tomaculous neuropathy (HNPP): results of a collaborative german belgium study. Europ J Hum Genet 1996; 4/1: 129 (Abstract 9.042) (London, UK) |
(o) | CG |
| 31 |
A Dimmler, T
Liehr,
H Schell, E Gebhart. Chromosome abnormalities detected by interphase-FISH in precancerous lesions and epithelial neoplasias of the skin. Med Genetik 1996; 8: 60 (Abstract W6-26*) (Göttingen, Germany) |
(p) | TCG |
| 30 |
WG Ballhausen, C Kraus, B
Wolff, T
Liehr.
A novel evolutionary high conserved heavy metal transporter gene with a somatostatin receptor domain (SHMT1) on human chromosome 5q13. Med Genetik 1996; 8: 92 (Abstractnr. W12-20*) (Göttingen, Germany) |
(p) | CG |
| 29 |
KD Bathke, T
Liehr,
A Ekici, H Grehl, D Claus, B Neundörfer, B
Rautenstrauss. Duplication and deletion analysis in hereditary peripheral neuropathies - evaluation of chromosome 17p11.2 specific probes for diagnostic purposes. Med Genetik 1996; 8: 98 (Abstract W12-49*) (Göttingen, Germany) |
(p) | CG |
| 28 |
O Park, T
Liehr,
H Altenberger, S Reiprich, K Rautenstrauss, F
Pröls, B Rautenstrauss. High dosage of human peripheral myelin protein PMP22 induces dramatically prolonged cell cycles for the yeast Saccharomyces cervisiae and growth arrest for E. coli bacteria. Med Genetik 1996; 8: 109 (Abstract P4-12*) (Göttingen, Germany) |
(p) | CG |
| 27 |
A Ekici, T
Liehr,
K D Bathke, H Grehl, B Rautenstrauss. A Charcot-Marie-Tooth type 1A (CMT1A) patient with different mosaicism patterns in blood and nerve tissue concerning the duplication in 17p11.2 - a casereport. Med Genetik 1996; 8: 80-81 (Abstract W10-13*) (Göttingen, Germany) |
(p) | CG |
| 26 |
B Rautenstrauss, H Grehl, T
Liehr,
K D Bathke, D Lorek, E Nelis, V Timmerman, C Van
Broeckhoven, J R Lupski, L Reiter, A Ekici, A
Götz, O Park, A Heiland, D Claus, H Schuch, A
Paulini, E Gebhart, HD Rott, B Neundörfer, RA
Pfeiffer. Charcot-Marie-Tooth (CMT) disease, Déjérine-Sottas syndrome (DSS) and tomaculous neuropathy (HNPP): results of a collaborative study. Med Genetik 1996; 8: 89 (Abstract W12-5) (Göttingen, Germany) |
(o) | CG |
| 25 |
T
Liehr,
U Zechner, H Hameister, H Grehl, U Suter, B
Rautenstrauss. Expression of Pmp22 in tissues of adult wildtype (wt) and tremblerJ (tr) mice: a comparative in situ study. Med Genetik 1996; 8: 28 (Abstract S1-6*) (Göttingen, Germany) |
(o) |
CG |
1995
| Number |
Authors/
Title/ Where Contribution was Published |
Poster (p)
or oral (o) |
Topic |
| 24 |
E Gebhart, T
Liehr,
S Neubauer, P Hofbeck, Y Hübner, A Stübinger, R
Lerch, S Reichardt. Experiences with interphase-FISH in solid tumors. Int J Oncol 1995; 7: S967 (Abstract 157) (Crete, Greece) |
(p) | TCG |
| 23 |
H Grehl, A Tiebe, T
Liehr,
A Engelhardt, B Rautenstrauss. Morphometry of sural nerve biopsies in genetically characterized hereditary demyelinating neuropathies. Clin Neuropathol 1995; 14: 260 (?) |
(p) | CG |
| 22 |
B Rautenstrauss, A Götz, T
Liehr,
H Grehl, M Sostarko, K D Bathke, A Ekici, O
Park, T Dumser, R Hausmann, R Hillenbrand, M
Schachner, R A Pfeiffer, B Neundörfer. Myelin associated glycoprotein immunoreactivity and Charcot-Marie-Tooth (CMT) disease type 1A: association of CMT and Multiple Sclerosis. Am J Hum Genet 1995; 57: SA340 (Abstract 1975) (Minneapolis, USA) |
(o) |
CG |
| 21 |
T
Liehr,
A Ekici, R Hillenbrand, M Schachner, B
Rautenstrauss. Assignment of Pmp22 and P0, candidate genes for Charcot-Marie-Tooth (CMT) disease type 1A and 1B, to rat chr. 10q22 and 13q24-26 by FISH. Am J Hum Genet 1995; 57: SA325 (Abstract 1888) (Minneapolis, USA) |
(p) | CG |
| 20 |
KD Bathke, T
Liehr,
A Ekici, V Timmerman, C Van Broeckhoven, H
Grehl, B Neundörfer, B Rautenstrauss. Evidence for a modified recombinant event in hereditary neuropathy with liability to pressure palsies (HNPP). Am J Hum Genet 1995; 57: SA207 (Abstract 1195) (Minneapolis, USA) |
(p) | CG |
| 19 |
H Grehl, A Tiebe, T
Liehr,
A Engelhardt, B Rautenstrauss. Molekulargenetische und morphologische Diagnostik der hereditären Neuropathie mit Neigung zu Druckläsionen (HNPP). Aktuelle Neurologie 1995; 22: S2 (Abstract P10) (Erlangen, Germany) |
(p) | CG |
| 18 |
A Götz, T
Liehr,
H Grehl, M Sostarka, K D Bathke, A Ekici, O
Park, T Dumser, R Hausmann, R Hillenbrand, M
Schachner, B Rautenstrauss. Genetic and immunological analysis of two female patients suffering from Charcot-Marie-Tooth disease and Multiple Sclerosis. Aktuelle Neurologie 1995; 22: S13 (Abstract P35) (Erlangen, Germany) |
(p) | CG |
| 17 |
B Rautenstrauss, T
Liehr,
C Gehring, K Thoma, K D Bathke, H Grehl. Genetic analysis of clinically determined hereditary neuropathy with liability to pressure palsies (HNPP) patient DNA: detection of an unusual recombination event leading to 17p11.2 deletion. Aktuelle Neurologie 1995; 22: S6 (Abstract P9) (Erlangen, Germany) |
(p) | CG |
| 16 |
D Lorek, K D Bathke, T
Liehr,
A Ekici, H Grehl, B Rautenstrauss. X-linked
dominantly inherited Charcot-Marie-Tooth
disease: differences in sequence analysis with
and without cloning of Cx32 specific PCR
products from one female patient. Aktuelle Neurologie 1995; 22: S17 (Abstract P34) (Erlangen, Germany) |
(p) | CG |
| 15 |
T
Liehr,
G Schmitt, H Grehl, B Rautenstrauss.
Charcot-Marie-Tooth (CMT) disease and hereditary
neuropathy with liability to pressure palsies
(HNPP): reactivation of archival sural nerve
biopsies for FISH-diagnostics. Aktuelle Neurologie 1995; 22: S17 (Abstract P31) (Erlangen, Germany) |
p | CG |
| 14 |
O Park, H Altenberger, S
Reiprich, T
Liehr,
H Grehl, B Rautenstrauss. High dosage of Charcot-Marie-Tooth type 1A disease candidate gene, human peripheral myelin protein PMP22 alias growth arrest specific gene 3 (GAS3), induces growth arrest in the yeast Saccharomyces cerevisae and E. coli bacteria. Aktuelle Neurologie 1995; 22: S19 (Abstract P30) (Erlangen, Germany) |
(p) | CG |
| 13 |
H Grehl, B Rautenstrauss, T
Liehr,
K D Bathke, A Ekici, E Nelis, C Van
Broeckhoven, D Claus, B Neundörfer. Clinical course in patients with demyelinating forms of hereditary motor and sensory neuropathies (HMSN) and confirmed mutations. J Neurol 1995; 42: S150 (Abstract 813) (?) |
(p) | CG |
| 12 |
KD Bathke, T
Liehr,
D Lorek, A Ekici, E Nelis, C Van Broeckhoven, H
Grehl, D Claus, B Neundörfer, B Rautenstrauss. Molecular analysis of Charcot-Marie-Tooth (CMT) disease and HNPP: gene dosage differences of PMP22 and point mutations of P0- and Cx32 gene. Med. Genetik 1995; 7: 189 (Abstract 133) (Berlin, Germany) |
(p) | CG |
| 11 |
T
Liehr,
G Schmitt, E Ganzmann, H Grehl, B Rautenstrauss.
FISH-studies on archival sural biopsies of Charcot-Marie-Tooth (CMT) disease and hereditary neuropathy with liability to pressure palsies (HNPP) patients. Med Genetik 1995; 7: 189 (Abstract 134) (Berlin, Germany) |
p |
CG |
| 10 |
B Rautenstrauss, T
Liehr,
D Bächner, H Grehl, H Hameister. Determination of the tissue specific expression pattern for peripheral myelin protein 22 (PMP22) during murine development and in different tissues of rat, cattle and humans. Med Genetik 1995; 7: 189 (Abstract 135) (Berlin, Germany) |
(o) |
CG |
1994
| Number |
Authors/
Title/ Where Contribution was
Published |
Poster
(p) or oral (o) |
Topic |
| 9 |
H
Grehl, D Bächner, T
Liehr,
H Hameister, B Rautenstrauss. Expression of the peripheral myelin protein 22 (PMP-22) during myelin development in two weeks old mice. J Neuroimmunol 1994; 54: 165 (Abstract P13.07) (?) |
(p) | CG |
| 8 |
KD
Bathke, H Grehl, T
Liehr,
A Ekici, E Nelis, C Van Broeckhoven, D
Claus, B Neundörfer, R A Pfeiffer, B
Rautenstrauss. Progress in molecular diagnosis of Charcot-Marie-Tooth disease type 1 (CMT1, HMSN 1) and hereditary neuropathy with liability to pressure palsies (HNPP) by fluorescence in situ hybridization (FISH) - detection of a potential genetic mosaicism. Am J Hum Genet 1994; 55: A211 (Abstract 1229) (Montreal, Canada) |
(p) | CG |
| 7 |
T
Liehr,
H Grehl, E Ganzmann, B Rautenstrauss. Anti-sense fluorescence in situ hybridization in human and rat tissue used for detection of PMP-22 mRNA. J Neurol 1994; 241: S21 (Abstract 123) (Barcelona, Spain) |
(p) | CG |
| 6 |
T
Liehr,
H Grehl, E Ganzmann, B Rautenstrauss. Detection of candidate gene mRNA (PMP-22) by flourescence anti-sense in situ hybridization in human and rat tissue. Med Genetik 1994; 6: 142 (Abstract P-6-14) (Düsseldorf, Germany) |
(p) | CG |
| 5 |
P
Harrer, T
Liehr,
E Gebhart. FISH analyses on classical bone marrow smears. Med Genetik 1994; 6: 157 (Abstract P-9-19)(Düsseldorf, Germany) |
(p) | TCG |
| 4 |
E
Gebhart, S Reichardt, T
Liehr,
P Harrer, U Trautmann. Do single aberrant karyotypes represent a clone detectable by FISH in interphase nuclei of human hematologic neoplasias? Med Genetik 1994; 6: 156 (Abstract P-9-16) (Düsseldorf, Germany) |
(p) | TCG |
| 3 |
W
Fiedler, T
Liehr,
U Claussen, R Fahsold. Towards a new gene on chromosome 22q12-q13.1. Med Genetik 1994; 6: 138 (Abstract P-6-17) (Düsseldorf, Germany) |
(p) | TCG |
1993
| Number |
Authors/
Title/ Where Contribution was
Published |
Poster
(p) or oral (o) |
Topic |
| 2 |
T
Liehr,
E Gebhart. Comparative interphase cytogenetics on human ovarian carcinomas using FISH. Med Genetik 1993; 5: 154 (Würzburg, Germany) |
p | TCG |
| 1 |
P
Binder-Wirth, R A Pfeiffer, H
Scherthan, U Trautmann, R Fahsold, T
Liehr,
K Romanakis. Detection of aneuploidy in sperm nuclei and examination of a male heterozygote for rob dic (14q15q) by bi-colour FISH. Med Genetik 1993; 5: 117 (Würzburg, Germany) |
(p) | CG |
