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 Abstractbooks)
|
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 |
2022
| Number |
Authors/ Title/ Where Contribution was
Published |
Poster (p) or oral (o) |
Topic |
2021
| Number |
Authors/ Title/ Where Contribution was
Published |
Poster (p) or oral (o) |
Topic |
| 344 |
T
Liehr, S Azawi. Molecular cytogenomic characterization of the murine cancer cell line C-127I identifies it a model for metastatic breast cancer. 2nd International Conference “Cancer Metastasis”, Austria, Virtual Event Abstract P14 |
p |
TCG |
| 343 |
I
Dietze-Armana, M Wanzel, T Liehr, K
Mehnert. Three additional marker chromosomes in a girls with global developmental delay and microcephaly. ESHG 2021- Virtual Conference. Abstract / Poster P14.018.C |
p |
CG |
| 342 |
T
Liehr. From cytogenetics to cytogenomics – what is the underlying idea? ESHG 2021- Virtual Conference. Abstract / Poster P14.019.C; P14.010.C |
p |
CG |
| 341 |
I
Tkach, N Huleyuk, D Zastavna, T Liehr,
E Ciszkowicz. The contribution of chromosomal abnormalities in the formation of sporadic and recurrent early reproductive losses. ESHG 2021- Virtual Conference. Abstract / Poster P01.079.C |
p |
CG |
| 340 |
P
Li, B Dupont, Y Shen, Q Hu, M Crimi, T
Liehr,
I Lebedev. An international collaboration for human ring chromosomes (ICHRC) towards developing standards and guidelines for best practice in laboratory diagnosis clinical management and collaborative research. ECA-Newsletter 2021, 48, pp18-19. Poster 1.P1 |
p |
CG |
2020
| Number |
Authors/ Title/ Where Contribution was
Published |
Poster (p) or oral (o) |
Topic |
| 339 |
R
Hochstenbach, T
Liehr,
R Hastings. Chromosomes in the DNA world - preserving cytogenomic competence of diagnostic medical genetic laboratories. ESHG Online Conference 2020. Poster P16.27.C. |
p |
CG |
| 338 |
A
Weber, T
Liehr,
S Bilgen, M Stumm. Complex small supernumerary marker chromosome sSMC originates from 6 different parts of 5 chromosomes. ESHG Online Conference 2020. Poster P14.43.C. |
p |
sSMC |
| 337 |
J
Jungnitsch, M Klever, U Melo, R Schöpflin, CA
Prada-Medina, T
Liehr,
S Mundlos, M Spielmann. Hi-C enables the 3D characterization of small supernumerary marker chromosomes. ESHG Online Conference 2020. Poster P14.42.B. |
p |
sSMC |
| 336 |
B
Gläser, K Komlosi, T Haack, S Waldmüller, A Gazou,
A Müller, T
Liehr,
J Fischer, A Tzschach. Interstitial 11q12.1q13.1 duplication in patients with intellectual disability. ESHG Online Conference 2020. Poster P14.18.B. |
p |
CG |
| 335 |
RA
Pilz, K Schwefel, AWeise, T
Liehr,
P Demmer, A Spuler, S Spiegler, E Gilberg, CA
Hübner, U Felbor, M Rath. Structural genome variations in cerebral cavernous malformations. ESHG Online Conference 2020. Poster P09.031.B. |
p |
CG |
| 334 |
V Langhof, J Naab, C Bartaun, S Anders, S Demuth,
T
Liehr,
M Klaus. Characterization of a unique karyotype resulting from a complex rearrangement involving the chromosomes 3 and 4 using chromosome analysis, FISH and array-CGH in a girl with facial dysmorphism. ESHG Online Conference 2020. Poster P11.82.A. |
p |
CG |
| 333 |
T
Liehr,
A Al-Rikabi. Towards next-generation phenotyping (NPG) for cat-eye syndrome. ESHG Online Conference 2020. E-poster E-P15.04 |
p |
sSMC |
2019
| Number |
Authors/ Title/ Where Contribution
was Published |
Poster (p) or oral (o) |
Topic |
| 332 |
T
Liehr.
(Molekulare) Zytogenetik in Zeiten von NGS. Abstractbook: 19. Jahrestagung der Österreichischen Gesellschaft für Humangenetik. Salzburg, Austria; 4. October 2019: 9 |
o |
M |
| 331 |
T
Liehr.
Small supernumerary marker chromosomes (sSMC) - genotype-phenotype correlation complicated by chromothripsis leading to discontinuous structure. Abstractbook: VII Congress of Vavilov Society of Geneticist and Breeders (VSG&B) and associate symposiums. St. Petersburg, Russia: 18.-22.06.2019: 325 |
o |
sSMC |
2018
| Number |
Authors/ Title/ Where Contribution
was Published |
Poster (p) or oral (o) |
Topic |
| 330 |
A García
Angulo, MA Merlo Torres , S Portela Bens, ME
Rodríguez Jiménez, I Cross Pacheco, E García
Suárez, A Al-Rikabi, T Liehr, L
Rebordinos González. Evidencia de una fusion Robertsoniana en Solea senegalensis (Kaup, 1858) mediante ZOO-FISH y analysis de genomic comparativa. Abstractbook of 'I Congresso de Jovenes Investigadores del Mar', Cadiz, Spain, 3-5.10.2018: 285-286 |
(p) |
EVO |
| 329 |
EA
Oliveira, LA Bertollo, P Rab, T
Liehr,
T Ezaz, CF Yano, T Hatanaka, MB Cioffi. Cytogenetics, genomics and historical biogeography of the South American and African Arapaimidae fish family (Teleostei, Osteoglossiformes). 2 Abstractbook: 22nd International Chromosome Conference. Prague, Czech; 2.-5. September 2018: 139-140 (Abstract PS-P-1590). |
(p) |
EVO |
| 328 |
MB
Cioffi, FF Barby, EA Oliveira, T Hatanaka, T
Liehr,
T Ezaz, P Rab, LA Bertollo. From chromosomes to genome: insights into the evolutionary relationships and biogeography of Old World knife fishes (Notopteridae; Osteoglossiformes). Abstractbook: 22nd International Chromosome Conference. Prague, Czech; 2.-5. September 2018: 137-138 (Abstract PS-P-1589) |
(p) | EVO |
| 327 |
A
Krasikova, V Fishman, M Nuriddinov, N
Battulin, O Serov, T
Liehr,
A Maslova, A Surkova, A Kulikova, A Zlotina. Chromatin domains in chicken interphase nucleus and lampbrush chromosomes. Abstractbook: 22nd International Chromosome Conference. Prague, Czech; 2.-5. September 2018: 105 (Abstract PS-P-1503) |
(p) | EVO |
| 326 |
T
Liehr.
Parental origin of deletions and duplications; about the necessity to check for cryptic inversions. Abstractbook: International Chromosome Conference Chromosome 2018. Novosibirsk, Russia; 20.-24. August 2018 (no abstract printed) |
o |
CG |
| 325 |
T
Liehr,
I Schreyer, A Kuechler, E Manolakos, S Singer,
A Dufke. Parental origin of deletions and duplications; about the necessity to check for cryptic inversions. Online abstracts: European Society of Human Genetics. 2018: Abstract n.a. |
(p) |
CG |
| 324 |
M
Moyses-Oliveira, A Di-Battista, M Zamariolli,
V Meloni, S Bragagnolo, D Christofolini, C
Steiner, L Sisdelli, N Kosyakova, T
Liehr,
A Reymond, M Melaragno. Breakpoint mapping at nucleotide resolution in balanced translocations associated with clinical phenotypes. Online abstracts: European Society of Human Genetics. 2018: Abstract P13.05A / A |
(p) | CG |
| 323 |
IA
Pessôa, MAK Othman, CKN Amorim, WAS Ferreira,
RJRN Brito, T
Liehr,
EHC de Oliveira. Genetic alterations of gliomas. Online abstracts: European Society of Human Genetics. 2018: Abstract P12.093A / A |
(p) | TCG |
| 322 |
YB Yurov,
SG Vorsanova, T
Liehr,
IY Iourov. Replication stress-mediated chromosome instability in the Alzheimer’s disease brain. Online abstracts: European Society of Human Genetics. 2018: Abstract P09.037A / A |
(p) | INT |
| 321 |
AM
Zlotina, AV Maslova, NV Kosyakova, T
Liehr,
AV Krasikova. 3D architecture of Japanese quail DNA repeats in interphase nucleus. Abstractbook: 23. International Colloquium on Animal Cytogenetics and Genomics. St. Petersburg, Russia; 9.-12. June 2018: 80 (Abstract P33) |
(o) |
EVO |
| 320 |
TV
Kulikova, LV Kazakova, AV Maslova, DV Dedukh,
IL Trofimova,
T Liehr,
A Krasikova. Loci-specific RNP-rich nuclear domains on lampbruch chromosomes: data pointing at RNA editing. Abstractbook: 23. International Colloquium on Animal Cytogenetics and Genomics. St. Petersburg, Russia; 9.-12. June 2018: 59 (Abstract P12) |
(o) |
EVO |
| 319 |
T
Liehr.
Molecular cytogenetics in Zoo-FISH-studies – still urgently needed. Abstractbook: 23. International Colloquium on Animal Cytogenetics and Genomics. St. Petersburg, Russia; 9.-12. June 2018: 21 |
o |
M EVO |
| 318 |
M Othman,
B Grygalewicz, D Vujić, J Melo, I Carreira, A
Ejduk, A Glaser, T
Liehr.
Acquired marker chromosomes and complex karyotypes in acute lymphoblastic leukemia can emerge from chromothripsis. Abstractbook: EHA-SWG Scientific Meeting, New Molecular Insights and Innovative Management Approaches for Acute Lymphoblastic Leukemia. Barcelona, Spain. 12.-14. April 2018: 46-47 |
(p) |
TCG |
2017
| Number |
Authors/ Title/ Where Contribution
was Published |
Poster (p) or oral (o) |
Topic |
| 317 |
R Capela, MAK Othman, DR
Ney-Garcia, S Rouxinol, M Tavares de Souza, BA
Lopes, T
Liehr,
P Ribeiro, MLM Silva. Molecular characterization of complex karyotypes in pediatric acute myeloid leukemia: report of a rapidly progressive myeloid neoplasm harboring a cryptic mecom rearrangement. Abstractbook: International Meeting in Oncology Research. In Celebration of 80 Years of the Brazilian National Cancer Institute (INCA). 2017: 33-34 (Abstract CG5) |
(p) |
TCG |
| 316 |
M Tavares de Souza, M
Bizzarro, I Aguiar Pepeira, M Othman, MG Vera, P
Ribeiro, T
Liehr,
TdJ Marques Salles, R Hassan, MLM Silva. Molecular characterization of secondary chromosome abnormalities in childhood Brukitt lymphoma/ leukemia. Abstractbook: International Meeting in Oncology Research. In Celebration of 80 Years of the Brazilian National Cancer Institute (INCA). 2017: 52-53 (Abstract CG39) |
(p) | TCG |
| 315 |
AD Kolotii, SG Vorsanova, YB
Yurov, IA Demidova, KS Vasin, OS Kurinnaia, MA
Zelenova, ML Gordeeva, NV Ziablova, VO Sharonin,
IV Soloviev, T
Liehr,
IY Iourov. Turner syndrome’s mosaicism revisited: a FISH/MCB study of 96 cases. Online abstracts: European Society of Human Genetics. Copenhagen, Denmark; 2017: E-P13.16 |
(p) | CG |
| 314 |
T
Liehr,
N Acquarola, K Pyle, S St-Pierre, M Rinholm, I
Schreyer. Next generation phenotyping in Emanuel and Pallister Killian syndrome using computer-aided facial dysmorphology analysis of 2D photos. Online abstracts: European Society of Human Genetics. Copenhagen, Denmark; 2017: P14.003C |
o |
sSMC |
| 313 |
FJ Sheth, S Tewari, J
Andrieux, T
Liehr,
KM Gabu, M Desai, M Mistri, B Patel, A Valodara,
S Trivedi, J Sheth. Homozygous variant of PGAP1 as a cause of severe developmental delay and intellectual disability identified by exome sequencing. Online abstracts: European Society of Human Genetics. Copenhagen, Denmark; 2017: E-P08.18 |
(p) | CG |
| 312 |
YB Yurov, SG Vorsanova, IA
Demidova, AD Kolotii, OA Smirnova, T
Liehr,
IY Iourov. DNA damage, aneuploidy and chromosome instability in the Alzheimer’s disease and autism brain. Online abstracts: European Society of Human Genetics. Copenhagen, Denmark; 2017: P09.030B |
(p) | INT |
| 311 |
G Jedraszak, F Jobic, N
Celton, T Dery, M Gallet, M Mathieu-Dramard, H
Copin, T
Liehr,
G Morin. Cat-Eye Syndrome: Phenotype and cytogenetic analyses of a cohort of 44 patients from an international collaborative study. Online abstracts: European Society of Human Genetics. Copenhagen, Denmark; 2017: Abstract P11.019C |
(p) | sSMC |
| 310 |
T
Liehr.
What about benign chromosomal imbalances in cancer genetics? Abstractbook: 3rd Conference on Aneuploidy and Cancer – Clinical and Experimental Aspects. Berkeley, USA, 26.-29. January 2017: 16 (Abstract 11) |
o |
TCG HET |
2016
| Number |
Authors/ Title/
Where Contribution was Published |
Poster (p) or
oral (o) |
Topic |
| 309 |
R
Neroutsou, M Lagou, A Spring, M Robola, E
Dim, M Donat, M Duesberg, T
Liehr,
M Syrrou, V Velissariou. Pericentric inversion of chromosome 9 inv(9)(p23q22.3) in the Greek population. Abstractbook: Panhellenic Congress of The National Greek Society of Medical Genetics, SIGE. Athens, Greece; 4-6 November 2016 (in Greek): no page# |
(p) | CG |
| 308 |
I
Louizou, R Neroutsou, A Vasiageorgi, S
Protopsalti, S Rapti, C Ifanti, T
Liehr,
E Tsitsopoulos, V Velissariou. Supernumerary marker derived from chromosome 2 during prenatal diagnosis: Molecular cytogenetic investigation necessary for clarification of CMA findings. Abstractbook: Panhellenic Congress of The National Greek Society of Medical Genetics, SIGE, Athens, 4-6 November 2016 (in Greek): no page# |
(p) | sSMC |
| 307 |
D
Ribeiro Ney Garcia,T
Liehr
, MAK Othman, K Rittscher, M Tavares de
Souza, R Capela, A Caetano Moreti, E Cifoni
Batista, E Abdelhay, E Sobral da Costa, R
Correa Ribeiro, MG Poirot Land, MLM Silva. Prevalencia de cariotipos complexos em un estudo consecutive de 146 criancas Brasileiras com leucemia linfoblastica aguda: um estudo conventional e molecular. Anais do Sobope: XV Congresso Brasileiro de Oncologia Pediatrica. Rio de Janeiro, Brazil; 15.-19. November 2016: 156 |
(p) | TCG |
| 306 |
M
Tavares de Souza, G Vera-Lozada, TJ
Marques-Salles, E Nogueira dos Santos, LW
Pinto, S Rouxinol, T
Liehr,
MG Poirot Land, R Correa Ribeiro, R Hassan,
MLM Silva. Perfil molecular do linfomy de Burkitt com um isocromossomoi (8)(q10) como unica anormalidade citogenetica em um paciente pediatrico com ataxia telabgiectasia. Anais do Sobope: XV Congresso Brasileiro de Oncologia Pediatrica. Rio de Janeiro, Brazil; 15.-19. November 2016: 155 |
(p) | TCG |
| 305 |
A Faria
de Figueiredo, AL Mencalha, R Capela, E
Cifoni Batista, A Caetano Moreti, E Nogueira
dos Santos, T
Liehr,
R Correa Ribeiro, MLM Silva, MG Poirot Land.
Perfil citogenetico e mutacional do gene FLT3 em 70 casos de leucemia mieloide aguda da infancia. Anais do Sobope: XV Congresso Brasileiro de Oncologia Pediatrica. Rio de Janeiro, Brazil; 15.-19. November 2016: 154 |
(p) | TCG |
| 304 |
R
Capela, EC Batista, D Ribeiro Ney Garcia,
MAK Othman, A Faria de Figueiredo, E
Carboni, T
Liehr,
G Moura Ferreira, R Correa Ribeiro, MLM
Silva. Hiperdiploidia, um caso raro de leukemia mieloide aguda pediatrica envolvendo a duplicacao da fusao reversa MLLT3-KMT2A e do gene GAS6, revelado por abordagens citogeneticas moleculares modernas. Anais do Sobope: XV Congresso Brasileiro de Oncologia Pediatrica. Rio de Janeiro, Brazil; 15.-19. November 2016: 147 |
(p) | TCG |
| 303 |
EC
Batista, AC Moreti, R Capela, A Faria de
Figueiredo, D Ribeiro Ney Garcia, MAK
Othman, MG Poirot Land, T
Liehr,
MLM Silva. Caracterizacao molecular dos genes paraceiros de fusao do KMT2A em 6 casos de leukemia aguda do lacente > 12 meses de idade com caritipos complexos ou cripticos. Anais do Sobope: XV Congresso Brasileiro de Oncologia Pediatrica. Rio de Janeiro, Brazil; 15.-19. November 2016: 139 |
(p) | TCG |
| 302 |
T
Harutunyan, G Hovhannisyan, N Babayan, T
Liehr,
A Arakelyan, R Aroutiounian, M Malakyan. Protective effects of Schiff base cyclic amino acid derivatives against mycotoxins geno- and cytotoxicity. Abstractbook: International Symposium of Mycotoxicology. Tokyo, Japan; 2016: 64 (Abstract YS09) |
(p) | TCG |
| 301 |
H
Merhni, M Zerkaoui, A Natiq, A Sbiti, T
Liehr,
A Sefiani. Unusual partial trisomy of long arm of chromosome 14 about two Moroccan cases. Abstractbook: Assises de Génétique Humaine et Médicale. Lyon, France. 4.-5. February 2016: Abstract 2874 |
(p) |
sSMC |
| 300 |
T
Liehr,
N Kosyakova. Principle of fluorescence in situ hybridization (FISH) technique and applications towards biodiversity, including fishery researches. Abstracts of the 5thInternational Conference on Sciences and Social Sciences 2015 (ICSSS 2015): Research and Innovation for Community and Regional Development September 17-18, 2015 at Rajabhat Maha Sarakham University, p26. |
(p) |
EVO |
| 299 |
H
Merhni, Y Doubaj, A Natiq, A Sbiti, T
Liehr,
A Sefiani. Syndrome myélodysplastique avec un rearrangement chromosomique complexe: à propos d’une observation et revue de la littérature. Abstractbook: Assises de Génétique Humaine et Médicale. Lyon, France. 4.-5. February 2016: Abstract CA05 |
(p) |
TCG |
| 298 |
RM
Aroutiounian, TA Harutyunyan, T
Liehr,
GG Hovhannisyan. Localisation of DNA-damage on human chromosomes - methods of molecular cytogenetics (in Russian). Abstractbook: Biomedicine. Novosibirsk , Russia; 2016: no page# |
(o) |
M |
| 297 |
AB
Hamid Al-Rikabi, N Fleischer, M Rinholm, S
St-Pierre, I Schreyer, T
Liehr.
Phenotyping Emanuel Syndrome using computer-aided facial dysmorphology analysis of 2D photos. Abstractbook: European Society of Human Genetics. Barcelona, Spain; 2016: Abstract P14.030 |
(p) |
sSMC |
| 296 |
YB
Yurov, SG Vorsanova, T
Liehr,
AD Kolotii, IY Iourov. Structural chromosome 21-specific instability in the diseased brain. Abstractbook: European Society of Human Genetics. Barcelona, Spain; 2016: Abstract P09.046 |
(p) | INT |
| 295 |
M
Rincic, Z Krsnik, K Gotovac, T
Liehr,
F Borovecki, L Brecevic. Customized high resolution arrayCGH for neurodevelopmental disorders: our experience. Abstractbook: European Society of Human Genetics. Barcelona, Spain; 2016: Abstract P08.21 |
(p) | CG |
| 294 |
M
Macejova, L Zejskova, R Plachy, T
Jancuskova, DW Hardekopf, J Stika, M
Ondrackova, N Kosyakova, T
Liehr,
A Zavrelova, P Zak, V Petecukova, J Novak, T
Kozak, S Pekova, M Karas. The characterization of KMT2A (MLL) chromosomal breakpoints. Abstractbook: European Society of Human Genetics. Barcelona, Spain; 2016: Abstract P07.18 |
(p) | TCG |
| 293 |
I
Tkach, N Huleyuk, D Zastavna, A Weise, N
Kosyakova, T
Liehr,
E Ciszkowicz. Cytogenetics study of 468 sample of products of conception. Abstractbook: European Society of Human Genetics. Barcelona, Spain; 2016: Abstract E-P01.71 |
(p) | CG |
| 292 |
T
Liehr.
Cytogenetically visible copy number variations (CG-CNVs) in banding and molecular cytogenetics of human; about heteromorphisms and euchromatic variants. Abstractbook: European Society of Human Genetics. Barcelona, Spain; 2016: Abstract E-P13.08 |
p | HET |
| 291 |
S
Teofilova, O Miljanovic, T Ostoji, M
Bulatovi, T
Liehr.
Small supernumerary marker chromosome 15 identified in prenatal diagnosis due to advanced maternal age. Abstractbook: European Society of Human Genetics. Barcelona, Spain; 2016: Abstract E-P01.69 |
(p) |
sSMC |
| 290 |
MAK
Othman, M Rincic, K Rittscher, T
Liehr.
High rates of submicroscopic aberrations in karyotypically normal acute lymphoblastic leukemia. Abstractbook: Postgraduate-Symposium on Cancer Research. Dornburg, Germany; 23. April 2016: Abstract 2 |
(o) |
TCG |
2015
| Number |
Authors/ Title/
Where Contribution was Published |
Poster (p) or
oral (o) |
Topic |
| 288 |
N
Kosyakova, T
Liehr.
Principles of fluorescence in situ hybridization (FISH) technique and applications towards biodiversity, including fishery research.
Abstracts
of 5th
International
Conference on
Science and
Social
Sciences 2015
(ICSSS 20159
Research and
Innovation for
Community and
Regional
Development.
17.-18.
September
2015, Rajabhat
Maha Sarakham
University,
Thailand
|
(o) |
M |
| 288 |
AB
Perez, MES Colovati, N Kosyakova, T
Liehr,
AB Hamid, MI Melaragno, ACM Malinverni. A possible chromosome 9 new heteromorphic variant in a patient with phenotypic alterations. Proceedings 65th Annual Meeting of the American Society of Human Genetics. Baltimore, USA; 2015: 845 (Abstract 2358F) |
(p) | HET |
| 287 |
M
Moysés-Oliveira, R Guilherme, V Meloni, A Di
Battista, C Mello, S Bragagnolo, D
Moretti-Ferreira, K Popadin, N Kosyakova, T
Liehr,
G Carvalheira, A Reymond, MI Melaragno. X-linked intellectual disability related genes disrupted by balanced X-autosome translocations. Proceedings 65th Annual Meeting of the American Society of Human Genetics. Baltimore, USA; 2015: 1115 (Abstract 2992F) |
(p) | CG |
| 286 |
MI
Melaragno, M Moysés-Oliveira, MAP Ramos, MCP
Crnach, MZ de Souza, N Kosyakova, T
Liehr,
D Hardekopf, J Stika, R Plachy, T
Jancuskova. Breakpoint mapping by chromosome microdissection and next generation sequencing in patients with balanced chromosomal rearrangements and correlation to phenotype. Proceedings 65th Annual Meeting of the American Society of Human Genetics. Baltimore, USA; 2015: 843 (Abstract 2355F) |
(p) | CG |
| 285 |
Y
Yurov, S Vorsanova, T
Liehr,
I Iourov. Somatic genetic and epigenetic mosaicism in the diseased brain: molecular-cytogenetic evaluation of aneuploidy and spatial chromosome organization in human brain cells. Abstractbook: Annual Conference of the German Genetics Society (GfG), Genetics 2015. Kiel, Germany: 28.-30. September 2015: 39 |
(p) |
INT |
| 284 |
S
Vorsanova, Y Yurov, T
Liehr,
I Iourov. Mitotic mechanisms of psychiatric disorders (autism, intellectual disability, epilepsy) uncovered by addressing mosaic genetic variation. Abstractbook: Annual Conference of the German Genetics Society (GfG), Genetics 2015. Kiel, Germany: 28.-30. September 2015: 36 |
(p) | INT |
| 283 |
R
Aroutiounian, G Hovhannisyan, T
Liehr.
Non-random distribution of cytogenetic damage. Abstractbook: Disordered and Ordered Materials Analysis and Characterization. DOM2015 International Symposium and Young Scientist School. Yerevan, Armenia; 24.-30. September 2015: 12-13 |
(o) |
TCG |
| 282 |
M
Toljic, T
Liehr,
A Egic, N Karadzov-Orlic, Z Milovanovic, Z
Mikovic, S Niksic, I Joksic. Molecular cytogenetic characterization of partial trisomy 12q (12q24.2->qter) and partial monosomy 2q (2q37.3->qter) detected prenatally. Abstractbook: 11. Balkan Congress of Human Genetics. Belgrade, Serbia; 17.-20.09.2015: 85 |
(p) | CG |
| 281 |
T
Liehr.
Small supernumerary marker chromosomes (sSMC); genotype-phenotype correlation complicated by a yet underestimated factor: their discontinuous structure. Abstractbook: 11. Balkan Congress of Human Genetics. Belgrade, Serbia; 17.-20.09.2015: 11 |
o |
sSMC |
| 280 |
A
Bugrov, O Buleu, T Karamysheva, T
Liehr.
New molecular cytological features of the stick insects (Phasmida). Abstractbook: The International Conference Chromosome 2015. Novosibirsk, Russia; 24-28. August 2015:16 |
(p) |
EVO |
| 279 |
T
Liehr.
Benign and pathological chromosomal imbalances - microscopic and submicroscopic copy number variations (CNVs) in human genetics. Abstractbook: The International Conference Chromosome 2015. Novosibirsk, Russia; 24-28. August 2015: 34 |
o |
HET |
| 278 |
M
Mulatinho, C Serao, K Mrasek, T
Liehr,
A Weise, J Llerena Jr. A de novo trisomy 3q delineated by multicolor chromosome banding (MCB), in a patient with mild Cornelia de Lange phenotype. Abstractbook: 4. Reuniao Brasileira de Citogenética. Atibaia, Brazil; 26.-29. May 2015: no page# |
(p) |
CG |
| 277 |
K
Rittscher, MAK Othman, B Grygalewicz, B
Pienkowska-Grela, M Rincic, J Melo, IM
Carreira, B Meyer, W Marzena, T
Liehr.
Novel cryptic rearrangements in adult B-cell precursor acute lymphoplastic leukemia involving MLL-gene. Abstractbook: 7. Postgraduate-Symposium on Cancer Research. Dornburg, Germany; 25. April 2015: Abstract 21 |
(o) | TCG |
| 276 |
MAK
Othman, K Rittscher, T
Liehr.
MLL gene displaying an important molecular biomarker in acute leukaemia. Abstractbook: 7. Postgraduate-Symposium on Cancer Research. Dornburg, Germany; 25. April 2015: Abstract 13 |
(o) | TCG |
| 275 |
E
Alhourani, MAK Othman, JB Melo, IM Carreira,
S Hauke, A Glaser, T
Liehr.
BIRC3 aberrations in chronic and B-cell acute lymphocytic leukemia patients. Abstractbook: 7. Postgraduate-Symposium on Cancer Research. Dornburg, Germany; 25. April 2015: Abstract 11 |
(o) |
TCG |
2014
| Number |
Authors/ Title/ Where Contribution was Published |
Poster (p) or oral (o) |
Topic |
| 274 |
OS Kurinnaya, SG Vorsanova,
VU Voinova, T
Liehr,
AD Kolotii, YB Yurov, OA Smirnova, IY Iourov. A case of autism, mental retardation and multiple congenital malformations caused by complex genomic anomalies. Proceedings 13. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 21-23. October 2014: 181 |
(p) | CG |
| 273 |
SG Vorsanova, YB Yurov, MA
Zelenova, OS Kurinnaya, T
Liehr,
AD Kolotii, IA Demidova, VS Kravets, SA
Korostelev, VO Sharonin, IY Iourov. Characteristic structural genomic variations in children with mental retardation, congenital malformations and autism. Proceedings 13. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 21-23. October 2014: 166 |
(p) | CG |
| 272 |
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. Proceedings 13. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 21-23. October 2014: 159-160 |
(p) | EVO |
| 271 |
K Varvagiannis, I Papoulidis,
T Koromila, K Kefalas, M Ziegler, T
Liehr,
MB Petersen, Y Gyftodimou, E Manolakos. De novo 393 kb microdeletion of 7p11.2 characterized by aCGH in a boy with psychomotor retardation and dysmorphic features. Proceedings 13. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 21-23. October 2014: 159 |
(p) | CG |
| 270 |
M Rincic, L Brecevic, AB
Hamid, T
Liehr,
N Kosyakova. Neocentric small supernumerary marker chromosome r(1)(p21.3p21.2) in a mentally retarded male patient. Proceedings 13. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 21-23. October 2014: 158-159 |
(p) | sSMC |
| 269 |
A Natiq, SC Elalaoui, T
Liehr,
S Amzazi, A Sefiani. Characterization of a rare short arm heteromorphism of chromosome 22 in a girl with Down-syndrome like facies. Proceedings 13. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 21-23. October 2014: 158 |
(p) | HET |
| 268 |
M Manvelyan, I Simonyan, G
Hovhannisyan, R Aroutiounian, AB Hamid, T
Liehr.
A new case of a complex small supernumerary marker chromosome, a der(9)t(7;9)(p22;q22) due to a maternal balanced rearrangement. Proceedings 13. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 21-23. October 2014: 158 |
(p) | sSMC |
| 267 |
N Guediche Armanet, L Tosca,
S Brisset, T
Liehr,
G Tachdjian. Small supernumerary marker chromosomes in human infertility. Proceedings 13. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 21-23. October 2014: 157-158 |
(p) | sSMC |
| 266 |
X Fan, A Tanomtong, A
Chaveerach, K Pinthong, S Pornnarong, W
Supiwong, V Trifonov, G Hovhannisyan, K Loth, C
Hensel, T
Liehr,
A Weise. Comprehensive molecular cytogenetic analysis of Barbary macaque (Macaca sylvanus). Proceedings 13. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 21-23. October 2014: 157 |
(p) | EVO |
| 265 |
X Fan, A Tanomtong, A
Chaveerach, K Pinthong, S Pornnarong, W
Supiwong, V Trifonov, G Hovhannisyan, R
Aroutiounian, T
Liehr,
A Weise. Molecular cytogenetic analysis of Thai southern pig-tailed macaque (Macaca nemestrina) by multicolor banding. Proceedings 13. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 21-23. October 2014: 157 |
(p) | EVO |
| 264 |
X Fan, A Tanomtong, A
Chaveerach, K Pinthong, S Pornnarong, W
Supiwong, T
Liehr,
A Weise. High resolution karyotype of Thai crab-eating macaque (Macaca fascicularis). Comprehensive molecular cytogenetic analysis of Barbary macaque (Macaca sylvanus). Proceedings 13. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 21-23. October 2014: 156-157 |
(p) | EVO |
| 263 |
E Alhourani, M Rincic, MAK
Othman, T
Liehr.
Cryptic chromosomal aberrations in chronic lymphoid leukemia. Proceedings 13. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 21-23. October 2014: 156 |
(p) |
TCG |
| 262 |
M Melaragno, RS Guilherme,CE
Steiner, GM Carvalheira, N Kosyakova, T
Liehr,
MM Oliveira. Pigmentary mosaicism type Ito in a balanced X-autosome translocation with no gene disruption at the breakpoint. Abstractbook: 64. Annual Meeting of the American Society of Human Genetics. San Diego, USA; 18.-22. October 2014: 650 (Abstract 2615S) |
(p) |
CG |
| 261 |
MM Oliveira, RS Guilherme, VA
Meloni, N Kosyakova, T
Liehr,
G Carvalheira, MI Melaragno. AMMECR1 gene disruption and expression impairment in a balanced X-autosome translocation patient. Abstractbook: 64. Annual Meeting of the American Society of Human Genetics. San Diego, USA; 18.-22. October 2014: 647 (Abstract 2604M) |
(p) |
CG |
| 260 |
T
Liehr.
Small supernumerary marker chromosomes – an update. Abstractbook: VI Meeting of Vavilov Society of Geneticists and Breeders and Associated Genetics Symposia. Belgrade (moved from Kladovo), Serbia ; 28. September-2. October 2014: 12 (Abstractnummer PL-02) |
o |
sSMC |
| 259 |
RM Aroutyounyan, T
Liehr,
GG Hovhannisyan. Analysis of DNA and chromosomal damage by hybrid methods of molecular cytogenetics. Abstractbook: VI Meeting of Vavilov Society of Geneticists and Breeders and Associated Genetics Symposia. Rostov-on-Don, Russia; 15.-20. June 2014: 106 (Abstract C5-38) |
(o) |
TCG |
| 258 |
EM Soares-Ventura, CB
Cavlcant, U Montarroyos, BdA Silva Amaral, EP
Leite, MLM Silva, T
Liehr,
MSPd Oliveira, TdJ Marques Salles, MTMN
Cornélio. Clinical and cytogenetic profile of children with acute myeloid leukemia experience in a single institution in the Northeastern of Brazil. Abstracts of ‘9th Biennal Symposium on Childhood Leukemia (CSL)’, Praha, Czech Republic, 28-29 April 2014, p.108 (Abstractnummer P158) |
(p) |
TCG |
| 257 |
MAF Hernandes, EM
Soares-Ventura, MTMN Cornélio, M Mafra, BdA
Silva Amaral, T
Liehr,
MS Pombo de Oliveira, TdJ Marques-Salles, MTC
Muniz. Additional aberrations to the ETV6/RUNX1 gene fusion in Brazilian children with acute lymphoblastic leukemia: experience in a single institution. Abstractbook: ‘9th Biennal Symposium on Childhood Leukemia (CSL)’, Prague, Czech; 28-29 April 2014: 108 (Abstract P157) |
(p) |
TCG |
| 256 |
MS Pombo de Oliveira, EM
Soares-Ventura, MLR Borges, MAF Hernandes, EFd
Silva, T Liehr, H Mkrtchyan, MTMN
Cornélio. Clinical significance and cytogenetic analysis of chromosome 7 aberrations in childhood leukemia: experiency of CEONHPE/UPE/Brazil. Abstractbook: ‘9th Biennal Symposium on Childhood Leukemia (CSL)’, Prague, Czech; 28-29 April 2014: 89 (Abstract P123) |
(p) |
TCG |
| 255 |
MS Pombo de Oliveira, TdJ
Marques-Salles, MLR Borges, AdJ Amral, MMPdL
Pinto, T
Liehr,
H Mkrtchyan, MTMN Cornélio, BdA Silva Amaral, EM
Soares-Ventura. Molecular cytogenetic studies unmasked chromosomal abnromalities in 4 cases of Fanconi anemia. Abstractbook: ‘9th Biennal Symposium on Childhood Leukemia (CSL)’, Prague, Czech; 28-29 April 2014: 89 (Abstract P122) |
(p) |
TCG |
| 254 |
MAK Othman, M Rincic, IM
Carreira, J Melo, B Grygalewicz, T
Liehr.
A novel chromosomal rearrangement involving the
IGH gene with inverted duplication of
(14)(q32q21)in a young adult B-cell acute
lymphoblastic leukemia (B-ALL) patient. Abstractbook: From Omics to Novel Therapies in Cancer. Berlin, Germany; 23-24 May 2014: 75-76 (Abstract 15) |
(o) |
TCG |
| 253 |
M Othman, M Rincic, J Melo,
IM Carreira, E Alhourani, A Glaser, T
Liehr.
A novel cryptic three way translocation t(2;9;18)(p23.2;p21.3;q21.33) involving BCL2, ALK and MLLT3 in a T-cell acute lymphoblastic leukemia. Abstractbook: 5. Postgraduate-Symposium on Cancer Research. Dornburg, Germany; 26. April 2014: Abstract 11 |
(o) |
TCG |
| 252 |
E Alhourani, M Othman, M
Rincic, T
Liehr.
Cryptic chromosomal aberrations in chronic lymphoid leukemia. Abstractbook: 5. Postgraduate-Symposium on Cancer Research. Dornburg, Germany; 26. April 2014: Abstract 10 |
(o) |
TCG |
| 251 |
AB Hamid, K Kreskowski, M
Ziegler, E. Klein, N Kosyakova, G Radhakrishnan,
X Fan, SS Hussein, M Volleth, T
Liehr.
Mitotic stability of small supernumerary marker chromosomes – a study based on 93 immortalized cell lines. Abstractbook: 3. B-Chromosome Conference. Gatersleben, Germany; 7.-9. April 2014: 35 |
(o) |
sSMC |
| 250 |
TV Karamysheva, T
Liehr,
NB Rubtsov. B chromosomes in the interphase nucleus in Korean field mice (Apodemus peninsulae). Abstractbook: 3. B-Chromosome Conference. Gatersleben, Germany; 7.-9. April 2014: 26 |
(o) |
EVO |
| 249 |
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. Abstractbook: 39. Meeting of the Indian Society of Human Genetics. Ahmedabad, India; Jan 2014: P-148 (Abstract P-80) |
(p) |
sSMC |
| 248 |
T
Liehr.
Uniparental disomy - clinical consequences due to imprinting and activation of recessive genes. Abstractbook: 39. Meeting of the Indian Society of Human Genetics. Ahmedabad, India; Jan 2014: S-2511 (Abstract S-31) |
o |
sSMC |
| 247 |
T
Liehr.
Small supernumerary marker chromosomes – an update. Abstractbook: 39. Meeting of the Indian Society of Human Genetics. Ahmedabad, India; Jan 2014: pS-11 (Abstract S-15) |
o |
sSMC |
2013
| Number |
Authors/ Title/ Where Contribution
was Published |
Poster (p) or oral (o) |
Topic |
| 246 |
YB
Yurov, SG Vorsanova, T
Liehr,
IY Iourov. 3D nuclear chromosome organization and epigenomic variation in the brain exhibiting neurodegeneration. Abstractbook: 10. Balkan Congress of Human Genetics and 2. Alpe Adria Meeting of Human Genetics, AABC2013. Bled, Slovenia; 10.-12. October 2013: 155 (Abstract P8.1) |
(p) |
INT |
| 245 |
IY
Iourov, SG Vorsanova, IA Demidova, OS
Kurinnajy, AD Kolotii, WS Kravec, MA Zelowa, T
Liehr,
Yurov YB. Mosaic variations of DNA copies in brain cells of autism and schizophrenic patients. Basis for mitotic concept of the pathogenesis of psychiatric illness (in Russian). Proceedings 12. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 2013: 103 |
(p) | INT |
| 244 |
T
Schmidt, T Bierhals, F Kortüm, I Bartels, T
Liehr,
P Burfeind, M Shoukier, V Frank, C Bergmann, K
Kutsche. Branchio-Otic syndrome caused by a genomic rearrangement: clinical findings and molecular cytogenetic studies in a patient with a pericentric inversion of chromosome 8. Proceedings 12. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 2013: 83-8 |
(p) | CG |
| 243 |
L
Rodriguez, SS Bhatt, M Garcia-Castro, A
Plasencia, J Fernandez-Toral, E Abarca, T
Liehr.
A unique case of a discontinous duplication of 3q26.1-1q28 region resulted from segregation error of a maternal insertion and its phenotypic consequences. Proceedings 12. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 2013: 83 |
(p) | CG |
| 242 |
M Rincic,
K Gotovac, T
Liehr,
L Brecevic, F Brancovecki. Evaluation of chromosomal mosaicism, by aCGH and MLPA: molecular characterization of mosaic ring chromosome 22. XII Russian Federation Congress “Modern technologies in pediatrics and pediatric surgery” Moscow, Russia, 2013, pp 82-83 |
(p) | CG |
| 241 |
A Natiq,
SC Elalaoui, T
Liehr,
A Amzazi, A Sefiani. Characterization of a rare short arm heteromorphism of chromosome 22 in a girl with Down-syndrome like facies. Proceedings 12. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 2013: 82 |
(p) | CG |
| 240 |
E
Manolakos, A Vetro, E Papadopoulou, K Kefalas,
M Lagou, L Thomaidis, P Peitsidis, S Sifakis,
A Divane, M Ziegler, T
Liehr,
O Zuffardi, I Papoulidis. Partial trisomy 2p and partial monosomy 2q arising from a paternal intrachromosomal 2q-into-2p between-arm insertion and paracentric inversion: molecular cytogenetic characterization of a four break rearrangement. Proceedings 12. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 2013: 81-82 |
(p) | CG |
| 239 |
T
Jancuskova, R Plachy, J Stika, L Zemankova, DW
Hardekopf, T
Liehr,
N Kosyakova, R Cmejla, L Zejskova, T Kozak, P
Zak, A Zavrelova, P Havlikova, M Karas, A
Junge, C Ramel, S Pekova. A method to identify new molecular markers for assessing minimal residual disease in acute leukemia patients. Proceedings 12. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 2013: 81 |
(p) | TCG |
| 238 |
RS
Guilherme, E Klein, AB Hamid, S Bhatt, M
Volleth, A Polityko, A Kulpanovich, A Dufke, B
Albrecht, S Morlot, L Brecevic, MB Petersen, E
Manolakos, N Kosyakova, T
Liehr.
Human ring chromosomes – new insights for their clinical significance. Proceedings 12. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 2013: 80-81 |
(p) | CG |
| 237 |
Y
AbdElmontalab Farah, I Fadl Elmula, HM
Abushama, K Kreskowski, T
Liehr.
Molecular cytogenetic study of NF2 gene deletion in meningioma IN Sudanese patients. Proceedings 12. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 2013: 80 |
(p) | TCG |
| 236 |
E
Ergul, T
Liehr,
H Mkrtchyan, A Sazci, B Kara. A de novo complex chromosome rearrangement involving five chromosomes (2, 3, 8, 10 and 13) in a boy with mental retardation. Proceedings 12. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 2013: 79-80 |
(p) | CG |
| 235 |
AV
Sales Bispo, P Buerégia-Frota, L Oliveira de
Santos, G Ferrez Leal, AR Duarte, J Araújo, V
Cavalcante da Silva, MT Cartaxo Muniz, T
Liehr,
N Santos. Clinical relevance of hidden Y-chromosome material in patients with Turner syndrome. Proceedings 12. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 2013: 79 |
(p) | CG |
| 234 |
N Aust, S
Schüle, AK Altendorf-Hofmann, Y Chen, T
Knösel, O Dirsch, U Settmacher, A Weise, K
Mrasek, T
Liehr.
Loss of chromosome 4 correlates with better long-term survival and lower relapse rate after R0-resection of colorectal liver metastases. Proceedings 12. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 2013: 78-79 |
(p) | TCG |
| 233 |
W
Al-Achkar, F Moassass, A Ikhtiar, MAK Othman,
T
Liehr,
A Wafa. Cytogenetic evolution in a patient with chronic developing a secondary acute meylogeneous leukemia subtype M5 resistant to imatinib mesylate therapy. Proceedings 12. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 2013: 78 |
(p) | TCG |
| 232 |
W
Al-Achkar, A Wafa, A Al-Ablog, F Moassass, T
Liehr.
Molecular characterization of an inv(Y)(p11.2q11.221~q222) in a Syrian family. Proceedings 12. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 2013: 77 |
(p) | CG |
| 231 |
W
Al-Achkar, A Wafa, A Aljapawe, T
Liehr.
Acquired del(9)(p22.3) in a primary plasma cell leukemia. Proceedings 12. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 2013: 77 |
(p) | CG |
| 230 |
M Rincic,
K Gotovac, T
Liehr,
L Brecevic, F Brancovecki. Evaluation of chromosomal mosaicism, by aCGH and MLPA: molecular characterization of mosaic ring chromosome 22. Abstractbook: 12. European Syposium on Congenital Anomalies. Zabreb, Croatia; 13. June 2013: 71 (Abstract 28) |
(o) | CG |
| 229 |
RS
Guilherme, MM Oliveira, T
Liehr,
N Kosyakova, AM Spinola-Castro, VA Meloni, MI
Melaragno. Chromosomal microdissection and array-CGH as a tool to determine the breakpoints in a patient with balanced translocation t(X;9). Abstractbook: 3. Reuniao Brasileira de Cytogenética. Guaruja, SP, Brazil; 26-29. May 2013: no page# |
(p) | CG |
| 228 |
RS
Guilherme, MCP Cernach, 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. Abstractbook: 3. Reuniao Brasileira de Cytogenética. Guaruja, SP, Brazil; 26-29. May 2013: no page# |
(p) | CG |
| 227 |
MM
Oliveira, RS Guilherme, VFA Meloni, SS Takeno,
ABA Perez, MAP Ramos, M Haidar, D
Moretti-Ferreira, L Martelli, JD Grzesiuk, CE
Steiner, N Kosyakova, T
Liehr,
GM Carvalheira, MI Melaragno. Balanced X-autosome translocations with variable phenotypes and different breakpoints defined by chromosomal microdissection and array-CGH. Abstractbook: 3. Reuniao Brasileira de Cytogenética. Guaruja, SP, Brazil; 26-29. May 2013: no page# |
(p) | CG |
| 226 |
N Aust, A
Altendorf-Hofmann, T
Liehr,
Y Chen, T Knösel, U Settmacher, A Weise, K
Mrasek, S Schüle. Loss of chromosome 4 correlates with better long term survival and lower relapse rate after R0-resection of colorectal liver metastasis. Abstractbook: 4. Postgraduate-Symposium on Cancer Research. Dornburg, Germany; 27. April 2013: 12 (Abstract 11) |
(o) | CG |
2012
| Number |
Authors/ Title/ Where Contribution
was Published |
Poster (p) or oral (o) |
Topic |
| 225 |
YB Yourov, SG Vorsanova, T
Liehr,
AD Kolotii, YB Yourov. X chromosome aneuploidy in brain cells of patients with autism, and its possible role in disease’s prevalence among boys. Proceedings 11. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 2012: 132 |
(p) |
INT |
| 224 |
IY Iourov, SG Vorsanova, T
Liehr,
YB Yourov. Nuclear organization of genome in brain neurons and the pathogenesis of neurodegenerative and psychiatric diseases in children. Proceedings 11. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 2012: 131 |
(p) | INT |
| 223 |
OS Kurinnaya, SG Vorsanova,
AD Kolotii, YB Yourov, GY Semina, VY Voinova , T
Liehr,
YB Yourov. A case of interstitial deletion in the q-arm of chromosome 4 in a child with developmental delay and multiple congenital abnomalities: application of FISH and MCB methods. Proceedings 11. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 2012: 113 |
(p) | CG |
| 222 |
AD Kolotii, IY Iourov, IA
Demidova, VS Kravets, OS Kurinnaya, T
Liehr,
YB Yourov, SG Vorsanova. Molecular cytogenetic analysis of 28 cases with additional chromosomal material of unknown origin in children with developmental delay and multiple congenital abnormalities. Proceedings 11. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 2012: 108 |
(p) | CG |
| 221 |
AD Kolotii, IA Demidova, GA
Alyamovskaya, T
Liehr,
YB Yourov, SG Vorsanova. A case of partial trisomy of chromosome 14 and partial monosomy of chromosome 4 confirmed by molecular cytogenetics methods. Proceedings 11. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 2012: 107 |
(p) | CG |
| 220 |
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. Proceedings 11. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 2012: 92-93 |
(p) | EVO |
| 219 |
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. Proceedings 11. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 2012: 92 |
(p) | sSMC |
| 218 |
L Theuss, T
Liehr,
N Kosayakova, J Schröder, M Ziegler, K
Kreskowski, B Pohle, S Bhatt, K Wilhelm, A
Weise, K Mrasek. Evidence for correlation of fragile sites and chromosomal breakpoints in carriers of constitutional balanced chromosomal rearrangements. Proceedings 11. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 2012: 91-92 |
(p) | INT CG |
| 217 |
MAK Othman, A Wafa, F
Moassass, E Klein, W Al-Achkar, T
Liehr.
Cytogenetically unusual Philadelphia chromosome positive chronic myeloid leukemia cases. Proceedings 11. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 2012: 91 |
(p) | TCG |
| 216 |
T
Liehr,
H Mkrtchyan, M Manvelyan, T Karamysheva, E
Klein, S Bhatt. Chromosome architecture studied by high resolution FISH-banding in three-dimensionally preserved human interphase nuclei. Proceedings 11. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 2012: 91 |
(p) | INT |
| 215 |
AB Hamid, A Weise, M Voigt, M
Bucksch, N Kosyakova, T
Liehr,
E Klein. Clinical impact of proximal autosomal imbalances. Proceedings 11. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 2012: 90 |
(p) | sSMC |
| 214 |
B Hamid, K Kreskowski, A
Weise, N Kosayakova, K Mrasek, M Voigt, RS
Guilherme, R Wagner, D Hardekopf, S Pekova, T
Karamysheva, T
Liehr,
E Klein. How to narrow down chromosomal breakpoints in small and large derivative chromosomes – a new probe set. Proceedings 11. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 2012: 90 |
(p) | M |
| 213 |
E Ewers, H Mkrtchyan, A
Weise, K Mrasek, AB Hamid, R Santos Guilherme, T
Liehr.
Centromere activity in dicentric small supernumerary marker chromosomes – a study in 100 cases. Proceedings 11. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 2012: 89-90 |
(p) | sSMC |
| 212 |
NLL Corrales, K Mrasek, M
Voigt, T
Liehr,
N Kosyakova. Comprehensive characterization of genomic instability in pluripotent stem cells and their derived neuroprogenitor cell lines. Proceedings 11. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 2012: 89 |
(p) | CG |
| 211 |
M Bucksch, M Ziegler, N
Kosayakova, AD Polityko, AI Kulpanovich, A
Weise, T
Liehr,
AB Hamid. A new multicolor-fluorescence in situ hybridization probe set directed against human heterochromatin: HCM-FISH. Proceedings 11. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 2012: 88-89 |
(p) | HET |
| 210 |
W Al-Achkar, A Wafa, T
Liehr,
E Klein, F Moassass. Detailed analysis of an idic(Y)(q11.21) in a mosaic karyotype. Proceedings 11. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 2012: 88 |
(p) | CG |
| 209 |
W Al-Achkar, F Moassass, A
Ikhtiar, MAK Othman, T
Liehr,
A Wafa. A double t(9;22)(q34;q11, a t(3;21) and multiple trisomies in a patient with chronic developing to secondary acute myelogenous leukemia subtype M5 resistant to imatinib mesylate therapy. Proceedings 11. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 2012: 87-88 |
(p) | TCG |
| 208 |
W Al-Achkar, A Wafa, A
Ikhtiar, T
Liehr.
Three-way Philadelphia translocation t(9;10;22)(q34;p11.2;q11.2) as a secondary abnormality in an imatinib mesylate resistant chronic myeloid leukemia patient. Proceedings 11. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 2012: 87 |
(p) | TCG |
| 207 |
W Al-Achkar, A Wafa, A
Aljapawe, MAK Othman, T
Liehr.
A novel cytogenetic abnormality r(7)(::p11.2->q36.3::) in a Philadelphia-positive chronic myeloid leukemia case. Proceedings 11. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 2012: 86-87 |
(p) | TCG |
| 206 |
W Al-Achkar, A Wafa, A
Aljapawe, T
Liehr.
A de novo del(9)(p22.3) in a primary plasma cell leukemia case: A case study and review of the literature. Proceedings 11. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 2012: 86 |
(p) | TCG |
| 205 |
MAM Abo-Zeid, T
Liehr,
SM El-Daly, AM Gamal-Eldeen, M Glei, A Shabaka,
S Bhatt, A Hamid. Molecular cytogenetic evaluation of the efficacy of photodynamic therapy by Indocyanine Green in breast adenocarcinoma MCF-7 cells. Proceedings 11. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 2012: 85-86 |
(p) | TCG |
| 204 |
T
Liehr.
Small supernumerary marker chromosomes. Abstractbook: 2. International Conference Chromosome. Novosibirsk, Russia; 2012: 17 |
o |
sSMC |
| 203 |
N Kosyakova, V Trifonov, H
Mkrtchyan, A Graphodatsky, T
Liehr.
Murine multicolor banding. Abstractbook: 2. International Conference Chromosome. Novosibirsk, Russia; 2012: 15 |
(o) |
M |
| 202 |
AD Polityko, OM Khurs, T
Liehr.
Human genomic diseases: analysis of a critical genomic region in the chromosomal segment 22q11.2. Abstractbook: V. Russian conference with international participation “Prenatal Diagnostics and Genetical Passport - Basis for Preventive Medicine in the Age of Nanotechnology”, Novosibirsk, Russia; 2012: 93 |
(p) |
CG |
| 201 |
TP Vieira, DR Ney-Garcia, AF
de Figueiredo, MT de Souza, S Bhatt, T
Liehr,
RC Ribeiro, E Abdelhay, ML Macedo-Silva. Identificação e Caracterização Citogenética Molecular de Rearranjos do Gene MLL em Leucemias Agudas da Infância. Abstractbook: II EPACITO - ENCONTRO PAULISTA DE CITOGENÉTICA: Centro de Convenções de Ribeirão Preto. Ribeirão Preto, Brazil. 22.-24. April 2012: Abstract CH026 |
(p) |
TCG |
| 200 |
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. Abstractbook: 20. International Colloquium on Animal Cytogenetics and Gene Mapping. Cordoba, Spain; 25-28. April 2012: 131 |
(o) |
EVO |
| 199 |
L Theuss, T
Liehr,
N Kosayakova, J Schröder, M Ziegler, K
Kreskowski, B Pohle, S Bhatt, K Wilhelm, A
Weise, K Mrasek. Evidence for correlation of fragile sites and chromosomal breakpoints in carriers of constitutional balanced chromosomal rearrangements. Abstractbook: 3. Postgraduate-Symposium on Cancer Research. Dornburg, Germany; 28. April 2012: 30 (Abstract 29) |
(o) |
CG |
| 198 |
C Wölfel, C Nitz, T
Liehr,
T Knösel, J Hartmann, I Petersen. c-MYC status in primary and secondary angiosarcomas. Abstractbook: 3. Postgraduate-Symposium on Cancer Research. Dornburg, Germany; 28. April 2012: 26 (Abstract 25) |
(o) |
TCG |
| 197 |
MAK Othman, A Wafa, F
Moassass, E Klein, W Al-Achkar, T
Liehr.
Cytogenetically unusual Philadelphia chromosome positive chronic myeloid leukemia cases. Abstractbook: 3. Postgraduate-Symposium on Cancer Research. Dornburg, Germany; 28. April 2012: 14 (Abstract 13) |
(o) |
TCG |
| 196 |
E Klein, H Mkrtchyan, A
Weise, K Mrasek, AB Hamid, R Santos Guilherme, T
Liehr.
Centromere activity in dicentric small supernumerary marker chromosomes – a study in 100 cases. Abstractbook: Gatersleben Research Conference 2012. Gatersleben; Germany 23.-25. April 2012: 49 |
(o) |
sSMC |
2011
| Number |
Authors/ Title/ Where Contribution
was Published |
Poster (p) or oral (o) |
Topic |
| 195 |
YB Yurov,
SG Vorsanova, AD Kolotii, T
Liehr,
IY Iourov. Molecular cytogenetic analysis of brain cells in autism as a novel method of search for biomarkers of this disorder (Russian). Proceedings 10. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 2011: 107-108 |
(p) | INT |
| 194 |
YB Yurov,
SG Vorsanova, AD Kolotii, MK Tagirova, T
Liehr,
IY Iourov. Neuroprotective processes in brain tissues of children with ataxia-telangiectasia: application of innovative molecular-cytogenetic techniques for developing of potential target therapy (Russian). Proceedings 10. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 2011: 107 |
(p) | INT |
| 193 |
MK
Tagirova, YB Yurov, SG Vorsanova, AD Kolotii,
T
Liehr,
IY Iourov. Somatic pairing of homologous chromosomes in interphase nuclei of brain cells in ataxia-telangiectasia (Louis–Bar syndrome) (Russian). Proceedings 10. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 2011: 97-98 |
(p) | INT |
| 192 |
OS
Kurinnaya, SG Vorsanova, AD Kolotii, IY
Iourov, MN Kharabadze, EG Agapov, T
Liehr,
YB Yurov. A case of rearranged chromosome 16 revealed by MCB method in a child with mental retardation, developmental delay and multiple congenital anomalies (Russian). Proceedings 10. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 2011: 83-84 |
(p) | CG |
| 191 |
VS
Kravets, EA Nikolaeva, IY Iourov, AD Kolotii,
T
Liehr,
SG Vorsanova. Rare case of chromosome 22 duplication in a child with mental retardation and developmental delay (Russian). Proceedings 10. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 2011: 82-83 |
(p) | CG |
| 190 |
EP
Bogatyreva, GG Listopad, EE Shipovskaya, SV
Pestretsova, T
Liehr,
AD Kolotii, IY Iourov. Molecular cytogenetic and molecular examination of a case of a boy with congenital anomalies and 46,XX karyotype (Russian). Proceedings 10. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 2011: 68 |
(p) | CG |
| 189 |
EP
Bogatyreva, GG Listopad, EE Shipovskaya, SV
Pestretsova, T
Liehr,
AD Kolotii, IY Iourov. Unusual case of Cri du chat syndrome as a result of unbalanced translocation between chromosomes 5 and 21: application of FISH method in diagnostics (Russian). Proceedings 10. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 2011: 67-68 |
(p) | CG |
| 188 |
A Weise,
K Mrasek, N Kosyakova, T
Liehr.
Comparative cytogenetic technologies. Proceedings 10. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 2011: 65-66 |
(p) | EVO |
| 187 |
O Villa,
M Mallo, N Kosyakova, M Salido, T
Liehr,
L Martínez-Avilés, C Pedro, M García-Aragonés,
B Espinet, L Florensa, L Arenillas, I Cuscó,
LA Pérez Jurado, F Solé. Deletion of TET2 gene in an acute myeloid leukemia case with a t(4;15)(q24;q26) characterized by glass needle based chromosome microdissection and oligonucleotide array. Proceedings 10. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 2011: 65 |
(p) | TCG |
| 186 |
K Mrasek,
N Kosayakova, J Schröder, M Ziegler, K
Kreskowski, B Pohle, S Bhatt, L Theuss, K
Wilhelm, A Weise, T
Liehr.
Evidence for correlation of fragile sites and chromosomal breakpoints in carriers of constitutional balanced chromosomal rearrangements. Proceedings 10. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 2011: 64-65 |
(p) | INT |
| 185 |
M
Manvelyan, FW Cremer, J Lancé, R Kläs, C
Kelbova, C Ramel, H Reichenbach, C Schmidt, E
Ewers, K Kreskowski, M Ziegler, N Kosyakova, T
Liehr.
New cytogenetically visible copy number variant in region 8q21.2. Proceedings 10. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 2011: 64 |
(p) | HET |
| 184 |
T
Liehr,
E Ewers, AB Hamid, N Kosyakova, M Voigt, A
Weise, M Manvelyan. Small supernumerary marker chromosomes and uniparental disomy have a story to tell. Proceedings 10. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 2011: 63-64 |
(p) | sSMC |
| 183 |
L Kraoua,
M Chaabouni, E Ewers, I Chelly, I Ouertani, LB
Jemaa, F Maazoul, T
Liehr,
H Chaabouni. Hexasomy of the Prader-Willi/Angelman critical region, including the OCA2 gene in a patient with pigmentary dysplasia: case report. Proceedings 10. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 2011: 63 |
(p) | sSMC |
| 182 |
AB Hamid,
E Klein, A Weise, M Voigt, T
Liehr,
N Kosyakova. Clinical impact of proximal autosomal imbalances. Proceedings 10. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 2011: 63 |
(p) | sSMC |
| 181 |
J
Gebhardt, H Mkrtchyan, M Manvelyan, P Kempf, T
Liehr,
S Bhatt. Cryptic aberrations in acute lymphocytic leukemia with apparently normal karyotype. Proceedings 10. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 2011: 61 |
(p) | TCG |
| 180 |
A Faria
de Figueiredo, T
Liehr,
S Bhatt, R Binato, M Tavares de Souza, R
Rodrigues Capela de Matos, T de Jesus Marques
Salles, FC Jordy, RC Ribeiro, E Abdelhay, ML
Macedo Silva. A complex karyotype masked a cryptic variant t(8;21)(q22;q22) in a child with acute myeloid leukemia. Proceedings 10. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 2011: 60-61 |
(p) | TCG |
| 179 |
F Dorka,
M Manvelyan, S Bhatt, T
Liehr.
Do position effects drive t(8;21) in acute myelogenous leukemia? Proceedings 10. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 2011: 60 |
(p) | TCG INT |
| 178 |
F
Braulke, R Steffens, T
Liehr,
M Manvelyan, I Chudoba, D Haase. Two different del(5q) clones in a patient with myelodysplastic syndrome. Proceedings 10. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 2011: 60 |
(p) | TCG |
| 177 |
T
Liehr,
M Manvelyan, A Lier, S Junker, P Kempf, F
Dorka, J Gebhardt, S Bhatt, A Weise, K Mrasek.
Do position effects drive t(8;21) in acute myelogenous leukemia? Abstracts of 22nd Wilhelm Bernhard Workshop, Riga, Latvia, 25.-29.08.2011, p 26 |
o |
TCG INT |
| 176 |
M
Weber, A Weise, K Mrasek, L Khachaturyan, DM
Morales, T
Liehr,
UR Markert, JS Fitzgerald. Cytogenetic and STAT3 expression analysis of HTR8/SVneo. Abstractbook: 3. Postgraduate-Symposium on Cancer Research. Dornburg, Germany; 30. April 2011: 46 |
(o) |
TCG |
| 175 |
J
Gebhardt, H Mkrtchyan, M Manvelyan, P Kempf, T
Liehr,
S Bhatt. Cryptic aberrations in acute lymphocytic leukemia with apparently normal karyotype. Abstractbook: 3. Postgraduate-Symposium on Cancer Research. Dornburg, Germany; 30. April 2011: 16 |
(o) |
TCG |
| 174 |
F Dorka,
M Manvelyan, S Bhatt, T
Liehr.
Interphase architecture in myeloid bone marrow cells possibly promotes t(8;21) in AML. Abstractbook: 3. Postgraduate-Symposium on Cancer Research. Dornburg, Germany; 30. April 2011: 15 |
(o) |
TCG |
| 173 |
M
Garcia-Castro, A Plasencia, IHernando, A
Benavides, L Rodriguez, T
Liehr,
J Fernandez-Toral. Holoprosencephalia alobar y monosomia 18p en un caso de translocation desequilibrada (Y;18). Abstractbook: Spanish Human Genetic Conference. Mucia, Spain; 30.03.-01. April 2011: 193 (Abstract P-109) |
(p) | CG |
| 172 |
L
Rodriguez, J Fernandez-Toral, A Plasencia, S
Bhatt, T
Liehr,
E Abarca. La citogenetica junto con la genetica molecular, esenciales para la correcta caracterization de un CCR (3;8). Abstractbook: Spanish Human Genetic Conference. Mucia, Spain; 30.03.-01. April 2011: 80 (Abstract O-027) |
(p) |
CG |
2010
| Number |
Authors/ Title/ Where Contribution
was Published |
Poster (p) or oral (o) |
Topic |
| 171 |
FJ Sheth, J Pani, M
Desai, J Andrieux, H Patil, S Mehta, A Weise, T
Liehr,
H Sheth, JJ Sheth. Usefulness of molecular techniques in characterization of sSMCT. Abstractbook: 60. Annual Meeting of the American Society of Human Genetics. Philadelphia, USA. 2007: 160 (Abstract 1241) |
(p) |
sSMC |
| 170 |
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. Proceedings 9. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 2010: 11 |
(p) | sSMC |
| 169 |
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. Proceedings 9. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 2010: 117-118 |
(p) | sSMC |
| 168 |
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. Proceedings 9. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 2010: 117 |
(p) | INT |
| 167 |
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. Proceedings 9. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 2010: 116 |
(p) | sSMC |
| 166 |
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 multicolor-FISH. Proceedings 9. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 2010: 116 |
(p) | M CG |
| 165 |
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. Proceedings 9. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 2010: 115-116 |
(p) | CG |
| 164 |
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. Proceedings 9. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 2010: 115 |
(p) | sSMC |
| 163 |
AB Hamid, NS Brancovic, DV
Ivanovic, PR Radivojevic, E Ewers, M Merkas, M
Ziegler, T
Liehr.
Trisomy 21 with a small supernumerary marker chromosome derived from chromosomes 13/21 and 18. Proceedings 9. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 2010: 115 |
(p) | sSMC |
| 162 |
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. Proceedings 9. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 2010: 114 |
(p) | sSMC |
| 161 |
YB Yurov, SG Vorsanova, AD
Kolotii, MK Tagirova, T
Liehr,
IY Iourov. Possible mechanisms of neurodegeneration in children with ataxia-telangiectasia: application of modern genomic and bioinformatic technologies for characterization of pathogenetic processes in the human brain (in Russian). Proceedings 9. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 2010: 113 |
(p) |
INT |
| 160 |
K Mrasek, T
Liehr,
A Weise. Evolutionary conserved breakpoints and fragile sites. Abstractbook: Annual Conference of the German Genetics Society (GfG), Evolution of Primates. Jena, Germany; 16.-18. September 2010: 22 |
(o) |
EVO |
| 159 |
T
Liehr,
K Mrasek, N Kosyakova, A Weise. Comparative cytogenetic technologies. Abstractbook: Annual Conference of the German Genetics Society (GfG), Evolution of Primates. Jena, Germany; 16.-18. September 2010: 21-22 |
o |
EVO |
| 158 |
T
Liehr.
Small supernumerary marker chromosomes in humans. Abstractbook: The Young Scientists School Bioinformatics and Systems Biology. Novosibirsk, Russia, 28.-29. June 2010: 10 |
o |
sSMC |
| 157 |
T
Liehr,
N Kosyakova, K Mrasek, E Ewers, SW Cheung, A
Weise. Detailed characterization of small supernumerary marker chromosomes reveals breakpoint hot spots. Abstractbook: 7. International Conference on Bioinformatics of Genome Regulation and Structur /System Biology. Novosibirsk, Russia; 20.-27. June 2010: 166 |
o |
sSMC |
| 156 |
C Wölfel, T
Liehr,
A Weise, I Petersen. Characterisation of epitheloid haemangioendothelioma with a new interphase-FISH-test. Abstractbook: 2. Postgraduate Symposium on Cancer Research. Dornburg, Germany; 24. April 2010: 19 |
(o) |
TCG |
| 155 |
K Wilhelm, N Blaurock, K
Behr, A-C Teichmann, T
Liehr,
A Weise, C Schoder, K Mrasek. Fanconi anemia as model for mapping of rarely observable FS. Abstractbook: 2. Postgraduate Symposium on Cancer Research. Dornburg, Germany; 24. April 2010: 15 |
(o) |
INT |
2009
| Number |
Authors/ Title/ Where Contribution
was Published |
Poster (p) or oral (o) |
Topic |
| 154 |
A Polityko, T
Liehr.
Diagnostics of small supernumerary marker chromosomes using fluorescence in situ hybridization (FISH) in Belarus Materials of II Meeting of Gynaecologists, Pediatricians, Surgeons of Kyrgyz Republic “Medicine priority in health of women and children”. Bishkek; Kirkisia. 29.-30. Oktober 2009: V.1.-App.1. Abstract Р.122-124 (in Russian) |
(o) |
sSMC |
| 153 |
MS Manvelyan, RM
Aroutiounian, IV Simonyan, T
Liehr.
Chromosome distribution in human sperm – a 3D multicolor banding-study. Proceedings Scientific-practical Conference ‘Actual Problems of Obstetrics and Gynecology’. Yerevan Armenia; 13. November 2009: 88-94 |
(o) |
INT |
| 152 |
ID Papoulidis, E Simou, E
Manolakos, T
Liehr,
A Vetro, AP Athanasiadis, C Malamaki, O
Zuffardi, MB Petersen. Prenatal diagnosis of a fetus with ring chromosome 21 characterized by molecular cytogenetic methods. Abstractbook: 59. Annual Meeting of the American Society of Human Genetics. Honolulu, Hawaii, USA; 20-24. October 2009: Abstract 1620T |
(p) |
CG |
| 151 |
H Sheth, F Sheth, J Andrieux,
A Weise, E Ewers, J Sheth, T
Liehr.
Small supernumerary marker chromosomes (sSMC) characterized by molecular cytogenetic technique: FISH. Abstractbook: 59. Annual Meeting of the American Society of Human Genetics. Honolulu, Hawaii, USA; 20-24. October 2009: Abstract 1423W |
(p) |
sSMC |
| 150 |
T
Liehr,
F Hunstig, S Bhatt, F Pellestor, K Mrasek, A
Weise, I Simonyan, R Aroutiounian, M Manvelyan.
The 3-dimensional distribution of human chromosomes in sperm. Abstractbook: 59. Annual Meeting of the American Society of Human Genetics. Honolulu, Hawaii, USA; 20-24. October 2009: Abstract 1661T. |
p |
INT |
| 149 |
I Iourov, A Kolotii, S
Vorsanova, T
Liehr,
Y Yurov. Multicolor Immuno-FISH: a new molecular technology for detection of chromosomal abnormalities in specific cell types. Proceedings 8. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 20-22. October 2009: 101 |
(p) |
CG M |
| 148 |
Y Yurov, S Vorsanova, A
Kolotii, V Kravetc, I Demidova, A Beresheva, O
Kurinnaya, I Solovyov, M Tagirova, T
Liehr,
I Iourov. Genomic instability in celebellum in ataxia-telangienctasia: application of new technologies for identification of molecular model of childhood neurodegenerative disease. Proceedings 8. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 20-22. October 2009: 102 |
(p) | CG |
| 147 |
A Weise, C Schoder, AC
Teichmann, K Behr, U Claussen, T
Liehr,
K Mrasek. Global screening and extended nomenclature for 230 aphidicolin-inducible fragile sites – including 61 yet unreported ones. Proceedings 8. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 20-22. October 2009: 109 |
(p) | INT |
| 146 |
V Trifonov, N Kosyakova, S
Romanenko, R Wagner, H Mkrtchyan, A Weise, T
Liehr.
Generation of murine whole and partial chromosome painting probes based on FISH-microdissection. Proceedings 8. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 20-22. October 2009: 108-109 |
(p) | M |
| 145 |
C Schoder, A Weise, K Mrasek,
E Velleuer, N Blaurock, K Wilhelm, T
Liehr.
Fragile sites show colocalization with breakpoints in chromosomes of Fanconi anemia patients. Proceedings 8. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 20-22. October 2009: 108 |
(p) | INT |
| 144 |
H Nelle, 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. Proceedings 8. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 20-22. October 2009: 107-108 |
(p) | sSMC |
| 143 |
K Mrasek, C Schoder, AC
Teichmann, K Behr, U Claussen, T
Liehr,
A Weise. The ‘fragile secret’ of 32 new molecular mapped aphidicolin induced fragile sites. Proceedings 8. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 20-22. October 2009: 107 |
(p) | INT |
| 142 |
H Mkrtchyan, K Mrasek, U
Claussen, SW Cheung, WW Cai, T
Liehr,
N Kosyakova, A Weise. Molecular definition of high resolution multicolor banding (MCB) probes – first within the human DNA-sequence anchored FISH-banding probe set. Proceedings 8. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 20-22. October 2009: 107 |
(p) | M |
| 141 |
JB Melo, N Kosyakova, T
Liehr,
L Backx, J Vermeesch, IM Carreira. Multicolor FISH versus array CGH techniques. Which to choose for the characterization of small supernumerary marker chromosomes? Proceedings 8. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 20-22. October 2009: 106-107 |
(p) | sSMC |
| 140 |
M Manvelyan, F Hunstig, S
Bhatt, F Pellestor, K Mrasek, A Weise, I
Simonyan, R Aroutiounian, T
Liehr.
The 3-dimensional distribution of human chromosomes in sperm. Proceedings 8. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 20-22. October 2009: 106 |
(p) | INT |
| 139 |
T
Liehr,
E Ewers, K Mrasek, H Mkrtchyan, N Kosyakova, L
Brecevic, J Wagner, A Weise. Marker chromosomes and mosaicism. Proceedings 8. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 20-22. October 2009: 105-106 |
(p) | sSMC |
| 138 |
N Kosyakova, A Weise, K
Mrasek, E Ewers, H Mkrtchyan, T
Liehr.
Multi-color FISH assays for characterization of marker chromosomes and epigenetic changes. Proceedings 8. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 20-22. October 2009: 105 |
(p) | sSMC |
| 137 |
P Kempf, H Mkrtchyan, M
Manvelyan, A Lier, A Heller, K Mrasek, F
Hunstig, A Weise, T
Liehr.
3D-interphase FISH studies of chromosomes 8 and 21 in AML patients with trisomy 8. Proceedings 8. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 20-22. October 2009: 105 |
(p) | TCG |
| 136 |
E Ewers, M Stumm, RD 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. Proceedings 8. Russian Congress Modern Methods in Pediatry and Childrensurgery. Moscow, Russia; 20-22. October 2009: 104 |
(p) |
CG |
| 135 |
IY Iourov, SG Vorsanova, T
Liehr,
YB Yurov. Nuclear organization of interphase chromosomes in the human brain. Abstractbook: International Conference "Chromosome 2009". Novosibirsk, Russia; 2009: 7-8 |
(o) |
INT |
| 134 |
C Wölfel, T
Liehr,
I Petersen. Interphase FISH analysis of epitheloid haemangioendothelioma. Abstractbook: Postgraduate-Symposium on Cancer Research. Dornburg, Germany. 9. May 2009: 8-9 (Abstract 20) |
(o) |
TCG |
| 133 |
P Kempf, H Mkrtchyan, M
Manvelyan, 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. Abstractbook: Postgraduate-Symposium on Cancer Research. Dornburg, Germany. 9. May 2009: 1-2 (Abstract A3) |
(o) |
TCG |
| 132 |
C Schoder, A Weise, K
Mrasek, E Velleuer, T
Liehr.
Break points in chromosomes of Fanconi Anemia patients show colocalisation with so called Fragile Sites. Abstractbook: Postgraduate-Symposium on Cancer Research. Dornburg, Germany. 9. May 2009: 1 (Abstract A1) |
(o) |
INT |
| 131 |
T
Liehr,
A Weise, K Mrasek, E Ewers, H Mkrtchyan, N
Kosyakova. Multi-color FISH assays for characterization of marker chromosomes and epigenetic changes. Abstractbook: Experimental Biology 2009. New Orleans, USA; 18.-22. April 2009: 44 |
o |
sSMC |
| 130 |
N Blaurock, C Schoder, A
Weise, K Mrasek, E Velleuer, T
Liehr.
Break points in chromosomes of Fanconi Anemia patients show colocalisation with Fragile Sites. Abstractbook: 15. International AEK Cancer Congress. Berlin, Germany; 18.-20. March 2009: 32 (Abstract C-08) |
(p) |
INT |
2008
| Number |
Authors/ Title/
Where Contribution was Published |
Poster (p) or oral
(o) |
Topic |
| 129 |
AD
Polityko, GI Lazjuk, T
Liehr.
Supernumerary marker chromosomes in human karyotype. Abstractbook: 4. congress of Medical Genetics of Ukraine. Lviv, Ukraine; 9.-11. October 2008: 42 (in Russian) |
(o) |
sSMC |
| 128 |
IY
Iourov, SG Vorsanova, T
Liehr,
YB Yurov. Intercellular genomic variations manifesting as aneuploidy in the normal, Alzheimer’s disease and ataxia-telangiectasia brain. Abstractbook: HGM2008, HUGO-meeting. Hyderabad, India. 27.-30. September 2008: 199 |
(p) |
INT |
| 127 |
YB
Yurov, IY Iourov, SG Vorsanova, T
Liehr,
AD Kolotii, AK Beresheva, IA Demidova, VS
Kravets, MK Tagirovam OS Kurinnaya, VV
Monakhov, IV Soloviev. Somatic genome instability closely associates with cerebellar neurodegeneration in the ataxia telangiectasia. Abstractbook: HGM2008, HUGO-meeting. Hyderabad, India. 27.-30. September 2008: 213 |
(p) |
INT |
| 126 |
T
Liehr,
A Weise, K Mrasek, H Mkrtchyan, N Kosyakova. Recent developments and applications in multicolor fluorescence in situ hybridization. Abstractbook: 38. Annual Meeting of the European Environmental Mutagen Society. Cavtat, Croatia; 21-25. September 2008: 70 |
o |
M TCG |
| 125 |
H
Mkrtchyan, K Mrasek, U Claussen, S W Cheung, W
W Cai, T
Liehr,
N Kosyakova, A Weise. Molecular definition of high resolution multicolor banding (MCB) probes – first within the human DNA-sequence anchored FISH-banding probe set. Abstractbook: 21. "Tumorzytogenetischen Arbeitstagung". Uslar-Volpriehausen, Germany; 22.-24. May 2008:10 |
(o) |
TCG M |
| 124 |
T
Liehr,
H Mkrtchyan, V Witthuhn, S Hinreiner, M Gross,
K Mrasek, K Behr, C Schoder, A Weise. Molecular cytogenetics in tumor cells - A review. Proceedings of the 27. Annual Convention of Indian Association for Cancer Research and International Symposium on Functional Genomics. Ahmedabad, India, 07.-09. February 2008: Abstract GS-25 |
o |
TCG |
2007
| Number |
Authors/ Title/ Where Contribution
was Published |
Poster (p) or oral (o) |
Topic |
| 123 |
S Bhatt, K Moradkhani, K
Mrasek, J Puechberty, G Lefort, J Lespinasse, P
Sarda, T
Liehr.
The direct characterization of breakpoints: a new approach for the segregation analysis of paracentric inversions in human sperm. Abstractbook: 57. Annual Meeting of the American Society of Human Genetics. San Diego, USA, 23.-27. October 2007: 328 (Abstract 1667) |
(p) |
CG INT |
| 122 |
T
Liehr,
K Mrasek, N Kosyakova, J Vermeesch, SW Cheung, A
Weise. A genotype-phenotype correlation of small supernumerary marker chromosomes (sSMC) in human. Abstractbook: 57. Annual Meeting of the American Society of Human Genetics. San Diego, USA, 23.-27. October 2007: 328 (Abstract 1663) |
p |
sSMC |
| 121 |
YB Yurov, SG Vorsanova, I
Iourov, T
Liehr,
IA Demidova, AK Beresheva, AD Kolotii, VS
Kravrts, VV Monakhov, F Pellestor, IV Soloviev.
Spontaneous rate of chromosomal mutations in fetal tissues. Proceedings of VI congress “Modern technologies in pediatrics and children surgery”. Moscow, Russia; 2007: 73 (in Russian) |
(p) | CG |
| 120 |
IY Iourov, OS Kurinnaya, AD
Kolotii, VY Voinova-Ulas, T
Liehr,
YB Yurov, SG Vorsanova. Inverted duplication of 2q11.2 in a child with congenital malformations: a need of modern molecular cytogenetic technologies. Proceedings of VI congress “Modern technologies in pediatrics and children surgery”. Moscow, Russia; 2007: 71-72 (in Russian) |
(p) | CG |
| 119 |
IY Iourov, AD Kolotii,
SG Vorsanova, VV Monakhov, T
Liehr,
YB Yurov. An euchromatic variant of chromosome 21 in mother of a child with autism. Proceedings of VI congress “Modern technologies in pediatrics and children surgery”. Moscow, Russia; 2007: 70 (in Russian) |
(p) | CG |
| 118 |
IY Iourov, SG Vorsanova, AD
Kolotii, VY Voinova-Ulas, AK Beresheva, T
Liehr,
YB Yurov. Mapping of a new fragile site on chromosome 9 of a mentally retarded child: identification of preneoplastic condition due to Philadelphia chromosome formation. Proceedings of VI congress “Modern technologies in pediatrics and children surgery”. Moscow, Russia; 2007: 69 (in Russian) |
(p) | CG |
| 117 |
AD Kolotii, IY Iourov, VI
Yablonskaya, T
Liehr,
IA Kozlova, YB Yurov, SG Vorsanova. A rare case of interstitial microdeletion of chromosome 12 in severely mentally retarded child with multiple congenital malformations. Proceedings of VI congress “Modern technologies in pediatrics and children surgery”. Moscow, Russia; 2007: 60 (in Russian) |
(p) | CG |
| 116 |
AD Kolotii, IY Iourov, T
Liehr,
ES Sakharova, SG Vorsanova. Interstitial microdeletion of chromosome 20 in a child with severe congenital malformations: the application of modern technologies. Proceedings of VI congress “Modern technologies in pediatrics and children surgery”. Moscow, Russia; 2007: 59 (in Russian) |
(p) |
CG |
| 115 |
I Iourov, S Vorsanova, T
Liehr,
A Kolotii, V Vostrkov, I Soloviev, N Uranova, Y
Yurov. First direct evidence for aneuploidy of chromosome 21 to affect the Alzheimer’s disease cerebral cortex and hippocampus, but not the cerebellum. Abstractbook: Genetics of Aging. Jena, Germany; 11.-13. October 2007: 30 (Abstract POS 20) |
(o) |
INT |
| 114 |
I Iourov, T
Liehr,
S Vorsanova, A Kolotii, Y Yurov. Chromosome instability in the Ataxia-telangiectasia cerebellum increase with age. Implications for genetic studies of aging. Abstractbook: Genetics of Aging. Jena, Germany; 11.-13. October 2007: 29-30 (Abstract POS 19) |
(o) |
INT |
| 113 |
IY Iourov, SG
Vorsanova, T
Liehr,
YB Yurov. Diagnosis of chromosome abnormalities in non-dividing cells by interphase chromosome-specific multicolor banding (ISC-MCB). Abstractbook: Actual Problems in Medical Genetics dedicated to the XXth anniversary of Department of Medical Genetics at NMAPO. Kiev, Ukraine; 2007: 140-142 |
(p) | INT |
| 112 |
IY Iourov, SG
Vorsanova, T
Liehr,
AD Kolotii, YB Yurov. Chromosome instability in the neuronal cells in ataxia-telangiectasia. Abstractbook: Actual Problems in Medical Genetics dedicated to the XXth anniversary of Department of Medical Genetics at NMAPO. Kiev, Ukraine; 2007: 139-140 |
(p) |
CG |
| 111 |
M Manvelyan, F Hunstig, F
Pellestor, S Bhatt, R Aroutionouan, T
Liehr.
3-D multicolor banding reveals the orientation of chromosomes in human sperm – a pilot study. Abstractbook: 2 International Medical Congress of Armenia. Yerevan, Armenia; 28.-30. June 2007: 22 |
(o) |
INT |
| 110 |
M Manvelyan, I Schreyer, A
Weise, T
Liehr,
K Mrasek, I Simonyan, R Aroutiounian. 48 new cases with infertility due to balanced chromosomal rearrangements – detailed molecular cytogenetic analysis of the 90 involved breakpoints. Abstractbook: 2 International Medical Congress of Armenia. Yerevan, Armenia; 28.-30. June 2007: 22 |
(o) |
CG |
| 109 |
N Kosyakova, K Mrasek, J
Vermeesch, L Brecevic, SW Cheung, A Weise, T
Liehr.
Towards a genotype-phenotype correlation of
small supernumerary marker chromosomes (sSMC) in
human. Abstractbook: 3. International Meeting on Cryptic Chromosomal Rearrangements in Mental Retardation and Autism. Troina, Italy; 13-14. April 2007: |
(p) | sSMC |
| 108 |
M Santos, M Mila, K
Mrasek, T
Liehr,
C Fuster. Cytogenetic characterization of small supernumerary marker chromosomes in 25 cases. Abstractbook: 3. International Meeting on Cryptic Chromosomal Rearrangements in Mental Retardation and Autism. Troina, Italy; 13-14. April 2007: no page# |
(p) |
sSMC |
| 107 |
H Mkrtchyan, M Gross, T
Liehr,
A Weise. Characterization of the parental origin of human chromosomes on a single cell level. Abstractbook: Genomic Disorders 2007 Congress. Hinxton, UK; 21.-23 March 2007: 72 |
(p) |
M |
| 106 |
N Kosyakova, H Nelle,
U Claussen, A Weise, T
Liehr.
The splitting of human chromosome bands into sub-bands. Abstractbook: Genomic Disorders 2007 Congress. Hinxton, UK; 21.-23 March 2007: 69 |
(p) |
INT |
| 105 |
M Gross, V Trifonov, T
Liehr,
A Weise. Of human and apes: A molecular cytogenetic study of chromosome evolution in chimpanzee. Abstractbook: Genomic Disorders 2007 Congress. Hinxton, UK; 21.-23 March 2007: 65 |
(p) |
EVO |
| 104 |
T
Liehr,
K Mrasek, N Kosyakova, J Vermeesch, L Brecevic,
S W Cheung, A Weise. Towards a genotype-phenotype correlation of small supernumerary marker chromosomes (sSMC) in human. Abstractbook: 12. Southafrican Society of Human Genetics (SASHG) Congress. Golden Gate, South-Africa; 1.-3. March 2007: 65-66 |
o |
sSMC |
| 103 |
M Gross, H Mkrtchyan, H
Thieme, F von Eggeling, B Horsthemke, C Jonsrud,
U Claussen, T
Liehr,
A Weise. Single cell epigenetics by parental origin determination (POD) FISH. Abstractbook: EHA scientific workshop on role of epigenetics in hematological malignancies. Mandelieu, France; 9.-11. February 2007: (Abstract 11) |
(p) |
M |
| 102 |
H Mkrtchyan, M Gross, H
Thieme, F von Eggeling, U Claussen, T
Liehr,
A Weise. How informative are microsatellite-analysis? Towards analyzing of epigenetic changes by differentiation of homologous chromosomes. Abstractbook: EHA scientific workshop on role of epigenetics in hematological malignancies. Mandelieu, France; 9.-11. February 2007: (Abstract 19) |
(p) |
M |
2006
see also here
| Number |
Authors/ Title/ Where Contribution
was Published |
Poster (p) or oral (o) |
Topic |
| 101 |
J Seidel, D Schumann, A
Meiner, T
Liehr,
U Claussen. Subtelomeres Duplikationssyndrom – eine neue genetische Entität. Abstractbook: 102. Jahrestagung der Deutschen Gesellschaft für Kinder- und Jugendmedizin. Mainz, Germany; 14.-17. September 2006: 164 (Abstract: DGKJ_PS-170) |
(o) |
CG |
| 100 |
IY Iourov, T
Liehr,
SG Vorsanova, AD Kolotii, YB Yurov. Chromosome specific multicolor banding — a new approach for identification of chromosome abnormalities in non-dividing cells. Proceedings of V Congress Current Technologies in Pediatrics and Child Surgery. Moscow, Russia. 2006: 67 |
(p) |
CG INT |
| 99 |
IY Iourov, SG Vorsanova, VV
Monakhov, T
Liehr,
YB Yurov. Two cases of chromosomal heteromorphisms characterized by unusual localization and size variation in alphoid DNA of chromosome 21. Proceedings of V Congress Current Technologies in Pediatrics and Child Surgery. Moscow, Russia. 2006: 66 |
(p) | CG |
| 98 |
VV Monakhov, AD Kolotii, IY
Iourov, T
Liehr,
VY Voinova-Ulas, PV Novikov, YB Yurov, SG
Vorsanova. Partial trisomy of 12p and monosomy of 13q due to translocation t(12;13)mat in a 5-year-aged infant. Proceedings of V Congress Current Technologies in Pediatrics and Child Surgery. Moscow, Russia. 2006: 60 |
(p) | CG |
| 97 |
AD Kolotii, IY Iourov, T
Liehr,
OS Kurinnaya, LA Havhun, EA Nikolaeva, YB Yurov,
SG Vorsanova. Multiple chromosome abnormalities addressed by FISH in a case of Angelman syndrome. Proceedings of V Congress Current Technologies in Pediatrics and Child Surgery. Moscow, Russia. 2006: 56 |
(p) | CG |
| 96 |
IA Demidova, IY Iourov, AD
Kolotii, OS Kurinnaya, T
Liehr,
SG Vorsanova. A rare case of partial monosomy of chromosome 7p associated with mental retardation and acrocephalosyndactily. Proceedings of V Congress Current Technologies in Pediatrics and Child Surgery. Moscow, Russia. 2006: 52-53 |
(p) | CG |
| 95 |
SG Vorsanova, IY Iourov, AD
Kolotii, NI Kononenko, T
Liehr,
VY Voinova-Ulas, YB Yurov. Chromosome instability associated with mosaic subtelomeric deletion 9p in an infant with mental retardation and congenital malformations. Proceedings of V Congress Current Technologies in Pediatrics and Child Surgery. Moscow, Russia. 2006: 51 |
(p) | CG |
| 94 |
S Bhatt, K Moradkhani, J
Puechberty, B Andreo, G Lefort, P Sarda, T
Liehr,
F Pellestor. Caracterisation des points de cassure, une approche efficace pour l’analyse de la segregation des inversions paracentriques dans sperme humain. Abstractbook: 18. Colloque de l’association des cytogeneticiens de langue francaise. Reims, France. 2006: 14 |
(o) |
CG INT |
| 93 |
E Matoso, J Ferrao, M
Venancio, J Saraiva, T
Liehr,
IM Carreira. Mosaicismo invulgar de uma deleccao 4p e revelado pela FISH. Abstractbook: 10. Reunioia da Sociedade Portuguesa de Genetica Humana. Coimbra, Portugal; 10.-11. November 2006: 73 |
(p) |
CG |
| 92 |
JB Melo, E Matoso, A Jardim,
M Amorim, JM Saraiva, T
Liehr,
IM Carreira. Characterizao de dois marcadores derivados do cromossoma 22 por citogenetica molecular. Abstractbook: 10. Reunioia da Sociedade Portuguesa de Genetica Humana. Coimbra, Portugal; 10.-11. November 2006: 37 |
(o) |
sSMC |
| 91 |
T
Liehr,
M Gross, B Horsthemke, C Jonsrud, U Claussen, H
Mkrtchyan, A Weise. Characterization of the parental origin of human chromosomes on a single cell level. Abstractbook: 10. Reunioia da Sociedade Portuguesa de Genetica Humana. Coimbra, Portugal; 10.-11. November 2006: 19 |
o |
M |
| 90 |
F Hunstig, F Pellestor, U
Steinhaeuser, H Starke, M Ziegler, U
Claussen, T
Liehr.
Multicolor banding studies on the ‘Barr-body’ in 3D-presevered human lymphocytes and on chromosomal orientation in human sperm interphase nuclei. Abstractbook: 2. Conference on X-inactivation. Paris, France; 17.-22. September 2006: 72 |
(o) |
INT |
| 89 |
L Brecevic, S Michel, H
Starke, K Müller, N Kosyakova, K Mrasek, A
Weise, T
Liehr. Multicolor FISH used for the characterization of small supernumerary marker chromosomes (sSMC) in commercially available immortalized cell lines. Proceedings of the 2. Croatian Congress on Microscopy with International Participation. Topusko, Croatia; 18.-21.05.2006: 92-93 |
(p) |
sSMC |
| 88 |
YB Yurov, IY Iourov, AD
Kolotii, AK Beresheva, T
Liehr,
SG Vorsanova SG. Interphase FISH study of aneuploidy rate in the brain tissues of patients with Ataxia-telangiectasia. Proceedings of the 7. Balkan Meeting of Human Genetics. Skopje, Macedonia; 31. August- 2. September 2006: 33 |
(p) |
INT |
| 87 |
L Míguez, M Santos, K Mrasek,
M Sostoa, H Starke, M Alegre, V Blasco, T
Liehr,
C Fuster. Caracterizacion de dos sSMC (13/21) en una mujer fertile fenotipicamente normal. Abstractbook: XXIIIth Spanish Congress of Human Genetics, July 2006: no page# |
(p) |
sSMC |
| 86 |
C Fuster, M Santos, K Mrasek,
H Starke, A González-Meneses, T
Liehr.
Identificación de un pequeno cromosoma marcador supernumerario (sSMC), derivado del chromosome X, en un nino von malformaciones congenitas. Abstractbook: XXIIIth Spanish Congress of Human Genetics, July 2006: no page# |
(p) |
sSMC |
| 85 |
T
Liehr,
K Mrasek, A Weise, N Kosyakova, J Vermeesch, L
Brecevic, S W Cheung, H Starke. Towards a genotype-phenotype correlation of small supernumerary marker chromosomes (sSMC). Abstractbook: 11. International Congress of Human Genetics. Brisbane, Australia; 06-11. Australia 2006: 108 (Abstract 0323) |
p |
sSMC |
| 84 |
A Weise, M Gross, B
Horsthemke, U Claussen, T
Liehr.
Parental-determination-FISH (pod-FISH) can distinguish homologues chromosomes. Abstractbook: 2nd Congress of the International Cytogenetics and Genome Society. Canterbury, UK, 25.-29. June 2006: 23 (Abstract O08) |
(o) |
M |
| 83 |
A Heller, T
Liehr.
Emerging technologies for aneuploidy screening: Recent possibilities of prenatal molecular cytogenetic diagnostics. Abstractbook: Workshop ‘Preimplantation testing using FISH’. Prague, Czech; 22-23. June 2006: 38-41 |
(o) |
CG |
| 82 |
D Mitter, K Buiting, A
Kuechler, T
Liehr,
UA Mau-Holzmann, E-C Prott, D Wieczorek, G
Gillessen-Kaesbach. Maternal uniparental disomy 14 (upd(14)mat) presents with an age dependent phenotype. Detection of 10 new patients by DNA methylation assay. Abstractbook: 19. course of Medical Genetics. Bertinoro, Italy; 24.04.-02.05.2006: no page# |
(o) |
CG |
| 81 |
T
Liehr,
H Mkrtchyan, C Karst, M Gross, F Hunstig, A
Polityko, A Weise. Multicolor-FISH approaches applied in tumor cytogenetics. Abstractbook: IV Annual conference of south district of Russian Federation: Current advances in human genetics: clinical aspects. Kislovodsk, Russia; 27-29. April 2006:112-118. |
o |
TCG |
2005
| Number |
Authors/ Title/ Where Contribution
was Published |
Poster (p) or oral (o) |
Topic |
| 80 |
IY Iourov, AD Kolotii, SG
Vorsanova, VY Voinova-Ulas, VV Monakhov, IM
Novikova, PV Novilov, IV Soloviev, T
Liehr,
YB Yurov. Application of modern molecular cytogenetic techniques for refinement of diagnosis of cryptic chromosome abnormality involving chromosomes 7 and 21. Proceedings of XIV Congress of Psychiatrists of Russia. Moscow, Russia; 2005: 75 (in Russian) |
(p) |
CG |
| 79 |
IY Iourov, SG
Vorsanova, T
Liehr,
F Pellestor. IV Soloviev, YB Yurov. Modern molecular cytogenetic techniques for diagnosis of chromosomal mosaicism. Proceedings of XIV Congress of Psychiatrists of Russia. Moscow, Russia; 2005: 74 (in Russian) |
(p) |
CG |
| 78 |
IY Iourov, SG
Vorsanova, IV Soloviev, T
Liehr,
YB Yurov. Current molecular cytogenetic approaches towards identification of chromosome abnormalities and chromosome organization in the neurons of the brain. Proceedings of XIV Congress of Psychiatrists of Russia. Moscow, Russia; 2005: 502 (in Russian) |
(p) |
CG |
| 77 |
A Weise, K Mrasek, N
Kosyakova, T
Liehr,
P Stankiewicz, SW Cheung, WW Cai. Towards a molecular genotype-phenotype correlation of small supernumeraray marker chromosomes (sSMC) by applying microdissected sSMC probes on a 21.5 k BAC array-CGH. Abstractbook: 55. Annual Meeting of the American Society of Human Genetics. Salt Lake City, USA; 25.-29. October 2005: 164 (Abstract 815) |
(p) |
sSMC |
| 76 |
F Sun, M Oliver-Bonet, T
Liehr,
H Starke, P Turek, E Ko, A Redamaker, RH Martin.
Analysis of achiasmate bivalents in pachytene cells from 8 normal male. Abstractbook: 55. Annual Meeting of the American Society of Human Genetics. Salt Lake City, USA; 25.-29. October 2005: 156 (Abstract 766) |
(p) |
CG |
| 75 |
R Martin, F Sun, M
Oliver-Bonet, T
Liehr,
H Starke, P Turek, E Ko, A Redamaker. Variation in meiotic recombination frequency for individual chromosomes. Abstractbook: 55 Annual Meeting of the American Society of Human Genetics. Salt Lake City, USA; 25.-29. October 2005: 60 (Abstract 214) |
(p) |
CG |
| 74 |
ES Sidneva, NV Kosyakova, AA
Rzhaninova, DV Goldstein, T
Liehr,
NP Bochkov. Chromosomal characteristics of human mesenchymal stem cell cultures. Abstractbook: 2. International Conference “Molecular Medicine and Biosafety”. Moscow, Russia; 20.-21. October 2005: P.246 (in Russian) |
(p) |
CG |
| 73 |
NV Kosyakova, H Starke, T
Liehr,
JR Vermeesch, L Backx., C Melotte. Application of microdissection and DNA-microarray for breakpoint characterization in human small supernumerary marker chromosomes (sSMC). Abstractbook: 2. International Conference “Molecular Medicine and Biosafety”. Moscow, Russia; 20.-21. October 2005: P.164 (in Russian) |
(p) |
sSMC |
| 72 |
H Mkrtchyan, C Karst, R
Aroutiounian, T
Liehr.
Multicolor FISH technique as powerful tools to study cryptic chromosomal aberrations in acute lymphoblastic leukemia. Abstractbook: Modern problems of genetics, radiobiology, radioecology and evolution. Yerevan, Armenia; 8.-11. September 2005: 233-235 |
(p) |
TCG |
| 71 |
A Polityko, N Rumyantseva, H
Starke, T
Liehr.
Investigation of the origin of small supernumerary marker chromosomes in constitutional karyotype using molecular cytogenetic approaches of multicolor fluorescent in situ hybridization (FISH). Abstractbook: Modern problems of genetics, radiobiology, radioecology and evolution. Yerevan, Armenia; 8.-11. September 2005: 84 |
(p) |
sSMC |
| 70 |
S Balci, Ö Engiz, D Aktas, I
Vargel, MS Beksac, K Mrasek, T
Liehr.
Ring kromozom 4 anomalili ve wolf-Hirschhorn sendromlu yarik damak-dudakli, iris kolobomlu, midgut malrotasyonlu, hipospadias ve korpus kallozum hipoplazili bir vakanin sunumu. Abstractbook: Maternal- Fetal Tip & Perinatoloji Dernegi. Antalya, Turkey; 30. April-2. May 2005: 97 (Abstract P37) |
(p) |
CG |
| 69 |
T
Liehr.
The database on sSMC. Abstractbook: 1. Course in pre-natal and post-natal clinical cytogenetics. Beirut, Lebanon; 12.-15. February 2005: 44-45 |
o |
sSMC |
| |
T
Liehr.
Small supernumerary marker chromosomes (sSMC). Abstractbook: 1. Course in pre-natal and post-natal clinical cytogenetics. Beirut, Lebanon; 12.-15. February 2005: 38-39 |
o |
sSMC |
2004
| Number |
Authors/ Title/ Where Contribution
was Published |
Poster (p) or oral (o) |
Topic |
| 67 |
C Karst, H Mkrtchyan, U
Claussen, T
Liehr.
Fluorescence in situ hybridzation improves the detection of cryptic chromosomal aberrations in acute lymphoblastic leukaemia. Abstractbook: Winter Confernce 2004 of the Cancer Genetics Group in U.K. London, UK; 10. December 2004: no page# |
(o) |
TCG |
| 66 |
J
Puechberty, G Lefort, A Weise, T
Liehr,
P Sarda, F Pellestor. FISH analysis of meiotic segregation in the sperm of a complex chromosome rearrangement carrier. Abstractbook: 54. Annual Meeting of the American Society of Human Genetics. Toronoto, USA; 26.-30. October 2004: 170 (Abstract 921) |
(p) |
CG |
| 65 |
T
Liehr,
K Mrasek, U Claussen, H Starke. Towards a first genotype-phenotype correlation of small supernumerary marker chromosomes (sSMC). Abstractbook: 54. Annual Meeting of the American Society of Human Genetics. Toronoto, USA; 26.-30. October 2004: 170 (Abstract 848) |
p |
sSMC |
| 64 |
U Claussen, H Lehrer, R
Hliscs , A Kuechler, A Weise, T
Liehr.
The splitting of chromosome bands into sub-bands analyzed by multicolor-banding (MCB) and chromosome stretching. Abstractbook: 54. Annual Meeting of the American Society of Human Genetics. Toronoto, USA; 26.-30. October 2004: 50 (Abstract 164) |
(o) |
INT |
| 63 |
S
Rudnik-Schöneborn, I Heil, T
Liehr,
HM Schüler. Ein Kind mit einem Fehlbildungskomplex und Duplikation 17p13. Abstractbook: Arbeitstreffen Klinische Genetik Nordrhein. Essen 12. October 2004: no page# |
(o) |
CG |
| 62 |
T
Liehr. Application of mFISH probe sets. Abstractbook: 6. Course in Molecular Cytogenetics and DNA Microarrays. Bertinoro, Italy; 27.-29. September 2004: 52-54. |
o |
M |
| 61 |
T
Liehr.
Multicolor FISH probe sets. Abstractbook: 6. Course in Molecular Cytogenetics and DNA Microarrays. Bertinoro, Italy; 27.-29. September 2004: 46-48 |
o |
M |
2003
| Number |
Authors/ Title/
Where Contribution was Published |
Poster (p) or oral
(o) |
Topic |
| 60 |
J
Seidel, T
Liehr.
Fallvorstellung: P.S., weibl., 10/95 Abstractbook: 27. Tagung des Sächsisch-Thüringischen Syndromclubs, Jena, 01.11.2003 |
(o) |
CG |
| 59 |
dim(9p21) im Gesamtmuster genomischer Imbalancen bei Plattenepithelkarziniomen der Mundhöhle. Abstractbook: 16. "Tumorzytogenetischen Arbeitstagung". Zelle, Germany; 15.-17. May 2003: 53 |
(o) |
TCG |
2002
| Number |
Authors/ Title/
Where Contribution was Published |
Poster (p) or oral
(o) |
Topic |
| 58 |
B
Grygalewiz, T
Liehr,
M Debiec-Rychter, A Hagemeijer. Application of FISH technique using new chromosome 12 band specific probe in four testicular germ cell i(12p)-negative tumors. Abstractbook: 8 Europ. Workshop on Cytogentics and Molecular Gentics of Human Solid Tumors. Barcelona, Spain; 12.-15. September 2002: 63 (Abstract P-25) |
(p) |
TCG |
| 57 |
U
Claussen, J Lemke, J Claussen, R Hliscs, S
Michel, I Chudoba, P Mühlig, M Westermann, K
Sperling, N Rubtsov, U-W Grumm, P Ullmann, K
Krohmeyer-Hauschild, T
Liehr.
The DNA-based structure of human chromosomes in interphase nuclei. Abstractbook: 8 Europ. Workshop on Cytogentics and Molecular Gentics of Human Solid Tumors. Barcelona, Spain; 12.-15. September 2002: 30 (Abstract L-8) |
(o) |
INT |
| 56 |
T
Liehr,
A Heller, H Starke, A Weise, K Mrasek, V
Trifonov, N Rubtsov, U Claussen. Multicolor banding (MCB) - a versatile tool for characterization of exact chromosomal breakpoints. Abstractbook: HGM2002 (Human Genome Meeting). Schanghai, China; 14.-17. April 2002: 248 (Abstract 629) |
p |
M |
| 55 |
T
Liehr,
A Heller, H Starke, A Weise, K Mrasek, V
Trifonov, N Rubtsov, U Claussen. Multicolor banding (MCB) - a versatile tool for characterization of exact chromosomal breakpoints. Abstractbook: HGM2002 (Human Genome Meeting). Schanghai, China; 14.-17. April 2002: 63 (Abstract 80) |
o |
M |
2001
| Number |
Authors/ Title/ Where Contribution
was Published |
Poster (p) or oral (o) |
Topic |
| 54 |
T
Liehr.
Present state and perspectives of centromere specific multicolor FISH (cenM-FISH) – a new approach for the PGD and prenatal diagnosis. Abstractbook: 12. Fetal Cell Workshop. Prague, Czech Republic; 12.-13. May 2001: 97 |
o | CG |
| 53 |
T
Liehr,
A Nietzel, M Rocchi, H Starke, A Heller, U
Claussen. Centromere specific multicolor FISH (cenM-FISH) – a new approach for the characterization of marker chromosomes. Abstractbook: 12. Fetal Cell Workshop. Prague, Czech Republic; 12.-13. May 2001: 72 |
o |
CG sSMC |
| 52 |
M
Stumm, S Schünemann, T
Liehr,
A Kuechler, H Geiger. Automated analysis of chromosomal aberrations in WCP124-metaphases. Proceedings of the 2. Euroconference on Quantitative Molecular Cytogenetics. Salamanca, Spain; 26.-28. April 2001: 44-47 |
(o) | TCG |
| 51 |
T
Liehr,
A Heller, H Starke, V Trifonov, N Rubtsov, K
Mrasek, A Weise, U Claussen. High resolution multicolour banding (MCB) for the entire human karyotype. Proceedings of the 2. Euroconference on Quantitative Molecular Cytogenetics. Salamanca, Spain; 26.-28. April 2001: 39-41 |
o | M |
| 50 |
Nachweis der AML-spezifischen Translokation t(16,21)(p11;q22) bei einem Patienten mit Akuter Lymphatischer Leukämie (ALL). Abstractbook: 14. "Tumorzytogenetischen Arbeitstagung". Weilburg, Germany; 26.-28. April 2001: 43 |
|
TCG |
| 49 |
S Scheil, S
Brüderlein, T
Liehr,
H Starke, J Herms, M Schulte, P Möller. Genome wide analysis of 16 chordomas by comparative genomic hybridization and cytogenetics of the first human chordoma cell line, U-CH1. Abstractbook: 14. "Tumorzytogenetischen Arbeitstagung". Weilburg, Germany; 26.-28. April 2001: 18 |
(o) |
TCG |
| 48 |
IF Loncarevic, J Römer, A
Heller, T
Liehr,
H Starke, H Sayer, C Bleck, I Hartmann, M
Ziegler, U Claussen. Kann der ABL-BCR RNA Verlust als Indikator für einen Deletion in Chromosom der(9)t(9;22) dienen? Abstractbook: 14. "Tumorzytogenetischen Arbeitstagung". Weilburg, Germany; 26.-28. April 2001: 22 |
(o) |
TCG |
| |
B Albrecht, T
Liehr.
Ringchromosom 8 im Mosaik bei einem Jungen mit Entwicklungsverzögerung. Abstractbook: 32. Arbeitstreffen “Klinische Genetik Nordrhein”. Essen, Germany; 03. April 2001: no page# |
(o) |
CG |
2000
| Number |
Authors/ Title/
Where Contribution was Published |
Poster (p) or oral
(o) |
Topic |
| 46 |
A
Heller, A Sauerbrey, C Bleck, I Loncarevic, V
Trifonov, I Chudoba, U Claussen, T
Liehr.
24 color-FISH und Multicolor-Bänderungsanalysen eines Falles mit komplexen Karyotypveränderungen bei sekundärem Myelodysplastischen Syndrom. Abstractbook: 13. "Tumorzytogenetischen Arbeitstagung". Otzenhausen, Germany; 01.-03. June 2000: 41 |
(o) |
TCG |
| 45 |
C
Knebelmann-Betzing, K Seeger, A Kulozik, R
Fengler, G Körner, L Badiali, A Prokopp, A
Heller, T
Liehr,
G Henze. Secondary acute myeloblastic leukemia after treatment of acute monoblastic leukemia. Abstractbook: 13. "Tumorzytogenetischen Arbeitstagung". Otzenhausen, Germany; 01.-03. June 2000: 33 |
(o) |
TCG |
| 44 |
IF
Loncarevic, H Starke, A Heller, C Bleck, M
Ziegler, T
Liehr,
J Clement, W Fiedler, C Kelbova, U Claussen. Ein Verlust der ABL- und BCR-Sequenzen auf dem Chromosom der(9)t(9;22) ist in ca. 25% der CML-Patienten nachweisbar. Abstractbook: 13. "Tumorzytogenetischen Arbeitstagung". Otzenhausen, Germany; 01.-03. June 2000: 31 |
(o) |
TCG |
| 43 |
T
Liehr,
A Nietzel, A Heller, H Starke, M Rocchi, U
Claussen. Zentromer-spezifische 24-Farben FISH: Einsatz einer neuen M-FISH Technik in der Tumorzytogenetik. Abstractbook: 13. "Tumorzytogenetischen Arbeitstagung". Otzenhausen, Germany; 01.-03. June 2000: 11 |
o |
TCG M |
| 42 |
M Stumm,
S Kleindorff, M Volleth, G Bollmann, A
Heller, T
Liehr,
S Neubauer. The quantification of spontaneous and radiation induced chromosomal aberrations by three color FISH. Proceedings of the 1. Euroconference on quantitative molecular cytogenetics. Bari, Italy; 13-15. April 2000: 28-31 |
(o) |
TCG |
| 41 |
T
Liehr,
A Nietzel, A Heller, H Starke, V Trifonov, M
Rocchi, W Fiedler, U Claussen. A new M-FISH technique: centromere specific 24-color FISH (cenM-FISH). Proceedings of the 1. Euroconference on quantitative molecular cytogenetics. Bari, Italy; 13-15. April 2000: 36-38 |
o |
M |
1999
| Number |
Authors/ Title/
Where Contribution was Published |
Poster (p) or oral
(o) |
Topic |
| 40 |
T
Liehr,
H Starke, U Claussen. Painting from microdissection. Abstractbook: 1. Course in Molecular Cytogenetics. Sestri Levante, Italy, 14.-18.November 1999; no page# |
o |
M |
| 39 |
T
Liehr,
H Starke, U Claussen. Microdissection of chromosomes – protocol. Abstractbook: 1. Course in Molecular Cytogenetics. Sestri Levante, Italy, 14.-18.November 1999; no page# |
o |
M |
| 38 |
Loncarevic IF, Starke H, Bleck C, Ziegler M,
JH Clement, T
Liehr,
U Claussen. Ph-negative chronische myeloische Leukämie mit BCR-ABL Genfusion auf Chromosom 22 oder Chromosom 9. Abstractbook: 12. "Tumorzytogenetischen Arbeitstagung". Berlin, Germany; 27.-29. May 1999: 30 |
(o) |
TCG |
| 37 |
T
Liehr,
H Starke, IF Loncarevic, A Heller, M Ziegler,
U Claussen. Einsatz der p53 FISH-Sonde zur Prognosedifferenzierung bei Leukämien. Abstractbook: 12. "Tumorzytogenetischen Arbeitstagung". Berlin, Germany; 27.-29. May 1999: 26 |
o |
TCG |
| 36 |
H Starke, A Heller, M Ziegler, IF Loncarevic,
U Claussen, E Gebhart, T
Liehr.
Eine neue Dreifarb-FISH-Methode zur Verlaufskontrolle Ph-positiver CML-Fälle nach gegengeschlechtlicher KMT. Abstractbook: 12. "Tumorzytogenetischen Arbeitstagung". Berlin, Germany; 27.-29. May 1999: 24 |
(o) |
TCG |
| 35 |
A
Heller, H Starke, M Ziegler, IF Loncarevic, U
Claussen, T
Liehr.
Ist der Ausschluß eines Sub-Klones mit numerischen Veränderungen der Chromosomen 7 und/oder 8 mittels FISH bei der ALL von Relevanz? Abstractbook: 12. "Tumorzytogenetischen Arbeitstagung". Berlin, Germany; 27.-29. May 1999: 27 |
(o) |
TCG |
1998
| Number |
Authors/ Title/
Where Contribution was Published |
Poster (p) or oral
(o) |
Topic |
| 34 |
T
Liehr,
S Girod, U Claussen, E Gebhart. Nucleus extraction from one paraffin-embedded section mounted on a slide for two-color FISH. Abstractbook: 6. European Conference on Cytogenetics and Molecular Genetics of Solid Tumors. Saarbrücken, Germany; 15.-18. October 1998: 104 |
o |
M |
| 33 |
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). Abstractbook: 6. European Conference on Cytogenetics and Molecular Genetics of Solid Tumors. Saarbrücken, Germany; 15.-18. October 1998: 76 |
(o) |
TCG |
| 32 |
T
Liehr.
An efficient nucleus extraction method from paraffin- and cryo-fixed material for up to three color-FISH analysis. Abstractbook: 1. Nordic Meeting on Molecular Cytogenetics. Aarhus, Denmark. 20.-22. August 1998: 28 |
o |
M |
| 31 |
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. Abstractbook: 7. CMTBelgium-Consortium Meeting. Antwerp, Belgium; 3.-5. July 1998: 42 |
o |
CG |
| 30 |
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. Abstractbook: 7. CMT-Consortium Meeting. Antwerp, Belgium; 3.-5. July 1998: 55 |
(o) |
CG |
| 29 |
E
Gebhart, T
Liehr.
Betrachtungen zu den Verteilungsmustern CGH-detektierter genomischer Imbalanzen. Abstractbook: 11. "Tumorzytogenetischen Arbeitstagung". Jena, Germany; 22.-24. May 1998: 36 |
(o) |
TCG |
| 28 |
T
Liehr,
W Fiedler, J Ries, S Girod, R Dahse, G Ernst,
S Koscielny, E Gebhart. HN-SCCs verschiedener Lokalisation charakterisiert mittels CGH und Telomerase-Assay. Abstractbook: 11. "Tumorzytogenetischen Arbeitstagung". Jena, Germany; 22.-24. May 1998: 35 |
o |
TCG |
1997
| Number |
Authors/ Title/
Where Contribution was Published |
Poster (p) or oral
(o) |
Topic |
| 27 |
C Fuchs,
M Hölzenbein, F H Hermann, C Kraus, T
Liehr,
C Opelz, B Rautenstrauss. A family affected by CMT1A and mental retardation shows a duplication of the PMP22 and the FALDH2 (Sjoergren-Larson) gene. Abstractbook: MDA Charcot-Marie-Tooth Disease Workshop. Baltimore, USA; 27.October 1997: 8 |
(o) |
CG |
| 26 |
T
Liehr,
C Fuchs, A Bevot, R Michaelis, A Bornemann, E
Postler, R Meyermann, W Friedl, H Grehl, B
Rautenstrauss. Mosaicism for two unrelated CMT1A patients - two casereports suggesting somatic reversion. Abstractbook: MDA Charcot-Marie-Tooth Disease Workshop. Baltimore, USA; 27.October 1997: 7 |
o |
CG |
| 25 |
C Fuchs, T
Liehr,
H Grehl, C Opelz, M Murakami, J R 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. Abstractbook: 6. European CMT-Consortium Meeting, Antwerp, Netherlands; 4.-5. July 1997: 26 |
(o) |
CG |
| 24 |
E
Gebhart, E Wolff, T
Liehr.
Genomische Imbalancen in Ovarial- und Mundhölenkarzinomen: Ein Vergleich mittels CGH-Analysen. Abstractbook: 10. "Tumorzytogenetischen Arbeitstagung". Friedrichsdorf, Germany; 22.-24. Mai 1997. 44 |
(o) |
TCG |
| 23 |
T
Liehr,
K Thoma, O Park, BG Feuerstein, T Murakami, JR
Lupski, E Gebhart, B Rautenstrauss. Das Periphere Myelin Protein 22kDa (PMP22) Gen liegt einer Glioblastom- und einer Osteosarkom-Zellinien amplifiziert vor; ein neuer Kandidat für ein Onkogen? Abstractbook: 10. "Tumorzytogenetischen Arbeitstagung". Friedrichsdorf, Germany; 22.-24. Mai 1997: 13 |
o |
TCG |
| 22 |
L
Reiter, T
Liehr,
B Rautenstrauss, J R Lupski. A possible role for the Mariner family of transposons in the generation of human chromosomal deletions and duplications. Abstractbook: Keystone Symposia. Santa Fe, New Mexico, USA; 1.-7. March 1997. Abstract 233 |
(o) |
CG |
1996
| Number |
Authors/ Title/ Where Contribution
was Published |
Poster (p) or oral (o) |
Topic |
| 21 |
T
Liehr,
H Grehl, B Rautenstrauss. CMT1A/HNPP-diagnostics by means of interphase FISH is possible on various kinds of tissue. Proceedings of the Symposium on Update in Neurogenetics. Ljubljana, Slovenia; 1996: 84 |
(p) |
CG |
| 20 |
T
Liehr,
B Rautenstrauss, H Grehl, UMH Schrell, E
Gebhart. Eine effiziente Kern-Extraktionsmethodik aus paraffin- und cryo-fixiertem Archivmaterial für anschliessende Mehrfarb-FISH Analysen. Abstractbook: 9. "Tumorzytogenetischen Arbeitstagung". Kitzbühel, Austria; 9.-11. Mai 1996: 13 |
o |
TCG |
| 19 |
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. Abstractbook: 5. Annual European Charcot-Marie-Tooth-Consortium Meeting. London, UK; 14. April 1996: 8 |
(o) |
CG |
| 18 |
B Rautenstrauss, K
Rautenstrauss, T Koeuth, T Murakami, L
Reiter, T
Liehr,
H Grehl, V Timmerman, KD Bathke, A Ekici, L
Shaffer, C Van Broeckhoven, J R Lupski. A 1.5 Mb deletion in 17p11.2 causing tomacolous neuropathy due to a mutation outside the recombination "hot spot" in CMT-REP elements. Abstractbook: 5. Annual European Charcot-Marie-Tooth-Consortium Meeting. 14. April 1996; London, UK: 12 |
(o) |
CG |
| 17 |
KD Bathke, T
Liehr,
A Ekici, L Reiter, J R Lupski, H Grehl, B
Neundörfer, B Rautenstrauss. A recesssive point mutation in the PMP22 gene determines the Charcot-Marie-Tooth disease phenotype in presence of a deletion in the homologous cromosome 17. Abstractbook: 5. Annual European Charcot-Marie-Tooth-Consortium Meeting. London, UK; 14. April 1996: 14 |
(o) |
CG |
| 16 |
T
Liehr,
H Grehl, A Ekici, KD Bathke, A Rauch, B
Rautenstrauss. Mosaicism for a CMT1A patient detected in four different tissue-types - a casereport suggesting somatic reversion. Abstractbook: 5. Annual European Charcot-Marie-Tooth-Consortium Meeting. London, UK; 14. April 1996: 13 |
o |
CG |
| 15 |
B Rautenstrauss, T
Liehr,
K D Bathke, H Grehl, K Rautenstrauss, T Koeuth,
M Tatsufumi, L Reiter, B Neundörfer, R A
Pfeiffer, J R Lupski. Charcot-Marie-Tooth disease and tomacolous neuropathy: identification of a recombination "hot spot" in a German study. Abstractbook: 16. International Winter Meeting of the Swiss Society of Neuropathology 1996. St. Moritz, Switzerland; 20.- 23. March 1996: 33 |
(p) |
CG |
| 14 |
KD Bathke, T
Liehr,
A Ekici, H Grehl, D Claus, B Neundörfer, R A
Pfeiffer, B Rautenstrauss. Molecular analyses of hereditary motor sensory neuropathy (HMSN) and tomacolous neuropathy (HNPP) patients using chromosome 17p11.2 specific probes. Abstractbook: 16. International Winter Meeting of the Swiss Society of Neuropathology 1996. St. Moritz, Switzerland; 20.- 23. March 1996: 24 |
(p) |
CG |
1995
| Number |
Authors/ Title/
Where Contribution was Published |
Poster (p) or oral
(o) |
Topic |
| 13 |
KD Bathke, D
Lorek, T
Liehr, A
Ekici, E Nelis, C Van Broeckhoven, H Grehl, D
Claus, B Neundörfer, B Rautenstrauss. Molecular analysis in Charcot-Marie-Tooth (CMT) disease and hereditary neuropathy with liability to pressure palsies (HNPP). Abstractbook: 2. Workshop Neurogenetics in Germany. Munich, Germany; 19.-21. October 1995: 26 |
(p) |
CG |
| 12 |
KD
Bathke, D Lorek, T
Liehr,
A Ekici, E Nelis, C Van Broeckhoven, H Grehl,
D Claus, B Rautenstrauss, B Neundörfer. Screening for point mutations in Chracot-Marie-Tooth patients without duplication at the chromosomal locus 17p11.2. Abstractbook: 2. joint meeting of the Benelux and German Neurological Societies, Neuroreunion. Maastricht, Netherlands; 21.-23. September 1995: Abstract OC-72. |
(o) |
CG |
| 11 |
T
Liehr,
P Hofbeck, Y Hübner, R Lerch, E Gebhart. Zweifarb-FISH-Analysen an alten zytogenetischen Präparaten solider Tumore (Interphasezytogenetik). Abstractbook: 8. "Tumorzytogenetischen Arbeitstagung". Bremen, Germany; 3.-6. Mai 1995: 40 |
o | TCG |
| 10 |
E
Gebhart, T
Liehr,
S Reichardt, K Thoma, U Trautmann. Betrachtungen zur Zuverlässigkeit von Interphase-FISH-Analysen bei Leukämien - Eine Analyse der Erlanger Befunde. Abstractbook: 8. "Tumorzytogenetischen Arbeitstagung". Bremen, Germany; 3.-6. Mai 1995: 50 |
(o) |
TCG |
1994
| Number |
Authors/ Title/
Where Contribution was Published |
Poster (p) or oral
(o) |
Topic |
| 9 |
C Kraus, T
Liehr, J Hülsken,
J Behrens, W Birchmeier, K H Greschick, W G
Ballhausen. Localization of the human ß-catenin gene (CTNNB1) to 3p21: a locus potentially associated with non-allelic heterogeneity in familial adenomatous polyposis (FAP). Abstractbook: EUROFAP; in Proceedings of the 5th workshop on Genetics of FAP and HNPCC. Budapest - Hungary, 2.-4.12.1994: Abstract 26 |
(p) |
TCG |
| 8 |
B
Schmucker, T
Liehr, H
Schmidt, M Hauser. Xq deletion of more than 40 Mb in a female with mild phenotype - evidence of most genes in Xq22-28 to be subject to X inactivation. Abstractbook: 26th Annual Meeting of the European Society of Human Genetics. Paris, France; 1.-5. Juni 1994: Abstract 149 |
(p) |
CG |
| 7 |
S
Neubauer, T
Liehr, A
Stübinger, E Gebhart. Vergleichende FISH-Studien an Interphasekernen von Suspensionspräparaten und Paraffinschnitten von Ovarialkarzinomen. Abstractbook: 7. "Tumorzytogenetischen Arbeitstagung". Schloß Salzau/Holstein, Germany; 28.-30. April 1994: 23 |
(o) |
TCG |
| 6 |
T
Liehr, P Harrer,
S Reichardt, E Gebhart. Vergleichende Interphasezytogenetik an klassischen Knochenmarks - Ausstrichen und - Suspensionspräparaten mittels FISH. Abstractbook: 7. "Tumorzytogenetischen Arbeitstagung". Schloß Salzau/Holstein, Germany; 28.-30. April 1994: 5 |
o |
TCG |
1993
| Number |
Authors/ Title/
Where Contribution was Published |
Poster (p) or oral
(o) |
Topic |
| 5 |
T
Liehr, S Reichardt, K
Thoma, A H Tulusan, E Gebhart. Interphasenzytogenetik mittels FISH bei menschlichen Ovarial-Karzinomen. Abstractbook: 6. "Tumorzytogenetischen Arbeitstagung". Kloster Banz, Germany; 16.-18. May 1993: 33 |
o |
TCG |
1992
| Number |
Authors/ Title/
Where Contribution was Published |
Poster (p) or oral
(o) |
Topic |
| 4 |
T
Liehr, N Atanasov, A H Tulusan,
E Gebhart. Proto-oncogene amplification and polymorphisms in human primary ovarian carcinomas. Abstractbook: 4. Convention of the (German) Society of Human Genetics; 08.-11. April 1992: T15/359 |
p |
TCG |
| 3 |
T
Liehr, E
Gebhart. Onkogen-Amplifikation in Ovarialkarzinomen - molekulare Identifizierung und zytogenetische Aspekte. Abstractbook: 5. "Tumorzytogenetischen Arbeitstagung". Vienna, Austria; 21.-23. May 1992: 37-39 |
o |
TCG |
| Number |
Authors/ Title/ Where Contribution
was Published |
Poster (p) or oral (o) |
Topic |
|
| 2 |
W Fiedler, T Liehr,
U Claussen, U Trautmann, Ad H M Geurts van
Kessel, R Fahsold. Regional mapping of new DNA markers flanking the Ewing sarcoma breakpoint on chromosome 22. Abstractbook: 2. international workshop on the mapping of human chromosome 22. Montreal, Canada, 10.-13. September 1991: 30 |
(p) |
TCG |
|
| 1 |
W Fiedler, T Liehr,
U Claussen, U Trautmann, G Senger, Ad H M Geurts
van Kessel, R Fahsold. Regional mapping of new DNA markers flanking the Ewing sarcoma breakpoint on chromosome 22. Abstractbook: 3. Convention of the (German) Society of Human Genetics; Ulm, Germany, 10.-13. April 1991: 227 |
(p) |
TCG |
