| Year |
Citation |
Score |
| 2016 |
Wafa A, Moassass F, Liehr T, Bhatt S, Aljapawe A, Al Achkar W. A high complex karyotype involving eleven chromosomes including three novel chromosomal aberrations and monoallelic loss of TP53 in case of follicular lymphoma transformed into B-cell lymphoblastic leukemia. Molecular Cytogenetics. 9: 91. PMID 28031746 DOI: 10.1186/S13039-016-0300-6 |
0.497 |
|
| 2016 |
Weise A, Bhatt S, Piaszinski K, Kosyakova N, Fan X, Altendorf-Hofmann A, Tanomtong A, Chaveerach A, de Cioffi MB, de Oliveira E, Walther JU, Liehr T, Chaudhuri JP. Chromosomes in a genome-wise order: evidence for metaphase architecture. Molecular Cytogenetics. 9: 36. PMID 27123045 DOI: 10.1186/S13039-016-0243-Y |
0.351 |
|
| 2015 |
Weise A, Othman MA, Bhatt S, Löhmer S, Liehr T. Application of BAC-probes to visualize copy number variants (CNVs). Methods in Molecular Biology (Clifton, N.J.). 1227: 299-307. PMID 25239754 DOI: 10.1007/978-1-4939-1652-8_16 |
0.48 |
|
| 2015 |
Gomaa IE, Abdel Gaber SA, Bhatt S, Liehr T, Glei M, El-Tayeb TA, Abdel-Kader MH. In vitro cytotoxicity and genotoxicity studies of gold nanoparticles-mediated photo-thermal therapy versus 5-fluorouracil Journal of Nanoparticle Research. 17: 1-11. DOI: 10.1007/S11051-015-2912-X |
0.335 |
|
| 2014 |
Rodríguez L, Bhatt SS, García-Castro M, Plasencia A, Fernández-Toral J, Abarca E, de Bello Cioffi M, Liehr T. A unique case of a discontinuous duplication 3q26.1-3q28 resulting from a segregation error of a maternal complex chromosomal rearrangement involving an insertion and an inversion. Gene. 535: 165-9. PMID 24316129 DOI: 10.1016/j.gene.2013.11.041 |
0.43 |
|
| 2014 |
Bhatt SS, Manvelyan M, Moradkhani K, Hunstig F, Mrasek K, Puechberty J, Lefort G, Sarda P, Weise A, Liehr T, Pellestor F. Inverted segment size and the presence of recombination hot spot clusters matter in sperm segregation analysis. Cytogenetic and Genome Research. 142: 145-9. PMID 24217531 DOI: 10.1159/000356142 |
0.668 |
|
| 2013 |
Guilherme R, Klein E, Hamid A, Bhatt S, Volleth M, Polityko A, Kulpanovich A, Dufke A, Albrecht B, Morlot S, Brecevic L, Petersen M, Manolakos E, Kosyakova N, Liehr T. Human Ring Chromosomes - New Insights for their Clinical Significance. Balkan Journal of Medical Genetics : Bjmg. 16: 13-20. PMID 24265580 DOI: 10.2478/Bjmg-2013-0013 |
0.517 |
|
| 2013 |
Guilherme RS, Cernach MC, Sfakianakis TE, Takeno SS, Nardozza LM, Rossi C, Bhatt SS, Liehr T, Melaragno MI. A complex chromosome rearrangement involving four chromosomes, nine breakpoints and a cryptic 0.6-Mb deletion in a boy with cerebellar hypoplasia and defects in skull ossification. Cytogenetic and Genome Research. 141: 317-23. PMID 23817307 DOI: 10.1159/000353302 |
0.467 |
|
| 2013 |
Kosyakova N, Grigorian A, Liehr T, Manvelyan M, Simonyan I, Mkrtchyan H, Aroutiounian R, Polityko AD, Kulpanovich AI, Egorova T, Jaroshevich E, Frolova A, Shorokh N, Naumchik IV, Volleth M, ... ... Bhatt S, et al. Heteromorphic variants of chromosome 9. Molecular Cytogenetics. 6: 14. PMID 23547710 DOI: 10.1186/1755-8166-6-14 |
0.567 |
|
| 2013 |
Ney-Garcia DR, Vieira TP, Liehr T, Bhatt S, de Souza MT, de Figueiredo AF, Ribeiro RC, Silva ML. A case of childhood T cell acute lymphoblastic leukemia with a complex t(9;9) and homozygous deletion of CDKN2A gene associated with a Philadelphia-positive minor subclone. Blood Cells, Molecules & Diseases. 50: 131-3. PMID 23044159 DOI: 10.1016/J.Bcmd.2012.09.005 |
0.327 |
|
| 2012 |
Guilherme RS, Klein E, Venner C, Hamid AB, Bhatt S, Melaragno MI, Volleth M, Polityko A, Kulpanovich A, Kosyakova N, Liehr T. Human ring chromosomes and small supernumerary marker chromosomes - Do they have telomeres? Chromosome Research. 20: 825-835. PMID 23076733 DOI: 10.1007/S10577-012-9316-X |
0.551 |
|
| 2012 |
Weise A, Mrasek K, Klein E, Mulatinho M, Llerena JC, Hardekopf D, Pekova S, Bhatt S, Kosyakova N, Liehr T. Microdeletion and microduplication syndromes. The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society. 60: 346-58. PMID 22396478 DOI: 10.1369/0022155412440001 |
0.338 |
|
| 2012 |
Ney-Garcia DR, Liehr T, Bhatt S, Souza MTd, Matos RRCd, Pimenta G, Pulcheri W, Ribeiro RC, Abdelhay E, Silva MLM. Childhood B-cell progenitor acute lymphoblastic leukemia presenting a three-way t(11;12;21)(q14;p13;q22) with a RUNX1 gene signal on chromosome 11 International Journal of Hematology. 95: 112-114. PMID 22215484 DOI: 10.1007/S12185-011-0981-X |
0.437 |
|
| 2012 |
Stankiewicz P, Kulkarni S, Dharmadhikari AV, Sampath S, Bhatt SS, Shaikh TH, Xia Z, Pursley AN, Cooper ML, Shinawi M, Paciorkowski AR, Grange DK, Noetzel MJ, Saunders S, Simons P, et al. Recurrent deletions and reciprocal duplications of 10q11.21q11.23 including CHAT and SLC18A3 are likely mediated by complex low-copy repeats. Human Mutation. 33: 165-79. PMID 21948486 DOI: 10.1002/Humu.21614 |
0.409 |
|
| 2012 |
Ney-Garcia DR, Liehr T, Bhatt S, de Souza MT, de Matos RR, Binato R, Jordy FC, Abdelhay E, Ribeiro RC, Silva ML. Molecular cytogenetics studies reveal unexpected chromosomal inversion as variant of t(12;21)(p13;q22) in child with B-cell precursor acute lymphoblastic leukemia. Leukemia & Lymphoma. 53: 342-4. PMID 21848362 DOI: 10.3109/10428194.2011.613134 |
0.499 |
|
| 2011 |
Liehr T, Kosayakova N, Schröder J, Ziegler M, Kreskowski K, Pohle B, Bhatt S, Theuss L, Wilhelm K, Weise A, Mrasek K. Evidence For Correlation Of Fragile Sites And Chromosomal Breakpoints In Carriers Of Constitutional Balanced Chromosomal Rearrangements Balkan Journal of Medical Genetics. 14: 13-16. PMID 24052707 DOI: 10.2478/V10034-011-0042-Z |
0.563 |
|
| 2011 |
Garcia DR, Bhatt S, Manvelyan M, de Souza MT, Binato R, Aguiar TF, Abdelhay E, Silva ML. An unusual T-cell childhood acute lymphoblastic leukemia harboring a yet unreported near-tetraploid karyotype. Molecular Cytogenetics. 4: 20. PMID 21936943 DOI: 10.1186/1755-8166-4-20 |
0.318 |
|
| 2011 |
De Figueiredo AF, Liehr T, Bhatt S, Binato R, De Souza MT, De Matos RR, Salles Tde J, Jordy FC, Ribeiro RC, Abdelhay E, Silva ML. A complex karyotype masked a cryptic variant t(8;21)(q22;q22) in a child with acute myeloid leukemia. Leukemia & Lymphoma. 52: 1593-6. PMID 21657952 DOI: 10.3109/10428194.2011.576286 |
0.431 |
|
| 2010 |
Mkrtchyan H, Gross M, Hinreiner S, Polytiko A, Manvelyan M, Mrasek K, Kosyakova N, Ewers E, Nelle H, Liehr T, Bhatt S, Thoma K, Gebhart E, Wilhelm S, Fahsold R, et al. The human genome puzzle - the role of copy number variation in somatic mosaicism. Current Genomics. 11: 426-31. PMID 21358987 DOI: 10.2174/138920210793176047 |
0.328 |
|
| 2009 |
Shinawi M, Schaaf CP, Bhatt SS, Xia Z, Patel A, Cheung SW, Lanpher B, Nagl S, Herding HS, Nevinny-Stickel C, Immken LL, Patel GS, German JR, Beaudet AL, Stankiewicz P. A small recurrent deletion within 15q13.3 is associated with a range of neurodevelopmental phenotypes. Nature Genetics. 41: 1269-71. PMID 19898479 DOI: 10.1038/ng.481 |
0.424 |
|
| 2009 |
Stankiewicz P, Sen P, Bhatt SS, Storer M, Xia Z, Bejjani BA, Ou Z, Wiszniewska J, Driscoll DJ, Maisenbacher MK, Bolivar J, Bauer M, Zackai EH, McDonald-McGinn D, Nowaczyk MM, et al. Genomic and genic deletions of the FOX gene cluster on 16q24.1 and inactivating mutations of FOXF1 cause alveolar capillary dysplasia and other malformations. American Journal of Human Genetics. 84: 780-91. PMID 19500772 DOI: 10.1016/J.Ajhg.2009.05.005 |
0.309 |
|
| 2009 |
Liehr T, Stumm M, Wegner RD, Bhatt S, Hickmann P, Patsalis PC, Meins M, Morlot S, Klaschka V, Ewers E, Hinreiner S, Mrasek K, Kosyakova N, Cai WW, Cheung SW, et al. 10p11.2 to 10q11.2 is a yet unreported region leading to unbalanced chromosomal abnormalities without phenotypic consequences Cytogenetic and Genome Research. 124: 102-105. PMID 19372675 DOI: 10.1159/000200094 |
0.569 |
|
| 2009 |
Bhatt S, Moradkhani K, Mrasek K, Puechberty J, Manvelyan M, Hunstig F, Lefort G, Weise A, Lespinasse J, Sarda P, Liehr T, Hamamah S, Pellestor F. Breakpoint mapping and complete analysis of meiotic segregation patterns in three men heterozygous for paracentric inversions. European Journal of Human Genetics : Ejhg. 17: 44-50. PMID 18685557 DOI: 10.1038/Ejhg.2008.144 |
0.761 |
|
| 2008 |
Manvelyan M, Hunstig F, Bhatt S, Mrasek K, Pellestor F, Weise A, Simonyan I, Aroutiounian R, Liehr T. Chromosome distribution in human sperm - a 3D multicolor banding-study. Molecular Cytogenetics. 1: 25. PMID 19014589 DOI: 10.1186/1755-8166-1-25 |
0.671 |
|
| 2008 |
Manvelyan M, Hunstig F, Mrasek K, Bhatt S, Pellestor F, Weise A, Liehr T. Position of chromosomes 18, 19, 21 and 22 in 3D-preserved interphase nuclei of human and gorilla and white hand gibbon. Molecular Cytogenetics. 1: 9. PMID 18471270 DOI: 10.1186/1755-8166-1-9 |
0.68 |
|
| 2008 |
Pellestor F, Bhatt S, Puechberty J, Lefort G, Liehr T, Sarda P, Hamamah S. The meiotic segregation of paracentric inversions: how breakpoint mapping can make the difference Reproductive Biomedicine Online. 16. DOI: 10.1016/S1472-6483(10)61357-0 |
0.548 |
|
| 2008 |
Bhatt S, Liehr T, Lefort G, Sarda P, Hamamah S, Pellestor F. Segregation analysis of paracentric inversions in human sperm: inverted segment size, low copy repeats (LCRs) and recombination hot spots have a story to tell Fertility and Sterility. 90. DOI: 10.1016/J.Fertnstert.2008.07.1678 |
0.619 |
|
| 2007 |
Bhatt S, Moradkhani K, Mrasek K, Puechberty J, Lefort G, Lespinasse J, Sarda P, Liehr T, Hamamah S, Pellestor F. Breakpoint characterization: a new approach for segregation analysis of paracentric inversion in human sperm. Molecular Human Reproduction. 13: 751-756. PMID 17913851 DOI: 10.1093/Molehr/Gam048 |
0.757 |
|
| 2007 |
Bhatt S, Puechberty J, Thomas L, Sarda P, Hamamah S, Pellestor F. Segregation analysis of two paracentric inversions using a new approach of breakpoint characterization Fertility and Sterility. 88. DOI: 10.1016/J.Fertnstert.2007.07.1143 |
0.546 |
|
| 2006 |
Moradkhani K, Puechberty J, Bhatt S, Lespinasse J, Vago P, Lefort G, Sarda P, Hamamah S, Pellestor F. Rare Robertsonian translocations and meiotic behaviour: sperm FISH analysis of t(13;15) and t(14;15) translocations: A Case Report Human Reproduction. 21: 3193-3198. PMID 16917122 DOI: 10.1093/Humrep/Del314 |
0.741 |
|
| 2006 |
Moradkhani K, Puechberty J, Bhatt S, Vago P, Janny L, Lefort G, Hamamah S, Sarda P, Pellestor F. Meiotic segregation of rare Robertsonian translocations: sperm analysis of three t(14q;22q) cases Human Reproduction. 21: 1166-1171. PMID 16439506 DOI: 10.1093/Humrep/Dei477 |
0.759 |
|
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