| Genomic and genic deletions of the FOX gene cluster on 16q24. 1 and inactivating mutations of FOXF1 cause alveolar capillary dysplasia and other malformations P Stankiewicz, P Sen, SS Bhatt, M Storer, Z Xia, BA Bejjani, Z Ou, ... The American Journal of Human Genetics 84 (6), 780-791, 2009 | 438 | 2009 |
| Insights into Sex Chromosome Evolution and Aging from the Genome of a Short-Lived Fish K Reichwald, A Petzold, P Koch, BR Downie, N Hartmann, S Pietsch, ... Cell 163 (6), 1527-1538, 2015 | 276 | 2015 |
| Prenatal Maternal Stress Predicts Methylation of Genes Regulating the Hypothalamic-Pituitary-Adrenocortical System in Mothers and Newborns in the Democratic Republic of Congo DA Kertes, HS Kamin, H D A, NC Rodney, S Bhatt, CJ Mulligan Child Development 87 (1), 61-72, 2016 | 214 | 2016 |
| A small recurrent deletion within 15q13. 3 is associated with a range of neurodevelopmental phenotypes M Shinawi, CP Schaaf, SS Bhatt, Z Xia, A Patel, SW Cheung, B Lanpher, ... Nature genetics 41 (12), 1269-1271, 2009 | 214 | 2009 |
| Microdeletion and microduplication syndromes A Weise, K Mrasek, E Klein, M Mulatinho, JC Llerena Jr, D Hardekopf, ... Journal of Histochemistry & Cytochemistry 60 (5), 346-358, 2012 | 212 | 2012 |
| Rare pathogenic microdeletions and tandem duplications are microhomology-mediated and stimulated by local genomic architecture LELM Vissers, SS Bhatt, IM Janssen, Z Xia, SR Lalani, R Pfundt, ... Human molecular genetics 18 (19), 3579-3593, 2009 | 173 | 2009 |
| Effect of Pet Dogs on Children's Perceived Stress and Cortisol Stress Response DA Kertes, J Liu, NJ Hall, NA Hadad, CDL Wynne, SS Bhatt Social Development 26 (2), 382-401, 2017 | 121 | 2017 |
| Chromosome distribution in human sperm–a 3D multicolor banding-study M Manvelyan, F Hunstig, S Bhatt, K Mrasek, F Pellestor, A Weise, ... Molecular cytogenetics 1, 1-8, 2008 | 90 | 2008 |
| BNDF methylation in mothers and newborns is associated with maternal exposure to war trauma DA Kertes, SS Bhatt, HS Kamin, DA Hughes, NC Rodney, CJ Mulligan Clinical Epigenetics 9 (1), 68, 2017 | 83 | 2017 |
| Heteromorphic variants of chromosome 9 N Kosyakova, A Grigorian, T Liehr, M Manvelyan, I Simonyan, ... Molecular cytogenetics 6, 1-11, 2013 | 73 | 2013 |
| Recurrent deletions and reciprocal duplications of 10q11. 21q11. 23 including CHAT and SLC18A3 are likely mediated by complex low‐copy repeats P Stankiewicz, S Kulkarni, AV Dharmadhikari, S Sampath, SS Bhatt, ... Human mutation 33 (1), 165-179, 2012 | 56 | 2012 |
| The human genome puzzle—the role of copy number variation in somatic mosaicism H Mkrtchyan, M Gross, S Hinreiner, A Polytiko, M Manvelyan, K Mrasek, ... Current genomics 11 (6), 426-431, 2010 | 51 | 2010 |
| Alu-specific microhomology-mediated deletions in CDKL5 in females with early-onset seizure disorder A Erez, AJ Patel, X Wang, Z Xia, SS Bhatt, W Craigen, SW Cheung, ... Neurogenetics 10, 363-369, 2009 | 49 | 2009 |
| Rare Robertsonian translocations and meiotic behaviour: sperm FISH analysis of t (13; 15) and t (14; 15) translocations: a case report K Moradkhani, J Puechberty, S Bhatt, J Lespinasse, P Vago, G Lefort, ... Human Reproduction 21 (12), 3193-3198, 2006 | 45 | 2006 |
| Position of chromosomes 18, 19, 21 and 22 in 3D-preserved interphase nuclei of human and gorilla and white hand gibbon M Manvelyan, F Hunstig, K Mrasek, S Bhatt, F Pellestor, A Weise, T Liehr Molecular cytogenetics 1 (1), 1-7, 2008 | 34 | 2008 |
| Human ring chromosomes–new insights for their clinical significance RS Guilherme, E Klein, AB Hamid, S Bhatt, M Volleth, A Polityko, ... Balkan Journal of Medical Genetics 16 (1), 13-19, 2013 | 30 | 2013 |
| Complex translocation disrupting TCF4 and altering TCF4 isoform expression segregates as mild autosomal dominant intellectual disability V Maduro, BN Pusey, PF Cherukuri, P Atkins, C du Souich, R Rupps, ... Orphanet journal of rare diseases 11 (1), 1-15, 2016 | 27 | 2016 |
| Meiotic segregation of rare Robertsonian translocations: sperm analysis of three t (14q; 22q) cases K Moradkhani, J Puechberty, S Bhatt, P Vago, L Janny, G Lefort, ... Human Reproduction 21 (5), 1166-1171, 2006 | 27 | 2006 |
| Evidence for correlation of fragile sites and chromosomal breakpoints in carriers of constitutional balanced chromosomal rearrangements T Liehr, N Kosayakova, J Schröder, M Ziegler, K Kreskowski, B Pohle, ... Balkan Journal of Medical Genetics 14 (2), 13-16, 2011 | 24 | 2011 |
| Breakpoint mapping and complete analysis of meiotic segregation patterns in three men heterozygous for paracentric inversions S Bhatt, K Moradkhani, K Mrasek, J Puechberty, M Manvelyan, F Hunstig, ... European Journal of Human Genetics 17 (1), 44-50, 2009 | 23 | 2009 |
Darlene KertesUniversity of FloridaVerified email at ufl.edu
