Gene regulatory elements, major drivers of human disease S Chatterjee, N Ahituv Annual review of genomics and human genetics 18, 45-63, 2017 | 162 | 2017 |
Molecular genetic anatomy and risk profile of Hirschsprung’s disease JM Tilghman, AY Ling, TN Turner, MX Sosa, N Krumm, S Chatterjee, ... New England Journal of Medicine 380 (15), 1421-1432, 2019 | 148 | 2019 |
Enhancer variants synergistically drive dysfunction of a gene regulatory network in Hirschsprung disease S Chatterjee, A Kapoor, JA Akiyama, DR Auer, D Lee, S Gabriel, ... Cell 167 (2), 355-368. e10, 2016 | 120 | 2016 |
An enhancer polymorphism at the cardiomyocyte intercalated disc protein NOS1AP locus is a major regulator of the QT interval A Kapoor, RB Sekar, NF Hansen, K Fox-Talbot, M Morley, V Pihur, ... The American Journal of Human Genetics 94 (6), 854-869, 2014 | 102 | 2014 |
A symphony of inner ear developmental control genes S Chatterjee, P Kraus, T Lufkin BMC genetics 11, 1-15, 2010 | 75 | 2010 |
Population variation in total genetic risk of Hirschsprung disease from common RET, SEMA3 and NRG1 susceptibility polymorphisms A Kapoor, Q Jiang, S Chatterjee, P Chakraborty, MX Sosa, C Berrios, ... Human molecular genetics 24 (10), 2997-3003, 2015 | 73 | 2015 |
Effects of RET and NRG1 polymorphisms in Indonesian patients with Hirschsprung disease A Kapoor, AY Ling, A Makhmudi, ES Herini, MX Sosa, S Chatterjee, ... Journal of pediatric surgery 49 (11), 1614-1618, 2014 | 42 | 2014 |
Conserved and non-conserved enhancers direct tissue specific transcription in ancient germ layer specific developmental control genes S Chatterjee, G Bourque, T Lufkin BMC developmental biology 11, 1-16, 2011 | 35 | 2011 |
A gene regulatory network explains RET–EDNRB epistasis in Hirschsprung disease S Chatterjee, A Chakravarti Human Molecular Genetics 28 (18), 3137-3147, 2019 | 25 | 2019 |
Genome-wide association study of Hirschsprung disease detects a novel low-frequency variant at the RET locus J Fadista, M Lund, L Skotte, F Geller, P Nandakumar, S Chatterjee, ... European Journal of Human Genetics 26 (4), 561-569, 2018 | 25 | 2018 |
Intestinal neuronal dysplasia-like submucosal ganglion cell hyperplasia at the proximal margins of Hirschsprung disease resections M Swaminathan, AP Oron, S Chatterjee, H Piper, S Cope-Yokoyama, ... Pediatric and Developmental Pathology 18 (6), 466-476, 2015 | 25 | 2015 |
Coding and noncoding variants in EBF3 are involved in HADDS and simplex autism EM Padhi, TJ Hayeck, Z Cheng, S Chatterjee, BJ Mannion, ... Human genomics 15, 1-15, 2021 | 21 | 2021 |
In vivo genome-wide analysis of multiple tissues identifies gene regulatory networks, novel functions and downstream regulatory genes for Bapx1 and its co-regulation with … S Chatterjee, V Sivakamasundari, SP Yap, P Kraus, V Kumar, X Xing, ... BMC genomics 15, 1-18, 2014 | 20 | 2014 |
Gene-and tissue-level interactions in normal gastrointestinal development and Hirschsprung disease S Chatterjee, P Nandakumar, DR Auer, SB Gabriel, A Chakravarti Proceedings of the National Academy of Sciences 116 (52), 26697-26708, 2019 | 19 | 2019 |
An integrative developmental genomics and systems biology approach to identify an in vivo sox trio‐mediated gene regulatory network in murine embryos WJ Lee, S Chatterjee, SP Yap, SL Lim, X Xing, P Kraus, W Sun, X Hu, ... BioMed Research International 2017 (1), 8932583, 2017 | 19 | 2017 |
The sound of silence: mouse models for hearing loss S Chatterjee, T Lufkin Genetics research international 2011 (1), 416450, 2011 | 17 | 2011 |
The role of post-transcriptional RNA processing and plasmid vector sequences on transient transgene expression in zebrafish S Chatterjee, L Min, RKM Karuturi, T Lufkin Transgenic research 19, 299-304, 2010 | 17 | 2010 |
Effects of MTHFR c.677C>T, F2 c.20210G>A and F5 Leiden Polymorphisms in Gastroschisis A Makhmudi, AH Sadewa, T Aryandono, S Chatterjee, HA Heij, Gunadi Journal of Investigative Surgery 29 (2), 88-92, 2016 | 13 | 2016 |
Fishing for function: zebrafish BAC transgenics for functional genomics S Chatterjee, T Lufkin Molecular BioSystems 7 (8), 2345-2351, 2011 | 13 | 2011 |
A multi-enhancer RET regulatory code is disrupted in Hirschsprung disease S Chatterjee, KM Karasaki, LE Fries, A Kapoor, A Chakravarti Genome Research 31 (12), 2199-2208, 2021 | 12 | 2021 |