Sumantra Chatterjee
Sumantra Chatterjee
Senior Research Scientist, NYU Langone Health
Verified email at
Cited by
Cited by
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
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
Gene regulatory elements, major drivers of human disease
S Chatterjee, N Ahituv
Annual review of genomics and human genetics 18, 45-63, 2017
A symphony of inner ear developmental control genes
S Chatterjee, P Kraus, T Lufkin
BMC genetics 11 (1), 68, 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
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
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
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), 63, 2011
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
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 Sox9 …
S Chatterjee, V Sivakamasundari, SP Yap, P Kraus, V Kumar, X Xing, ...
BMC genomics 15 (1), 1-18, 2014
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, 2017
Fishing for function: zebrafish BAC transgenics for functional genomics
S Chatterjee, T Lufkin
Molecular BioSystems 7 (8), 2345-2351, 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 (2), 299-304, 2010
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
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
Regulatory genomics: Insights from the zebrafish
S Chatterjee, T Lufkin
Current topics in genetics 5, 1, 2012
The sound of silence: mouse models for hearing loss
S Chatterjee, T Lufkin
Genetics research international 2011, 2011
Making no bones about it: transcription factors in vertebrate skeletogenesis and disease
S Chatterjee, V Sivakamasundari, WJ Lee, HY Chan, T Lufkin
Trends in developmental biology 6, 45, 2012
A gene regulatory network explains RETEDNRB epistasis in Hirschsprung disease
S Chatterjee, A Chakravarti
Human molecular genetics 28 (18), 3137-3147, 2019
A conditional mouse line for lineage tracing of Sox9 loss-of-function cells using enhanced green fluorescent protein
S Chatterjee, P Kraus, V Sivakamasundari, X Xing, SP Yap, S Jie, T Lufkin
Biotechnology letters 35 (12), 1991-1996, 2013
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