Author

Ashish Kapoor

Observed names: A Kapoor, A. Kapoor

Institution: Harcourt Butler Technical University

Observed institutions: University of Geneva, Howard Hughes Medical Institute, Johns Hopkins University, Jawaharlal Nehru Centre for Advanced Scientific Research, University of Washington, Johns Hopkins Medicine, Harcourt Butler Technical University, The University of Texas Health Science Center at Houston

ORCID: 0000-0003-3977-6140

Observed ORCID: 0000-0003-3977-6140

OpenAlex ID: A5078150431

Molecular Genetic Anatomy and Risk Profile of Hirschsprung’s Disease

2019 · Joseph M. Tilghman, Albee Y. Ling, et al. · New England Journal of Medicine · 193

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Enhancer Variants Synergistically Drive Dysfunction of a Gene Regulatory Network In Hirschsprung Disease

2016 · Sumantra Chatterjee, Ashish Kapoor, et al. · Cell · 140

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Functional Loss of Semaphorin 3C and/or Semaphorin 3D and Their Epistatic Interaction with Ret Are Critical to Hirschsprung Disease Liability

2015 · Qian Jiang, Stacey Arnold, et al. · The American Journal of Human Genetics · 136

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An Enhancer Polymorphism at the Cardiomyocyte Intercalated Disc Protein NOS1AP Locus Is a Major Regulator of the QT Interval

2014 · Ashish Kapoor, Rajesh B. Sekar, et al. · The American Journal of Human Genetics · 82

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An idiopathic epilepsy syndrome linked to 3q13.3‐q21 and missense mutations in the extracellular calcium sensing receptor gene

2008 · Ashish Kapoor, Parthasarathy Satishchandra, et al. · Annals of Neurology · 78

Population variation in total genetic risk of Hirschsprung disease from common RET, SEMA3 and NRG1 susceptibility polymorphisms

2015 · Ashish Kapoor, Qian Jiang, et al. · Human Molecular Genetics · 68

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A Multicenter Study of BRD2 as a Risk Factor for Juvenile Myoclonic Epilepsy

2007 · Gianpiero L. Cavalleri, Nicole M. Walley, et al. · Epilepsia · 63

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Trans-ethnic meta-analysis of genome-wide association studies for Hirschsprung disease

2016 · Clara Sze-man Tang, Hongsheng Gui, et al. · Human Molecular Genetics · 42

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Effects of RET and NRG1 polymorphisms in Indonesian patients with Hirschsprung disease

2014 · Gunadi, Ashish Kapoor, et al. · Journal of Pediatric Surgery · 41

Human genome meeting 2016

2016 · GUSTO study group, A. K. Srivastava, et al. · Human Genomics · 40

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Human cardiac cis -regulatory elements, their cognate transcription factors, and regulatory DNA sequence variants

2018 · Dongwon Lee, Ashish Kapoor, et al. · Genome Research · 28

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A multi-enhancer RET regulatory code is disrupted in Hirschsprung disease

2021 · Sumantra Chatterjee, Kameko M Karasaki, et al. · Genome Research · 27

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Multiple SCN5A variant enhancers modulate its cardiac gene expression and the QT interval

2019 · Ashish Kapoor, Dongwon Lee, et al. · Proceedings of the National Academy of Sciences · 22

Mendelian Puzzles

2012 · Aravinda Chakravarti, Ashish Kapoor · Science · 18

Absence ofGABRA1 Ala322Asp mutation in juvenile myoclonic epilepsy families from India

2003 · A. Kapoor, J. Vijai, et al. · Journal of Genetics · 18

Combined Genetic Effects of RET and NRG1 Susceptibility Variants on Multifactorial Hirschsprung Disease in Indonesia

2018 · Gunadi, Kristy Iskandar, et al. · Journal of Surgical Research · 16

Genetic association analysis of KCNQ3 and juvenile myoclonic epilepsy in a South Indian population

2003 · J. Vijai, A. Kapoor, et al. · Human Genetics · 16

HPASubC: A suite of tools for user subclassification of human protein atlas tissue images

2015 · Toby C. Cornish, Aravinda Chakravarti, et al. · Journal of Pathology Informatics · 14

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A novel genetic locus for juvenile myoclonic epilepsy at chromosome 5q12–q14

2007 · Ashish Kapoor, R. Ratnapriya, et al. · Human Genetics · 14

Rare coding TTN variants are associated with electrocardiographic QT interval in the general population

2016 · Ashish Kapoor, Kiranmayee Bakshy, et al. · Scientific Reports · 12

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Testing the Ret and Sema3d genetic interaction in mouse enteric nervous system development

2017 · Ashish Kapoor, Dallas R. Auer, et al. · Human Molecular Genetics · 9

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Protective and susceptibility effects of hSKCa3 allelic variants on juvenile myoclonic epilepsy

2005 · J Vijai, A Kapoor, et al. · Journal of Medical Genetics · 9

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Sequence-based correction of barcode bias in massively parallel reporter assays

2021 · Dongwon Lee, Ashish Kapoor, et al. · Genome Research · 8

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Multiple, independent, common variants at RET, SEMA3 and NRG1 gut enhancers specify Hirschsprung disease risk in European ancestry subjects

2020 · Ashish Kapoor, Priyanka Nandakumar, et al. · Journal of Pediatric Surgery · 7

Cardiac muscle–restricted partial loss of Nos1ap expression has limited but significant impact on electrocardiographic features

2023 · Alexa Smith, Dallas Auer, et al. · G3 Genes Genomes Genetics · 5

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Works count: 34

Citation count: 1,120

H-index: 16

I10-index: 20