2026 Namrata Gupta: Genetics Researcher – H-Index, Publications & Awards

Discipline name	D-Index	World Ranking	Current World Ranking	National Ranking	Current National Ranking	Publications	Citations
Genetics	69	2300	2186	1033	971	140	80501

Overview

Namrata Gupta is affiliated with the Broad Institute in the United States and has a research portfolio primarily situated within the fields of Biochemistry, Genetics and Molecular Biology, as well as Medicine. The scientist's work prominently addresses key areas of Genetics, Molecular Biology, and specialties including Pulmonary and Respiratory Medicine, Epidemiology, and Cardiology and Cardiovascular Medicine.

The research conducted by Namrata Gupta covers a spectrum of topics with a focus on Genetic Associations and Epidemiology, Genomics and Rare Diseases, as well as Bioinformatics and Genomic Networks. Further work includes investigations into Genomic variations and chromosomal abnormalities, Chronic Obstructive Pulmonary Disease (COPD) Research, Genomics and Phylogenetic Studies, and Epigenetics and DNA Methylation.

Gupta has contributed to multiple publications, with notable papers including:

The mutational constraint spectrum quantified from variation in 141,456 humans, 2020, Nature
A structural variation reference for medical and population genetics, 2020, Nature
A genomic mutational constraint map using variation in 76,156 human genomes, 2023, Nature
Pangenomics enables genotyping of known structural variants in 5202 diverse genomes, 2021, Science
A genome-wide mutational constraint map quantified from variation in 76,156 human genomes, 2022, bioRxiv (Cold Spring Harbor Laboratory)

The scientist frequently collaborates with peers such as Stacey Gabriel, Stephen S. Rich, Jerome I. Rotter, Diego Ardissino, and Mark J. Daly.

Namrata Gupta's research has been published extensively in outlets such as bioRxiv (Cold Spring Harbor Laboratory), Nature Communications, Nature, UNC Libraries, and The American Journal of Human Genetics.

Best Publications

A global reference for human genetic variation.

Adam Auton;Gonçalo R. Abecasis;David M. Altshuler;Richard M. Durbin

18403
Citations
An integrated map of genetic variation from 1,092 human genomes

Goncalo R Abecasis;Adam Auton;Lisa D Brooks

13558
Citations
Analysis of protein-coding genetic variation in 60,706 humans

Monkol Lek;Konrad J. Karczewski;Konrad J. Karczewski;Eric V. Minikel;Eric V. Minikel;Kaitlin E. Samocha

10685
Citations
The mutational constraint spectrum quantified from variation in 141,456 humans

Konrad J. Karczewski;Laurent C. Francioli;Grace Tiao;Beryl B. Cummings

8404
Citations
The mutational constraint spectrum quantified from variation in 141,456 humans

Konrad J. Karczewski;em> ..] Laurent C. Francioli;Daniel G. MacArthur

6800
Citations
Genetics of rheumatoid arthritis contributes to biology and drug discovery

Yukinori Okada;Yukinori Okada;Di Wu;Di Wu;Di Wu;Gosia Trynka;Gosia Trynka;Towfique Raj;Towfique Raj

2654
Citations
Clonal Hematopoiesis and risk of atherosclerotic cardiovascular disease

Siddhartha Jaiswal;Pradeep Natarajan;Pradeep Natarajan;Alexander J. Silver;Christopher J. Gibson

2130
Citations
The major genetic determinants of HIV-1 control affect HLA class I peptide presentation

Pereyra F;Jia X;McLaren Pj

1679
Citations
A structural variation reference for medical and population genetics

Ryan L Collins;Ryan L Collins;Harrison Brand;Harrison Brand;Konrad J Karczewski;Konrad J Karczewski;Xuefang Zhao;Xuefang Zhao

1135
Citations
A global reference for human genetic variation

Adam Auton;Gonçalo R. Abecasis;David M. Altshuler;Richard M. Durbin

963
Citations
Diagnostic Yield and Clinical Utility of Sequencing Familial Hypercholesterolemia Genes in Patients With Severe Hypercholesterolemia

Amit V. Khera;Amit V. Khera;Hong Hee Won;Gina M. Peloso;Gina M. Peloso;Kim S. Lawson

909
Citations
Loss-of-function mutations in APOC3, triglycerides, and coronary disease

Jacy Crosby;Gina M. Peloso;Gina M. Peloso;Paul L. Auer;David R. Crosslin

892
Citations
Multi-Ethnic Genome-wide Association Study for Atrial Fibrillation

Carolina Roselli;Mark D. Chaffin;Lu Chen Weng;Lu Chen Weng;Stefanie Aeschbacher

769
Citations
Somatic ERCC2 Mutations Correlate with Cisplatin Sensitivity in Muscle-Invasive Urothelial Carcinoma

Eliezer M Van Allen;Kent W. Mouw;Philip Kim;Gopa Iyer

598
Citations
Inactivating mutations in NPC1L1 and protection from coronary heart disease

Nathan O. Stitziel;Hong Hee Won;Alanna C. Morrison;Gina M. Peloso

565
Citations
Exome sequencing and the genetic basis of complex traits

Adam Kiezun;Kiran Garimella;Ron Do;Ron Do;Nathan O Stitziel;Nathan O Stitziel

491
Citations
ANGPTL3 Deficiency and Protection Against Coronary Artery Disease

Nathan O. Stitziel;Amit V. Khera;Xiao Wang;Andrew J. Bierhals

424
Citations
Human knockouts and phenotypic analysis in a cohort with a high rate of consanguinity.

Danish Saleheen;Pradeep Natarajan;Pradeep Natarajan;Irina M. Armean;Irina M. Armean;Wei Zhao

332
Citations
Genetic Interleukin 6 Signaling Deficiency Attenuates Cardiovascular Risk in Clonal Hematopoiesis

Alexander G. Bick;James P. Pirruccello;Gabriel K. Griffin;Gabriel K. Griffin;Gabriel K. Griffin;Namrata Gupta

325
Citations
Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci

Alexandra Zhernakova;Alexandra Zhernakova;Alexandra Zhernakova;Eli A. Stahl;Eli A. Stahl;Gosia Trynka;Soumya Raychaudhuri;Soumya Raychaudhuri

1
Citations

Frequent Co-Authors

Sekar Kathiresan Harvard University

Stacey Gabriel Broad Institute

Mark J. Daly Massachusetts General Hospital

Eric S. Lander Broad Institute

Amit Khera Harvard University

Daniel G. MacArthur Garvan Institute of Medical Research

Anne H. O’Donnell-Luria Broad Institute

Benjamin M. Neale Harvard University

Konrad J. Karczewski Harvard University

Eric Boerwinkle The University of Texas Health Science Center at Houston

External Links

Personal website of Namrata Gupta

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