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Genetics
USA
2026

D-Index & Metrics

Genetics

D-Index
138
Citations
136697
World Ranking
193
National Ranking
101

Medicine

D-Index
137
Citations
136615
World Ranking
1851
National Ranking
1054

Research.com Recognitions

  • 2026 - Research.com Genetics in United States Leader Award
  • 2025 - Research.com Genetics in United States Leader Award
  • 2024 - Research.com Genetics in United States Leader Award
  • 2023 - Research.com Genetics in United States Leader Award
  • 2015 - Member of the National Academy of Sciences
  • 2014 - Fellow of the American Association for the Advancement of Science (AAAS)

Overview

Aravinda Chakravarti is affiliated with New York University Langone Medical Center in the United States. Their research primarily spans the fields of Biochemistry, Genetics and Molecular Biology, and Medicine, with a substantial body of work focused on subfields including Molecular Biology, Genetics, Surgery, Cardiology and Cardiovascular Medicine, and Infectious Diseases.

The main topics of Chakravarti's research encompass congenital gastrointestinal and neural anomalies, genetic associations and epidemiology, intestinal malrotation and obstruction disorders, genetic mapping and diversity in plants and animals, bioinformatics and genomic networks, congenital anomalies and fetal surgery, and digestive system and related health.

Frequent publication venues for Chakravarti include:

  • bioRxiv (Cold Spring Harbor Laboratory)
  • UNC Libraries
  • Genome Research
  • Proceedings of the National Academy of Sciences
  • Zenodo (CERN European Organization for Nuclear Research)

Some of their recent papers are:

  • The road ahead in genetics and genomics, 2020, Nature Reviews Genetics
  • Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16p, 2022, Nature Genetics
  • Pathogenic alleles in microtubule, secretory granule and extracellular matrix-related genes in familial keratoconus, 2021, Human Molecular Genetics
  • Insights From a Large-Scale Whole-Genome Sequencing Study of Systolic Blood Pressure, Diastolic Blood Pressure, and Hypertension, 2022, Hypertension
  • Ret deficiency decreases neural crest progenitor proliferation and restricts fate potential during enteric nervous system development, 2023, Proceedings of the National Academy of Sciences

Chakravarti has collaborated frequently with several co-authors, including:

  • Dongwon Lee
  • Or Yaacov
  • Nora Franceschini
  • Sumantra Chatterjee
  • Hanna Berk-Rauch

In recognition of their scientific contributions, Chakravarti was appointed as a Fellow of the American Association for the Advancement of Science (AAAS) in 2014 and was elected as a Member of the National Academy of Sciences in 2015.

Best Publications

  • A global reference for human genetic variation.

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

  • Finding the missing heritability of complex diseases

    Teri A. Manolio;Francis S. Collins;Nancy J. Cox;David B. Goldstein

  • The International HapMap Project

    John W. Belmont;Paul Hardenbol;Thomas D. Willis;Fuli Yu

  • A haplotype map of the human genome

    John W. Belmont;Andrew Boudreau;Suzanne M. Leal;Paul Hardenbol

  • Identification of the cystic fibrosis gene: genetic analysis.

    Bat Sheva Kerem;Johanna M. Rommens;Janet A. Buchanan;Danuta Markiewicz

  • A second generation human haplotype map of over 3.1 million SNPs

    Kelly A. Frazer;Dennis G. Ballinger;David R. Cox;David A. Hinds

  • Discovery and refinement of loci associated with lipid levels

    Cristen J. Willer;Ellen M. Schmidt;Sebanti Sengupta;Gina M. Peloso;Gina M. Peloso;Gina M. Peloso

  • Genome-wide detection and characterization of positive selection in human populations

    Pardis C. Sabeti;Pardis C. Sabeti;Patrick Varilly;Patrick Varilly;Ben Fry;Jason Lohmueller

  • Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

    S. Hong Lee;Stephan Ripke;Stephan Ripke;Benjamin M. Neale;Benjamin M. Neale;Stephen V. Faraone

  • Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk

    Georg B. Ehret;Georg B. Ehret;Georg B. Ehret;Patricia B. Munroe;Kenneth M. Rice;Murielle Bochud

  • Defining the role of common variation in the genomic and biological architecture of adult human height

    Andrew R. Wood;Tonu Esko;Jian Yang;Sailaja Vedantam

  • Association between Microdeletion and Microduplication at 16p11.2 and Autism

    Lauren A. Weiss;Yiping Shen;Joshua M. Korn;Joshua M. Korn;Dan E. Arking

  • Genome-wide association scan shows genetic variants in the FTO gene are associated with obesity-related traits.

    Angelo Scuteri;Serena Sanna;Wei-Min Chen;Manuela Uda

  • Genetic studies of body mass index yield new insights for obesity biology

    Adam E. Locke;Bratati Kahali;Sonja I. Berndt;Anne E. Justice

  • Genome-wide association study of blood pressure and hypertension

    Daniel Levy;Georg B. Ehret;Georg B. Ehret;Kenneth Rice;Germaine C. Verwoert

  • DNA duplication associated with Charcot-Marie-Tooth disease type 1A

    James R. Lupski;Roberto Montes de Oca-Luna;Susan Slaugenhaupt;Liu Pentao

  • VARIATIONS ON A THEME : CATALOGING HUMAN DNA SEQUENCE VARIATION

    Francis S. Collins;Mark S. Guyer;Aravinda Chakravarti

  • Patterns of single-nucleotide polymorphisms in candidate genes for blood-pressure homeostasis

    Marc K. Halushka;Jian Bing Fan;Kimberly Bentley;Linda Hsie

  • Development of Human Protein Reference Database as an Initial Platform for Approaching Systems Biology in Humans

    Suraj Peri;Suraj Peri;J. Daniel Navarro;J. Daniel Navarro;Ramars Amanchy;Troels Z. Kristiansen;Troels Z. Kristiansen

  • Mapping copy number variation by population-scale genome sequencing

    Ryan E. Mills;Klaudia Walter;Chip Stewart;Robert E. Handsaker

Frequent Co-Authors

Georg B. Ehret
Georg B. Ehret University of Geneva
Eric Boerwinkle
Eric Boerwinkle The University of Texas Health Science Center at Houston
Bruce M. Psaty
Bruce M. Psaty University of Washington
Dan E. Arking
Dan E. Arking Johns Hopkins University School of Medicine
Jaspal S. Kooner
Jaspal S. Kooner Imperial College London
Christopher Newton-Cheh
Christopher Newton-Cheh Harvard University
Jerome I. Rotter
Jerome I. Rotter UCLA Medical Center
Nilesh J. Samani
Nilesh J. Samani University of Leicester
Tonu Esko
Tonu Esko University of Tartu
André G. Uitterlinden
André G. Uitterlinden Erasmus University Rotterdam

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