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Biology and Biochemistry

D-Index
62
Citations
125745
World Ranking
10491
National Ranking
4551

Overview

Stephen T. Sherry is affiliated with the National Institutes of Health in the United States. Their research primarily focuses on the fields of biochemistry, genetics, and molecular biology, spanning a total of 30 publications in these areas. The scientist's subfields of study include molecular biology, genetics, ecology, cancer research, and plant science.

The work of Stephen T. Sherry covers a range of topics, including:

  • Genomics and Phylogenetic Studies
  • Genomics and Rare Diseases
  • Molecular Biology Techniques and Applications
  • Cancer Genomics and Diagnostics
  • Genetics, Bioinformatics, and Biomedical Research
  • Bacteriophages and microbial interactions
  • RNA and protein synthesis mechanisms

The scientist has contributed frequently to notable publication venues such as:

  • Nucleic Acids Research
  • Nature Biotechnology
  • UNC Libraries
  • Genome Biology

Recent papers associated with Stephen T. Sherry include:

  • Database resources of the national center for biotechnology information, 2021, published in Nucleic Acids Research
  • Database resources of the National Center for Biotechnology Information, 2020, published in Nucleic Acids Research
  • A robust benchmark for detection of germline large deletions and insertions, 2020, published in Nature Biotechnology
  • Database resources of the National Center for Biotechnology Information in 2023, 2022, published in Nucleic Acids Research
  • GenBank, 2020, published in Nucleic Acids Research

Stephen T. Sherry has collaborated frequently with several coauthors, including:

  • Eric W Sayers
  • Kim D. Pruitt
  • Chunlin Xiao
  • Evan Bolton
  • Donald C. Comeau

Best Publications

  • A global reference for human genetic variation.

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

  • The variant call format and VCFtools

    Petr Danecek;Adam Auton;Goncalo Abecasis;Cornelis A. Albers

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

    Goncalo R Abecasis;Adam Auton;Lisa D Brooks

  • dbSNP: the NCBI database of genetic variation

    Stephen T. Sherry;Minghong Ward;M. Kholodov;J. Baker

  • Table S2: Trans-factors and trinucleotide repeat instability Trans-factor

    Arturo López Castel;John D Cleary;Christopher E Pearson

  • 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

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

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

  • 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

  • Mapping copy number variation by population-scale genome sequencing

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

  • The NCBI dbGaP database of genotypes and phenotypes.

    Matthew D Mailman;Michael Feolo;Yumi Jin;Masato Kimura

  • ClinGen — The Clinical Genome Resource

    Heidi L. Rehm;Jonathan S. Berg;Lisa D. Brooks;Carlos D. Bustamante

  • dbSNP-database for single nucleotide polymorphisms and other classes of minor genetic variation.

    Stephen T. Sherry;Minghong Ward;Karl Sirotkin

  • A global reference for human genetic variation

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

  • The Genetic Structure of Ancient Human Populations

    Henry C. Harpending;Stephen T. Sherry;Alan R. Rogers;Mark Stoneking

  • Genetic traces of ancient demography

    Henry C. Harpending;Mark A. Batzer;Michael Gurven;Lynn B. Jorde

  • Extensive sequencing of seven human genomes to characterize benchmark reference materials

    Justin M. Zook;David Catoe;Jennifer McDaniel;Lindsay Vang

  • dbSNP: a database of single nucleotide polymorphisms.

    Elizabeth M. Smigielski;Karl Sirotkin;Minghong Ward;Stephen T. Sherry

  • A map of human genome variation from population-scale sequencing

    Richard M. Durbin;David L. Altshuler;Gonçalo R. Abecasis;David R. Bentley

  • Integrative Annotation of 21,037 Human Genes Validated by Full-Length cDNA Clones

    Tadashi Imanishi;Takeshi Itoh;Yutaka Suzuki;Claire O'Donovan

Frequent Co-Authors

Mark A. Batzer
Mark A. Batzer Louisiana State University
Mark Stoneking
Mark Stoneking Max Planck Society
Paul Flicek
Paul Flicek The Jackson Laboratory
Mark J. Daly
Mark J. Daly Massachusetts General Hospital
Bartha Maria Knoppers
Bartha Maria Knoppers McGill University Health Centre
Gonçalo R. Abecasis
Gonçalo R. Abecasis University of Michigan–Ann Arbor
Aravinda Chakravarti
Aravinda Chakravarti New York University Langone Medical Center
David Altshuler
David Altshuler Harvard University
Richard A. Gibbs
Richard A. Gibbs Baylor College of Medicine
Stephen F. Schaffner
Stephen F. Schaffner Broad Institute

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