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Author Details

Stephen T Sherry
National Center for Biotechnology Information, National Institutes of Health
1991
72
47
PMIDPaper TitleJournal TitlePublished Year
37889039GenBank 2024 Update.Nucleic Acids Res2024
36350640GenBank 2023 update.Nucleic Acids Res2023
36370100Database resources of the National Center for Biotechnology Information in 2023.Nucleic Acids Res2023
34850943GenBank.Nucleic Acids Res2022
34850941Database resources of the national center for biotechnology information.Nucleic Acids Res2022
33095870Database resources of the National Center for Biotechnology Information.Nucleic Acids Res2021
34504347Establishing community reference samples, data and call sets for benchmarking cancer mutation detection using whole-genome sequencing.Nat Biotechnol2021
34504346Toward best practice in cancer mutation detection with whole-genome and whole-exome sequencing.Nat Biotechnol2021
33196830GenBank.Nucleic Acids Res2021
32541955A robust benchmark for detection of germline large deletions and insertions.Nat Biotechnol2020
32699374Author Correction: A robust benchmark for detection of germline large deletions and insertions.Nat Biotechnol2020
30936564An open resource for accurately benchmarking small variant and reference calls.Nat Biotechnol2019
31201313High-coverage, long-read sequencing of Han Chinese trio reference samples.Sci Data2019
30894680Publisher Correction: Federated discovery and sharing of genomic data using Beacons.Nat Biotechnol2019
30069064Registered access: authorizing data access.Eur J Hum Genet2018
27899644The dbGaP data browser: a new tool for browsing dbGaP controlled-access genomic data.Nucleic Acids Res2017
28609482Quickly identifying identical and closely related subjects in large databases using genotype data.PLoS One2017
26796797Consent Codes: Upholding Standard Data Use Conditions.PLoS Genet2016
27643465DNA Commission of the International Society for Forensic Genetics: Recommendations on the validation of software programs performing biostatistical calculations for forensic genetics applications.Forensic Sci Int Genet2016
27271295Extensive sequencing of seven human genomes to characterize benchmark reference materials.Sci Data2016
26014595ClinGen--the Clinical Genome Resource.N Engl J Med2015
23695286Phenotype-Genotype Integrator (PheGenI): synthesizing genome-wide association study (GWAS) data with existing genomic resources.Eur J Hum Genet2014
25162809Data use under the NIH GWAS data sharing policy and future directions.Nat Genet2014
24634402Characterizing genetic variants for clinical action.Am J Med Genet C Semin Med Genet2014
23561843A mechanism for controlled access to GWAS data: experience of the GAIN Data Access Committee.Am J Hum Genet2013
22140104Database resources of the National Center for Biotechnology Information.Nucleic Acids Res2012
22543379The 1000 Genomes Project: data management and community access.Nat Methods2012
21097890Database resources of the National Center for Biotechnology Information.Nucleic Acids Res2011
21921928Assessing and managing risk when sharing aggregate genetic variant data.Nat Rev Genet2011
21653522The variant call format and VCFtools.Bioinformatics2011
21103945A mathematical approach to the analysis of multiplex DNA profiles.Bull Math Biol2011
19910364Database resources of the National Center for Biotechnology Information.Nucleic Acids Res2010
18940862Database resources of the National Center for Biotechnology Information.Nucleic Acids Res2009
19381300Supplementing high-density SNP microarrays for additional coverage of disease-related genes: addiction as a paradigm.PLoS One2009
18045790Database resources of the National Center for Biotechnology Information.Nucleic Acids Res2008
17170002Database resources of the National Center for Biotechnology Information.Nucleic Acids Res2007
17898773The NCBI dbGaP database of genotypes and phenotypes.Nat Genet2007
17943131Genome-wide detection and characterization of positive selection in human populations.Nature2007
17943122A second generation human haplotype map of over 3.1 million SNPs.Nature2007
17728769New models of collaboration in genome-wide association studies: the Genetic Association Information Network.Nat Genet2007
17495918Completing the map of human genetic variation.Nature2007
17392799Recommendations of the 2006 Human Variome Project meeting.Nat Genet2007
16381840Database resources of the National Center for Biotechnology Information.Nucleic Acids Res2006
15608222Database resources of the National Center for Biotechnology Information.Nucleic Acids Res2005
16293742Epidemiology. DNA identifications after the 9/11 World Trade Center attack.Science2005
16251470Inference and analysis of haplotypes from combined genotyping studies deposited in dbSNP.Genome Res2005
15103394Integrative annotation of 21,037 human genes validated by full-length cDNA clones.PLoS Biol2004
15214060Mitochondrial DNA and Y chromosome diversity and the peopling of the Americas: evolutionary and demographic evidence.Am J Hum Biol2004
15020430The allele frequency spectrum in genome-wide human variation data reveals signals of differential demographic history in three large world populations.Genetics2004
12502794Sequence variations in the public human genome data reflect a bottlenecked population history.Proc Natl Acad Sci U S A2003
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Collaborators

Kim D Pruitt
National Center for Biotechnology Information, National Institutes of Health
Co-authored papers 15
Michael Feolo
University of Massachusetts Medical School
Co-authored papers 15
Donna R Maglott
National Center for Biotechnology Information, National Institutes of Health
Co-authored papers 13
Deanna M Church
Present address: Inscripta Inc.
Co-authored papers 10
Mark A Batzer
Louisiana State University
Co-authored papers 10
Chunlin Xiao
Chongqing Aier Eye Hospital
Co-authored papers 8
Wolfgang Helmberg
Medical University of Graz
Co-authored papers 8
Ilene Karsch-Mizrachi
Co-authored papers 8
Stephen H Bryant
National Center for Biotechnology Information
Co-authored papers 8
Tanya Barrett
National Center for Biotechnology Information, National Institutes of Health
Co-authored papers 8
Michael DiCuccio
National Center for Biotechnology Information, National Institutes of Health
Co-authored papers 8
Alexandre Souvorov
Co-authored papers 7
Yuri Kapustin
National Center for Biotechnology Information, National Institutes of Health
Co-authored papers 7
Erin M Ramos
National Human Genome Research Institute
Co-authored papers 6
Evan E Bolton
National Center for Biotechnology Information, National Institutes of Health
Co-authored papers 6
James C Mullikin
National Human Genome Research Institute, National Institutes of Health
Co-authored papers 6
Zhiyong Lu
National Center for Biotechnology Information, National Institutes of Health.
Co-authored papers 6
Lisa D Brooks
National Human Genome Research Institute, National Institutes of Health
Co-authored papers 6
Aron Marchler-Bauer
National Center for Biotechnology Information, National Institutes of Health
Co-authored papers 6
Laura Lyman Rodriguez
Patient-Centered Outcomes Research Institute
Co-authored papers 5
Christopher E Mason
Feil Family Brain and Mind Research Institute.
Co-authored papers 5
Marc Salit
Stanford University
Co-authored papers 5
Ron Edgar
Co-authored papers 5
Paul Flicek
European Bioinformatics Institute
Co-authored papers 5
Pui-Yan Kwok
Cardiovascular Research Institute, University of California San Francisco
Co-authored papers 5
Justin M Zook
National Institute of Standards and Technology
Co-authored papers 5
Anthony J Brookes
University of Leicester
Co-authored papers 5
Nathan D Olson
National Institute of Standards and Technology
Co-authored papers 4
Lincoln Stein
Ontario Institute for Cancer Research, University Avenue
Co-authored papers 4
Mark J Daly
Massachusetts General Hospital
Co-authored papers 4
Release 1.2