List of works - Stephen T Sherry

A mathematical approach to the analysis of multiplex DNA profiles

scientific article

A mechanism for controlled access to GWAS data: experience of the GAIN Data Access Committee

scientific article (publication date: 4 April 2013)

A robust benchmark for detection of germline large deletions and insertions

scientific article published on 15 June 2020

A second generation human haplotype map of over 3.1 million SNPs

scientific article

An open resource for accurately benchmarking small variant and reference calls

scientific article published on 01 April 2019

Assessing and managing risk when sharing aggregate genetic variant data

scientific article (publication date: 16 September 2011)

Assessing reproducibility of inherited variants detected with short-read whole genome sequencing

scientific article published on 03 January 2022

Author Correction: A robust benchmark for detection of germline large deletions and insertions

scientific article published on 22 July 2020

Characterizing genetic variants for clinical action

scientific article

ClinGen--the Clinical Genome Resource

scientific article

Completing the map of human genetic variation

scientific article published on May 2007

Consent Codes: Upholding Standard Data Use Conditions

scientific article

Data use under the NIH GWAS data sharing policy and future directions

scientific article published in September 2014

Database resources of the National Center for Biotechnology Information

scientific article (published 2012-01-01)

Database resources of the National Center for Biotechnology Information

scientific article

Database resources of the National Center for Biotechnology Information

scientific article (published 2010-01-01)

Database resources of the National Center for Biotechnology Information

scientific article (published 2006-01-01)

Database resources of the National Center for Biotechnology Information

scientific article (publication date: 2009)

Database resources of the National Center for Biotechnology Information

scientific article published on 23 October 2020

Databases in Human and Medical Genetics

article

Epidemiology. DNA identifications after the 9/11 World Trade Center attack

scientific article

Extensive sequencing of seven human genomes to characterize benchmark reference materials

scientific article

Federated discovery and sharing of genomic data using Beacons

scientific article published on 01 March 2019

GenBank

scientific article published on 16 November 2020

GenBank

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

scientific article

High-coverage, long-read sequencing of Han Chinese trio reference samples.

scientific article

Indexing pharmacogenetic knowledge on the World Wide Web.

scientific article published in January 2003

Inference and analysis of haplotypes from combined genotyping studies deposited in dbSNP

scientific article

Integrative annotation of 21,037 human genes validated by full-length cDNA clones

scientific article

Mitochondrial DNA and Y chromosome diversity and the peopling of the Americas: evolutionary and demographic evidence

scientific article published on July 2004

New approaches to dating suggest a recent age for the human mtDNA ancestor

scientific article published on August 29, 1992

Phenotype-Genotype Integrator (PheGenI): synthesizing genome-wide association study (GWAS) data with existing genomic resources

scientific article

Publisher Correction: Federated discovery and sharing of genomic data using Beacons

scientific article published on 01 April 2019

Quickly identifying identical and closely related subjects in large databases using genotype data

scientific article

Recommendations of the 2006 Human Variome Project meeting

scientific article published in April 2007

Registered access: authorizing data access

scientific article published on 2 August 2018

Sequence variations in the public human genome data reflect a bottlenecked population history

scientific article

Supplementing high-density SNP microarrays for additional coverage of disease-related genes: addiction as a paradigm

scientific article

The 1000 Genomes Project: data management and community access

scientific article (publication date: 27 April 2012)

The NCBI dbGaP database of genotypes and phenotypes

scientific article

The allele frequency spectrum in genome-wide human variation data reveals signals of differential demographic history in three large world populations

scientific article

The dbGaP data browser: a new tool for browsing dbGaP controlled-access genomic data

scientific article

Toward best practice in cancer mutation detection with whole-genome and whole-exome sequencing

scientific article published on 09 September 2021

List of works by Stephen T Sherry

A mathematical approach to the analysis of multiplex DNA profiles

A mechanism for controlled access to GWAS data: experience of the GAIN Data Access Committee

A robust benchmark for detection of germline large deletions and insertions

A second generation human haplotype map of over 3.1 million SNPs

An open resource for accurately benchmarking small variant and reference calls

Assessing and managing risk when sharing aggregate genetic variant data

Assessing reproducibility of inherited variants detected with short-read whole genome sequencing

Author Correction: A robust benchmark for detection of germline large deletions and insertions

Characterizing genetic variants for clinical action

ClinGen--the Clinical Genome Resource

Completing the map of human genetic variation

Consent Codes: Upholding Standard Data Use Conditions

Data use under the NIH GWAS data sharing policy and future directions

Database resources of the National Center for Biotechnology Information

Database resources of the National Center for Biotechnology Information

Database resources of the National Center for Biotechnology Information

Database resources of the National Center for Biotechnology Information

Database resources of the National Center for Biotechnology Information

Database resources of the National Center for Biotechnology Information

Database resources of the National Center for Biotechnology Information

Databases in Human and Medical Genetics

Epidemiology. DNA identifications after the 9/11 World Trade Center attack

Extensive sequencing of seven human genomes to characterize benchmark reference materials

Federated discovery and sharing of genomic data using Beacons

GenBank

GenBank

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

High-coverage, long-read sequencing of Han Chinese trio reference samples.

Indexing pharmacogenetic knowledge on the World Wide Web.

Inference and analysis of haplotypes from combined genotyping studies deposited in dbSNP

Integrative annotation of 21,037 human genes validated by full-length cDNA clones

Mitochondrial DNA and Y chromosome diversity and the peopling of the Americas: evolutionary and demographic evidence

New approaches to dating suggest a recent age for the human mtDNA ancestor

Phenotype-Genotype Integrator (PheGenI): synthesizing genome-wide association study (GWAS) data with existing genomic resources

Publisher Correction: Federated discovery and sharing of genomic data using Beacons

Quickly identifying identical and closely related subjects in large databases using genotype data

Recommendations of the 2006 Human Variome Project meeting

Registered access: authorizing data access

Sequence variations in the public human genome data reflect a bottlenecked population history

Supplementing high-density SNP microarrays for additional coverage of disease-related genes: addiction as a paradigm

The 1000 Genomes Project: data management and community access

The NCBI dbGaP database of genotypes and phenotypes

The allele frequency spectrum in genome-wide human variation data reveals signals of differential demographic history in three large world populations

The dbGaP data browser: a new tool for browsing dbGaP controlled-access genomic data

Toward best practice in cancer mutation detection with whole-genome and whole-exome sequencing