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

Por Marth, Gabor T, Czabarka, Eva, Murvai, Janos, Sherry, Stephen T
Publicado em 2004

dbSNP: a database of single nucleotide polymorphisms

Por Smigielski, Elizabeth M., Sirotkin, Karl, Ward, Minghong, Sherry, Stephen T.
Publicado em 2000

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

Por Jin, Yumi, Schäffer, Alejandro A., Sherry, Stephen T., Feolo, Michael
Publicado no PLoS One (2017)

A Mathematical Approach to the Analysis of Multiplex DNA Profiles

Por Goor, Robert M., Neall, Lisa Forman, Hoffman, Douglas, Sherry, Stephen T.
Publicado em 2010

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

Por Zaitlen, Noah A., Kang, Hyun Min, Feolo, Michael L., Sherry, Stephen T., Halperin, Eran, Eskin, Eleazar
Publicado em 2005

Genetic traces of ancient demography

Por Harpending, Henry C., Batzer, Mark A., Gurven, Michael, Jorde, Lynn B., Rogers, Alan R., Sherry, Stephen T.
Publicado em 1998

Assessing and Managing Risk when Sharing Aggregate Genetic Variant Data

Por Craig, David W., Goor, Robert, Wang, Zhenyan, Paschall, Justin, Ostell, Jim, Feolo, Mike, Sherry, Stephen T., Manolio, Teri A.
Publicado em 2011

Patterns of Human Diversity, within and among Continents, Inferred from Biallelic DNA Polymorphisms

Por Romualdi, Chiara, Balding, David, Nasidze, Ivane S., Risch, Gregory, Robichaux, Myles, Sherry, Stephen T., Stoneking, Mark, Batzer, Mark A., Barbujani, Guido
Publicado em 2002

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

Por Ramos, Erin M, Hoffman, Douglas, Junkins, Heather A, Maglott, Donna, Phan, Lon, Sherry, Stephen T, Feolo, Mike, Hindorff, Lucia A
Publicado em 2014

Reading between the LINEs: Human Genomic Variation Induced by LINE-1 Retrotransposition

Por Sheen, Fang-miin, Sherry, Stephen T., Risch, Gregory M., Robichaux, Myles, Nasidze, Ivane, Stoneking, Mark, Batzer, Mark A., Swergold, Gary D.
Publicado em 2000

The 1000 Genomes Project: Data Management and Community Access

Por Clarke, Laura, Zheng-Bradley, Xiangqun, Smith, Richard, Kulesha, Eugene, Xiao, Chunlin, Toneva, Iliana, Vaughan, Brendan, Preuss, Don, Leinonen, Rasko, Shumway, Martin, Sherry, Stephen, Flicek, Paul
Publicado em 2012

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

Por Wong, Kira M., Langlais, Kristofor, Tobias, Geoffrey S., Fletcher-Hoppe, Colette, Krasnewich, Donna, Leeds, Hilary S., Rodriguez, Laura Lyman, Godynskiy, Georgy, Schneider, Valerie A., Ramos, Erin M., Sherry, Stephen T.
Publicado no Nucleic Acids Res (2017)

The variant call format and VCFtools

Por Danecek, Petr, Auton, Adam, Abecasis, Goncalo, Albers, Cornelis A., Banks, Eric, DePristo, Mark A., Handsaker, Robert E., Lunter, Gerton, Marth, Gabor T., Sherry, Stephen T., McVean, Gilean, Durbin, Richard
Publicado em 2011

Supplementing High-Density SNP Microarrays for Additional Coverage of Disease-Related Genes: Addiction as a Paradigm

Por Saccone, Scott F., Bierut, Laura J., Chesler, Elissa J., Kalivas, Peter W., Lerman, Caryn, Saccone, Nancy L., Uhl, George R., Li, Chuan-Yun, Philip, Vivek M., Edenberg, Howard J., Sherry, Stephen T., Feolo, Michael, Moyzis, Robert K., Rutter, Joni L.
Publicado em 2009

A Mechanism for Controlled Access to GWAS Data: Experience of the GAIN Data Access Committee

Por Ramos, Erin M., Din-Lovinescu, Corina, Bookman, Ebony B., McNeil, Lisa J., Baker, Carl C., Godynskiy, Georgy, Harris, Emily L., Lehner, Thomas, McKeon, Catherine, Moss, Joel, Starks, Vaurice L., Sherry, Stephen T., Manolio, Teri A., Rodriguez, Laura Lyman
Publicado em 2013

ClinGen — The Clinical Genome Resource

Por Rehm, Heidi L., Berg, Jonathan S., Brooks, Lisa D., Bustamante, Carlos D., Evans, James P., Landrum, Melissa J., Ledbetter, David H., Maglott, Donna R., Martin, Christa Lese, Nussbaum, Robert L., Plon, Sharon E., Ramos, Erin M., Sherry, Stephen T., Watson, Michael S.
Publicado no N Engl J Med (2015)

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

Por Marth, Gabor, Schuler, Greg, Yeh, Raymond, Davenport, Ruth, Agarwala, Richa, Church, Deanna, Wheelan, Sarah, Baker, Jonathan, Ward, Ming, Kholodov, Michael, Phan, Lon, Czabarka, Eva, Murvai, Janos, Cutler, David, Wooding, Stephen, Rogers, Alan, Chakravarti, Aravinda, Harpending, Henry C., Kwok, Pui-Yan, Sherry, Stephen T.
Publicado em 2003

Consent Codes: Upholding Standard Data Use Conditions

Por Dyke, Stephanie O. M., Philippakis, Anthony A., Rambla De Argila, Jordi, Paltoo, Dina N., Luetkemeier, Erin S., Knoppers, Bartha M., Brookes, Anthony J., Spalding, J. Dylan, Thompson, Mark, Roos, Marco, Boycott, Kym M., Brudno, Michael, Hurles, Matthew, Rehm, Heidi L., Matern, Andreas, Fiume, Marc, Sherry, Stephen T.
Publicado no PLoS Genet (2016)

Completing the map of human genetic variation: A plan to identify and integrate normal structural variation into the human genome sequence.

Por Eichler, Evan E., Nickerson, Deborah A., Altshuler, David, Bowcock, Anne M., Brooks, Lisa D., Carter, Nigel P., Church, Deanna M., Felsenfeld, Adam, Guyer, Mark, Lee, Charles, Lupski, James R., Mullikin, James C., Pritchard, Jonathan K., Sebat, Jonathan, Sherry, Stephen T., Smith, Douglas, Valle, David, Waterston, Robert H.
Publicado em 2007

The NCBI dbGaP database of genotypes and phenotypes

Por Mailman, Matthew D., Feolo, Michael, Jin, Yumi, Kimura, Masato, Tryka, Kimberly, Bagoutdinov, Rinat, Hao, Luning, Kiang, Anne, Paschall, Justin, Phan, Lon, Popova, Natalia, Pretel, Stephanie, Ziyabari, Lora, Shao, Yu, Wang, Zhen Y., Sirotkin, Karl, Ward, Minghong, Kholodov, Michael, Zbicz, Kerry, Beck, Jeffrey, Kimelman, Michael, Shevelev, Sergey, Preuss, Don, Yaschenko, Eugene, Graeff, Alan, Ostell, James, Sherry, Stephen T.
Publicado em 2007