The mutational dynamics of short tandem repeats in large, multigenerational families Autor Cody J. Steely, W. Scott Watkins, Lisa Baird, Lynn B. Jorde

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Discovery of rare, diagnostic AluYb8/9 elements in diverse human populations Autor Julie Feusier, David J. Witherspoon, W. Scott Watkins, Clément Goubert, Thomas A. Sasani, Lynn B. Jorde

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Large, three-generation human families reveal post-zygotic mosaicism and variability in germline mutation accumulation Autor Thomas A Sasani, Brent S Pedersen, Ziyue Gao, Lisa Baird, Molly Przeworski, Lynn B Jorde, Aaron R Quinlan

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Modeling the amplification dynamics of human Alu retrotransposons. Autor Dale J Hedges, Richard Cordaux, Jinchuan Xing, David J Witherspoon, Alan R Rogers, Lynn B Jorde, Mark A Batzer

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Shared and unique signals of high-altitude adaptation in geographically distinct Tibetan populations. Autor Tana Wuren, Tatum S Simonson, Ga Qin, Jinchuan Xing, Chad D Huff, David J Witherspoon, Lynn B Jorde, Ri-Li Ge

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Shared genomic segments analysis identifies MHC class I and class III molecules as genetic risk factors for juvenile idiopathic arthritis Autor Cecile N. Avery, Nicole D. Russell, Cody J. Steely, Aimee O. Hersh, John F. Bohnsack, Sampath Prahalad, Lynn B. Jorde

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A Genome-Wide Search for Greek and Jewish Admixture in the Kashmiri Population. Autor Jonathan M Downie, Tsewang Tashi, Felipe Ramos Lorenzo, Julie Ellen Feusier, Hyder Mir, Josef T Prchal, Lynn B Jorde, Parvaiz A Koul

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Extremely low-coverage whole genome sequencing in South Asians captures population genomics information Autor Navin Rustagi, Anbo Zhou, W. Scott Watkins, Erika Gedvilaite, Shuoguo Wang, Naveen Ramesh, Donna Muzny, Richard A. Gibbs, Lynn B. Jorde, Fuli Yu, Jinchuan Xing

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Genomic analysis of natural selection and phenotypic variation in high-altitude mongolians. Autor Jinchuan Xing, Tana Wuren, Tatum S Simonson, W Scott Watkins, David J Witherspoon, Wilfred Wu, Ga Qin, Chad D Huff, Lynn B Jorde, Ri-Li Ge

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Relationship estimation from whole-genome sequence data. Autor Hong Li, Gustavo Glusman, Hao Hu, Shankaracharya, Juan Caballero, Robert Hubley, David Witherspoon, Stephen L Guthery, Denise E Mauldin, Lynn B Jorde, Leroy Hood, Jared C Roach, Chad D Huff

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Whole-genome sequencing analysis in families with recurrent pregnancy loss: A pilot study. Autor Tsegaselassie Workalemahu, Cecile Avery, Sarah Lopez, Nathan R Blue, Amelia Wallace, Aaron R Quinlan, Hilary Coon, Derek Warner, Michael W Varner, D Ware Branch, Lynn B Jorde, Robert M Silver

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Clinical and biochemical function of polymorphic NR0B1 GGAA-microsatellites in Ewing sarcoma: a report from the Children's Oncology Group. Autor Michael J Monument, Kirsten M Johnson, Elizabeth McIlvaine, Lisa Abegglen, W Scott Watkins, Lynn B Jorde, Richard B Womer, Natalie Beeler, Laura Monovich, Elizabeth R Lawlor, Julia A Bridge, Joshua D Schiffman, Mark D Krailo, R Lor Randall, Stephen L Lessnick

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A comprehensive map of mobile element insertion polymorphisms in humans. Autor Chip Stewart, Deniz Kural, Michael P Strömberg, Jerilyn A Walker, Miriam K Konkel, Adrian M Stütz, Alexander E Urban, Fabian Grubert, Hugo Y K Lam, Wan-Ping Lee, Michele Busby, Amit R Indap, Erik Garrison, Chad Huff, Jinchuan Xing, Michael P Snyder, Lynn B Jorde, Mark A Batzer, Jan O Korbel, Gabor T Marth, 1000 Genomes Project

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Correction: Alternating Hemiplegia of Childhood: Retrospective Genetic Study and Genotype-Phenotype Correlations in 187 Subjects from the US AHCF Registry. Autor Louis Viollet, Gustavo Glusman, Kelley J Murphy, Tara M Newcomb, Sandra P Reyna, Matthew Sweney, Benjamin Nelson, Frederick Andermann, Eva Andermann, Gyula Acsadi, Richard L Barbano, Candida Brown, Mary E Brunkow, Harry T Chugani, Sarah R Cheyette, Abigail Collins, Suzanne D DeBrosse, David Galas, Jennifer Friedman, Lee Hood, Chad Huff, Lynn B Jorde, Mary D King, Bernie LaSalle, Richard J Leventer, Aga J Lewelt, Mylynda B Massart, Mario R Mérida, Louis J Ptáček, Jared C Roach, Robert S Rust, Francis Renault, Terry D Sanger, Marcio A Sotero de Menezes, Rachel Tennyson, Peter Uldall, Yue Zhang, Mary Zupanc, Winnie Xin, Kenneth Silver, Kathryn J Swoboda

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Alternating Hemiplegia of Childhood: Retrospective Genetic Study and Genotype-Phenotype Correlations in 187 Subjects from the US AHCF Registry. Autor Louis Viollet, Gustavo Glusman, Kelley J Murphy, Tara M Newcomb, Sandra P Reyna, Matthew Sweney, Benjamin Nelson, Frederick Andermann, Eva Andermann, Gyula Acsadi, Richard L Barbano, Candida Brown, Mary E Brunkow, Harry T Chugani, Sarah R Cheyette, Abigail Collins, Suzanne D DeBrosse, David Galas, Jennifer Friedman, Lee Hood, Chad Huff, Lynn B Jorde, Mary D King, Bernie LaSalle, Richard J Leventer, Aga J Lewelt, Mylynda B Massart, Mario R Mérida, Louis J Ptáček, Jared C Roach, Robert S Rust, Francis Renault, Terry D Sanger, Marcio A Sotero de Menezes, Rachel Tennyson, Peter Uldall, Yue Zhang, Mary Zupanc, Winnie Xin, Kenneth Silver, Kathryn J Swoboda

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