The mutational dynamics of short tandem repeats in large, multigenerational families by 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 by Julie Feusier, David J. Witherspoon, W. Scott Watkins, Clément Goubert, Thomas A. Sasani, Lynn B. Jorde

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Extremely low-coverage whole genome sequencing in South Asians captures population genomics information by 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. by 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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Targeted Gene Sequencing in Children with Crohn’s Disease and Their Parents: Implications for Missing Heritability by Jiun-Sheng Chen, Fulan Hu, Subra Kugathasan, Lynn B. Jorde, David Nix, Ann Rutherford, Lee Denson, W. Scott Watkins, Sampath Prahalad, Chad Huff, Stephen L. Guthery

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Common Variation in Cytoskeletal Genes Is Associated with Conotruncal Heart Defects by Fadi I. Musfee, A. J. Agopian, Elizabeth Goldmuntz, Hakon Hakonarson, Bernice E. Morrow, Deanne M. Taylor, Martin Tristani-Firouzi, W. Scott Watkins, Mark Yandell, Laura E. Mitchell

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Clinical and biochemical function of polymorphic NR0B1 GGAA-microsatellites in Ewing sarcoma: a report from the Children's Oncology Group. by 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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De novo and recessive forms of congenital heart disease have distinct genetic and phenotypic landscapes by W. Scott Watkins, E. Javier Hernandez, Sergiusz Wesolowski, Brent W. Bisgrove, Ryan T. Sunderland, Edwin Lin, Gordon Lemmon, Bradley L. Demarest, Thomas A. Miller, Daniel Bernstein, Martina Brueckner, Wendy K. Chung, Bruce D. Gelb, Elizabeth Goldmuntz, Jane W. Newburger, Christine E. Seidman, Yufeng Shen, H. Joseph Yost, Mark Yandell, Martin Tristani-Firouzi

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The history and geographic distribution of a KCNQ1 atrial fibrillation risk allele by Shannon Hateley, Angelica Lopez-Izquierdo, Chuanchau J. Jou, Scott Cho, Joshua G. Schraiber, Shiya Song, Colin T. Maguire, Natalia Torres, Michael Riedel, Neil E. Bowles, Cammon B. Arrington, Brett J. Kennedy, Susan P. Etheridge, Shuping Lai, Chase Pribble, Lindsay Meyers, Derek Lundahl, Jake Byrnes, Julie M. Granka, Christopher A. Kauffman, Gordon Lemmon, Steven Boyden, W. Scott Watkins, Mary Anne Karren, Stacey Knight, J. Brent Muhlestein, John F. Carlquist, Jeffrey L. Anderson, Kenneth G. Chahine, Khushi U. Shah, Catherine A. Ball, Ivor J. Benjamin, Mark Yandell, Martin Tristani-Firouzi

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