Integrating common and rare genetic variation in diverse human populations

作者：David Altshuler, S. F. Schaffner, Stacey B. Gabriel, Xiaoming Jia, Joshua M. Korn, James Nemesh, Samuela Pollack, Wendy Brodeur, Huy Nguyen, Ilya Shlyakhter, Richard A. Gibbs, Fuli Yu, Penelope E. Bonnen, Kyle Chang, Alicia Hawes, Lora Lewis, Yanru Ren, David A. Wheeler, Donna M. Muzny, Claudia Gonzaga‐Jauregui, Emmanouil T. Dermitzakis, Stephen B. Montgomery, Rhian Gwilliam, Sarah Hunt, Aarno Palotie, Pamela Whittaker, C. Barnes, Kati Kristiansson, Nicole Soranzo, Verneri Anttila, Qingrun Zhang, Mohammed J. R. Ghori, WJ McLaren, Fumihiko Takeuchi, Katayoon Darvishi, Charles Lee, Alon Keinan, Alkes L. Price, Mark J. Daly, Stephen Leslie, Gil McVean, Loukas Moutsianas, Sharon R. Grossman, Elizabeth B. Hostetter, Clement A. Adebamowo, Morris W. Foster, Deborah R. Gordon, J Licinio, María Cristina Manca, Patricia A. Marshall, Ichiro Matsuda, Duncan Ngare, Vivian Ota Wang, Deepa Reddy, Charles N. Rotimi, Charmaine D. Royal, Richard R. Sharp, Changqing Zeng, Lisa D. Brooks, Jean E. McEwen · 发表于：Nature · 年份：2010 · DOI：10.1038/nature09298 · 被引用次数：3231 · 研究领域：Genomics and Rare Diseases、Genomics and Phylogenetic Studies、Genomic variations and chromosomal abnormalities