Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis

作者：Linda M. Polfus, Rajiv K. Khajuria, Ursula M. Schick, Nathan Pankratz, Raha Pazoki, Jennifer A. Brody, Ming‐Huei Chen, Paul L. Auer, James S. Floyd, Jie Huang, Leslie A. Lange, Frank J.A. van Rooij, Richard A. Gibbs, Ginger Metcalf, Donna M. Muzny, Narayanan Veeraraghavan, Klaudia Walter, Lu Chen, Lisa R. Yanek, Lewis C. Becker, Gina M. Peloso, Aoi Wakabayashi, Mart Kals, Andres Metspalu, Tõnu Esko, Keolu Fox, Robert W. Wallace, Nora Franceschini, Nena Matijevic, Kenneth Rice, Traci M. Bartz, Leo‐Pekka Lyytikäinen, Mika Kähönen, Terho Lehtimäki, Olli Raitakari, Ruifang Li‐Gao, Dennis O. Mook‐Kanamori, Guillaume Lettre, Cornelia M. van Duijn, Oscar H. Franco, Stephen S. Rich, Fernando Rivadeneira, Albert Hofman, André G. Uitterlinden, James Wilson, Bruce M. Psaty, Nicole Soranzo, Abbas Dehghan, Eric Boerwinkle, Xiaoling Zhang, Andrew D. Johnson, Christopher J. O’Donnell, Jill M. Johnsen, Alex P. Reiner, Santhi K. Ganesh, Vijay G. Sankaran · 发表于：The American Journal of Human Genetics · 年份：2016 · DOI：10.1016/j.ajhg.2016.08.002 · 被引用次数：18 · 研究领域：Blood disorders and treatments、Blood groups and transfusion