Open AccessWhole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis
Author(s) -
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 B. Wallace,
Nora Franceshini,
Nena Matijevic,
Kenneth Rice,
Traci M. Bartz,
Leo-Pekka Lyytikäinen,
Mika Kähönen,
Terho Lehtimäki,
Olli Raitakari,
Ruifang LiGao,
Dennis O. MookKanamori,
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,
Alexander P. Reiner,
Santhi K. Ganesh,
Vijay G. Sankaran
Publication year - 2016
Publication title -
carolina digital repository (university of north carolina at chapel hill)
Language(s) - English
DOI - 10.17615/vn1s-8a35
Subject(s) - exome sequencing , biology , splice , genetics , exome , haematopoiesis , computational biology , stem cell , gene , phenotype