Whole-exome sequencing of 14 389 individuals from the ESP and CHARGE consortia identifies novel rare variation associated with hemostatic factors

Nathan Pankratz(University of Minnesota), Nicholas L. Smith(University of Washington), Peng Wei(Creighton University), Ming‐Huei Chen(Boston University), Mary Cushman(University of Vermont), André G. Uitterlinden(Erasmus MC), Jeroen van Rooij(Erasmus MC), Ginger Metcalf(Baylor College of Medicine), Robert Kraaij(Erasmus MC), Donna M. Muzny(Baylor College of Medicine), Albert Hofman(Harvard University), Eric Boerwinkle(Training Programs in Epidemiology and Public Health Interventions Network), Moniek P.M. de Maat, Paul S. de Vries(The University of Texas Health Science Center at Houston), Oscar H. Franco(University Medical Center Utrecht), Richard A. Gibbs(Baylor College of Medicine), Paul L. Auer(Cape Town HVTN Immunology Laboratory / Hutchinson Centre Research Institute of South Africa), Weihong Tang, Jill M. Johnsen(University of Washington), Jennifer A. Brody(Cincinnati Children's Hospital Medical Center), Aaron R. Folsom(University of Minnesota), Kelly K Haagenson(University of Minnesota), Alex P. Reiner(Brigham and Women's Hospital), Alanna C. Morrison(The University of Texas Health Science Center at Houston), Abbas Dehghan(UK Dementia Research Institute), Christopher J. O’Donnell(National Heart Lung and Blood Institute), Barbara McKnight(University of Washington), Christie Kovar(Baylor College of Medicine), Bruce M. Psaty(Services Hospital), Mary Rachel Stimson(University of Minnesota), Jennifer E. Huffman(Harvard University)

Human Molecular Genetics

May 10, 2022

Cited by 17

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