Genome-wide rare variant analysis for thousands of phenotypes in over 70,000 exomes from two cohorts

Elizabeth T. Cirulli (), Simon White, Robert W. Read, Gai Elhanan, William J. Metcalf, Francisco Tanudjaja, Donna M. Fath, Efren Sandoval, Magnus Isaksson, Karen A. Schlauch, Joseph J. Grzymski, James T. Lu and Nicole L. Washington
Additional contact information
Elizabeth T. Cirulli: Helix
Simon White: Helix
Robert W. Read: Desert Research Institute
Gai Elhanan: Desert Research Institute
William J. Metcalf: Desert Research Institute
Francisco Tanudjaja: Helix
Donna M. Fath: Helix
Efren Sandoval: Helix
Magnus Isaksson: Helix
Karen A. Schlauch: Desert Research Institute
Joseph J. Grzymski: Desert Research Institute
James T. Lu: Helix
Nicole L. Washington: Helix

Nature Communications, 2020, vol. 11, issue 1, 1-10

Abstract: Abstract Understanding the impact of rare variants is essential to understanding human health. We analyze rare (MAF

Date: 2020
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DOI: 10.1038/s41467-020-14288-y

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