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Identification of novel and rare variants associated with handgrip strength using whole genome sequence data from the NHLBI Trans-Omics in Precision Medicine (TOPMed) Program.

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Title: Identification of novel and rare variants associated with handgrip strength using whole genome sequence data from the NHLBI Trans-Omics in Precision Medicine (TOPMed) Program.
Authors: Sarnowski, Chloé1,2 (AUTHOR) Chloe.Sarnowski@uth.tmc.edu, Chen, Han2,3 (AUTHOR), Biggs, Mary L.4,5 (AUTHOR), Wassertheil-Smoller, Sylvia6 (AUTHOR), Bressler, Jan2 (AUTHOR), Irvin, Marguerite R.7 (AUTHOR), Ryan, Kathleen A.8 (AUTHOR), Karasik, David9,10 (AUTHOR), Arnett, Donna K.11 (AUTHOR), Cupples, L. Adrienne1,12 (AUTHOR), Fardo, David W.13 (AUTHOR), Gogarten, Stephanie M.5 (AUTHOR), Heavner, Benjamin D.5 (AUTHOR), Jain, Deepti5 (AUTHOR), Kang, Hyun Min14 (AUTHOR), Kooperberg, Charles15 (AUTHOR), Mainous, Arch G.16 (AUTHOR), Mitchell, Braxton D.8,17 (AUTHOR), Morrison, Alanna C.2 (AUTHOR), O'Connell, Jeffrey R.8 (AUTHOR)
Source: PLoS ONE. 7/2/2021, Vol. 16 Issue 7, p1-19. 19p.
Database: Academic Search Ultimate
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