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C.J.Williams K.Williams L.K.Wilson C.Wilson J.G.Wong Q.Wu J.Xu H.Yanek L.R.Yang I.Yang R.Zaghloul N.Zekavat M.Zhang Y.Zhao S.X.Zhao W.Zhi D.Zhou X.Zhu X.Zody M.Zoellner S.Abdalla M.Abecasis G.R.Assimes T.Atkinson E.Beitelshees A.Bis J.Bodea C.Brody J.Cade B.Carlson J.Chang I.-S.Chen Y.-D.I.Chun S.Chung R.-H.Damcott C.de Vries P.Do R.Elliott A.Fu M.Ganna A.Gong D.-W.Graham S.Haas M.Haring B.He J.Heckbert S.Himes B.Hixson J.Jain D.Jarvik G.Jhun M.A.Jiang J.Jun G.Kalyani R.Khera A.Klarin D.Kral B.Lange L.Laurie C.Lemaitre R.Li Z.Li X.Lin X.Mathur R.McHugh C.McLenithan J.Mikulla J.Moran A.Morrison A.C.Nakao T.Natarajan P.Nickerson D.North K.O’Donnell C.Pampana A.Patel A.Peloso G.M.Perry J.Peters U.Pirruccello J.Pollin T.Preuss M.Rao D.C.Reed R.Reiner A.Rosenthal S.Rotter J.I.Schoenberg J.Selvaraj M.S.Sheu W.H.-H.Sofer T.Stilp A.M.Sunyaev S.R.Surakka I.Sztalryd C.Tang H.Taylor K.D.Uddin M.M.Urbut S.Verbanck M.Von Holle A.Wang H.Wiggins K.Willer C.J.Wolford B.Xu H.Zaghloul N.Zekavat M.Zhang J.Neale B.M.Sunyaev S.R.Peloso G.M.NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium, TOPMed Lipids Working GroupTOPMed Lipids Working GroupNHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium2021-04-282021-04-2820201061-4036https://www.scopus.com/inward/record.uri?eid=2-s2.0-85089736482&doi=10.1038%2fs41588-020-0676-4&partnerID=40&md5=b4a4b841f51e2b103d11de251f4027b7https://scholars.lib.ntu.edu.tw/handle/123456789/557963[SDGs]SDG3high density lipoprotein cholesterol; low density lipoprotein cholesterol; spacer DNA; triacylglycerol; low density lipoprotein cholesterol; Article; biobank; cohort analysis; computer model; controlled study; epigenetics; gene disruption; gene replication; genetic association; genetic variability; human; large scale production; missense mutation; population structure; priority journal; single nucleotide polymorphism; whole genome sequencing; biological model; computer simulation; genetic predisposition; genetic variation; genetics; genome; genome-wide association study; molecular genetics; phenotype; procedures; whole genome sequencing; Cholesterol, LDL; Computer Simulation; Genetic Predisposition to Disease; Genetic Variation; Genome; Genome-Wide Association Study; Humans; Models, Genetic; Molecular Sequence Annotation; Phenotype; Whole Genome Sequencingjournal article10.1038/s41588-020-0676-4328396062-s2.0-85089736482