| 2022 | Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data | Wainschtein, P; Jain, D; Zheng, Z; Cupples, LA; Shadyab, AH; McKnight, B; Shoemaker, BM; Mitchell, BD; Psaty, BM; Kooperberg, C; Liu, CT; Albert, CM; Roden, D; Chasman, DI; Darbar, D; Lloyd-Jones, DM; Arnett, DK; Regan, EA; Boerwinkle, E; Rotter, JI; O'Connell, JR; Yanek, LR; de Andrade, M; Allison, MA; McDonald, MN; Chung, MK; Fornage, M; Chami, N; Smith, NL; Ellinor, PT; Vasan, RS; Mathias, RA; Loos, RJF; Rich, SS; Lubitz, SA; Heckbert, SR; Redline, S; Guo, X; Chen, Y-I; Laurie, CA; Hernandez, RD; McGarvey, ST; Goddard, ME; Laurie, CC; North, KE; Lange, LA; Weir, BS; Yengo, L; Yang, J; Visscher, PM; TOPMed Anthropometry Working Group; Chang, YC ; NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium | Nature genetics 54(3), 263-273 | | | |
