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Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data.
Wainschtein P, Jain D, Zheng Z; TOPMed Anthropometry Working Group; NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium; 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. Wainschtein P, et al. Among authors: arnett dk. Nat Genet. 2022 Mar;54(3):263-273. doi: 10.1038/s41588-021-00997-7. Epub 2022 Mar 7. Nat Genet. 2022. PMID: 35256806 Free PMC article.
A genome-wide scan for urinary albumin excretion in hypertensive families.
Freedman BI, Beck SR, Rich SS, Heiss G, Lewis CE, Turner S, Province MA, Schwander KL, Arnett DK, Mellen BG; HyperGEN Investigators. Freedman BI, et al. Among authors: arnett dk. Hypertension. 2003 Sep;42(3):291-6. doi: 10.1161/01.HYP.0000087890.33245.41. Epub 2003 Aug 18. Hypertension. 2003. PMID: 12925555
Genes for left ventricular hypertrophy.
Arnett DK, de las Fuentes L, Broeckel U. Arnett DK, et al. Curr Hypertens Rep. 2004 Feb;6(1):36-41. doi: 10.1007/s11906-004-0009-5. Curr Hypertens Rep. 2004. PMID: 14972088 Review.
635 results