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Transethnic Transferability of a Genome-Wide Polygenic Score for Coronary Artery Disease.
Fahed AC, Aragam KG, Hindy G, Chen YI, Chaudhary K, Dobbyn A, Krumholz HM, Sheu WHH, Rich SS, Rotter JI, Chowdhury R, Cho J, Do R, Ellinor PT, Kathiresan S, Khera AV. Fahed AC, et al. Circ Genom Precis Med. 2021 Feb;14(1):e003092. doi: 10.1161/CIRCGEN.120.003092. Epub 2020 Dec 7. Circ Genom Precis Med. 2021. PMID: 33284643 Free PMC article. No abstract available.
Association of Rare Pathogenic DNA Variants for Familial Hypercholesterolemia, Hereditary Breast and Ovarian Cancer Syndrome, and Lynch Syndrome With Disease Risk in Adults According to Family History.
Patel AP, Wang M, Fahed AC, Mason-Suares H, Brockman D, Pelletier R, Amr S, Machini K, Hawley M, Witkowski L, Koch C, Philippakis A, Cassa CA, Ellinor PT, Kathiresan S, Ng K, Lebo M, Khera AV. Patel AP, et al. Among authors: fahed ac. JAMA Netw Open. 2020 Apr 1;3(4):e203959. doi: 10.1001/jamanetworkopen.2020.3959. JAMA Netw Open. 2020. PMID: 32347951 Free PMC article.
Physiology as a Lingua Franca for Clinical Machine Learning.
Sarma GP, Reinertsen E; ML4CVD Group. Sarma GP, et al. Patterns (N Y). 2020 May 8;1(2):100017. doi: 10.1016/j.patter.2020.100017. eCollection 2020 May 8. Patterns (N Y). 2020. PMID: 33205094 Free PMC article.
Exploring the link between Gilbert's syndrome and atherosclerotic cardiovascular disease: insights from a subpopulation-based analysis of over one million individuals.
Kartoun U, Fahed AC, Kany S, Singh P, Khurshid S, Patel AP, Batra P, Philippakis A, Khera AV, Lubitz SA, Ellinor PT, Anand V, Ng K. Kartoun U, et al. Among authors: fahed ac. Eur Heart J Open. 2023 Jun 9;3(3):oead059. doi: 10.1093/ehjopen/oead059. eCollection 2023 May. Eur Heart J Open. 2023. PMID: 37377635 Free PMC article. No abstract available.
63 results