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Exome sequence analysis identifies rare coding variants associated with a machine learning-based marker for coronary artery disease.
Petrazzini BO, Forrest IS, Rocheleau G, Vy HMT, Márquez-Luna C, Duffy Á, Chen R, Park JK, Gibson K, Goonewardena SN, Malick WA, Rosenson RS, Jordan DM, Do R. Petrazzini BO, et al. Among authors: jordan dm. Nat Genet. 2024 Jul;56(7):1412-1419. doi: 10.1038/s41588-024-01791-x. Epub 2024 Jun 11. Nat Genet. 2024. PMID: 38862854
Population-Based Penetrance of Deleterious Clinical Variants.
Forrest IS, Chaudhary K, Vy HMT, Petrazzini BO, Bafna S, Jordan DM, Rocheleau G, Loos RJF, Nadkarni GN, Cho JH, Do R. Forrest IS, et al. Among authors: jordan dm. JAMA. 2022 Jan 25;327(4):350-359. doi: 10.1001/jama.2021.23686. JAMA. 2022. PMID: 35076666 Free PMC article.
87 results