Assessing the contribution of rare genetic variants to phenotypes of chronic obstructive pulmonary disease using whole-genome sequence data.
Kim W, Hecker J, Barr RG, Boerwinkle E, Cade B, Correa A, Dupuis J, Gharib SA, Lange L, London SJ, Morrison AC, O'Connor GT, Oelsner EC, Psaty BM, Vasan RS, Redline S, Rich SS, Rotter JI, Yu B, Lange C, Manichaikul A, Zhou JJ, Sofer T, Silverman EK, Qiao D, Cho MH; NHLBI Trans-Omics in Precision Medicine (TOPMed) Consortium and TOPMed Lung Working Group.
Kim W, et al. Among authors: morrison ac.
Hum Mol Genet. 2022 Nov 10;31(22):3873-3885. doi: 10.1093/hmg/ddac117.
Hum Mol Genet. 2022.
PMID: 35766891
Free PMC article.