Association of Genetic Variants and Incident Coronary Heart Disease in Multiethnic Cohorts: The PAGE Study
Year: 2020
Type: article
Study design: Observational Study
Abstract: Genome wide association studies identified several single nucleotide polymorphisms (SNPs) associated with prevalent coronary heart disease (CHD) but less is known of associations with incident CHD. The association of thirteen published CHD SNPs was examined in five ancestry groups of four large US prospective cohorts.
DOI: 10.17615/4n1y-v979
Authors: Kooperberg, Charles, Best, Lyle G., Lin, Dan Yu, Taverna, Darin, Franceschini, Nora, North, Kari E., Boerwinkle, Eric, Jenny, Nancy, Vöckler, Jens S., Bookman, Ebony, Reiner, Alex P., Eaton, Charles, Bella, Jonathan N., Carty, Cara, Greenland, Philip, Deelman, Ewa, Heiss, Gerardo, Lin, Yi, Cole, Shelley A., Young, Alicia M., Psaty, Bruce, Bužková, Petra, Hindorff, Lucia A., Garrett, Tiana
Institution: University of North Carolina at Chapel Hill
Language: English
Subfield: Genetics
Domain: Life Sciences
Open Access status: green
Funders: U.S. Department of Health and Human Services, Women's Health Initiative, Cedars-Sinai Medical Center, Strong, Ministerio de Economía y Competitividad, National Institutes of Health, National Heart, Lung, and Blood Institute, National Human Genome Research Institute, National Institute of Diabetes and Digestive and Kidney Diseases, National Center for Research Resources
Awards: G1028935811, Cardiovascular Disease in Sioux Indians, G109231058, G1107292973, G118440752, G1188197595, G1241292848, Epidemiology of putative genuine genetic variant: The Women's Health Intiative, G1332411685, G136105103, G1462415530, The Strong Heart Study, Phase V, G156924709, G1593340546, G1617453120, G1646017446, G164614106, G1746001450, G1909643007, G191650467, G206718646, G215333750, G2215229, G2253702613, G2295046671, Epidemiology of Putative Causal Variants in the Multiethnic Cohort, G2417273319, G2547046739, G2555954497, G257474614, G25881238, G277826483, G2800149121, Strong Heart Family Study, G2852769941, G305513510, G309550730, G3134865449, Cardiovascular Evaluation for the SHS Phase V, G3191277318, G3226848658, G3544793024, G3642616392, G4145745212, G4214622172, G4216744017, G423252844, G4281851297, G4289235060, G4302802884, G4321061599, G4401737188, G4454202622, G4560602636, G4671189754, G4738207643, G484043965, G4932516547, G4940723635, G4987078009, G510023084, G5183277930, G528395701, G530368906, G532295152, G5428688682, G5522185877, G555506801, G5566602938, G582705428, G593087434, CHS Events Follow-up Study, G603760282, G6094799806, G6204895930, G6464247198, G6576172577, G6860406196, G6917805344, G7066869570, G7071300326, G709210845, G715477388, G7272550893, G7323080267, G7582705761, G7775492603, G786153652, G793702358, G8176111713, G8181733155, Epidemiologic Architecture for Genes Linked to Environment (EAGLE), CHS-Transition Phase -268055222, G863538970, G8650178004, G8650184350, G8780700017, G8934942062, Cardiovascular Disease in Pima Indians, G9000007515, G9000015747, G9000027259, G9000028181, G9000028264, G9000039132, G9000069887, G9000080822, G9000108254, G9000112759, G9000121483, G9000124754, G9000126117, G9000140433, G9000145448, G9000152345, G9000155493, G9000195409, G9000205553, G9000239991, G9000294209, G9000350284, G905887895, G920255405, G939135972, G960597250, G999174792
OpenAlex ID: W4300436275