| Literature DB >> 26092349 |
Timothy J Hohman1, Jessica N Cooke-Bailey1, Christiane Reitz2, Gyungah Jun3, Adam Naj4, Gary W Beecham5, Zhi Liu5, Regina M Carney6, Jeffrey M Vance7, Michael L Cuccaro8, Ruchita Rajbhandary5, Badri Narayan Vardarajan2, Li-San Wang9, Otto Valladares9, Chiao-Feng Lin9, Eric B Larson10, Neill R Graff-Radford11, Denis Evans12, Philip L De Jager13, Paul K Crane10, Joseph D Buxbaum14, Jill R Murrell15, Towfique Raj13, Nilufer Ertekin-Taner11, Mark W Logue16, Clinton T Baldwin17, Robert C Green18, Lisa L Barnes19, Laura B Cantwell9, M Daniele Fallin20, Rodney C P Go21, Patrick Griffith22, Thomas O Obisesan23, Jennifer J Manly2, Kathryn L Lunetta24, M Ilyas Kamboh25, Oscar L Lopez25, David A Bennett26, John Hardy27, Hugh C Hendrie28, Kathleen S Hall28, Alison M Goate29, Rosalyn Lang30, Goldie S Byrd30, Walter A Kukull31, Tatiana M Foroud32, Lindsay A Farrer33, Eden R Martin34, Margaret A Pericak-Vance7, Gerard D Schellenberg9, Richard Mayeux2, Jonathan L Haines1, Tricia A Thornton-Wells35.
Abstract
INTRODUCTION: African-American (AA) individuals have a higher risk for late-onset Alzheimer's disease (LOAD) than Americans of primarily European ancestry (EA). Recently, the largest genome-wide association study in AAs to date confirmed that six of the Alzheimer's disease (AD)-related genetic variants originally discovered in EA cohorts are also risk variants in AA; however, the risk attributable to many of the loci (e.g., APOE, ABCA7) differed substantially from previous studies in EA. There likely are risk variants of higher frequency in AAs that have not been discovered.Entities:
Keywords: Admixture mapping; African-American; Alzheimer's disease; Genome-wide association analysis (GWAS); Local admixture; Local ancestry
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Year: 2015 PMID: 26092349 PMCID: PMC4681680 DOI: 10.1016/j.jalz.2015.02.012
Source DB: PubMed Journal: Alzheimers Dement ISSN: 1552-5260 Impact factor: 21.566