全基因组关联研究
单核苷酸多态性
生物
载脂蛋白E
疾病
遗传学
遗传关联
阿尔茨海默病
基因座(遗传学)
荟萃分析
基因型
基因
医学
内科学
作者
Jean‐Charles Lambert,Carla A. Ibrahim‐Verbaas,Denise Harold,Adam C. Naj,Rebecca Sims,Céline Bellenguez,Gyungah Jun,Anita L. DeStefano,Joshua C. Bis,Gary W. Beecham,Benjamin Grenier‐Boley,Giancarlo Russo,Tricia A. Thornton‐Wells,Nicola Jones,Albert V. Smith,Vincent Chouraki,Charlene Thomas,M. Arfan Ikram,Diana Zélénika,Badri N. Vardarajan
出处
期刊:Nature Genetics
[Nature Portfolio]
日期:2013-10-27
卷期号:45 (12): 1452-1458
被引量:4130
摘要
Philippe Amouyel, Julie Williams, Gerard Schellenberg, Sudha Seshadri and colleagues report a meta-analysis of genome-wide association studies for late-onset Alzheimer's disease in 17,008 cases and 37,154 controls with replication in an additional 8,572 cases and 11,312 controls. They identify 11 loci newly associated with Alzheimer's disease. Eleven susceptibility loci for late-onset Alzheimer's disease (LOAD) were identified by previous studies; however, a large portion of the genetic risk for this disease remains unexplained. We conducted a large, two-stage meta-analysis of genome-wide association studies (GWAS) in individuals of European ancestry. In stage 1, we used genotyped and imputed data (7,055,881 SNPs) to perform meta-analysis on 4 previously published GWAS data sets consisting of 17,008 Alzheimer's disease cases and 37,154 controls. In stage 2, 11,632 SNPs were genotyped and tested for association in an independent set of 8,572 Alzheimer's disease cases and 11,312 controls. In addition to the APOE locus (encoding apolipoprotein E), 19 loci reached genome-wide significance (P < 5 × 10−8) in the combined stage 1 and stage 2 analysis, of which 11 are newly associated with Alzheimer's disease.
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