全基因组关联研究
生物
表达数量性状基因座
连锁不平衡
遗传关联
遗传学
基因座(遗传学)
数量性状位点
疾病
单核苷酸多态性
基因
基因型
内科学
医学
作者
Diana Chang,Mike A. Nalls,Ingileif B. Hallgrímsdóttir,Julie Hunkapiller,Marcel van der Brug,Fang Cai,Geoffrey A. Kerchner,Gai Ayalon,Baris Bingol,Morgan Sheng,David A. Hinds,Timothy W. Behrens,Andrew Singleton,Tushar Bhangale,Robert Graham
出处
期刊:Nature Genetics
[Nature Portfolio]
日期:2017-09-11
卷期号:49 (10): 1511-1516
被引量:1210
摘要
Common variant genome-wide association studies (GWASs) have, to date, identified >24 risk loci for Parkinson's disease (PD). To discover additional loci, we carried out a GWAS comparing 6,476 PD cases with 302,042 controls, followed by a meta-analysis with a recent study of over 13,000 PD cases and 95,000 controls at 9,830 overlapping variants. We then tested 35 loci (P < 1 × 10-6) in a replication cohort of 5,851 cases and 5,866 controls. We identified 17 novel risk loci (P < 5 × 10-8) in a joint analysis of 26,035 cases and 403,190 controls. We used a neurocentric strategy to assign candidate risk genes to the loci. We identified protein-altering or cis-expression quantitative trait locus (cis-eQTL) variants in linkage disequilibrium with the index variant in 29 of the 41 PD loci. These results indicate a key role for autophagy and lysosomal biology in PD risk, and suggest potential new drug targets for PD.
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