疾病
生物
全基因组关联研究
遗传学
遗传关联
基因
联想(心理学)
单核苷酸多态性
计算生物学
基因型
医学
内科学
认识论
哲学
作者
Douglas P. Wightman,Iris E. Jansen,Jeanne E. Savage,Alexey Shadrin,Shahram Bahrami,Dominic Holland,Arvid Rongve,Sigrid Børte,Bendik S. Winsvold,Ole Kristian Drange,Amy E. Martinsen,Anne Heidi Skogholt,Cristen J. Willer,Geir Bråthen,Ingunn Bosnes,Jonas B. Nielsen,Lars G. Fritsche,Laurent F. Thomas,Linda M. Pedersen,Maiken E. Gabrielsen
出处
期刊:Nature Genetics
[Nature Portfolio]
日期:2021-09-01
卷期号:53 (9): 1276-1282
被引量:713
标识
DOI:10.1038/s41588-021-00921-z
摘要
Late-onset Alzheimer's disease is a prevalent age-related polygenic disease that accounts for 50-70% of dementia cases. Currently, only a fraction of the genetic variants underlying Alzheimer's disease have been identified. Here we show that increased sample sizes allowed identification of seven previously unidentified genetic loci contributing to Alzheimer's disease. This study highlights microglia, immune cells and protein catabolism as relevant to late-onset Alzheimer's disease, while identifying and prioritizing previously unidentified genes of potential interest. We anticipate that these results can be included in larger meta-analyses of Alzheimer's disease to identify further genetic variants that contribute to Alzheimer's pathology.
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