Funder
U.S. Department of Health & Human Services | NIH | National Human Genome Research Institute
U.S. Department of Health & Human Services | NIH | National Heart, Lung, and Blood Institute
Burroughs Wellcome Fund
Broad Institute
Alfred P. Sloan Foundation
Massachusetts Institute of Technology
U.S. Department of Health & Human Services | NIH | National Institute of Mental Health
NSF | Directorate for Mathematical & Physical Sciences | Division of Mathematical Sciences
Publisher
Springer Science and Business Media LLC
Reference56 articles.
1. International Multiple Sclerosis Genetics Consortium. Low-frequency and rare-coding variation contributes to multiple sclerosis risk. Cell 175, 1679–1687.e7 (2018).
2. Marouli, E. et al. Rare and low-frequency coding variants alter human adult height. Nature 542, 186–190 (2017).
3. Liu, D. J. et al. Exome-wide association study of plasma lipids in >300,000 individuals. Nat. Genet. 49, 1758–1766 (2017).
4. Liu, C. et al. Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci. Nat. Genet. 48, 1162–1170 (2016).
5. Fu, W. et al. Analysis of 6,515 exomes reveals a recent origin of most human protein-coding variants. Nature 493, 216–220 (2013).
Cited by
79 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献