Integration of rare expression outlier-associated variants improves polygenic risk prediction
Craig Smail(Children's Mercy Hospital), Stephen B. Montgomery(Stanford University), Themistocles L. Assimes(Stanford University), Nicole M. Ferraro, Johanne Marie Justesen(University of Copenhagen), Marissa R. Keever-Keigher(Children's Mercy Hospital), Yan V. Sun(Utah State University), Matthew Aguirre(Broad Institute), Abhiram Rao(Stanford University), Matthew G. Durrant(Palo Alto Institute), Michael J. Gloudemans, Manuel A. Rivas(Stanford University), Alex P. Reiner(Brigham and Women's Hospital), Christopher J. O’Donnell(Harvard University), Qin Hui(China-Japan Friendship Hospital), Xin Li(BaiCheng Normal University), Yosuke Tanigawa(Broad Institute), Jie Huang(VA Boston Healthcare System), Charles Kooperberg(Fred Hutch Cancer Center)
Cited by 32
Related Papers
Analysis of protein-coding genetic variation in 60,706 humans
|Nature|2016|10.3k
A cross-population atlas of genetic associations for 220 human phenotypes
|Nature Genetics|2021|2.4k
Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease
|Nature Genetics|2011|2k
Genome-wide association study of blood pressure and hypertension
|Nature Genetics|2009|1.4k