作者
Sara R Rashkin, Rebecca E Graff, Linda Kachuri, Khanh K Thai, Stacey E Alexeeff, Maruta A Blatchins, Taylor B Cavazos, Douglas A Corley, Nima C Emami, Joshua D Hoffman, Eric Jorgenson, Lawrence H Kushi, Travis J Meyers, Stephen K Van Den Eeden, Elad Ziv, Laurel A Habel, Thomas J Hoffmann, Lori C Sakoda, John S Witte
发表日期
2020/9/4
期刊
Nature Communications
卷号
11
期号
1
页码范围
1-14
出版商
Nature Publishing Group
简介
Deciphering the shared genetic basis of distinct cancers has the potential to elucidate carcinogenic mechanisms and inform broadly applicable risk assessment efforts. Here, we undertake genome-wide association studies (GWAS) and comprehensive evaluations of heritability and pleiotropy across 18 cancer types in two large, population-based cohorts: the UK Biobank (408,786 European ancestry individuals; 48,961 cancer cases) and the Kaiser Permanente Genetic Epidemiology Research on Adult Health and Aging cohorts (66,526 European ancestry individuals; 16,001 cancer cases). The GWAS detect 21 genome-wide significant associations independent of previously reported results. Investigations of pleiotropy identify 12 cancer pairs exhibiting either positive or negative genetic correlations; 25 pleiotropic loci; and 100 independent pleiotropic variants, many of which are regulatory elements and/or …
引用总数
20202021202220232024737516136