Ontology highlight
ABSTRACT:
SUBMITTER: Han Y
PROVIDER: S-EPMC4572069 | biostudies-literature | 2015 Oct
REPOSITORIES: biostudies-literature
Han Ying Y Hazelett Dennis J DJ Wiklund Fredrik F Schumacher Fredrick R FR Stram Daniel O DO Berndt Sonja I SI Wang Zhaoming Z Rand Kristin A KA Hoover Robert N RN Machiela Mitchell J MJ Yeager Merideth M Burdette Laurie L Chung Charles C CC Hutchinson Amy A Yu Kai K Xu Jianfeng J Travis Ruth C RC Key Timothy J TJ Siddiq Afshan A Canzian Federico F Takahashi Atsushi A Kubo Michiaki M Stanford Janet L JL Kolb Suzanne S Gapstur Susan M SM Diver W Ryan WR Stevens Victoria L VL Strom Sara S SS Pettaway Curtis A CA Al Olama Ali Amin AA Kote-Jarai Zsofia Z Eeles Rosalind A RA Yeboah Edward D ED Tettey Yao Y Biritwum Richard B RB Adjei Andrew A AA Tay Evelyn E Truelove Ann A Niwa Shelley S Chokkalingam Anand P AP Isaacs William B WB Chen Constance C Lindstrom Sara S Le Marchand Loic L Giovannucci Edward L EL Pomerantz Mark M Long Henry H Li Fugen F Ma Jing J Stampfer Meir M John Esther M EM Ingles Sue A SA Kittles Rick A RA Murphy Adam B AB Blot William J WJ Signorello Lisa B LB Zheng Wei W Albanes Demetrius D Virtamo Jarmo J Weinstein Stephanie S Nemesure Barbara B Carpten John J Leske M Cristina MC Wu Suh-Yuh SY Hennis Anselm J M AJ Rybicki Benjamin A BA Neslund-Dudas Christine C Hsing Ann W AW Chu Lisa L Goodman Phyllis J PJ Klein Eric A EA Zheng S Lilly SL Witte John S JS Casey Graham G Riboli Elio E Li Qiyuan Q Freedman Matthew L ML Hunter David J DJ Gronberg Henrik H Cook Michael B MB Nakagawa Hidewaki H Kraft Peter P Chanock Stephen J SJ Easton Douglas F DF Henderson Brian E BE Coetzee Gerhard A GA Conti David V DV Haiman Christopher A CA
Human molecular genetics 20150710 19
Interpretation of biological mechanisms underlying genetic risk associations for prostate cancer is complicated by the relatively large number of risk variants (n = 100) and the thousands of surrogate SNPs in linkage disequilibrium. Here, we combined three distinct approaches: multiethnic fine-mapping, putative functional annotation (based upon epigenetic data and genome-encoded features), and expression quantitative trait loci (eQTL) analyses, in an attempt to reduce this complexity. We examine ...[more]