Ontology highlight
ABSTRACT:
SUBMITTER: Schumacher FR
PROVIDER: S-EPMC4967357 | biostudies-literature | 2015 Jul
REPOSITORIES: biostudies-literature
Schumacher Fredrick R FR Schmit Stephanie L SL Jiao Shuo S Edlund Christopher K CK Wang Hansong H Zhang Ben B Hsu Li L Huang Shu-Chen SC Fischer Christopher P CP Harju John F JF Idos Gregory E GE Lejbkowicz Flavio F Manion Frank J FJ McDonnell Kevin K McNeil Caroline E CE Melas Marilena M Rennert Hedy S HS Shi Wei W Thomas Duncan C DC Van Den Berg David J DJ Hutter Carolyn M CM Aragaki Aaron K AK Butterbach Katja K Caan Bette J BJ Carlson Christopher S CS Chanock Stephen J SJ Curtis Keith R KR Fuchs Charles S CS Gala Manish M Giovannucci Edward L EL Gogarten Stephanie M SM Hayes Richard B RB Henderson Brian B Hunter David J DJ Jackson Rebecca D RD Kolonel Laurence N LN Kooperberg Charles C Küry Sébastien S LaCroix Andrea A Laurie Cathy C CC Laurie Cecelia A CA Lemire Mathieu M Levine David D Ma Jing J Makar Karen W KW Qu Conghui C Taverna Darin D Ulrich Cornelia M CM Wu Kana K Kono Suminori S West Dee W DW Berndt Sonja I SI Bezieau Stéphane S Brenner Hermann H Campbell Peter T PT Chan Andrew T AT Chang-Claude Jenny J Coetzee Gerhard A GA Conti David V DV Duggan David D Figueiredo Jane C JC Fortini Barbara K BK Gallinger Steven J SJ Gauderman W James WJ Giles Graham G Green Roger R Haile Robert R Harrison Tabitha A TA Hoffmeister Michael M Hopper John L JL Hudson Thomas J TJ Hudson Thomas J TJ Jacobs Eric E Jacobs Eric E Iwasaki Motoki M Jee Sun Ha SH Jenkins Mark M Jia Wei-Hua WH Joshi Amit A Li Li L Lindor Noralene M NM Matsuo Keitaro K Moreno Victor V Mukherjee Bhramar B Newcomb Polly A PA Potter John D JD Potter John D JD Raskin Leon L Rennert Gad G Rosse Stephanie S Severi Gianluca G Schoen Robert E RE Seminara Daniela D Shu Xiao-Ou XO Slattery Martha L ML Tsugane Shoichiro S White Emily E Xiang Yong-Bing YB Zanke Brent W BW Zheng Wei W Le Marchand Loic L Casey Graham G Gruber Stephen B SB Peters Ulrike U
Nature communications 20150707
Genetic susceptibility to colorectal cancer is caused by rare pathogenic mutations and common genetic variants that contribute to familial risk. Here we report the results of a two-stage association study with 18,299 cases of colorectal cancer and 19,656 controls, with follow-up of the most statistically significant genetic loci in 4,725 cases and 9,969 controls from two Asian consortia. We describe six new susceptibility loci reaching a genome-wide threshold of P<5.0E-08. These findings provide ...[more]