A novel colorectal cancer risk locus at 4q32.2 identified from an international genome-wide association study

Only a fraction of colorectal cancer heritability is explained by known risk-conferring genetic variation. This study was designed to identify novel risk alleles in Europeans. We conducted a genome-wide association study (GWAS) meta-analysis of colorectal cancer in participants from a population-bas...

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書誌詳細
出版年:Carcinogenesis
主要な著者: Schmit, Stephanie L., Schumacher, Fredrick R., Edlund, Christopher K., Conti, David V., Raskin, Leon, Lejbkowicz, Flavio, Pinchev, Mila, Rennert, Hedy S., Jenkins, Mark A., Hopper, John L., Buchanan, Daniel D., Lindor, Noralane M., Le Marchand, Loic, Gallinger, Steven, Haile, Robert W., Newcomb, Polly A., Huang, Shu-Chen, Rennert, Gad, Casey, Graham, Gruber, Stephen B.
フォーマット: Artigo
言語:Inglês
出版事項: Oxford University Press 2014
主題:
Original Manuscript
オンライン･アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC4271131/
https://ncbi.nlm.nih.gov/pubmed/25023989
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/carcin/bgu148
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