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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Detalhes bibliográficos
Publicado no:Carcinogenesis
Principais autores: 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.
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2014
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Original Manuscript
Acesso em linha: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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