Large-scale fine mapping of the HNF1B locus and prostate cancer risk

Previous genome-wide association studies have identified two independent variants in HNF1B as susceptibility loci for prostate cancer risk. To fine-map common genetic variation in this region, we genotyped 79 single nucleotide polymorphisms (SNPs) in the 17q12 region harboring HNF1B in 10 272 prosta...

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Detalhes bibliográficos
Main Authors: Berndt, Sonja I., Sampson, Joshua, Yeager, Meredith, Jacobs, Kevin B., Wang, Zhaoming, Hutchinson, Amy, Chung, Charles, Orr, Nick, Wacholder, Sholom, Chatterjee, Nilanjan, Yu, Kai, Kraft, Peter, Feigelson, Heather Spencer, Thun, Michael J., Diver, W. Ryan, Albanes, Demetrius, Virtamo, Jarmo, Weinstein, Stephanie, Schumacher, Fredrick R., Cancel-Tassin, Geraldine, Cussenot, Olivier, Valeri, Antoine, Andriole, Gerald L., Crawford, E. David, Haiman, Christopher, Henderson, Brian, Kolonel, Laurence, Le Marchand, Loic, Siddiq, Afshan, Riboli, Elio, Travis, Ruth C., Kaaks, Rudolf, Isaacs, William, Isaacs, Sarah, Wiley, Kathleen E., Gronberg, Henrik, Wiklund, Fredrik, Stattin, Pär, Xu, Jianfeng, Zheng, S. Lilly, Sun, Jielin, Vatten, Lars J., Hveem, Kristian, Njølstad, Inger, Gerhard, Daniela S., Tucker, Margaret, Hayes, Richard B., Hoover, Robert N., Fraumeni, Joseph F., Hunter, David J., Thomas, Gilles, Chanock, Stephen J.
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2011
Assuntos:
Association Studies Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3140817/
https://ncbi.nlm.nih.gov/pubmed/21576123
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddr213
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