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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Autors principals: 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.
Format: Artigo
Idioma:Inglês
Publicat: Oxford University Press 2011
Matèries:
Association Studies Articles
Accés en línia: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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