FGFR2 variants and breast cancer risk: fine-scale mapping using African American studies and analysis of chromatin conformation

Genome-wide association studies have identified FGFR2 as a breast cancer (BC) susceptibility gene in populations of European and Asian descent, but a causative variant has not yet been conclusively identified. We hypothesized that the weaker linkage disequilibrium across this associated region in po...

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Detalhes bibliográficos
Main Authors: Udler, Miriam S., Meyer, Kerstin B., Pooley, Karen A., Karlins, Eric, Struewing, Jeffery P., Zhang, Jinghui, Doody, David R., MacArthur, Stewart, Tyrer, Jonathan, Pharoah, Paul D., Luben, Robert, Bernstein, Leslie, Kolonel, Laurence N., Henderson, Brian E., Le Marchand, Loic, Ursin, Giske, Press, Michael F., Brennan, Paul, Sangrajrang, Suleeporn, Gaborieau, Valerie, Odefrey, Fabrice, Shen, Chen-Yang, Wu, Pei-Ei, Wang, Hui-Chun, Kang, Daehee, Yoo, Keun-Young, Noh, Dong-Young, Ahn, Sei-Hyun, Ponder, Bruce A.J., Haiman, Christopher A., Malone, Kathleen E., Dunning, Alison M., Ostrander, Elaine A., Easton, Douglas F.
Formato: Artigo
Idioma:English
Publicado em: Oxford University Press 2009
Assuntos:
Association Studies Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2733817/
https://ncbi.nlm.nih.gov/pubmed/19223389
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddp078
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Internet

https://ncbi.nlm.nih.gov/pmc/articles/PMC2733817/
https://ncbi.nlm.nih.gov/pubmed/19223389
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddp078

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