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Genome-wide association study identifies breast cancer risk variant at 10q21.2: results from the Asia Breast Cancer Consortium.

Cai Q, Long J, Lu W, Qu S, Wen W, Kang D, Lee JY, Chen K, Shen H, Shen CY, Sung H, Matsuo K, Haiman CA, Khoo US, Ren Z, Iwasaki M, Gu K, Xiang YB, Choi JY, Park SK, Zhang L, Hu Z, Wu PE, Noh DY, Tajima K, Henderson BE, Chan KY, Su F, Kasuga Y, Wang W, Cheng JR, Yoo KY, Lee JY, Zheng H, Liu Y, Shieh YL, Kim SW, Lee JW, Iwata H, Le Marchand L, Chan SY, Xie X, Tsugane S, Lee MH, Wang S, Li G, Levy S, Huang B, Shi J, Delahanty R, Zheng Y, Li C, Gao YT, Shu XO, Zheng W
Hum Mol Genet. 2011 20 (24): 4991-9

PMID: 21908515 · PMCID: PMC3221542 · DOI:10.1093/hmg/ddr405

MeSH Terms (15)

Adult Aged Alleles Asia Breast Neoplasms Cell Line, Tumor Chromosomes, Human, Pair 10 Female Genetic Predisposition to Disease Genome-Wide Association Study Humans Menopause Middle Aged Odds Ratio Polymorphism, Single Nucleotide

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