Common non-synonymous SNPs associated with breast cancer susceptibility: findings from the Breast Cancer Association Consortium
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Title
Common non-synonymous SNPs associated with breast cancer susceptibility: findings from the Breast Cancer Association Consortium
Authors
Keywords
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Journal
HUMAN MOLECULAR GENETICS
Volume 23, Issue 22, Pages 6096-6111
Publisher
Oxford University Press (OUP)
Online
2014-06-19
DOI
10.1093/hmg/ddu311
References
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- Genome-wide association study identifies breast cancer risk variant at 10q21.2: results from the Asia Breast Cancer Consortium
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- 7q21-rs6964587 and breast cancer risk: an extended case-control study by the Breast Cancer Association Consortium
- (2011) R. L. Milne et al. JOURNAL OF MEDICAL GENETICS
- Novel Breast Cancer Susceptibility Locus at 9q31.2: Results of a Genome-Wide Association Study
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- (2011) Christopher A Haiman et al. NATURE GENETICS
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- A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1)
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- Association of a Common AKAP9 Variant With Breast Cancer Risk: A Collaborative Analysis
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- Common variants on chromosome 5p12 confer susceptibility to estrogen receptor–positive breast cancer
- (2008) Simon N Stacey et al. NATURE GENETICS
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