A systematic analysis of the association studies between CASP8 D302H polymorphisms and breast cancer risk
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics
Link
http://link.springer.com/article/10.1007/s12041-017-0774-y/fulltext.html
Reference25 articles.
1. Breast Cancer Association C 2006 Commonly studied single-nucleotide polymorphisms and breast cancer: results from the Breast Cancer Association Consortium. J. Natl. Cancer Inst. 98, 1382–1396.
2. Campa D., Kaaks R., Le Marchand L., Haiman C. A., Travis R. C., Berg C. D. et al. 2011 Interactions between genetic variants and breast cancer risk factors in the breast and prostate cancer cohort consortium. J. Natl. Cancer Inst. 103, 1252–1263.
3. Couch F. J., Wang X., McWilliams R. R., Bamlet W. R., de Andrade M. and Petersen G. M. 2009 Association of breast cancer susceptibility variants with risk of pancreatic cancer. Cancer Epidemiol. Biomarkers Prev. 18, 3044–3048.
4. Cox A., Dunning A. M., Garcia-Closas M., Balasubramanian S., Reed M. W., Pooley K. A. et al. 2007 A common coding variant in CASP8 is associated with breast cancer risk. Nat. Genet. 39, 352–358.
5. Fletcher O. and Dudbridge F. 2014 Candidate gene-environment interactions in breast cancer. BMC Med. 12, 195.
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