Breast cancer risk for noncarriers of family-specific BRCA1 and BRCA2 mutations: more trouble with phenocopies
- PMID: 22370324
- DOI: 10.1200/JCO.2011.40.8021
Breast cancer risk for noncarriers of family-specific BRCA1 and BRCA2 mutations: more trouble with phenocopies
Comment on
-
Breast cancer risk for noncarriers of family-specific BRCA1 and BRCA2 mutations: findings from the Breast Cancer Family Registry.J Clin Oncol. 2011 Dec 1;29(34):4505-9. doi: 10.1200/JCO.2010.34.4440. Epub 2011 Oct 31. J Clin Oncol. 2011. PMID: 22042950 Free PMC article.
Similar articles
-
Contribution of germline BRCA1 and BRCA2 sequence alterations to breast cancer in Northern India.BMC Med Genet. 2006 Oct 4;7:75. doi: 10.1186/1471-2350-7-75. BMC Med Genet. 2006. PMID: 17018160 Free PMC article.
-
BRCA1 and BRCA2 mutation predictions using the BOADICEA and BRCAPRO models and penetrance estimation in high-risk French-Canadian families.Breast Cancer Res. 2006;8(1):R3. doi: 10.1186/bcr1365. Epub 2005 Dec 12. Breast Cancer Res. 2006. PMID: 16417652 Free PMC article.
-
Prevalence of BRCA1 and BRCA2 mutations in women diagnosed with ductal carcinoma in situ.JAMA. 2005 Feb 23;293(8):964-9. doi: 10.1001/jama.293.8.964. JAMA. 2005. PMID: 15728167
-
Comprehensive spectrum of BRCA1 and BRCA2 deleterious mutations in breast cancer in Asian countries.J Med Genet. 2016 Jan;53(1):15-23. doi: 10.1136/jmedgenet-2015-103132. Epub 2015 Jul 17. J Med Genet. 2016. PMID: 26187060 Free PMC article. Review.
-
Genomic rearrangements in the BRCA1 and BRCA2 genes.Hum Mutat. 2005 May;25(5):415-22. doi: 10.1002/humu.20169. Hum Mutat. 2005. PMID: 15832305 Review.
Cited by
-
Clinical follow-up and breast and ovarian cancer screening of true BRCA1/2 noncarriers: a qualitative investigation.Genet Med. 2016 Jun;18(6):627-34. doi: 10.1038/gim.2015.135. Epub 2015 Nov 5. Genet Med. 2016. PMID: 26540155
-
Genetic tests as prophecy: understanding self-defeating and self-fulfilling mechanisms in (predictive) genetic testing.Eur J Hum Genet. 2025 Aug;33(8):1051-1056. doi: 10.1038/s41431-025-01874-1. Epub 2025 Jun 5. Eur J Hum Genet. 2025. PMID: 40473778 Free PMC article. Review.
-
Phenocopies in melanoma-prone families with germ-line CDKN2A mutations.Genet Med. 2018 Sep;20(9):1087-1090. doi: 10.1038/gim.2017.216. Epub 2017 Dec 7. Genet Med. 2018. PMID: 29215650 Free PMC article.
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Medical
Miscellaneous
