Cancer genetics and reproduction.
Explore this paper's citation graph
Summary
Recognition of individuals and families with inherited cancer predisposition syndromes and individuals at high risk due to familial cancer clustering is fundamentally important for the management and treatment of the current cancer and for future prevention of further cancers for the individual and their extended family.
- Type
- article
- Published
- 2010-02-01
- Cited by
- 5
- References
- 95
- OpenAlex
- https://openalex.org/W19864186
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:21356206
Keywords
Humanities, Art
References
- Germ-line BRCA1 mutations in Jewish and non-Jewish women with early-onset breast cancer.
- BRCA1, BRCA2, and hereditary nonpolyposis colorectal cancer gene mutations in an unselected ovarian cancer population: relationship to family history and implications for genetic testing.
- Breast and ovarian cancer incidence in BRCA1-mutation carriers. Breast Cancer Linkage Consortium.
- BRCA1 and BRCA2 mutations account for a large proportion of ovarian carcinoma cases
- Breast cancer and hormonal contraceptives: Collaborative reanalysis of individual data on 53 297 women with breast cancer and 100 239 women without breast cancer from 54 epidemiological studies
- Survival in familial, BRCA1-associated, and BRCA2-associated epithelial ovarian cancer. United Kingdom Coordinating Committee for Cancer Research (UKCCCR) Familial Ovarian Cancer Study Group.
- Risks and benefits of estrogen plus progestin in healthy postmenopausal women: principal results From the Women's Health Initiative randomized controlled trial.
- Heredity and human cancer.
- Survival of BRCA1 breast and ovarian cancer patients: a population-based study from southern Sweden.
- High frequency of BRCA1 and BRCA2 germline mutations in Ashkenazi Jewish ovarian cancer patients, regardless of family history.
- Surveillance for endometrial cancer in hereditary nonpolyposis colorectal cancer syndrome
- Primary peritoneal carcinoma after prophylactic oophorectomy in women with a family history of ovarian cancer. A report of the gilda radner familial ovarian cancer registry
- Cancer risk in hereditary nonpolyposis colorectal cancer due to MSH6 mutations: impact on counseling and surveillance.
- Specific keynote: hereditary ovarian cancer: what we know.
- Multiple newly identified loci associated with prostate cancer susceptibility
- Recurrent BRCA2 6174delT mutations in Ashkenazi Jewish women affected by breast cancer
- Phenotypic and genotypic heterogeneity in the Lynch syndrome: diagnostic, surveillance and management implications
- The contribution of germline BRCA1 and BRCA2 mutations to familial ovarian cancer: no evidence for other ovarian cancer-susceptibility genes.
- Genome-wide association study identifies novel breast cancer susceptibility loci
- PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene
Cited by
- Adenocarcinoma oncocítico oxifílico de endometrio: reporte de caso
- Pre-operative gynecologic evaluation of bariatric surgery patients: improving cancer detection in a high-risk population.
- Association of intimate partner vasectomy, use of long-acting progestogen-based contraceptives and intra-uterine contraceptive devices with risk of ovarian cancer.
- The Frequency of the Different Kinds of Ovarian Cancer in Shahid Sadoughi Hospital, Yazd, Iran
- Screening and Prevention of Ovarian Cancer
- Chapter 149 – Skin Cancer
Related papers
No related papers recorded.