Autosomal dominant inheritance of early‐onset breast cancer. Implications for risk prediction
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Summary
A large number of women with a family history of breast cancer face the task of providing appropriate screening schedules for their patients, and one group for whom this is particularly important are those Women with aFamily history of Breast cancer.
- Type
- article
- Published
- 1994-02-01
- Cited by
- 993
- References
- 43
- Access
- Open access
- OpenAlex
- https://openalex.org/W1968813862
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:12731524
Keywords
Medicine, Epidemiology, Breast cancer, Medical school, Haven
References
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- Segregation and linkage analysis of nine Utah breast cancer pedigrees
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- Familial breast-ovarian cancer locus on chromosome 17q12-q23.
- Breast cancer genes: how many, where and who are they?
- Genetic epidemiology of breast cancer in Britain
- Genetic study of breast cancer: Identification of a high risk group
- Inherited breast and ovarian cancer. What are the risks? What are the choices?
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- Germ line p53 mutations in a familial syndrome of breast cancer, sarcomas, and other neoplasms.
- Family history, age, and risk of breast cancer. Prospective data from the Nurses' Health Study.
- Risk of familial breast cancer
- Histologic types of benign breast disease and the risk for breast cancer
- Breast and other cancers in families with ataxia-telangiectasia.
- Inheritance of human breast cancer: evidence for autosomal dominant transmission in high-risk families.
- Recommendations on predictive testing for germ line p53 mutations among cancer-prone individuals.
- Family history and the risk of breast cancer.
- Genetic counseling for families with inherited susceptibility to breast and ovarian cancer.
Cited by
- Promoting breast health among women in the U.S. Virgin Islands: a focused study of the needs of Caribbean women.
- Chromosomal instability and double minute chromosomes in a breast cancer patient.
- Risk of breast and ovarian cancer in women with strong family histories.
- Effectiveness of breast cancer surveillance in BRCA1/2 gene mutation carriers and women with high familial risk.
- Understanding Mathematical Models for Breast Cancer Risk Assessment and Counseling
- Heightened Psychobiological Reactivity to Laboratory Stressors in Healthy Women at Familial Risk for Breast Cancer
- Assessing the Sensitivity of Decision-Analytic Results to Unobserved Markers of Risk: Defining the Effects of Heterogeneity Bias
- Life insurance and breast cancer risk assessment: Adverse selection, genetic testing decisions, and discrimination
- Perception of breast cancer risk and surveillance behaviours of women with family history of breast cancer: A brief report on a Spanish cohort
- Psychological Distress and Breast Self-Examination Frequency in Women at Increased Risk for Hereditary or Familial Breast Cancer
- A multidisciplinary approach to the management of breast cancer, part 1: prevention and diagnosis.
- Unraveling the Next Chapter: Sexual Development, Body Image, and Sexual Functioning in Female BRCA Carriers
- Quality of care review: some progress, and toward what goal?
- Breast cancer risk assessment in a mammography screening program and participation in the IBIS-II chemoprevention trial
- A clinical trial of lovastatin for modification of biomarkers associated with breast cancer risk
- Prophylactic bilateral mastectomy and contralateral prophylactic mastectomy.
- Complexities in Cancer Risk Counseling: Presentation of Three Cases
- Novel loss-of-function mutation in BRCA2 gene identified in a Chinese female with a family history of ovarian cancer: A case report
- Risk assessment & genetic testing.
- An Evaluation of the Effectiveness of a Nurse-Run Clinic for Women at Increased Risk for Breast Cancer on Anxiety, Depression, and Cancer Worry
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