Genetic epidemiology of breast cancer in Britain
- 1 May 1991
- journal article
- case report
- Published by Wiley in Annals of Human Genetics
- Vol. 55 (2) , 151-159
- https://doi.org/10.1111/j.1469-1809.1991.tb00408.x
Abstract
A complex segregation analysis was conducted on two British series (one consecutive series of probands with breast cancer and one series ascertained through a normal consultand). Altogether there were 1248 nuclear families with breast cancer. A dominant gene with a frequency of 0.003 giving a lifetime penetrance of 0.83 is favoured. Ovarian, endometrial and cancers associated with the SBLA syndrome, as well as benign breast disease, were significantly more common in familial breast cancer than in families of single cases. Probands in families with more than one individual with breast cancer were non-significantly younger than isolated probands.Keywords
This publication has 12 references indexed in Scilit:
- Malignancies in families of women with medullary, tubular and invasive ductal breast cancerEuropean Journal of Cancer and Clinical Oncology, 1990
- Inheritance of human breast cancer: evidence for autosomal dominant transmission in high-risk families.Proceedings of the National Academy of Sciences, 1988
- Genetic analysis of human breast cancer: Implications for family study designsGenetic Epidemiology, 1988
- Segregation and linkage analysis of nine Utah breast cancer pedigreesGenetic Epidemiology, 1987
- FAMILIAL BREAST CANCER IN A POPULATION-BASED SERIESAmerican Journal of Epidemiology, 1986
- Segregation analysis of the Jacobsen dataGenetic Epidemiology, 1986
- Segregation and linkage analysis of breast cancer in the Dutch and Utah familiesGenetic Epidemiology, 1986
- Genetic epidemiology of breast cancer: Segregation analysis of 200 Danish pedigreesGenetic Epidemiology, 1984
- Early Age of Onset in Familial Breast CancerArchives of Surgery, 1976
- Soft-Tissue Sarcomas, Breast Cancer, and Other NeoplasmsAnnals of Internal Medicine, 1969