{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,18]],"date-time":"2026-08-18T01:38:37Z","timestamp":1787017117556,"version":"build-2736575974"},"reference-count":5,"publisher":"BMJ","issue":"11","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["J Med Genet"],"published-print":{"date-parts":[[1995,11]]},"abstract":"<jats:p>Breast cancer is a multifactorial disease with an inherited predisposition being implicated in around 5% of all cases. Using previous epidemiological data assessing risks for the relatives of women with breast cancer, we have identified 154 women (from a screened population of 35,505) and 289 of their relatives between 50 and 64 years who have more than twice the age related risk of developing breast cancer. This constitutes 1.24% of the breast screening population attending the North East Scotland NHSBSP. For each woman identified to be at high risk, we have found 1.87 female relatives between 50 and 64 years and 1.85 relatives under 50 years also to be at high risk. Around 78% of the women identified with a significant family history of breast or other cancer have attended for counselling about their risks. The breast screening programme can be used to identify women at high risk of breast cancer in order to offer them (and their relatives) access to genetic counselling and appropriate screening.<\/jats:p>","DOI":"10.1136\/jmg.32.11.862","type":"journal-article","created":{"date-parts":[[2008,11,10]],"date-time":"2008-11-10T15:23:16Z","timestamp":1226330596000},"page":"862-866","source":"Crossref","is-referenced-by-count":8,"title":["Identification of women at high genetic risk of breast cancer through the National Health Service Breast Screening Programme (NHSBSP)."],"prefix":"10.1136","volume":"32","author":[{"given":"D","family":"de Silva","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"F","family":"Gilbert","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"G","family":"Needham","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"H","family":"Deans","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"P","family":"Turnpenny","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"N","family":"Haites","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"239","published-online":{"date-parts":[[1995,11,1]]},"reference":[{"key":"ref_1","article-title":"Registrar General for Scotland annual report 1992","year":"1992","unstructured":"Registrar General for Scotland annual report 1992. London: HMSO, 1992."},{"key":"ref_2","first-page":"455","volume":"71","author":"Segregation aansasloycsiisa.teJd Natl Cancer Inst","year":"1983","unstructured":"Segregation aansasloycsiisa.teJd Natl Cancer Inst 1983;71:455-61."},{"key":"ref_3","first-page":"7","article-title":"Genetic epidemiology of breast cancer: segregation analysis","volume-title":"Danish pedigrees","volume":"1","author":"Williams, W.; Anderson, D.","year":"1984","unstructured":"Williams W, Anderson D. Genetic epidemiology of breast cancer: segregation analysis of 200 Danish pedigrees. Genet Epidemiol 1984;1:7-20."},{"key":"ref_4","first-page":"286","article-title":"Effects of individualised breast cancer risk counselling: a randomized trial","volume":"87","author":"Lerman, C.; Lustbader, E.; Rimer, B.","year":"1995","unstructured":"Lerman C, Lustbader E, Rimer B, et al. Effects of individualised breast cancer risk counselling: a randomized trial. J7 Nad Cancer Inst 1995;87:286-92."},{"key":"ref_5","first-page":"1074","article-title":"Mammography adhoefrbernecaestacnadncpesry.cJhoNloagdicCalandciesrtrIenssst among women at risk","volume":"85","author":"Lerman, C.; Daly, M.; Sands, C.","year":"1993","unstructured":"Lerman C, Daly M, Sands C, et al. Mammography adhoefrbernecaestacnadncpesry.cJhoNloagdicCalandciesrtrIenssst among women at risk 1993;85:1074-80."}],"container-title":["Journal of Medical Genetics"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/syndication.highwire.org\/content\/doi\/10.1136\/jmg.32.11.862","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2025,10,18]],"date-time":"2025-10-18T05:22:06Z","timestamp":1760764926000},"score":1,"resource":{"primary":{"URL":"https:\/\/jmg.bmj.com\/lookup\/doi\/10.1136\/jmg.32.11.862"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1995,11]]},"references-count":5,"journal-issue":{"issue":"11","published-online":{"date-parts":[[1995,11,1]]},"published-print":{"date-parts":[[1995,11]]}},"alternative-id":["10.1136\/jmg.32.11.862"],"URL":"https:\/\/doi.org\/10.1136\/jmg.32.11.862","relation":{},"ISSN":["0022-2593","1468-6244"],"issn-type":[{"value":"0022-2593","type":"print"},{"value":"1468-6244","type":"electronic"}],"subject":[],"published":{"date-parts":[[1995,11]]}}}