HBOC in Europe

Abstract Europe has contributed to the majority of high-impact papers on genes and risk alleles in breast cancer and ovarian cancer susceptibility. Consortia like the Breast Cancer Linkage Consortium, Breast Cancer Association Consortium, and the Consortium of Investigators on Modifying genes in BR...

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Main Author: Hanne Meijers Heijboer
Format: Article
Language:English
Published: Universitas Gadjah Mada 2017-02-01
Series:Journal of the Medical Sciences
Online Access:https://jurnal.ugm.ac.id/bik/article/view/13617
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spelling doaj-d0253c41204242f9b5d4d5e802c7e9522020-11-24T22:26:51ZengUniversitas Gadjah MadaJournal of the Medical Sciences0126-13122356-39312017-02-0148410.19106/JMedScieSup004804201601110748HBOC in EuropeHanne Meijers HeijboerAbstract Europe has contributed to the majority of high-impact papers on genes and risk alleles in breast cancer and ovarian cancer susceptibility. Consortia like the Breast Cancer Linkage Consortium, Breast Cancer Association Consortium, and the Consortium of Investigators on Modifying genes in BRCA1/2, started from the nineties of the last century on.  Many highly motivated participants throughout Europe, the US, Australia and elsewhere contributed to the formation of huge datasets. Instrumental of the success of the consortia was also the leadership and knowledge of Dough Easton, UK, on the statistics of cancer genetics. The consortia papers have produced the data on which national guidelines in HBOC were formulated in West-Europe, the US and worldwide.   Genetic testing for HBOC is in most Western-European countries accepted and funded. Two decades after the identification of BRCA1 and BRCA2, attitudes towards genetic testing for HBOC are changing and becoming more ‘common’ practice. This offers opportunities to organize cancer genetic care more efficiently and at lower costs while informed decision making and consent of the patients remain in place. Keywords: BRCA1, BRCA2, HBOC, Europe, Founder mutations, linkagehttps://jurnal.ugm.ac.id/bik/article/view/13617
collection DOAJ
language English
format Article
sources DOAJ
author Hanne Meijers Heijboer
spellingShingle Hanne Meijers Heijboer
HBOC in Europe
Journal of the Medical Sciences
author_facet Hanne Meijers Heijboer
author_sort Hanne Meijers Heijboer
title HBOC in Europe
title_short HBOC in Europe
title_full HBOC in Europe
title_fullStr HBOC in Europe
title_full_unstemmed HBOC in Europe
title_sort hboc in europe
publisher Universitas Gadjah Mada
series Journal of the Medical Sciences
issn 0126-1312
2356-3931
publishDate 2017-02-01
description Abstract Europe has contributed to the majority of high-impact papers on genes and risk alleles in breast cancer and ovarian cancer susceptibility. Consortia like the Breast Cancer Linkage Consortium, Breast Cancer Association Consortium, and the Consortium of Investigators on Modifying genes in BRCA1/2, started from the nineties of the last century on.  Many highly motivated participants throughout Europe, the US, Australia and elsewhere contributed to the formation of huge datasets. Instrumental of the success of the consortia was also the leadership and knowledge of Dough Easton, UK, on the statistics of cancer genetics. The consortia papers have produced the data on which national guidelines in HBOC were formulated in West-Europe, the US and worldwide.   Genetic testing for HBOC is in most Western-European countries accepted and funded. Two decades after the identification of BRCA1 and BRCA2, attitudes towards genetic testing for HBOC are changing and becoming more ‘common’ practice. This offers opportunities to organize cancer genetic care more efficiently and at lower costs while informed decision making and consent of the patients remain in place. Keywords: BRCA1, BRCA2, HBOC, Europe, Founder mutations, linkage
url https://jurnal.ugm.ac.id/bik/article/view/13617
work_keys_str_mv AT hannemeijersheijboer hbocineurope
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