Genotype-first approach to the detection of hereditary breast and ovarian cancer risk, and effects of risk disclosure to biobank participants

Genotype-first approach allows to systematically identify carriers of pathogenic variants in BRCA1/2 genes conferring a high risk of familial breast and ovarian cancer. Participants of the Estonian biobank have expressed support for the disclosure of clinically significant findings. With an Estonian...

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Библиографические подробности
Опубликовано в: :Eur J Hum Genet
Главные авторы: Leitsalu, Liis, Palover, Marili, Sikka, Timo Tõnis, Reigo, Anu, Kals, Mart, Pärn, Kalle, Nikopensius, Tiit, Esko, Tõnu, Metspalu, Andres, Padrik, Peeter, Tõnisson, Neeme
Формат: Artigo
Язык:Inglês
Опубликовано: Springer International Publishing 2020
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Article
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC7940387/
https://ncbi.nlm.nih.gov/pubmed/33230308
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41431-020-00760-2
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