Communicating polygenic risk scores in the familial breast cancer clinic
Author:
Funder
National Breast Cancer Foundation
Cancer Council NSW
National Health and Medical Research Council
Publisher
Elsevier BV
Subject
General Medicine
Reference46 articles.
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3. A role for common genomic variants in the assessment of familial breast Cancer;Sawyer;J. Clin. Oncol.,2012
4. Addition of a 161-SNP polygenic risk score to family history-based risk prediction: impact on clinical management in non-BRCA1/2 breast cancer families;Lakeman;J. Med. Genet.,2019
5. The impact of a panel of 18 SNPs on breast cancer risk in women attending a UK familial screening clinic: a case-control study;Evans;J. Med. Genet.,2017
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