The benefit of adding polygenic risk scores, lifestyle factors, and breast density to family history and genetic status for breast cancer risk and surveillance classification of unaffected women from germline CHEK2 c.1100delC families
Author:
Funder
KWF Kankerbestrijding
Publisher
Elsevier BV
Reference40 articles.
1. Low-penetrance susceptibility to breast cancer due to CHEK2(*)1100delC in noncarriers of BRCA1 or BRCA2 mutations;Meijers-Heijboer;Nat Genet,2002
2. CHEK2*1100delC and susceptibility to breast cancer: a collaborative analysis involving 10,860 breast cancer cases and 9,065 controls from 10 studies;Consortium;Am J Hum Genet,2004
3. CHEK2*1100delC genotyping for clinical assessment of breast cancer risk: meta-analyses of 26,000 patient cases and 27,000 controls;Weischer;J Clin Oncol,2008
4. Excess breast cancer risk in first degree relatives of CHEK2*1100delC positive familial breast cancer cases;Adank;Eur J Cancer,2013
5. Frequency of the CHEK2 1100delC mutation among women with breast cancer: an international study;Zhang;Cancer Res,2008
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