Common variants at the 19p13.1 and ZNF365 loci are associated with ER subtypes of breast cancer and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
Genome-wide association studies (GWAS) identified variants at 19p13.1 and ZNF365 (10q21.2) as risk factors for breast cancer among BRCA1 and BRCA2 mutation carriers, respectively. We explored associations with ovarian cancer and with breast cancer by tumor histopathology for these variants in mutation carriers from the Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA).
| Originalsprog | Engelsk |
|---|---|
| Tidsskrift | Cancer Epidemiology, Biomarkers & Prevention |
| Vol/bind | 21 |
| Udgave nummer | 4 |
| Sider (fra-til) | 645-57 |
| Antal sider | 13 |
| ISSN | 1055-9965 |
| DOI | |
| Status | Udgivet - 2012 |
ID: 48450631