A risk prediction algorithm for ovarian cancer incorporatingBRCA1, BRCA2, common alleles and other familial effects
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Title
A risk prediction algorithm for ovarian cancer incorporatingBRCA1, BRCA2, common alleles and other familial effects
Authors
Keywords
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Journal
JOURNAL OF MEDICAL GENETICS
Volume 52, Issue 7, Pages 465-475
Publisher
BMJ
Online
2015-05-30
DOI
10.1136/jmedgenet-2015-103077
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Note: Only part of the references are listed.- Identification of six new susceptibility loci for invasive epithelial ovarian cancer
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- Germline Mutation in BRCA1 or BRCA2 and Ten-Year Survival for Women Diagnosed with Epithelial Ovarian Cancer
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- Prospective validation of the breast cancer risk prediction model BOADICEA and a batch-mode version BOADICEACentre
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- Genome-Wide Association Study in BRCA1 Mutation Carriers Identifies Novel Loci Associated with Breast and Ovarian Cancer Risk
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- Ovarian cancer susceptibility alleles and risk of ovarian cancer inBRCA1andBRCA2mutation carriers
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- Genetic Variation at 9p22.2 and Ovarian Cancer Risk for BRCA1 and BRCA2 Mutation Carriers
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- A genome-wide association study identifies susceptibility loci for ovarian cancer at 2q31 and 8q24
- (2010) Ellen L Goode et al. NATURE GENETICS
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- A genome-wide association study identifies a new ovarian cancer susceptibility locus on 9p22.2
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