Germline mutation in the RAD51B gene confers predisposition to breast cancer

Rare Mutations in XRCC2 Increase the Risk of Breast Cancer

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Guidelines for splicing analysis in molecular diagnosis derived from a set of 327 combined in silico/in vitro studies on BRCA1 and BRCA2 variants

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Rare variants in XRCC2 as breast cancer susceptibility alleles: Table 1

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Exome sequencing reveals a novel Fanconi group defined by XRCC2 mutation: Figure 1

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Genome-wide association study identifies a common variant in RAD51B associated with male breast cancer risk

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Germline RAD51C mutations confer susceptibility to ovarian cancer

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A HRM-based screening method detects RAD51C germ-line deleterious mutations in Spanish breast and ovarian cancer families

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Mutation analysis of RAD51L1 (RAD51B/REC2) in multiple-case, non-BRCA1/2 breast cancer families

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Global cancer statistics

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Analysis of RAD51C germline mutations in high-risk breast and ovarian cancer families and ovarian cancer patients

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Association between the XRCC3 polymorphisms and breast cancer risk: meta-analysis based on case–control studies

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Germline mutations in RAD51D confer susceptibility to ovarian cancer

(2011) Chey Loveday et al.   NATURE GENETICS

RAD51 paralogs: Roles in DNA damage signalling, recombinational repair and tumorigenesis

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EMMA, a cost- and time-effective diagnostic method for simultaneous detection of point mutations and large-scale genomic rearrangements: application to BRCA1 and BRCA2 in 1,525 patients

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Mutation of the RAD51C gene in a Fanconi anemia–like disorder

(2010) Fiona Vaz et al.   NATURE GENETICS

Germline mutations in breast and ovarian cancer pedigrees establish RAD51C as a human cancer susceptibility gene

(2010) Alfons Meindl et al.   NATURE GENETICS

A method and server for predicting damaging missense mutations

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Rare Variants Create Synthetic Genome-Wide Associations

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A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1)

(2009) Gilles Thomas et al.   NATURE GENETICS

Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm

(2009) Prateek Kumar et al.   Nature Protocols

Inherited Susceptibility to Common Cancers

(2008) William D. Foulkes   NEW ENGLAND JOURNAL OF MEDICINE

Polygenes, Risk Prediction, and Targeted Prevention of Breast Cancer

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