DNA repair variants and breast cancer risk

Author:

Grundy Anne1,Richardson Harriet2,Schuetz Johanna M.3,Burstyn Igor4,Spinelli John J.56,Brooks-Wilson Angela37,Aronson Kristan J.2

Affiliation:

1. CRCHUM (Centre de Recherche du CHUM), Montreal, Quebec, Canada

2. Department of Public Health Sciences and Cancer Research Institute; Queen's University; Kingston Ontario Canada

3. Canada's Michael Smith Genome Sciences Centre; British Columbia Cancer Agency; Vancouver British Columbia Canada

4. Department of Environmental and Occupational Health; Drexel University; Philadelphia Pennsylvania

5. Department of Cancer Control Research; British Columbia Cancer Agency; Vancouver British Columbia Canada

6. School of Population and Public Health; University of British Columbia; Vancouver British Columbia Canada

7. Department of Physiology and Kinesiology; Simon Fraser University; Burnaby British Columbia Canada

Funder

Canadian Institutes of Health Research

Publisher

Wiley

Subject

Health, Toxicology and Mutagenesis,Genetics(clinical),Epidemiology

Reference47 articles.

1. GRR: Graphical representation of relationship errors;Abecasis;Bioinformatics,2001

2. Haploview: Analysis and visualization of LD and haplotype maps;Barrett;Bioinformatics,2005

3. Common variants in the ATM, BRCA1, BRCA2, CHEK2 and TP53 cancer susceptibility genes are unlikely to increase breast cancer risk;Baynes;Breast Cancer Res,2007

4. Controlling the false discovery rate: A practical and powerful approach to multiple testing;Benjamini;J Royal Stat Soc Ser B,1995

5. Genetic association and functional studies of major polymorphic variants of MGMT;Bugni;DNA Repair (Amst),2007

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