CASP8 variants D302H and −652 6N ins/del do not influence the risk of colorectal cancer in the United Kingdom population
Open Access
- 25 March 2008
- journal article
- research article
- Published by Springer Science and Business Media LLC in British Journal of Cancer
- Vol. 98 (8), 1434-1436
- https://doi.org/10.1038/sj.bjc.6604314
Abstract
No abstract availableKeywords
This publication has 12 references indexed in Scilit:
- National study of colorectal cancer geneticsBritish Journal of Cancer, 2007
- The CASP8 -652 6N del promoter polymorphism and breast cancer risk: a multicenter studyBreast Cancer Research and Treatment, 2007
- A common genetic risk factor for colorectal and prostate cancerNature Genetics, 2007
- Genome-wide association scan identifies a colorectal cancer susceptibility locus on chromosome 8q24Nature Genetics, 2007
- A genome-wide association scan of tag SNPs identifies a susceptibility variant for colorectal cancer at 8q24.21Nature Genetics, 2007
- A common coding variant in CASP8 is associated with breast cancer riskNature Genetics, 2007
- Explaining the Familial Colorectal Cancer Risk Associated with Mismatch Repair (MMR)-Deficient and MMR-Stable TumorsClinical Cancer Research, 2007
- Association of the CASP10 V410I variant with reduced familial breast cancer risk and interaction with the CASP8 D302H variantCarcinogenesis: Integrative Cancer Research, 2005
- 'Racial' differences in genetic effects for complex diseasesNature Genetics, 2004
- Environmental and Heritable Factors in the Causation of Cancer — Analyses of Cohorts of Twins from Sweden, Denmark, and FinlandNew England Journal of Medicine, 2000