A genome-wide scan of 10 000 gene-centric variants and colorectal cancer risk.
Genome scans based on gene-centric single nucleotide polymorphisms (SNPs) have been proposed as an efficient approach to identify disease-causing variants that is complementary to scans based on tagging SNPs. Adopting this approach to identify low-penetrance susceptibility alleles for colorectal can...
Main Authors: | Webb, E, Broderick, P, Lubbe, S, Chandler, I, Tomlinson, I, Houlston, R |
---|---|
Format: | Journal article |
Language: | English |
Published: |
2009
|
Similar Items
-
Comprehensive analysis of common mitochondrial DNA variants and colorectal cancer risk.
by: Webb, E, et al.
Published: (2008) -
A genome-wide association scan of tag SNPs identifies a susceptibility variant for colorectal cancer at 8q24.21.
by: Tomlinson, I, et al.
Published: (2007) -
Evaluation of <it>NTHL1</it>, <it>NEIL1</it>, <it>NEIL2</it>, <it>MPG</it>, <it>TDG</it>, <it>UNG </it>and <it>SMUG1 </it>genes in familial colorectal cancer predisposition
by: Chandler Ian, et al.
Published: (2006-10-01) -
Validation of Recently Proposed Colorectal Cancer Susceptibility Gene Variants in an Analysis of Families and Patients-a Systematic Review.
by: Broderick, P, et al.
Published: (2016) -
CASP8 variants D302H and -652 6N ins/del do not influence the risk of colorectal cancer in the United Kingdom population.
by: Pittman, A, et al.
Published: (2008)