Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer

Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer

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Λεπτομέρειες βιβλιογραφικής εγγραφής
Κύριοι συγγραφείς:	Houlston, R, Webb, E, Broderick, P, Pittman, A, Bernardo, D, Lubbe, S, Chandler, I, Vijayakrishnan, J, Sullivan, K, Penegar, S, Carvajal-Carmona, L, Howarth, K, Jaeger, E, Spain, S, Walther, A, Barclay, E, Martin, L, Gorman, M, Domingo, E, Teixeira, A, Kerr, D, Cazier, J, Niittymaki, I, Tuupanen, S, Karhu, A
Μορφή:	Journal article
Έκδοση:	2008

Παρόμοια τεκμήρια

Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer.
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A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3.
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A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3.
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Comprehensive analysis of common mitochondrial DNA variants and colorectal cancer risk.
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Systematic search for enhancer elements and somatic allelic imbalance at seven low-penetrance colorectal cancer predisposition loci.
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Common genetic variants at the CRAC1 (HMPS) locus on chromosome 15q13.3 influence colorectal cancer risk.
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Refinement of the basis and impact of common 11q23.1 variation to the risk of developing colorectal cancer.
ανά: Pittman, A, κ.ά.
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A genome-wide association study shows that common alleles of SMAD7 influence colorectal cancer risk.
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Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33.
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Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33
ανά: Houlston, R, κ.ά.
Έκδοση: (2010)

Systematic search for enhancer elements and somatic allelic imbalance at seven low-penetrance colorectal cancer predisposition loci
ανά: Houlston Richard S, κ.ά.
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CASP8 variants D302H and -652 6N ins/del do not influence the risk of colorectal cancer in the United Kingdom population.
ανά: Pittman, A, κ.ά.
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A genome-wide association scan of tag SNPs identifies a susceptibility variant for colorectal cancer at 8q24.21.
ανά: Tomlinson, I, κ.ά.
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A genome-wide scan of 10 000 gene-centric variants and colorectal cancer risk.
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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
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Fine Mapping of Colorectal Cancer Low Penetrance Susceptibility Loci
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Common variation at the adiponectin locus is not associated with colorectal cancer risk in the UK.
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Colorectal cancer risk is not associated with increased levels of homozygosity in a population from the United Kingdom.
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Multiple common susceptibility variants near BMP pathway loci GREM1, BMP4, and BMP2 explain part of the missing heritability of colorectal cancer.
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Fine-mapping of colorectal cancer susceptibility loci at 8q23.3, 16q22.1 and 19q13.11: refinement of association signals and use of in silico analysis to suggest functional variation and unexpected candidate target genes.
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Deciphering the genetics of hereditary non-syndromic colorectal cancer.
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Imputation as a method to fine map cancer susceptibility loci
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Evidence of linkage to chromosome 9q22.33 in colorectal cancer kindreds from the United Kingdom.
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Common variation near CDKN1A, POLD3 and SHROOM2 influences colorectal cancer risk
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Common variation near CDKN1A, POLD3 and SHROOM2 influences colorectal cancer risk.
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Evidence for a colorectal cancer susceptibility locus on chromosome 3q21-q24 from a high-density SNP genome-wide linkage scan (vol 15, pg 2903, 2006)
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The common colorectal cancer predisposition SNP rs6983267 at chromosome 8q24 confers potential to enhanced Wnt signaling.
ανά: Tuupanen, S, κ.ά.
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Germline mutations affecting the proofreading domains of POLE and POLD1 predispose to colorectal adenomas and carcinomas.
ανά: Palles, C, κ.ά.
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Multiple common susceptibility variants near BMP pathway loci GREM1, BMP4, and BMP2 explain part of the missing heritability of colorectal cancer.
ανά: Ian P M Tomlinson, κ.ά.
Έκδοση: (2011-06-01)

Loci on 7p12.2, 10q21.2 and 14q11.2 are associated with risk of childhood acute lymphoblastic leukemia.
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Erratum: Germline mutations affecting the proofreading domains of POLE and POLD1 predispose to colorectal adenomas and carcinomas (Nature Genetics (2013) 45 (136-144))
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Multiple Hodgkin lymphoma-associated loci within the HLA region at chromosome 6p21.3.
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Association between chromosomal instability and prognosis in colorectal cancer: a meta-analysis.
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Identification of susceptibility loci for colorectal cancer in a genome-wide meta-analysis.
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Allelic variation at the 8q23.3 colorectal cancer risk locus functions as a cis-acting regulator of EIF3H.
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Multiple segmental uniparental disomy associated with abnormal DNA methylation of imprinted Loci in silver-russell syndrome.
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Effect of SNP haplotypes associated with colorectal cancer risk on outcome
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