Authors Govindarajan A, Fraser N, Cranford V, et al. Citation Ann Surg Oncol. 2008 Jul;15(7):1923-30. PubMedLink https://pubmed.ncbi.nlm.nih.gov/18473145/ PMCID PMC2770244
Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer.
Authors Houlston RS, Webb E, Broderick P, et al. Citation Nat Genet. 2008 Dec;40(12):1426-35. PubMedLink https://pubmed.ncbi.nlm.nih.gov/19011631/ PMCID PMC2836775
Family history and colorectal cancer survival in women.
Authors Kirchhoff AC, Newcomb PA, Trentham-Dietz A, et al. Citation Fam Cancer. 2008;7(4):287-92. PubMedLink https://pubmed.ncbi.nlm.nih.gov/18360806/ PMCID NA
Efficient p-value estimation in massively parallel testing problems.
Authors Kustra R, Shi X, Murdoch DJ, et al. Citation Biostatistics. 2008 Oct;9(4):601-12. PubMedLink https://pubmed.ncbi.nlm.nih.gov/18304995/ PMCID PMC2536722
Pathological features of colorectal carcinomas in MYH-associated polyposis.
Authors O’Shea AM, Cleary SP, Croitoru MA, et al. Citation Histopathology. 2008 Aug;53(2):184-94. PubMedLink https://pubmed.ncbi.nlm.nih.gov/18564191/ PMCID PMC2754312
Molecular characterization of MSI-H colorectal cancer by MLHI promoter methylation, immunohistochemistry, and mismatch repair germline mutation screening.
Authors Poynter JN, Siegmund KD, Weisenberger DJ, et al. Citation Cancer Epidemiol Biomarkers Prev. 2008 Nov;17(11):3208-15. PubMedLink https://pubmed.ncbi.nlm.nih.gov/18990764/ PMCID PMC2628332
Activation of Notch signaling in human colon adenocarcinoma.
Authors Reedijk M, Odorcic S, Zhang H, et al. Citation Int J Oncol. 2008 Dec;33(6):1223-9. PubMedLink https://pubmed.ncbi.nlm.nih.gov/19020755/ PMCID PMC2739737
The clinical phenotype of Lynch syndrome due to germ-line PMS2 mutations.
Authors Senter L, Clendenning M, Sotamaa K, et al. Citation Gastroenterology. 2008 Aug;135(2):419-28. PubMedLink https://pubmed.ncbi.nlm.nih.gov/18602922/ PMCID PMC2759321
Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21.
Authors Tenesa A, Farrington SM, Prendergast JG, et al. Citation Nat Genet. 2008 May;40(5):631-7. PubMedLink https://pubmed.ncbi.nlm.nih.gov/18372901/ PMCID PMC2778004
Germline EPHB2 receptor variants in familial colorectal cancer.
Authors Zogopoulos G, Jorgensen C, Bacani J, et al. Citation PLoS One. 2008 Aug 6;3(8):e2885. PubMedLink https://pubmed.ncbi.nlm.nih.gov/18682749/ PMCID PMC2483346