Authors Schmit SL, Schumacher FR, Edlund CK, et al. Citation Carcinogenesis. 2014 Nov;35(11):2512-9. PubMedLink https://pubmed.ncbi.nlm.nih.gov/25023989/ PMCID PMC4271131
Genetic variation in UGT genes modify the associations of NSAIDs with risk of colorectal cancer: Colon Cancer Family Registry.
Authors Scherer D, Koepl LM, Poole EM, et al. Citation Genes Chromosomes Cancer. 2014 Jul;53(7):568-78. PubMedLink https://pubmed.ncbi.nlm.nih.gov/24677636/ PMCID PMC4326223
High prevalence of mismatch repair deficiency in prostate cancers diagnosed in mismatch repair gene mutation carriers from the Colon Cancer Family Registry.
Authors Rosty C, Walsh MD, Lindor NM, et al. Citation Fam Cancer. 2014 Dec;13(4):573-82. PubMedLink https://pubmed.ncbi.nlm.nih.gov/25117503/ PMCID PMC4329248
Genetic Variation in prostaglandin synthesis and related pathways, NSAID use, and colorectal cancer risk in the Colon Cancer Family Registry.
Authors Resler AJ, Makar KW, Heath L, et al. Citation Carcinogenesis. 2014 Sep;35(9):2121-6. PubMedLink https://pubmed.ncbi.nlm.nih.gov/24908683/ PMCID PMC4146420
Family History of Colorectal Cancer is not Associated with Colorectal Cancer Survival Regardless of Microsatellite Instability Status.
Authors Phipps A, Ahnen DJ, Campbell PT, et al. Citation Cancer Epidemiol Biomarkers Prev. 2014 Aug;23(8):1700-4. PubMedLink https://pubmed.ncbi.nlm.nih.gov/24891550/ PMCID PMC4119483
Identification of genes expressed by immune cells of the colon that are regulated by colorectal cancer-associated variants.
Authors Peltekova VD, Lemire M, Qazi AM, et al. Citation Int J Cancer. 2014 May 15;134(10):2330-41. PubMedLink https://pubmed.ncbi.nlm.nih.gov/24154973/ PMCID PMC3949167
A genome-wide association study of early-onset breast cancer identifies PFKM as a novel breast cancer gene and supports a common genetic spectrum for breast cancer at any age.
Authors Ahsan H, Halpern J, Kibriya MG, et al. Citation Cancer Epidemiol Biomarkers Prev. 2014 Apr;23(4):658-69. PubMedLink https://pubmed.ncbi.nlm.nih.gov/24493630/ PMCID PMC3990360
Tumour MLH1 promoter region methylation testing is an effective prescreen for Lynch Syndrome (HNPCC).
Authors Newton K, Jorgensen NM, Wallace AJ, et al. Citation J Med Genet. 2014 Dec;51(12):789-96. PubMedLink https://pubmed.ncbi.nlm.nih.gov/25280751/ PMCID PMC5159427
A randomized trial to increase colonoscopy screening in members of high risk families in the Colorectal Cancer Family Registry and Cancer Genetics Network.
Authors Lowery JT, Horick N, Kinney AY, et al. Citation Cancer Epidemiol Biomarkers Prev. 2014 Apr;23(4):601-10. PubMedLink https://pubmed.ncbi.nlm.nih.gov/24501379/ PMCID PMC3976708
Colorectal cancer and self-reported tooth agenesis.
Authors Lindor NM, Win AK, Gallinger S, et al. Citation Hered Cancer Clin Pract. 2014 Mar 10;12(1):7. PubMedLink https://pubmed.ncbi.nlm.nih.gov/24607150/ PMCID PMC3975307