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GWASeq: targeted re-sequencing follow up to GWAS.
Authors Salomon PM, Li WG, Edlund CK, et al. Citation BMC Genomics. 2016 Mar 3;17:176. PubMedLink https://pubmed.ncbi.nlm.nih.gov/26940994/ PMCID PMC4776370
Germline mutations in PMS2 and MLH1 in individuals with solitary loss of PMS2 expression in colorectal carcinomas from the Colon Cancer Family Registry Cohort.
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Knowledge and Uptake of Genetic Counseling and Colonoscopic Screening Among Individuals at Increased Risk for Lynch Syndrome and their Endoscopists from the Family Health Promotion Project.
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Variation at 2q35 (PNKD and TMBIM1) influences colorectal cancer risk and identifies a pleiotropic effect with inflammatory bowel disease.
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Quality of Life and Mortality of Long-Term Colorectal Cancer Survivors in the Seattle Colorectal Cancer Family Registry.
Authors Adams SV, Ceballos R, Newcomb PA. Citation PLoS One. 2016 Jun 2;11(6):e0156534. PubMedLink https://pubmed.ncbi.nlm.nih.gov/27253385/ PMCID PMC4890809
Clinicopathologic Risk Factor Distributions for MLH1 Promoter Region Methylation in CIMP-Positive Tumors.
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SNP rs16906252C>T is an expression and methylation quantitative trait locus associated with an increased risk of developing MGMT-methylated colorectal cancer.
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The Impact of Receiving Predictive Genetic Information about Lynch Syndrome on Individual Colonoscopy and Smoking Behaviors.
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Telomere structure and maintenance gene variants and risk of five cancer types.
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