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A high-resolution copy-number variation resource for clinical and population genetics.
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Association of the colorectal CpG island methylator phenotype with molecular features, risk factors and family history.
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Role of tumour molecular and pathology features to estimate colorectal cancer risk for first-degree relatives.
Authors Win AK, Buchanan DD, Rosty C, et al. Citation Gut. 2015 Jan;64(1):101-10. PubMedLink https://pubmed.ncbi.nlm.nih.gov/24615377/ PMCID PMC4180004
Genetic variants within the hTERT gene and the risk of colorectal cancer in Lynch syndrome.
Authors Win AK, Clendenning M, Crawford W, et al. Citation Genes Cancer. 2015 Nov; 6(11-12): 445–451. PubMedLink https://pubmed.ncbi.nlm.nih.gov/26807197/ PMCID PMC4701223
Risk of colorectal cancer for people with a mutation in both a MUTYH and a DNA mismatch repair gene.
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Germline TP53 mutations in patients with early-onset colorectal cancer in the Colon Cancer Family Registry.
Authors Yurgelun MB, Masciari S, Joshi VA, et al. Citation JAMA Oncol. 2015 May;1(2):214-21. PubMedLink https://pubmed.ncbi.nlm.nih.gov/26086041/ PMCID PMC4465271
Genetic determinants of telomere length and risk of common cancers: a Mendelian randomization study.
Authors Zhang C, Doherty JA, Burgess S, et al. Citation Hum Mol Genet. 2015 Sep 15;24(18):5356-66. PubMedLink https://pubmed.ncbi.nlm.nih.gov/26138067/ PMCID PMC4550826
Long-term psychosocial and behavioral adjustment in individuals receiving genetic test results in Lynch syndrome.
Authors Esplen JM, Won J, Aronson M, et al. Citation Clin Genet. 2015 Jun;87(6):525-32. PubMedLink https://pubmed.ncbi.nlm.nih.gov/25297893/ PMCID PMC4391982
A new GWAS and meta-analysis with 1000Genomes imputation identifies novel risk variants for colorectal cancer.
Authors Al-Tassan NA, Whiffin N, Hosking FJ, et al. Citation Sci Rep. 2015 May 20;5:10442. PubMedLink https://pubmed.ncbi.nlm.nih.gov/25990418/ PMCID PMC4438486