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Large-Scale Genome-Wide Association Study of East Asians Identifies Loci Associated With Risk for Colorectal Cancer.

Authors Lu Y, Kweon SS, Tanikawa C, et al.
Citation Gastroenterology. 2019 Apr;156(5):1455-1466.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/30529582/
PMCID PMC6441622
DNA repair and cancer in colon and rectum: novel players in genetic susceptibility.

Authors Pardini B, Corrado A, Paolicchi E, et al.
Citation Int J Cancer. 2019 Jun 17.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/31209889/
PMCID PMC7301215
Genome-wide association study of circulating folate one-carbon metabolites.

Authors Wang J, Asante I, Baron JA, et al.
Citation Genet Epidemiol. 2019 Sep 10.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/31502714/
PMCID PMC6829035
Mendelian randomization analysis of C-reactive protein on colorectal cancer risk.

Authors Wang X, Dai JY, Albanes D, et al.
Citation Int J Epidemiol. 2018 Nov 21.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/30476131/
PMCID PMC6659358
Combined effect of modifiable and non-modifiable risk factors for colorectal cancer risk in a pooled analysis of 11 population-based studies.

Authors Wang X, O’Connell K, Jeon J, et al.
Citation BMJ Open Gastroenterol. 2019 Dec 2;6(1):e000339.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/31875139/
PMCID PMC6904202
Association Between Intake of Red and Processed Meat and Survival in Patients With Colorectal Cancer in a Pooled Analysis.

Authors Carr PR, Banbury B, Berndt SI, et al.
Citation Clin Gastroenterol Hepatol. 2018 Nov 23. pii: S1542-3565(18)31279-5.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/30476588/
PMCID PMC6533164
Costs and outcomes of Lynch syndrome screening in the Australian colorectal cancer population.

Authors Cenin DR, Naber SK, Lansdorp-Vogelaar I, et al.
Citation J Gastroenterol Hepatol. 2018 Oct;33(10):1737-1744.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/29645364/
PMCID PMC6403824
Risks of Colorectal Cancer and Cancer-Related Mortality in Familial Colorectal Cancer Type X and Lynch Syndrome Families.

Authors Choi YH, Lakhal-Chaieb L, Kröl A, et al.
Citation J Natl Cancer Inst. 2018 Oct 30.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/30380125/
PMCID PMC7514801
Association of family history and survival in patients with colorectal cancer: a pooled analysis of eight epidemiologic studies.

Authors Chong DQ, Banbury BL, Phipps AI, et al.
Citation Cancer Med. 2018 May;7(5):2192-2199.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/29582567/
PMCID PMC5943468
Leptin gene variants and colorectal cancer risk: Sex-specific associations.

Authors Chun KA, Kocarnik JM, Hardikar SS, et al.
Citation PLoS One. 2018 Oct 31;13(10):e0206519.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/30379922/
PMCID PMC6209341
Laxative type in relation to colorectal cancer risk.

Authors Citronberg JS, Hardikar S, Phipps A, et al.
Citation Ann Epidemiol. 2018 Jul 9. pii: S1047-2797(18)30109-1.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/30150160/
PMCID PMC6415945
Somatic mutations of the coding microsatellites within the beta-2-microglobulin gene in mismatch repair-deficient colorectal cancers and adenomas.

Authors Clendenning M, Huang A, Jayasekara H, et al.
Citation Fam Cancer. 2018 Jan;17(1):91-100.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/28616688/
PMCID PMC6129400
Diagnostics of Pleiotropy in Mendelian randomization Studies: Global and Individual Tests for Direct Effects.

Authors Dai JY, Peters U, Wang X, et al.
Citation Am J Epidemiol. 2018 Sep 5.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/30188971/
PMCID PMC6269243
Physical activity and the risk of colorectal cancer in Lynch syndrome.

Authors Dashti SG, Win AK, Hardikar SS, et al.
Citation Int J Cancer. 2018 Jun 14.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/29904935/
PMCID PMC6195467
Family history-based colorectal cancer screening in Australia: a modelling study of the costs, benefits and harms of different participation scenarios.

Authors Dillon M, Flander L, Buchanan DD, et al.
Citation Plos Medicine. 2018 Aug 16;15(8):e1002630.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/30114221/
PMCID PMC6095490
Genomic Characterization of Upper-Tract Urothelial Carcinoma in Patients with Lynch Syndrome.

Authors Donahue TF, Bagrodia A, Audenet F, et al.
Citation JCO Precision Oncology. 2018 Jan 23.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/30854504/
PMCID PMC6404976
RNF43 is mutated less frequently in Lynch Syndrome compared with sporadic microsatellite unstable colorectal cancers.

Authors Fennell LJ, Clendenning M, McKeone DM, et al.
Citation Fam Cancer. 2018 Jan;17(1):63-69.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/28573495/
PMCID PMC6086823
Symptom Severity and Quality of Life Among Long-Term Colorectal Cancer Survivors Compared with Matched Control Subjects: A Population-Based Study.

Authors Hart TL, Charles ST, Gunaratne M, et al.
Citation Dis Colon Rectum. 2018 Jan 24.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/29377871/
PMCID PMC5805591
Exploring causality in the association between circulating 25-hydroxyvitamin D and colorectal cancer risk: a large Mendelian randomisation study.

Authors He Y, Timofeeva M, Farrington SM, et al.
Citation BMC Med. 2018 Aug 14;16(1):142.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/30103784/
PMCID PMC6090711
Cohort Profile: The Colon Cancer Family Registry Cohort (CCFRC).

Authors Jenkins MA, Win AK, Templeton AS, et al.
Citation Int J Epidemiol. 2018 Feb 27.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/29490034/
PMCID PMC5913593
Discussions about predictive genetic testing for Lynch syndrome: the role of health professionals and families in decisions to decline.

Authors Kanga-Parabia A, Gaff C, Flander L, et al.
Citation Fam Cancer. 2018 Feb 20.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/29464398/
PMCID PMC6102092
Mendelian randomisation study of age at menarche and age at menopause and the risk of colorectal cancer.

Authors Neumeyer S, Banbury BL, Arndt V, et al.
Citation Br J Cancer. 2018 Jun;118(12):1639-1647.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/29795306/
PMCID PMC6008474
DNA mismatch repair protein deficient non-neoplastic colonic crypts: a novel indicator of Lynch syndrome.

Authors Pai RK, Dudley B, Karloski E, et al.
Citation Mod Pathol. 2018 Jun 8.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/29884888/
PMCID PMC6396289
Genetic susceptibility markers for a breast-colorectal cancer phenotype: Exploratory results from genome-wide association studies.

Authors Pande M, Joon A, Brewster AM, et al.
Citation PLoS One. 2018 Apr 26;13 (4): e0196245.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/29698419/
PMCID PMC5919670
Novel common genetic susceptibility loci for colorectal cancer.

Authors Schmit SL, Edlund CK, Schumacher FR, et al.
Citation J Natl Cancer Inst. 2019 Feb 1;111(2):146-157.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/29917119/
PMCID PMC6555904
Interaction between polymorphisms in aspirin metabolic pathways, regular aspirin use and colorectal cancer risk: A case-control study in unselected white European populations.

Authors Sheth H, Northwood E, Ulrich CM, et al.
Citation PloS One. 2018 Feb 9;13(2):e0192223.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/29425227/
PMCID PMC5806861
A Mixed-Effects Model for Powerful Association Tests in Integrative Functional Genomics.

Authors Su YR, Di C, Bien S, et al.
Citation Am J Hum Genet. 2018 May 3;102(5):904-919.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/29727690/
PMCID PMC5986723
Genome-wide association study and meta-analysis in Northern European populations replicate multiple colorectal cancer risk loci.

Authors Tanskanen T, van den Berg L, Välimäki N, et al.
Citation Int J Cancer. 2018 Feb 1;142(3):540-546.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/28960316/
PMCID PMC6383773
Cancer risks for PMS2-associated Lynch syndrome.

Authors ten Broeke SW, van der Klift H, Tops C, et al.
Citation J Clin Oncol. 2018 Oct 10;36(29):2961-2968.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/30161022/
PMCID PMC6349460
Influence of Smoking, Body Mass Index, and Other Factors on the Preventive Effect of Nonsteroidal Anti-Inflammatory Drugs on Colorectal Cancer Risk.

Authors Wang X, Chan AT, Slattery ML, et al.
Citation Cancer Res. 2018 Aug 15;78(16):4790-4799.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/29921691/
PMCID PMC6095723
Enrichment of colorectal cancer associations in functional regions: Insight for using epigenomics data in the analysis of whole genome sequence-imputed GWAS data.

Authors Bien SA, Auer PL, Harrison TA, et al.
Citation PLoS One. 2017 Nov 21;12(11):e0186518.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/29161273/
PMCID PMC5697874
Tumor testing to identify lynch syndrome in two Australian colorectal cancer cohorts.

Authors Buchanan DD, Clendenning M, Rosty C, et al.
Citation J Gastroenterol Hepatol. 2017 Feb;32(2):427-438.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/27273229/
PMCID PMC5140773
Lack of evidence for germline RNF43 mutations in patients with serrated polyposis syndrome from a large multinational study.

Authors Buchanan DD, Clendenning M, Zhuoer L, et al.
Citation Gut. 2017 Jun;66(6):1170-1172.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/27582512/
PMCID NA
Risk of colorectal cancer for carriers of a germ-line mutation in POLE or POLD1.

Authors Buchanan DD, Stewart JR, Clendenning M, et al.
Citation Genet Med. 2017 Nov 9.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/29120461/
PMCID PMC5943186
Modeling of successive cancer risks in Lynch syndrome families in the presence of competing risks using copulas.

Authors Choi YH, Briollais L, Win AK, et al.
Citation Biometrics. 2017 Mar;73(1):271-282.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/27378229/
PMCID PMC5319907
Alcohol Consumption and the Risk of Colorectal Cancer in Mismatch Repair Gene Mutation Carriers.

Authors Dashti SG, Buchanan DD, Jayasekara H, et al.
Citation Cancer Epidemiol Biomarkers Prev. 2017 Mar;26(3):366-375.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/27811119/
PMCID PMC5336397
Targeted sequencing of 36 known or putative colorectal cancer susceptibility genes.

Authors DeRycke MS, Gunawardena S, Balcom JR, et al.
Citation Mol Genet Genomic Med. 2017 Jul 23;5(5):553-569.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/28944238/
PMCID PMC5606870
Prediction of overall survival in stage II and III colon cancer beyond TNM system: a retrospective, pooled biomarker study.

Authors Dienstmann R, Mason MJ, Sinicrope FA, et al.
Citation Ann Oncol. 2017 May 1;28(5):1023-1031.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/28453697/
PMCID PMC5406760
Circulating vitamin D concentration and risk of seven cancers: Mendelian randomisation study.

Authors Dimitrakopoulou VI, Tsilidis KK, Haycock PC, et al.
Citation BMJ. 2017 Oct 31;359.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/29089348/
PMCID PMC5666592
Testing for Gene-Environment Interactions Using a Prospective Family Cohort Design: Body Mass Index in Early and Later Adulthood and Risk of Breast Cancer.

Authors Dite GS, MacInnis RJ, Bickerstaffe A, et al.
Citation Am J Epidemiol. 2017 Mar 15;185(6):487-500.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/28399571/
PMCID PMC6158796
Inherited variation in circadian rhythm genes and risks of prostate cancer and three other cancer sites in combined cancer consortia.

Authors Gu F, Zhang H, Hyland PL, et al.
Citation Int J Cancer. 2017 Nov 1;141(9):1794-1802.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/28699174/
PMCID PMC5907928
Timing of Aspirin and Other Nonsteroidal Anti-Inflammatory Drug Use Among Patients with Colorectal Cancer in Relation to Tumor Markers and Survival.

Authors Hua X, Phipps AI, Burnett-Hartman AN, et al.
Citation J Clin Oncol. 2017 Aug 20;35(24):2806-2813.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/28617623/
PMCID PMC5562174
Choosing not to undergo predictive genetic testing for hereditary colorectal cancer syndromes: expanding our understanding of decliners and declining.

Authors Keogh LA, Niven H, Rutstein A, et al.
Citation J Behav Med. 2017 Aug;40(4):583-594.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/28197815/
PMCID PMC6057776
Long-term weight loss after colorectal cancer diagnosis is associated with lower survival: The Colon Cancer Family Registry.

Authors Kocarnik JM, Hua X, Hardikar S, et al.
Citation Cancer. 2017 Aug 25.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/28841225/
PMCID PMC5693760
Clinical verification of genetic results returned to research participants: findings from a Colon Cancer Family Registry.

Authors Laurino MY, Truitt AR, Tenney L, et al.
Citation Mol Genet Genomic Med. 2017 Nov;5(6):700-708.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/29178651/
PMCID PMC5702564
Germline miRNA DNA variants and the risk of colorectal cancer by subtype.

Authors Lindor NM, Larson MC, DeRycke MS, et al.
Citation Genes Chromosomes Cancer. 2017 Mar;56(3):177-184.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/27636879/
PMCID PMC5245119
Quantifying the Genetic Correlation between Multiple Cancer Types.

Authors Lindström S, Finucane H, Bulik-Sullivan B, et al.
Citation Cancer Epidemiol Biomarkers Prev. 2017 Sep;26(9):1427-1435.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/28637796/
PMCID PMC5582139
Pro-inflammatory fatty acid profile and colorectal cancer risk: A Mendelian randomisation analysis.

Authors May-Wilson S, Sud A, Law PJ, et al.
Citation Eur J Cancer. 2017 Aug 19;84:228-238.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/28829991/
PMCID PMC5630201
Prediagnostic alcohol consumption and colorectal cancer survival: The Colon Cancer Family Registry.

Authors Phipps AI, Robinson JR, Campbell PT, et al.
Citation Cancer. 2017 May 15;123(6):1035-1043.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/27861761/
PMCID PMC5339045
Targeted sequencing of established and candidate colorectal cancer genes in the Colon Cancer Family Registry Cohort.

Authors Raskin L, Guo Y, Du L, et al.
Citation Oncotarget. 2017 Jun 21;8(55):93450-93463.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/29212164/
PMCID PMC5706810
Mendelian randomisation implicates hyperlipidaemia as a risk factor for colorectal cancer.

Authors Rodriguez-Broadbent H, Law PJ, Sud A, et al.
Citation Int J Cancer. 2017 Jun 15;140(12):2701-2708.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/28340513/
PMCID PMC6135234
The dynamic DNA methylation landscape of the mutL homolog 1 shore is altered by MLH1-93G>A polymorphism in normal tissues and colorectal cancer.

Authors Savio AJ, Mrkonjic, Lemire M, et al.
Citation Clin. Epigenetics. 2017 Mar 9;9:26.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/28293327/
PMCID PMC5345264
How does genetic risk information for Lynch syndrome translate to risk management behaviours?

Authors Steel E, Robbins A, Jenkins M, et al.
Citation Hered Cancer Clin Pract. 2017 Jan 5;15:1.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/28070225/
PMCID PMC5217251
Genetic Variants in Epigenetic Pathways and Risks of Multiple Cancers in the GAME-ON Consortium.

Authors Toth R, Scherer D, Kelemen LE, et al.
Citation Cancer Epidemiol Biomarkers Prev. 2017 Jan 23.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/28115406/
PMCID PMC6054308
Novel colon cancer susceptibility variants identified from a genome-wide association study in African Americans.

Authors Wang H, Schmit SL, Haiman CA, et al.
Citation Int J Cancer. 2017 Jun 15;140(12):2728-2733.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/28295283/
PMCID PMC5505639
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
A Bayesian graphical model for genome-wide association studies (GWAS).

Authors Briollais L, Dobra A, Liu J, et al.
Citation Ann Appl Stat. 2016 Jun;10(2):786-811.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/33907591/
PMCID PMC8075301
Multivitamin, calcium and folic acid supplements and the risk of colorectal cancer in Lynch syndrome.

Authors Chau R, Dashti SG, Ait Ouakrim D, et al.
Citation Int J Epidemiol. 2016 Jun;45(3):940-53.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/27063605/
PMCID PMC5697347
Fine-Mapping of Common Genetic Variants Associated with Colorectal Tumor Risk Identified Potential Functional Variants.

Authors Du M, Jiao S, Bien S, et al.
Citation PLoS One. 2016 Jul 5;11(7):e0157521.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/27379672/
PMCID PMC4933364
Nonsyndromic cleft lip with or without cleft palate and cancer: Evaluation of a possible common genetic background through the analysis of GWAS data.

Authors Dunkhase E, Ludwig KU, Knapp M, et al.
Citation Genom Data. 2016;10:22–29.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/27630819/
PMCID PMC5013250
Cross-Cancer Genome-Wide Analysis of Lung, Ovary, Breast, Prostate, and Colorectal Cancer Reveals Novel Pleiotropic Associations.

Authors Fehringer G, Kraft P, Pharoah PD, et al.
Citation Cancer Res. 2016 Sep 1;76(17):5103-14.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/27197191/
PMCID PMC5010493
CYP24A1 variant modifies the association between use of oestrogen plus progestogen therapy and colorectal cancer risk.

Authors Garcia-Albeniz X, Rudolph A, Hutter C, et al.
Citation Br J Cancer. 2016 Jan 19;114(2):221-9.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/26766742/
PMCID PMC4815813
Genome-Wide Interaction Analyses between Genetic Variants and Alcohol Consumption and Smoking for Risk of Colorectal Cancer.

Authors Gong J, Hutter CM, Newcomb PA, et al.
Citation PLoS Genet. 2016 Oct 10;12(10):e1006296.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/27723779/
PMCID PMC5065124
PMS2 monoallelic mutation carriers: the known unknown.

Authors Goodenberger ML, Thomas BC, Riegert-Johnson D, et al.
Citation Genet Med. 2016 Jan;18(1):13-9.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/25856668/
PMCID PMC4834863
Mendelian randomisation analysis strongly implicates adiposity with risk of developing colorectal cancer.

Authors Jarvis D, Mitchell JS, Law PJ, et al.
Citation Br J Cancer. 2016 Jul 12;115(2):266-72.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/27336604/
PMCID PMC4947703
Risk factors for metachronous colorectal cancer following a primary colorectal cancer: A prospective cohort study.

Authors Jayasekara H, Reece JC, Buchanan DD, et al.
Citation Int J Cancer. 2016. 139, 1081-1090.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/27098183/
PMCID PMC4911232
Telomere structure and maintenance gene variants and risk of five cancer types.

Authors Karami S, Han Y, Pande M, et al.
Citation Int J Cancer. 2016 Dec 15;139(12):2655-2670.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/27459707/
PMCID PMC5198774
The Impact of Receiving Predictive Genetic Information about Lynch Syndrome on Individual Colonoscopy and Smoking Behaviors.

Authors Kim JS, Coyte PC, Cotterchio M, et al.
Citation Cancer Epidemiol Biomarkers Prev. 2016 Nov;25(11):1524-1533.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/27528600/
PMCID PMC5274544
SNP rs16906252C>T is an expression and methylation quantitative trait locus associated with an increased risk of developing MGMT-methylated colorectal cancer.

Authors Kuroiwa-Trzmielina J, Wang F, Rapkins RW, et al.
Citation Clin Cancer Res. 2016 Dec 15;22(24):6266-6277.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/27267851/
PMCID PMC5143212
Clinicopathologic Risk Factor Distributions for MLH1 Promoter Region Methylation in CIMP-Positive Tumors.

Authors Levine AJ, Phipps AI, Baron JA, et al.
Citation Cancer Epidemiol Biomarkers Prev. 2016 Jan;25(1):68-75.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/26512054/
PMCID PMC4713308
Risk Factors for Early-Onset and Very-Early-Onset Pancreatic Adenocarcinoma: A Pancreatic Cancer Case-Control Consortium (PanC4) Analysis.

Authors McWilliams RR, Maisonneuve P, Bamlet WR, et al.
Citation Pancreas. 2016 Feb;45(2):311-6.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/26646264/
PMCID PMC4710562
Variation at 2q35 (PNKD and TMBIM1) influences colorectal cancer risk and identifies a pleiotropic effect with inflammatory bowel disease.

Authors Orlando G, Law PJ, Palin K, et al.
Citation Hum Mol Genet. 2016 Jun 1;25(11):2349-2359.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/27005424/
PMCID PMC5081051
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.

Authors Patel SG, Ahnen DJ, Kinney AY, et al.
Citation Am J Gastroenterol. 2016 Feb;111(2):285-93.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/26856748/
PMCID PMC5193129
Germline mutations in PMS2 and MLH1 in individuals with solitary loss of PMS2 expression in colorectal carcinomas from the Colon Cancer Family Registry Cohort.

Authors Rosty C, Clendenning M, Walsh MD, et al.
Citation BMJ Open. 2016 Feb 19;6(2):e010293.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/26895986/
PMCID PMC4762074
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
Promoter methylation of ITF2, but not APC, is associated with microsatellite instability in two populations of colorectal cancer patients.

Authors Savio AJ, Daftary D, Dicks E, et al.
Citation BMC Cancer. 2016 Feb 17;16(1):113.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/26884349/
PMCID PMC4756469
A Cross-Cancer Genetic Association Analysis of the DNA Repair and DNA Damage Signaling Pathways for Lung, Ovary, Prostate, Breast, and Colorectal Cancer.

Authors Scarbrough PM, Weber RP, Iversen ES, et al.
Citation Cancer Epidemiol Biomarkers Prev 2016 Jan;25(1):193-200.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/26637267/
PMCID PMC4713268
Cholecystectomy and the risk of colorectal cancer by tumor mismatch repair deficiency status.

Authors Shang J, Reece JC, Buchanan DD, et al.
Citation Int J Colorectal Dis. 2016 Aug;31(8):1451-7.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/27286977/
PMCID PMC4949040
Winner’s Curse Correction and Variable Thresholding Improve Performance of Polygenic Risk Modeling Based on Genome-Wide Association Study Summary-Level Data.

Authors Shi J, Park JH, Duan J, et al.
Citation PLoS Genet. 2016 Dec 30;12(12):e1006493.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/28036406/
PMCID PMC5201242
The Experience of Extended Bowel Resection in Individuals With a High Metachronous Colorectal Cancer Risk: A Qualitative Study.

Authors Steel EJ, Trainer AH, Heriott AG, et al.
Citation Oncol Nurs Forum. 2016 Jul 1;43(4):444-52.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/27314187/
PMCID PMC5114664
Prevalence and penetrance of major genes and polygenes for colorectal cancer.

Authors Win AK, Jenkins MA, Dowty JG, et al.
Citation Cancer Epidemiol Biomarkers Prev. 2016 Oct 31.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/27799157/
PMCID PMC5336409
Risk of extracolonic cancers for people with biallelic and monoallelic mutations in MUTYH.

Authors Win AK, Reece JC, Dowty JG, et al.
Citation Int J Cancer. 2016 Oct 1;139(7):1557-63.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/27194394/
PMCID PMC5094810
Association of a let-7 miRNA binding region of TGFBR1 with hereditary mismatch repair proficient colorectal cancer (MSS HNPCC).

Authors Xicola RM, Bontu S, Doyle BJ, et al.
Citation Carcinogenesis. 2016 Aug;37(8):751-8.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/27234654/
PMCID PMC4967215
Common variants in the obesity-associated genes FTO and MC4R are not associated with risk of colorectal cancer.

Authors Yang B, Thrift AP, Figueiredo JC, et al.
Citation Cancer Epidemiol. 2016 Oct;44:1-4.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/27449576/
PMCID PMC5125024
Identification of Susceptibility Loci and Genes for Colorectal Cancer Risk.

Authors Zeng C, Matsuda K, Jia WG, et al.
Citation Gastroenterology. 2016 Jun;150(7):1633-45.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/26965516/
PMCID PMC4909543
Aspirin, Ibuprofen, and the Risk of Colorectal Cancer in Lynch Syndrome.

Authors Ait Ouakrim D, Dashti SG, Chau R, et al.
Citation J Natl Cancer Inst. 2015 Jun 24;107(9).
PubMedLink https://pubmed.ncbi.nlm.nih.gov/26109217/
PMCID PMC4651105
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
Red meat intake, NAT2, and risk of colorectal cancer: A pooled analysis of 11 studies.

Authors Ananthakrishnan AN, Du M, Berndt SI, et al.
Citation Cancer Epidemiol Biomarkers Prev. 2015 Jan;24(1):198-205.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/25342387/
PMCID PMC4294960
Lynch syndrome and cervical cancer.

Authors Antill YC, Dowty JG, Win AK, et al.
Citation Int J Cancer. 2015 Dec 1;137(11):2757-61.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/26077226/
PMCID PMC4573262
Association between body mass index and mortality for colorectal cancer survivors: overall and by tumor molecular phenotype.

Authors Campbell PT, Newton CC, Newcomb PA, et al.
Citation Cancer Epidemiol Biomarkers Prev. 2015 Aug;24(8):1229-38.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/26038390/
PMCID PMC4526409
Determining the familial risk distribution of colorectal cancer: a data mining approach.

Authors Chau R, Jenkins MA, Buchanan DD, et al.
Citation Fam Cancer. 2015 Dec 17.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/26681340/
PMCID PMC4803603
Common colorectal cancer risk alleles contribute to the multiple colorectal adenoma phenotype, but do not influence colonic polyposis in FAP.

Authors Cheng TH, Gorman M, Martin L, et al.
Citation Eur J Hum Genet. 2015 Feb;23(2):260-3.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/24801760/
PMCID PMC4140766
Meta-analysis of genome-wide association studies identifies common susceptibility polymorphisms for colorectal and endometrial cancer near SH2B3 and TSHZ1.

Authors Cheng TH, Thompson D, Painter J, et al.
Citation Sci Rep. 2015 Dec 1;5:17369.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/26621817/
PMCID PMC4664893
Female Hormonal Factors and the Risk of Endometrial Cancer in Lynch Syndrome.

Authors Dashti SG, Chau R, Quakrim DA, et al.
Citation JAMA. 2015 Jul 7;314(1):61-71.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/26151267/
PMCID PMC4688894
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
Mutation Spectrum and Risk of Colorectal Cancer in African American Families with Lynch Syndrome.

Authors Guindalini RS, Win AK, Gulden C, et al.
Citation Gastroenterology. 2015 Nov;149(6):1446-53.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/26248088/
PMCID PMC4648287
Prediagnostic Physical Activity and Colorectal Cancer Survival: Overall and Stratified by Tumor Characteristics.

Authors Hardikar S, Newcomb PA, Campbell PT, et al.
Citation Cancer Epidemiol Biomarkers Prev. 2015 Jul;24(7):1130-7.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/25976417/
PMCID PMC4491038
Childhood Cancers in families with and without Lynch syndrome.

Authors Heath JA, Reece JC, Buchanan DD, et al.
Citation Fam Cancer. 2015 Dec;14(4):545-51.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/25963852/
PMCID PMC4631656
Cross Cancer Genomic Investigation of Inflammation Pathway for Five Common Cancers: Lung, Ovary, Prostate, Breast, and Colorectal Cancer.

Authors Hung RJ, Ulrich CM, Goode EL, et al.
Citation J Natl Cancer Inst. 2015 Aug 29;107(11).
PubMedLink https://pubmed.ncbi.nlm.nih.gov/26319099/
PMCID PMC4675100
Meat intake, cooking methods, dietary carcinogens, and colorectal cancer risk: findings from the Colorectal Cancer Family Registry.

Authors Joshi AD, Kim A, Lewinger JP, et al.
Citation Cancer Med. 2015 Jun;4(6):936-52.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/25846122/
PMCID PMC4472216

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Large-Scale Genome-Wide Association Study of East Asians Identifies Loci Associated With Risk for Colorectal Cancer.

DNA repair and cancer in colon and rectum: novel players in genetic susceptibility.

Genome-wide association study of circulating folate one-carbon metabolites.

Mendelian randomization analysis of C-reactive protein on colorectal cancer risk.

Combined effect of modifiable and non-modifiable risk factors for colorectal cancer risk in a pooled analysis of 11 population-based studies.

Association Between Intake of Red and Processed Meat and Survival in Patients With Colorectal Cancer in a Pooled Analysis.

Costs and outcomes of Lynch syndrome screening in the Australian colorectal cancer population.

Risks of Colorectal Cancer and Cancer-Related Mortality in Familial Colorectal Cancer Type X and Lynch Syndrome Families.

Association of family history and survival in patients with colorectal cancer: a pooled analysis of eight epidemiologic studies.

Leptin gene variants and colorectal cancer risk: Sex-specific associations.

Laxative type in relation to colorectal cancer risk.

Somatic mutations of the coding microsatellites within the beta-2-microglobulin gene in mismatch repair-deficient colorectal cancers and adenomas.

Diagnostics of Pleiotropy in Mendelian randomization Studies: Global and Individual Tests for Direct Effects.

Physical activity and the risk of colorectal cancer in Lynch syndrome.

Family history-based colorectal cancer screening in Australia: a modelling study of the costs, benefits and harms of different participation scenarios.

Genomic Characterization of Upper-Tract Urothelial Carcinoma in Patients with Lynch Syndrome.

RNF43 is mutated less frequently in Lynch Syndrome compared with sporadic microsatellite unstable colorectal cancers.

Symptom Severity and Quality of Life Among Long-Term Colorectal Cancer Survivors Compared with Matched Control Subjects: A Population-Based Study.

Exploring causality in the association between circulating 25-hydroxyvitamin D and colorectal cancer risk: a large Mendelian randomisation study.

Cohort Profile: The Colon Cancer Family Registry Cohort (CCFRC).

Discussions about predictive genetic testing for Lynch syndrome: the role of health professionals and families in decisions to decline.

Mendelian randomisation study of age at menarche and age at menopause and the risk of colorectal cancer.

DNA mismatch repair protein deficient non-neoplastic colonic crypts: a novel indicator of Lynch syndrome.

Genetic susceptibility markers for a breast-colorectal cancer phenotype: Exploratory results from genome-wide association studies.

Novel common genetic susceptibility loci for colorectal cancer.

Interaction between polymorphisms in aspirin metabolic pathways, regular aspirin use and colorectal cancer risk: A case-control study in unselected white European populations.

A Mixed-Effects Model for Powerful Association Tests in Integrative Functional Genomics.

Genome-wide association study and meta-analysis in Northern European populations replicate multiple colorectal cancer risk loci.

Cancer risks for PMS2-associated Lynch syndrome.

Influence of Smoking, Body Mass Index, and Other Factors on the Preventive Effect of Nonsteroidal Anti-Inflammatory Drugs on Colorectal Cancer Risk.

Enrichment of colorectal cancer associations in functional regions: Insight for using epigenomics data in the analysis of whole genome sequence-imputed GWAS data.

Tumor testing to identify lynch syndrome in two Australian colorectal cancer cohorts.

Lack of evidence for germline RNF43 mutations in patients with serrated polyposis syndrome from a large multinational study.

Risk of colorectal cancer for carriers of a germ-line mutation in POLE or POLD1.

Modeling of successive cancer risks in Lynch syndrome families in the presence of competing risks using copulas.

Alcohol Consumption and the Risk of Colorectal Cancer in Mismatch Repair Gene Mutation Carriers.

Targeted sequencing of 36 known or putative colorectal cancer susceptibility genes.

Prediction of overall survival in stage II and III colon cancer beyond TNM system: a retrospective, pooled biomarker study.

Circulating vitamin D concentration and risk of seven cancers: Mendelian randomisation study.

Testing for Gene-Environment Interactions Using a Prospective Family Cohort Design: Body Mass Index in Early and Later Adulthood and Risk of Breast Cancer.

Inherited variation in circadian rhythm genes and risks of prostate cancer and three other cancer sites in combined cancer consortia.

Timing of Aspirin and Other Nonsteroidal Anti-Inflammatory Drug Use Among Patients with Colorectal Cancer in Relation to Tumor Markers and Survival.

Choosing not to undergo predictive genetic testing for hereditary colorectal cancer syndromes: expanding our understanding of decliners and declining.

Long-term weight loss after colorectal cancer diagnosis is associated with lower survival: The Colon Cancer Family Registry.

Clinical verification of genetic results returned to research participants: findings from a Colon Cancer Family Registry.

Germline miRNA DNA variants and the risk of colorectal cancer by subtype.

Quantifying the Genetic Correlation between Multiple Cancer Types.

Pro-inflammatory fatty acid profile and colorectal cancer risk: A Mendelian randomisation analysis.

Prediagnostic alcohol consumption and colorectal cancer survival: The Colon Cancer Family Registry.

Targeted sequencing of established and candidate colorectal cancer genes in the Colon Cancer Family Registry Cohort.

Mendelian randomisation implicates hyperlipidaemia as a risk factor for colorectal cancer.

The dynamic DNA methylation landscape of the mutL homolog 1 shore is altered by MLH1-93G>A polymorphism in normal tissues and colorectal cancer.

How does genetic risk information for Lynch syndrome translate to risk management behaviours?

Genetic Variants in Epigenetic Pathways and Risks of Multiple Cancers in the GAME-ON Consortium.

Novel colon cancer susceptibility variants identified from a genome-wide association study in African Americans.

Quality of Life and Mortality of Long-Term Colorectal Cancer Survivors in the Seattle Colorectal Cancer Family Registry.

A Bayesian graphical model for genome-wide association studies (GWAS).

Multivitamin, calcium and folic acid supplements and the risk of colorectal cancer in Lynch syndrome.

Fine-Mapping of Common Genetic Variants Associated with Colorectal Tumor Risk Identified Potential Functional Variants.

Nonsyndromic cleft lip with or without cleft palate and cancer: Evaluation of a possible common genetic background through the analysis of GWAS data.

Cross-Cancer Genome-Wide Analysis of Lung, Ovary, Breast, Prostate, and Colorectal Cancer Reveals Novel Pleiotropic Associations.

CYP24A1 variant modifies the association between use of oestrogen plus progestogen therapy and colorectal cancer risk.

Genome-Wide Interaction Analyses between Genetic Variants and Alcohol Consumption and Smoking for Risk of Colorectal Cancer.

PMS2 monoallelic mutation carriers: the known unknown.

Mendelian randomisation analysis strongly implicates adiposity with risk of developing colorectal cancer.

Risk factors for metachronous colorectal cancer following a primary colorectal cancer: A prospective cohort study.

Telomere structure and maintenance gene variants and risk of five cancer types.

The Impact of Receiving Predictive Genetic Information about Lynch Syndrome on Individual Colonoscopy and Smoking Behaviors.

SNP rs16906252C>T is an expression and methylation quantitative trait locus associated with an increased risk of developing MGMT-methylated colorectal cancer.

Clinicopathologic Risk Factor Distributions for MLH1 Promoter Region Methylation in CIMP-Positive Tumors.

Risk Factors for Early-Onset and Very-Early-Onset Pancreatic Adenocarcinoma: A Pancreatic Cancer Case-Control Consortium (PanC4) Analysis.

Variation at 2q35 (PNKD and TMBIM1) influences colorectal cancer risk and identifies a pleiotropic effect with inflammatory bowel disease.

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.

Germline mutations in PMS2 and MLH1 in individuals with solitary loss of PMS2 expression in colorectal carcinomas from the Colon Cancer Family Registry Cohort.

GWASeq: targeted re-sequencing follow up to GWAS.

Promoter methylation of ITF2, but not APC, is associated with microsatellite instability in two populations of colorectal cancer patients.

A Cross-Cancer Genetic Association Analysis of the DNA Repair and DNA Damage Signaling Pathways for Lung, Ovary, Prostate, Breast, and Colorectal Cancer.

Cholecystectomy and the risk of colorectal cancer by tumor mismatch repair deficiency status.

Winner’s Curse Correction and Variable Thresholding Improve Performance of Polygenic Risk Modeling Based on Genome-Wide Association Study Summary-Level Data.