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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
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
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
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
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
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
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
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
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
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
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
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
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
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
The Influence of Screening for Precancerous Lesions on Family-Based Genetic Association Tests: An Example of Colorectal Polyps and Cancer.

Authors Schmit SL, Figueiredo JC, Cortessis VK.
Citation Am J of Epidemiol. 2015 Oct 15;182(8):714-22.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/26306664/
PMCID PMC4597802
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
Genome-wide association study of colorectal cancer identifies six new susceptibility loci.

Authors Schumacher FR, Schmit SL, Jiao S, et al.
Citation Nat Commun. 2015 Jul 7;6:7138.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/26151821/
PMCID PMC4967357
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
Fertility after young-onset colorectal cancer: a study of subjects with Lynch syndrome.

Authors Stupart D, Win AK, Winship IM.
Citation Colorectal Dis. 2015 Sep;17(9):787-93.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/25754680/
PMCID PMC4766107
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
Mendelian randomization study of height and risk of colorectal cancer.

Authors Thrift AP, Gong J, Peters U, et al.
Citation Int J Epidemiol. 2015 Apr;44(2):662-72.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/25997436/
PMCID PMC4481609
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
Mendelian randomization study of body mass index and colorectal cancer risk.

Authors Thrift AP, Gong J, Peters U, et al.
Citation Cancer Epidemiol Biomarkers Prev. 2015 Jul;24(7):1024-31.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/25976416/
PMCID PMC4490960
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
A high-resolution copy-number variation resource for clinical and population genetics.

Authors Uddin M, Thiruvahindrapuram B, Walker S, et al.
Citation Genet Med. 2015 Sep;17(9):747-52.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/25503493/
PMCID PMC4752593
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
Association of the colorectal CpG island methylator phenotype with molecular features, risk factors and family history.

Authors Weisenberger DJ, Levine AJ, Long TI, et al.
Citation Cancer Epidemiol Biomarkers Prev. 2015 Mar;24(3):512-9.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/25587051/
PMCID PMC4355081
Comparison of Prediction Models for Lynch Syndrome Among Individuals with Colorectal Cancer.

Authors Kastrinos F, Ojha RP, Leenen C, et al.
Citation J Natl Cancer Inst. 2015 Nov 18;108(2).
PubMedLink https://pubmed.ncbi.nlm.nih.gov/26582061/
PMCID PMC4862416
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
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
Identification of a common variant with potential pleiotropic effect on risk of inflammatory bowel disease and colorectal cancer.

Authors Khalili H, Gong J, Brenner H, et al.
Citation Carcinogenesis. 2015 Sep;36(9):999-1007.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/26071399/
PMCID PMC4573660
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
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
A genome-wide association study for colorectal cancer identifies a risk locus in 14q23.1.

Authors Lemire M, Qu C, Loo LWM, et al.
Citation Hum Genet. 2015 Nov;134(11-12):1249-62.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/26404086/
PMCID PMC4687971
Risk of colorectal cancer for people with a mutation in both a MUTYH and a DNA mismatch repair gene.

Authors Win AK, Reece JC, Buchanan DD, et al.
Citation Fam Cancer. 2015 Dec;14(4):575-83.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/26202870/
PMCID PMC4631636
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
Long-range epigenetic regulation is conferred by genetic variation located at thousands of independent loci.

Authors Lemire M, Zaidi SH, Ban M, et al.
Citation Nat Commun. 2015 Feb 26;6:6326.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/25716334/
PMCID PMC4351585
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
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
The effect of 5-fluorouracil/leucovorin chemotherapy on CpG methylation, or the confounding role of leukocyte heterogeneity: an illustration.

Authors Lemire M, Zaidi SH, Zanke BW, et al.
Citation Genomics. 2015 Dec;106(6):340-7.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/26368860/
PMCID PMC4722538
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
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
Association of aspirin and NSAID use with risk of colorectal cancer according to genetic variants.

Authors Nan H, Hutter CM, Lin Y, et al.
Citation JAMA. 2015 Mar 17;313(11):1133-42.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/25781442/
PMCID PMC4382867
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
Consequences of germline variation disrupting the constitutional translational initiation codon start sites of MLH1 and BRCA2: Use of potential alternative start sites and implications for predicting variant pathogenicity.

Authors Parsons MT, Whiley PJ, Beesley J, et al.
Citation Mol Carcinog. 2015 Jul;54(7):513-22.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/24302565/
PMCID PMC4041856
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
PIK3CA Somatic Mutation Status in Relation to Patient and Tumor Factors in Racial/Ethnic Minorities with Colorectal Cancer.

Authors Phipps AI, Ahnen DJ, Cheng I, et al.
Citation Cancer Epidemiol Biomarkers Prev. 2015 Jul;24(7):1046-51.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/25994739/
PMCID PMC4490937
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
Association between molecular subtypes of colorectal cancer and patient survival.

Authors Phipps AI, Limburg PJ, Baron JA, et al.
Citation Gastroenterology. 2015 Jan;148(1):77-87.e2.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/25280443/
PMCID PMC4274235
Diabetes, antidiabetic medications, and pancreatic cancer risk: an analysis from the International Pancreatic Cancer Case-Control Consortium.

Authors Bosetti C, Rosato V, Li D, et al.
Citation Ann Oncol. 2014 Oct;25(10):2065-72.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/25057164/
PMCID PMC4176453
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
Pleiotropic effects of genetic risk variants for other cancers on colorectal cancer risk: PAGE, GECCO and CCFR consortia.

Authors Cheng I, Kocarnik JM, Dumitrescu L, et al.
Citation Gut. 2014 May;63(5):800-7.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/23935004/
PMCID PMC3918490
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
No evidence of gene-calcium interactions in genome-wide analysis of colorectal cancer risk.

Authors Du M, Zhang X, Hoffmeister M, et al.
Citation Cancer Epidemiol Biomarkers Prev. 2014 Dec;23(12):2971-6.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/25192705/
PMCID PMC4257872
A novel colorectal cancer risk locus at 4q32.2 identified from an international genome-wide association study.

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
Genome-wide diet-gene interaction analyses for risk of colorectal cancer.

Authors Figueiredo JC, Hsu L, Hutter CM, et al.
Citation PLoS Genet. 2014 Apr 17;10(4):e1004228.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/24743840/
PMCID PMC3990510
Characterisation of Familial Colorectal Cancer Type X, Lynch syndrome, and non-familial colorectal cancer.

Authors Shiovitz S, Copeland WK, Passarelli MN, et al.
Citation Br J Cancer. 2014 Jul 29;111(3):598-602.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/24918813/
PMCID PMC4119982
Perceived versus predicted risks of colorectal cancer and self-reported colonoscopies by members of mismatch repair gene mutation-carrying families who have declined genetic testing.

Authors Flander L, Speirs-Bridge A, Rutstein A, et al.
Citation J Genet Couns. 2014 Feb;23(1):79-88.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/23748873/
PMCID PMC3838501
Fertility and apparent genetic anticipation in Lynch syndrome.

Authors Stupart D, Win AK, Jenkins M, et al.
Citation Fam Cancer. 2014 Sep;13(3):369-74.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/24677027/
PMCID PMC4357528
Functional normalization of 450k methylation array data improves replication in large cancer studies.

Authors Fortin JP, Labbe A, Lemire M, et al.
Citation Genome Biol. 2014 Dec 3;15(12):503.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/25599564/
PMCID PMC4283580
Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific database.

Authors Thompson BA, Spurdle AB, Plazzer JP, et al.
Citation Nat Genet. 2014 Feb;46(2):107-15.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/24362816/
PMCID PMC4294709
Communication of genetic test results to family and health-care providers following disclosure of research results.

Authors Graves KD, Sinicrope PS, Esplen MJ, et al.
Citation Genet Med. 2014 Apr;16(4):294-301.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/24091800/
PMCID PMC4009372
Trans-ethnic genome-wide association study of colorectal cancer identifies a new susceptibility locus in VT11A.

Authors Wang H, Burnett T, Kono S, et al.
Citation Nat Commun. 2014 Aug 8;5:4613.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/25105248/
PMCID PMC4180879
Gene-environment interaction involving recently identified colorectal cancer susceptibility loci.

Authors Kantor ED, Hutter CM, Minnier J, et al.
Citation Cancer Epidemiol Biomarkers Prev. 2014 Sep;23(9):1824-33.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/24994789/
PMCID PMC4209726
Identification of susceptibility loci for colorectal cancer in a genome-wide meta-analysis.

Authors Whiffin N, Hosking FJ, Farrington SM, et al.
Citation Hum Mol Genet. 2014 Sep 1;23(17):4729-37.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/24737748/
PMCID PMC4133584
How do researchers manage genetic results in practice? The experience of the multinational Colon Cancer Family Registry.

Authors Keogh LA, Fisher D, Sheinfeld Gorin S, et al.
Citation J Community Genet. 2014 Apr;5(2):99-108.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/23703702/
PMCID PMC3955463
Risk of colorectal cancer for carriers of mutations in MUTYH, with and without a family history of cancer.

Authors Win AK, Dowty JG, Cleary SP, et al.
Citation Gastroenterology. 2014 May;146(5):1208-11.e1-5.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/24444654/
PMCID PMC3992182
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
Large-scale genetic study in East Asians identifies six new loci associated with colorectal cancer risk.

Authors Zhang B, Jia WH, Matsuda K, et al.
Citation Nat Genet. 2014 Jun;46(6):533-42.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/24836286/
PMCID PMC4068797
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
Dietary N-nitroso compounds and risk of colorectal cancer: a case-control study in Newfoundland and Labrador and Ontario, Canada.

Authors Zhu Y, Wang PP, Zhao J, et al.
Citation Br J Nutr. 2014 Mar 28;111(6):1109-17.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/24160559/
PMCID PMC4339287
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 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
No association between germline variation in catechol-O-methyltransferase and colorectal cancer survival in postmenopausal women.

Authors Passarelli MN, Newcomb PA, Makar KW, et al.
Citation Menopause. 2014 Apr;21(4):415-20.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/23880798/
PMCID PMC3865220
Does risk of endometrial cancer for women without a germline mutation in a DNA mismatch repair gene depend on family history of endometrial cancer or colorectal cancer?

Authors Bharati R, Jenkins MA, Lindor NM, et al.
Citation Gynecol Oncol. 2014 May;133(2):287-92.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/24631449/
PMCID PMC4016812
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
The association of telomere length with colorectal cancer differs by the age of cancer onset.

Authors Boardman LA, Litzelman K, Seo S, et al.
Citation Clin Transl Gastroenterol. 2014 Mar 6;5:e52.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/24598784/
PMCID PMC3972691
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
A genome-wide association study of anorexia nervosa.

Authors Boraska V, Franklin C , Floyd JAB, et al.
Citation Mol Psychiatry. 2014 Oct;19(10):1085-94.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/24514567/
PMCID PMC4325090
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
Ulcer, gastric surgery and pancreatic cancer risk: an analysis from the International Pancreatic Cancer Case-Control Consortium (PanC4).

Authors Bosetti C, Lucenteforte E, Bracci PM, et al.
Citation Ann Oncol. 2013 Nov;24(11):2903-10.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/23970016/
PMCID PMC3811904
SBERIA: set-based gene-environment interaction test for rare and common variants in complex diseases.

Authors Jiao S, Hsu L, Bezieau S, et al.
Citation Genet Epidemiol. 2013 Jul;37(5):452-64.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/23720162/
PMCID PMC3713231
Lynch syndrome-associated breast cancers do not overexpress chromosome 11-encoded mucins.

Authors Walsh MD, Cummings MC, Pearson SA, et al.
Citation Mod Pathol. 2013 Jul;26(7):944-54.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/23370770/
PMCID PMC4204018
Family history of colorectal cancer in BRAF p.V600E-mutated colorectal cancer cases.

Authors Buchanan DD, Win AK, Walsh MD, et al.
Citation Cancer Epidemiol Biomarkers Prev. 2013 May;22(5):917-26.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/23462926/
PMCID PMC4024397
Comparison of the clinical prediction model PREMM(1,2,6) and molecular testing for the systematic identification of Lynch syndrome in colorectal cancer.

Authors Kastrinos F, Steyerberg EW, Balmaña J, et al.
Citation Gut. 2013 Feb;62(2):272-9.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/22345660/
PMCID PMC3470824
Association between hypermethylation of DNA repetitive elements in white blood cell DNA and early-onset colorectal cancer.

Authors Walters RJ, Williamson EJ, English DR, et al.
Citation Epigenetics. 2013 Jul;8(7):748-55.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/23804018/
PMCID PMC3781194
Human papillomavirus DNA is rarely detected in colorectal carcinomas and not associated with microsatellite instability: the Seattle Colon Cancer Family Registry.

Authors Burnett-Hartman AN, Feng Q, Popov V, et al.
Citation Cancer Epidemiol Biomarkers Prev. 2013 Feb;22(2):317-9.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/23250932/
PMCID PMC3565050
Polymorphisms in genes related to one-carbon metabolism are not related to pancreatic cancer in PanScan and PanC4.

Authors Leenders M, Bhattacharjee S, Vineis P, et al.
Citation Cancer Causes Control. 2013 Mar;24(3):595-602.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/23334854/
PMCID PMC4127987
Fine-mapping of genome-wide association study-identified risk loci for colorectal cancer in African Americans.

Authors Wang H, Haiman CA, Burnett T, et al.
Citation Hum Mol Genet. 2013 Dec 15;22(24):5048-55.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/23851122/
PMCID PMC3836473
Much of the genetic risk of colorectal cancer is likely to be mediated through susceptibility to adenomas.

Authors Carvajal-Carmona LG, Zauber AG, Jones AM, et al.
Citation Gastroenterology. 2013 Jan;144(1):53-5.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/22999960/
PMCID PMC3572711
CCAT2, a novel noncoding RNA mapping to 8q24, underlies metastatic progression and chromosomal instability in colon cancer.

Authors Ling H, Spizzo R, Atlasi Y, et al.
Citation Genome Res. 2013 Sep;23(9):1446-61.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/23796952/
PMCID PMC3759721
Genetic variation in the inflammation and innate immunity pathways and colorectal cancer risk.

Authors Wang H, Taverna D, Stram DO, et al.
Citation Cancer Epidemiol Biomarkers Prev. 2013 Nov;22(11):2094-101.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/24045924/
PMCID PMC3836607
Innate immunity gene polymorphisms and the risk of colorectal neoplasia.

Authors Chang CM, Chia VM, Gunter MJ, et al.
Citation Carcinogenesis. 2013 Nov;34(11):2512-20.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/23803696/
PMCID PMC3810838
Integrated analysis of genome-wide copy number alterations and gene expression in microsatellite stable, CpG island methylator phenotype-negative colon cancer.

Authors Loo LW, Tiirikainen M, Cheng I, et al.
Citation Genes Chromosomes Cancer. 2013 May;52(5):450-66.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/23341073/
PMCID PMC4019504
Germline variants and advanced colorectal adenomas: adenoma prevention with celecoxib trial genome-wide association study.

Authors Wang J, Carvajal-Carmona LG, Chu JH, et al.
Citation Clin Cancer Res. 2013 Dec 1;19(23):6430-7.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/24084763/
PMCID PMC4037290
Absence of PMS2 mutations in Colon-CFR participants whose colorectal cancers demonstrate unexplained loss of MLH1 expression.

Authors Clendenning M, Macrae FA, Walsh MD, et al.
Citation Clin Genet. 2013 Jun;83(6):591-3.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/23017166/
PMCID PMC3557751
Colorectal cancer survival by location and microsatellite status: data from the Colon Cancer Family Registries and their implications.

Authors Lynch PM.
Citation Dis Colon Rectum. 2013 Aug;56(8):935-6.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/23838860/
PMCID NA
Deciphering the genetic architecture of low-penetrance susceptibility to colorectal cancer.

Authors Whiffin N, Dobbins SE, Hosking FJ, et al.
Citation Hum Mol Genet. 2013 Dec 15;22(24):5075-82.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/23904454/
PMCID PMC3836483
Detection of large scale 3′ deletions in the PMS2 gene amongst Colon-CFR participants: have we been missing anything?

Authors Clendenning M, Walsh MD, Gelpi JB, et al.
Citation Fam Cancer. 2013 Sep;12(3):563-6.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/23288611/
PMCID PMC3639299

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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.

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

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

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

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.

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

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

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

GWASeq: targeted re-sequencing follow up to GWAS.

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

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

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

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

Female Hormonal Factors and the Risk of Endometrial Cancer in Lynch Syndrome.

The Influence of Screening for Precancerous Lesions on Family-Based Genetic Association Tests: An Example of Colorectal Polyps and Cancer.

Long-term psychosocial and behavioral adjustment in individuals receiving genetic test results in Lynch syndrome.

Genome-wide association study of colorectal cancer identifies six new susceptibility loci.

Mutation Spectrum and Risk of Colorectal Cancer in African American Families with Lynch Syndrome.

Fertility after young-onset colorectal cancer: a study of subjects with Lynch syndrome.

Prediagnostic Physical Activity and Colorectal Cancer Survival: Overall and Stratified by Tumor Characteristics.

Mendelian randomization study of height and risk of colorectal cancer.

Childhood Cancers in families with and without Lynch syndrome.

Mendelian randomization study of body mass index and colorectal cancer risk.

Cross Cancer Genomic Investigation of Inflammation Pathway for Five Common Cancers: Lung, Ovary, Prostate, Breast, and Colorectal Cancer.

A high-resolution copy-number variation resource for clinical and population genetics.

Meat intake, cooking methods, dietary carcinogens, and colorectal cancer risk: findings from the Colorectal Cancer Family Registry.

Association of the colorectal CpG island methylator phenotype with molecular features, risk factors and family history.

Comparison of Prediction Models for Lynch Syndrome Among Individuals with Colorectal Cancer.

Role of tumour molecular and pathology features to estimate colorectal cancer risk for first-degree relatives.

Aspirin, Ibuprofen, and the Risk of Colorectal Cancer in Lynch Syndrome.

Identification of a common variant with potential pleiotropic effect on risk of inflammatory bowel disease and colorectal cancer.

Genetic variants within the hTERT gene and the risk of colorectal cancer in Lynch syndrome.

A new GWAS and meta-analysis with 1000Genomes imputation identifies novel risk variants for colorectal cancer.

A genome-wide association study for colorectal cancer identifies a risk locus in 14q23.1.

Risk of colorectal cancer for people with a mutation in both a MUTYH and a DNA mismatch repair gene.

Red meat intake, NAT2, and risk of colorectal cancer: A pooled analysis of 11 studies.

Long-range epigenetic regulation is conferred by genetic variation located at thousands of independent loci.

Germline TP53 mutations in patients with early-onset colorectal cancer in the Colon Cancer Family Registry.

Lynch syndrome and cervical cancer.

The effect of 5-fluorouracil/leucovorin chemotherapy on CpG methylation, or the confounding role of leukocyte heterogeneity: an illustration.

Genetic determinants of telomere length and risk of common cancers: a Mendelian randomization study.

Association between body mass index and mortality for colorectal cancer survivors: overall and by tumor molecular phenotype.

Association of aspirin and NSAID use with risk of colorectal cancer according to genetic variants.

Determining the familial risk distribution of colorectal cancer: a data mining approach.

Consequences of germline variation disrupting the constitutional translational initiation codon start sites of MLH1 and BRCA2: Use of potential alternative start sites and implications for predicting variant pathogenicity.

Common colorectal cancer risk alleles contribute to the multiple colorectal adenoma phenotype, but do not influence colonic polyposis in FAP.

PIK3CA Somatic Mutation Status in Relation to Patient and Tumor Factors in Racial/Ethnic Minorities with Colorectal Cancer.

Meta-analysis of genome-wide association studies identifies common susceptibility polymorphisms for colorectal and endometrial cancer near SH2B3 and TSHZ1.

Association between molecular subtypes of colorectal cancer and patient survival.

Diabetes, antidiabetic medications, and pancreatic cancer risk: an analysis from the International Pancreatic Cancer Case-Control Consortium.

High prevalence of mismatch repair deficiency in prostate cancers diagnosed in mismatch repair gene mutation carriers from the Colon Cancer Family Registry.

Pleiotropic effects of genetic risk variants for other cancers on colorectal cancer risk: PAGE, GECCO and CCFR consortia.

Genetic variation in UGT genes modify the associations of NSAIDs with risk of colorectal cancer: Colon Cancer Family Registry.

No evidence of gene-calcium interactions in genome-wide analysis of colorectal cancer risk.

A novel colorectal cancer risk locus at 4q32.2 identified from an international genome-wide association study.

Genome-wide diet-gene interaction analyses for risk of colorectal cancer.

Characterisation of Familial Colorectal Cancer Type X, Lynch syndrome, and non-familial colorectal cancer.

Perceived versus predicted risks of colorectal cancer and self-reported colonoscopies by members of mismatch repair gene mutation-carrying families who have declined genetic testing.

Fertility and apparent genetic anticipation in Lynch syndrome.

Functional normalization of 450k methylation array data improves replication in large cancer studies.

Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific database.

Communication of genetic test results to family and health-care providers following disclosure of research results.

Trans-ethnic genome-wide association study of colorectal cancer identifies a new susceptibility locus in VT11A.

Gene-environment interaction involving recently identified colorectal cancer susceptibility loci.

Identification of susceptibility loci for colorectal cancer in a genome-wide meta-analysis.

How do researchers manage genetic results in practice? The experience of the multinational Colon Cancer Family Registry.

Risk of colorectal cancer for carriers of mutations in MUTYH, with and without a family history of cancer.

Colorectal cancer and self-reported tooth agenesis.

Large-scale genetic study in East Asians identifies six new loci associated with colorectal cancer risk.

A randomized trial to increase colonoscopy screening in members of high risk families in the Colorectal Cancer Family Registry and Cancer Genetics Network.

Dietary N-nitroso compounds and risk of colorectal cancer: a case-control study in Newfoundland and Labrador and Ontario, Canada.

Tumour MLH1 promoter region methylation testing is an effective prescreen for Lynch Syndrome (HNPCC).

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.

No association between germline variation in catechol-O-methyltransferase and colorectal cancer survival in postmenopausal women.

Does risk of endometrial cancer for women without a germline mutation in a DNA mismatch repair gene depend on family history of endometrial cancer or colorectal cancer?

Identification of genes expressed by immune cells of the colon that are regulated by colorectal cancer-associated variants.

The association of telomere length with colorectal cancer differs by the age of cancer onset.

Family History of Colorectal Cancer is not Associated with Colorectal Cancer Survival Regardless of Microsatellite Instability Status.