Our Publications

Click on a year to expand publications for that year.

Alternatively, click the search icon in the top right corner of this page to search for the publication.

2025

2024

2023

2022

2021

2020

2019

2018

2017

2016

2015

2014

2013

2012

2011

2010

2009

2008

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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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.

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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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 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
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
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
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
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
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
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
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
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
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
Phospholipase A2G1B polymorphisms and risk of colorectal neoplasia.

Authors Abbenhardt C, Poole EM, Kulmacz RJ, et al.
Citation Int J Mol Epidemiol Genet. 2013 Sep 12;4(3):140-9.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/24046806/
PMCID PMC3773565
Survival after inflammatory bowel disease-associated colorectal cancer in the Colon Cancer Family Registry.

Authors Adams SV, Ahnen DJ, Baron JA, et al.
Citation World J Gastroenterol. 2013 Jun 7;19(21):3241-8.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/23745025/
PMCID PMC3671075
Screening participation for people at increased risk of colorectal cancer due to family history: a systematic review and meta-analysis.

Authors Ait Ouakrim D, Lockett T, Boussioutas A, et al.
Citation Fam Cancer. 2013 Sep;12(3):459-72.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/23700069/
PMCID NA
Germline HOXB13 p.Gly84Glu mutation and risk of colorectal cancer.

Authors Akbari MR, Anderson LN, Buchanan DD, et al.
Citation Cancer Epidemiol. 2013 Aug;37(4):424-7.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/23541221/
PMCID PMC3684005
Genetic variants in vitamin d pathway genes and risk of pancreas cancer; results from a population-based case-control study in ontario, Canada.

Authors Anderson LN, Cotterchio M, Knight JA, et al.
Citation PLoS One. 2013 Jun 24;8(6):e66768.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/23826131/
PMCID PMC3691295
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
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
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
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
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
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
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
Germline Mutations in the Polyposis-Associated Genes BMPR1A, SMAD4, PTEN, MUTYH and GREM1 Are Not Common in Individuals with Serrated Polyposis Syndrome.

Authors Clendenning M, Young JP, Walsh MD, et al.
Citation PLoS One. 2013 Jun 21;8(6):e66705.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/23805267/
PMCID PMC3689730
Telomere length varies by DNA extraction method: implications for epidemiologic research.

Authors Cunningham JM, Johnson RA, Litzelman K, et al.
Citation Cancer Epidemiol Biomarkers Prev. 2013 Nov;22(11):2047-54.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/24019396/
PMCID PMC3827976
Identification of novel variants in colorectal cancer families by high-throughput exome sequencing.

Authors DeRycke MS, Gunawardena SR, Middha S, et al.
Citation Cancer Epidemiol Biomarkers Prev. 2013 Jul;22(7):1239-51.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/23637064/
PMCID PMC3704223
Cancer risks for MLH1 and MSH2 mutation carriers.

Authors Dowty JG, Win AK, Buchanan DD, et al.
Citation Hum Mutat. 2013 Mar;34(3):490-7.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/23255516/
PMCID PMC3887142
Cumulative impact of common genetic variants and other risk factors on colorectal cancer risk in 42,103 individuals.

Authors Dunlop MG, Tenesa A, Farrington SM, et al.
Citation Gut. 2013 Jun;62(6):871-81.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/22490517/
PMCID PMC5105590
Genetic Predictors of Circulating 25-Hydroxyvitamin D and Risk of Colorectal Cancer.

Authors Hiraki LT, Qu C, Hutter CM, et al.
Citation Cancer Epidemiol Biomarkers Prev. 2013 Nov;22(11):2037-46.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/23983240/
PMCID PMC3818310
Receptivity and preferences in cancer risk reduction lifestyle programs: A survey of colorectal cancer family members.

Authors Howell LA, Brockman TA, Sinicrope PS, et al.
Citation J Behav Health. 2013; 2(4): 279-290.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/25606348/
PMCID PMC4297662
Interaction of polymorphisms in mitotic regulator genes with cigarette smoking and pancreatic cancer risk.

Authors Jang JH, Cotterchio M, Borgida A, et al.
Citation Mol Carcinog. 2013 Nov;52 Suppl 1:E103-9.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/23908141/
PMCID PMC4533929
Genetic variations in SMAD7 are associated with colorectal cancer risk in the Colon Cancer Family Registry.

Authors Jiang X, Castelao JE, Vandenberg D, et al.
Citation PLoS One. 2013;8(4):e60464.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/23560096/
PMCID PMC3616155
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
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
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
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
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
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
COX-1 (PTGS1) and COX-2 (PTGS2) polymorphisms, NSAID interactions, and risk of colon and rectal cancers in two independent populations.

Authors Makar KW, Poole EM, Resler AJ, et al.
Citation Cancer Causes Control. 2013 Dec;24(12):2059-75.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/24022467/
PMCID PMC3913564
Allergies and risk of pancreatic cancer: a pooled analysis from the Pancreatic Cancer Case-Control Consortium.

Authors Olson SH, Hsu M, Satagopan JM, et al.
Citation Am J Epidemiol. 2013 Sep 1;178(5):691-700.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/23820785/
PMCID PMC3755648
Common single-nucleotide polymorphisms in the estrogen receptor β promoter are associated with colorectal cancer survival in postmenopausal women.

Authors Passarelli MN, Phipps AI, Potter JD, et al.
Citation Cancer Res. 2013 Jan 15;73(2):767-75.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/23149914/
PMCID PMC3588850
Identification of Genetic Susceptibility Loci for Colorectal Tumors in a Genome-wide Meta-analysis.

Authors Peters U, Jiao S, Schumacher FR, et al.
Citation Gastroenterology. 2013 Apr;144(4):799-807.e24.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/23266556/
PMCID PMC3636812
KRAS-mutation status in relation to colorectal cancer survival: the joint impact of correlated tumour markers.

Authors Phipps AI, Buchanan DD, Makar KW, et al.
Citation Br J Cancer. 2013 Apr 30;108(8):1757-64.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/23511557/
PMCID PMC3668469
Colon and rectal cancer survival by tumor location and microsatellite instability: The Colon Cancer Family Registry.

Authors Phipps AI, Lindor NM, Jenkins MA, et al.
Citation Dis Colon Rectum. 2013 Aug;56(8):937-44.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/23838861/
PMCID PMC3708260
Multiplicity and molecular heterogeneity of colorectal carcinomas in individuals with serrated polyposis.

Authors Rosty C, Walsh MD, Walters RJ, et al.
Citation Am J Surg Pathol. 2013 Mar;37(3):434-42.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/23211288/
PMCID PMC3567207
IÎºBKÎ² and NFÎºB1, NSAID use and risk of colorectal cancer in the Colon Cancer Family Registry.

Authors Seufert BL, Poole EM, Whitton J, et al.
Citation Carcinogenesis. 2013 Jan;34(1):79-85.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/23002237/
PMCID PMC3534188
Two-phase and family-based designs for next-generation sequencing studies.

Authors Thomas DC, Yang Z, Yang F.
Citation Front Genet. 2013 Dec 13;4:276.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/24379824/
PMCID PMC3861783
BRAFV600E immunohistochemistry facilitates universal screening of colorectal cancers for Lynch syndrome.

Authors Toon CW, Walsh MD, Chou A, et al.
Citation Am J Surg Pathol. 2013 Oct;37(10):1592-602.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/23797718/
PMCID PMC3773060
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
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
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
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
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
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
Are the common genetic variants associated with colorectal cancer risk for DNA mismatch repair gene mutation carriers?

Authors Win AK, Hopper JL, Buchanan DD, et al.
Citation Eur J Cancer. 2013 May;49(7):1578-87.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/23434150/
PMCID PMC3625445
Risks of colorectal and other cancers after endometrial cancer for women with lynch syndrome.

Authors Win AK, Lindor NM, Winship I, et al.
Citation J Natl Cancer Inst. 2013 Feb 20;105(4):274-9.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/23385444/
PMCID PMC3576323
Risk of metachronous colon cancer following surgery for rectal cancer in mismatch repair gene mutation carriers.

Authors Win AK, Parry S, Parry B, et al.
Citation Ann Surg Oncol. 2013 Jun;20(6):1829-36.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/23358792/
PMCID PMC4041733
Dietary patterns and colorectal cancer recurrence and survival: a cohort study.

Authors Zhu Y, Wu H, Wang PP, et al.
Citation BMJ Open. 2013 Feb 7;3(2). pii: e002270.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/23396503/
PMCID PMC3586110
Screening practices of unaffected people at familial risk of colorectal cancer.

Authors Ait Ouakrim D, Boussioutas A, Lockett T, et al.
Citation Cancer Prev Res (Phila). 2012 Feb;5(2):240-7.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/22030089/
PMCID PMC3273548

2007

2006

2005

2004

2003

2002

2001

2000

1999

Click on a year to expand publications for that year.

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

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

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

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

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

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

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.

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

Association between molecular subtypes of colorectal cancer and patient survival.

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

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

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

Mendelian randomization study of height and risk of colorectal cancer.

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

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

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

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

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

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

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

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

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.

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?

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

A genome-wide association study of anorexia nervosa.

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

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

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

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

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

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

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

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

Colorectal cancer and self-reported tooth agenesis.

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

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

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

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

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

Genetic Variation in prostaglandin synthesis and related pathways, NSAID use, and colorectal cancer risk in the Colon Cancer Family Registry.

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

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

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

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

Fertility and apparent genetic anticipation in Lynch syndrome.

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

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

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

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

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

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

Phospholipase A2G1B polymorphisms and risk of colorectal neoplasia.

Survival after inflammatory bowel disease-associated colorectal cancer in the Colon Cancer Family Registry.

Screening participation for people at increased risk of colorectal cancer due to family history: a systematic review and meta-analysis.

Germline HOXB13 p.Gly84Glu mutation and risk of colorectal cancer.

Genetic variants in vitamin d pathway genes and risk of pancreas cancer; results from a population-based case-control study in ontario, Canada.

Ulcer, gastric surgery and pancreatic cancer risk: an analysis from the International Pancreatic Cancer Case-Control Consortium (PanC4).

Family history of colorectal cancer in BRAF p.V600E-mutated colorectal cancer cases.

Human papillomavirus DNA is rarely detected in colorectal carcinomas and not associated with microsatellite instability: the Seattle Colon Cancer Family Registry.

Much of the genetic risk of colorectal cancer is likely to be mediated through susceptibility to adenomas.

Innate immunity gene polymorphisms and the risk of colorectal neoplasia.

Absence of PMS2 mutations in Colon-CFR participants whose colorectal cancers demonstrate unexplained loss of MLH1 expression.

Detection of large scale 3′ deletions in the PMS2 gene amongst Colon-CFR participants: have we been missing anything?

Germline Mutations in the Polyposis-Associated Genes BMPR1A, SMAD4, PTEN, MUTYH and GREM1 Are Not Common in Individuals with Serrated Polyposis Syndrome.

Telomere length varies by DNA extraction method: implications for epidemiologic research.

Identification of novel variants in colorectal cancer families by high-throughput exome sequencing.

Cancer risks for MLH1 and MSH2 mutation carriers.

Cumulative impact of common genetic variants and other risk factors on colorectal cancer risk in 42,103 individuals.

Genetic Predictors of Circulating 25-Hydroxyvitamin D and Risk of Colorectal Cancer.

Receptivity and preferences in cancer risk reduction lifestyle programs: A survey of colorectal cancer family members.

Interaction of polymorphisms in mitotic regulator genes with cigarette smoking and pancreatic cancer risk.

Genetic variations in SMAD7 are associated with colorectal cancer risk in the Colon Cancer Family Registry.

SBERIA: set-based gene-environment interaction test for rare and common variants in complex diseases.

Comparison of the clinical prediction model PREMM(1,2,6) and molecular testing for the systematic identification of Lynch syndrome in colorectal cancer.

Polymorphisms in genes related to one-carbon metabolism are not related to pancreatic cancer in PanScan and PanC4.

CCAT2, a novel noncoding RNA mapping to 8q24, underlies metastatic progression and chromosomal instability in colon cancer.

Integrated analysis of genome-wide copy number alterations and gene expression in microsatellite stable, CpG island methylator phenotype-negative colon cancer.

Colorectal cancer survival by location and microsatellite status: data from the Colon Cancer Family Registries and their implications.