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Promoter methylation of Wnt antagonists DKK1 and SFRP1 is associated with opposing tumor subtypes in two large populations of colorectal cancer patients.

Authors Rawson JB, Manno M, Mrkonjic M, et al.
Citation Carcinogenesis. 2011 May;32(5):741-7.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/21304055/
PMCID PMC3140140
Promoter methylation of Wnt5a is associated with microsatellite instability and BRAF V600E mutation in two large populations of colorectal cancer patients.

Authors Rawson JB, Mrkonjic M, Daftary D, et al.
Citation Br J Cancer. 2011 Jun 7;104(12):1906-12.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/21587258/
PMCID PMC3111198
Linkage to chromosome 2q32.2-q33.3 in familial serrated neoplasia (Jass syndrome).

Authors Roberts A, Nancarrow D, Clendenning M, et al.
Citation Fam Cancer. 2011 Jun;10(2):245-54.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/21165777/
PMCID PMC3100490
Frequency of deletions of EPCAM (TACSTD1) in MSH2-associated lynch syndrome cases.

Authors Rumilla K, Schowalter KV, Lindor NM, et al.
Citation J Mol Diagn. 2011 Jan;13(1):93-9.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/21227399/
PMCID PMC3069927
Calcium and vitamin D and risk of colorectal cancer: results from a large population-based case-control study in Newfoundland and Labrador and Ontario.

Authors Sun Z, Wang PP, Roebothan B, et al.
Citation Can J Public Health. 2011 Sep-Oct;102(5):382-9.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/22032106/
PMCID PMC6973686
Multiple common susceptibility variants near BMP pathway loci GREM1, BMP4, and BMP2 explain part of the missing heritability of colorectal cancer.

Authors Tomlinson IP, Carvajal-Carmona LG, Dobbins SE, et al.
Citation PLoS Genet. 2011 Jun;7(6):e1002105.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/21655089/
PMCID PMC3107194
Dependence of colorectal cancer risk on the parent-of-origin of mutations in DNA mismatch repair genes.

Authors van Vliet CM, Dowty JG, van Vliet JL, et al.
Citation Hum Mutat. 2011 Feb;32(2):207-12.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/21120946/
PMCID PMC3228833
Cancer: Lynch syndrome–how should colorectal cancer be managed?

Authors Vasen HF, de Vos tot Nederveen Cappel WH.
Citation Nat Rev Gastroenterol Hepatol. 2011 Apr;8(4):184-6.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/21460875/
PMCID NA
Germline PKHD1 mutations are protective against colorectal cancer.

Authors Ward CJ, Wu Y, Johnson RA, et al.
Citation Hum Genet. 2011 Mar;129(3):345-9.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/21274727/
PMCID PMC3102497
Lynch syndrome: barriers to and facilitators of screening and disease management.

Authors Watkins KE, Way CY, Fiander JJ, et al.
Citation Hered Cancer Clin Pract. 2011 Sep 7;9:8.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/21899746/
PMCID PMC3180430
Cancer risks for monoallelic MUTYH mutation carriers with a family history of colorectal cancer.

Authors Win AK, Cleary SP, Dowty JG, et al.
Citation Int J Cancer. 2011 Nov 1;129(9):2256-62.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/21171015/
PMCID PMC3291738
Body mass index in early adulthood and endometrial cancer risk for mismatch repair gene mutation carriers.

Authors Win AK, Dowty JG, Antill YC, et al.
Citation Obstet Gynecol. 2011 Apr;117(4):899-905.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/21422863/
PMCID PMC3084323
Body mass index in early adulthood and colorectal cancer risk for carriers and non-carriers of germline mutations in DNA mismatch repair genes.

Authors Win AK, Dowty JG, English DR, et al.
Citation Br J Cancer. 2011 Jun 28;105(1):162-9.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/21559014/
PMCID PMC3137400
Association between monoallelic MUTYH mutation and colorectal cancer risk: a meta-regression analysis.

Authors Win AK, Hopper JL, Jenkins MA.
Citation Fam Cancer. 2011 Mar;10(1):1-9.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/21061173/
PMCID PMC3228836
Determining the frequency of de novo germline mutations in DNA mismatch repair genes.

Authors Win AK, Jenkins MA, Buchanan DD, et al.
Citation J Med Genet. 2011 Aug;48(8):530-4.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/21636617/
PMCID PMC3436601
Risks of Lynch syndrome cancers for MSH6 mutation carriers.

Authors Baglietto L, Lindor NM, Dowty JG, et al.
Citation J Natl Cancer Inst. 2010 Feb 3;102(3):193-201.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/20028993/
PMCID PMC2815724
Polymorphisms in base excision repair genes as colorectal cancer risk factors and modifiers of the effect of diets high in red meat.

Authors Brevik A, Joshi AD, Corral R, et al.
Citation Cancer Epidemiol Biomarkers Prev. 2010 Dec;19(12):3167-73.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/21037106/
PMCID PMC3058341
Lessons from Lynch syndrome: a tumor biology-based approach to familial colorectal cancer.

Authors Buchanan DD, Roberts A, Walsh MD, et al.
Citation Future Oncol. 2010 Apr;6(4):539-49.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/20373868/
PMCID PMC2896690
Risk factors for colorectal cancer in patients with multiple serrated polyps: a cross-sectional case series from genetics clinics.

Authors Buchanan DD, Sweet K, Drini M, et al.
Citation PLoS One. 2010 Jul 16;5(7):e11636.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/20661287/
PMCID PMC2905435
Phenotypic diversity in patients with multiple serrated polyps: a genetics clinic study.

Authors Buchanan DD, Sweet K, Drini M, et al.
Citation Int J Colorectal Dis. 2010 Jun;25(6):703-12.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/20213458/
PMCID PMC2862176
Case-control study of overweight, obesity, and colorectal cancer risk, overall and by tumor microsatellite instability status.

Authors Campbell PT, Jacobs ET, Ulrich CM, et al.
Citation J Natl Cancer Inst. 2010 Mar 17;102(6):391-400.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/20208017/
PMCID PMC2841037
Cigarette smoking, genetic variants in carcinogen-metabolizing enzymes, and colorectal cancer risk.

Authors Cleary SP, Cotterchio M, Shi E, et al.
Citation Am J Epidemiol. 2010 Nov 1;172(9):1000-14.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/20937634/
PMCID PMC2984254
Genes involved with folate uptake and distribution and their association with colorectal cancer risk.

Authors Figueiredo JC, Levine AJ, Lee WH, et al.
Citation Cancer Causes Control. 2010 Apr;21(4):597-608.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/20037791/
PMCID PMC2904058
Bayesian mixture models for the incorporation of prior knowledge to inform genetic association studies.

Authors Fridley BL, Serie D, Jenkins G, et al.
Citation Genet Epidemiol. 2010 Jul;34(5):418-26.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/20583285/
PMCID PMC2910528
Confirmation of linkage to and localization of familial colon cancer risk haplotype on chromosome 9q22.

Authors Gray-McGuire C, Guda K, Adrianto I, et al.
Citation Cancer Res. 2010 Jul 1;70(13):5409-18.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/20551049/
PMCID PMC2896448
Use of folic acid-containing supplements after a diagnosis of colorectal cancer.

Authors Holmes RS, Li L, Zheng Y, et al.
Citation Cancer Epidemiol Biomarkers Prev. 2010 Aug;19(8):2023-34.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/20696661/
PMCID PMC3523172
Genetic variation in the retinoid X receptor and calcium-sensing receptor and risk of colorectal cancer in the Colon Cancer Family Registry.

Authors Jacobs ET, Martínez ME, Campbell PT, et al.
Citation Carcinogenesis. 2010 Aug;31(8):1412-6.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/20558521/
PMCID PMC2915636
Report of the combined meeting of the International Society for Gastrointestinal Hereditary Tumours, the Human Variome Project and the National Cancer Institute Colon Cancer Family Registry, Duesseldorf, Germany, 24 June 2009.

Authors Kohonen-Corish M, Weber TK, Lindblom A.
Citation Fam Cancer. 2010 Dec;9(4):705-11.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/20532640/
PMCID NA
A candidate gene study of folate-associated one carbon metabolism genes and colorectal cancer risk.

Authors Levine AJ, Figueiredo JC, Lee W, et al.
Citation Cancer Epidemiol Biomarkers Prev. 2010 Jul;19(7):1812-21.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/20615890/
PMCID PMC2950115
Genetic variability in the MTHFR gene and colorectal cancer risk using the Colorectal Cancer Family Registry.

Authors Levine AJ, Figueiredo JC, Lee W, et al.
Citation Cancer Epidemiol Biomarkers Prev. 2010 Jan;19(1):89-100.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/20056627/
PMCID PMC2805460
Parent of origin effects on age at colorectal cancer diagnosis.

Authors Lindor NM, Rabe KG, Petersen GM, et al.
Citation Int J Cancer. 2010 Jul 15;127(2):361-6.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/19904757/
PMCID PMC2877160
Alpha-1-antitrypsin deficiency and smoking as risk factors for mismatch repair deficient colorectal cancer: a study from the Colon Cancer Family Registry.

Authors Lindor NM, Yang P, Evans I, et al.
Citation Mol Genet Metab. 2010 Feb;99(2):157-9.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/19853488/
PMCID PMC2818220
Colon cancer information as a source of exercise motivation in first- and second-degree relatives of colon cancer patients.

Authors McGowan E, Prapavessis H.
Citation Psychology, Health, & Medicine. 2010 Dec;15(6):729-41.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/21154024/
PMCID NA
Specific variants in the MLH1 gene region may drive DNA methylation, loss of protein expression, and MSI-H colorectal cancer.

Authors Mrkonjic M, Roslin NM, Greenwood CM, et al.
Citation PLoS One. 2010 Oct 13;5(10):e13314.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/20967208/
PMCID PMC2954166
Risk of endometrial cancer for women diagnosed with HNPCC-related colorectal carcinoma.

Authors Obermair A, Youlden DR, Young JP, et al.
Citation Int J Cancer. 2010 Dec 1;127(11):2678-84.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/20533284/
PMCID PMC2947566
Smoking and colorectal cancer in Lynch syndrome: results from the Colon Cancer Family Registry and the University of Texas M.D. Anderson Cancer Center.

Authors Pande M, Lynch PM, Hopper JL, et al.
Citation Clin Cancer Res. 2010 Feb 15;16(4):1331-9.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/20145170/
PMCID PMC2822883
A genome-wide association study identifies pancreatic cancer susceptibility loci on chromosomes 13q22.1, 1q32.1 and 5p15.33.

Authors Petersen GM, Amundadottir L, Fuchs CS, et al.
Citation Nat Genet. 2010 Mar;42(3):224-8.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/20101243/
PMCID PMC2853179
Genetic variation in the vitamin D receptor (VDR) and the vitamin D-binding protein (GC) and risk for colorectal cancer: results from the Colon Cancer Family Registry.

Authors Poynter JN, Jacobs ET, Figueiredo JC, et al.
Citation Cancer Epidemiol Biomarkers Prev. 2010 Feb;19(2):525-36.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/20086113/
PMCID PMC2819604
Will Knowledge of Gene-based Colorectal Cancer Disease Risk Influence Quality of Life and Screening Behavior? Findings from a Population-based Study.

Authors Ramsey S, Blough D, McDermott C, et al.
Citation Public Health Genomics. 2010;13(1):1-12.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/20160979/
PMCID PMC2760996
Lower gastrointestinal tract cancer predisposition syndromes.

Authors Shah NB, Lindor NM.
Citation Hematol Oncol Clin North Am. 2010 Dec;24(6):1229-52.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/21075290/
PMCID PMC4103645
Pickled meat consumption and colorectal cancer (CRC): a case-control study in Newfoundland and Labrador, Canada.

Authors Squires J, Roebothan B, Buehler S, et al.
Citation Cancer Causes Control. 2010 Sep;21(9):1513-21.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/20506038/
PMCID NA
A large-scale meta-analysis to refine colorectal cancer risk estimates associated with MUTYH variants.

Authors Theodoratou E, Campbell H, Tenesa A, et al.
Citation Br J Cancer. 2010 Dec 7;103(12):1875-84.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/21063410/
PMCID PMC3008602
Lynch syndrome-associated breast cancers: clinicopathologic characteristics of a case series from the Colon Cancer Family Registry.

Authors Walsh MD, Buchanan DD, Cummings MC, et al.
Citation Clin Cancer Res. 2010 Apr 1;16(7):2214-24.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/20215533/
PMCID PMC2848890
Risk factors: Hyperplastic polyposis syndrome and risk of colorectal cancer.

Authors Young JP, Parry S.
Citation Nat Rev Gastroenterol Hepatol. 2010 Nov;7(11):594-5.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/21042338/
PMCID NA
Tobacco smoking and colorectal cancer: a population-based case-control study in Newfoundland and Labrador.

Authors Zhao J, Halfyard B, Roebothan B, et al.
Citation Can J Public Health. 2010 Jul-Aug;101(4):281-9.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/21033532/
PMCID NA
On combining family-based and population-based case-control data in association studies.

Authors Zheng Y, Heagerty PJ, Hsu L.
Citation Biometrics. 2010 Dec;66(4):1024-33.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/20163402/
PMCID PMC3038246
Genome-wide association study identifies variants in the ABO locus associated with susceptibility to pancreatic cancer.

Authors Amundadottir L, Kraft P, Stolzenberg-Solomon RZ, et al.
Citation Nat Genet. 2009 Sep;41(9):986-90.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/19648918/
PMCID PMC2839871
Lifestyle, dietary, and medical history factors associated with pancreatic cancer risk in Ontario, Canada.

Authors Anderson LN, Cotterchio M, Gallinger S.
Citation Cancer Causes Control. 2009 Aug; 20(6): 825–834.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/19194662/
PMCID PMC3907069
Classifying MLH1 and MSH2 variants using bioinformatic prediction, splicing assays, segregation, and tumor characteristics.

Authors Arnold S, Buchanan DD, Barker M, et al.
Citation Hum Mutat. 2009 May;30(5):757-70.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/19267393/
PMCID PMC2707453
The association of tumor microsatellite instability phenotype with family history of colorectal cancer.

Authors Bapat B, Lindor NM, Baron J, et al.
Citation Cancer Epidemiol Biomarkers Prev. 2009 Mar;18(3):967-75.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/19258475/
PMCID PMC2763617
Penetrance of colorectal cancer among MLH1/MSH2 carriers participating in the Colorectal Cancer Familial Registry in Ontario.

Authors Choi YH, Cotterchio M, McKeown-Eyssen G, et al.
Citation Hered Cancer Clin Pract. 2009 Aug 23;7(1):14.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/19698169/
PMCID PMC2744657
Germline MutY human homologue mutations and colorectal cancer: a multisite case-control study.

Authors Cleary SP, Cotterchio M, Jenkins MA, et al.
Citation Gastroenterology. 2009 Apr;136(4):1251-60.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/19245865/
PMCID PMC2739726
Family history of hormonal cancers and colorectal cancer risk: a case-control study conducted in Ontario.

Authors Jang JH, Cotterchio M, Gallinger S, et al.
Citation Int J Cancer. 2009 Aug 15;125(4):918-25.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/19437533/
PMCID PMC2767328
Role of MSH6 and PMS2 in the dna mismatch repair process and carcinogenesis.

Authors Jenkins MA.
Citation Surg Oncol Clin N Am. 2009 Oct;18(4):625-36.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/19793570/
PMCID NA
Red meat and poultry intake, polymorphisms in the nucleotide excision repair and mismatch repair pathways, and colorectal cancer risk.

Authors Joshi AD, Corral R, Siegmund KD, et al.
Citation Carcinogenesis. 2009 Mar;30(3):472-9.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/19029193/
PMCID PMC2722151
Making a case for surveillance colonoscopy in Lynch syndrome.

Authors Lindor NM.
Citation Colorectal Dis. 2009 Feb;11(2):131-2.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/19160466/
PMCID NA
Hereditary colorectal cancer: MYH-associated polyposis and other newly identified disorders.

Authors Lindor NM.
Citation Best Pract Res Clin Gastroenterol. 2009;23(1):75-87.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/19258188/
PMCID NA
Familial Colorectal Cancer Type X: the other half of hereditary nonpolyposis colon cancer syndrome.

Authors Lindor NM.
Citation Surg Oncol Clin N Am. 2009 Oct;18(4):637-45.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/19793571/
PMCID PMC3454516
Association of apolipoprotein E polymorphisms and dietary factors in colorectal cancer.

Authors Mrkonjic M, Chappell E, Pethe VV, et al.
Citation Br J Cancer. 2009 Jun 16;100(12):1966-74.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/19455140/
PMCID PMC2714237
Associations between smoking, alcohol consumption, and colorectal cancer, overall and by tumor microsatellite instability status.

Authors Poynter JN, Haile RW, Siegmund KD, et al.
Citation Cancer Epidemiol Biomarkers Prev. 2009 Oct;18(10):2745-50.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/19755657/
PMCID PMC2759847
Analysis of families with Lynch syndrome complicated by advanced serrated neoplasia: the importance of pathology review and pedigree analysis.

Authors Walsh MD, Buchanan DD, Walters R, et al.
Citation Fam Cancer. 2009;8(4):313-23.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/19241144/
PMCID PMC2783449
Validity of random-digit-dialing in recruiting controls in a case-control study.

Authors Wang PP, Dicks E, Gong X, et al.
Citation Am J Health Behav. 2009 Sep-Oct;33(5):513-20.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/19296741/
PMCID NA
The Relationship between Gravidity and Parity and Colorectal Cancer Risk.

Authors Wernli KJ, Wang Y, Zheng Y, et al.
Citation J Womens Health (Larchmt). 2009 Jul;18(7):995-1001.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/19575687/
PMCID PMC2851134
Concordance with clinical practice guidelines for adjuvant chemotherapy in patients with stage I–III colon cancer: experience in 2 Canadian provinces.

Authors Wirtzfeld DA, Mikula L, Gryfe R, et al.
Citation Can J Surg. 2009 Apr;52(2):92-7.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/19399202/
PMCID PMC2663496
Characterization of mutant MUTYH proteins associated with familial colorectal cancer.

Authors Ali M, Kim H, Cleary S, et al.
Citation Gastroenterology. 2008 Aug;135(2):499-507.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/18534194/
PMCID PMC2761659
Infectious agents and colorectal cancer: a review of Helicobacter pylori, Streptococcus bovis, JC virus, and human papillomavirus.

Authors Burnett-Hartman AN, Newcomb PA, Potter JD.
Citation Cancer Epidemiol Biomarkers Prev. 2008 Nov;17(11):2970-9.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/18990738/
PMCID PMC2676114
Colorectal cancer cases and relatives of cases indicate similar willingness to receive and disclose genetic information.

Authors Ceballos RM, Newcomb PA, Beasley JM, et al.
Citation Genet Test. 2008 Sep;12(3):415-20.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/18752450/
PMCID PMC2683753
Reproducibility of serum leptin, insulin-like growth factor-I, and insulin-like growth factor-binding protein-3 measurements.

Authors Chia VM, Newcomb PA, White E, et al.
Citation Horm Res. 2008;69(5):295-300.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/18259109/
PMCID NA
Missense polymorphisms in the adenomatous polyposis coli gene and colorectal cancer risk.

Authors Cleary SP, Kim H, Croitoru ME, et al.
Citation Dis Colon Rectum. 2008 Oct;51(10):1467-73; discussion 1473-4.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/18612690/
PMCID PMC2768068
A frame-shift mutation of PMS2 is a widespread cause of Lynch syndrome.

Authors Clendenning M, Senter L, Hampel H, et al.
Citation J Med Genet. 2008 Jun;45(6):340-5.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/18178629/
PMCID PMC4339871
Red meat intake, doneness, polymorphisms in genes that encode carcinogen-metabolizing enzymes, and colorectal cancer risk.

Authors Cotterchio M, Boucher BA, Manno M, et al.
Citation Cancer Epidemiol Biomarkers Prev. 2008 Nov;17(11):3098-107.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/18990750/
PMCID PMC2751598
Predictors of multivisceral resection in patients with locally advanced colorectal cancer.

Authors Govindarajan A, Fraser N, Cranford V, et al.
Citation Ann Surg Oncol. 2008 Jul;15(7):1923-30.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/18473145/
PMCID PMC2770244
Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer.

Authors Houlston RS, Webb E, Broderick P, et al.
Citation Nat Genet. 2008 Dec;40(12):1426-35.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/19011631/
PMCID PMC2836775
Family history and colorectal cancer survival in women.

Authors Kirchhoff AC, Newcomb PA, Trentham-Dietz A, et al.
Citation Fam Cancer. 2008;7(4):287-92.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/18360806/
PMCID NA
Efficient p-value estimation in massively parallel testing problems.

Authors Kustra R, Shi X, Murdoch DJ, et al.
Citation Biostatistics. 2008 Oct;9(4):601-12.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/18304995/
PMCID PMC2536722
Pathological features of colorectal carcinomas in MYH-associated polyposis.

Authors O’Shea AM, Cleary SP, Croitoru MA, et al.
Citation Histopathology. 2008 Aug;53(2):184-94.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/18564191/
PMCID PMC2754312
Molecular characterization of MSI-H colorectal cancer by MLHI promoter methylation, immunohistochemistry, and mismatch repair germline mutation screening.

Authors Poynter JN, Siegmund KD, Weisenberger DJ, et al.
Citation Cancer Epidemiol Biomarkers Prev. 2008 Nov;17(11):3208-15.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/18990764/
PMCID PMC2628332
Activation of Notch signaling in human colon adenocarcinoma.

Authors Reedijk M, Odorcic S, Zhang H, et al.
Citation Int J Oncol. 2008 Dec;33(6):1223-9.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/19020755/
PMCID PMC2739737
The clinical phenotype of Lynch syndrome due to germ-line PMS2 mutations.

Authors Senter L, Clendenning M, Sotamaa K, et al.
Citation Gastroenterology. 2008 Aug;135(2):419-28.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/18602922/
PMCID PMC2759321
Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21.

Authors Tenesa A, Farrington SM, Prendergast JG, et al.
Citation Nat Genet. 2008 May;40(5):631-7.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/18372901/
PMCID PMC2778004
Germline EPHB2 receptor variants in familial colorectal cancer.

Authors Zogopoulos G, Jorgensen C, Bacani J, et al.
Citation PLoS One. 2008 Aug 6;3(8):e2885.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/18682749/
PMCID PMC2483346
Colorectal Cancer Risks in Relatives of Young-Onset Cases: Is Risk the Same Across All First-Degree Relatives?

Authors Boardman LA, Morlan BW, Rabe KG, et al.
Citation Clin Gastroenterol Hepatol. 2007 Oct;5(10):1195-8.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/17702662/
PMCID PMC2180165
Excess body weight and colorectal cancer risk in Canada: associations in subgroups of clinically defined familial risk of cancer.

Authors Campbell PT, Cotterchio M, Dicks E, et al.
Citation Cancer Epidemiol Biomarkers Prev. 2007 Sep;16(9):1735-44.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/17855691/
PMCID NA
Exogenous hormones and colorectal cancer risk in Canada: associations stratified by clinically defined familial risk of cancer.

Authors Campbell PT, Newcomb P, Gallinger S, et al.
Citation Cancer Causes Control. 2007 Sep;18(7):723-33.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/17549595/
PMCID NA
Allergies are associated with reduced pancreas cancer risk: A population-based case-control study in Ontario, Canada.

Authors Eppel A, Cotterchio M, Gallinger S.
Citation Int J Cancer. 2007 Nov 15;121(10):2241-5.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/17582608/
PMCID NA
Colorectal cancer survivors undergoing genetic testing for hereditary non-polyposis colorectal cancer: motivational factors and psychosocial functioning.

Authors Esplen MJ, Madlensky L, Aronson M, et al.
Citation Clin Genet. 2007 Nov;72(5):394-401.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/17892499/
PMCID NA
Very high incidence of familial colorectal cancer in Newfoundland: a comparison with Ontario and 13 other population-based studies.

Authors Green RC, Green JS, Buehler SK, et al.
Citation Fam Cancer 2007;6:53-62.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/17039269/
PMCID NA
Optimal selection of markers for validation or replication from genome-wide association studies.

Authors Greenwood CM, Rangrej J, Sun L.
Citation Genet Epidemiol. 2007 Jul;31(5):396-407.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/17410553/
PMCID NA
Stability of BAT26 in Lynch syndrome colorectal tumours.

Authors Jaskowski L, Young J, Jackson L, et al.
Citation Eur J Hum Genet. 2007 Feb;15(2):139-41; author reply 141-2.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/17133259/
PMCID NA
Pathology features in Bethesda guidelines predict colorectal cancer microsatellite instability: a population-based study.

Authors Jenkins MA, Hayashi S, O’Shea AM, et al.
Citation Gastroenterology. 2007 Jul;133(1):48-56.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/17631130/
PMCID PMC2933045
Rationale for, and approach to, studying modifiers of risk in persons with a genetic predisposition to colorectal cancer.

Authors Jenkins MA, Southey MC, Giles GG.
Citation Curr Oncol Rep. 2007 May;9(3):202-7.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/17430691/
PMCID NA
Should health care providers have a duty to warn family members of individuals with an HNPCC-predisposing mutation? A survey of patients from the Ontario Familial Colon Cancer Registry.

Authors Kohut K, Manno M, Gallinger S.
Citation J Med Genet. 2007 Jun;44(6):404-7.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/17551085/
PMCID PMC2740891
Accuracy of colorectal polyp self-reports: findings from the Colon Cancer Family Registry.

Authors Madlensky L, Daftary D, Burnett T, et al.
Citation Cancer Epidemiol Biomarkers Prev. 2007 Sep;16(9):1898-901.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/17726139/
PMCID NA
MSH2 118T>C and MSH6 159C>T promoter polymorphisms and the risk of colorectal cancer.

Authors Mrkonjic M, Raptis S, Green RC, et al.
Citation Carcinogenesis. 2007 Dec;28(12):2575-80.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/17942459/
PMCID NA
Helicobacter pylori infection in Ontario: prevalence and risk factors.

Authors Naja F, Krieger N, Sullivan T.
Citation Can J Gastroenterol. 2007 Aug;21(8):501-6.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/17703249/
PMCID PMC2657974
Colon Cancer Family Registry: An International Resource for Studies of the Genetic Epidemiology of Colon Cancer.

Authors Newcomb PA, Baron J, Cotterchio M, et al.
Citation Cancer Epidemiol Biomarkers Prev. 2007 Nov;16(11):2331-43.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/17982118/
PMCID NA
Estrogen plus progestin use, microsatellite instability, and the risk of colorectal cancer in women.

Authors Newcomb PA, Zheng Y, Chia VM, et al.
Citation Cancer Res. 2007 Aug 1;67(15):7534-9.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/17671225/
PMCID NA
Variants on 9p24 and 8q24 are associated with risk of colorectal cancer: results from the Colon Cancer Family Registry.

Authors Poynter JN, Figueiredo JC, Conti DV, et al.
Citation Cancer Res. 2007 Dec 1;67(23):11128-32.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/18056436/
PMCID NA
MLH1 -93 G>A promoter polymorphism and the risk for microsatellite unstable colorectal cancer.

Authors Raptis S, Mrkonjic M, Green R,et al
Citation J Natl Cancer Inst. 2007 Mar 21;99(6):463-74.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/17374836/
PMCID NA
Genetic association studies of cancer: where do we go from here?

Authors Rebbeck TR, Khoury MJ, Potter JD.
Citation Cancer Epidemiol Biomarkers Prev. 2007 May;16(5):864-5.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/17507606/
PMCID NA

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Click on a year to expand publications for that year.

Promoter methylation of Wnt antagonists DKK1 and SFRP1 is associated with opposing tumor subtypes in two large populations of colorectal cancer patients.

Promoter methylation of Wnt5a is associated with microsatellite instability and BRAF V600E mutation in two large populations of colorectal cancer patients.

Linkage to chromosome 2q32.2-q33.3 in familial serrated neoplasia (Jass syndrome).

Frequency of deletions of EPCAM (TACSTD1) in MSH2-associated lynch syndrome cases.

Calcium and vitamin D and risk of colorectal cancer: results from a large population-based case-control study in Newfoundland and Labrador and Ontario.

Multiple common susceptibility variants near BMP pathway loci GREM1, BMP4, and BMP2 explain part of the missing heritability of colorectal cancer.

Dependence of colorectal cancer risk on the parent-of-origin of mutations in DNA mismatch repair genes.

Cancer: Lynch syndrome–how should colorectal cancer be managed?

Germline PKHD1 mutations are protective against colorectal cancer.

Lynch syndrome: barriers to and facilitators of screening and disease management.

Cancer risks for monoallelic MUTYH mutation carriers with a family history of colorectal cancer.

Body mass index in early adulthood and endometrial cancer risk for mismatch repair gene mutation carriers.

Body mass index in early adulthood and colorectal cancer risk for carriers and non-carriers of germline mutations in DNA mismatch repair genes.

Association between monoallelic MUTYH mutation and colorectal cancer risk: a meta-regression analysis.

Determining the frequency of de novo germline mutations in DNA mismatch repair genes.

Risks of Lynch syndrome cancers for MSH6 mutation carriers.

Polymorphisms in base excision repair genes as colorectal cancer risk factors and modifiers of the effect of diets high in red meat.

Lessons from Lynch syndrome: a tumor biology-based approach to familial colorectal cancer.

Risk factors for colorectal cancer in patients with multiple serrated polyps: a cross-sectional case series from genetics clinics.

Phenotypic diversity in patients with multiple serrated polyps: a genetics clinic study.

Case-control study of overweight, obesity, and colorectal cancer risk, overall and by tumor microsatellite instability status.

Cigarette smoking, genetic variants in carcinogen-metabolizing enzymes, and colorectal cancer risk.

Genes involved with folate uptake and distribution and their association with colorectal cancer risk.

Bayesian mixture models for the incorporation of prior knowledge to inform genetic association studies.

Confirmation of linkage to and localization of familial colon cancer risk haplotype on chromosome 9q22.

Use of folic acid-containing supplements after a diagnosis of colorectal cancer.

Genetic variation in the retinoid X receptor and calcium-sensing receptor and risk of colorectal cancer in the Colon Cancer Family Registry.

Report of the combined meeting of the International Society for Gastrointestinal Hereditary Tumours, the Human Variome Project and the National Cancer Institute Colon Cancer Family Registry, Duesseldorf, Germany, 24 June 2009.

A candidate gene study of folate-associated one carbon metabolism genes and colorectal cancer risk.

Genetic variability in the MTHFR gene and colorectal cancer risk using the Colorectal Cancer Family Registry.

Parent of origin effects on age at colorectal cancer diagnosis.

Alpha-1-antitrypsin deficiency and smoking as risk factors for mismatch repair deficient colorectal cancer: a study from the Colon Cancer Family Registry.

Colon cancer information as a source of exercise motivation in first- and second-degree relatives of colon cancer patients.

Specific variants in the MLH1 gene region may drive DNA methylation, loss of protein expression, and MSI-H colorectal cancer.

Risk of endometrial cancer for women diagnosed with HNPCC-related colorectal carcinoma.

Smoking and colorectal cancer in Lynch syndrome: results from the Colon Cancer Family Registry and the University of Texas M.D. Anderson Cancer Center.

A genome-wide association study identifies pancreatic cancer susceptibility loci on chromosomes 13q22.1, 1q32.1 and 5p15.33.

Genetic variation in the vitamin D receptor (VDR) and the vitamin D-binding protein (GC) and risk for colorectal cancer: results from the Colon Cancer Family Registry.

Will Knowledge of Gene-based Colorectal Cancer Disease Risk Influence Quality of Life and Screening Behavior? Findings from a Population-based Study.

Lower gastrointestinal tract cancer predisposition syndromes.

Pickled meat consumption and colorectal cancer (CRC): a case-control study in Newfoundland and Labrador, Canada.

A large-scale meta-analysis to refine colorectal cancer risk estimates associated with MUTYH variants.

Lynch syndrome-associated breast cancers: clinicopathologic characteristics of a case series from the Colon Cancer Family Registry.

Risk factors: Hyperplastic polyposis syndrome and risk of colorectal cancer.

Tobacco smoking and colorectal cancer: a population-based case-control study in Newfoundland and Labrador.

On combining family-based and population-based case-control data in association studies.

Genome-wide association study identifies variants in the ABO locus associated with susceptibility to pancreatic cancer.

Lifestyle, dietary, and medical history factors associated with pancreatic cancer risk in Ontario, Canada.

Classifying MLH1 and MSH2 variants using bioinformatic prediction, splicing assays, segregation, and tumor characteristics.

The association of tumor microsatellite instability phenotype with family history of colorectal cancer.

Penetrance of colorectal cancer among MLH1/MSH2 carriers participating in the Colorectal Cancer Familial Registry in Ontario.

Germline MutY human homologue mutations and colorectal cancer: a multisite case-control study.

Family history of hormonal cancers and colorectal cancer risk: a case-control study conducted in Ontario.

Role of MSH6 and PMS2 in the dna mismatch repair process and carcinogenesis.

Red meat and poultry intake, polymorphisms in the nucleotide excision repair and mismatch repair pathways, and colorectal cancer risk.

Making a case for surveillance colonoscopy in Lynch syndrome.

Hereditary colorectal cancer: MYH-associated polyposis and other newly identified disorders.

Familial Colorectal Cancer Type X: the other half of hereditary nonpolyposis colon cancer syndrome.

Association of apolipoprotein E polymorphisms and dietary factors in colorectal cancer.

Associations between smoking, alcohol consumption, and colorectal cancer, overall and by tumor microsatellite instability status.

Analysis of families with Lynch syndrome complicated by advanced serrated neoplasia: the importance of pathology review and pedigree analysis.

Validity of random-digit-dialing in recruiting controls in a case-control study.

The Relationship between Gravidity and Parity and Colorectal Cancer Risk.

Concordance with clinical practice guidelines for adjuvant chemotherapy in patients with stage I–III colon cancer: experience in 2 Canadian provinces.

Characterization of mutant MUTYH proteins associated with familial colorectal cancer.

Infectious agents and colorectal cancer: a review of Helicobacter pylori, Streptococcus bovis, JC virus, and human papillomavirus.

Colorectal cancer cases and relatives of cases indicate similar willingness to receive and disclose genetic information.

Reproducibility of serum leptin, insulin-like growth factor-I, and insulin-like growth factor-binding protein-3 measurements.

Missense polymorphisms in the adenomatous polyposis coli gene and colorectal cancer risk.

A frame-shift mutation of PMS2 is a widespread cause of Lynch syndrome.

Red meat intake, doneness, polymorphisms in genes that encode carcinogen-metabolizing enzymes, and colorectal cancer risk.

Predictors of multivisceral resection in patients with locally advanced colorectal cancer.

Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer.

Family history and colorectal cancer survival in women.

Efficient p-value estimation in massively parallel testing problems.

Pathological features of colorectal carcinomas in MYH-associated polyposis.

Molecular characterization of MSI-H colorectal cancer by MLHI promoter methylation, immunohistochemistry, and mismatch repair germline mutation screening.

Activation of Notch signaling in human colon adenocarcinoma.

The clinical phenotype of Lynch syndrome due to germ-line PMS2 mutations.