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2008

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
Genome-wide association scan identifies a colorectal cancer susceptibility locus on chromosome 8q24.

Authors Zanke BW, Greenwood CM, Rangrej J, et al.
Citation Nat Genet. 2007 Aug;39(8):989-94.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/17618283/
PMCID NA
Germ-line DNA copy number variation frequencies in a large North American population.

Authors Zogopoulos G, Ha KC, Naqib F, et al.
Citation Hum Genet. 2007 Nov;122(3-4):345-53.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/17638019/
PMCID NA
Hawaii Colorectal Cancer Family Registry.

Authors Burnett T, Miller-Pakvasa H, Saltzman B, et al.
Citation Hawaii Med J. 2006 Jul;65(7):208-10.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/16948402/
PMCID NA
Prediction of germline mutations and cancer risk in the Lynch syndrome.

Authors Chen S, Wang W, Lee S, et al.
Citation JAMA. 2006 Sep 27;296(12):1479-87.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/17003396/
PMCID PMC2538673
Risk of microsatellite-unstable colorectal cancer is associated jointly with smoking and nonsteroidal anti-inflammatory drug use.

Authors Chia VM, Newcomb PA, Bigler J, et al.
Citation Cancer Res. 2006 Jul 1;66(13):6877-83.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/16818666/
PMCID NA
Dietary phytoestrogen intake is associated with reduced colorectal cancer risk.

Authors Cotterchio M, Boucher BA, Manno M, et al.
Citation J Nutr. 2006 Dec;136(12):3046-53.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/17116718/
PMCID PMC1850957
Body mass index and the risk of death following the diagnosis of colorectal cancer in postmenopausal women (United States).

Authors Doria-Rose VP, Newcomb PA, Morimoto LM, et al.
Citation Cancer Causes Control. 2006 Feb;17(1):63-70.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/16411054/
PMCID NA
Cancer risks for mismatch repair gene mutation carriers: a population-based early onset case-family study.

Authors Jenkins MA, Baglietto L, Dowty JG, et al.
Citation Clin Gastroenterol Hepatol. 2006 Apr;4(4):489-98.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/16616355/
PMCID NA
Risk of colorectal cancer in monoallelic and biallelic carriers of MYH mutations: a population-based case-family study.

Authors Jenkins MA, Croitoru ME, Monga N, et al.
Citation Cancer Epidemiol Biomarkers Prev. 2006 Feb;15(2):312-4.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/16492921/
PMCID NA
Recommendations for the care of individuals with an inherited predisposition to Lynch syndrome: a systematic review.

Authors Lindor NM, Petersen GM, Hadley DW, et al.
Citation JAMA. 2006 Sep 27;296(12):1507-17.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/17003399/
PMCID NA
Ascending the learning curve–MSI testing experience of a six-laboratory consortium.

Authors Lindor NM, Smalley R, Barker M, et al.
Citation Cancer Biomark. 2006;2(1-2):5-9.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/17192055/
PMCID NA
Population-based study of the prevalence of family history of cancer: implications for cancer screening and prevention.

Authors Ramsey SD, Yoon P, Moonesinghe R.
Citation Genet Med. 2006 Sep;8(9):571-5.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/16980813/
PMCID PMC2726801
Chromosomal instability in microsatellite-unstable and stable colon cancer.

Authors Trautmann K, Terdiman JP, French AJ, et al.
Citation Clin Cancer Res. 2006 Nov 1;12(21):6379-85.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/17085649/
PMCID NA
Molecular predictors of lymph node metastasis in colon cancer: increased risk with decreased thymidylate synthase expression.

Authors Artinyan A, Essani R, Lake J, et al.
Citation J Gastrointest Surg. 2005 Dec;9(9):1216-21; discussion 1221.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/16332476/
PMCID NA
Use of microsatellite instability and immunohistochemistry testing for the identification of individuals at risk for Lynch syndrome.

Authors Baudhuin LM, Burgart LJ, Leontovich O.
Citation Fam Cancer. 2005;4(3):255-65.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/16136387/
PMCID NA
Conversion analysis for mutation detection in MLH1 and MSH2 in patients with colorectal cancer.

Authors Casey G, Lindor NM, Papadopoulos N, et al.
Citation JAMA. 2005 Feb 16;293(7):799-809.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/15713769/
PMCID PMC2933041
Environmental risk factors and colorectal neoplasia: Recent developments.

Authors Chia V, Newcomb PA.
Citation Current Colorectal Cancer Reports. 2005;1(2):67-72.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/NA/
PMCID NA
Colorectal screening is associated with reduced colorectal cancer risk: a case-control study within the population-based Ontario Familial Colorectal Cancer Registry.

Authors Cotterchio M, Manno M, Klar N, et al.
Citation Cancer Causes Control. 2005 Sep;16(7):865-75.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/16132797/
PMCID NA
Association between colonic screening, subject characteristics, and stage of colorectal cancer.

Authors Fazio L, Cotterchio M, Manno M, et al.
Citation Am J Gastroenterol. 2005 Nov;100(11):2531-9.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/16279911/
PMCID NA
Isolated loss of PMS2 expression in colorectal cancers: frequency, patient age, and familial aggregation.

Authors Gill S, Lindor NM, Burgart LJ, et al.
Citation Clin Cancer Res. 2005 Sep 15;11(18):6466-71.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/16166421/
PMCID NA
Identifying target populations for screening or not screening using logic regression.

Authors Janes H, Pepe M, Kooperberg C.
Citation Stat Med. 2005 May 15;24(9):1321-38.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/15568185/
PMCID NA
Lower cancer incidence in Amsterdam-I criteria families without mismatch repair deficiency: Familial Colorectal Cancer Type X.

Authors Lindor NM, Rabe K, Petersen GM, et al.
Citation JAMA. 2005 Apr 27;293(16):1979-85.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/15855431/
PMCID PMC2933042
Variation in plasma insulin-like growth factor-1 and insulin-like growth factor binding protein-3: genetic factors.

Authors Morimoto LM, Newcomb PA, Bigler J, et al.
Citation Cancer Epidemiol Biomarkers Prev. 2005 Jun;14(6):1394-401.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/15941947/
PMCID NA
Insulin-like growth factor polymorphisms and colorectal cancer risk.

Authors Morimoto LM, Newcomb PA, White E, et al.
Citation Cancer Epidemiol Biomarkers Prev. 2005 May;14(5):1204-11.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/15894673/
PMCID NA
Variation in plasma insulin-like growth factor-1 and insulin-like growth factor binding protein-3: personal and lifestyle factors (United States).

Authors Morimoto LM, Newcomb PA, White E, et al.
Citation Cancer Causes Control. 2005 Oct;16(8):917-27.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/16132801/
PMCID NA
Association between subject factors and colorectal cancer screening participation in Ontario, Canada.

Authors Ramji F, Cotterchio M, Manno M, et al.
Citation Cancer Detect Prev. 2005;29:221-6.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/15896925/
PMCID NA
Family history assessment to detect increased risk for colorectal cancer: conceptual considerations and a preliminary economic analysis.

Authors Ramsey SD, Burke W, Pinsky L, et al.
Citation Cancer Epidemiol Biomarkers Prev. 2005 Nov;14(11 Pt 1):2494-500.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/16284369/
PMCID PMC2692569
Clinical Significance of tumor microsatellite instability and immunohistochemistry for mismatch repair deficiency in colorectal cancers.

Authors Thomas BC, Thibodeau SN, Lindor NM.
Citation Current Colorectal Cancer Reports. 2005 Vol 1:no. 1; 1-6.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/NA/
PMCID NA
Recent developments in genomewide association scans: a workshop summary and review.

Authors Thomas DC, Haile RW, Duggan D.
Citation Am J Hum Genet. 2005 Sep;77(3):337-45.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/16080110/
PMCID PMC1226200
High frequency of hereditary colorectal cancer in Newfoundland likely involves novel susceptibility genes.

Authors Woods MO, Hyde AJ, Curtis FK, et al.
Citation Clin Cancer Res. 2005 Oct 1;11(19 Pt 1):6853-61.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/16203774/
PMCID NA
Familial mutations in PMS2 can cause autosomal dominant hereditary nonpolyposis colorectal cancer.

Authors Worthley DL, Walsh MD, Barker M, et al.
Citation Gastroenterology. 2005 May;128(5):1431-6.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/15887124/
PMCID NA
Evidence for an association between JC virus and colorectal neoplasia.

Authors Boland CR, Bigler J, Newcomb PA, et al.
Citation Cancer Epidemiol Biomarkers Prev. 2004 Dec;13(12):2285-6; author reply 2286.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/15598796/
PMCID NA
Association between biallelic and monoallelic germline MYH mutations and colorectal cancer risk.

Authors Croitoru ME, Cleary SP, Di Nicola N, et al.
Citation J Natl Cancer Inst. 2004;96(21):1631-4.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/15523092/
PMCID NA
The incidence of colorectal cancer following a negative screening sigmoidoscopy: implications for screening interval.

Authors Doria-Rose VP, Levin TR, Selby JV, et al.
Citation Gastroenterology. 2004; 127:714-722.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/15362026/
PMCID NA
BRAF mutation is associated with DNA methylation in serrated polyps and cancers of the colorectum.

Authors Kambara T, Simms LA, Whitehall VL, et al.
Citation Gut. 2004 Aug;53(8):1137-44.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/15247181/
PMCID PMC1774130
Role of inherited defects of MYH in the development of sporadic colorectal cancer.

Authors Kambara T, Whitehall VL, Spring KJ, et al.
Citation Genes Chromosomes Cancer. 2004 May;40(1):1-9.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/15034862/
PMCID NA
Colorectal tumour microsatellite instability test results: perspectives from patients.

Authors Lindor NM, Sloan J, Goldberg R, et al.
Citation Hered Cancer Clin Pract. 2004 May 15;2(2):69-75.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/20233473/
PMCID PMC2839997
Recognition of genetic syndromes in families with suspected hereditary colon cancer syndromes.

Authors Lindor NM.
Citation Clin Gastroenterol Hepatol. 2004 May;2(5):366-75.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/15118973/
PMCID NA
Reasons given by relatives of colorectal cancer patients for not undergoing screening.

Authors Madlensky L, Esplen MJ, Goel V.
Citation Prev Med. 2004 Oct;39(4):643-8.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/15351528/
PMCID NA
No evidence of an association of JC virus and colon neoplasia.

Authors Newcomb PA, Bush AC, Stoner GL, et al.
Citation Cancer Epidemiol Biomarkers Prev. 2004 Apr;13(4):662-6.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/15066935/
PMCID NA
Limitations of the odds ratio in gauging the performance of a diagnostic, prognostic, or screening marker.

Authors Pepe MS, Janes H, Longton G, et al.
Citation Am J Epidemiol. 2004 May 1;159(9):882-90.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/15105181/
PMCID NA

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Click on a year to expand publications for that year.

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.

Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21.

Germline EPHB2 receptor variants in familial colorectal cancer.

Colorectal Cancer Risks in Relatives of Young-Onset Cases: Is Risk the Same Across All First-Degree Relatives?

Excess body weight and colorectal cancer risk in Canada: associations in subgroups of clinically defined familial risk of cancer.

Exogenous hormones and colorectal cancer risk in Canada: associations stratified by clinically defined familial risk of cancer.

Allergies are associated with reduced pancreas cancer risk: A population-based case-control study in Ontario, Canada.

Colorectal cancer survivors undergoing genetic testing for hereditary non-polyposis colorectal cancer: motivational factors and psychosocial functioning.

Very high incidence of familial colorectal cancer in Newfoundland: a comparison with Ontario and 13 other population-based studies.

Optimal selection of markers for validation or replication from genome-wide association studies.

Stability of BAT26 in Lynch syndrome colorectal tumours.

Pathology features in Bethesda guidelines predict colorectal cancer microsatellite instability: a population-based study.

Rationale for, and approach to, studying modifiers of risk in persons with a genetic predisposition to colorectal cancer.

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.

Accuracy of colorectal polyp self-reports: findings from the Colon Cancer Family Registry.

MSH2 118T>C and MSH6 159C>T promoter polymorphisms and the risk of colorectal cancer.

Helicobacter pylori infection in Ontario: prevalence and risk factors.

Colon Cancer Family Registry: An International Resource for Studies of the Genetic Epidemiology of Colon Cancer.

Estrogen plus progestin use, microsatellite instability, and the risk of colorectal cancer in women.

Variants on 9p24 and 8q24 are associated with risk of colorectal cancer: results from the Colon Cancer Family Registry.

MLH1 -93 G>A promoter polymorphism and the risk for microsatellite unstable colorectal cancer.

Genetic association studies of cancer: where do we go from here?

Genome-wide association scan identifies a colorectal cancer susceptibility locus on chromosome 8q24.

Germ-line DNA copy number variation frequencies in a large North American population.

Hawaii Colorectal Cancer Family Registry.

Prediction of germline mutations and cancer risk in the Lynch syndrome.

Risk of microsatellite-unstable colorectal cancer is associated jointly with smoking and nonsteroidal anti-inflammatory drug use.

Dietary phytoestrogen intake is associated with reduced colorectal cancer risk.

Body mass index and the risk of death following the diagnosis of colorectal cancer in postmenopausal women (United States).

Cancer risks for mismatch repair gene mutation carriers: a population-based early onset case-family study.

Risk of colorectal cancer in monoallelic and biallelic carriers of MYH mutations: a population-based case-family study.

Recommendations for the care of individuals with an inherited predisposition to Lynch syndrome: a systematic review.

Ascending the learning curve–MSI testing experience of a six-laboratory consortium.

Population-based study of the prevalence of family history of cancer: implications for cancer screening and prevention.

Chromosomal instability in microsatellite-unstable and stable colon cancer.

Molecular predictors of lymph node metastasis in colon cancer: increased risk with decreased thymidylate synthase expression.

Use of microsatellite instability and immunohistochemistry testing for the identification of individuals at risk for Lynch syndrome.

Conversion analysis for mutation detection in MLH1 and MSH2 in patients with colorectal cancer.

Environmental risk factors and colorectal neoplasia: Recent developments.

Colorectal screening is associated with reduced colorectal cancer risk: a case-control study within the population-based Ontario Familial Colorectal Cancer Registry.

Association between colonic screening, subject characteristics, and stage of colorectal cancer.

Isolated loss of PMS2 expression in colorectal cancers: frequency, patient age, and familial aggregation.