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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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
Genetic variants in carcinogen-metabolizing enzymes, cigarette smoking and pancreatic cancer risk.

Authors Jang JH, Cotterchio M, Borgida A, et al.
Citation Carcinogenesis. 2012 Apr;33(4):818-27.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/22301281/
PMCID PMC3324443
Meta-analysis of new genome-wide association studies of colorectal cancer risk.

Authors Peters U, Hutter CM, Hsu L, et al.
Citation Hum Genet. 2012 Feb;131(2):217-34.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/21761138/
PMCID PMC3257356
Cancer risks for relatives of patients with serrated polyposis.

Authors Win AK, Walters RJ, Buchanan DD, et al.
Citation Am J Gastroenterol. 2012 May;107(5):770-8.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/22525305/
PMCID PMC3488375
Letter: Kaplan-Meier failure estimate for metachronous colorectal cancer risk is clinically relevant.

Authors Jenkins MA, Gurrin LC, Parry S.
Citation Gut 2012;61:5 783-784 Published Online First: 24 October 2011.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/NA/
PMCID NA
BRAF mutation status and survival after colorectal cancer diagnosis according to patient and tumor characteristics.

Authors Phipps AI, Buchanan DD, Makar KW, et al.
Citation Cancer Epidemiol Biomarkers Prev. 2012 Oct;21(10):1792-8.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/22899730/
PMCID PMC3467328
Colorectal and Other Cancer Risks for Carriers and Noncarriers From Families With a DNA Mismatch Repair Gene Mutation: A Prospective Cohort Study.

Authors Win AK, Young JP, Lindor NM, et al.
Citation J Clin Oncol. 2012 Mar 20;30(9):958-64.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/22331944/
PMCID PMC3341109
Genome-wide association analyses in East Asians identify new susceptibility loci for colorectal cancer.

Authors Jia WH, Zhang B, Matsuo K, et al.
Citation Nat Genet. 2013 Feb;45(2):191-6.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/23263487/
PMCID PMC3679924
A comparison of approaches for association studies of polymorphisms and colorectal cancer risk.

Authors Ramsey SD, Holmes RS, McDermott CL, et al.
Citation Colorectal Dis. 2012 Sep;14(9):e573-86.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/22390411/
PMCID PMC3471808
The Australasian Colorectal Cancer Family Registry: Reducing the impact of colorectal cancer.

Authors Winship I, Win AK.
Citation Med J Aust 2012; 197 (9): 480-481.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/23121570/
PMCID NA
Genome-wide search for gene-gene interactions in colorectal cancer.

Authors Jiao S, Hsu L, Berndt S, et al.
Citation PLoS One. 2012;7(12):e52535.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/23300701/
PMCID PMC3530500
Vitamin D intake is negatively associated with promoter methylation of the Wnt antagonist gene DKK1 in a large group of colorectal cancer patients.

Authors Rawson JB, Sun Z, Dicks E, et al.
Citation Nutr Cancer. 2012;64(7):919-28.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/22966878/
PMCID PMC4323165
Interaction between alcohol drinking and obesity in relation to colorectal cancer risk: a case-control study in Newfoundland and Labrador, Canada.

Authors Zhao J, Zhu Y, Wang PP, et al.
Citation BMC Public Health. 2012 Feb 1;12:94.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/22296784/
PMCID PMC3280927
The TERT variant rs2736100 is associated with colorectal cancer risk.

Authors Kinnersley B, Migliorini G, Broderick P, et al.
Citation Br J Cancer. 2012 Sep 4;107(6):1001-8.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/22878375/
PMCID PMC3464867
Phenotype and polyp landscape in serrated polyposis syndrome: a series of 100 patients from genetics clinics.

Authors Rosty C, Buchanan DD, Walsh MD, et al.
Citation Am J Surg Pathol 2012 Jun;36(6):876-82.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/22510757/
PMCID PMC3354022
Cancer risks for the relatives of colorectal cancer cases with a methylated MLH1 promoter region: data from the Colorectal Cancer Family Registry.

Authors Levine AJ, Win AK, Buchanan DD, et al.
Citation Cancer Prev Res (Phila). 2012 Feb;5(2):328-35.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/22144422/
PMCID PMC3273599
MLH1 region polymorphisms show a significant association with CpG island shore methylation in a large cohort of healthy individuals.

Authors Savio AJ, Lemire M, Mrkonjic M, et al.
Citation PLoS One. 2012;7(12):e51531.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/23240038/
PMCID PMC3519863
cis-Expression QTL analysis of established colorectal cancer risk variants in colon tumors and adjacent normal tissue.

Authors Loo LW, Cheng I, Tiirikainen M, et al.
Citation PLoS One. 2012;7(2):e30477.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/22363440/
PMCID PMC3281844
A population-based study of prevalence and adherence trends in average risk colorectal cancer screening, 1997 to 2008.

Authors Sinicrope PS, Goode EL, Limburg PJ, et al.
Citation Cancer Epidemiol Biomarkers Prev. 2012 Feb;21(2):347-50.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/22144500/
PMCID PMC3339802
Lessons learned from the Family Health Promotion Project.

Authors Lowery JT, Ahnen DJ.
Citation Colorectal Cancer, June 2012, Vol. 1, No. 3, Pages 193-195.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/NA/
PMCID NA
Association of total energy intake and macronutrient consumption with colorectal cancer risk: results from a large population-based case-control study in Newfoundland and Labrador and Ontario, Canada.

Authors Sun Z, Liu L, Wang PP, et al.
Citation Nutr J. 2012 Mar 26;11:18.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/22449145/
PMCID PMC3378449
The Family Health Promotion Project (FHPP): design and baseline data from a randomized trial to increase colonoscopy screening in high risk families.

Authors Lowery JT, Marcus A, Kinney A, et al.
Citation Contemp Clin Trials. 2012 Mar;33(2):426-35.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/22101228/
PMCID PMC4303240
Reported intake of selected micronutrients and risk of colorectal cancer: results from a large population-based case-control study in Newfoundland, Labrador and Ontario, Canada.

Authors Sun Z, Zhu Y, Wang PP, et al.
Citation Anticancer Res. 2012 Feb;32(2):687-96.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/22287764/
PMCID NA
Informatics and data quality at collaborative multicenter Breast and Colon Cancer Family Registries.

Authors McGarvey PB, Ladwa S, Oberti M, et al.
Citation J Am Med Inform Assoc. 2012 Jun;19(e1):e125-8.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/22323393/
PMCID PMC3392863
A multifactorial likelihood model for MMR gene variant classification incorporating probabilities based on sequence bioinformatics and tumor characteristics: a report from the Colon Cancer Family Registry.

Authors Thompson BA, Goldgar DE, Paterson C, et al.
Citation Hum Mutat. 2013 Jan;34(1):200-9.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/22949379/
PMCID PMC3538359
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
The Effect of a Multifaceted Efficacy Intervention on Exercise Behavior in Relatives of Colon Cancer Patients.

Authors McGowan EL, Prapavessis H, Campbell N, et al.
Citation Int J Behav Med. 2012 Dec;19(4):550-62.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/21910025/
PMCID NA
Calibration of multiple in silico tools for predicting pathogenicity of mismatch repair gene missense substitutions.

Authors Thompson BA, Greenblatt MS, Vallee MP, et al.
Citation Hum Mutat. 2013 Jan;34(1):255-65.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/22949387/
PMCID PMC4318556
Screening practices of Australian men and women categorized as “at or slightly above average risk” of colorectal cancer.

Authors Ait Ouakrim D, Lockett T, Boussioutas A, et al.
Citation Cancer Causes Control. 2012 Nov;23(11):1853-64.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/23011536/
PMCID PMC3508400
The germline MLH1 K618A variant and susceptibility to Lynch syndrome-associated tumors.

Authors Medeiros F, Lindor NM, Couch FJ.
Citation J Mol Diagn. 2012 May-Jun;14(3):264-73.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/22426235/
PMCID PMC4432490
Recurrent and founder mutations in the PMS2 gene.

Authors Tomsic J, Senter L, Liyanarachchi S, et al.
Citation Clin Genet. 2013 Mar;83(3):238-43.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/22577899/
PMCID PMC3445698
Colorectal cancer linkage on chromosomes 4q21, 8q13, 12q24, and 15q22.

Authors Cicek MS, Cunningham JM, Fridley BL, et al.
Citation PLoS One. 2012;7(5):e38175.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/22675446/
PMCID PMC3364975
Performance of PREMM(1,2,6), MMRpredict, and MMRpro in detecting Lynch syndrome among endometrial cancer cases.

Authors Mercado RC, Hampel H, Kastrinos F, et al.
Citation Genet Med. 2012 Jul;14(7):670-80.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/22402756/
PMCID PMC3396560
Immunohistochemical testing of conventional adenomas for loss of expression of mismatch repair proteins in Lynch syndrome mutation carriers: a case series from the Australasian site of the Colon Cancer Family Registry.

Authors Walsh MD, Buchanan DD, Pearson SA, et al.
Citation Mod Pathol. 2012 May;25(5):722-30.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/22322191/
PMCID PMC3477239
Common variation near CDKN1A, POLD3 and SHROOM2 influences colorectal cancer risk.

Authors Dunlop MG, Dobbins SE, Farrington SM, et al.
Citation Nat Genet. 2012 May 27;44(7):770-6.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/22634755/
PMCID PMC4747430
Identification of Lynch syndrome among patients with colorectal cancer.

Authors Moreira L, Balaguer F, Lindor N, et al.
Citation JAMA. 2012 Oct 17;308(15):1555-65.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/23073952/
PMCID PMC3873721
Carcinogen metabolism genes, red meat and poultry intake, and colorectal cancer risk.

Authors Wang J, Joshi AD, Corral R, et al.
Citation Int J Cancer. 2012 Apr 15;130(8):1898-907.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/21618522/
PMCID PMC3883510
A pooled analysis of smoking and colorectal cancer: timing of exposure and interactions with environmental factors.

Authors Gong J, Hutter C, Baron JA, et al.
Citation Cancer Epidemiol Biomarkers Prev. 2012 Nov;21(11):1974-85.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/23001243/
PMCID PMC3493822
Impact of colon cancer screening on family history phenotype.

Authors Newcomb PA, Savu A, Phipps AI, et al.
Citation Epidemiology. 2012 Mar;23(2):308-10.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/22252410/
PMCID PMC3299289
Identification of constitutional MLH1 epimutations and promoter variants in colorectal cancer patients from the Colon Cancer Family Registry.

Authors Ward RL, Dobbins T, Lindor NM, et al.
Citation Genet Med. 2013 Jan;15(1):25-35.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/22878509/
PMCID PMC3908650
Characterization of Gene-Environment Interactions for Colorectal Cancer Susceptibility Loci.

Authors Hutter CM, Chang-Claude J, Slattery ML, et al.
Citation Cancer Res. 2012 Apr 15;72(8):2036-44.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/22367214/
PMCID PMC3374720
Correlation of tumour BRAF mutations and MLH1 methylation with germline mismatch repair (MMR) gene mutation status: a literature review assessing utility of tumour features for MMR variant classification.

Authors Parsons MT, Buchanan DD, Thompson B, et al.
Citation J Med Genet. 2012 Mar;49(3):151-7.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/22368298/
PMCID NA
Risks of primary extracolonic cancers following colorectal cancer in lynch syndrome.

Authors Win AK, Lindor NM, Young JP, et al.
Citation J Natl Cancer Inst. 2012 Sep 19;104(18):1363-72.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/22933731/
PMCID PMC3529597
Prevalence of Alternations in DNA mismatch repair gene alterations in a population-based sample of young-onset colorectal cancer patients.

Authors Limburg PJ, Harmsen WS, Chen HH, et al.
Citation Clin Gastroenterol Hepatol. 2011 Jun;9(6):497-502.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/21056691/
PMCID PMC3058119
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
Pancreatic cancer and a novel MSH2 germline alteration.

Authors Lindor NM, Petersen GM, Spurdle AB, et al.
Citation Pancreas. 2011 Oct;40(7):1138-40.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/21926548/
PMCID PMC3425611
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
Metachronous colorectal cancer risk for mismatch repair gene mutation carriers: the advantage of more extensive colon surgery.

Authors Parry S, Win AK, Parry B, et al.
Citation Gut. 2011 Jul;60(7):950-7.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/21193451/
PMCID PMC3848416
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
Common colorectal cancer risk variants in SMAD7 are associated with survival among prediagnostic nonsteroidal anti-inflammatory drug users: a population-based study of postmenopausal women.

Authors Passarelli MN, Coghill AE, Hutter CM, et al.
Citation Genes Chromosomes Cancer. 2011 Nov;50(11):875-86.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/21910156/
PMCID PMC3201720
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
Cigar and pipe smoking, smokeless tobacco use and pancreatic cancer: an analysis from the International Pancreatic Cancer Case-Control Consortium (PanC4).

Authors Bertuccio P, La Vecchia C, Silverman DT, et al.
Citation Ann Oncol. 2011 Jun;22(6):1420-6.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/21245160/
PMCID PMC3139985
Prediagnostic smoking history, alcohol consumption, and colorectal cancer survival: The Seattle Colon Cancer Family Registry.

Authors Phipps AI, Baron J, Newcomb PA.
Citation Cancer. 2011 Nov 1;117(21):4948-57.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/21495019/
PMCID PMC3138819
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
Management of pancreatic adenocarcinoma in Ontario, Canada: a population-based study using novel case ascertainment.

Authors Borgida AE, Ashamalla S, Al-Sukhni W, et al.
Citation Can J Surg. 2011 Feb;54(1):54-60.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/21251433/
PMCID PMC3038358
Modeling measurement error in tumor characterization studies.

Authors Rakovski C, Weisenberger DJ, Marjoram P, et al.
Citation BMC Bioinformatics. 2011 Jul 13;12:284.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/21752297/
PMCID PMC3213130
Meta-analysis of 8q24 for seven cancers reveals a locus between NOV and ENPP2 associated with cancer development.

Authors Brisbin AG, Asmann YW, Song H, et al.
Citation BMC Med Genet. 2011 Dec 5;12:156.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/22142333/
PMCID PMC3267702
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
Fine-mapping of colorectal cancer susceptibility loci at 8q23.3, 16q22.1 and 19q13.11: refinement of association signals and use of in silico analysis to suggest functional variation and unexpected candidate target genes.

Authors Carvajal-Carmona LG, Cazier JB, Jones AM, et al.
Citation Hum Mol Genet. 2011 Jul 15;20(14):2879-88.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/21531788/
PMCID PMC3118761
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
Quality Assessment and Correlation of Microsatellite Instability and Immunohistochemical Markers among Population- and Clinic-Based Colorectal Tumors Results from the Colon Cancer Family Registry.

Authors Cicek MS, Lindor NM, Gallinger S, et al.
Citation J Mol Diagn. 2011 May;13(3):271-81.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/21497289/
PMCID PMC3077724
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
Mutation deep within an intron of MSH2 causes Lynch syndrome.

Authors Clendenning M, Buchanan DD, Walsh MD, et al.
Citation Fam Cancer. 2011 Jun;10(2):297-301.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/21360204/
PMCID PMC4580736
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
Prediagnostic non-steroidal anti-inflammatory drug use and survival after diagnosis of colorectal cancer.

Authors Coghill AE, Newcomb PA, Campbell PT, et al.
Citation Gut. 2011 Apr;60(4):491-8.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/21051449/
PMCID PMC3049822
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
Pre-diagnostic NSAID use but not hormone therapy is associated with improved colorectal cancer survival in women.

Authors Coghill AE, Newcomb PA, Chia VM, et al.
Citation Br J Cancer. 2011 Mar 1;104(5):763-8.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/21304527/
PMCID PMC3048198
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
Genetic variation in inflammatory pathways is related to colorectal cancer survival.

Authors Coghill AE, Newcomb PA, Poole EM, et al.
Citation Clin Cancer Res. 2011 Nov 15;17(22):7139-47.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/21976545/
PMCID PMC3218294
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
Development and Validation of an Instrument to Measure the Impact of Genetic Testing on Self-Concept in Lynch Syndrome (LS).

Authors Esplen MJ, Stuckless N, Wong J, et al.
Citation Clin Genet. 2011 Nov;80(5):415-23.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/21883167/
PMCID PMC3237954
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
Genotype-environment interactions in microsatellite stable/microsatellite instability-low colorectal cancer: results from a genome-wide association study.

Authors Figueiredo JC, Lewinger JP, Song C, et al.
Citation Cancer Epidemiol Biomarkers Prev. 2011 May;20(5):758-66.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/21357381/
PMCID PMC3089660

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COX-1 (PTGS1) and COX-2 (PTGS2) polymorphisms, NSAID interactions, and risk of colon and rectal cancers in two independent populations.

Are the common genetic variants associated with colorectal cancer risk for DNA mismatch repair gene mutation carriers?

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

Allergies and risk of pancreatic cancer: a pooled analysis from the Pancreatic Cancer Case-Control Consortium.

Risks of colorectal and other cancers after endometrial cancer for women with lynch syndrome.

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

Common single-nucleotide polymorphisms in the estrogen receptor β promoter are associated with colorectal cancer survival in postmenopausal women.

Risk of metachronous colon cancer following surgery for rectal cancer in mismatch repair gene mutation carriers.

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

Identification of Genetic Susceptibility Loci for Colorectal Tumors in a Genome-wide Meta-analysis.

Dietary patterns and colorectal cancer recurrence and survival: a cohort study.

Cancer risks for MLH1 and MSH2 mutation carriers.

KRAS-mutation status in relation to colorectal cancer survival: the joint impact of correlated tumour markers.

Phospholipase A2G1B polymorphisms and risk of colorectal neoplasia.

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

Colon and rectal cancer survival by tumor location and microsatellite instability: The Colon Cancer Family Registry.

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

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

Multiplicity and molecular heterogeneity of colorectal carcinomas in individuals with serrated polyposis.

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

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

IÎºBKÎ² and NFÎºB1, NSAID use and risk of colorectal cancer in the Colon Cancer Family Registry.

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

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

Two-phase and family-based designs for next-generation sequencing studies.

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

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

BRAFV600E immunohistochemistry facilitates universal screening of colorectal cancers for Lynch syndrome.

Genetic variants in carcinogen-metabolizing enzymes, cigarette smoking and pancreatic cancer risk.

Meta-analysis of new genome-wide association studies of colorectal cancer risk.

Cancer risks for relatives of patients with serrated polyposis.

Letter: Kaplan-Meier failure estimate for metachronous colorectal cancer risk is clinically relevant.

BRAF mutation status and survival after colorectal cancer diagnosis according to patient and tumor characteristics.

Colorectal and Other Cancer Risks for Carriers and Noncarriers From Families With a DNA Mismatch Repair Gene Mutation: A Prospective Cohort Study.

Genome-wide association analyses in East Asians identify new susceptibility loci for colorectal cancer.

A comparison of approaches for association studies of polymorphisms and colorectal cancer risk.

The Australasian Colorectal Cancer Family Registry: Reducing the impact of colorectal cancer.

Genome-wide search for gene-gene interactions in colorectal cancer.

Vitamin D intake is negatively associated with promoter methylation of the Wnt antagonist gene DKK1 in a large group of colorectal cancer patients.

Interaction between alcohol drinking and obesity in relation to colorectal cancer risk: a case-control study in Newfoundland and Labrador, Canada.

The TERT variant rs2736100 is associated with colorectal cancer risk.

Phenotype and polyp landscape in serrated polyposis syndrome: a series of 100 patients from genetics clinics.

Cancer risks for the relatives of colorectal cancer cases with a methylated MLH1 promoter region: data from the Colorectal Cancer Family Registry.

MLH1 region polymorphisms show a significant association with CpG island shore methylation in a large cohort of healthy individuals.

cis-Expression QTL analysis of established colorectal cancer risk variants in colon tumors and adjacent normal tissue.

A population-based study of prevalence and adherence trends in average risk colorectal cancer screening, 1997 to 2008.

Lessons learned from the Family Health Promotion Project.

Association of total energy intake and macronutrient consumption with colorectal cancer risk: results from a large population-based case-control study in Newfoundland and Labrador and Ontario, Canada.

The Family Health Promotion Project (FHPP): design and baseline data from a randomized trial to increase colonoscopy screening in high risk families.

Reported intake of selected micronutrients and risk of colorectal cancer: results from a large population-based case-control study in Newfoundland, Labrador and Ontario, Canada.

Informatics and data quality at collaborative multicenter Breast and Colon Cancer Family Registries.

A multifactorial likelihood model for MMR gene variant classification incorporating probabilities based on sequence bioinformatics and tumor characteristics: a report from the Colon Cancer Family Registry.

Screening practices of unaffected people at familial risk of colorectal cancer.

The Effect of a Multifaceted Efficacy Intervention on Exercise Behavior in Relatives of Colon Cancer Patients.

Calibration of multiple in silico tools for predicting pathogenicity of mismatch repair gene missense substitutions.

Screening practices of Australian men and women categorized as “at or slightly above average risk” of colorectal cancer.

The germline MLH1 K618A variant and susceptibility to Lynch syndrome-associated tumors.

Recurrent and founder mutations in the PMS2 gene.

Colorectal cancer linkage on chromosomes 4q21, 8q13, 12q24, and 15q22.

Performance of PREMM(1,2,6), MMRpredict, and MMRpro in detecting Lynch syndrome among endometrial cancer cases.

Immunohistochemical testing of conventional adenomas for loss of expression of mismatch repair proteins in Lynch syndrome mutation carriers: a case series from the Australasian site of the Colon Cancer Family Registry.

Common variation near CDKN1A, POLD3 and SHROOM2 influences colorectal cancer risk.

Identification of Lynch syndrome among patients with colorectal cancer.

Carcinogen metabolism genes, red meat and poultry intake, and colorectal cancer risk.

A pooled analysis of smoking and colorectal cancer: timing of exposure and interactions with environmental factors.

Impact of colon cancer screening on family history phenotype.

Identification of constitutional MLH1 epimutations and promoter variants in colorectal cancer patients from the Colon Cancer Family Registry.

Characterization of Gene-Environment Interactions for Colorectal Cancer Susceptibility Loci.

Correlation of tumour BRAF mutations and MLH1 methylation with germline mismatch repair (MMR) gene mutation status: a literature review assessing utility of tumour features for MMR variant classification.

Risks of primary extracolonic cancers following colorectal cancer in lynch syndrome.

Prevalence of Alternations in DNA mismatch repair gene alterations in a population-based sample of young-onset colorectal cancer patients.

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

Pancreatic cancer and a novel MSH2 germline alteration.

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

Metachronous colorectal cancer risk for mismatch repair gene mutation carriers: the advantage of more extensive colon surgery.

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

Common colorectal cancer risk variants in SMAD7 are associated with survival among prediagnostic nonsteroidal anti-inflammatory drug users: a population-based study of postmenopausal women.

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

Cigar and pipe smoking, smokeless tobacco use and pancreatic cancer: an analysis from the International Pancreatic Cancer Case-Control Consortium (PanC4).