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

Authors Burnett-Hartman AN, Feng Q, Popov V, et al.
Citation Cancer Epidemiol Biomarkers Prev. 2013 Feb;22(2):317-9.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/23250932/
PMCID PMC3565050
Much of the genetic risk of colorectal cancer is likely to be mediated through susceptibility to adenomas.

Authors Carvajal-Carmona LG, Zauber AG, Jones AM, et al.
Citation Gastroenterology. 2013 Jan;144(1):53-5.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/22999960/
PMCID PMC3572711
Innate immunity gene polymorphisms and the risk of colorectal neoplasia.

Authors Chang CM, Chia VM, Gunter MJ, et al.
Citation Carcinogenesis. 2013 Nov;34(11):2512-20.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/23803696/
PMCID PMC3810838
Absence of PMS2 mutations in Colon-CFR participants whose colorectal cancers demonstrate unexplained loss of MLH1 expression.

Authors Clendenning M, Macrae FA, Walsh MD, et al.
Citation Clin Genet. 2013 Jun;83(6):591-3.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/23017166/
PMCID PMC3557751
Detection of large scale 3′ deletions in the PMS2 gene amongst Colon-CFR participants: have we been missing anything?

Authors Clendenning M, Walsh MD, Gelpi JB, et al.
Citation Fam Cancer. 2013 Sep;12(3):563-6.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/23288611/
PMCID PMC3639299
Germline Mutations in the Polyposis-Associated Genes BMPR1A, SMAD4, PTEN, MUTYH and GREM1 Are Not Common in Individuals with Serrated Polyposis Syndrome.

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

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

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

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

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

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

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

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

Authors Jiang X, Castelao JE, Vandenberg D, et al.
Citation PLoS One. 2013;8(4):e60464.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/23560096/
PMCID PMC3616155
SBERIA: set-based gene-environment interaction test for rare and common variants in complex diseases.

Authors Jiao S, Hsu L, Bezieau S, et al.
Citation Genet Epidemiol. 2013 Jul;37(5):452-64.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/23720162/
PMCID PMC3713231
Comparison of the clinical prediction model PREMM(1,2,6) and molecular testing for the systematic identification of Lynch syndrome in colorectal cancer.

Authors Kastrinos F, Steyerberg EW, Balmaña J, et al.
Citation Gut. 2013 Feb;62(2):272-9.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/22345660/
PMCID PMC3470824
Polymorphisms in genes related to one-carbon metabolism are not related to pancreatic cancer in PanScan and PanC4.

Authors Leenders M, Bhattacharjee S, Vineis P, et al.
Citation Cancer Causes Control. 2013 Mar;24(3):595-602.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/23334854/
PMCID PMC4127987
CCAT2, a novel noncoding RNA mapping to 8q24, underlies metastatic progression and chromosomal instability in colon cancer.

Authors Ling H, Spizzo R, Atlasi Y, et al.
Citation Genome Res. 2013 Sep;23(9):1446-61.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/23796952/
PMCID PMC3759721
Integrated analysis of genome-wide copy number alterations and gene expression in microsatellite stable, CpG island methylator phenotype-negative colon cancer.

Authors Loo LW, Tiirikainen M, Cheng I, et al.
Citation Genes Chromosomes Cancer. 2013 May;52(5):450-66.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/23341073/
PMCID PMC4019504
Colorectal cancer survival by location and microsatellite status: data from the Colon Cancer Family Registries and their implications.

Authors Lynch PM.
Citation Dis Colon Rectum. 2013 Aug;56(8):935-6.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/23838860/
PMCID NA
COX-1 (PTGS1) and COX-2 (PTGS2) polymorphisms, NSAID interactions, and risk of colon and rectal cancers in two independent populations.

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

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

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

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

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

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

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

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

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

Authors Toon CW, Walsh MD, Chou A, et al.
Citation Am J Surg Pathol. 2013 Oct;37(10):1592-602.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/23797718/
PMCID PMC3773060
Lynch syndrome-associated breast cancers do not overexpress chromosome 11-encoded mucins.

Authors Walsh MD, Cummings MC, Pearson SA, et al.
Citation Mod Pathol. 2013 Jul;26(7):944-54.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/23370770/
PMCID PMC4204018
Association between hypermethylation of DNA repetitive elements in white blood cell DNA and early-onset colorectal cancer.

Authors Walters RJ, Williamson EJ, English DR, et al.
Citation Epigenetics. 2013 Jul;8(7):748-55.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/23804018/
PMCID PMC3781194
Fine-mapping of genome-wide association study-identified risk loci for colorectal cancer in African Americans.

Authors Wang H, Haiman CA, Burnett T, et al.
Citation Hum Mol Genet. 2013 Dec 15;22(24):5048-55.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/23851122/
PMCID PMC3836473
Genetic variation in the inflammation and innate immunity pathways and colorectal cancer risk.

Authors Wang H, Taverna D, Stram DO, et al.
Citation Cancer Epidemiol Biomarkers Prev. 2013 Nov;22(11):2094-101.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/24045924/
PMCID PMC3836607
Germline variants and advanced colorectal adenomas: adenoma prevention with celecoxib trial genome-wide association study.

Authors Wang J, Carvajal-Carmona LG, Chu JH, et al.
Citation Clin Cancer Res. 2013 Dec 1;19(23):6430-7.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/24084763/
PMCID PMC4037290
Deciphering the genetic architecture of low-penetrance susceptibility to colorectal cancer.

Authors Whiffin N, Dobbins SE, Hosking FJ, et al.
Citation Hum Mol Genet. 2013 Dec 15;22(24):5075-82.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/23904454/
PMCID PMC3836483
Are the common genetic variants associated with colorectal cancer risk for DNA mismatch repair gene mutation carriers?

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

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

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

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

Authors Ait Ouakrim D, Boussioutas A, Lockett T, et al.
Citation Cancer Prev Res (Phila). 2012 Feb;5(2):240-7.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/22030089/
PMCID PMC3273548
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
The PREMM(1,2,6) model predicts risk of MLH1, MSH2, and MSH6 germline mutations based on cancer history.

Authors Kastrinos F, Steyerberg EW, Mercado R, et al.
Citation Gastroenterology. 2011 Jan;140(1):73-81.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/20727894/
PMCID PMC3125673
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
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
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
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
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
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

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

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

Innate immunity gene polymorphisms and the risk of colorectal neoplasia.

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

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

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

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

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

Cancer risks for MLH1 and MSH2 mutation carriers.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Lynch syndrome-associated breast cancers do not overexpress chromosome 11-encoded mucins.

Association between hypermethylation of DNA repetitive elements in white blood cell DNA and early-onset colorectal cancer.

Fine-mapping of genome-wide association study-identified risk loci for colorectal cancer in African Americans.

Genetic variation in the inflammation and innate immunity pathways and colorectal cancer risk.

Germline variants and advanced colorectal adenomas: adenoma prevention with celecoxib trial genome-wide association study.

Deciphering the genetic architecture of low-penetrance susceptibility to colorectal cancer.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

The TERT variant rs2736100 is associated with colorectal cancer risk.

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

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

Lessons learned from the Family Health Promotion Project.

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

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

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

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

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

Identification of Lynch syndrome among patients with colorectal cancer.

Impact of colon cancer screening on family history phenotype.

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.

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

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

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

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

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

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

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

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.

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.

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.

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

Recurrent and founder mutations in the PMS2 gene.

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.

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

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

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

Cancer risks for relatives of patients with serrated polyposis.