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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