Authors Fernandez-Rozadilla C, Timofeeva M, Chen Z. et alCitation Nat Genet. 2023 Mar;55(3):519-520.PubMedLink https://pubmed.ncbi.nlm.nih.gov/36782065/PMCID Erratum
Genome-wide interaction study with smoking for colorectal cancer risk identifies novel genetic loci related to tumor suppression, inflammation and immune response
Authors Carreras-Torres R, Kim AE, Lin Y. et alCitation Cancer Epidemiol Biomarkers Prev. 2023 Mar 6;32(3):315-328.PubMedLink https://pubmed.ncbi.nlm.nih.gov/36576985/PMCID PMC9992283
A validation of models for prediction of mismatch repair gene mutations
Authors Shyr C, Blackford AL, Huang T. et alCitation Genet Med. 2022 Oct;24(10):2155-2166.PubMedLink https://pubmed.ncbi.nlm.nih.gov/35997715/PMCID NIHMID: 1910759
Cancer Risk C (CR-C), a functional genomics test, is a sensitive and rapid test for germline mismatch repair deficiency
Authors Alim I, Loke J, Yam S. et alCitation Genet Med. 2022 Sep;24(9):1821-1830.PubMedLink https://pubmed.ncbi.nlm.nih.gov/35616648/PMCID PMC10072225
Risk Stratification for Early-Onset Colorectal Cancer Using a Combination of Genetic and Environmental Risk Scores: An International Multi-Center Study
Authors Archambault AN, Jeon J, Lin Y. et alCitation JNCI. 2022 Apr 11;114(4):528-539.PubMedLink https://pubmed.ncbi.nlm.nih.gov/35026030/PMCID PMC9002285
Association between germline variants and somatic mutations in colorectal cancer
Authors Barfield R, Qu C, Steinfelder RS. et alCitation Sci Rep. 2022 Jun 17;12(1):10207.PubMedLink https://pubmed.ncbi.nlm.nih.gov/35715570/PMCID PMC9205954
Genetic regulation of DNA methylation yields novel discoveries in GWAS of colorectal cancer
Authors Barfield R, Huyghe JR, Lemire M, et al.Citation Cancer Epidemiol Biomarkers Prev. 2022 Mar3;cebp.0724.2021.PubMedLink https://pubmed.ncbi.nlm.nih.gov/35247911/PMCID PMC9081265
Assessing the causal role of epigenetic clocks in the development of multiple cancers: a Mendelian randomization study
Authors Berstein FM, McCartney DL, Lu AT. et alCitation eLife. 2022 Mar 29;11:e75374.PubMedLink https://pubmed.ncbi.nlm.nih.gov/35346416/PMCID PMC9049976
Large-scale cross-cancer fine-mapping of the 5p15.33 region reveals multiple independent signals
Authors Chen H, Majumdar A, Wang L, et al. Citation HGG Adv. 2021 Jul 8;2(3):100041. PubMedLink https://pubmed.ncbi.nlm.nih.gov/34355204/ PMCID PMC8336922
Identifying colorectal cancer caused by biallelic MUTYH pathogenic variants using tumor mutational signatures
Authors Georgeson P, Harrison TA, Pope BJ. et alCitation Nat Commun. 2022 Jun 6;13(1):3254.PubMedLink https://pubmed.ncbi.nlm.nih.gov/35668106/PMCID PMC9170691