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Carcinogenesis|December 10, 2020
Germline variation in the insulin-like growth factor pathway and risk of Barrett's esophagus and esophageal adenocarcinomaShruti G Dighe, Jianhong Chen, Li Yan, et al.Medrxiv : the Preprint Server for Health Sciences|May 25, 2026
Exome sequencing directly implicates 68 genes in inflammatory bowel diseaseRuifei Zhu, Qian Zhang, Kai Yuan, et al.Scientific Reports|November 11, 2015
Recurrent Coding Sequence Variation Explains Only A Small Fraction of the Genetic Architecture of Colorectal CancerMaria N Timofeeva, Ben Kinnersley, Susan M Farrington, et al.Gastroenterology|April 28, 2012
Consensus statements for management of Barrett's dysplasia and early-stage esophageal adenocarcinoma, based on a Delphi processCathy Bennett, Nimish Vakil, Jacques Bergman, et al.Gastroenterology|December 3, 2014
Polymorphisms near TBX5 and GDF7 are associated with increased risk for Barrett's esophagusClaire Palles, Laura Chegwidden, Xinzhong Li, et al.Nature Genetics|August 29, 2022
Large-scale sequencing identifies multiple genes and rare variants associated with Crohn's disease susceptibilityAleksejs Sazonovs, Christine R Stevens, Guhan R Venkataraman, et al.Nature Genetics|September 11, 2012
Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagusZhan Su, Laura J Gay, Amy Strange, et al.Nature Genetics|December 5, 2018
Discovery of common and rare genetic risk variants for colorectal cancerJeroen R Huyghe, Stephanie A Bien, Tabitha A Harrison, et al.Pageof 45