Understanding Association and Causality in the Genetic Studies of Inflammatory Bowel Disease
Author:
Publisher
Elsevier BV
Subject
Gastroenterology,Hepatology
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1. Autophagy genes variants and paediatric Crohn's disease phenotype: A single-centre experience;Digestive and Liver Disease;2014-06
2. IL23R, NOD2/CARD15, ATG16L1 and PHOX2B polymorphisms in a group of patients with Crohn's disease and correlation with sub-phenotypes;International Journal of Molecular Medicine;2011-03-01
3. Clinical significance of NOD2/CARD15 and Toll-like receptor 4 gene single nucleotide polymorphisms in inflammatory bowel disease;World Journal of Gastroenterology;2008
4. Evaluating the role of the genetic variations of PTPN22, NFKB1, and FcGRIIIA genes in inflammatory bowel disease: A meta-analysis;Inflammatory Bowel Diseases;2007-10
5. Functional effects of protein sequence polymorphisms in the organic cation/ergothioneine transporter OCTN1 (SLC22A4);PHARMACOGENET GENOM;2007
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