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Gut|June 15, 2004
A microarray screen for novel candidate genes in coeliac disease pathogenesisB Diosdado, M C Wapenaar, L Franke, et al.Arthritis and Rheumatism|March 27, 2013
Association of variants in IL2RA with progression of joint destruction in rheumatoid arthritisR Knevel, D P C de Rooy, A Zhernakova, et al.European Journal of Human Genetics : EJHG|August 13, 2009
Association of the TGF-beta receptor genes with abdominal aortic aneurysmA F Baas, J Medic, R van 't Slot, et al.Journal of Medical Genetics|December 14, 2007
Myosin IXB gene region and gluten intolerance: linkage to coeliac disease and a putative dermatitis herpetiformis associationL L E Koskinen, I R Korponay-Szabo, K Viiri, et al.Human Mutation|January 11, 2000
Genetic variation in ICF syndrome: evidence for genetic heterogeneityC Wijmenga, R S Hansen, G Gimelli, et al.Neurology|November 23, 2005
Lack of association between VEGF polymorphisms and ALS in a Dutch populationP W J Van Vught, N A Sutedja, J H Veldink, et al.American Journal of Human Genetics|August 27, 1998
Localization of the ICF syndrome to chromosome 20 by homozygosity mappingC Wijmenga, L P van den Heuvel, E Strengman, et al.Nutrition & Diabetes|February 10, 2015
Determining the association between adipokine expression in multiple tissues and phenotypic features of non-alcoholic fatty liver disease in obesityM G M Wolfs, N Gruben, S S Rensen, et al.International Journal of Obesity (2005)|August 5, 2009
Genetic variations in regulatory pathways of fatty acid and glucose metabolism are associated with obesity phenotypes: a population-based cohort studyS W van den Berg, M E T Dollé, S Imholz, et al.Neurogastroenterology and Motility|April 20, 2018
A GWAS meta-analysis from 5 population-based cohorts implicates ion channel genes in the pathogenesis of irritable bowel syndromeF Bonfiglio, M Henström, A Nag, et al.Pageof 12