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Stephan R. Targan
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Altered Intestinal ACE2 Levels Are Associated With Inflammation, Severe Disease, and Response to Anti-Cytokine Therapy in Inflammatory Bowel Disease
Prevalence and Associations of Avascular Necrosis of the Hip in a Large Well-characterized Cohort of Patients With Inflammatory Bowel Disease
Late-Onset Crohn's Disease Is A Subgroup Distinct in Genetic and Behavioral Risk Factors With UC-Like Characteristics
Plasma N-Glycan Signatures Are Associated With Features of Inflammatory Bowel Diseases
Colonic Phenotypes Are Associated with Poorer Response to Anti-TNF Therapies in Patients with IBD
Association of Ribonuclease T2 Gene Polymorphisms With Decreased Expression and Clinical Characteristics of Severity in Crohn's Disease
Genome-Wide Association Study Identifies African-Specific Susceptibility Loci in African Americans With Inflammatory Bowel Disease
Myeloid ATG16L1 Facilitates Host-Bacteria Interactions in Maintaining Intestinal Homeostasis
The TNF family member TL1A induces IL-22 secretion in committed human Th17 cells via IL-9 induction
Gene-microbiota interactions contribute to the pathogenesis of inflammatory bowel disease
Perianal Crohn's Disease is Associated with Distal Colonic Disease, Stricturing Disease Behavior, IBD-Associated Serologies and Genetic Variation in the JAK-STAT Pathway
A Pleiotropic Missense Variant in SLC39A8 Is Associated With Crohn's Disease and Human Gut Microbiome Composition
Ocular Manifestations in Inflammatory Bowel Disease Are Associated with Other Extra-intestinal Manifestations, Gender, and Genes Implicated in Other Immune-related Traits
Characterization of genetic loci that affect susceptibility to inflammatory bowel diseases in African Americans
Human NK cells licensed by killer Ig receptor genes have an altered cytokine program that modifies CD4+ T cell function
Clinical, serologic, and genetic factors associated with pyoderma gangrenosum and erythema nodosum in inflammatory bowel disease patients
Genetic variants synthesize to produce paneth cell phenotypes that define subtypes of Crohn's disease
Multidimensional prognostic risk assessment identifies association between IL12B variation and surgery in Crohn's disease
Assessing health status in inflammatory bowel disease using a novel single-item numeric rating scale
Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease
Variants in ZNF365 isoform D are associated with Crohn's disease
Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47
Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci
Fucosyltransferase 2 (FUT2) non-secretor status is associated with Crohn's disease
Genome wide association (GWA) predictors of anti-TNFalpha therapeutic responsiveness in pediatric inflammatory bowel disease
Genome-wide association identifies multiple ulcerative colitis susceptibility loci
Genetic epistasis of IL23/IL17 pathway genes in Crohn's disease
Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study
IL23R haplotypes provide a large population attributable risk for Crohn's disease
Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease
Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis
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