Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

CARD15 polymorphisms in Behçet's disease.

Scandinavian journal of rheumatology - 1 Jan 2000

Ahmad T, Zhang L, Gogus F, Verity D, Wallace G, Madanat W, Fayyad F, James T, Neville M, Kanawati C, Fortune F, Celik A, Stanford M, Jewell D P, Marshall S E

Abstract excerpt

BACKGROUND: Behçet's disease (BD) is a chronic multi-system inflammatory disorder of unknown aetiology, which shares many features of the inflammatory bowel diseases (IBDs). CARD15 has recently been identified as the first susceptibility gene in Crohn's disease (CD). OBJECTIVE: Given certain clinical and pathological similarities between CD and BD, and recent evidence of linkage of BD to the CARD15 genomic...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Arabs
Share to Behcet Syndrome

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to England

Share to HLA-B Antigens

Share to HLA-B51 Antigen

Share to Jordan

Share to Nod2 Signaling Adaptor Protein

Share to Turkey

Source

Identifiers

PMID: 16134731
DOI: 10.1080/03009740510018714

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

CARD15 polymorphisms in Behçet's disease.PMID 16134731Read ↗

Common Crohn's disease-predisposing variants of the CARD15/NOD2 gene are not associated with Behçet's disease in Turkey.Semantic proximity Read ↗

Variants of CARD15 are associated with an aggressive clinical course of Crohn's disease--an IG-IBD study.Semantic proximity Read ↗

CARD15 genetic variation in a Quebec population: prevalence, genotype-phenotype relationship, and haplotype structure.Semantic proximity Read ↗

Association of CARD15 polymorphisms with atopy-related traits in a population-based cohort of Caucasian adults.Semantic proximity Read ↗

NOD2/CARD15 mutations in Croatian patients with Crohn's disease: prevalence and genotype-phenotype relationship.Semantic proximity Read ↗

Association between mutations in the CARD15 (NOD2) gene and Crohn's disease in Israeli Jewish patients.Semantic proximity Read ↗

CARD15 gene polymorphisms in Serbian patients with Crohn's disease: genotype-phenotype analysis.Semantic proximity Read ↗

Diverse effects of the CARD15 and IBD5 loci on clinical phenotype in 630 patients with Crohn's disease.Semantic proximity Read ↗

CARD15 mutation analysis in an Italian population: Leu1007fsinsC but neither Arg702Trp nor Gly908Arg mutations are associated with Crohn's disease.Semantic proximity Read ↗

Role of the CARD15 gene in the pathogenesis of Crohn disease: phenotypic classification and prognostic implications.Semantic proximity Read ↗

CARD15 and IL23R influences Crohn's disease susceptibility but not disease phenotype in a Brazilian population.Semantic proximity Read ↗

Stratification by CARD15 variant genotype in a genome-wide search for inflammatory bowel disease susceptibility loci.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.