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

Comparative phenotypic and CARD15 mutational analysis among African American, Hispanic, and White children with Crohn's disease.

Inflammatory bowel diseases - 1 Jul 2005

Kugathasan Subra, Loizides Anthony, Babusukumar Umesh, McGuire Erin, Wang Tao, Hooper Pleasant, Nebel Justin, Kofman Galina, Noel Richard, Broeckel Ulrich, Tolia Vasundhara

Abstract excerpt

BACKGROUND: Despite a large body of literature on the subject of Crohn's disease (CD), very little information is available on racial/ethnic differences related to disease presentation, clinical course, and genetics. The first identified CD susceptibility gene, CARD15, seems to be present in up t...

Read the complete abstract on PubMed

Topics

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

Share to Age of Onset
Share to Black or African American

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Crohn Disease

Share to Hispanic or Latino

Share to Intracellular Signaling Peptides and Proteins

Share to Nod2 Signaling Adaptor Protein

Share to United States

Share to White People

Source

Identifiers

PMID: 15973116
DOI: 10.1097/01.mib.0000171279.05471.21

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-15973116-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Comparative phenotypic and CARD15 mutational analysis among African American, Hispanic, and White children with Crohn's disease.PMID 15973116Read ↗

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

Molecular genetics of Crohn's disease.Semantic proximity Read ↗

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

NOD2/CARD15 variants are associated with lower weight at diagnosis in children with Crohn's disease.Semantic proximity Read ↗

Advances in the genetics of inflammatory bowel disease.Semantic proximity Read ↗

The molecular classification of the clinical manifestations of Crohn's disease.Semantic proximity Read ↗

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

NOD2/CARD15 mutations in Polish and Bosnian populations with and without Crohn's disease: prevalence and genotype-phenotype analysis.Semantic proximity Read ↗

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

Diverse effects of the CARD15 and IBD5 loci on clinical phenotype in 630 patients 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 ↗

NOD2/CARD15: geographic differences in the Spanish population and clinical applications in Crohn's disease.Semantic proximity Read ↗

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