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

Association of NOD2 (CARD 15) genotype with clinical course of Crohn's disease: a cohort study.

Lancet (London, England) - 11 May 2002

Hampe Jochen, Grebe Jochen, Nikolaus Susanna, Solberg Camilla, Croucher Peter J P, Mascheretti Silvia, Jahnsen Jörgen, Moum Björn, Klump Bodo, Krawczak Michael, Mirza Muddassar M, Foelsch Ulrich R, Vatn Morten, Schreiber Stefan

Abstract excerpt

BACKGROUND: Crohn's disease is a heterogeneous disorder for which NOD2 (CARD 15) has been identified as a susceptibility gene. We investigate the relation between NOD2 genotype and phenotypic characteristics of patients with Crohn's disease. METHODS: Hypotheses about the relation between NOD2 genotype and Crohn's disease phenotype were generated retrospectively from a group of 446 German patients with this...

Read the complete abstract on PubMed

Topics

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

Share to Carrier Proteins
Share to Chi-Square Distribution

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Chromosomes, Human, Pair 16

Share to Crohn Disease

Share to Germany

Share to Intracellular Signaling Peptides and Proteins

Share to Nod2 Signaling Adaptor Protein

Share to Norway

Source

Identifiers

PMID: 12020527
DOI: 10.1016/S0140-6736(02)08590-2

Genes

NOD2

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

Association of NOD2 (CARD 15) genotype with clinical course of Crohn's disease: a cohort study.PMID 12020527Read ↗

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

Associations between NOD2/CARD15 genotype and phenotype in Crohn's disease--Are we there yet?Semantic proximity Read ↗

NOD2/CARD15 gene polymorphisms in Crohn's disease: a genotype- phenotype analysis.Semantic proximity Read ↗

Prevalence of mutations of the NOD2/CARD15 gene and relation to phenotype in Spanish patients with Crohn disease.Semantic proximity Read ↗

Association of NOD2/CARD15 mutations on Crohn's disease phenotype in an Italian population.Semantic proximity Read ↗

Alterations of the CARD15/NOD2 gene and the impact on management and treatment of Crohn's disease patients.Semantic proximity Read ↗

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

NOD2/CARD15 gene polymorphisms and Crohn's disease in the Chinese population.Semantic proximity Read ↗

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

CARD15/NOD2 mutations in Crohn's disease.Semantic proximity Read ↗

[NOD2/CARD15 mutations and genotype-phenotype correlations in patients with Crohn's disease. Hungarian multicenter study].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 ↗

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