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

A functional candidate screen for coeliac disease genes.

European journal of human genetics : EJHG - 1 Nov 2006

Curley Christine R, Monsuur Alienke J, Wapenaar Martin C, Rioux John D, Wijmenga Cisca

Abstract excerpt

It is increasingly evident that different inflammatory disorders show some overlap in their pathological features, concurrence in families and individuals, and shared genetic factors. This might also be true for coeliac disease, a chronic inflammatory disorder of the gastrointestinal system, which shares two linkage regions with inflammatory bowel disease: on chromosome 5q31 (CELIAC2 and IBD5) and 19p13 (CELIAC4...

Read the complete abstract on PubMed

Topics

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

Share to Chromosome Mapping
Share to Celiac Disease
Share to Chromosomes, Human, Pair 19

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Chromosomes, Human, Pair 5

Share to Cohort Studies

Share to Cytochrome P-450 Enzyme System

Share to Cytochrome P450 Family 4

Share to Netherlands

Source

Identifiers

PMID: 16835590
DOI: 10.1038/sj.ejhg.5201687

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

A functional candidate screen for coeliac disease genes.PMID 16835590Read ↗

Genomewide search in Canadian families with inflammatory bowel disease reveals two novel susceptibility loci.Semantic proximity Read ↗

Evaluation of 6 candidate genes on chromosome 11q23 for coeliac disease susceptibility: a case control study.Semantic proximity Read ↗

A combined genetics and genomics approach to unravelling molecular pathways in coeliac disease.Semantic proximity Read ↗

Analysis of marker genes contributing to coeliac disease susceptibility.Semantic proximity Read ↗

Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci.Semantic proximity Read ↗

Haplotype-based association analysis of 56 functional candidate genes in the IBD6 locus on chromosome 19.Semantic proximity Read ↗

A genetic perspective on coeliac disease.Semantic proximity Read ↗

Common polygenic variation in coeliac disease and confirmation of ZNF335 and NIFA as disease susceptibility loci.Semantic proximity Read ↗

Variants within protectin (CD59) and CD44 genes linked to an inherited haplotype in a family with coeliac disease.Semantic proximity Read ↗

Analysis of candidate genes on chromosomes 5q and 19p in celiac disease.Semantic proximity Read ↗

Analysis of candidate genes on chromosome 19 in coeliac disease: an association study of the KIR and LILR gene clusters.Semantic proximity Read ↗

Searching for genes influencing a complex disease: the case of coeliac disease.Semantic proximity Read ↗

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