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

Genome-wide linkage analysis of 160 North American families with celiac disease.

Genes and immunity - 1 Mar 2007

Garner C P, Ding Y C, Steele L, Book L, Leiferman K, Zone J J, Neuhausen S L

Abstract excerpt

Celiac disease (CD) is a common autoimmune disease caused by exposure to the protein gliadin in wheat, and related prolamins in barley and rye. The prevalence of the disease in the US is 1:133. The aim of this study was to identify non-human leukocyte antigen (HLA) loci that predispose to CD. A g...

Read the complete abstract on PubMed

Topics

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

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

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genomics

Share to Lod Score

Share to Major Histocompatibility Complex

Share to Microsatellite Repeats

Share to North America

Source

Identifiers

PMID: 17136122
DOI: 10.1038/sj.gene.6364361

Genes

NPL

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-17136122-2026-09-02.2. 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

Genome-wide linkage analysis of 160 North American families with celiac disease.PMID 17136122Read ↗

Genome-wide linkage analysis for celiac disease in North American families.Semantic proximity Read ↗

Genome-wide linkage analysis of Scandinavian affected sib-pairs supports presence of susceptibility loci for celiac disease on chromosomes 5 and 11.Semantic proximity Read ↗

Genomewide linkage analysis of celiac disease in Finnish families.Semantic proximity Read ↗

From genome-wide association studies to disease mechanisms: celiac disease as a model for autoimmune diseases.Semantic proximity Read ↗

Genomewide search and association studies in a Finnish celiac disease population: Identification of a novel locus and replication of the HLA and CTLA4 loci.Semantic proximity Read ↗

The genetics of celiac disease: A comprehensive review of clinical implications.Semantic proximity Read ↗

Genetics of celiac disease.Semantic proximity Read ↗

Understanding Celiac Disease by Genomics.Semantic proximity Read ↗

Celiac disease genetics: past, present and future challenges.Semantic proximity Read ↗

Association analysis of the extended MHC region in celiac disease implicates multiple independent susceptibility loci.Semantic proximity Read ↗

Celiac disease susceptibility: The genome and beyond.Semantic proximity Read ↗

Genetics in coeliac disease.Semantic proximity Read ↗

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