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

Celiac disease: moving from genetic associations to causal variants.

Clinical genetics - 1 Sept 2011

Hrdlickova B, Westra H-J, Franke L, Wijmenga C

Abstract excerpt

Genome-wide association studies are providing insight into the genetic basis of common complex diseases: more than 1150 genetic loci [2165 unique single nucleotide polymorphisms (SNPs)] have recently been associated to 159 complex diseases. The hunt for genes contributing to immune-related diseases has been particularly successful in celiac disease, for example, with 27 genome-wide significantly associated loci...

Read the complete abstract on PubMed

Topics

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

Share to Quantitative Trait Loci
Share to CD4-Positive T-Lymphocytes
Share to Celiac Disease

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Gene Expression Profiling

Share to Gene Expression Regulation

Share to Genome, Human

Share to HLA-DQ Antigens

Share to Intestine, Small

Source

Identifiers

PMID: 21595655
DOI: 10.1111/j.1399-0004.2011.01707.x

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

Celiac disease: moving from genetic associations to causal variants.PMID 21595655Read ↗

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

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

Understanding Celiac Disease by Genomics.Semantic proximity Read ↗

Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease.Semantic proximity Read ↗

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

Expression analysis in intestinal mucosa reveals complex relations among genes under the association peaks in celiac disease.Semantic proximity Read ↗

Combined functional and positional gene information for the identification of susceptibility variants in celiac disease.Semantic proximity Read ↗

Replication of celiac disease UK genome-wide association study results in a US population.Semantic proximity Read ↗

Fine mapping of the celiac disease-associated LPP locus reveals a potential functional variant.Semantic proximity Read ↗

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

A genetic perspective on coeliac disease.Semantic proximity Read ↗

Genome-wide association study identifies novel risk variants for celiac disease in the 5p15.33 locus: insights from a population-based screening of adults, the HUNT studySemantic proximity Read ↗

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