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 analysis of 944 133 individuals provides insights into the etiology of haemorrhoidal disease

22 Apr 2021

Abstract excerpt

OBJECTIVE: Haemorrhoidal disease (HEM) affects a large and silently suffering fraction of the population but its aetiology, including suspected genetic predisposition, is poorly understood. We report the first genome-wide association study (GWAS) meta-analysis to identify genetic risk factors for HEM to date. DESIGN: We conducted a GWAS meta-analysis of 218 920 patients with HEM and 725 213 controls of European...

Read the complete abstract on PubMed

Topics

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

Share to Anorectal Disease Treatments and Outcomes
Share to Congenital gastrointestinal and neural anomalies
Share to Fibromyalgia and Chronic Fatigue Syndrome Research

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 33888516
DOI: 10.1136/gutjnl-2020-323868

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genome-wide analysis of 944 133 individuals provides insights into the etiology of haemorrhoidal diseasePMID 33888516Read ↗

Genome-wide analysis of 944,133 individuals provides insights into the etiology of hemorrhoidal diseaseSemantic proximity Read ↗

Research Letter: Therapeutic targets for haemorrhoidal disease: proteome-wide Mendelian randomisation and colocalization analysesSemantic proximity Read ↗

Genome-wide association analysis and replication in 810,625 individuals with varicose veinsSemantic proximity Read ↗

Hereditary haemorrhagic telangiectasia: a clinical and scientific review.Semantic proximity Read ↗

Genome-wide association analyses identify 39 new susceptibility loci for diverticular disease.Semantic proximity Read ↗

Varicose veins of lower extremities: insights from the first large-scale genetic studySemantic proximity Read ↗

Hemostatic phenotypes and genetic disordersSemantic proximity Read ↗

Updates on diagnostic criteria for hereditary haemorrhagic telangiectasia in the light of whole genome sequencing of 'gene-negative' individuals recruited to the 100 000 Genomes Project.Semantic proximity Read ↗

Genetics of Behçet's Disease: Functional Genetic Analysis and Estimating Disease HeritabilitySemantic proximity Read ↗

Genome-wide association analysis and replication in 810,625 individuals identifies novel therapeutic targets for varicose veinsSemantic proximity Read ↗

Exome sequencing and analysis of 44,028 British South Asians enriched for high autozygositySemantic proximity Read ↗

Multi-ancestry proteogenomic analysis identifies risk proteins for intracranial aneurysmsSemantic proximity Read ↗

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