Identification of genetic loci associated with nocturnal enuresis: a genome-wide association study.

doi:10.1016/S2352-4642(20)30350-3

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

Community

Back to search

Article

Identification of genetic loci associated with nocturnal enuresis: a genome-wide association study.

The Lancet. Child & adolescent health - 1 Mar 2021

Jørgensen Cecilie S, Horsdal Henriette T, Rajagopal Veera M, Grove Jakob, Als Thomas D, Kamperis Konstantinos, Nyegaard Mette, Walters G Bragi, Eðvarðsson Viðar Örn, Stefánsson Hreinn, Nordentoft Merete, Hougaard David Michael, Werge Thomas, Mors Ole, Mortensen Preben Bo, Agerbo Esben, Rittig Søren, Stefánsson Kári, Børglum Anders D, Demontis Ditte, Christensen Jane H

Abstract excerpt

BACKGROUND: Nocturnal enuresis (bedwetting) is a common disorder affecting 10-16% of 7-year-old children globally. Nocturnal enuresis is highly heritable, but its genetic determinants remain unknown. We aimed to identify genetic variants associated with nocturnal enuresis and explore its genetic architecture and underlying biology. METHODS: We did a genome-wide association study (GWAS) of nocturnal enuresis....

Read the complete abstract on PubMed

Topics

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

Share to Attention Deficit Disorder with Hyperactivity

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Autism Spectrum Disorder

Share to Child

Share to Chromosomes, Human, Pair 13

Share to Chromosomes, Human, Pair 6

Share to Deamino Arginine Vasopressin

Share to Genetic Loci

Share to Genome-Wide Association Study

Source

Open in PubMed

Identifiers

PMID: 33453761
DOI: 10.1016/S2352-4642(20)30350-3

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Identification of genetic loci associated with nocturnal enuresis: a genome-wide association study.PMID 33453761Read ↗

THE GENETICS OF ENURESIS:Semantic proximity Read ↗

Nocturnal enuresis: a suggestive endophenotype marker for a subgroup of inattentive attention-deficit/hyperactivity disorder.Semantic proximity Read ↗

Genetic and biological mechanisms of pediatric enuresis: integrating pathophysiology, GWAS associations, and multi-omics research.Semantic proximity Read ↗

Exploring the Genetic Risk of Childhood Daytime Urinary Incontinence: A Genome-Wide Association Study.Semantic proximity Read ↗

Molecular genetics of nocturnal enuresis: clinical and genetic heterogeneity.Semantic proximity Read ↗

Molecular genetics of nocturnal enuresis: linkage to a locus on chromosome 22.Semantic proximity Read ↗

Clinical enuresis phenotypes in familial nocturnal enuresis.Semantic proximity Read ↗

Clinical phenotyping of children with nocturnal enuresis: A key classification to improve the approach.Semantic proximity Read ↗

Genetic Contributions to Lower Urinary Tract Dysfunction.Semantic proximity Read ↗

The effect of familial aggregation on the children with primary nocturnal enuresis.Semantic proximity Read ↗

Prevalence of enuresis and its association with attention-deficit/hyperactivity disorder among U.S. children: results from a nationally representative study.Semantic proximity Read ↗

Hereditary phenotypes in nocturnal enuresis.Semantic proximity Read ↗

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