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

Variants in the circadian clock genes PER2 and PER3 associate with familial sleep phase disorders.

Chronobiology international - 1 May 2024

Plavc Laura, Skubic Cene, Dolenc Grošelj Leja, Rozman Damjana

Abstract excerpt

Delayed sleep phase disorder and advanced sleep phase disorder cause disruption of the circadian clock and present with extreme morning/evening chronotype with unclear role of the genetic etiology, especially for delayed sleep phase disorder. To assess if genotyping can aid in clinical diagnosis, we examined the presence of genetic variants in circadian clock genes previously linked to both sleep disorders in...

Read the complete abstract on PubMed

Topics

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

Share to Circadian Clocks
Share to Circadian Rhythm
Share to Pedigree

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Period Circadian Proteins

Share to Polymorphism, Single Nucleotide

Share to Slovenia

Share to Young Adult

Source

Identifiers

PMID: 38695651
DOI: 10.1080/07420528.2024.2348016

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

Variants in the circadian clock genes PER2 and PER3 associate with familial sleep phase disorders.PMID 38695651Read ↗

The impact of Mendelian sleep and circadian genetic variants in a population settingSemantic proximity Read ↗

The impact of Mendelian sleep and circadian genetic variants in a population setting.Semantic proximity Read ↗

PER2 gene and its association with sleep-related disorders: A review.Semantic proximity Read ↗

Screening of clock gene polymorphisms demonstrates association of a PER3 polymorphism with morningness-eveningness preference and circadian rhythm sleep disorder.Semantic proximity Read ↗

Circadian Gene Variants in Diseases.Semantic proximity Read ↗

Phenotyping of PER3 variants reveals widespread effects on circadian preference, sleep regulation, and health.Semantic proximity Read ↗

Genome-wide association analyses in > 119,000 individuals identifies thirteen morningness and two sleep duration lociSemantic proximity Read ↗

Single nucleotide polymorphisms (SNPs) in circadian genes: Impact on gene function and phenotype.Semantic proximity Read ↗

Circadian clock gene polymorphisms implicated in human pathologies.Semantic proximity Read ↗

Genome-Wide Association Analyses in 128,266 Individuals Identifies New Morningness and Sleep Duration LociSemantic proximity Read ↗

A common polymorphism near PER1 and the timing of human behavioral rhythms.Semantic proximity Read ↗

Novel insights from genetic and molecular characterization of the human clock.Semantic proximity Read ↗

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