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

HTR2A variation and sudden infant death syndrome: a case-control analysis.

Acta paediatrica (Oslo, Norway : 1992) - 1 Jan 2009

Rand Casey M, Berry-Kravis Elizabeth M, Fan Wenqing, Weese-Mayer Debra E

Abstract excerpt

AIM: The serotonergic (5-HT) system functions in central autonomic regulation with homeostatic roles in cardiorespiratory control, thermoregulation, arousal and sleep-wake cycling. Altered function and development of this system in cases of sudden infant death syndrome (SIDS) have been established, but the aetiology of these disturbances remains unclear. The serotonin receptor, HTR2A, functions within this system...

Read the complete abstract on PubMed

Topics

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

Share to Autonomic Nervous System
Share to Case-Control Studies

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Hypoxia

Share to Infant

Share to Receptor, Serotonin, 5-HT2A

Share to Risk Factors

Share to Serotonin

Share to Sudden Infant Death

Source

Identifiers

PMID: 18771483
DOI: 10.1111/j.1651-2227.2008.01018.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

HTR2A variation and sudden infant death syndrome: a case-control analysis.PMID 18771483Read ↗

Serotonin gene variants are unlikely to play a significant role in the pathogenesis of the sudden infant death syndrome.Semantic proximity Read ↗

High serum serotonin in sudden infant death syndrome.Semantic proximity Read ↗

Serotonin transporter gene variation in sudden infant death syndrome.Semantic proximity Read ↗

Identifying infants at risk for sudden infant death syndrome.Semantic proximity Read ↗

Sudden infant death syndrome: rare mutation in the serotonin system FEV gene.Semantic proximity Read ↗

Association between polymorphisms in the P2RY1 and SSTR2 genes and sudden infant death syndrome.Semantic proximity Read ↗

Association of the serotonin transporter gene with sudden infant death syndrome: a haplotype analysis.Semantic proximity Read ↗

Sudden Infant Death Syndrome: review of implicated genetic factors.Semantic proximity Read ↗

Genetic variation in the monoamine oxidase A and serotonin transporter genes in sudden infant death syndrome.Semantic proximity Read ↗

Genes regulating the serotonin metabolic pathway in the brain stem and their role in the etiopathogenesis of the sudden infant death syndrome.Semantic proximity Read ↗

Gene variants predisposing to SIDS: current knowledge.Semantic proximity Read ↗

Genomic risk factors in sudden infant death syndromeSemantic proximity Read ↗

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