Evidence map›Paper›PMID 24814480›Full record

ArticleDevelopmental cognitive neuroscience2014

Social cognition, face processing, and oxytocin receptor single nucleotide polymorphisms in typically developing children.

Mylissa M Slane, Laina G Lusk, K B Boomer, Abby E Hare, Margaret K King, David W Evans

Open access · goldAbstract read
In one paragraph

Article in Developmental cognitive neuroscience, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 2 pooled it
3.2field-weighted citation impact, top 9% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

15 citing papers in PubMed, 2 syntheses or guidelines pooled it, 36 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Genetic and epigenetic signatures associated with plasma oxytocin levels in children and adolescents with autism spectrum disorder.Autism research : official journal of the International Society for Autism Research · 2023
    Trial
  4. OXTR rs53576 Variation with Breast and Nipple Pain in Breastfeeding Women.Pain management nursing : official journal of the American Society of Pain Management Nurses · 2021
    Trial
  5. Article
  6. Article
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  11. Article
  12. Neurobiological Aspects of Face Recognition: The Role of Oxytocin.Frontiers in behavioral neuroscience · 2018
    Review
  13. Article
  14. Article
  15. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

Mylissa M SlaneBucknell University, Department of Psychology, Program in Neuroscience, 701 Moore Avenue, Lewisburg, PA 17837, USA.
Laina G LuskBucknell University, Department of Psychology, Program in Neuroscience, 701 Moore Avenue, Lewisburg, PA 17837, USA.
K B BoomerBucknell University, Department of Mathematics, 701 Moore Avenue, Lewisburg, PA 17837, USA.
Abby E HareGeisinger-Bucknell Autism and Developmental Medicine Center, 120 Hamm Drive, Suite 2, Lewisburg, PA 17837, USA.
Margaret K KingGeisinger-Bucknell Autism and Developmental Medicine Center, 120 Hamm Drive, Suite 2, Lewisburg, PA 17837, USA.
David W EvansBucknell University, Department of Psychology, Program in Neuroscience, 701 Moore Avenue, Lewisburg, PA 17837, USA. Electronic address: dwevans@bucknell.edu.
Bucknell University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recent research has provided evidence of a link between behavioral measures of social cognition (SC) and neural and genetic correlates. Differences in face processing and variations in the oxytocin receptor (OXTR) gene have been associated with SC deficits and autism spectrum disorder (ASD) traits. Much work has examined the qualitative differences between those with ASD and typically developing (TD) individuals, but very little has been done to quantify the natural variation in ASD-like traits in the typical population. The present study examines this variation in TD children using a multidimensional perspective involving behavior assessment, neural electroencephalogram (EEG) testing, and OXTR genotyping. Children completed a series of neurocognitive assessments, provided saliva samples for sequencing, and completed a face processing task while connected to an EEG. No clear pattern emerged for EEG covariates or genotypes for individual OXTR single nucleotide polymorphisms (SNPs). However, SNPs rs2254298 and rs53576 consistently interacted such that the AG/GG allele combination of these SNPs was associated with poorer performance on neurocognitive measures. These results suggest that neither SNP in isolation is risk-conferring, but rather that the combination of rs2254298(A/G) and rs53576(G/G) confers a deleterious effect on SC across several neurocognitive measures.

Indexed as

Child DevelopmentFaceSocial BehaviorAdolescentAllelesChildChild Development Disorders, PervasiveChild, PreschoolCognitionElectroencephalographyFemaleGenetic MarkersGenotypeHumansMaleOxytocinGenetic MarkersOxytocinReceptors, OxytocinAutism spectrum disorderEvent-related potential-N170OxytocinSocial cognitionTypically developing children

Identifiers

PMID24814480
PMCPMC6989749
OpenAlexW2076208856

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.