Evidence map›Paper›PMID 28338743›Full record

ArticleSocial cognitive and affective neuroscience2017

Incidental memory for faces in children with different genetic subtypes of Prader-Willi syndrome.

Alexandra P Key, Elisabeth M Dykens

Open access · goldAbstract read
In one paragraph

Article in Social cognitive and affective neuroscience, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

9 citing papers in PubMed, 19 citations in OpenAlex.

  1. Trial
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  7. The Unfulfilled Promise of the N170 as a Social Biomarker.Biological psychiatry. Cognitive neuroscience and neuroimaging · 2020
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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

2 authors at 2 institutions in 2 countries.

Alexandra P KeyVanderbilt Kennedy Center for Research on Human Development.
Elisabeth M DykensVanderbilt Kennedy Center for Research on Human Development.
Kennedy Center · DKVanderbilt University · US

Funding

THREE-TIERED PREVENTION MODEL TO BETTER SERVE ALL STUDENP30HD015052 · NICHD · VANDERBILT UNIVERSITY · PI DYKENS, ELISABETH MAY · 1985 to 2014
$18.6M
Research Project: Sensory and Multisensory Contributions to AutismU54HD083211 · NICHD · VANDERBILT UNIVERSITY MEDICAL CENTER · PI DYKENS, ELISABETH MAY · 2015 to 2019
$7.1M
Predicting Phenotypic Trajectories in Prader-Willi SyndromeR01HD035684 · NICHD · VANDERBILT UNIVERSITY · PI DYKENS, ELISABETH MAY · 1997 to 2014
$3.3M
NICHD NIH HHS P30 HD015052NICHD NIH HHS R01 HD035684NICHD NIH HHS U54 HD083211
6 · The paper itself

Abstract

The present study examined the effects of genetic subtype on social memory in children (7-16 years) with Prader-Willi syndrome (PWS). Visual event-related potentials (ERPs) during a passive viewing task were used to compare incidental memory traces for repeated vs single presentations of previously unfamiliar social (faces) and nonsocial (houses) images in 15 children with the deletion subtype and 13 children with maternal uniparental disomy (mUPD). While all participants perceived faces as different from houses (N170 responses), repeated faces elicited more positive ERP amplitudes ('old/new' effect, 250-500ms) only in children with the deletion subtype. Conversely, the mUPD group demonstrated reduced amplitudes suggestive of habituation to the repeated faces. ERP responses to repeated vs single house images did not differ in either group. The results suggest that faces hold different motivational value for individuals with the deletion vs mUPD subtype of PWS and could contribute to the explanation of subtype differences in the psychiatric symptoms, including autism symptomatology.

Indexed as

FaceMemoryAdolescentBrainChildElectroencephalographyEvoked Potentials, VisualFemaleGene DeletionHumansMaleMemory DisordersMotivationPhenotypePhotic StimulationPrader-Willi SyndromeERPfacememoryPrader–Willi syndromesocial

Identifiers

PMID28338743
PMCPMC5472135
OpenAlexW2589715463

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.