Evidence map›Paper›PMID 31228678›Full record

ArticleDevelopmental cognitive neuroscience2019

Neural dynamics underlying coherent motion perception in children and adults.

Catherine Manning, Blair Kaneshiro, Peter J Kohler, Mihaela Duta, Gaia Scerif, Anthony M Norcia

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Developmental cognitive neuroscience, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

11 citing papers in PubMed, 15 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Visual Motion and Decision-Making in Dyslexia: Reduced Accumulation of Sensory Evidence and Related Neural Dynamics.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2022
    Article
  6. Review
  7. Article
  8. Global motion evoked potentials in autistic and dyslexic children: A cross-syndrome approach.Cortex; a journal devoted to the study of the nervous system and behavior · 2021
    Article
  9. Article
  10. Review
  11. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 2 countries.

Catherine ManningDepartment of Experimental Psychology, University of Oxford, Anna Watts Building, Radcliffe Observatory Quarter, Woodstock Road, Oxford, OX2 6GG, UK. Electronic address: catherine.manning@psy.ox.ac.uk.
Blair KaneshiroDepartment of Otolaryngology Head and Neck Surgery, Stanford University School of Medicine, Stanford University, 2452 Watson Court, Palo Alto, CA, 94303, USA.
Peter J KohlerDepartment of Psychology, Stanford University, Jordan Hall, 450 Serra Mall, Stanford, CA, 94305, USA.
Mihaela DutaDepartment of Experimental Psychology, University of Oxford, Anna Watts Building, Radcliffe Observatory Quarter, Woodstock Road, Oxford, OX2 6GG, UK.
Gaia ScerifDepartment of Experimental Psychology, University of Oxford, Anna Watts Building, Radcliffe Observatory Quarter, Woodstock Road, Oxford, OX2 6GG, UK.
Anthony M NorciaDepartment of Psychology, Stanford University, Jordan Hall, 450 Serra Mall, Stanford, CA, 94305, USA.
Stanford University · USUniversity of Oxford · GB

Funding

Wellcome TrustWellcome Trust 204685/Z/16/Z
6 · The paper itself

Abstract

Motion sensitivity increases during childhood, but little is known about the neural correlates. Most studies investigating children's evoked responses have not dissociated direction-specific and non-direction-specific responses. To isolate direction-specific responses, we presented coherently moving dot stimuli preceded by incoherent motion, to 6- to 7-year-olds (n = 34), 8- to 10-year-olds (n = 34), 10- to 12-year-olds (n = 34) and adults (n = 20). Participants reported the coherent motion direction while high-density EEG was recorded. Using a data-driven approach, we identified two stimulus-locked EEG components with distinct topographies: an early component with an occipital topography likely reflecting sensory encoding and a later, sustained positive component over centro-parietal electrodes that we attribute to decision-related processes. The component waveforms showed clear age-related differences. In the early, occipital component, all groups showed a negativity peaking at ˜300 ms, like the previously reported coherent-motion N2. However, the children, unlike adults, showed an additional positive peak at ˜200 ms, suggesting differential stimulus encoding. The later positivity in the centro-parietal component rose more steeply for adults than for the youngest children, likely reflecting age-related speeding of decision-making. We conclude that children's protracted development of coherent motion sensitivity is associated with maturation of both early sensory and later decision-related processes.

Indexed as

AdolescentAdultBrainChildChild DevelopmentElectroencephalographyEvoked Potentials, VisualFemaleHumansMaleMotion PerceptionPhotic StimulationReaction TimeYoung AdultComponent decompositionDirection perceptionElectroencephalographyEvoked potentialsMotion perceptionVisual development

Identifiers

PMID31228678
PMCPMC6688051
OpenAlexW2950422226

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.