Evidence map›Paper›PMID 38026686›Full record

ReviewFrontiers in cellular neuroscience2023

Altered motor learning and coordination in mouse models of autism spectrum disorder.

Katherine R Cording, Helen S Bateup

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in cellular neuroscience, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
7.7field-weighted citation impact, top 2% 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

32 citing papers in PubMed, 44 citations in OpenAlex.

  1. Article
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  6. CTRP10 is required for optimal motor function.The Journal of biological chemistry · 2026
    Article
  7. Article
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  9. Novel mouse line with D277N mutation in theFrontiers in cell and developmental biology · 2026
    Article
  10. Article
  11. A Novel Mouse Model for Developmental and Epileptic Encephalopathy by Purkinje Cell-Specific Deletion ofThe Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Article
  12. Article
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  20. Review
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 1 country.

Katherine R CordingHelen Wills Neuroscience Institute, University of California, Berkeley, Berkeley, CA, United States.
Helen S BateupHelen Wills Neuroscience Institute, University of California, Berkeley, Berkeley, CA, United States.
Chan Zuckerberg Initiative (United States) · USUniversity of California, Berkeley · US

Funding

Investigating Syngap1 as a regulator of striatal synaptic functionR01MH130839 · NIMH · UNIVERSITY OF CALIFORNIA BERKELEY · PI Helen S. Bateup · 2022 to 2026
$1.9M
The impact of Tsc-mTOR signaling on basal ganglia functionR01NS105634 · NINDS · UNIVERSITY OF CALIFORNIA BERKELEY · PI BATEUP, HELEN S. · 2019 to 2022
$1.3M
Examining striatal synaptic function across mouse models of autism spectrum disorder (ASD)F31NS124499 · NINDS · UNIVERSITY OF CALIFORNIA BERKELEY · PI CORDING, KATIE · 2022 to 2023
$87k
NIMH NIH HHS R01 MH130839NINDS NIH HHS F31 NS124499NINDS NIH HHS R01 NS105634
6 · The paper itself

Abstract

Autism spectrum disorder (ASD) is a complex neurodevelopmental disorder with increasing prevalence. Over 1,000 risk genes have now been implicated in ASD, suggesting diverse etiology. However, the diagnostic criteria for the disorder still comprise two major behavioral domains - deficits in social communication and interaction, and the presence of restricted and repetitive patterns of behavior (RRBs). The RRBs associated with ASD include both stereotyped repetitive movements and other motor manifestations including changes in gait, balance, coordination, and motor skill learning. In recent years, the striatum, the primary input center of the basal ganglia, has been implicated in these ASD-associated motor behaviors, due to the striatum's role in action selection, motor learning, and habit formation. Numerous mouse models with mutations in ASD risk genes have been developed and shown to have alterations in ASD-relevant behaviors. One commonly used assay, the accelerating rotarod, allows for assessment of both basic motor coordination and motor skill learning. In this corticostriatal-dependent task, mice walk on a rotating rod that gradually increases in speed. In the extended version of this task, mice engage striatal-dependent learning mechanisms to optimize their motor routine and stay on the rod for longer periods. This review summarizes the findings of studies examining rotarod performance across a range of ASD mouse models, and the resulting implications for the involvement of striatal circuits in ASD-related motor behaviors. While performance in this task is not uniform across mouse models, there is a cohort of models that show increased rotarod performance. A growing number of studies suggest that this increased propensity to learn a fixed motor routine may reflect a common enhancement of corticostriatal drive across a subset of mice with mutations in ASD-risk genes.

Indexed as

autism spectrum disordercorticostriataldirect pathwayindirect pathwaymotor learningmouse modelsrotarodstriatum

Identifiers

PMID38026686
PMCPMC10663323
OpenAlexW4388540438

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.