Evidence map›Paper›PMID 40478461›Full record

ReviewNeurogenetics2025

Zebrafish as a tool for autism research: unraveling the roles of Shank3, Cntnap2, Neuroligin3, and Arid1b in synaptic and behavioral abnormalities.

Akansha Pal, Falguni Goel, Vipin Kumar Garg

Abstract readReview
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In one paragraph

Review in Neurogenetics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
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

8 citing papers in PubMed.

  1. Article
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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

3 authors.

Akansha PalDepartment of Pharmaceutical Technology, Meerut Institute of Engineering & Technology (MIET), Meerut, India.
Falguni GoelDepartment of Pharmaceutical Technology, Meerut Institute of Engineering & Technology (MIET), Meerut, India.
Vipin Kumar GargDepartment of Pharmaceutical Technology, Meerut Institute of Engineering & Technology (MIET), Meerut, India. vipin.garg@miet.ac.in.ORCID http://orcid.org/0000-0003-4263-002X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autism Spectrum Disorder, a complex neurodevelopmental disorder, is manifested by deficits in social communication and restricted, repetitive patterns of behavior, interests, or activities. Its molecular mechanism of pathology is not that much understood, though various genetic mutations have been established in its causation. The most important genes are Shank3, Cntnap2, Neuroligin3, and Arid1b. Recently, zebrafish (Danio rerio) have emerged as a highly valuable model organism to study these genetic contributions to ASD, given their genetic tractability, transparent embryos, and ease of behavioral assessment. This review discusses the models of zebrafish used to examine the roles of Shank3, Cntnap2, Neuroligin3, and Arid1b in synaptic function, neuronal connectivity, and behavioral abnormalities characteristic of ASD. We discuss the molecular pathways affected by mutations in these genes, including synapse formation, excitatory/inhibitory balance, and neuronal signaling, which lead to the neurodevelopmental impairments observed in ASD. We have also highlighted the various behavioral assays in zebrafish, such as social interaction tests, sensory processing assays, and repetitive behavior measurements, which are used to study ASD-like phenotypes. The unique advantages of zebrafish include high-throughput potential, the ability to monitor real-time neuronal activity, and the ease with which genetic manipulations can be done. The review focuses on the advancement of zebrafish in understanding ASD and their potential for rising targeted interventions to address core symptoms of the disorder.

Indexed as

Autism Spectrum DisorderAutistic DisorderDisease Models, AnimalMembrane ProteinsNerve Tissue ProteinsZebrafish ProteinsAnimalsBehavior, AnimalCell Adhesion Molecules, NeuronalDNA-Binding ProteinsHumansMutationSynapsesTranscription FactorsZebrafishCell Adhesion Molecules, NeuronalDNA-Binding ProteinsMembrane ProteinsNerve Tissue Proteinsneuroligin 3Transcription FactorsZebrafish ProteinsAutism spectrum disorderBehavioral assaysGenetic mutationsNeurodevelopmental disordersSocial interactionSynaptic disfunction

Identifiers

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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.