Evidence map›Paper›PMID 42804154›Full record

ArticleNeuroscience bulletin2026

Aberrant Neural Outputs and Disrupted Neural Oscillations of the Cerebellar Nuclei in a Mouse Model of Fragile X Syndrome.

Jing-Wen Guo, En-Wei Shen, Wan-Qi Huang, Long-Yu Guo, Martijn Schonewille, Chris De Zeeuw, Wei Chen, Lin Zhou, Ying Shen, Luxi Wang

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In one paragraph

Article in Neuroscience bulletin, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Jing-Wen Guo *Department of Psychiatry, Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou, 310016, China.
En-Wei Shen *Department of Psychiatry, Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou, 310016, China.
Wan-Qi Huang *Department of Psychiatry, Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou, 310016, China.
Long-Yu GuoKey Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, Department of Neurology, The Second Affiliated Hospital, Institute of Neuroscience, Guangzhou Medical University, Guangzhou, 510260, China.
Martijn SchonewilleDepartment of Neuroscience, Erasmus University Medical Center, 3000 CA, Rotterdam, The Netherlands.
Chris De ZeeuwDepartment of Neuroscience, Erasmus University Medical Center, 3000 CA, Rotterdam, The Netherlands.
Wei ChenDepartment of Psychiatry, Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou, 310016, China.
Lin ZhouDepartment of Psychiatry, Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou, 310016, China. lynchow@zju.edu.cn.
Ying ShenDepartment of Psychiatry, Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou, 310016, China. yshen@zju.edu.cn.ORCID http://orcid.org/0000-0001-7034-5328
Luxi WangDepartment of Psychiatry, Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou, 310016, China. luxiwang@zju.edu.cn.ORCID http://orcid.org/0000-0002-7822-6566

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The cerebellum is heavily connected to other brain regions, playing a role in both motor and non-motor functions. Genetic mutations leading to cerebellar dysfunction are associated with autism spectrum disorder (ASD); however, cerebellar output has not yet been systematically studied in this context. Here, using Fmr1-knockout mice, a model for Fragile X syndrome, we mapped the three-dimensional distributions of target neurons in the deep cerebellar nuclei (DCN). We found that projections from the DCN to various forebrain nuclei were differentially and specifically altered in Fmr1-knockout mice. Furthermore, in vivo electrophysiology revealed disrupted neuronal firing patterns, loss of specific neuronal subtypes, and aberrant local field potential oscillations within the DCN of Fmr1-knockout mice, all in the absence of any morphological changes. Notably, these oscillations exhibited weakened θ, α, and β powers, while the γ power remained unchanged. Our study further demonstrated the nucleus-specific dysregulation of cerebellar outputs and associated network dysfunction in an ASD model, highlighting the cerebellum as a key node in the pathophysiology of different neurodevelopmental disorders.

Indexed as

Autism spectrum disorderCerebellumFragile X syndromeLarge-scale tracingNeural oscillation

Identifiers

PMID42804154

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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.