Evidence map›Paper›PMID 41667422›Full record

ArticleTranslational psychiatry2026

Early-life sleep disruption in Shank3-deficient rats: A preclinical model for autism-related sleep mechanisms and interventions.

Mei-Hong Qiu, Zhi-Gang Zhong, Pei-Wen Song, Gui-Jin Tao, Jin-Tao Zhang, Yong-Hua Chen, Tian-Jia Song, Wei-Min Qu, Rong Zhang, Zhi-Li Huang

Abstract read
In one paragraph

Article in Translational psychiatry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. 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

10 authors.

Mei-Hong Qiu *Department of Neurobiology, Institute for Basic Research on Aging and Medicine, School of Basic Medical Sciences, Fudan University, Shanghai, 200032, China. mhqiu@shmu.edu.cn.ORCID http://orcid.org/0000-0002-3462-1724
Zhi-Gang Zhong *Department of Neurobiology, Institute for Basic Research on Aging and Medicine, School of Basic Medical Sciences, Fudan University, Shanghai, 200032, China.
Pei-Wen Song *Department of Neurobiology, Institute for Basic Research on Aging and Medicine, School of Basic Medical Sciences, Fudan University, Shanghai, 200032, China.
Gui-Jin Tao *Department of Neurobiology, Institute for Basic Research on Aging and Medicine, School of Basic Medical Sciences, Fudan University, Shanghai, 200032, China.
Jin-Tao ZhangDepartment of Neurobiology, Institute for Basic Research on Aging and Medicine, School of Basic Medical Sciences, Fudan University, Shanghai, 200032, China.
Yong-Hua ChenDepartment of Physiology, School of Basic Medical Sciences, Fudan University, Shanghai, 200032, China.
Tian-Jia SongNeuroscience Research Institute, Department of Neurobiology, Department of Integration of Chinese and Western Medicine, School of Basic Medical Sciences, Peking University, Key Laboratory for Neuroscience (Ministry of Education), Key Laboratory for Neuroscience (Ministry of Health), Autism Research Center, Peking University Health Science Center, Beijing, 100191, China.
Wei-Min QuDepartment of Pharmacology, School of Basic Medical Sciences, State Key Laboratory of Medical Neurobiology and MOE Frontiers Center for Brain Science, Institutes of Brain Science, Fudan University, Shanghai, 200032, China.ORCID http://orcid.org/0000-0002-0251-5214
Rong ZhangNeuroscience Research Institute, Department of Neurobiology, Department of Integration of Chinese and Western Medicine, School of Basic Medical Sciences, Peking University, Key Laboratory for Neuroscience (Ministry of Education), Key Laboratory for Neuroscience (Ministry of Health), Autism Research Center, Peking University Health Science Center, Beijing, 100191, China.ORCID http://orcid.org/0000-0002-6889-5571
Zhi-Li HuangDepartment of Pharmacology, School of Basic Medical Sciences, State Key Laboratory of Medical Neurobiology and MOE Frontiers Center for Brain Science, Institutes of Brain Science, Fudan University, Shanghai, 200032, China.ORCID http://orcid.org/0000-0001-9359-1150

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sleep disturbances are among the most prevalent and early-emerging features of autism spectrum disorder (ASD), often preceding core behavioral symptoms. Despite their clinical relevance, the neurobiological mechanisms driving early-life sleep disruption in ASD remain poorly understood. Shank3, encoding a synaptic scaffolding protein at excitatory synapses, is one of the most well-established monogenic risk factors for ASD. Here, we systematically investigated sleep architecture and homeostatic regulation in juvenile Shank3

Indexed as

Autism Spectrum DisorderNerve Tissue ProteinsSleep Wake DisordersAnimalsCircadian RhythmDisease Models, AnimalElectroencephalographyFemaleHomeostasisMaleMicrofilament ProteinsRatsSleep DeprivationMicrofilament ProteinsNerve Tissue ProteinsShank3 protein, rat

Identifiers

PMID41667422
PMCPMC13004876

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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.