Evidence map›Paper›PMID 30574290›Full record

ArticleMolecular autism2018

Autism-associated CHD8 deficiency impairs axon development and migration of cortical neurons.

Qiong Xu, Yuan-Yuan Liu, Xiaoming Wang, Guo-He Tan, Hui-Ping Li, Samuel W Hulbert, Chun-Yang Li, Chun-Chun Hu, Zhi-Qi Xiong, Xiu Xu and 1 more

Open access · goldAbstract read
In one paragraph

Article in Molecular autism, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
5.6field-weighted citation impact, top 3% 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

54 citing papers in PubMed, 90 citations in OpenAlex.

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  3. bioRxiv : the preprint server for biology · 2026
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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

11 authors at 4 institutions in 2 countries.

Qiong Xu *1Department of Child Health Care, Children's Hospital of Fudan University, Shanghai, 201102 China.
Yuan-Yuan Liu *2Guangxi Key Laboratory of Regenerative Medicine & Guangxi Collaborative Innovation Center for Biomedicine, School of Preclinical Medicine, Guangxi Medical University, Nanning, 530021 Guangxi China.
Xiaoming Wang3Department of Pediatrics, Duke University School of Medicine, Durham, 27710 NC USA.
Guo-He Tan2Guangxi Key Laboratory of Regenerative Medicine & Guangxi Collaborative Innovation Center for Biomedicine, School of Preclinical Medicine, Guangxi Medical University, Nanning, 530021 Guangxi China.
Hui-Ping Li1Department of Child Health Care, Children's Hospital of Fudan University, Shanghai, 201102 China.
Samuel W Hulbert4Department of Neurobiology, Duke University School of Medicine, Durham, 27710 NC USA.
Chun-Yang Li1Department of Child Health Care, Children's Hospital of Fudan University, Shanghai, 201102 China.
Chun-Chun Hu1Department of Child Health Care, Children's Hospital of Fudan University, Shanghai, 201102 China.
Zhi-Qi Xiong5Institute of Neuroscience & State Key Laboratory of Neuroscience, CAS Center for Excellence in Brain Science and Intelligence Technology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai, 200031 China.
Xiu Xu1Department of Child Health Care, Children's Hospital of Fudan University, Shanghai, 201102 China.
Yong-Hui Jiang3Department of Pediatrics, Duke University School of Medicine, Durham, 27710 NC USA.
Children's Hospital of Fudan University · CNDuke University · USGuangxi Medical University · CNChinese Academy of Sciences · CN

Funding

Analysis of Shank3 Complete and Temporal and Spatial Specific Knockout MiceR01MH098114 · NIMH · DUKE UNIVERSITY · PI JIANG, YONG-HUI · 2012 to 2016
$2.2M
A novel neural circuit analysis paradigm to model autism in miceR21MH104316 · NIMH · DUKE UNIVERSITY · PI JIANG, YONG-HUI · 2014 to 2015
$435k
A novel paradigm to dissect the function connectivity in Shank3 autism modelR21HD087795 · NICHD · YALE UNIVERSITY · PI JIANG, YONG-HUI · 2017 to 2018
$434k
NICHD NIH HHS R21 HD087795NIMH NIH HHS R01 MH098114NIMH NIH HHS R21 MH104316
6 · The paper itself

Abstract

Background: Mutations in Methods: We examined the expression of Results: We discovered that CHD8 is expressed highly in neurons and at low levels in glia cells in both humans and mice. Specifically, CHD8 is localized predominately in the nucleus of both MAP2 and parvalbumin-positive neurons. In the developing mouse brain, expression of Conclusion: Our findings indicate an important role for CHD8 in dendritic and axon development and neuronal migration and thus offer novel insights to further dissect the underlying molecular and circuit mechanisms of ASD caused by CHD8 deficiency.

Indexed as

NeurogenesisAnimalsAutistic DisorderCells, CulturedCerebral CortexDNA-Binding ProteinsHumansMiceMice, Inbred C57BLNeuronsDNA-Binding Proteinsduplin protein, mouseAutism spectrum disorder (ASD)CHD8Chromatin remodelingNeurite growthNeurodevelopment

Identifiers

PMID30574290
PMCPMC6299922
OpenAlexW2905167454

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.