Evidence map›Paper›PMID 32815320›Full record

ArticleAutism research : official journal of the International Society for Autism Research2020

A Novel Chd8 Mutant Mouse Displays Altered Ultrasonic Vocalizations and Enhanced Motor Coordination.

Samuel W Hulbert, Xiaoming Wang, Simisola O Gbadegesin, Qiong Xu, Xiu Xu, Yong-Hui Jiang

Open access · greenAbstract read
In one paragraph

Article in Autism research : official journal of the International Society for Autism Research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.9field-weighted citation impact, top 28% 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

13 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. CTRP10 is required for optimal motor function.The Journal of biological chemistry · 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

6 authors at 2 institutions in 2 countries.

Samuel W HulbertDepartment of Genetics, Yale University School of Medicine, New Haven, Connecticut, USA.ORCID 0000-0003-0369-0150
Xiaoming WangDepartment of Pediatrics, Duke University School of Medicine, Durham, North Carolina, USA.
Simisola O GbadegesinDepartment of Pediatrics, Duke University School of Medicine, Durham, North Carolina, USA.
Qiong XuThe Children's Hospital of Fudan University, Shanghai, China.
Xiu XuThe Children's Hospital of Fudan University, Shanghai, China.
Yong-Hui JiangDepartment of Genetics, Yale University School of Medicine, New Haven, Connecticut, USA.
Duke University · USChildren's Hospital of Fudan University · CN

Funding

Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
Molecular and circuitry mechanism underlying autism behaviors in Shank3 mouse modelsR01MH117289 · NIMH · YALE UNIVERSITY · PI JIANG, YONG-HUI · 2019 to 2023
$3.2M
Epigenetic Therapy and Prader-Willi SyndromeR01HD088626 · NICHD · YALE UNIVERSITY · PI JIANG, YONG-HUI, JIN, JIAN · 2017 to 2021
$2.8M
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
NCATS NIH HHS UL1 TR001863NICHD NIH HHS R01 HD088626NICHD NIH HHS R21 HD087795NIMH NIH HHS R01 MH098114NIMH NIH HHS R01MH098114NIMH NIH HHS R01 MH117289NIMH NIH HHS R21 MH104316NIMH NIH HHS R21MH104316
6 · The paper itself

Abstract

Mutations in CHD8 are among the most common autism-causing genetic defects identified in human genomics studies. Therefore, many labs have attempted to model this disorder by generating mice with mutations in Chd8. Using a gene trap inserted after Exon 31, we created a novel Chd8 mutant mouse (Chd8

Indexed as

Autistic DisorderSocial Communication DisorderAnimalsDisease Models, AnimalDNA-Binding ProteinsFemaleMaleMiceTranscription FactorsUltrasonicsVocalization, AnimalDNA-Binding ProteinsTranscription FactorsASDautismCHD8mouse behaviormouse models

Identifiers

PMID32815320
PMCPMC7780289
OpenAlexW3056678179

What OpenQuestion holds

Textmetadata
LicenceTDM
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.