Evidence map›Paper›PMID 36375841›Full record

ArticleLife science alliance2023

Loss of autism-candidate CHD8 perturbs neural crest development and intestinal homeostatic balance.

Gaëlle Hayot, Mathieu Massonot, Céline Keime, Elodie Faure, Christelle Golzio

Open access · goldAbstract read
In one paragraph

Article in Life science alliance, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
4.1field-weighted citation impact, top 5% 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

9 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
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  4. SINEUP RNA rescues molecular phenotypes associated with CHD8 suppression in autism spectrum disorder model systems.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Article
  5. Article
  6. Review
  7. Review
  8. Review
  9. Article
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

5 authors at 1 institution in 1 country.

Gaëlle HayotInstitut de Génétique et de Biologie Moléculaire et Cellulaire, Illkirch, France.
Mathieu MassonotInstitut de Génétique et de Biologie Moléculaire et Cellulaire, Illkirch, France.ORCID 0000-0003-4718-9798
Céline KeimeInstitut de Génétique et de Biologie Moléculaire et Cellulaire, Illkirch, France.ORCID 0000-0001-7604-3814
Elodie FaureInstitut de Génétique et de Biologie Moléculaire et Cellulaire, Illkirch, France.
Christelle GolzioInstitut de Génétique et de Biologie Moléculaire et Cellulaire, Illkirch, France christelle.golzio@igbmc.fr.ORCID 0000-0002-4420-3921
Centre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Individuals with mutations in

Indexed as

Autistic DisorderNeural CrestAnimalsCell MovementHomeostasisIntestinesSerotoninZebrafishSerotonin

Identifiers

PMID36375841
PMCPMC9664244
OpenAlexW4308997492

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.