Evidence map›Paper›PMID 30733854›Full record

ArticleMolecular autism2019

Intestinal dysmotility in a zebrafish (

David M James, Robert A Kozol, Yuji Kajiwara, Adam L Wahl, Emily C Storrs, Joseph D Buxbaum, Mason Klein, Baharak Moshiree, Julia E Dallman

Open access · goldAbstract read
In one paragraph

Article in Molecular autism, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
4.7field-weighted citation impact, top 4% 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

49 citing papers in PubMed, 80 citations in OpenAlex.

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  8. A Frank Assessment of SHANK: Impacts of Pathogenic Variations in SHANK3 on Preclinical Models of Phelan McDermid Syndrome.Autism research : official journal of the International Society for Autism Research · 2025
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  13. Frontiers in neuroscience · 2025
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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

9 authors at 4 institutions in 1 country.

David M James *1Department of Biology, University of Miami, Coral Gables, FL USA.
Robert A Kozol *1Department of Biology, University of Miami, Coral Gables, FL USA.
Yuji Kajiwara2Seaver Autism Center for Research and Treatment, Department of Psychiatry, Friedman Brain Institute and Mindich Child Health and Development Institute, Icahn School of Medicine at Mount Sinai, New York, NY USA.
Adam L Wahl1Department of Biology, University of Miami, Coral Gables, FL USA.
Emily C Storrs1Department of Biology, University of Miami, Coral Gables, FL USA.
Joseph D Buxbaum2Seaver Autism Center for Research and Treatment, Department of Psychiatry, Friedman Brain Institute and Mindich Child Health and Development Institute, Icahn School of Medicine at Mount Sinai, New York, NY USA.
Mason Klein3Department of Physics, University of Miami, Coral Gables, FL USA.
Baharak MoshireeDivision of Gastroenterology, Atrium Health, University of North Carolina, Charlotte, NC USA.
Julia E Dallman1Department of Biology, University of Miami, Coral Gables, FL USA.
University of Miami · USChild Health and Development Institute · USIcahn School of Medicine at Mount Sinai · USUniversity of North Carolina at Charlotte · US

Funding

University of Miami IMSD ProgramR25GM076419 · NIGMS · UNIVERSITY OF MIAMI CORAL GABLES · PI GAINES, MICHAEL S. · 2006 to 2016
$4.2M
Prefrontal function in the Shank3-deficient rat: A first rat model for ASDR01MH101584 · NIMH · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI BUXBAUM, JOSEPH D., HOF, PATRICK R · 2014 to 2018
$2.4M
Gastrointestinal Comorbidities in Autism Spectrum DisordersR21HD093021 · NICHD · UNIVERSITY OF MIAMI CORAL GABLES · PI DALLMAN, JULIA EVE · 2018 to 2019
$403k
Stable Zebrafish Models of Autism Spectrum DisorderR03MH103857 · NIMH · UNIVERSITY OF MIAMI CORAL GABLES · PI DALLMAN, JULIA EVE · 2014 to 2015
$151k
Howard Hughes Medical InstituteNICHD NIH HHS R21 HD093021NIGMS NIH HHS R25 GM076419NIMH NIH HHS R01 MH101584NIMH NIH HHS R03 MH103857
6 · The paper itself

Abstract

Background and aims: Autism spectrum disorder (ASD) is currently estimated to affect more than 1% of the world population. For people with ASD, gastrointestinal (GI) distress is a commonly reported but a poorly understood co-occurring symptom. Here, we investigate the physiological basis for GI distress in ASD by studying gut function in a zebrafish model of Phelan-McDermid syndrome (PMS), a condition caused by mutations in the Methods: To generate a zebrafish model of PMS, we used CRISPR/Cas9 to introduce clinically related C-terminal frameshift mutations in Results: Significantly slower rates of DT peristaltic contractions ( Conclusions: Our data and rescue experiments support mutations in

Indexed as

Gastrointestinal MotilityAnimalsAutistic DisorderEnteric Nervous SystemEnteroendocrine CellsIntestinal MucosaIntestinesMutationNerve Tissue ProteinsNeuronsProtein IsoformsSerotoninZebrafishZebrafish ProteinsNerve Tissue ProteinsProtein IsoformsSerotoninSHANK3 protein, zebrafishZebrafish ProteinsDigestive transitEnteroendocrinePeristaltic ratePhelan-McDermid syndrome

Identifiers

PMID30733854
PMCPMC6357389
OpenAlexW2914944728

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.