Evidence map›Paper›PMID 41446048›Full record

ArticlebioRxiv : the preprint server for biology2025

Insertion of rare autism variants in synaptic genes induce novel behavioral phenotypes in

Dustin Haskell, William R Haury, Myra Granato, Brandon L Bastien, Michael P Hart

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Dustin HaskellDepartment of Genetics, Perelman School of Medicine, University of Pennsylvania.
William R HauryDepartment of Genetics, Perelman School of Medicine, University of Pennsylvania.
Myra GranatoDepartment of Genetics, Perelman School of Medicine, University of Pennsylvania.
Brandon L BastienDepartment of Genetics, Perelman School of Medicine, University of Pennsylvania.
Michael P HartDepartment of Genetics, Perelman School of Medicine, University of Pennsylvania.ORCID 0000-0001-8865-3062

Funding

Translational Research Support CoreP30ES013508 · NIEHS · UNIVERSITY OF PENNSYLVANIA · PI A. Clementina Mesaros · 2006 to 2026
$35.3M
Enhancing and expanding the CGC Strain CollectionP40OD010440 · OD · UNIVERSITY OF MINNESOTA · PI Aric L Daul, Ann E. Rougvie · 2012 to 2026
$7.5M
Molecular coordination of adhesion molecules in foraging behaviors and circuitsR35GM146782 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI Michael P Hart · 2022 to 2026
$2.0M
Dissecting neural mechanisms integrating multiple inputs in C. elegansR56MH096881 · NIMH · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI CHALASANI, SREEKANTH H., HART, MICHAEL P · 2023 to 2024
$1.2M
NIEHS NIH HHS P30 ES013508NIGMS NIH HHS R35 GM146782NIH HHS P40 OD010440NIMH NIH HHS R56 MH096881
6 · The paper itself

Abstract

Neurodevelopmental conditions and disorders, including autism, involve a complex interplay of genetic, environmental, and developmental factors. Despite this complexity, genetic studies have identified more than 150 candidate genes that increase risk for autism and related neurodevelopmental and neuropsychiatric conditions. Unsurprisingly, synaptic genes are a large proportion of these genes, likely due to their roles in the formation and maintenance of synaptic architecture, function, and the plasticity of neurons and circuits. The association of synaptic genes with autism and similar conditions is driven by all types of genetic variation, including inherited and

Identifiers

PMID41446048
PMCPMC12724498

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.