Evidence map›Paper›PMID 40801227›Full record

ReviewAnnals of neurology2025

Molecular and Genetic Mechanisms in Autism Spectrum Disorder.

April Pruitt, Abha R Gupta, Ellen J Hoffman

Abstract readReview
In one paragraph

Review in Annals of neurology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. 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

3 authors.

April PruittChild Study Center, Yale School of Medicine, New Haven, CT.ORCID 0000-0002-5807-5422
Abha R GuptaChild Study Center, Yale School of Medicine, New Haven, CT.ORCID 0000-0001-8030-0078
Ellen J HoffmanChild Study Center, Yale School of Medicine, New Haven, CT.ORCID 0000-0002-5083-1369

Funding

Multimodal Developmental Neurogenetics of Females with ASDR01MH100028 · NIMH · YALE UNIVERSITY · PI Allison Elizabeth Jack, LAUREN KENWORTHY · 2012 to 2026
$37.8M
Interdepartmental Neuroscience Program (INP)T32NS041228 · NINDS · YALE UNIVERSITY · PI Charles A Greer, Marina R Picciotto · 2001 to 2026
$12.0M
High-throughput in vivo and in vitro functional and multi-omics screens of neuropsychiatric and neurodevelopmental disorder risk genesRM1MH132648 · NIMH · YALE UNIVERSITY · PI Kristen Jennifer Brennand, Rong Fan · 2023 to 2026
$5.6M
High-throughput Functional Analysis of Autism Risk GenesR01MH116002 · NIMH · YALE UNIVERSITY · PI ELLEN J HOFFMAN · 2018 to 2026
$4.5M
Investigating the Translatome in Genetic Models of AutismR21MH133245 · NIMH · YALE UNIVERSITY · PI HOFFMAN, ELLEN J · 2023 to 2024
$459k
Autism Science Foundation 22-005Howard Hughes Medical Institute GT16695Interdepartmental Neuroscience Program at YaleNIMH NIH HHS R01 MH100028NIMH NIH HHS R01MH100028NIMH NIH HHS R01 MH116002NIMH NIH HHS R01MH116002NIMH NIH HHS R21 MH133245NIMH NIH HHS R21MH133245NIMH NIH HHS RM1 MH132648NIMH NIH HHS RM1MH132648NINDS NIH HHS T32 NS041228The O'Sullivan FoundationYale Department of Pediatrics
6 · The paper itself

Abstract

Autism spectrum disorders (ASDs) are a group of neurodevelopmental disorders characterized by deficits in social communication and interaction and the presence of repetitive and restricted behaviors. ASDs are clinically and genetically heterogeneous with hundreds of genes identified through large-scale whole exome and genome sequencing studies contributing to risk. Recent studies are beginning to illuminate shared mechanisms across ASD-associated genes at the molecular, cellular, circuit, and behavioral levels, identifying neurogenesis and excitatory-inhibitory neuron development as points of biological convergence. These functional analyses of ASD genes provide substantial promise for gaining a deeper understanding of ASD pathophysiology and elucidating novel therapeutic targets. ANN NEUROL 2025;98:1163-1177.

Indexed as

Autism Spectrum DisorderGenetic Predisposition to DiseaseAnimalsHumans

Identifiers

PMID40801227
PMCPMC13159706

What Socratic 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 Socratic graph.