Evidence map›Paper›PMID 39994426›Full record

ArticleMolecular psychiatry2025

Polygenic scores for autism are associated with reduced neurite density in adults and children from the general population.

Yuanjun Gu, Eva Maria-Stauffer, Saashi A Bedford, APEX consortium, iPSYCH-autism consortium, Rafael Romero-Garcia, Jakob Grove, Anders D Børglum, Hilary Martin, Simon Baron-Cohen and 2 more

Abstract read
In one paragraph

Article in Molecular psychiatry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Decreased BOLD Signal Variability in Middle-Aged and Older Adults on the Autism Spectrum.Autism research : official journal of the International Society for Autism Research · 2026
    Article
  4. Article
  5. Review
  6. Article
  7. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors.

Yuanjun GuDepartment of Psychiatry, University of Cambridge, Cambridge, CB2 8AH, UK. yg330@cam.ac.uk.ORCID 0000-0001-9475-0010
Eva Maria-StaufferDepartment of Psychiatry, University of Cambridge, Cambridge, CB2 8AH, UK.
Saashi A BedfordDepartment of Psychiatry, University of Cambridge, Cambridge, CB2 8AH, UK.
APEX consortium
iPSYCH-autism consortium
Rafael Romero-GarciaDepartment of Psychiatry, University of Cambridge, Cambridge, CB2 8AH, UK.ORCID 0000-0002-5199-4573
Jakob GroveThe Lundbeck Foundation Initiative for Integrative Psychiatric Research, iPSYCH, Aarhus, 8000, Denmark.ORCID 0000-0003-2284-5744
Anders D BørglumThe Lundbeck Foundation Initiative for Integrative Psychiatric Research, iPSYCH, Aarhus, 8000, Denmark.ORCID 0000-0001-8627-7219
Hilary MartinHuman Genetics Programme, Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, CB10 1SA, UK.
Simon Baron-CohenAutism Research Centre, Department of Psychiatry, University of Cambridge, Cambridge, CB2 8AH, UK.
Richard A I BethlehemDepartment of Psychology, University of Cambridge, Cambridge, CB2 3EB, UK.ORCID 0000-0002-0714-0685
Varun WarrierDepartment of Psychiatry, University of Cambridge, Cambridge, CB2 8AH, UK. vw260@cam.ac.uk.

Funding

2/7 Psychiatric Genomics Consortium: Advancing Discovery and ImpactR01MH124851 · NIMH · MASSACHUSETTS GENERAL HOSPITAL · PI BOERGLUM, ANDERS, DAVIS, LEA K · 2021 to 2025
$5.4M
EC | Horizon 2020 Framework Programme (EU Framework Programme for Research and Innovation H2020) 101057385NIMH NIH HHS R01 MH124851Wellcome TrustWellcome Trust (Wellcome) 214322\Z\18\Z
6 · The paper itself

Abstract

Genetic variants linked to autism are thought to change cognition and behaviour by altering the structure and function of the brain. Although a substantial body of literature has identified structural brain differences in autism, it is unknown whether autism-associated common genetic variants are linked to changes in cortical macro- and micro-structure. We investigated this using neuroimaging and genetic data from adults (UK Biobank, N = 31,748) and children (ABCD, N = 4928). Using polygenic scores and genetic correlations we observe a robust negative association between common variants for autism and a magnetic resonance imaging derived phenotype for neurite density (intracellular volume fraction) in the general population. This result is consistent across both children and adults, in both the cortex and in white matter tracts, and confirmed using polygenic scores and genetic correlations. There were no sex differences in this association. Mendelian randomisation analyses provide no evidence for a causal relationship between autism and intracellular volume fraction, although this should be revisited using better powered instruments. Overall, this study provides evidence for shared common variant genetics between autism and cortical neurite density.

Indexed as

Autistic DisorderNeuritesAdultAutism Spectrum DisorderBrainCerebral CortexChildFemaleGenetic Predisposition to DiseaseGenome-Wide Association StudyHumansMagnetic Resonance ImagingMaleMendelian Randomization AnalysisMiddle AgedMultifactorial Inheritance

Identifiers

PMID39994426
PMCPMC12240833

What OpenQuestion holds

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Registered trials

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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.