Evidence map›Paper›PMID 41263488›Full record

ArticlePsychiatric genetics2026

Shared genetic architecture between autism spectrum disorder, loneliness, and social isolation reveals novel genetic loci.

Sigrun Hope, Aihua Lin, Linn Rodevand, Saira Jameela Hübenette, Daniel S Quintana, Ida E Sønderby, Weiqiu Cheng, Oleksandr Frei, Shahram Bahrami, Guy F L Hindley and 7 more

Abstract read
In one paragraph

Article in Psychiatric genetics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Quo Vadis translational neuroscience?Translational neuroscience · 2026
    Review
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

17 authors.

Sigrun HopeK.G. Jebsen Centre for Neurodevelopmental Disorders, University of Oslo and Oslo University Hospital.
Aihua LinNorwegian Centre for Mental Disorders Research (NORMENT), Institute of Clinical Medicine, University of Oslo and Division of Mental Health and Addiction, Oslo University Hospital.
Linn RodevandNorwegian Centre for Mental Disorders Research (NORMENT), Institute of Clinical Medicine, University of Oslo and Division of Mental Health and Addiction, Oslo University Hospital.
Saira Jameela HübenetteK.G. Jebsen Centre for Neurodevelopmental Disorders, University of Oslo and Oslo University Hospital.
Daniel S QuintanaK.G. Jebsen Centre for Neurodevelopmental Disorders, University of Oslo and Oslo University Hospital.
Ida E SønderbyK.G. Jebsen Centre for Neurodevelopmental Disorders, University of Oslo and Oslo University Hospital.
Weiqiu ChengNorwegian Centre for Mental Disorders Research (NORMENT), Institute of Clinical Medicine, University of Oslo and Division of Mental Health and Addiction, Oslo University Hospital.
Oleksandr FreiNorwegian Centre for Mental Disorders Research (NORMENT), Institute of Clinical Medicine, University of Oslo and Division of Mental Health and Addiction, Oslo University Hospital.
Shahram BahramiNorwegian Centre for Mental Disorders Research (NORMENT), Institute of Clinical Medicine, University of Oslo and Division of Mental Health and Addiction, Oslo University Hospital.
Guy F L HindleyNorwegian Centre for Mental Disorders Research (NORMENT), Institute of Clinical Medicine, University of Oslo and Division of Mental Health and Addiction, Oslo University Hospital.
Anett KaaleNevSom, Department of Rare Disorders and Disabilities.
Alexey A ShadrinNorwegian Centre for Mental Disorders Research (NORMENT), Institute of Clinical Medicine, University of Oslo and Division of Mental Health and Addiction, Oslo University Hospital.
Kevin S O'ConnellNorwegian Centre for Mental Disorders Research (NORMENT), Institute of Clinical Medicine, University of Oslo and Division of Mental Health and Addiction, Oslo University Hospital.
Nadine ParkerNorwegian Centre for Mental Disorders Research (NORMENT), Institute of Clinical Medicine, University of Oslo and Division of Mental Health and Addiction, Oslo University Hospital.
Srdjan DjurovicNorwegian Centre for Mental Disorders Research (NORMENT), Institute of Clinical Medicine, University of Oslo and Division of Mental Health and Addiction, Oslo University Hospital.
Terje NærlandK.G. Jebsen Centre for Neurodevelopmental Disorders, University of Oslo and Oslo University Hospital.
Ole A AndreassenK.G. Jebsen Centre for Neurodevelopmental Disorders, University of Oslo and Oslo University Hospital.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveDeficits in social communication and social interaction are core features of autism spectrum disorder (ASD), and studies suggest that loneliness and social isolation are common. ASD has a strong genetic basis, but the genetic architecture and overlap with social phenotypes are not clear.

methodsWe analyzed summary statistics from genome-wide association studies on ASD (46 350), loneliness (452 302), and social isolation (288 950), using linkage disequilibrium score regression, local analysis of covariant annotation (LAVA), bivariate causal mixture model (MiXeR), and the conditional/conjunctional false discovery rate (cond/conjFDR).

resultsFor ASD and social isolation, we found nonsignificant global genetic correlation ( rg = 0.02, P  = 0.8), but LAVA identified 72 genomic regions with bidirectional correlations, and MiXeR estimated that 8.7 k of 13.1 k variants (81%) were shared, of which 53% had concordant effect directions. For ASD and loneliness, we found a positive genetic correlation ( rg = 0.26, P  = 2e-10), LAVA identified 80 genomic regions with bidirectional genetic correlations, and MiXeR suggested that at least 3.8 k variants were shared. We identified nine specific shared genetic loci between ASD and loneliness and eight between ASD and social isolation (conjFDR < 0.05). Of these, 12 loci were novel for ASD. Genes mapped to these loci are involved in γ-aminobutyric acid (GABA), glutamate, calcium, and stress hormone signaling, cerebral glucose transport, TAU-accumulation, and immune function.

conclusionWe found extensive overlap in genetic architecture between ASD, loneliness, and social isolation, with bidirectional effects. By leveraging data for ASD and social traits, we identified 12 novel ASD related genetic loci implicating several genes, thereby elucidating potential pathways underlying their shared genetic architecture.

Indexed as

Autism Spectrum DisorderLonelinessSocial IsolationGenetic LociGenetic Predisposition to DiseaseGenome-Wide Association StudyHumansLinkage DisequilibriumMalePolymorphism, Single Nucleotideautismgenome-wide association studylonelinesssocial isolation

Identifiers

PMID41263488
PMCPMC12834293

What Socratic holds

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LicenceCC BY-NC-ND
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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 Socratic graph.