Evidence map›Paper›PMID 42823405›Full record

ArticleNature communications2026

Common alleles associated with connectivity within and across the brain's main functional networks.

Xavier Caseras, Tom Chambers, Lynsey Hall, Antonio F Pardiñas, Kevin Murphy, Richard Jl Anney

Abstract read
PubMed Publisher
In one paragraph

Article in Nature communications, 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. 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

6 authors.

Xavier CaserasCentre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, School of Medicine, Cardiff University, Cardiff Wales, UK. caserasx@cardiff.ac.uk.ORCID 0000-0002-8490-6891
Tom ChambersCentre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, School of Medicine, Cardiff University, Cardiff Wales, UK.
Lynsey HallCentre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, School of Medicine, Cardiff University, Cardiff Wales, UK.
Antonio F PardiñasCentre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, School of Medicine, Cardiff University, Cardiff Wales, UK.ORCID 0000-0001-6845-7590
Kevin MurphyCardiff University Brain Research Imaging Centre (CUBRIC), School of Physics and Astronomy, Cardiff University, Cardiff Wales, UK.
Richard Jl AnneyCentre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, School of Medicine, Cardiff University, Cardiff Wales, UK.ORCID 0000-0002-6083-407X

Funding

Wellcome Trust (Wellcome) ISSF3 ref. AC1130IF04Wellcome Trust (Wellcome) WT224267
6 · The paper itself

Abstract

Previous GWAS of brain's connectivity have been challenged by the difficulty of best representing the complexity of this phenotype. Here we report the results from a multivariate GWAS approach that allows for a better representation of this complexity, while boosting statistical power. This strategy notably increases the detection of significant signals to 114 independent SNPs, pointing at 315 candidate genes. Our results show a large overlap of the genetic makeup associated with functional connectivity across brain networks but also identify network specific signals, suggesting a potential genetic stratification between cognitive and sensory-motor networks. We also identify a large genetic overlap between functional connectivity and risk for neuropsychiatric disorders, suggesting that regions of the genome important for neuronal communication are enriched for neuropsychiatric risk SNPs. The work presented here expands our understanding of the common allele architecture of brain connectivity, as well as provides novel targets to functional genomics research.

Indexed as

AllelesBrainNerve NetGenetic Predisposition to DiseaseGenome-Wide Association StudyHumansPolymorphism, Single Nucleotide

Identifiers

What OpenQuestion holds

Textmetadata
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.