Evidence map›Paper›PMID 39009701›Full record

ArticleMolecular psychiatry2025

Genetic neurodevelopmental clustering and dyslexia.

Austeja Ciulkinyte, Hayley S Mountford, Pierre Fontanillas, 23andMe Research Team, Timothy C Bates, Nicholas G Martin, Simon E Fisher, Michelle Luciano

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 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Article
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  8. Shared and distinct phenotypic profiles among neurodevelopmental disorder genes.medRxiv : the preprint server for health sciences · 2026
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  11. Review
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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

8 authors.

Austeja CiulkinyteTranslational Neuroscience PhD Programme, University of Edinburgh, Edinburgh, UK.ORCID 0000-0001-5268-5492
Hayley S MountfordSchool of Philosophy, Psychology and Language Sciences, University of Edinburgh, Edinburgh, UK.ORCID 0000-0002-7663-6326
Pierre Fontanillas23andMe, Inc., Sunnyvale, CA, USA.ORCID 0000-0002-8944-4454
23andMe Research Team
Timothy C BatesSchool of Philosophy, Psychology and Language Sciences, University of Edinburgh, Edinburgh, UK.ORCID 0000-0002-1153-9007
Nicholas G MartinGenetic Epidemiology, QIMR Berghofer Medical Research Institute, Herston, QLD, Australia.ORCID 0000-0003-4069-8020
Simon E FisherLanguage and Genetics Department, Max Planck Institute for Psycholinguistics, Nijmegen, Netherlands.ORCID 0000-0002-3132-1996
Michelle LucianoSchool of Philosophy, Psychology and Language Sciences, University of Edinburgh, Edinburgh, UK. michelle.luciano@ed.ac.uk.ORCID 0000-0002-7306-3008

Funding

RCUK | Biotechnology and Biological Sciences Research Council (BBSRC) BB/T000813/1Wellcome TrustWellcome Trust (Wellcome) 218493/Z/19/Z
6 · The paper itself

Abstract

Dyslexia is a learning difficulty with neurodevelopmental origins, manifesting as reduced accuracy and speed in reading and spelling. It is substantially heritable and frequently co-occurs with other neurodevelopmental conditions, particularly attention deficit-hyperactivity disorder (ADHD). Here, we investigate the genetic structure underlying dyslexia and a range of psychiatric traits using results from genome-wide association studies of dyslexia, ADHD, autism, anorexia nervosa, anxiety, bipolar disorder, major depressive disorder, obsessive compulsive disorder, schizophrenia, and Tourette syndrome. Genomic Structural Equation Modelling (GenomicSEM) showed heightened support for a model consisting of five correlated latent genomic factors described as: F1) compulsive disorders (including obsessive-compulsive disorder, anorexia nervosa, Tourette syndrome), F2) psychotic disorders (including bipolar disorder, schizophrenia), F3) internalising disorders (including anxiety disorder, major depressive disorder), F4) neurodevelopmental traits (including autism, ADHD), and F5) attention and learning difficulties (including ADHD, dyslexia). ADHD loaded more strongly on the attention and learning difficulties latent factor (F5) than on the neurodevelopmental traits latent factor (F4). The attention and learning difficulties latent factor (F5) was positively correlated with internalising disorders (.40), neurodevelopmental traits (.25) and psychotic disorders (.17) latent factors, and negatively correlated with the compulsive disorders (-.16) latent factor. These factor correlations are mirrored in genetic correlations observed between the attention and learning difficulties latent factor and other cognitive, psychological and wellbeing traits. We further investigated genetic variants underlying both dyslexia and ADHD, which implicated 49 loci (40 not previously found in GWAS of the individual traits) mapping to 174 genes (121 not found in GWAS of individual traits) as potential pleiotropic variants. Our study confirms the increased genetic relation between dyslexia and ADHD versus other psychiatric traits and uncovers novel pleiotropic variants affecting both traits. In future, analyses including additional co-occurring traits such as dyscalculia and dyspraxia will allow a clearer definition of the attention and learning difficulties latent factor, yielding further insights into factor structure and pleiotropic effects.

Indexed as

Attention Deficit Disorder with HyperactivityDyslexiaGenome-Wide Association StudyNeurodevelopmental DisordersAutistic DisorderBipolar DisorderFemaleGenetic Predisposition to DiseaseHumansMajor Depressive DisorderMaleObsessive-Compulsive DisorderPhenotypePolymorphism, Single NucleotideSchizophreniaTourette Syndrome

Identifiers

PMID39009701
PMCPMC11649571

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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.