Shared genetic architecture of cortical morphology and psychiatric disorders: insights from a cross-trait analyses across 180 cortical regions

The shared genetic liability between cortical morphology and psychiatric disorders remains unclear. We aimed to identify whether the genetic loci shared between cortical morphology and six psychiatric disorders show regional or global effects. We identified substantial pairwise genetic overlaps of cortical surface area or thickness with psychiatric disorders; however, these loci lacked a uniform direction (∼50% concordance). Cross-trait analyses revealed distinct architectures: internalizing disorders and schizophrenia/bipolar disorder shared more genetic loci with localized effects, whereas neurodevelopmental disorders shared fewer loci but more with widespread effects. We identified 17 genomic loci shared across all disorders, most of which had opposing directional effects across cortical regions. Only one locus (rs2431112) had region-specific and unidirectional effects (reduced primary visual and posterior cingulate surface area). This directional heterogeneity within and across pleiotropic loci reveals complex shared genetic architectures and likely limits the genetic predictive performance of brain morphology for psychiatric disorders.

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Journal
medRxiv
Published
2026-04-13
DOI
https://doi.org/10.64898/2026.04.10.26349224
Primary Topic
Genetic Associations and Epidemiology
Type
article
Field-Weighted Citation Impact
0.00

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article

Shared genetic architecture of cortical morphology and psychiatric disorders: insights from a cross-trait analyses across 180 cortical regions

Karmel W. Choi, Sander Lamballais, Yingzhe Zhang, Henning Tiemeier et al.
medRxiv
Genetic Associations and Epidemiology
article

Shared genetic architecture of cortical morphology and psychiatric disorders: insights from a cross-trait analyses across 180 cortical regions

Karmel W. Choi, Sander Lamballais, Yingzhe Zhang, Henning Tiemeier, Travis Triplett Mallard
article en

Abstract

The shared genetic liability between cortical morphology and psychiatric disorders remains unclear. We aimed to identify whether the genetic loci shared between cortical morphology and six psychiatric disorders show regional or global effects. We identified substantial pairwise genetic overlaps of cortical surface area or thickness with psychiatric disorders; however, these loci lacked a uniform direction (∼50% concordance). Cross-trait analyses revealed distinct architectures: internalizing disorders and schizophrenia/bipolar disorder shared more genetic loci with localized effects, whereas neurodevelopmental disorders shared fewer loci but more with widespread effects. We identified 17 genomic loci shared across all disorders, most of which had opposing directional effects across cortical regions. Only one locus (rs2431112) had region-specific and unidirectional effects (reduced primary visual and posterior cingulate surface area). This directional heterogeneity within and across pleiotropic loci reveals complex shared genetic architectures and likely limits the genetic predictive performance of brain morphology for psychiatric disorders.

medRxiv
Harvard University (US), Erasmus MC (NL), Massachusetts General Hospital (US)
National Institute of Mental Health
Openalex Percentile: Top 22%
Genetic Associations and Epidemiology
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