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Author

A. Børglum

3 papers indexed here

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Open access Sep 2026

Analysis of Rare Coding Variation Identifies New Genetic Contributors to Schizophrenia

In this study, we present the largest rare coding variant association study of schizophrenia to date, with 87,959 schizophrenia cases and 150,587 controls. We identify 16 genes at exome-wide significance: SETD1A, ZMYM2, HERC1, RB1CC1, SCAF1, XPO7, SP4, FYN, PPP3CA, CUL1, HDAC9, JARID2, ATP9A, PTK2, STAG1, and SCN2A, an...

J. Sealock, C. Dowd, Calwing Liao et al. · 1 citation
Open access Sep 2026

Polygenic effects on cortical size and ADHD converge on a mid-gestational progenitor-to-neuron transition programme

Neurodevelopmental and psychiatric conditions have long been hypothesised to emerge from changes in the structure and function of the brain. However, the molecular and cellular mechanisms linking brain structure to these conditions remain unknown. Here, using genetic and structural/diffusion neuroimaging data from 59,2...

Y. He, A. Ebneabbasi, K. Rademaker et al. · 0 citations
Open access Sep 2026

Common genetic variants are associated with increased likelihood of latent co-occurring neurodevelopmental and mental health factors among autistic individuals.

Evidence is found for additive effects of other genetic factors in contributing to some latent co-occurring neurodevelopmental and mental health conditions in autism.

Adeniran Okewole, Vincent-Raphaël Bourque, M. Koko et al. · 1 citation

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