Open access
Sep 2026
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.
· bioRxiv · 1 citation
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Open access
Jul 2026
Introduction Limitations of current classifications of schizophrenia, schizoaffective disorder, and bipolar disorder are evident from their overlapping symptoms, aetiologies, treatments, and outcomes, and present a barrier to novel treatment discovery. Alternative conceptualisations are needed to address nosological va...
Charlotte A. Dennison, S. Legge, A. Cardno et al.
· medRxiv · 0 citations
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Open access
Aug 2026
A greater burden of common genetic variants is associated with more severe forms of illness in schizophrenia.
Urmi Das, J. Crowley, R. Karlsson et al.
· Molecular Psychiatry · 0 citations
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