Abstract

Given increasing recognition that psychosis onset is a late stage of a neurodevelopmental illness, and the importance of early intervention, efforts are focused on understanding the pathophysiology of early stages of psychosis. Here we characterize morphometric similarity networks (MSNs) using structural brain imaging measures in subjects at clinical high-risk (CHR) who converted (CHRc) or did not convert (CHRnc) to psychosis relative to healthy comparison (HC) subjects. We incorporate postmortem transcriptomic data from the Allen Human Brain Atlas (AHBA) to relate transcriptomic and MSN cortical spatial patterns.

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