Findings support the face validity and potential clinical utility of a circadian subtype of depression as a clinical profile and support the face validity and potential clinical utility of its biology and predictive utility.
E. Tonini, J. Crouse, M. Shin et al.· The British journal of psych...· 1 citation
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
Together, these results implicate a constellation of rare variants that map onto neuronal biology and demonstrate that diverse global populations converge on shared genetic signals underlying BD risk.
Calwing Liao, Robert Ye, J. Sealock et al.· medRxiv· 0 citations
Background and aims Digital addiction is highly prevalent among emerging adults and is associated with significant detrimental health outcomes. Through the lens of the Interaction of Person-Affect-Cognition-Execution model, attention-deficit/hyperactivity disorder (ADHD) symptoms and autistic traits may increase vulner...
M. J. Giblett, C. Jaklich, B. Andrew et al.· medRxiv· 0 citations
Bipolar disorder’s genetic architecture appears hierarchical—a general liability resolving into dimensions of course and comorbidity, beyond subtypes, beyond subtypes.
Tracey van der Veen, M. Tesfaye, J. M. K. Yang et al.· Research Square· 0 citations
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