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Interaction Testing and Polygenic Risk Scoring to Estimate the Association of Common Genetic Variants With Treatment Resistance in Schizophrenia
Rare coding variants in ten genes confer substantial risk for schizophrenia
DNA sequence-level analyses reveal potential phenotypic modifiers in a large family with psychiatric disorders
Gene–Brain Structure Relationships: Arbitrary Assumptions of Heterogeneity Generate Unfalsifiable Claims—Reply
Haplotype Analysis and a Novel Allele-Sharing Method Refines a Chromosome 4p Locus Linked to Bipolar Affective Disorder
DISC1 and PDE4B are interacting genetic factors in schizophrenia that regulate cAMP signaling
Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders.
GWA study data mining and independent replication identify cardiomyopathy-associated 5 (CMYA5) as a risk gene for schizophrenia
Genetic association and brain morphology studies and the chromosome 8p22 pericentriolar material 1 (PCM1) gene in susceptibility to schizophrenia
