Background Cognitive impairment in schizophrenia is a major contributor to poor outcomes yet its causes are poorly understood. Some rare copy number variants (CNVs) are associated with schizophrenia risk and impact cognition in healthy populations but their contribution to cognitive impairment in schizophrenia has not been investigated. We examined the effect of 12 schizophrenia CNVs on cognition in those with schizophrenia. Methods General cognitive ability was measured using the MATRICS composite z-score in 875 schizophrenia cases, and in a replication sample of 519 schizophrenia cases using WAIS Full-Scale IQ. Using linear regression we tested for association between cognition and schizophrenia CNV status, covarying for age and sex. I...
Objective: Chromosome 22q11.2 deletion syndrome (22q11.2DS) is associated with a more than 20-fold i...
Background The UK Biobank is a unique resource for biomedical research, with extensive phenotypic an...
Copy number variants (CNVs) are associated with psychiatric conditions in clinical populations. The ...
Background Cognitive impairment in schizophrenia is a major contributor to poor outcomes yet its ca...
The burden of large and rare copy number genetic variants (CNVs) as well as certain specific CNVs in...
The burden of large and rare copy number genetic variants (CNVs) as well as certain specific CNVs in...
By performing a meta-analysis of rare coding variants in whole-exome sequences from 4,133 schizophre...
The burden of large and rare copy number genetic variants (CNVs) as well as certain specific CNVs in...
The burden of large and rare copy number genetic variants (CNVs) as well as certain specific CNVs in...
Copy number variation (CNV) is a widely replicated risk factor for psychiatric disorders such as sch...
Background Copy number variants (CNVs) play a significant role in disease pathogenesis in a small s...
Objective: Chromosome 22q11.2 deletion syndrome (22q11.2DS) is associated with a more than 20-fold i...
Background The UK Biobank is a unique resource for biomedical research, with extensive phenotypic an...
Copy number variants (CNVs) are associated with psychiatric conditions in clinical populations. The ...
Background Cognitive impairment in schizophrenia is a major contributor to poor outcomes yet its ca...
The burden of large and rare copy number genetic variants (CNVs) as well as certain specific CNVs in...
The burden of large and rare copy number genetic variants (CNVs) as well as certain specific CNVs in...
By performing a meta-analysis of rare coding variants in whole-exome sequences from 4,133 schizophre...
The burden of large and rare copy number genetic variants (CNVs) as well as certain specific CNVs in...
The burden of large and rare copy number genetic variants (CNVs) as well as certain specific CNVs in...
Copy number variation (CNV) is a widely replicated risk factor for psychiatric disorders such as sch...
Background Copy number variants (CNVs) play a significant role in disease pathogenesis in a small s...
Objective: Chromosome 22q11.2 deletion syndrome (22q11.2DS) is associated with a more than 20-fold i...
Background The UK Biobank is a unique resource for biomedical research, with extensive phenotypic an...
Copy number variants (CNVs) are associated with psychiatric conditions in clinical populations. The ...