A three-marker C-A-T dysbindin haplotype identified by Williams et al (PMID: 15066891) is associated with increased risk for schizophrenia, decreased mRNA expression, poorer cognitive performance, and early sensory processing deficits. We investigated whether this same dysbindin risk haplotype was also associated with structural variation in the gray matter volume (GMV). Using voxel-based morphometry, whole-volume analysis revealed significantly reduced GMVs in both the right dorsolateral prefrontal and left occipital cortex, corresponding to the behavioral findings of impaired spatial working memory and EEG findings of impaired visual processing already reported. These data provide important evidence of the influence of dysbindin risk vari...
DieThe etiology of schizophrenia and other psychiatric disorders is characterized by a strong geneti...
Objective: Converging evidence has demonstrated an associa-tion between variants in the dysbindin ge...
, which is expressed exclusively in the brain, has been observed in Brodmann areas (BA) 9 and 32 of ...
A three-marker C-A-T dysbindin haplotype identified by Williams et al (PMID: 15066891) is associated...
A three-marker C–A–T dysbindin haplotype identified by Williams et al (PMID: 15066891) is associated...
Working memory (WM) dysfunction is a hallmark feature of schizophrenia. Functional imaging studies u...
Schizophrenia is a neurodevelopmental disorder, and risk genes are thought to act through disruption...
DTNBP1 (dystrobrevin binding protein 1) remains a top candidate gene in schizophrenia. Reduced expre...
Reduced Gray matter (GM) volume is a core feature of schizophrenia. Mapping genes that is associated...
Eleven studies now report significant associations between schizophrenia and certain haplotypes of s...
Genetic variation in dysbindin 1 (DTNBP1) gene region tagged by SNP rs1018381 exhibits a linkage wit...
Behavioral genetic studies of humans have associated variation in the DTNBP1 gene with schizophrenia...
<div><p>Reduced Gray matter (GM) volume is a core feature of schizophrenia. Mapping genes that is as...
Background: Schizophrenia is a neurodevelopmental disorder, and risk genes are thought to act throu...
Schizophrenia is associated with brain structural abnormalities including gray and white matter volu...
DieThe etiology of schizophrenia and other psychiatric disorders is characterized by a strong geneti...
Objective: Converging evidence has demonstrated an associa-tion between variants in the dysbindin ge...
, which is expressed exclusively in the brain, has been observed in Brodmann areas (BA) 9 and 32 of ...
A three-marker C-A-T dysbindin haplotype identified by Williams et al (PMID: 15066891) is associated...
A three-marker C–A–T dysbindin haplotype identified by Williams et al (PMID: 15066891) is associated...
Working memory (WM) dysfunction is a hallmark feature of schizophrenia. Functional imaging studies u...
Schizophrenia is a neurodevelopmental disorder, and risk genes are thought to act through disruption...
DTNBP1 (dystrobrevin binding protein 1) remains a top candidate gene in schizophrenia. Reduced expre...
Reduced Gray matter (GM) volume is a core feature of schizophrenia. Mapping genes that is associated...
Eleven studies now report significant associations between schizophrenia and certain haplotypes of s...
Genetic variation in dysbindin 1 (DTNBP1) gene region tagged by SNP rs1018381 exhibits a linkage wit...
Behavioral genetic studies of humans have associated variation in the DTNBP1 gene with schizophrenia...
<div><p>Reduced Gray matter (GM) volume is a core feature of schizophrenia. Mapping genes that is as...
Background: Schizophrenia is a neurodevelopmental disorder, and risk genes are thought to act throu...
Schizophrenia is associated with brain structural abnormalities including gray and white matter volu...
DieThe etiology of schizophrenia and other psychiatric disorders is characterized by a strong geneti...
Objective: Converging evidence has demonstrated an associa-tion between variants in the dysbindin ge...
, which is expressed exclusively in the brain, has been observed in Brodmann areas (BA) 9 and 32 of ...