AbstractThe 22q11.2 deletion syndrome (22q11DS) is an uncommon genetic disorder with an increased risk of psychosis. Although the neural substrates of psychosis and schizophrenia are not well understood, aberrations in cortical networks represent intriguing potential mechanisms. Investigations of anatomic networks within 22q11DS are sparse. We investigated group differences in anatomic network structure in 48 individuals with 22q11DS and 370 typically developing controls by analyzing covariance patterns in cortical thickness among 68 regions of interest using graph theoretical models. Subjects with 22q11DS had less robust geographic organization relative to the control group, particularly in the occipital and parietal lobes. Multiple global...
Background: Dysconnectivity has been consistently proposed as a major key mechanism in psychosis. In...
Chromosome 22q11.2 deletion syndrome (22q11DS) is a genetic disease known to lead to cerebral struct...
The 22q11.2 deletion (22q11DS) is a common chromosomal microdeletion and a potent risk factor for ps...
The 22q11.2 deletion syndrome (22q11DS) is an uncommon genetic disorder with an increased risk of ps...
AbstractThe 22q11.2 deletion syndrome (22q11DS) is an uncommon genetic disorder with an increased ri...
Abstract The 22q11 deletion syndrome is a genetic disorder associated with a high risk of developing...
Chromosome 22q11.2 deletion syndrome (22q11DS) is a genetic disease known to lead to cerebral struct...
Although many genetic risk factors for psychiatric and neurodevelopmental disorders have been identi...
AbstractChromosome 22q11.2 deletion syndrome (22q11DS) is a genetic disease known to lead to cerebra...
BACKGROUND: 22q11.2 deletion syndrome (22q11DS) is the third-largest known genetic risk factor for t...
22q11.2 deletion syndrome (22q11DS) represents a homogeneous model of schizophrenia particularly sui...
The clinical picture associated with 22q11.2 deletion syndrome (22q11DS) includes mild mental retard...
The 22q11.2 deletion (22q11DS) is a common chromosomal microdeletion and a potent risk factor for ps...
The neural endophenotype associated with 22q11.2 deletion syndrome (22q11DS) includes deviant cortic...
The 22q11.2 deletion (22q11DS) is a common chromosomal microdeletion and a potent risk factor for ps...
Background: Dysconnectivity has been consistently proposed as a major key mechanism in psychosis. In...
Chromosome 22q11.2 deletion syndrome (22q11DS) is a genetic disease known to lead to cerebral struct...
The 22q11.2 deletion (22q11DS) is a common chromosomal microdeletion and a potent risk factor for ps...
The 22q11.2 deletion syndrome (22q11DS) is an uncommon genetic disorder with an increased risk of ps...
AbstractThe 22q11.2 deletion syndrome (22q11DS) is an uncommon genetic disorder with an increased ri...
Abstract The 22q11 deletion syndrome is a genetic disorder associated with a high risk of developing...
Chromosome 22q11.2 deletion syndrome (22q11DS) is a genetic disease known to lead to cerebral struct...
Although many genetic risk factors for psychiatric and neurodevelopmental disorders have been identi...
AbstractChromosome 22q11.2 deletion syndrome (22q11DS) is a genetic disease known to lead to cerebra...
BACKGROUND: 22q11.2 deletion syndrome (22q11DS) is the third-largest known genetic risk factor for t...
22q11.2 deletion syndrome (22q11DS) represents a homogeneous model of schizophrenia particularly sui...
The clinical picture associated with 22q11.2 deletion syndrome (22q11DS) includes mild mental retard...
The 22q11.2 deletion (22q11DS) is a common chromosomal microdeletion and a potent risk factor for ps...
The neural endophenotype associated with 22q11.2 deletion syndrome (22q11DS) includes deviant cortic...
The 22q11.2 deletion (22q11DS) is a common chromosomal microdeletion and a potent risk factor for ps...
Background: Dysconnectivity has been consistently proposed as a major key mechanism in psychosis. In...
Chromosome 22q11.2 deletion syndrome (22q11DS) is a genetic disease known to lead to cerebral struct...
The 22q11.2 deletion (22q11DS) is a common chromosomal microdeletion and a potent risk factor for ps...