22q11.2 deletion syndrome (22q11DS) is a recurrent genetic mutation that is highly penetrant for psychosis. Behavioral research suggests that 22q11DS patients exhibit a characteristic neurocognitive phenotype that includes differential impairment in spatial working memory (WM). Notably, spatial WM has also been proposed as an endophenotype for idiopathic psychotic disorder, yet little is known about the neurobiological substrates of WM in 22q11DS. In order to investigate the neural systems engaged during spatial WM in 22q11DS patients, we collected functional magnetic resonance imaging (fMRI) data while 41 participants (16 22q11DS patients, 25 demographically matched controls) performed a spatial capacity WM task that included manipulations...
22q11.2 deletion syndrome (22q11DS) is a genetic disorder associated with a microdeletion of chromos...
22q11.2 deletion syndrome (22q11DS) is associated with elevated levels of impulsivity, inattention, ...
The 22q11.2 deletion (22q11DS) is a common chromosomal microdeletion and a potent risk factor for ps...
22q11.2 deletion syndrome (22q11DS) is a recurrent genetic mutation that is highly penetrant for psy...
INTRODUCTION: Impaired spatial working memory is a core cognitive deficit observed in people with 22...
The 22q11.2 deletion is one of the most common copy number variants in humans. Carriers of the delet...
Background: Dysconnectivity has been consistently proposed as a major key mechanism in psychosis. In...
22q11.2 deletion syndrome (22q11DS) is a genetic disorder associated with a microdeletion of chromos...
AbstractThe 22q11.2 deletion syndrome (22q11DS) is an uncommon genetic disorder with an increased ri...
Background22q11.2 deletion syndrome (22q11DS) is a neurogenetic condition associated with deficits i...
Background: Children with chromosome 22q11.2 deletion syndrome (22q11.2DS) exhibit nonverbal learnin...
22q11.2 Deletion Syndrome is associated with cognitive, behavioural, and psychiatric problems and is...
Large-scale brain networks play a prominent role in cognitive abilities and their activity is impair...
The 22q11.2 deletion (22q11DS) is a common chromosomal microdeletion and a potent risk factor for ps...
The clinical picture associated with 22q11.2 deletion syndrome (22q11DS) includes mild mental retard...
22q11.2 deletion syndrome (22q11DS) is a genetic disorder associated with a microdeletion of chromos...
22q11.2 deletion syndrome (22q11DS) is associated with elevated levels of impulsivity, inattention, ...
The 22q11.2 deletion (22q11DS) is a common chromosomal microdeletion and a potent risk factor for ps...
22q11.2 deletion syndrome (22q11DS) is a recurrent genetic mutation that is highly penetrant for psy...
INTRODUCTION: Impaired spatial working memory is a core cognitive deficit observed in people with 22...
The 22q11.2 deletion is one of the most common copy number variants in humans. Carriers of the delet...
Background: Dysconnectivity has been consistently proposed as a major key mechanism in psychosis. In...
22q11.2 deletion syndrome (22q11DS) is a genetic disorder associated with a microdeletion of chromos...
AbstractThe 22q11.2 deletion syndrome (22q11DS) is an uncommon genetic disorder with an increased ri...
Background22q11.2 deletion syndrome (22q11DS) is a neurogenetic condition associated with deficits i...
Background: Children with chromosome 22q11.2 deletion syndrome (22q11.2DS) exhibit nonverbal learnin...
22q11.2 Deletion Syndrome is associated with cognitive, behavioural, and psychiatric problems and is...
Large-scale brain networks play a prominent role in cognitive abilities and their activity is impair...
The 22q11.2 deletion (22q11DS) is a common chromosomal microdeletion and a potent risk factor for ps...
The clinical picture associated with 22q11.2 deletion syndrome (22q11DS) includes mild mental retard...
22q11.2 deletion syndrome (22q11DS) is a genetic disorder associated with a microdeletion of chromos...
22q11.2 deletion syndrome (22q11DS) is associated with elevated levels of impulsivity, inattention, ...
The 22q11.2 deletion (22q11DS) is a common chromosomal microdeletion and a potent risk factor for ps...