Background: Chromosome 22q11.2 deletion syndrome (22q11.2DS) is a neurogenetic disorder that is associated with a 25-fold increase in schizophrenia. Both individuals with 22q11.2DS and those with schizophrenia present with social cognitive deficits, which are putatively subserved by a network of brain regions that are involved in the processing of social cognitive information. This study used two-tensor tractography to examine the white matter tracts believed to underlie the social brain network in a group of 57 young adults with 22q11.2DS compared to 30 unaffected controls. Results: Results indicated that relative to controls, participants with 22q11.2DS showed significant differences in several DTI metrics within the inferior fronto-occip...
The 22q11.2 deletion syndrome (22q11DS) is a widely recognized genetic model allowing the study of n...
BACKGROUND: Social impairments are described as a common feature of the 22q11.2 deletion syndrome (2...
22q11.2 deletion syndrome (22q11DS)—a neurodevelopmental condition caused by a hemizygous deletion o...
22q11.2 Microdeletion Syndrome (22q11DS) is a highly penetrant genetic mutation associated with a si...
Identifying the neural underpinnings of socio-emotional deficits in 22q11.2 deletion syndrome (22q11...
AIM: The 22q11.2 deletion (22q11DS) syndrome is a neurogenetic condition marked by social dysfunctio...
22q11.2 Microdeletion syndrome (22qDS) is caused by a recurrent genetic mutation associated with a h...
22q11.2 deletion syndrome (22q11DS) is a genetic mutation associated with disorders of cortical conn...
Background 22q11.2 Deletion Syndrome (22q11DS) represents one of the most important genetic risk fa...
Background: Dysconnectivity has been consistently proposed as a major key mechanism in psychosis. In...
The 22q11.2 deletion is one of the most common copy number variants in humans. Carriers of the delet...
Large-scale brain networks play a prominent role in cognitive abilities and their activity is impair...
22q11.2 Deletion Syndrome is associated with cognitive, behavioural, and psychiatric problems and is...
<div><p>The 22q11.2 deletion syndrome (22q11DS) is a widely recognized genetic model allowing the st...
22q11.2 Microdeletion Syndrome (22q11DS) is a highly penetrant genetic mutation associated with a si...
The 22q11.2 deletion syndrome (22q11DS) is a widely recognized genetic model allowing the study of n...
BACKGROUND: Social impairments are described as a common feature of the 22q11.2 deletion syndrome (2...
22q11.2 deletion syndrome (22q11DS)—a neurodevelopmental condition caused by a hemizygous deletion o...
22q11.2 Microdeletion Syndrome (22q11DS) is a highly penetrant genetic mutation associated with a si...
Identifying the neural underpinnings of socio-emotional deficits in 22q11.2 deletion syndrome (22q11...
AIM: The 22q11.2 deletion (22q11DS) syndrome is a neurogenetic condition marked by social dysfunctio...
22q11.2 Microdeletion syndrome (22qDS) is caused by a recurrent genetic mutation associated with a h...
22q11.2 deletion syndrome (22q11DS) is a genetic mutation associated with disorders of cortical conn...
Background 22q11.2 Deletion Syndrome (22q11DS) represents one of the most important genetic risk fa...
Background: Dysconnectivity has been consistently proposed as a major key mechanism in psychosis. In...
The 22q11.2 deletion is one of the most common copy number variants in humans. Carriers of the delet...
Large-scale brain networks play a prominent role in cognitive abilities and their activity is impair...
22q11.2 Deletion Syndrome is associated with cognitive, behavioural, and psychiatric problems and is...
<div><p>The 22q11.2 deletion syndrome (22q11DS) is a widely recognized genetic model allowing the st...
22q11.2 Microdeletion Syndrome (22q11DS) is a highly penetrant genetic mutation associated with a si...
The 22q11.2 deletion syndrome (22q11DS) is a widely recognized genetic model allowing the study of n...
BACKGROUND: Social impairments are described as a common feature of the 22q11.2 deletion syndrome (2...
22q11.2 deletion syndrome (22q11DS)—a neurodevelopmental condition caused by a hemizygous deletion o...