AbstractDysfunction of cerebral white matter (WM) is a potential factor underlying the neurobiology of schizophrenia. People with 22q11 deletion syndrome have altered brain morphology and increased risk for schizophrenia, therefore decreased WM integrity may be related to schizophrenia in 22q11DS. We measured fractional anisotropy (FA) and WM volume in 27 adults with 22q11DS with schizophrenia (n=12, 22q11DS SCZ+) and without schizophrenia (n=15, 22q11DS SCZ−), 12 individuals with idiopathic schizophrenia and 31 age-matched healthy controls. We found widespread decreased WM volume in posterior and temporal brain areas and decreased FA in areas of the frontal cortex in the whole 22q11DS group compared to healthy controls. In 22q11DS SCZ+ com...
Background: Chromosome 22q11.2 deletion syndrome (22q11.2DS) is a neurogenetic disorder that is asso...
The 22q11.2 deletion syndrome (22q11DS) is a widely recognized genetic model allowing the study of n...
The 22q11.2 deletion (22q11DS) is a common chromosomal microdeletion and a potent risk factor for ps...
Individuals with 22q11.2 deletion syndrome (22q11.2DS) evince a 30% incidence of schizophrenia. We c...
22q11.2 deletion syndrome (22q11DS)—a neurodevelopmental condition caused by a hemizygous deletion o...
Young people with 22q11 Deletion Syndrome (22q11DS) are at substantial risk for developing psychosis...
Background Patients with a deletion at chromosome 22q11.2 (22q11DS) have 30% lifetime risk of develo...
Background—The 22q11.2 Deletion Syndrome (22q11.2DS) is regarded as an etiologically homogenous mode...
22q11.2 deletion syndrome (22q11DS)—a neurodevelopmental condition caused by a hemizygous deletion o...
The 22q11.2 deletion syndrome (22q11DS) is a widely recognized genetic model allowing the study of n...
22q11.2 deletion syndrome (22q11DS)-a neurodevelopmental condition caused by a hemizygous deletion o...
22q11.2 deletion syndrome (22q11DS)-a neurodevelopmental condition caused by a hemizygous deletion o...
Disruptions of white matter microstructure have been widely reported in schizophrenia. However, the ...
The 22q11.2 deletion syndrome (22q11DS) is a widely recognized genetic model allowing the study of n...
22q11.2 deletion syndrome (22q11DS) is associated with an increased susceptibility to develop schizo...
Background: Chromosome 22q11.2 deletion syndrome (22q11.2DS) is a neurogenetic disorder that is asso...
The 22q11.2 deletion syndrome (22q11DS) is a widely recognized genetic model allowing the study of n...
The 22q11.2 deletion (22q11DS) is a common chromosomal microdeletion and a potent risk factor for ps...
Individuals with 22q11.2 deletion syndrome (22q11.2DS) evince a 30% incidence of schizophrenia. We c...
22q11.2 deletion syndrome (22q11DS)—a neurodevelopmental condition caused by a hemizygous deletion o...
Young people with 22q11 Deletion Syndrome (22q11DS) are at substantial risk for developing psychosis...
Background Patients with a deletion at chromosome 22q11.2 (22q11DS) have 30% lifetime risk of develo...
Background—The 22q11.2 Deletion Syndrome (22q11.2DS) is regarded as an etiologically homogenous mode...
22q11.2 deletion syndrome (22q11DS)—a neurodevelopmental condition caused by a hemizygous deletion o...
The 22q11.2 deletion syndrome (22q11DS) is a widely recognized genetic model allowing the study of n...
22q11.2 deletion syndrome (22q11DS)-a neurodevelopmental condition caused by a hemizygous deletion o...
22q11.2 deletion syndrome (22q11DS)-a neurodevelopmental condition caused by a hemizygous deletion o...
Disruptions of white matter microstructure have been widely reported in schizophrenia. However, the ...
The 22q11.2 deletion syndrome (22q11DS) is a widely recognized genetic model allowing the study of n...
22q11.2 deletion syndrome (22q11DS) is associated with an increased susceptibility to develop schizo...
Background: Chromosome 22q11.2 deletion syndrome (22q11.2DS) is a neurogenetic disorder that is asso...
The 22q11.2 deletion syndrome (22q11DS) is a widely recognized genetic model allowing the study of n...
The 22q11.2 deletion (22q11DS) is a common chromosomal microdeletion and a potent risk factor for ps...