Nearly one-third of individuals with 22q11.2 deletion syndrome (22q11.2DS) develop a psychotic disorder during life, most of them by early adulthood. Importantly, a full-blown psychotic episode is usually preceded by subthreshold symptoms. In the current study, 760 participants (aged 6-55 years) with a confirmed hemizygous 22q11.2 microdeletion have been recruited through 10 medical sites worldwide, as part of an international research consortium. Of them, 692 were nonpsychotic and with complete measurement data. Subthreshold psychotic symptoms were assessed using the Structured Interview for Prodromal Syndromes (SIPS). Nearly one-third of participants met criteria for positive subthreshold psychotic symptoms (32.8%), less than 1% qualified...
Objective: Genetic syndromes related to psychosis have become increasingly important for exploring t...
ObjectiveChromosome 22q11.2 deletion syndrome is a neurogenetic disorder associated with high rates ...
Objective: Chromosome 22q11.2 deletion syndrome is a neurogenetic disorder associated with high rate...
Nearly one-third of individuals with 22q11.2 deletion syndrome (22q11.2DS) develop a psychotic disor...
Nearly one-third of individuals with 22q11.2 deletion syndrome (22q11.2DS) develop a psychotic disor...
Abstract Background Pathways leading to psychosis in 22q11.2 deletion syndrome (22q11.2DS) have been...
BackgroundPathways leading to psychosis in 22q11.2 deletion syndrome (22q11.2DS) have been the focus...
22q11.2 deletion syndrome (22q11DS) is associated with increased risk for schizophrenia. Better iden...
Individuals with 22q11.2 Deletion Syndrome (22q11.2DS) are at substantially heightened risk for psy...
IMPORTANCE Patients with 22q11.2 deletion syndrome (22q11DS) have an elevated (25%) risk of developi...
ImportancePatients with 22q11.2 deletion syndrome (22q11DS) have an elevated (25%) risk of developin...
The present study sought to examine the longitudinal psychoeducational, neurocognitive, and psychiat...
Importance: Patients with 22q11.2 deletion syndrome (22q11DS) have an elevated (25%) risk of develop...
Individuals with 22q11.2 deletion syndrome (22q11DS) are at increased risk for developing schizophre...
Patients with 22q11.2 deletion syndrome (22q11DS) have an elevated (25%) risk for developing schizop...
Objective: Genetic syndromes related to psychosis have become increasingly important for exploring t...
ObjectiveChromosome 22q11.2 deletion syndrome is a neurogenetic disorder associated with high rates ...
Objective: Chromosome 22q11.2 deletion syndrome is a neurogenetic disorder associated with high rate...
Nearly one-third of individuals with 22q11.2 deletion syndrome (22q11.2DS) develop a psychotic disor...
Nearly one-third of individuals with 22q11.2 deletion syndrome (22q11.2DS) develop a psychotic disor...
Abstract Background Pathways leading to psychosis in 22q11.2 deletion syndrome (22q11.2DS) have been...
BackgroundPathways leading to psychosis in 22q11.2 deletion syndrome (22q11.2DS) have been the focus...
22q11.2 deletion syndrome (22q11DS) is associated with increased risk for schizophrenia. Better iden...
Individuals with 22q11.2 Deletion Syndrome (22q11.2DS) are at substantially heightened risk for psy...
IMPORTANCE Patients with 22q11.2 deletion syndrome (22q11DS) have an elevated (25%) risk of developi...
ImportancePatients with 22q11.2 deletion syndrome (22q11DS) have an elevated (25%) risk of developin...
The present study sought to examine the longitudinal psychoeducational, neurocognitive, and psychiat...
Importance: Patients with 22q11.2 deletion syndrome (22q11DS) have an elevated (25%) risk of develop...
Individuals with 22q11.2 deletion syndrome (22q11DS) are at increased risk for developing schizophre...
Patients with 22q11.2 deletion syndrome (22q11DS) have an elevated (25%) risk for developing schizop...
Objective: Genetic syndromes related to psychosis have become increasingly important for exploring t...
ObjectiveChromosome 22q11.2 deletion syndrome is a neurogenetic disorder associated with high rates ...
Objective: Chromosome 22q11.2 deletion syndrome is a neurogenetic disorder associated with high rate...