Abstract Background Pathways leading to psychosis in 22q11.2 deletion syndrome (22q11.2DS) have been the focus of intensive research during the last two decades. One of the common clinical risk factors for the evolution of psychosis in 22q11.2DS is the presence of positive and negative subthreshold psychotic symptoms. The gold standard for measuring subthreshold symptoms is the Structured Interview for Prodromal Syndromes (SIPS) and its accompanying Scale of Prodromal Symptoms (SOPS) ratings. Although the scale has been used by many centers studying 22q11.2DS, the inter-site reliability of the scale in this population has never been established. Methods In the present study, experienced clinical assessors from three large international cent...
22q11.2 deletion syndrome (22q11DS) is a genetic condition associated with a markedly increased risk...
22q11.2 deletion syndrome (22q.11.2DS) might be one of the strongest genetic risk factors for psycho...
Importance: Patients with 22q11.2 deletion syndrome (22q11DS) have an elevated (25%) risk of develop...
BackgroundPathways leading to psychosis in 22q11.2 deletion syndrome (22q11.2DS) have been the focus...
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...
22q11.2 deletion syndrome (22q11DS) is associated with increased risk for schizophrenia. Better iden...
Objective: Genetic syndromes related to psychosis have become increasingly important for exploring t...
BACKGROUND: The 22q11.2 deletion syndrome (22q11DS) is one of the highest known risk factors for sch...
Adults with 22q11.2 Deletion syndrome (22q11DS) have increased prevalence of schizophrenia features....
Individuals with 22q11.2 deletion syndrome (22q11DS) are at increased risk for developing schizophre...
22q11.2 deletion syndrome (22q11.2DS) is a neurogenetic condition associated with increased risk for...
Objectives: 22q11.2 deletion syndrome (22q11DS) is a genetic condition associated with a markedly in...
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...
22q11.2 deletion syndrome (22q11DS) is a genetic condition associated with a markedly increased risk...
22q11.2 deletion syndrome (22q.11.2DS) might be one of the strongest genetic risk factors for psycho...
Importance: Patients with 22q11.2 deletion syndrome (22q11DS) have an elevated (25%) risk of develop...
BackgroundPathways leading to psychosis in 22q11.2 deletion syndrome (22q11.2DS) have been the focus...
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...
22q11.2 deletion syndrome (22q11DS) is associated with increased risk for schizophrenia. Better iden...
Objective: Genetic syndromes related to psychosis have become increasingly important for exploring t...
BACKGROUND: The 22q11.2 deletion syndrome (22q11DS) is one of the highest known risk factors for sch...
Adults with 22q11.2 Deletion syndrome (22q11DS) have increased prevalence of schizophrenia features....
Individuals with 22q11.2 deletion syndrome (22q11DS) are at increased risk for developing schizophre...
22q11.2 deletion syndrome (22q11.2DS) is a neurogenetic condition associated with increased risk for...
Objectives: 22q11.2 deletion syndrome (22q11DS) is a genetic condition associated with a markedly in...
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...
22q11.2 deletion syndrome (22q11DS) is a genetic condition associated with a markedly increased risk...
22q11.2 deletion syndrome (22q.11.2DS) might be one of the strongest genetic risk factors for psycho...
Importance: Patients with 22q11.2 deletion syndrome (22q11DS) have an elevated (25%) risk of develop...