Psychotic symptoms in children and adolescents with 22q11.2 deletion syndrome: Neuropsychological and behavioral implications.

No abstract is available for this paper.

• Publication year

  2006

• Venue

  Schizophrenia Research

• Publication date

  2006-06-01

• Fields of study

  Medicine, Psychology

• Identifiers
  DOI 10.1016/J.SCHRES.2006.01.019PMID 16545541
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• No evidence for an effect of COMT Val158Met genotype on executive function in patients with 22q11 deletion syndrome.

  2006cited by this paper
• Annotation: velo-cardio-facial syndrome.

  2005cited by this paper
• Predicting schizophrenia: findings from the Edinburgh High-Risk Study

  2005cited by this paper
• Adolescents and young adults with 22qll deletion syndrome: psychopathology in an at-risk group

  2005cited by this paper
• Differential patterns of premorbid academic and social deterioration in patients with schizophrenia.

  2005cited by this paper
• COMT genotype predicts longitudinal cognitive decline and psychosis in 22q11.2 deletion syndrome

  2005cited by this paper
• Memory impairments identified in people at ultra-high risk for psychosis who later develop first-episode psychosis.

  2005cited by this paper
• Neuropsychological deficits in children associated with increased familial risk for schizophrenia.

  2004cited by this paper
• The schizophrenia phenotype in 22q11 deletion syndrome.

  2003cited by this paper
• Evidence for early-childhood, pan-developmental impairment specific to schizophreniform disorder: results from a longitudinal birth cohort.

  2002cited by this paper
• Schizotypal components in people at high risk of developing schizophrenia: early findings from the Edinburgh High-Risk Study

  2002cited by this paper
• Childhood behaviour, psychotic symptoms and psychosis onset in young people at high risk of schizophrenia: early findings from the Edinburgh High Risk Study

  2002cited by this paper
• The Neurocognitive Phenotype of the 22Q11.2 Deletion Syndrome: Selective Deficit in Visual-Spatial Memory

  2001cited by this paper
• Children's self-reported psychotic symptoms and adult schizophreniform disorder: a 15-year longitudinal study.

  2000cited by this paper
• Attention, memory, and motor skills as childhood predictors of schizophrenia-related psychoses: the New York High-Risk Project.

  2000cited by this paper
• High rates of schizophrenia in adults with velo-cardio-facial syndrome.

  1999cited by this paper
• Schedule for Affective Disorders and Schizophrenia for School-Age Children-Present and Lifetime Version (K-SADS-PL): initial reliability and validity data.

  1997cited by this paper
• IQ and risk for schizophrenia: a population-based cohort study

  1997cited by this paper
• Human catechol-O-methyltransferase pharmacogenetics: description of a functional polymorphism and its potential application to neuropsychiatric disorders.

  1996cited by this paper
• Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11.

  1995cited by this paper
• Putatively psychosis-prone subjects 10 years later.

  1994cited by this paper
• Evaluation in an inpatient setting of DTREE, a computer-assisted diagnostic assessment procedure.

  1993cited by this paper
• Late-onset psychosis in the velo-cardio-facial syndrome.

  1992cited by this paper
• Manual for the child behavior checklist/4-18 and 1991 profile

  1991cited by this paper
• Towards a Neuropsychology of Schizophrenia

  1988cited by this paper

• Adaptive and Behavioral Phenotype in Pediatric 22q11.2 Deletion Syndrome: Characterizing a High-Risk Neurogenetic Copy Number Variant.

  2026cites this paper
• Review of the Pathophysiology and Clinical Manifestations of 22q11.2 Deletion and Duplication Syndromes

  2025cites this paper
• Genetics and Schizophrenia

  2024cites this paper
• Multiscale characterization of cortical signatures in positive and negative schizotypy: A worldwide ENIGMA study

  2024cites this paper
• Psychosis

  2023cites this paper
• Adaptive living skills, sleep problems, and mental health disorders in adults with 22q11.21 deletion syndrome.

  2023cites this paper
• Adaptive behavior deficits in individuals with 3q29 deletion syndrome

  2023cites this paper
• Psychotic symptoms and its associated factors relating to psychoactive substance use among the youth population in Northwest Ethiopia

  2023cites this paper
• Adaptive behaviour deficits in individuals with 3q29 deletion syndrome.

  2023cites this paper
• Updated clinical practice recommendations for managing children with 22q11.2 deletion syndrome.

  2023cites this paper
• Synaptic Plasticity Dysfunctions in the Pathophysiology of 22q11 Deletion Syndrome: Is There a Role for Astrocytes?

  2022cites this paper
• Psychosis spectrum symptoms among individuals with schizophrenia-associated copy number variants and evidence of cerebellar correlates of symptom severity

  2022cites this paper
• A cross-comparison of cognitive ability across 8 genomic disorders.

  2021cites this paper
• Developmental trajectories and brain correlates of Directed Forgetting in 22q11.2 deletion syndrome.

  2021cites this paper
• Abnormal Development and Dysconnectivity of Distinct Thalamic Nuclei in Patients With 22q11.2 Deletion Syndrome Experiencing Auditory Hallucinations.

  2020cites this paper
• Social cognition in 22q11.2 deletion syndrome and idiopathic developmental neuropsychiatric disorders

  2020cites this paper
• Defects in thymic development

  2020cites this paper
• Vulnerability to Psychosis: A Psychoanalytical Perspective. The Paradigmatic Example of 22q11.2 Microdeletion Syndrome

  2020cites this paper
• Efficacy of Low-Dose Aripiprazole for Treatment of Psychotic Symptoms in a Patient with 22q11.2 Deletion Syndrome.

  2020cites this paper
• Prevalence, course and psychosis-predictive value of negative symptoms in 22q11.2 deletion syndrome.

  2019cites this paper
• Positive psychotic symptoms are associated with divergent developmental trajectories of hippocampal volume during late adolescence in patients with 22q11DS

  2019cites this paper
• Kliniese kenmerke van Afrikaner-skisofreniepasiënte

  2019cites this paper
• Genetiese bevindings in ‘n groep Afrikaners met skisofrenie

  2019cites this paper
• Agtergrond as rigtingaanwyser

  2019cites this paper
• Vroeë afwykende niepsigotiese gedrag in skisofrenie

  2019cites this paper
• Vatbaarheid vir skisofrenie by 22q11.2-mikroweglatings

  2019cites this paper
• An implicit and reliable neural measure quantifying impaired visual coding of facial expression: evidence from the 22q11.2 deletion syndrome

  2019cites this paper
• Alteration of functional brain architecture in 22q11.2 deletion syndrome - Insights into susceptibility for psychosis

  2019cites this paper
• Neurocognitive profile and onset of psychosis symptoms in children, adolescents and young adults with 22q11 deletion syndrome: A longitudinal study.

  2019cites this paper
• Spesifieke chromosoomgebiede en/of kandidaatgene geïdentifiseer by skisofrenie

  2019cites this paper
• Nader aan die siekbed

  2019cites this paper
• Genetic Basis of Auditory Verbal Hallucinations in Schizophrenia

  2018cites this paper
• 22q11 microdeletion syndrome and ultra‐high risk for psychosis: The role of neurological soft signs as an independent marker of vulnerability for psychosis

  2018cites this paper
• Remarques épistémologiques et cliniques sur la notion de vulnérabilité psychotique

  2018cites this paper
• Time-based prospective memory in children and adolescents with 22q11.2 deletion syndrome

  2018cites this paper
• Overview of Social Cognitive Dysfunctions in Rare Developmental Syndromes With Psychiatric Phenotype

  2018cites this paper
• Caracterización fenotípica de una muestra clínica de pacientes con síndrome de deleción 22q11

  2017cites this paper
• No age effect in the prevalence and clinical significance of ultra-high risk symptoms and criteria for psychosis in 22q11 deletion syndrome: Confirmation of the genetically driven risk for psychosis?

  2017cites this paper
• Implication of reward alterations in the expression of negative symptoms in 22q11.2 deletion syndrome: a behavioural and DTI study

  2017cites this paper
• Dilated Cardiomyopathy due to Hypocalcemia Secondary to Congenital Hypoparathyroidism in a Newborn with DiGeorge Syndrome

  2017cites this paper
• 22q11.2 deletion syndrome lowers seizure threshold in adult patients without epilepsy

  2017cites this paper
• Social cognitive impairment in 22q11 deletion syndrome: A review.

  2017cites this paper
• Multimodal investigation of triple network connectivity in patients with 22q11DS and association with executive functions

  2017cites this paper
• Visual processing deficits in 22q11.2 Deletion Syndrome

  2017cites this paper
• Working Memory Impairments in Chromosome 22q11.2 Deletion Syndrome: The Roles of Anxiety and Stress Physiology

  2017cites this paper
• Neurocognitive and Social Cognitive Impairments in Early-Onset Psychosis and At-Risk Youth: Implications for Intervention Strategies

  2017cites this paper
• Cortical-amygdala volumetric ratios predict onset of symptoms of psychosis in 22q11.2 deletion syndrome.

  2017cites this paper
• Negative and paranoid symptoms are associated with negative performance beliefs and social cognition in 22q11.2 deletion syndrome

  2017cites this paper
• Prospective memory in 22q11.2 DS 1 Time-based prospective memory in children and adolescents with 22q11.2 deletion syndrome

  2017cites this paper
• Ultra high risk status and transition to psychosis in 22q11.2 deletion syndrome

  2016cites this paper
• Chapter 9 – Schizophrenia

  2016cites this paper
• Cognitive behavioral therapy in 22q11.2 microdeletion with psychotic symptoms: What do we learn from schizophrenia?

  2016cites this paper
• CASE REPORT OF SMITH-MAGENIS SYNDROME IN LITHUANIAN UNIVERSITY OF HEALTH SCIENCES

  2016cites this paper
• Genetic Consideration of Schizotypal Traits: A Review

  2016cites this paper
• Associations between social cognition, skills, and function and subclinical negative and positive symptoms in 22q11.2 deletion syndrome

  2016cites this paper
• Visual processing of emotional dynamic faces in 22q11.2 deletion syndrome.

  2016cites this paper
• Facial emotion perception by intensity in children and adolescents with 22q11.2 deletion syndrome

  2016cites this paper
• Cognitive phenotype and psychiatric disorder in 22q11.2 deletion syndrome: A review.

  2016cites this paper
• Neurocognitive profile in psychotic versus nonpsychotic individuals with 22q11.2 deletion syndrome.

  2016cites this paper
• Social cognitive training in adolescents with chromosome 22q11.2 deletion syndrome: feasibility and preliminary effects of the intervention.

  2015cites this paper
• Schizotypal traits in adolescents with 22q11.2 deletion syndrome: validity, reliability and risk for psychosis

  2015cites this paper
• [Neurocognitive and psychiatric management of the 22q11.2 deletion syndrome].

  2015cites this paper
• Developmental Trajectories in 22q11.2 Deletion

  2015cites this paper
• Identifying patterns of anxiety and depression in children with chromosome 22q11.2 deletion syndrome: comorbidity predicts behavioral difficulties and impaired functional communications.

  2015cites this paper
• Developmental trajectories in 22q11.2 deletion syndrome

  2015cites this paper
• Expression of Parkinson's disease and associated neurophenotypes in 22q11.2 deletion syndrome

  2015cites this paper
• POLIMORFIZM KATECHOLO-O-METYLOTRANSFERAZY (COMT) ORAZ RECEPTORÓW DOPAMINY (DRD1, DRD4) W ETIOLOGII I TERAPII STANU PRZEDRZUCAWKOWEGO

  2014cites this paper
• Deviant dynamics of EEG resting state pattern in 22q11.2 deletion syndrome adolescents: A vulnerability marker of schizophrenia?

  2014cites this paper
• Predominant negative symptoms in 22q11.2 deletion syndrome and their associations with cognitive functioning and functional outcome.

  2014cites this paper
• The 22q11.2 deletion syndrome as a window into complex neuropsychiatric disorders over the lifespan.

  2014cites this paper
• Defects in Thymic Development: DiGeorge/CHARGE/Chromosome 22q11.2 Deletion

  2014cites this paper
• Genetically modified mice related to schizophrenia and other psychoses: seeking phenotypic insights into the pathobiology and treatment of negative symptoms.

  2014cites this paper
• Molecular Screening for 22 Q 11 . 2 Deletion Syndrome in Patients With Congenital Heart Disease

  2014cites this paper
• Molecular Screening for 22Q11.2 Deletion Syndrome in Patients With Congenital Heart Disease

  2014cites this paper
• Reduced Fronto-Temporal and Limbic Connectivity in the 22q11.2 Deletion Syndrome: Vulnerability Markers for Developing Schizophrenia?

  2013cites this paper
• Graph theory reveals dysconnected hubs in 22q11DS and altered nodal efficiency in patients with hallucinations

  2013cites this paper
• Clinical and cognitive risk factors for psychotic symptoms in 22q11.2 deletion syndrome: a transversal and longitudinal approach

  2013cites this paper
• 22q11 deletion syndrome: a review of the neuropsychiatric features and their neurobiological basis

  2013cites this paper
• The genomics of schizophrenia: update and implications.

  2013cites this paper
• Action simulation in hallucination-prone adolescents

  2013cites this paper
• Structural abnormalities in cortical volume, thickness, and surface area in 22q11.2 microdeletion syndrome: Relationship with psychotic symptoms☆

  2013cites this paper
• Prodromal and autistic symptoms in schizotypal personality disorder and 22q11.2 deletion syndrome.

  2013cites this paper
• Discussing the psychiatric manifestations of 22q11.2 deletion syndrome: an exploration of clinical practice among medical geneticists

  2013cites this paper
• Feasibility and preliminary efficacy data from a computerized cognitive intervention in children with chromosome 22q11.2 deletion syndrome.

  2013cites this paper
• Subtypes in 22q11.2 deletion syndrome associated with behaviour and neurofacial morphology.

  2013cites this paper
• Copy number variation at 22q11.2: from rare variants to common mechanisms of developmental neuropsychiatric disorders

  2013cites this paper
• Risk factors and the evolution of psychosis in 22q11.2 deletion syndrome: a longitudinal 2-site study.

  2013cites this paper
• Altered auditory processing in frontal and left temporal cortex in 22q11.2 deletion syndrome: a group at high genetic risk for schizophrenia.

  2013cites this paper
• 1 , 3-10 AN OVERVIEW OF CORRELATIONS BETWEEN SCHIZOPHRENIA AND 22 Q 11 . 2 DELETION SYNDROME

  2013influential citation
• Psychotic like experiences and 22q11 microdeletion syndrome: two possible models for the investigation of gene-enviroment interaction in psychotic onset

  2013cites this paper
• Analyzing quantitatively and topologically the white matter organization in 22Q11.2 deletion syndrome

  2013cites this paper
• Cognition, psychopathology and the role of genetic variation in Catechol-O-Methyltransferase in children at increased risk of schizophrenia

  2013cites this paper
• An overview of correlations between schizophrenia and 22q11.2 deletion syndrome

  2013cites this paper
• 22q11 deletion syndrome: a review of the neuropsychiatric features and their neurobiological basis

  2013cites this paper
• 22q11 deletion syndrome: a review of the neuropsychiatric features and their neurobiological basis

  2013cites this paper
• Mouse Models of 22q11.2-Associated Autism Spectrum Disorder

  2012cites this paper
• Is there a core neuropsychiatric phenotype in 22q11.2 deletion syndrome?

  2012cites this paper
• Alterations of social interaction through genetic and environmental manipulation of the 22q11.2 gene Sept5 in the mouse brain.

  2012cites this paper
• Adolescents at ultra-high risk for psychosis with and without 22q11 deletion syndrome: a comparison of prodromal psychotic symptoms and general functioning.

  2012cites this paper
• Wybrane zagadnienia z immunologii klinicznej – inne zdefiniowane niedobory odporności (część II)

  2012cites this paper