(Q33352752)

26 July 2017

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title

Genes, brain development and psychiatric phenotypes in velo-cardio-facial syndrome (English)

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26 July 2017

3

Stephan Eliez

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26 July 2017

2

Marie Schaer

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26 July 2017

Doron Gothelf

1

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26 July 2017

1 January 2008

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Developmental Disabilities Research Reviews

26 July 2017

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26 July 2017

14

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26 July 2017

59-68

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26 July 2017

1

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A gender-moderated effect of a functional COMT polymorphism on prefrontal brain morphology and function in velo-cardio-facial syndrome (22q11.2 deletion syndrome).

26 July 2017

1 reference

Prevalence of psychiatric disorders in 4 to 16-year-olds with Williams syndrome

21 January 2018

1 reference

Bipolar spectrum disorders in patients diagnosed with velo-cardio-facial syndrome: does a hemizygous deletion of chromosome 22q11 result in bipolar affective disorder?

21 January 2018

1 reference

Polymicrogyria and deletion 22q11.2 syndrome: window to the etiology of a common cortical malformation.

21 January 2018

1 reference

ADHD symptoms in children with FXS.

21 January 2018

1 reference

Impaired activation of face processing networks revealed by functional magnetic resonance imaging in 22q11.2 deletion syndrome.

21 January 2018

1 reference

7 January 2021

Manic symptoms and behavioral dysregulation in youth with velocardiofacial syndrome (22q11.2 deletion syndrome).

1 reference

7 January 2021

Autistic spectrum disorders in velo-cardio facial syndrome (22q11.2 deletion).

1 reference

7 January 2021

Behavior and corpus callosum morphology relationships in velocardiofacial syndrome (22q11.2 deletion syndrome).

1 reference

7 January 2021

ADHD, major depressive disorder, and simple phobias are prevalent psychiatric conditions in youth with velocardiofacial syndrome.

1 reference

7 January 2021

Screening for 22q11 deletions in a schizophrenia population.

1 reference

7 January 2021

Velo-cardio-facial syndrome: Implications of microdeletion 22q11 for schizophrenia and mood disorders

1 reference

7 January 2021

COMT Val108/158 Met modifies mismatch negativity and cognitive function in 22q11 deletion syndrome

1 reference

7 January 2021

Adolescents and young adults with 22q11 deletion syndrome: psychopathology in an at-risk group.

1 reference

7 January 2021

White matter tract alterations in fragile X syndrome: preliminary evidence from diffusion tensor imaging.

1 reference

7 January 2021

Arithmetic ability and parietal alterations: a diffusion tensor imaging study in velocardiofacial syndrome.

1 reference

7 January 2021

Catechol-O-methyl transferase and expression of schizophrenia in 73 adults with 22q11 deletion syndrome

1 reference

7 January 2021

The schizophrenia phenotype in 22q11 deletion syndrome

1 reference

7 January 2021

Cytogenetic Abnormalities in Attention-Deficit/Hyperactivity Disorder

1 reference

7 January 2021

Mapping cortical thickness in children with 22q11.2 deletions

1 reference

7 January 2021

Functional consequences of PRODH missense mutations

1 reference

7 January 2021

Thalamic reductions in children with chromosome 22q11.2 deletion syndrome

1 reference

7 January 2021

Specific cerebellar reductions in children with chromosome 22q11.2 deletion syndrome.

1 reference

7 January 2021

Psychotic illness in people with Prader Willi syndrome due to chromosome 15 maternal uniparental disomy.

1 reference

7 January 2021

Psychiatric morbidity and X-chromosomal origin in a Klinefelter sample.

1 reference

7 January 2021

Velocardiofacial syndrome associated with atrophy of the shoulder girdle muscles and cervicomedullary narrowing.

1 reference

7 January 2021

A population-based study of the 22q11.2 deletion: phenotype, incidence, and contribution to major birth defects in the population

1 reference

7 January 2021

Brain and behaviour in children with 22q11.2 deletion syndrome: a volumetric and voxel-based morphometry MRI study.

1 reference

7 January 2021

Functional analysis of genetic variation in catechol-O-methyltransferase (COMT): effects on mRNA, protein, and enzyme activity in postmortem human brain

1 reference

7 January 2021

Qualitative MRI findings in adults with 22q11 deletion syndrome and schizophrenia

1 reference

7 January 2021

Structural brain abnormalities in patients with schizophrenia and 22q11 deletion syndrome.

1 reference

7 January 2021

Association of Huntington's disease and schizophrenia-like psychosis in a Huntington's disease pedigree

1 reference

7 January 2021

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

1 reference

7 January 2021

Temporal perception in velo-cardio-facial syndrome

1 reference

7 January 2021

Hippocampal volume reduction in 22q11.2 deletion syndrome.

1 reference

7 January 2021

Hippocampal volume reduction in children with chromosome 22q11.2 deletion syndrome is associated with cognitive impairment

1 reference

7 January 2021

Three steps toward improving the measurement of behavior in behavioral phenotype research

1 reference

7 January 2021

Effect of COMT Val108/158 Met genotype on frontal lobe function and risk for schizophrenia

1 reference

7 January 2021

Increased basal ganglia volumes in velo-cardio-facial syndrome (deletion 22q11.2).

1 reference

7 January 2021

Functional brain imaging study of mathematical reasoning abilities in velocardiofacial syndrome (del22q11.2)

1 reference

7 January 2021

Velocardiofacial syndrome: are structural changes in the temporal and mesial temporal regions related to schizophrenia?

1 reference

7 January 2021

Children and adolescents with velocardiofacial syndrome: a volumetric MRI study.

1 reference

7 January 2021

A quantitative MRI study of posterior fossa development in velocardiofacial syndrome

1 reference

7 January 2021

Psychiatric disorders and behavioral problems in children with velocardiofacial syndrome: usefulness as phenotypic indicators of schizophrenia risk.

1 reference

7 January 2021

Autism spectrum disorders and symptoms in children with molecularly confirmed 22q11.2 deletion syndrome

1 reference

7 January 2021

Measuring the thickness of the human cerebral cortex from magnetic resonance images

1 reference

7 January 2021

Isolation and characterization of a novel gene containing WD40 repeats from the region deleted in velo-cardio-facial/DiGeorge syndrome on chromosome 22q11.

1 reference

7 January 2021

The development of face expertise

1 reference

7 January 2021

Brain development during childhood and adolescence: a longitudinal MRI study

1 reference

7 January 2021

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

1 reference

7 January 2021

Structural changes to the fusiform gyrus: A cerebral marker for social impairments in 22q11.2 deletion syndrome?

1 reference

7 January 2021

D(1) receptors in prefrontal cells and circuits

1 reference

7 January 2021

COMT genotype predicts longitudinal cognitive decline and psychosis in 22q11.2 deletion syndrome

1 reference

7 January 2021

Velocardiofacial manifestations and microdeletions in schizophrenic inpatients

1 reference

7 January 2021

Abnormal cortical activation during response inhibition in 22q11.2 deletion syndrome.

1 reference

7 January 2021

Association of the low-activity COMT 158Met allele with ADHD and OCD in subjects with velocardiofacial syndrome

1 reference

7 January 2021

Developmental trajectories of brain structure in adolescents with 22q11.2 deletion syndrome: a longitudinal study

1 reference

7 January 2021

Obsessive-compulsive disorder in patients with velocardiofacial (22q11 deletion) syndrome

1 reference

7 January 2021

Human cerebellar activity reflecting an acquired internal model of a new tool.

1 reference

7 January 2021

Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11.

1 reference

7 January 2021

3-Methoxytyramine Is the Major Metabolite of Released Dopamine in the Rat Frontal Cortex: Reassessment of the Effects of Antipsychotics on the Dynamics of Dopamine Release and Metabolism in the Frontal Cortex, Nucleus Accumbens, and Striatum by a Sim

1 reference

7 January 2021

Inroads to mechanisms of disease in child psychiatric disorders

1 reference

7 January 2021

Frontal and caudate alterations in velocardiofacial syndrome (deletion at chromosome 22q11.2)

1 reference

7 January 2021

Regional cortical white matter reductions in velocardiofacial syndrome: a volumetric MRI analysis.

1 reference

7 January 2021

The neural correlates of non-spatial working memory in velocardiofacial syndrome (22q11.2 deletion syndrome)

1 reference

7 January 2021

Temporal lobe anatomy and psychiatric symptoms in velocardiofacial syndrome (22q11.2 deletion syndrome).

1 reference

7 January 2021

Agenesis of the corpus callosum associated with DiGeorge-velocardiofacial syndrome: a case report and review of the literature

1 reference

7 January 2021

Association of codon 108/158 catechol-O-methyltransferase gene polymorphism with the psychiatric manifestations of velo-cardio-facial syndrome

1 reference

7 January 2021

Differential postnatal development of catecholamine and serotonin inputs to identified neurons in prefrontal cortex of rhesus monkey

1 reference

7 January 2021

Dopamine transporter immunoreactivity in monkey cerebral cortex: regional, laminar, and ultrastructural localization

1 reference

7 January 2021

Genetic variation at the 22q11 PRODH2/DGCR6 locus presents an unusual pattern and increases susceptibility to schizophrenia

1 reference

7 January 2021

Corpus callosum morphology and ventricular size in chromosome 22q11.2 deletion syndrome

1 reference

7 January 2021

Catechol O -methyltransferase val 158 -met genotype and individual variation in the brain response to amphetamine

1 reference

7 January 2021

Prefrontal cortex involvement in processing incorrect arithmetic equations: evidence from event-related fMRI.

1 reference

7 January 2021

Brain anomalies in velo-cardio-facial syndrome.

1 reference

7 January 2021

High rates of schizophrenia in adults with velo-cardio-facial syndrome.

1 reference

7 January 2021

Transcriptional and behavioral interaction between 22q11.2 orthologs modulates schizophrenia-related phenotypes in mice

1 reference

7 January 2021

Children's Self-Reported Psychotic Symptoms and Adult Schizophreniform Disorder

1 reference

7 January 2021

Involvement of hyperprolinemia in cognitive and psychiatric features of the 22q11 deletion syndrome.

1 reference

7 January 2021

Abnormal patterns of cortical gyrification in velo-cardio-facial syndrome (deletion 22q11.2): an MRI study

1 reference

7 January 2021

Visual category-selectivity for faces, places and objects emerges along different developmental trajectories.

1 reference

7 January 2021

The principal features and mechanisms of dopamine modulation in the prefrontal cortex

1 reference

7 January 2021

Abnormalities of the corpus callosum in nonpsychotic children with chromosome 22q11 deletion syndrome.

1 reference

7 January 2021

A review of MRI findings in schizophrenia

1 reference

7 January 2021

Late‐Onset psychosis in the velo‐cardio‐facial syndrome

1 reference

7 January 2021

Volumetric, connective, and morphologic changes in the brains of children with chromosome 22q11.2 deletion syndrome: an integrative study.

1 reference

7 January 2021

Neuromotor deficits in children with the 22q11 deletion syndrome

1 reference

7 January 2021

Mapping continued brain growth and gray matter density reduction in dorsal frontal cortex: Inverse relationships during postadolescent brain maturation.

1 reference

7 January 2021

22q11 deletion syndrome in childhood onset schizophrenia: an update

1 reference

7 January 2021

Intelligence and psychosocial adjustment in velocardiofacial syndrome: a study of 37 children and adolescents with VCFS.

1 reference

7 January 2021

Maturation of brain function associated with response inhibition.

1 reference

7 January 2021

Mapping cortical change in Alzheimer's disease, brain development, and schizophrenia

1 reference

7 January 2021

Brain anatomy in adults with velocardiofacial syndrome with and without schizophrenia: preliminary results of a structural magnetic resonance imaging study.

1 reference

7 January 2021

Structural brain abnormalities associated with deletion at chromosome 22q11: quantitative neuroimaging study of adults with velo-cardio-facial syndrome.

1 reference

7 January 2021

Processing facial emotions in adults with velo-cardio-facial syndrome: functional magnetic resonance imaging.

1 reference

7 January 2021

Effects of a functional COMT polymorphism on brain anatomy and cognitive function in adults with velo-cardio-facial syndrome.

1 reference

7 January 2021

The 22q11.2 deletion in children: high rate of autistic disorders and early onset of psychotic symptoms.

1 reference

7 January 2021

ADHD symptoms and insistence on sameness in Prader-Willi syndrome

1 reference

7 January 2021

Childhood autism and associated comorbidities

1 reference

7 January 2021

Identifiers

DOI

10.1002/DDRR.9

1 reference

26 July 2017

1 reference

PubMed ID

18636637