Annotation: velo-cardio-facial syndrome (Q36118609)

12 August 2017

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title

Annotation: velo-cardio-facial syndrome (English)

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12 August 2017

Murphy KC

1

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12 August 2017

1 June 2005

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The Journal of Child Psychology and Psychiatry

12 August 2017

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12 August 2017

46

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12 August 2017

563-571

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12 August 2017

6

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Screening for 22q11 deletions in a schizophrenia population.

12 August 2017

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.00408.X

Investigation of white matter structure in velocardiofacial syndrome: a diffusion tensor imaging study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.00408.X

The schizophrenia phenotype in 22q11 deletion syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.00408.X

22q11 deletion syndrome in adults with schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.00408.X

The neurocognitive phenotype of the 22q11.2 deletion syndrome: selective deficit in visual-spatial memory.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.00408.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.00408.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.00408.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.00408.X

Analysis of speech characteristics in children with velocardiofacial syndrome (VCFS) and children with phenotypic overlap without VCFS

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.00408.X

Possible role for COMT in psychosis associated with velo-cardio-facial syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.00408.X

Parental origin of the deletion 22q11.2 and brain development in velocardiofacial syndrome: a preliminary study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.00408.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.00408.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.00408.X

Language skills in children with velocardiofacial syndrome (deletion 22q11.2).

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.00408.X

The gene encoding proline dehydrogenase modulates sensorimotor gating in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.00408.X

Velo-cardio-facial syndrome: a review of 120 patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.00408.X

Clinical characteristics of schizophrenia associated with velo-cardio-facial syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.00408.X

An investigation of the neuropsychological profile in adults with velo-cardio-facial syndrome (VCFS).

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.00408.X

Genome scan meta-analysis of schizophrenia and bipolar disorder, part II: Schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.00408.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.00408.X

Brain anomalies in velo-cardio-facial syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.00408.X

Psychoeducational profile of the 22q11.2 microdeletion: A complex pattern.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.00408.X

An SNP map of human chromosome 22.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.00408.X

Schizophrenia and velo-cardio-facial syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.00408.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.00408.X

Velo-cardio-facial syndrome: a model for understanding the genetics and pathogenesis of schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.00408.X

Neuropsychiatric disorders in the 22q11 deletion syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.00408.X

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

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.00408.X

Early speech and language development in children with velocardiofacial syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.00408.X

A combined analysis of D22S278 marker alleles in affected sib-pairs: support for a susceptibility locus for schizophrenia at chromosome 22q12. Schizophrenia Collaborative Linkage Group (Chromosome 22).

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.00408.X

Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: genomic organization and deletion endpoint analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.00408.X

Communication issues in 22q11.2 deletion syndrome: children at risk.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.00408.X

Neuropsychological, learning and psychosocial profile of primary school aged children with the velo-cardio-facial syndrome (22q11 deletion): evidence for a nonverbal learning disability?

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.00408.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.00408.X

Research on behavioral phenotypes: velocardiofacial syndrome (deletion 22q11.2).

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.00408.X

Association between PRODH and schizophrenia is not confirmed

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.00408.X

Neuropsychological profile of children and adolescents with the 22q11.2 microdeletion.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.00408.X

Chromosome 22q11 deletions, velo-cardio-facial syndrome and early-onset psychosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.00408.X

22q11 deletion syndrome in childhood onset schizophrenia: an update

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.00408.X

10.1111/J.1469-7610.2005.00408.X

21 January 2018

Identifiers

DOI

1 reference

12 August 2017

1 reference

PubMed ID

15877762