(Q36772016)

English

A review of neurocognitive and behavioral profiles associated with 22q11 deletion syndrome: implications for clinical evaluation and treatment

scientific article published on April 2007

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scholarly article

1 reference

Europe PubMed Central

16 August 2017

1 reference

Europe PubMed Central

A review of neurocognitive and behavioral profiles associated with 22q11 deletion syndrome: implications for clinical evaluation and treatment (English)

1 reference

Europe PubMed Central

16 August 2017

22q11 deletion syndrome

1 reference

based on heuristic

inferred from title

author name string

Opal Ousley

1

1 reference

Europe PubMed Central

16 August 2017

Kimberly Rockers

2

1 reference

Europe PubMed Central

16 August 2017

Mary Lynn Dell

3

1 reference

Europe PubMed Central

16 August 2017

Karlene Coleman

4

1 reference

Europe PubMed Central

16 August 2017

Joseph F Cubells

5

1 reference

Europe PubMed Central

16 August 2017

language of work or name

0 references

publication date

1 April 2007

1 reference

Europe PubMed Central

16 August 2017

Current Psychiatry Reports

1 reference

Europe PubMed Central

16 August 2017

9

1 reference

Europe PubMed Central

16 August 2017

148-158

1 reference

Europe PubMed Central

16 August 2017

2

1 reference

Europe PubMed Central

16 August 2017

https://scigraph.springernature.com/pub.10.1007/s11920-007-0085-8

0 references

Velo-cardio-facial syndrome: a distinctive behavioral phenotype

1 reference

https://api.crossref.org/works/10.1007%2FS11920-007-0085-8

21 January 2018

Minor physical anomalies and their relationship to the aetiology of schizophrenia.

1 reference

https://api.crossref.org/works/10.1007%2FS11920-007-0085-8

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS11920-007-0085-8

21 January 2018

Health, education, work, and independence of young adults with disabilities

1 reference

https://api.crossref.org/works/10.1007%2FS11920-007-0085-8

21 January 2018

Thyroid abnormalities as a feature of DiGeorge syndrome: a patient report and review of the literature.

1 reference

https://api.crossref.org/works/10.1007%2FS11920-007-0085-8

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS11920-007-0085-8

21 January 2018

Cognitive deficits associated with schizophrenia in velo-cardio-facial syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/17389127

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dysphagia in children with a 22q11.2 deletion: unusual pattern found on modified barium swallow

1 reference

https://pubmed.ncbi.nlm.nih.gov/17389127

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Psychotic illness in patients diagnosed with velo-cardio-facial syndrome and their relatives

1 reference

https://pubmed.ncbi.nlm.nih.gov/17389127

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic abnormalities of chromosome 22 and the development of psychosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/17389127

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prevalence of ADHD in children with velocardiofacial syndrome: a preliminary report.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17389127

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17389127

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Velo-cardio-facial syndrome: language and psychological profiles.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17389127

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neuropsychological characteristics of children with the 22q11 Deletion Syndrome: a descriptive analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/17389127

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prevalence and clinical manifestations of 22q11.2 microdeletion in adults with selected conotruncal anomalies

1 reference

https://pubmed.ncbi.nlm.nih.gov/17389127

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetics of childhood disorders: XXV. Velocardiofacial syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/17389127

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deletions and microdeletions of 22q11.2 in velo-cardio-facial syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/17389127

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17389127

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Schizophrenia, CATCH 22 and FISH

1 reference

https://pubmed.ncbi.nlm.nih.gov/17389127

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Velocardiofacial syndrome in childhood-onset schizophrenia.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17389127

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17389127

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17389127

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prevalence of intellectual disability and comorbid mental illness in an Australian community sample.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17389127

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17389127

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Annotation: velo-cardio-facial syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/17389127

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cognitive and behavior profile of preschool children with chromosome 22q11.2 deletion.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17389127

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

22q11 deletion syndrome in adults with schizophrenia

1 reference

https://pubmed.ncbi.nlm.nih.gov/17389127

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17389127

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The neuropsychological phenotype of velocardiofacial syndrome (VCFS): relationship to psychopathology.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17389127

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17389127

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neuropsychiatric disorders in the 22q11 deletion syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/17389127

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17389127

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neuropsychological profile and neuroimaging in patients with 22Q11.2 Deletion Syndrome: a review

1 reference

https://pubmed.ncbi.nlm.nih.gov/17389127

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Can we improve the diagnostic efficiency and predictive power of prodromal symptoms for schizophrenia?

1 reference

https://pubmed.ncbi.nlm.nih.gov/17389127

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Velo-cardio-facial syndrome associated with chromosome 22 deletions encompassing the DiGeorge locus

1 reference

https://pubmed.ncbi.nlm.nih.gov/17389127

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17389127

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

22q11 deletion syndrome: a genetic subtype of schizophrenia

1 reference

https://pubmed.ncbi.nlm.nih.gov/17389127

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Incidence and prevalence of the 22q11 deletion syndrome: a population-based study in Western Sweden

1 reference

https://pubmed.ncbi.nlm.nih.gov/17389127

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Early motor development in young children with 22q.11 deletion syndrome and a conotruncal heart defect.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17389127

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Velo-cardio-facial syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17389127

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular analysis of velo-cardio-facial syndrome patients with psychiatric disorders.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17389127

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DiGeorge syndrome: new insights

1 reference

https://pubmed.ncbi.nlm.nih.gov/17389127

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17389127

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17389127

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Microdeletions within 22q11 associated with sporadic and familial DiGeorge syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17389127

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17389127

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Defining the clinical spectrum of deletion 22q11.2

1 reference

https://pubmed.ncbi.nlm.nih.gov/17389127

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17389127

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Predicting spoken language level in children with autism spectrum disorders.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17389127

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17389127

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17389127

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Early intervention and early experience

1 reference

https://pubmed.ncbi.nlm.nih.gov/17389127

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17389127

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17389127

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

22q11.2 deletion syndrome: genetics, neuroanatomy and cognitive/behavioral features keywords

1 reference

https://pubmed.ncbi.nlm.nih.gov/17389127

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Taking advantage of early diagnosis: preschool children with the 22q11.2 deletion

1 reference

https://pubmed.ncbi.nlm.nih.gov/17389127

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The New York high risk project to the Hillside recognition and prevention (RAP) program

1 reference

https://pubmed.ncbi.nlm.nih.gov/17389127

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Communication disorders in the 22Q11.2 microdeletion syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/17389127

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Aggressive behavior in patients with attention-deficit/hyperactivity disorder, conduct disorder, and pervasive developmental disorders.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17389127

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17389127

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17389127

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17389127

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S11920-007-0085-8

1 reference

Europe PubMed Central

16 August 2017

1 reference

Europe PubMed Central

16 August 2017

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