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The schizophrenia phenotype in 22q11 deletion syndrome
scientific article
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scholarly article
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title
The schizophrenia phenotype in 22q11 deletion syndrome
(English)
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main subject
schizophrenia
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22q11 deletion syndrome
1 reference
based on heuristic
inferred from title
phenotype
1 reference
based on heuristic
inferred from title
author
Philip AbdelMalik
object named as
Philip AbdelMalik
series ordinal
3
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author name string
Anne S Bassett
series ordinal
1
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Eva W C Chow
series ordinal
2
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Mirona Gheorghiu
series ordinal
4
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Janice Husted
series ordinal
5
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Rosanna Weksberg
series ordinal
6
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language of work or name
English
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publication date
September 2003
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published in
American Journal of Psychiatry
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volume
160
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page(s)
1580-6
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issue
9
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cites work
“Mini-mental state”
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276594
retrieved
7 April 2017
Chromosome 22q11 deletion syndrome: update and review of the clinical features, cognitive-behavioral spectrum, and psychiatric complications
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276594
retrieved
7 April 2017
Location of a major susceptibility locus for familial schizophrenia on chromosome 1q21-q22
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276594
retrieved
7 April 2017
'Pfropfschizophrenie' revisited. Schizophrenia in people with mild learning disability
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276594
retrieved
7 April 2017
The positive and negative syndrome scale (PANSS) for schizophrenia
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276594
retrieved
7 April 2017
Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276594
retrieved
7 April 2017
Implications of normal brain development for the pathogenesis of schizophrenia
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276594
retrieved
7 April 2017
A rating scale for mania: reliability, validity and sensitivity
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276594
retrieved
7 April 2017
Structural brain abnormalities in patients with schizophrenia and 22q11 deletion syndrome.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276594
retrieved
27 September 2017
Patterns of dysmorphic features in schizophrenia
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276594
retrieved
27 September 2017
Genetic insights into the neurodevelopmental hypothesis of schizophrenia
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276594
retrieved
27 September 2017
Brain imaging in neurogenetic conditions: realizing the potential of behavioral neurogenetics research
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276594
retrieved
27 September 2017
Chromosomal abnormalities and schizophrenia
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276594
retrieved
27 September 2017
Molecular genetics of Alzheimer's disease.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276594
retrieved
27 September 2017
Qualitative MRI findings in adults with 22q11 deletion syndrome and schizophrenia
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276594
retrieved
27 September 2017
22q11 deletion syndrome: a genetic subtype of schizophrenia
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276594
retrieved
27 September 2017
Phenotype of adults with the 22q11 deletion syndrome: A review
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276594
retrieved
27 September 2017
Clinical characteristics of schizophrenia associated with velo-cardio-facial syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276594
retrieved
27 September 2017
A population study of chromosome 22q11 deletions in infancy
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276594
retrieved
27 September 2017
22q11 deletion syndrome in adults with schizophrenia
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276594
retrieved
27 September 2017
Molecular analysis of velo-cardio-facial syndrome patients with psychiatric disorders.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276594
retrieved
27 September 2017
Mental retardation: genetic findings, clinical implications and research agenda
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276594
retrieved
27 September 2017
Positive and negative symptoms in families with schizophrenia
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276594
retrieved
27 September 2017
Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndromes: implications for genetic counselling and prenatal diagnosis
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276594
retrieved
27 September 2017
Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276594
retrieved
27 September 2017
The genetics of Alzheimer's disease: associations with hematologic malignancy and Down's syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276594
retrieved
27 September 2017
Clozapine in the treatment of refractory psychotic mania
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276594
retrieved
30 May 2018
Psychiatric disorders and behavioral problems in children with velocardiofacial syndrome: usefulness as phenotypic indicators of schizophrenia risk.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276594
retrieved
28 November 2018
Reaction time measures of sustained attention differentiate bipolar disorder from schizophrenia
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276594
retrieved
28 November 2018
Effects of clozapine, olanzapine, risperidone, and haloperidol on hostility among patients with schizophrenia
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276594
retrieved
28 November 2018
Catecholamines in patients with 22q11.2 deletion syndrome and the low-activity COMT polymorphism
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276594
retrieved
28 November 2018
High rates of schizophrenia in adults with velo-cardio-facial syndrome.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276594
retrieved
28 November 2018
Clinical and neurobiological correlates of cytogenetic abnormalities in childhood-onset schizophrenia
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276594
retrieved
28 November 2018
Psychopathology of Schizophrenia: initial validation of a 5-factor model
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/12944331
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Chromosome 21q21 sublocalisation of gene encoding beta-amyloid peptide in cerebral vessels and neuritic (senile) plaques of people with Alzheimer disease and Down syndrome
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/12944331
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1176/APPI.AJP.160.9.1580
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PMCID
3276594
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PubMed ID
12944331
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