Analyses of the associations between the genes of 22q11 deletion syndrome and schizophrenia (Q36592188)

15 August 2017

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title

Analyses of the associations between the genes of 22q11 deletion syndrome and schizophrenia (English)

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15 August 2017

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22q11 deletion syndrome

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Tadao Arinami

1

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15 August 2017

13 September 2006

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Journal of Human Genetics

15 August 2017

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15 August 2017

51

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15 August 2017

12

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15 August 2017

1037-1045

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https://scigraph.springernature.com/pub.10.1007/s10038-006-0058-5

15 August 2017

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cites work

Clinical features of 78 adults with 22q11 Deletion Syndrome.

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https://api.crossref.org/works/10.1007%2FS10038-006-0058-5

Hyperprolinemia is not associated with childhood onset schizophrenia

21 January 2018

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https://api.crossref.org/works/10.1007%2FS10038-006-0058-5

22q11.2 duplication syndrome: two new familial cases with some overlapping features with DiGeorge/velocardiofacial syndromes.

21 January 2018

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https://api.crossref.org/works/10.1007%2FS10038-006-0058-5

Implications of normal brain development for the pathogenesis of schizophrenia

21 January 2018

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https://api.crossref.org/works/10.1007%2FS10038-006-0058-5

A haplotype implicated in schizophrenia susceptibility is associated with reduced COMT expression in human brain

21 January 2018

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12 December 2020

Screening for 22q11 deletions in a schizophrenia population.

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12 December 2020

Identification of a novel nuclear localization signal in Tbx1 that is deleted in DiGeorge syndrome patients harboring the 1223delC mutation

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12 December 2020

VEGF: a modifier of the del22q11 (DiGeorge) syndrome?

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12 December 2020

Case-control study and transmission disequilibrium test provide consistent evidence for association between schizophrenia and genetic variation in the 22q11 gene ZDHHC8.

1 reference

12 December 2020

Neurocognitive profile in 22q11 deletion syndrome and schizophrenia

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12 December 2020

Human studies of prepulse inhibition of startle: normal subjects, patient groups, and pharmacological studies

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12 December 2020

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

1 reference

12 December 2020

Genetic factors are major determinants of phenotypic variability in a mouse model of the DiGeorge/del22q11 syndromes

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12 December 2020

Significant linkage to chromosome 22q for exploratory eye movement dysfunction in schizophrenia

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Lack of association of the COMT (Val158/108 Met) gene and schizophrenia: a meta-analysis of case-control studies

1 reference

12 December 2020

Tbx1 haploinsufficieny in the DiGeorge syndrome region causes aortic arch defects in mice

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Microduplication and triplication of 22q11.2: a highly variable syndrome

1 reference

12 December 2020

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

1 reference

12 December 2020

Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11.

1 reference

12 December 2020

A 200-kb region of human chromosome 22q11.2 confers antipsychotic-responsive behavioral abnormalities in mice

1 reference

12 December 2020

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

1 reference

12 December 2020

Prevalence of 22q11 microdeletion

1 reference

12 December 2020

Evidence that the gene encoding ZDHHC8 contributes to the risk of schizophrenia

1 reference

12 December 2020

ZDHHC8 as a candidate gene for schizophrenia: analysis of a putative functional intronic marker in case-control and family-based association studies

1 reference

12 December 2020

A complete genetic association scan of the 22q11 deletion region and functional evidence reveal an association between DGCR2 and schizophrenia.

1 reference

12 December 2020

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

1 reference

12 December 2020

The neurodevelopmental model of schizophrenia: update 2005.

1 reference

12 December 2020

The ZDHHC8 gene did not associate with bipolar disorder or schizophrenia

1 reference

12 December 2020

Multicenter linkage study of schizophrenia loci on chromosome 22q.

1 reference

12 December 2020

An Fgf8 mouse mutant phenocopies human 22q11 deletion syndrome

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12 December 2020

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

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12 December 2020

Protein palmitoylation: a regulator of neuronal development and function

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12 December 2020

Human catechol-O-methyltransferase pharmacogenetics: description of a functional polymorphism and its potential application to neuropsychiatric disorders.

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12 December 2020

A systematic genomewide linkage study in 353 sib pairs with schizophrenia

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12 December 2020

Psychiatric inpatients and chromosome deletions within 22q11.2.

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12 December 2020

Further study of a genetic association between the CLDN5 locus and schizophrenia

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12 December 2020

22q11 deletion syndrome: a genetic subtype of schizophrenia

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12 December 2020

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

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12 December 2020

Profiles of neuropsychologic function in schizophrenia

1 reference

12 December 2020

Hyperprolinemia is a risk factor for schizoaffective disorder

1 reference

12 December 2020

The 22q11 deletion syndromes

1 reference

12 December 2020

Lower prepulse inhibition in children with the 22q11 deletion syndrome

1 reference

12 December 2020

Failure to find association between PRODH deletion and schizophrenia

1 reference

12 December 2020

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

1 reference

12 December 2020

No association was found between a functional SNP in ZDHHC8 and schizophrenia in a Japanese case-control population

1 reference

12 December 2020

Microduplication 22q11.2, an emerging syndrome: clinical, cytogenetic, and molecular analysis of thirteen patients

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Linkage of a composite inhibitory phenotype to a chromosome 22q locus in eight Utah families

1 reference

12 December 2020

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

1 reference

12 December 2020

Theories of schizophrenia: a genetic-inflammatory-vascular synthesis

1 reference

12 December 2020

Interaction between NOTCH4 and catechol-O-methyltransferase genotypes in schizophrenia patients with poor response to typical neuroleptics

1 reference

12 December 2020

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

1 reference

12 December 2020

TBX1 is responsible for cardiovascular defects in velo-cardio-facial/DiGeorge syndrome

1 reference

12 December 2020

No association between the putative functional ZDHHC8 single nucleotide polymorphism rs175174 and schizophrenia in large European samples

1 reference

12 December 2020

A common molecular basis for rearrangement disorders on chromosome 22q11

1 reference

12 December 2020

A review of Disrupted-In-Schizophrenia-1 (DISC1): neurodevelopment, cognition, and mental conditions

1 reference

12 December 2020

A comprehensive analysis of 22q11 gene expression in the developing and adult brain

1 reference

12 December 2020

Transmission disequilibrium test provides evidence of association between promoter polymorphisms in 22q11 gene DGCR14 and schizophrenia

1 reference

12 December 2020

A functional polymorphism in the COMT gene and performance on a test of prefrontal cognition

1 reference

12 December 2020

Genetic, developmental, and physical factors associated with attention deficit hyperactivity disorder in patients with velocardiofacial syndrome.

1 reference

12 December 2020

Functional consequences of PRODH missense mutations

1 reference

12 December 2020

The schizophrenia phenotype in 22q11 deletion syndrome

1 reference

12 December 2020

Congenital heart disease in mice deficient for the DiGeorge syndrome region

1 reference

12 December 2020

Hyperprolinaemia in patients with deletion (22)(q11.2) syndrome

1 reference

12 December 2020

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

1 reference

12 December 2020

Catechol-O-methyltransferase gene Val/Met functional polymorphism and risk of schizophrenia: a large-scale association study plus meta-analysis

1 reference

12 December 2020

The molecular genetics of the 22q11-associated schizophrenia

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12 December 2020

Role of TBX1 in human del22q11.2 syndrome

1 reference

12 December 2020

Tbx1 haploinsufficiency is linked to behavioral disorders in mice and humans: implications for 22q11 deletion syndrome

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12 December 2020

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

1 reference

12 December 2020

Effects of a functional COMT polymorphism on prefrontal cognitive function in patients with 22q11.2 deletion syndrome

1 reference

12 December 2020

The quantification of COMT mRNA in post mortem cerebellum tissue: diagnosis, genotype, methylation and expression

1 reference

12 December 2020

Velocardiofacial syndrome in childhood-onset schizophrenia.

1 reference

12 December 2020

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

1 reference

12 December 2020

PRODH mutations and hyperprolinemia in a subset of schizophrenic patients

1 reference

12 December 2020

Functional analysis of polymorphisms in the promoter regions of genes on 22q11.

1 reference

12 December 2020

The CLDN5 locus may be involved in the vulnerability to schizophrenia

1 reference

12 December 2020

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

1 reference

12 December 2020

A highly significant association between a COMT haplotype and schizophrenia.

1 reference

12 December 2020

A new genomic duplication syndrome complementary to the velocardiofacial (22q11 deletion) syndrome

1 reference

12 December 2020

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

1 reference

12 December 2020

10.1007/S10038-006-0058-5

Identifiers

DOI

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15 August 2017

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PubMed ID

16969581