(Q36493850)

14 August 2017

1 reference

title

Chromosome 22 deletion syndrome and schizophrenia (English)

1 reference

14 August 2017

0 references

2

1 reference

14 August 2017

Nigel M Williams

1

1 reference

PubMed ID

16737900

14 August 2017

Michael J Owen

series ordinal

3

1 reference

14 August 2017

1 January 2006

1 reference

International Review of Neurobiology

14 August 2017

1 reference

14 August 2017

73

1 reference

14 August 2017

1-27

1 reference

Screening for 22q11 deletions in a schizophrenia population.

14 August 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

Microarray analysis of postmortem temporal cortex from patients with schizophrenia

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

Meta-analysis of whole-genome linkage scans of bipolar disorder and schizophrenia

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

Functional consequences of PRODH missense mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

Neurocognitive correlates of the COMT Val(158)Met polymorphism in chronic schizophrenia.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

Cloning a balanced translocation associated with DiGeorge syndrome and identification of a disrupted candidate gene

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

Abnormal fMRI response of the dorsolateral prefrontal cortex in cognitively intact siblings of patients with schizophrenia.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

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

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

Variants in the catechol-o-methyltransferase (COMT) gene are associated with schizophrenia in Irish high-density families

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

The effect of apomorphine on regional cerebral blood flow in schizophrenia

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

Dopamine in schizophrenia: a review and reconceptualization

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

White matter changes in schizophrenia: evidence for myelin-related dysfunction

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

A genome-wide scan for linkage to chromosomal regions in 382 sibling pairs with schizophrenia or schizoaffective disorder

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

Genetic and neurochemical modulation of prefrontal cognitive functions in children.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

The DNA sequence of human chromosome 22

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

A common molecular basis for rearrangement disorders on chromosome 22q11

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

Family-based association studies of COMT gene polymorphisms and schizophrenia in the Chinese population

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

A family-based association study of T1945C polymorphism in the proline dehydrogenase gene and schizophrenia in the Chinese population

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

COMT Val(158)Met and BDNF C(270)T polymorphisms in schizophrenia: a case-control study.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

Association between a functional catechol O-methyltransferase gene polymorphism and schizophrenia: meta-analysis of case-control and family-based studies

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

Catechol-O-methyltransferase-deficient mice exhibit sexually dimorphic changes in catecholamine levels and behavior

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

The gene encoding proline dehydrogenase modulates sensorimotor gating in mice

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

Executive subprocesses in working memory: relationship to catechol-O-methyltransferase Val158Met genotype and schizophrenia

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

Velocardiofacial manifestations and microdeletions in schizophrenic inpatients

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

Catecholamines in patients with 22q11.2 deletion syndrome and the low-activity COMT polymorphism

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

Soluble and particulate forms of rat catechol-O-methyltransferase distinguished by gel electrophoresis and immune fixation.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

Additional support for schizophrenia linkage on chromosomes 6 and 8: a multicenter study. Schizophrenia Linkage Collaborative Group for Chromosomes 3, 6 and 8

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

Genome-wide expression analysis reveals dysregulation of myelination-related genes in chronic schizophrenia

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

Separate and interacting effects within the catechol-O-methyltransferase (COMT) are associated with schizophrenia.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

Genes for schizophrenia? Recent findings and their pathophysiological implications

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

Schizophrenia genes, gene expression, and neuropathology: on the matter of their convergence

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

Catechol-O-methyl transferase Val158Met gene polymorphism in schizophrenia: working memory, frontal lobe MRI morphology and frontal cerebral blood flow.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

Effect of dopamine uptake inhibition on brain catecholamine levels and locomotion in catechol-O-methyltransferase-disrupted mice.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

PRODH mutations and hyperprolinemia in a subset of schizophrenic patients

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

Characterization of membrane-bound and soluble catechol-O-methyltransferase from human frontal cortex

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

Haplotype tagging for the identification of common disease genes

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

Homicidal behavior in schizophrenia associated with a genetic polymorphism determining low catechol O-methyltransferase (COMT) activity

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

Family‐based and case–control study of catechol‐O‐methyltransferase in schizophrenia among Palestinian Arabs

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

Catechol-O-methyltransferase polymorphisms and schizophrenia: a transmission disequilibrium study in multiply affected families

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

Follow-up report of potential linkage for schizophrenia on chromosome 22q: Part 3

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

Family-based linkage disequilibrium mapping using SNP marker haplotypes: application to a potential locus for schizophrenia at chromosome 22q11

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

Evidence for association between novel polymorphisms in the PRODH gene and schizophrenia in a Chinese population

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

Chromosomal microdeletions: dissecting del22q11 syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

Congenital heart disease in mice deficient for the DiGeorge syndrome region

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

Genetic variation in the 22q11 locus and susceptibility to schizophrenia

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

Kinetics of human soluble and membrane-bound catechol O-methyltransferase: a revised mechanism and description of the thermolabile variant of the enzyme

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

Comparative sequence analysis of 634 kb of the mouse chromosome 16 region of conserved synteny with the human velocardiofacial syndrome region on chromosome 22q11.2.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

Sequence-ready physical map of the mouse chromosome 16 region with conserved synteny to the human velocardiofacial syndrome region on 22q11.2.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

Catechol O-methyltransferase Val158Met polymorphism in schizophrenia: differential effects of Val and Met alleles on cognitive stability and flexibility.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

Association study of a functional catechol-O-methyltransferase gene polymorphism in Japanese schizophrenics

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

T-box genes in human disorders

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

COMT haplotypes suggest P2 promoter region relevance for schizophrenia.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

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/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

Mice deleted for the DiGeorge/velocardiofacial syndrome region show abnormal sensorimotor gating and learning and memory impairments.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

Comparative mapping of the human 22q11 chromosomal region and the orthologous region in mice reveals complex changes in gene organization

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

Novel subtype of peroxisomal acyl-CoA oxidase deficiency and bifunctional enzyme deficiency with detectable enzyme protein: identification by means of complementation analysis

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

New evidence of association between COMT gene and prefrontal neurocognitive function in healthy individuals from sibling pairs discordant for psychosis

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

Haplotypic association spanning the 22q11.21 genes COMT and ARVCF with schizophrenia

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

Catechol-O-methyltransferase gene Val108/158Met polymorphism, and susceptibility to schizophrenia: association is more significant in women

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

The 22q11 deletion syndromes

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

Family-based association studies of monoaminergic gene polymorphisms among North Indians with schizophrenia

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

Dopamine axon varicosities in the prelimbic division of the rat prefrontal cortex exhibit sparse immunoreactivity for the dopamine transporter.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

A genome-wide search for schizophrenia susceptibility genes

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

A highly significant association between a COMT haplotype and schizophrenia.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

COMT: a common susceptibility gene in bipolar disorder and schizophrenia.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

Variation in catechol-o-methyltransferase val158 met genotype associated with schizotypy but not cognition: a population study in 543 young men.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

Genomic organization of the human catechol O-methyltransferase gene and its expression from two distinct promoters.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

Oligodendrocyte dysfunction in schizophrenia and bipolar disorder

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

Catechol-o-methyltransferase inhibition improves set-shifting performance and elevates stimulated dopamine release in the rat prefrontal cortex

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

Expression of ARVCF in the human ganglionic eminence during fetal development

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

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

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

Thermal stability and the biochemical genetics of erythrocyte catechol-O-methyl-transferase and plasma dopamine-beta-hydroxylase.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

Association between PRODH and schizophrenia is not confirmed

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

Detailed analysis of PRODH and PsPRODH reveals no association with schizophrenia

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

A systematic genomewide linkage study in 353 sib pairs with schizophrenia

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

Mutation screening and LD mapping in the VCFS deleted region of chromosome 22q11 in schizophrenia using a novel DNA pooling approach.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

No association between schizophrenia and polymorphisms in COMT in two large samples

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

Association between Val108/158 Met polymorphism of the COMT gene and schizophrenia

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

Role of TBX1 in human del22q11.2 syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

Differential expression of human COMT alleles in brain and lymphoblasts detected by RT-coupled 5' nuclease assay

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2806%2973001-X

7 January 2021

10.1016/S0074-7742(06)73001-X

Identifiers

DOI

1 reference

14 August 2017

1 reference

PubMed ID

16737900