(Q34344833)

1 August 2017

title

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

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1 August 2017

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Sanders AR

1

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1 August 2017

Rusu I

2

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1 August 2017

Duan J

3

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1 August 2017

Vander Molen JE

4

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1 August 2017

Hou C

5

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1 August 2017

Schwab SG

6

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1 August 2017

Wildenauer DB

7

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1 August 2017

Martinez M

8

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1 August 2017

Gejman PV

9

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1 August 2017

language of work or name

English

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publication date

1 April 2005

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1 August 2017

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1 August 2017

volume

10

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1 August 2017

issue

4

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1 August 2017

page(s)

353-365

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

1 August 2017

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

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Identity of the organic cation transporter OCT3 as the extraneuronal monoamine transporter (uptake2) and evidence for the expression of the transporter in the brain

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Schizophrenia and functional polymorphisms in the MAOA and COMT genes: no evidence for association or epistasis.

21 January 2018

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Population variation in linkage disequilibrium across the COMT gene considering promoter region and coding region variation

21 January 2018

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Erythrocyte COMT-activity in patients with affective disorders

21 January 2018

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Human liver catechol-O-methyltransferase pharmacogenetics

21 January 2018

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A highly significant association between a COMT haplotype and schizophrenia.

21 January 2018

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

21 January 2018

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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

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A genome-wide search for schizophrenia susceptibility genes

21 January 2018

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Splitting schizophrenia: periodic catatonia-susceptibility locus on chromosome 15q15

21 January 2018

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A systematic genomewide linkage study in 353 sib pairs with schizophrenia

21 January 2018

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

21 January 2018

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A high-density genome scan detects evidence for a bipolar-disorder susceptibility locus on 13q32 and other potential loci on 1q32 and 18p11.2.

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001586

Cloning, sequencing and functional expression of a novel human thioredoxin reductase

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001586

Human mitochondrial thioredoxin reductase cDNA cloning, expression and genomic organization

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001586

Identification of a new human catenin gene family member (ARVCF) from the region deleted in velo-cardio-facial syndrome

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001586

Velo-cardio-facial syndrome: a distinctive behavioral phenotype

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001586

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

21 January 2018

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

21 January 2018

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

21 January 2018

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The schizophrenia phenotype in 22q11 deletion syndrome

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001586

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

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001586

Methylation pharmacogenetics: catechol O-methyltransferase, thiopurine methyltransferase, and histamine N-methyltransferase

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001586

Crystal structure of catechol O-methyltransferase

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001586

Human catechol O-methyltransferase genetic variation: gene resequencing and functional characterization of variant allozymes

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001586

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

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001586

Recent advances in the genetics of schizophrenia

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001586

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

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001586

Schizophrenia and velo-cardio-facial syndrome.

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001586

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

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001586

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001586

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

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001586

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001586

Catechol O-methyltransferase (COMT) mRNA expression in the dorsolateral prefrontal cortex of patients with schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001586

Catechol-o-methyltransferase (COMT) and proline dehydrogenase (PRODH) mRNAs in the dorsolateral prefrontal cortex in schizophrenia, bipolar disorder, and major depression.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001586

Velo-cardio-facial syndrome and psychotic disorders: implications for psychiatric genetics

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001586

Is schizophrenia a neurodevelopmental disorder?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001586

Implications of normal brain development for the pathogenesis of schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001586

The dopamine hypothesis of schizophrenia: focus on the dopamine receptor

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001586

A paradigm shift in brain research

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001586

Physiological dysfunction of dorsolateral prefrontal cortex in schizophrenia. III. A new cohort and evidence for a monoaminergic mechanism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001586

Gating of information flow within the limbic system and the pathophysiology of schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001586

Suggestive evidence for a schizophrenia susceptibility locus on chromosome 6q and a confirmation in an independent series of pedigrees

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001586

Merlin--rapid analysis of dense genetic maps using sparse gene flow trees

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001586

A unified approach to adjusting association tests for population admixture with arbitrary pedigree structure and arbitrary missing marker information.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001586

Multicenter linkage study of schizophrenia loci on chromosome 22q.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001586

Identification of Sequence Variants and Analysis of the Role of the Catechol-O-Methyl-Transferase Gene in Schizophrenia Susceptibility

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001586

Characterization of single-nucleotide polymorphisms in coding regions of human genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001586

Gene-based SNP discovery as part of the Japanese Millennium Genome Project: identification of 190,562 genetic variations in the human genome. Single-nucleotide polymorphism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001586

Single nucleotide variation analysis in 65 candidate genes for CNS disorders in a representative sample of the European population

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001586

Synonymous mutations in the human dopamine receptor D2 (DRD2) affect mRNA stability and synthesis of the receptor

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001586

Overexpression of cadherins and underexpression of beta-catenin inhibit dorsal mesoderm induction in early Xenopus embryos

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001586

Nature versus nurture revisited: an old idea with a new twist

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001586

Schizophrenia: the cellular biology of a functional psychosis

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001586

Advancing a neurodevelopmental origin for schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001586

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

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001586

Suggestive Linkage to Chromosomal Regions 13q31 and 22q12 in Families With Psychotic Bipolar Disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001586

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001586

Genomic scan for genes predisposing to schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001586

Influential ideas and experimental progress in schizophrenia genetics research

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001586

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/10.1038%2FSJ.MP.4001586

7 January 2021

Human neurons express the polyspecific cation transporter hOCT2, which translocates monoamine neurotransmitters, amantadine, and memantine

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001586

7 January 2021

Cloning, expression and structure of catechol-O-methyltransferase.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001586

7 January 2021

Characterization and implications of estrogenic down-regulation of human catechol-O-methyltransferase gene transcription

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001586

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001586

7 January 2021

Identification of 197 genetic variations in six human methyltranferase genes in the Japanese population

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001586

7 January 2021

Erythrocyte catechol-O-methyltransferase activity in a Swedish population

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001586

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001586

7 January 2021

Splitting Schizophrenia: Periodic Catatonia–Susceptibility Locus on Chromosome 15q15

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001586

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001586

7 January 2021

Initial genomic scan of the NIMH genetics initiative bipolar pedigrees: Chromosomes 3, 5, 15, 16, 17, and 22

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001586

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001586

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/10.1038%2FSJ.MP.4001586

7 January 2021

Genetic polymorphism of catechol-O-methyltransferase (COMT): correlation of genotype with individual variation of S-COMT activity and comparison of the allele frequencies in the normal population and Parkinsonian patients in Finland

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001586

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001586

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001586

7 January 2021

Does dopamine play a role in schizophrenia?

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001586

7 January 2021

Catechol-O-methyltransferase genotype and dopamine regulation in the human brain.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001586

7 January 2021

Projections from the rat prefrontal cortex to the ventral tegmental area: target specificity in the synaptic associations with mesoaccumbens and mesocortical neurons

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001586

7 January 2021

The role of endogenous sensitization in the pathophysiology of schizophrenia: implications from recent brain imaging studies

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001586

7 January 2021

Genome-wide search for schizophrenia susceptibility loci: The NIMH genetics initiative and millennium consortium

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001586

7 January 2021

GOLD--graphical overview of linkage disequilibrium

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001586

7 January 2021

Identifiers

DOI

10.1038/SJ.MP.4001586

1 reference

Dimensions Publication ID

1 August 2017

1029477722

0 references

1 reference