Haplotypic association spanning the 22q11.21 genes COMT and ARVCF with schizophrenia. (Q34344833)

From Wikidata

Revision as of 17:00, 21 December 2021 by KrBot (talk | contribs) (‎Changed Asturian label: Haplotypic association spanning the 22q11.21 genes COMT and ARVCF with schizophrenia)

(diff) ← Older revision | Latest revision (diff) | Newer revision → (diff)

Jump to navigation Jump to search

scientific article

Language	Label	Description	Also known as
English	Haplotypic association spanning the 22q11.21 genes COMT and ARVCF with schizophrenia.	scientific article

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

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

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

0 references

author name string

Sanders AR

1

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Rusu I

2

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Duan J

3

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Vander Molen JE

4

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Hou C

5

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Schwab SG

6

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Wildenauer DB

7

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Martinez M

8

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Gejman PV

9

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

language of work or name

0 references

publication date

1 April 2005

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Molecular Psychiatry

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

10

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

4

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

353-365

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

https://scigraph.springernature.com/pub.10.1038/sj.mp.4001586

0 references

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

1 reference

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

21 January 2018

Brain catecholamine metabolism in catechol-O-methyltransferase (COMT)-deficient mice

1 reference

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

21 January 2018

Catechol-O-methyltransferase (COMT) in rat brain: immunoelectron microscopic study with an antiserum against rat recombinant COMT protein

1 reference

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

21 January 2018

Catechol O-methyltransferase mRNA expression in human and rat brain: evidence for a role in cortical neuronal function

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

Cell-free synthesis of rat and human catechol O-methyltransferase. Insertion of the membrane-bound form into microsomal membranes in vitro

1 reference

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

21 January 2018

Human catechol-O-methyltransferase: cloning and expression of the membrane-associated form

1 reference

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

21 January 2018

Cloning and Characterization of Human Placental Catechol--Methyltransferase cDNA

1 reference

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

21 January 2018

Expression and intracellular localization of catechol O-methyltransferase in transfected mammalian cells.

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

Catecholamine metabolism in the brain by membrane-bound and soluble catechol-o-methyltransferase (COMT) estimated by enzyme kinetic values.

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

Pharmacological and physiological functions of the polyspecific organic cation transporters: OCT1, 2, and 3 (SLC22A1-3).

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

Erythrocyte COMT-activity in patients with affective disorders

1 reference

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

21 January 2018

Human liver catechol-O-methyltransferase pharmacogenetics

1 reference

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

21 January 2018

A highly significant association between a COMT haplotype and schizophrenia.

1 reference

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

21 January 2018

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/10.1038%2FSJ.MP.4001586

21 January 2018

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).

1 reference

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

21 January 2018

A genome-wide search for schizophrenia susceptibility genes

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

A systematic genomewide linkage study in 353 sib pairs with schizophrenia

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

Human mitochondrial thioredoxin reductase cDNA cloning, expression and genomic organization

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

Velo-cardio-facial syndrome: a distinctive behavioral phenotype

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

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/10.1038%2FSJ.MP.4001586

21 January 2018

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

1 reference

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

21 January 2018

The schizophrenia phenotype in 22q11 deletion syndrome

1 reference

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

21 January 2018

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/10.1038%2FSJ.MP.4001586

21 January 2018

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

1 reference

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

21 January 2018

Crystal structure of catechol O-methyltransferase

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

Recent advances in the genetics of schizophrenia

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

Schizophrenia and velo-cardio-facial syndrome.

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

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/10.1038%2FSJ.MP.4001586

21 January 2018

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/10.1038%2FSJ.MP.4001586

21 January 2018

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

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

Is schizophrenia a neurodevelopmental disorder?

1 reference

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

21 January 2018

Implications of normal brain development for the pathogenesis of schizophrenia

1 reference

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

21 January 2018

The dopamine hypothesis of schizophrenia: focus on the dopamine receptor

1 reference

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

21 January 2018

A paradigm shift in brain research

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

Multicenter linkage study of schizophrenia loci on chromosome 22q.

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

Schizophrenia: the cellular biology of a functional psychosis

1 reference

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

21 January 2018

Advancing a neurodevelopmental origin for schizophrenia

1 reference

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

21 January 2018

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/10.1038%2FSJ.MP.4001586

21 January 2018

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

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

Genomic scan for genes predisposing to schizophrenia

1 reference

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

21 January 2018

Influential ideas and experimental progress in schizophrenia genetics research

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

Erythrocyte catechol-O-methyltransferase activity in a Swedish population

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

Does dopamine play a role in schizophrenia?

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

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

based on heuristic

inferred from DOI database lookup

GOLD--graphical overview of linkage disequilibrium

1 reference

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

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1038/SJ.MP.4001586

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q34344833&oldid=1547733787"