A highly significant association between a COMT haplotype and schizophrenia. - Wikidata - wikimedia - TriplyDB

A highly significant association between a COMT haplotype and schizophrenia.

A highly significant association between a COMT haplotype and schizophrenia.

http://www.wikidata.org/entity/Q37203703

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Genome-wide association identifies a common variant in the reelin gene that increases the risk of schizophrenia only in women Matrix-assisted laser desorption/ionisation, time-of-flight mass spectrometry in genomics research The quantification of COMT mRNA in post mortem cerebellum tissue: diagnosis, genotype, methylation and expression Genotyping DNA pools on microarrays: tackling the QTL problem of large samples and large numbers of SNPs A catechol-O-methyltransferase that is essential for auditory function in mice and humans.Polymorphisms at the G72/G30 gene locus, on 13q33, are associated with bipolar disorder in two independent pedigree series Polymorphisms in the trace amine receptor 4 (TRAR4) gene on chromosome 6q23.2 are associated with susceptibility to schizophrenia Functional analysis of genetic variation in catechol-O-methyltransferase (COMT): effects on mRNA, protein, and enzyme activity in postmortem human brain Bipolar I disorder and schizophrenia: a 440-single-nucleotide polymorphism screen of 64 candidate genes among Ashkenazi Jewish case-parent trios Catechol-O-methyltransferase polymorphisms and some implications for cognitive therapeutics The genetics of schizophrenia COMT genetic variation confers risk for psychotic and affective disorders: a case control study Association of SNPs and haplotypes in GABAA receptor beta2 gene with schizophrenia Molecular genetic studies of schizophrenia A network of dopaminergic gene variations implicated as risk factors for schizophrenia Update on psychiatric genetics Orientation and cellular distribution of membrane-bound catechol-O-methyltransferase in cortical neurons: implications for drug development Genomewide association for schizophrenia in the CATIE study: results of stage 1 Schizophrenia genes, gene expression, and neuropathology: on the matter of their convergence Meta-Analysis of the COMT Val158Met Polymorphism in Major Depressive Disorder: Effect of Ethnicity.Dysbindin-1 mutant mice implicate reduced fast-phasic inhibition as a final common disease mechanism in schizophrenia.A B2 SINE insertion in the Comt1 gene (Comt1(B2i)) results in an overexpressing, behavior modifying allele present in classical inbred mouse strains Genetic variants of Nogo-66 receptor with possible association to schizophrenia block myelin inhibition of axon growth.Adherence to nicotine replacement therapy among pregnant smokers Nogo Receptor 1 (RTN4R) as a candidate gene for schizophrenia: analysis using human and mouse genetic approaches.Low enzymatic activity haplotypes of the human catechol-O-methyltransferase gene: enrichment for marker SNPs.Association between catechol-O-methyltrasferase Val108/158Met genotype and prefrontal hemodynamic response in schizophrenia Dysbindin regulates the transcriptional level of myristoylated alanine-rich protein kinase C substrate via the interaction with NF-YB in mice brain.Catechol-O-methyltransferase Val 158 Met polymorphism and antisaccade eye movements in schizophrenia Effects of COMT genotype on behavioral symptomatology in the 22q11.2 Deletion Syndrome.The complex global pattern of genetic variation and linkage disequilibrium at catechol-O-methyltransferase.Theranostic Biomarkers for Schizophrenia Prediction of psychosis onset in Alzheimer disease: the role of depression symptom severity and the HTR2A T102C polymorphism.Adolescent cannabis use increases risk for cocaine-induced paranoia.Genetics of Psychosis in Alzheimer Disease.Association study of CSF2RB with schizophrenia in Irish family and case - control samples.Sexual dimorphisms and prediction of conversion in the NAPLS psychosis prodrome A comprehensive analysis of 22q11 gene expression in the developing and adult brain.Dopamine and psychosis: theory, pathomechanisms and intermediate phenotypes Technologies in the Whole-Genome Age: MALDI-TOF-Based Genotyping.

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A highly significant association between a COMT haplotype and schizophrenia.

http://www.wikidata.org/entity/Q37203703

description

article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on 25 October 2002

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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name

A highly significant association between a COMT haplotype and schizophrenia.

@en

A highly significant association between a COMT haplotype and schizophrenia.

@nl

type

label

A highly significant association between a COMT haplotype and schizophrenia.

@en

A highly significant association between a COMT haplotype and schizophrenia.

@nl

prefLabel

A highly significant association between a COMT haplotype and schizophrenia.

@en

A highly significant association between a COMT haplotype and schizophrenia.

@nl

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American Journal of Human Genetics

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A highly significant association between a COMT haplotype and schizophrenia

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Anne Pisanté-Shalom

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Ariel Darvasi

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Baruch Spivak

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Benjamin Yakir

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Efrat Lev-Lehman

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Eilat Shinar

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Haim Y Knobler

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Ilya Reznik

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Leon Karp

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Marnina Swartz-Vanetik

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P2860

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

A protein kinase encoded by the t complex responder gene causes non-mendelian inheritance

The future of genetic studies of complex human diseases

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

Genetic analysis of case/control data using estimated haplotype frequencies: application to APOE locus variation and Alzheimer's disease.

Prefrontal neurons and the genetics of schizophrenia.

Search for schizophrenia susceptibility genes.

Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11.

A comparison of linkage disequilibrium measures for fine-scale mapping.

Parental origin-dependent, male offspring-specific transmission-ratio distortion at loci on the human X chromosome.

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1296-1302

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10.1086/344514

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6

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71

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Jacques S. Beckmann

Abraham Weizman

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2002-10-25T00:00:00Z

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11062067

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