The catechol-O-methyl transferase (COMT) gene as a candidate for psychiatric phenotypes: evidence and lessons.
about
Rethinking psychosis: the disadvantages of a dichotomous classification now outweigh the advantagesPersonality in relation to genetic liability for schizophrenia and bipolar disorder: differential associations with the COMT Val 108/158 Met polymorphismResearch review: DSM-V conduct disorder: research needs for an evidence baseConvergent evidence that oligodendrocyte lineage transcription factor 2 (OLIG2) and interacting genes influence susceptibility to schizophreniaA Review of Biomarkers in Mood and Psychotic Disorders: A Dissection of Clinical vs. Preclinical CorrelatesCOMT val158met moderation of dopaminergic drug effects on cognitive function: a critical reviewA pilot multivariate parallel ICA study to investigate differential linkage between neural networks and genetic profiles in schizophrenia.A genome-wide in vitro bacterial-infection screen reveals human variation in the host response associated with inflammatory diseaseDepression and anxiety in relation to catechol-O-methyltransferase Val158Met genotype in the general population: the Nord-Trøndelag Health Study (HUNT).Tourette syndrome and klippel-feil anomaly in a child with chromosome 22q11 duplication.Sex differences in magical ideation: a community-based twin studyCOMT Val108/158Met polymorphism and the modulation of task-oriented behavior in children with ADHD.Interaction of chronic stress with serotonin transporter and catechol-O-methyltransferase polymorphisms in predicting youth depressionThe impact of the Val158Met catechol-O-methyltransferase genotype on neural correlates of sad facial affect processing in patients with bipolar disorder and their relatives.Common genetic variations in CLOCK transcription factor are associated with nonalcoholic fatty liver diseaseThe genetic deconstruction of psychosisThe catechol-O-methyl transferase Val158Met polymorphism and experience of reward in the flow of daily life.How might stress contribute to increased risk for schizophrenia in children with chromosome 22q11.2 deletion syndrome?Strong genetic evidence for a selective influence of GABAA receptors on a component of the bipolar disorder phenotypeCatechol O-methyltransferase pharmacogenomics and selective serotonin reuptake inhibitor response.Prenatal vitamins, one-carbon metabolism gene variants, and risk for autismImaging genetics of mood disorders.Higher FKBP5, COMT, CHRNA5, and CRHR1 allele burdens are associated with PTSD and interact with trauma exposure: implications for neuropsychiatric research and treatment.Epigenetic modifications in frontal cortex from Alzheimer's disease and bipolar disorder patients.Association of FKBP5, COMT and CHRNA5 polymorphisms with PTSD among outpatients at risk for PTSD.Is COMT a susceptibility gene for schizophrenia?Genetics of obsessive-compulsive disorder: a research update.Neuroplasticity of neocortical circuits in schizophrenia.Neurotransmission and bipolar disorder: a systematic family-based association study.COMT Val(158) Met genotype is associated with reward learning: a replication study and meta-analysisAssociation between the catechol-O-methyltransferase Val158Met polymorphism and cocaine dependence.Genetic variation in catechol-O-methyltransferase: effects on working memory in schizophrenic patients, their siblings, and healthy controlsCatechol-O-methyltransferase contributes to genetic susceptibility shared among anxiety spectrum phenotypesNeural markers of errors as endophenotypes in neuropsychiatric disorders.Investigating the molecular basis of major depressive disorder etiology: a functional convergent genetic approachResilience in mental health: linking psychological and neurobiological perspectives.Attention Deficit Hyperactivity Disorder comorbid oppositional defiant disorder and its predominately inattentive type: evidence for an association with COMT but not MAOA in a Chinese sample.Endophenotypes, dimensions, risks: is psychosis analogous to common inherited medical illnesses?Pharmacogenomics with antidepressants in the STAR*D study.Evidence for single nucleotide polymorphisms and their association with bipolar disorder.
P2860
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P2860
The catechol-O-methyl transferase (COMT) gene as a candidate for psychiatric phenotypes: evidence and lessons.
description
2006 nî lūn-bûn
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2006 թուականի Մայիսին հրատարակուած գիտական յօդուած
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2006 թվականի մայիսին հրատարակված գիտական հոդված
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2006年の論文
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2006年論文
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2006年論文
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2006年論文
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2006年論文
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2006年論文
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2006年论文
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name
The catechol-O-methyl transfer ...... notypes: evidence and lessons.
@ast
The catechol-O-methyl transfer ...... notypes: evidence and lessons.
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type
label
The catechol-O-methyl transfer ...... notypes: evidence and lessons.
@ast
The catechol-O-methyl transfer ...... notypes: evidence and lessons.
@en
prefLabel
The catechol-O-methyl transfer ...... notypes: evidence and lessons.
@ast
The catechol-O-methyl transfer ...... notypes: evidence and lessons.
@en
P2860
P356
P1433
P1476
The catechol-O-methyl transfer ...... notypes: evidence and lessons.
@en
P2093
P2860
P2888
P304
P356
10.1038/SJ.MP.4001808
P407
P577
2006-05-01T00:00:00Z