Catechol-o-methyltransferase, cognition, and psychosis: Val158Met and beyond.

No abstract is available for this paper.

• Publication year

  2006

• Venue

  Biological Psychiatry

• Publication date

  2006-07-15

• Fields of study

  Medicine, Psychology

• Identifiers
  DOI 10.1016/J.BIOPSYCH.2005.10.024PMID 16476412
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• A novel protein isoform of catechol O-methyltransferase (COMT): brain expression analysis in schizophrenia and bipolar disorder and effect of Val158Met genotype

  2006cited by this paper
• Effect of Catechol-O-Methyltransferase val158met Genotype on Attentional Control

  2005cited by this paper
• Lack of association of the COMT (Val158/108 Met) gene and schizophrenia: a meta-analysis of case–control studies

  2005cited by this paper
• Midbrain dopamine and prefrontal function in humans: interaction and modulation by COMT genotype

  2005cited by this paper
• 22q11 deletion syndrome

  2005cited by this paper
• A survey of the 22q11 microdeletion in a large cohort of schizophrenia patients.

  2005cited by this paper
• Moderation of the effect of adolescent-onset cannabis use on adult psychosis by a functional polymorphism in the catechol-O-methyltransferase gene: longitudinal evidence of a gene X environment interaction.

  2005cited by this paper
• Catechol-O-Methyltransferase val158met Genotype Affects Processing of Emotional Stimuli in the Amygdala and Prefrontal Cortex

  2005cited by this paper
• The methionine allele of the COMT polymorphism impairs prefrontal cognition in children and adolescents with ADHD

  2005cited by this paper
• COMT genotype predicts longitudinal cognitive decline and psychosis in 22q11.2 deletion syndrome

  2005cited by this paper
• Cortical regulation of subcortical dopamine systems and its possible relevance to schizophrenia

  2005cited by this paper
• COMT Val108/158 Met modifies mismatch negativity and cognitive function in 22q11 deletion syndrome.

  2005cited by this paper
• Catechol-O-methyltransferase haplotypes are associated with psychosis in Alzheimer disease

  2005cited by this paper
• Catechol‐o‐methyltransferase (COMT) and proline dehydrogenase (PRODH) mRNAs in the dorsolateral prefrontal cortex in schizophrenia, bipolar disorder, and major depression

  2004cited by this paper
• The association between panic disorder and the L/L genotype of catechol-O-methyltransferase.

  2004cited by this paper
• Variation in catechol-o-methyltransferase val158 met genotype associated with schizotypy but not cognition: a population study in 543 young men.

  2004cited by this paper
• Variants in the catechol-o-methyltransferase (COMT) gene are associated with schizophrenia in Irish high-density families

  2004cited by this paper
• Genetic and neurochemical modulation of prefrontal cognitive functions in children.

  2004cited by this paper
• The Catechol-O-Methyltransferase Polymorphism: Relations to the Tonic–Phasic Dopamine Hypothesis and Neuropsychiatric Phenotypes

  2004cited by this paper
• Catechol O-methyltransferase Val158Met polymorphism in schizophrenia: differential effects of Val and Met alleles on cognitive stability and flexibility.

  2004cited by this paper
• Planning ability in Parkinson's disease is influenced by the COMT val158met polymorphism

  2004cited by this paper
• Effects of a functional COMT polymorphism on prefrontal cognitive function in patients with 22q11.2 deletion syndrome.

  2004cited by this paper
• The principal features and mechanisms of dopamine modulation in the prefrontal cortex.

  2004cited by this paper
• Targeting the dopamine D1 receptor in schizophrenia: insights for cognitive dysfunction

  2004cited by this paper
• Interaction of COMT (Val(108/158)Met) genotype and olanzapine treatment on prefrontal cortical function in patients with schizophrenia.

  2004cited by this paper
• Functional analysis of genetic variation in catechol-O-methyltransferase (COMT): effects on mRNA, protein, and enzyme activity in postmortem human brain.

  2004cited by this paper
• Catechol-O-Methyltransferase Inhibition Improves Set-Shifting Performance and Elevates Stimulated Dopamine Release in the Rat Prefrontal Cortex

  2004cited by this paper
• Catechol-O-methyltransferase gene polymorphism is associated with risk of psychosis in Alzheimer Disease.

  2004cited by this paper
• Genes, dopamine and cortical signal-to-noise ratio in schizophrenia.

  2004cited by this paper
• Catechol-O-methyltransferase val108/158met genotype predicts working memory response to antipsychotic medications.

  2004cited by this paper
• Genetic origins of anxiety in women: a role for a functional catechol-O-methyltransferase polymorphism

  2003cited by this paper
• MULTIPLE PROMOTERS OF CATECHOL-O-METHYLTRANSFERASE GENE ARE SELECTIVELY INACTIVATED BY CPG HYPERMETHYLATION IN ENDOMETRIAL CANCER

  2003cited by this paper
• Genome scan meta-analysis of schizophrenia and bipolar disorder, part III: Bipolar disorder.

  2003cited by this paper
• Human catechol-O-methyltransferase down-regulation by estradiol.

  2003cited by this paper
• Catechol-O-Methyltransferase Genotype and Dopamine Regulation in the Human Brain

  2003cited by this paper
• Executive subprocesses in working memory: relationship to catechol-O-methyltransferase Val158Met genotype and schizophrenia.

  2003cited by this paper
• Catechol O-methyltransferase val158-met genotype and individual variation in the brain response to amphetamine

  2003cited by this paper
• Genome scan meta-analysis of schizophrenia and bipolar disorder, part II: Schizophrenia.

  2003cited by this paper
• Catechol O-methyltransferase mRNA expression in human and rat brain: evidence for a role in cortical neuronal function.

  2003cited by this paper
• Association of the G1947A COMT (Val(108/158)Met) gene polymorphism with prefrontal P300 during information processing.

  2003cited by this paper
• Catechol O-Methyltransferase (COMT) mRNA Expression in the Dorsolateral Prefrontal Cortex of Patients with Schizophrenia

  2003cited by this paper
• Association between a functional catechol O-methyltransferase gene polymorphism and schizophrenia: meta-analysis of case-control and family-based studies.

  2003cited by this paper
• Ultrastructural localization of the norepinephrine transporter in superficial and deep layers of the rat prelimbic prefrontal cortex and its spatial relationship to probable dopamine terminals.

  2003cited by this paper
• A haplotype implicated in schizophrenia susceptibility is associated with reduced COMT expression in human brain.

  2003cited by this paper
• Effects of peripheral and central catechol-O-methyltransferase inhibition on striatal extracellular levels of dopamine: a microdialysis study in freely moving rats.

  2003cited by this paper
• COMT val158met Genotype Affects µ-Opioid Neurotransmitter Responses to a Pain Stressor

  2003cited by this paper
• A highly significant association between a COMT haplotype and schizophrenia.

  2002cited by this paper
• Dopaminergic modulation of cortical function in patients with Parkinson's disease

  2002cited by this paper
• A functional polymorphism in the COMT gene and performance on a test of prefrontal cognition.

  2002cited by this paper
• 18F‐dopa PET evidence that tolcapone acts as a central COMT inhibitor in Parkinson's disease

  2002cited by this paper
• Meta-analysis of whole-genome linkage scans of bipolar disorder and schizophrenia

  2002cited by this paper
• Family-based association studies of COMT gene polymorphisms and schizophrenia in the Chinese population

  2002cited by this paper
• Neurocognitive correlates of the COMT Val(158)Met polymorphism in chronic schizophrenia.

  2002cited by this paper
• Higher scores of self reported schizotypy in healthy young males carrying the COMT high activity allele

  2002cited by this paper
• Catechol-O-methyltransferase Val-108/158-Met gene variants associated with performance on the Wisconsin Card Sorting Test.

  2002cited by this paper
• Brain catecholamine metabolism in catechol‐O‐methyltransferase (COMT)‐deficient mice

  2002cited by this paper
• 22q11 DS: genomic mechanisms and gene function in DiGeorge/velocardiofacial syndrome

  2002cited by this paper
• Dopamine transporter immunoreactivity in monkey cerebral cortex: Regional, laminar, and ultrastructural localization

  2001cited by this paper
• Effect of COMT Val108/158 Met genotype on frontal lobe function and risk for schizophrenia

  2001cited by this paper
• Mice deleted for the DiGeorge/velocardiofacial syndrome region show abnormal sensorimotor gating and learning and memory impairments.

  2001cited by this paper
• Prefrontal neurons and the genetics of schizophrenia.

  2001cited by this paper
• D(1) receptors in prefrontal cells and circuits.

  2000cited by this paper
• Projections from the Rat Prefrontal Cortex to the Ventral Tegmental Area: Target Specificity in the Synaptic Associations with Mesoaccumbens and Mesocortical Neurons

  2000cited by this paper
• Gating of information flow within the limbic system and the pathophysiology of schizophrenia.

  2000cited by this paper
• Family-based linkage disequilibrium mapping using SNP marker haplotypes: application to a potential locus for schizophrenia at chromosome 22q11

  2000cited by this paper
• The effects of cannabinoids on the brain.

  1999cited by this paper
• High rates of schizophrenia in adults with velo-cardio-facial syndrome.

  1999cited by this paper
• Effect of a tyrosine-free amino acid mixture on regional brain catecholamine synthesis and release

  1999cited by this paper
• Global variation in the frequencies of functionally different catechol-O-methyltransferase alleles.

  1999cited by this paper
• 22q11 deletion syndrome: a genetic subtype of schizophrenia.

  1999cited by this paper
• Characterization and implications of estrogenic down-regulation of human catechol-O-methyltransferase gene transcription.

  1999cited by this paper
• Catechol-O-methyltransferase (COMT): biochemistry, molecular biology, pharmacology, and clinical efficacy of the new selective COMT inhibitors.

  1999cited by this paper
• Human neurons express the polyspecific cation transporter hOCT2, which translocates monoamine neurotransmitters, amantadine, and memantine.

  1998cited by this paper
• Catechol-O-methyltransferase-deficient mice exhibit sexually dimorphic changes in catecholamine levels and behavior.

  1998cited by this paper
• Dopamine Axon Varicosities in the Prelimbic Division of the Rat Prefrontal Cortex Exhibit Sparse Immunoreactivity for the Dopamine Transporter

  1998cited by this paper
• Distribution of catechol‐O‐methyltransferase expression in human central nervous system

  1998cited by this paper
• Chromosome 22q11.2 interstitial deletions among childhood-onset schizophrenics and "multidimensionally impaired".

  1998cited by this paper
• 22q11 deletion syndrome in adults with schizophrenia.

  1998cited by this paper
• Genotype determining low catechol-O-methyltransferase activity as a risk factor for obsessive-compulsive disorder.

  1997cited by this paper
• Supranormal Stimulation of D1 Dopamine Receptors in the Rodent Prefrontal Cortex Impairs Spatial Working Memory Performance

  1997cited by this paper
• Velocardiofacial manifestations and microdeletions in schizophrenic inpatients.

  1997cited by this paper
• Expression and intracellular localization of catechol O-methyltransferase in transfected mammalian cells.

  1997cited by this paper
• An association between the allele coding for a low activity variant of catechol-O-methyltransferase and the risk for breast cancer.

  1997cited by this paper
• The interface between dopamine neurons and the amygdala: implications for schizophrenia.

  1997cited by this paper
• Human catechol-O-methyltransferase pharmacogenetics: description of a functional polymorphism and its potential application to neuropsychiatric disorders.

  1996cited by this paper
• Modulation of memory fields by dopamine Dl receptors in prefrontal cortex

  1995cited by this paper
• Cloning, expression and structure of catechol-O-methyltransferase.

  1995cited by this paper
• Postnatal maturation of the dopaminergic innervation of monkey prefrontal and motor cortices: A tyrosine hydroxylase immunohistochemical analysis

  1995cited by this paper
• Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11.

  1995cited by this paper
• Kinetics of human soluble and membrane-bound catechol O-methyltransferase: a revised mechanism and description of the thermolabile variant of the enzyme.

  1995cited by this paper
• Genomic organization of the human catechol O-methyltransferase gene and its expression from two distinct promoters.

  1994cited by this paper
• Genomic scan for genes predisposing to schizophrenia.

  1994cited by this paper
• Immunohistochemical study of catechol-O-methyltransferase in the human mesostriatal system.

  1994cited by this paper
• Distribution of catechol-O-methyltransferase enzyme in rat tissues.

  1994cited by this paper
• Chromosomal mapping of the human catechol-O-methyltransferase gene to 22q11.1----q11.2.

  1992cited by this paper
• Membrane-bound catechol-O-methyltransferase: a reevaluation of its role in the O-methylation of the catecholamine neurotransmitters.

  1992cited by this paper
• D1 dopamine receptors in prefrontal cortex: involvement in working memory

  1991cited by this paper
• Cloning and Characterization of Human Placental Catechol--Methyltransferase cDNA

  1991cited by this paper
• Human catechol-O-methyltransferase: cloning and expression of the membrane-associated form.

  1991cited by this paper
• Behavioural and neurochemical effects of Ro 40-7592, a new COMT inhibitor with a potential therapeutic activity in Parkinson's disease

  1990cited by this paper

• Driven by Dopamine: Genetic Insights into Motivation and Performance in Sports and Esports.

  2026cites this paper
• Genetic Variation in Response to the Mediterranean–DASH Intervention for Neurodegenerative Delay (MIND): A Randomized Controlled Trial

  2026cites this paper
• Cognitive Deficits in Schizophrenia: Brain Deorganization and Neurorehabilitation.

  2026cites this paper
• COMT and ACE (Epi)genetic Variation Is Associated with Cognitive and Metabolic Resilience in Swiss Tactical Athletes

  2026cites this paper
• PROTAC-based degradation of catechol-O-methyltransferase for potential treatment of Parkinson’s disease

  2026cites this paper
• Relationships between addiction and the COMT rs4680 Gene Polymorphism

  2025cites this paper
• The Interaction Between Socioeconomic Status, Parent-Child Relationship, and the COMT Val158Met Polymorphism Predicts Chinese Preschoolers' Executive Function.

  2025cites this paper
• Assessment of Serum Dopamine and Catechol-O-methyltransferase (COMT) Levels in Patients with Sleep Parafunction

  2025cites this paper
• A proof-of-concept study: investigating the impact of COMT genotype and proline on negative symptoms in Alzheimer’s disease

  2025cites this paper
• Positive Associations between the Personality Trait of Openness and Verbal Learning and Memory in Individuals with Parkinson's Disease: A Pilot Study.

  2025cites this paper
• Females in Psychedelic Research: A Perspective for Advancing Research and Practice.

  2025cites this paper
• COMT rs4680 and DAOA rs947267 Polymorphism Interact to Influence Cognition and Psychiatric Symptoms in Chronic Schizophrenia.

  2025cites this paper
• The role of genetic factors in the occurrence of levodopa-induced motor complications in Parkinson’s disease

  2025cites this paper
• Not the same as it ever was: A review of memory modification, updating, and distortion in humans and rodents.

  2025cites this paper
• Single nucleotide polymorphisms of ANKK1, DDR4, and GRIN2B genes predict behavior in a prospective cohort of Mexican children and adolescents

  2024cites this paper
• Preliminary Evidence for a Positive Relation Between the COMT rs4680 Met/Met Genotype and Math Achievement

  2024cites this paper
• Association of catechol-O-methyltransferase gene polymorphisms with treatment response and levodopa-induced complications in Parkinson's disease: A summary of current knowledge

  2024cites this paper
• Dissociable effects of dopaminergic medications on depression symptom dimensions in Parkinson disease

  2024cites this paper
• The relationship between COMT, proline, and negative symptoms in clinical high risk and recent psychosis onset

  2024cites this paper
• Efficacy and safety of established and off‐label ADHD drug therapies for cognitive impairment or attention‐deficit hyperactivity disorder symptoms in bipolar disorder: A systematic review by the ISBD Targeting Cognition Task Force

  2024cites this paper
• Ödül Değerinde Kimyasal Dopamin ve İşlevleri

  2024cites this paper
• Smoking, coffee intake, and Parkinson's disease: potential protective mechanisms and components.

  2024cites this paper
• Cognitive impairment in patients with melanoma before adjuvant immune checkpoint inhibitor therapy and associations with brain gray matter, catechol‐O‐methyltransferase genotype, and psychological factors

  2024cites this paper
• Catechol-O-methyltransferase Inhibitors from Calendula officinalis Leaf

  2023cites this paper
• Toward a biopsychosocial model of hoarding disorder

  2023cites this paper
• Apathy and Motivation: Biological Basis and Drug Treatment.

  2023cites this paper
• Estradiol and the Catechol-o-methyltransferase Gene Interact to Predict Working Memory Performance: A Replication and Extension

  2023cites this paper
• The monoaminergic system is a bilaterian innovation

  2023cites this paper
• Associations between Catechol-O-methyltransferase (COMT) polymorphisms and cognitive impairments, psychiatric symptoms and tardive dyskinesia in schizophrenia.

  2023cites this paper
• The U-shaped relationship between dopaminergic genes and adolescent aggressive behavior: The moderating role of maternal negative parenting

  2023influential citation
• Dissociable effects of dopaminergic medications on depression symptom dimensions in Parkinson’s disease

  2023cites this paper
• Neurotransmission-related gene expression in the frontal pole is altered in subjects with bipolar disorder and schizophrenia

  2023cites this paper
• Genes and Sales

  2023cites this paper
• Thermostability and catechol-O-methyltransferase inhibitory activity of acylated anthocyanins from purple yam.

  2022cites this paper
• COMTVal158Met polymorphism is associated with ecstasy (MDMA)-induced psychotic symptoms in the Turkish population

  2022cites this paper
• Effects of Selen on the Antidepressant-like Activity of Agents Affecting the Adenosinergic Neurotransmission

  2022cites this paper
• Gender divergent effect of COMT gene rs4680 polymorphism on the association between executive dysfunction and psychotic-like experiences.

  2022cites this paper
• Prefrontal abnormalities, executive dysfunction and symptoms severity are modulated by COMT Val158Met polymorphism in first episode psychosis.

  2022cites this paper
• New drug targets in psychiatry: neurobiological considerations in the genomics era.

  2022cites this paper
• Cumulative Genetic Score of DRD2 Polymorphisms Is Associated with Impulsivity and Masked Semantic Priming

  2022cites this paper
• Cannabis induced psychosis: a systematic review on the role of genetic polymorphisms.

  2022cites this paper
• Neurotransmission-Related Gene Expression in the Frontal Pole (Brodmann Area 10) is Altered in Subjects with Bipolar Disorder and Schizophrenia

  2022cites this paper
• White-Matter Integrity and Working Memory: Links to Aging and Dopamine-Related Genes

  2022cites this paper
• Features of cognitive and non-cognitive indicators of mental health associated with the VAL158MET polymorphism of the COMT gene in adolescents of school age

  2022cites this paper
• Concussion-Associated Gene Variant COMT rs4680 Is Associated With Elite Rugby Athlete Status

  2022cites this paper
• Association of Two Variable Number of Tandem Repeats in the Monoamine Oxidase A Gene Promoter with Schizophrenia

  2021cites this paper
• Influence of Catechol-O-Methyltransferase Gene Polymorphism on the Correlation between Alexithymia and Hypervigilance to Pain

  2021cites this paper
• Insight into the Therapeutic Potential of a Bicyclic Hydroxypyridone Compound 2‐[(2,4‐Dichlorophenyl)methyl]‐7‐hydroxy‐1,2,3,4‐tetrahydro‐8H‐pyrido[1,2‐a]pyrazin‐8‐one as COMT Inhibitor in the Treatment of Parkinson's Disease: A Molecular Dynamic Simulation Approach

  2021cites this paper
• Dopamine-related receptors, substance dependence, behavioral problems and personality among juvenile delinquents

  2021cites this paper
• Oculomotor Control Asymmetry in Antisaccade Task in Carriers of Val158Met Polymorphic Variants of the Cateholamine-O-Methyltransferase Gene

  2021cites this paper
• Catechol-O-Methyltransferase Inhibitors Isolated From Thai Propolis

  2021cites this paper
• Working memory, cortical dopamine tone, and frontoparietal brain recruitment in post-traumatic stress disorder: a randomized controlled trial

  2021cites this paper
• Inhibitory Control Mediates the Associations Between Parenting Practices and Depressive Symptoms in Adolescents: The Moderating Role of Catechol-O-Methyltransferase (COMT) Gene

  2021cites this paper
• Dopaminergic modulation of regional cerebral blood flow: An arterial spin labelling study of genetic and pharmacological manipulation of COMT activity

  2021cites this paper
• Differential resting-state patterns across networks are spatially associated with Comt and Trmt2a gene expression patterns in a mouse model of 22q11.2 deletion

  2021cites this paper
• Detection of Morphological Abnormalities in Schizophrenia: An Important Step to Identify Associated Genetic Disorders or Etiologic Subtypes

  2021cites this paper
• Dimensions of Craving Interact with COMT Genotype to Predict Relapse in Individuals with Alcohol Use Disorder Six Months after Treatment

  2021cites this paper
• Deep analysis of the LRTOMTc.242G>A variant in non‐syndromic hearing loss North African patients and the Berber population: Implications for genetic diagnosis and genealogical studies

  2021cites this paper
• Dopaminergic and neurotrophic genetic polymorphisms modulate the implicit gender-science stereotype.

  2021cites this paper
• Strategies and cognitive reserve to preserve lexical production in aging

  2021cites this paper
• Dopamine and Risky Decision-Making in Gambling Disorder

  2020cites this paper
• Analytical methodologies for sensing catechol-O-methyltransferase activity and their applications

  2020cites this paper
• The effect of dopamine on the comprehension of spectrally-shifted noise-vocoded speech: a pilot study

  2020cites this paper
• Hydrogen deuterium exchange defines catalytically linked regions of protein flexibility in the catechol O-methyltransferase reaction

  2020cites this paper
• Factors Moderating the Association between Cannabis Use and Psychosis Risk: A Systematic Review

  2020cites this paper
• Effects of COMT rs4680 and BDNF rs6265 polymorphisms on brain degree centrality in Han Chinese adults who lost their only child

  2020cites this paper
• Motor learning and COMT Val158met polymorphism: analyses of oculomotor behavior and corticocortical communication.

  2020cites this paper
• Prediction of schizophrenia using MAOA-uVNTR polymorphism: A case–control study

  2020influential citation
• Evidence for the contribution of COMT gene Val158/108Met polymorphism (rs4680) to working memory training‐related prefrontal plasticity

  2020cites this paper
• Cancer Biology and Prevention in Diabetes

  2020cites this paper
• Genetic and psychological underpinnings of motivation and satisfaction of industrial salespeople

  2020cites this paper
• How Can Drug Metabolism and Transporter Genetics Inform Psychotropic Prescribing?

  2020cites this paper
• Mechanisms Underlying the Comorbidity of Schizophrenia and Type 2 Diabetes Mellitus

  2020cites this paper
• Title: The effect of dopamine on the comprehension of spectrally-shifted noise-vocoded speech: a pilot study

  2020cites this paper
• Genetic Determinants of Gating Functions: Do We Get Closer to Understanding Schizophrenia Etiopathogenesis?

  2020cites this paper
• The interactive effect of genetic polymorphisms of IL-10 and COMT on cognitive function in schizophrenia.

  2020cites this paper
• Hispidulin attenuates the social withdrawal in isolated disrupted‐in‐schizophrenia‐1 mutant and chronic phencyclidine‐treated mice

  2020cites this paper
• SNPs from BCHE and DRD3 genes associated to cocaine abuse amongst violent individuals from Sao Paulo, Brazil.

  2020cites this paper
• Interaction between the immune and metabolic systems in different stages of schizophrenia spectrum disorders

  2020cites this paper
• Influence of ovarian hormones on value-based decision-making systems: contribution to sexual dimorphisms in mental disorders.

  2020cites this paper
• The COMT rs4680 polymorphism, family functioning and preschoolers' attentional control indexed by intraindividual reaction time variability.

  2020cites this paper
• Povezanost polimorfizma Val 108/158Met katehol-o-metil transferaze i kliničkih simptoma posttraumatskog stresnog poremećaja

  2020cites this paper
• Adolescent cannabinoid exposure interacts with other risk factors in schizophrenia: a review of the evidence from animal models.

  2020cites this paper
• Zika Infection Disrupts Proteins Involved in the Neurosensory System

  2020cites this paper
• Effects of COMT Genotypes on Working Memory Performance in Fibromyalgia Patients

  2020cites this paper
• Pharmacogenomics and Psychopharmacology

  2020cites this paper
• Interaction of Catechol‐O‐methyltransferase Val158Met polymorphism and sex influences association of parietal intrinsic functional connectivity and immediate verbal memory

  2020cites this paper
• Effort-related decision making in humanized COMT mice: Effects of Val158Met polymorphisms and possible implications for negative symptoms in humans.

  2020cites this paper
• Female-specific effects of the catechol-O-methyl transferase Val158Met gene polymorphism on working memory-related brain function

  2020cites this paper
• Catechol-O-methyltransferase genotype differentially contributes to the flexibility and stability of cognitive sets in patients with psychotic disorders and their first-degree relatives.

  2020influential citation
• A novel pathogenic variant in the LRTOMT gene causes autosomal recessive non-syndromic hearing loss in an Iranian family

  2020cites this paper
• Associations of separate working memory parameters with comt genotypes in Western Siberia

  2019cites this paper
• THE INFLUENCE OF DOPAMINERGIC POLYMORPHISMS ON SELECTIVE STOPPING.

  2019cites this paper
• Acute effects of ∆9-tetrahydrocannabinol (THC) on resting state brain function and their modulation by COMT genotype.

  2019cites this paper
• Association Between the Catechol-O-Methyltransferase (COMT) Val158Met Polymorphism and Manual Performance Asymmetries

  2019influential citation
• The clinical applications and practical relevance of human conditioning paradigms for posttraumatic stress disorder

  2019cites this paper
• Genetic risk factors for schizophrenia associate with sleep spindle activity in healthy adolescents

  2019cites this paper
• Synthesis and Evaluation of Bicyclic Hydroxypyridones as Inhibitors of Catechol O-Methyltransferase

  2019cites this paper
• Lower folate levels in methamphetamine-induced psychosis: A cross-sectional study.

  2019cites this paper
• Association between the catechol-O-methyltransferase (COMT) Val158Met polymorphism and motor behavior in healthy adults: A study review.

  2019cites this paper