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COMT Val108/158Met Modifies Mismatch Negativity and Cognitive Function in 22q11 Deletion Syndrome

Data up to Jan 2025

Published2005
Citations151
References92

Total Citations Per Year

Abstract

References (92)

The Endophenotype Concept in Psychiatry: Etymology and Strategic Intentions

2003 • 5,516 citations

Effect of COMT Val 108/158 Met genotype on frontal lobe function and risk for schizophrenia

2001 • 2,408 citations

22q11.2 deletion syndrome

2015 • 2,036 citations

Functional Analysis of Genetic Variation in Catechol-O-Methyltransferase (COMT): Effects on mRNA, Protein, and Enzyme Activity in Postmortem Human Brain

2004 • 1,637 citations

Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study.

1997 • 1,187 citations

Genome Scan Meta-Analysis of Schizophrenia and Bipolar Disorder, Part II: Schizophrenia

2003 • 1,160 citations

High Rates of Schizophrenia in Adults With Velo-Cardio-Facial Syndrome

1999 • 1,013 citations

Tbx1 haploinsufficiency in the DiGeorge syndrome region causes aortic arch defects in mice

2001 • 996 citations

The Child and Adolescent Psychiatric Assessment (CAPA)

1995 • 968 citations

Catechol O -methyltransferase val 158 -met genotype and individual variation in the brain response to amphetamine

2003 • 900 citations

‘Primitive intelligence’ in the auditory cortex

2001 • 819 citations

D1 receptors in prefrontal cells and circuits

2000 • 804 citations

Prefrontal neurons and the genetics of schizophrenia

2001 • 738 citations

The Development of Working Memory in Normally Achieving and Subtypes of Learning Disabled Children

1989 • 734 citations

Schizophrenia and Affective Disorders—Cosegregation with a Translocation at Chromosome 1q42 That Directly Disrupts Brain-Expressed Genes: Clinical and P300 Findings in a Family

2001 • 729 citations

Mismatch negativity in schizophrenia: a meta-analysis

2005 • 702 citations

A Highly Significant Association between a COMT Haplotype and Schizophrenia

2002 • 701 citations

Role of cortical N-methyl-D-aspartate receptors in auditory sensory memory and mismatch negativity generation: implications for schizophrenia.

1996 • 647 citations

A Functional Polymorphism in the COMT Gene and Performance on a Test of Prefrontal Cognition

2002 • 613 citations

Genes, dopamine and cortical signal-to-noise ratio in schizophrenia

2004 • 596 citations

Executive Subprocesses in Working Memory

2003 • 591 citations

The Quick Test (QT): Provisional Manual,

1962 • 578 citations

The Development of Working Memory in Normally Achieving and Subtypes of Learning Disabled Children

1989 • 577 citations

Genome Scan Meta-Analysis of Schizophrenia and Bipolar Disorder, Part III: Bipolar Disorder

2003 • 573 citations

Attention, Memory, and Motor Skills as Childhood Predictors of Schizophrenia-Related Psychoses: The New York High-Risk Project

2000 • 507 citations

The 22q11 deletion syndromes

2000 • 492 citations

Association of Promoter Variants in the α7 Nicotinic Acetylcholine Receptor Subunit Gene With an Inhibitory Deficit Found in Schizophrenia

2002 • 446 citations

Psychotic Illness in Patients Diagnosed with Velo-Cardio-Facial Syndrome and Their Relatives

1994 • 434 citations

Mismatch negativity: An index of a preattentive processing deficit in schizophrenia

1991 • 408 citations

Brain potential evidence for an auditory sensory memory deficit in schizophrenia

1995 • 362 citations

Association Between a Functional Catechol O-Methyltransferase Gene Polymorphism and Schizophrenia: Meta-Analysis of Case-Control and Family-Based Studies

2003 • 348 citations

Premorbid Social Functioning in Schizophrenia and Bipolar Disorder: Similarities and Differences

1997 • 337 citations

The Schizophrenia Phenotype in 22q11 Deletion Syndrome

2003 • 329 citations

Neurocognitive correlates of the COMT Val158Met polymorphism in chronic schizophrenia

2002 • 327 citations

Genetic variation at the 22q11 PRODH2/DGCR6 locus presents an unusual pattern and increases susceptibility to schizophrenia

2002 • 322 citations

Catechol-O-Methyltransferase Genotype and Dopamine Regulation in the Human Brain

2003 • 321 citations

Impaired auditory frequency discrimination in dyslexia detected with mismatch evoked potentials

1999 • 319 citations

Mismatch negativity potentials and cognitive impairment in schizophrenia

2003 • 314 citations

Speech Disorder in Schizophrenia: Review of the Literature and Exploration of Its Relation to the Uniquely Human Capacity for Language

2001 • 312 citations

Evidence that the gene encoding ZDHHC8 contributes to the risk of schizophrenia

2004 • 310 citations

Association of codon 108/158 catechol-O-methyltransferase gene polymorphism with the psychiatric manifestations of velo-cardio-facial syndrome

1996 • 308 citations

Mismatch Negativity in Chronic Schizophrenia and First-Episode Schizophrenia

2002 • 285 citations

Impaired feedback regulation of XBP1 as a genetic risk factor for bipolar disorder

2003 • 272 citations

Associated deficits in mismatch negativity generation and tone matching in schizophrenia

2000 • 253 citations

Inheritance of low erythrocyte catechol-o-methyltransferase activity in man.

1977 • 248 citations

How specific are deficits in mismatch negativity generation to schizophrenia?

2003 • 244 citations

Catechol O-Methyltransferase Val158Met Polymorphism in Schizophrenia: Differential Effects of Val and Met Alleles on Cognitive Stability and Flexibility

2004 • 232 citations

Deficits in Auditory and Visual Context-Dependent Processing in Schizophrenia

2000 • 230 citations

The Neurocognitive Phenotype of the 22Q11.2 Deletion Syndrome: Selective Deficit in Visual-Spatial Memory

2001 • 222 citations

The behavioural phenotype in velo-cardio-facial syndrome (VCFS): from infancy to adolescence.

1999 • 205 citations

Cognition in schizophrenia

2001 • 187 citations

Duration mismatch negativity in biological relatives of patients with schizophrenia spectrum disorders

2002 • 186 citations

Neuropsychological change in young people at high risk for schizophrenia: results from the first two neuropsychological assessments of the Edinburgh High Risk Study

2000 • 184 citations

Duration and frequency mismatch negativity in schizophrenia

2000 • 180 citations

Association of the G1947A COMT (Val108/158Met) gene polymorphism with prefrontal P300 during information processing

2003 • 173 citations

Adolescents and young adults with 22qll deletion syndrome: psychopathology in an at-risk group

2005 • 170 citations

COMT: A common susceptibility gene in bipolar disorder and schizophrenia

2004 • 165 citations

Obsessive‐compulsive disorder in patients with velocardiofacial (22q11 deletion) syndrome

2003 • 154 citations

Cognition in schizophrenia : impairments, importance, and treatment strategies

2000 • 146 citations

Mismatch Negativity Event-Related Potential Elicited by Speech Stimuli

1992 • 139 citations

Subjective and objective neuropsychological abnormalities in a psychosis prodrome clinic

2002 • 138 citations

Effects of a Functional COMT Polymorphism on Prefrontal Cognitive Function in Patients With 22q11.2 Deletion Syndrome

2004 • 131 citations

Impairment in frontal but not temporal components of mismatch negativity in schizophrenia

2002 • 130 citations

Individual differences in spatial working memory in relation to schizotypy.

1995 • 130 citations

Impaired Cortical Network for Preattentive Detection of Change in Speech Sounds in Schizophrenia: A High-Resolution Event-Related Potential Study

2002 • 125 citations

THE QUICK TEST

1951 • 124 citations

Comparison of three WISC-III short forms: Weighing psychometric, clinical, and practical factors

1996 • 123 citations

Velo-cardio-facial syndrome

2005 • 123 citations

An investigation of the neuropsychological profile in adults with velo-cardio-facial syndrome (VCFS)

2002 • 116 citations

Velo‐cardio‐facial syndrome: Implications of microdeletion 22q11 for schizophrenia and mood disorders

2001 • 116 citations

Individual differences in spatial working memory in relation to schizotypy.

1995 • 110 citations

Automatic processing of tones and speech stimuli in children with specific language impairment

2002 • 108 citations

Association between reduced duration mismatch negativity (MMN) and raised temporal discrimination thresholds in schizophrenia

2003 • 106 citations

Event-related potential correlates of impaired selective attention in children at high risk for schizophrenia

1992 • 102 citations

Automatic processing of tones and speech stimuli in children with specific language impairment

2002 • 100 citations

Performance of patients with schizophrenia on a pen and paper visuospatial working memory task with short delay

1997 • 96 citations

Impairment in activation of a frontal attention-switch mechanism in schizophrenic patients

2002 • 89 citations

Genetic linkage and association between chromosome 1q and working memory function in schizophrenia

2002 • 88 citations

Language skills in children with velocardiofacial syndrome (deletion 22q11.2)

2002 • 88 citations

The methionine allele of the COMT polymorphism impairs prefrontal cognition in children and adolescents with ADHD

2005 • 87 citations

Separate and interacting effects within the catechol-O-methyltransferase (COMT) are associated with schizophrenia

2004 • 83 citations

Auditory sensory memory in schizophrenia: inadequate trace formation?

2000 • 75 citations

Selectivity of verbal memory deficit in schizophrenic patients and their relatives

2002 • 74 citations

The difference in Mismatch negativity between the acute and post-acute phase of schizophrenia

2002 • 73 citations

Catecholamines in patients with 22q11.2 deletion syndrome and the low-activity COMT polymorphism

2001 • 68 citations

The first neurophysiological evidence for cognitive brain dysfunctions in children with CATCH

1997 • 60 citations

Short‐forms of the UK WAIS—R: Regression equations and their predictive validity in a general population sample

1992 • 59 citations

language comprehension in schizophrenics and their brothers

1992 • 56 citations

Analysis of Speech Characteristics in Children With Velocardiofacial Syndrome (VCFS) and Children With Phenotypic Overlap Without VCFS

2001 • 53 citations

Schizotypy and patterns of lateral asymmetry on hemisphere-specific language tasks

2001 • 45 citations

Profiles of communication disorder in children with velocardiofacial syndrome: Comparison to children with Down syndrome

2001 • 37 citations

The neurocognitive phenotype of the 22Q11.2 deletion syndrome

1999 • 2 citations

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