(Q33608693)

28 July 2017

title

Effects of COMT genotype on behavioral symptomatology in the 22q11.2 Deletion Syndrome (English)

1 reference

28 July 2017

11

Elaine Zackai

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28 July 2017

Donna M McDonald-McGinn

6

object named as

Donna M McDonald-McGinn

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28 July 2017

1

Carrie E Bearden

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28 July 2017

Abbas F Jawad

2

1 reference

28 July 2017

David R Lynch

3

1 reference

28 July 2017

John R Monterossso

4

1 reference

28 July 2017

Set Sokol

5

1 reference

28 July 2017

Sulagna C Saitta

7

1 reference

28 July 2017

Stacy E Harris

8

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28 July 2017

Edward Moss

9

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28 July 2017

Paul P Wang

10

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28 July 2017

Beverly S Emanuel

12

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28 July 2017

Tony J Simon

13

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28 July 2017

publication date

1 February 2005

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28 July 2017

published in

Child Neuropsychology

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28 July 2017

volume

11

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28 July 2017

issue

1

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28 July 2017

page(s)

109-117

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

28 July 2017

cites work

1 reference

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21 June 2018

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Association between a functional catechol O-methyltransferase gene polymorphism and schizophrenia: meta-analysis of case-control and family-based studies

21 June 2018

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A highly significant association between a COMT haplotype and schizophrenia.

21 June 2018

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Schizophrenia and velo-cardio-facial syndrome.

21 June 2018

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Prefrontal neurons and the genetics of schizophrenia

21 June 2018

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

21 June 2018

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Neuropsychiatric disorders in the 22q11 deletion syndrome

21 June 2018

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A prospective cohort study of childhood behavioral deviance and language abnormalities as predictors of adult schizophrenia

21 June 2018

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22q11 deletion syndrome: a genetic subtype of schizophrenia

21 June 2018

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Haplotype relative risk study of catechol-O-methyltransferase (COMT) and attention deficit hyperactivity disorder (ADHD): association of the high-enzyme activity Val allele with ADHD impulsive-hyperactive phenotype

21 June 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810976

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

21 June 2018

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22q11 deletion syndrome in adults with schizophrenia

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810976

Premorbid social functioning in schizophrenia and bipolar disorder: similarities and differences.

21 June 2018

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Bipolar spectrum disorders in patients diagnosed with velo-cardio-facial syndrome: does a hemizygous deletion of chromosome 22q11 result in bipolar affective disorder?

21 June 2018

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810976

Child development risk factors for adult schizophrenia in the British 1946 birth cohort

21 June 2018

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Kinetics of human soluble and membrane-bound catechol O-methyltransferase: a revised mechanism and description of the thermolabile variant of the enzyme

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810976

Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810976

Velo-cardio-facial syndrome: language and psychological profiles.

21 June 2018

1 reference

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Chromosomal mapping of the human catechol-O-methyltransferase gene to 22q11.1----q11.2

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810976

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810976

Lack of effect of polymorphisms in dopamine metabolism related genes on imaging of TRODAT-1 in striatum of asymptomatic volunteers and patients with Parkinson's disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810976

Family‐based and case–control study of catechol‐O‐methyltransferase in schizophrenia among Palestinian Arabs

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810976

Catechol-O-methyltransferase genotype and dopamine regulation in the human brain.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810976

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

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810976

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

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810976

The neurocognitive phenotype of the 22q11.2 deletion syndrome: selective deficit in visual-spatial memory.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810976

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

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810976

MAO-A and COMT polymorphisms and gene effects in narcolepsy.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810976

Neuropsychological profile of children and adolescents with the 22q11.2 microdeletion.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810976

Association of anorexia nervosa with the high activity allele of the COMT gene: a family-based study in Israeli patients.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810976

Association study of the low-activity allele of catechol-O-methyltransferase and alcoholism using a family-based approach

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810976

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

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810976

Human catechol-O-methyltransferase pharmacogenetics: description of a functional polymorphism and its potential application to neuropsychiatric disorders.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2810976

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

30 October 2018

1 reference

12 December 2020

Catechol-O-methyltransferase polymorphisms and schizophrenia: a transmission disequilibrium study in multiply affected families

1 reference

12 December 2020

Catechol-O-methyltransferase Vall58Met polymorphism: frequency analysis in Han Chinese subjects and allelic association of the low activity allele with bipolar affective disorder

1 reference

12 December 2020

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

1 reference

12 December 2020

Ultra-ultra rapid cycling bipolar disorder is associated with the low activity catecholamine-O-methyltransferase allele

1 reference

12 December 2020

The 22q11.2 deletion: screening, diagnostic workup, and outcome of results; report on 181 patients

1 reference

12 December 2020

Confirmation of an excess of the high enzyme activity COMTval allele in heroin addicts in a family-based haplotype relative risk study

1 reference

12 December 2020

Meta-analysis of whole-genome linkage scans of bipolar disorder and schizophrenia

1 reference

12 December 2020

10.1080/09297040590911239

Identifiers

DOI

1 reference

28 July 2017

1 reference

28 July 2017

1 reference