COMT genetic variation confers risk for psychotic and affective disorders: a case control study (Q24816526)

6

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author name string

Birgit Funke

1

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Anil K Malhotra

2

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Christine T Finn

3

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Stephen L Lake

5

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Pamela DeRosse

7

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John M Kane

8

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Raju Kucherlapati

Behavioral and Brain Functions

9

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language of work or name

English

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publication date

18 October 2005

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published in

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volume

1

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issue

1

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page(s)

19

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Variants in the catechol-o-methyltransferase (COMT) gene are associated with schizophrenia in Irish high-density families

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Combined family trio and case-control analysis of the COMT Val158Met polymorphism in European patients with anorexia nervosa

28 November 2018

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Catechol-o-methyltransferase (COMT) and proline dehydrogenase (PRODH) mRNAs in the dorsolateral prefrontal cortex in schizophrenia, bipolar disorder, and major depression.

28 November 2018

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In Sickness or in Health?

28 November 2018

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Association between Val108/158 Met polymorphism of the COMT gene and schizophrenia

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1282571

A haplotype implicated in schizophrenia susceptibility is associated with reduced COMT expression in human brain

28 November 2018

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

28 November 2018

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Family-based and case-control association studies of catechol-O-methyltransferase in attention deficit hyperactivity disorder suggest genetic sexual dimorphism

28 November 2018

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Regarding "Testing for population subdivision and association in four case-control studies".

28 November 2018

1 reference

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Functional catechol-O-methyltransferase gene polymorphism and susceptibility to schizophrenia

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1282571

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

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1282571

Association between the COMT locus and obsessive-compulsive disorder in females but not males

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1282571

Catecholamine metabolism in the brain by membrane-bound and soluble catechol-o-methyltransferase (COMT) estimated by enzyme kinetic values.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1282571

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

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1282571

Homicidal behavior in schizophrenia associated with a genetic polymorphism determining low catechol O-methyltransferase (COMT) activity.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1282571

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

28 November 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1282571

Genomic organization of the human catechol O-methyltransferase gene and its expression from two distinct promoters

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1282571

Male gender is associated with deficit schizophrenia: a meta-analysis

28 November 2018

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12 December 2020

No association between anxiety disorders and catechol-O-methyltransferase polymorphism

1 reference

12 December 2020

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

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12 December 2020

Family-based linkage disequilibrium mapping using SNP marker haplotypes: application to a potential locus for schizophrenia at chromosome 22q11

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12 December 2020

The Familial Aggregation of Psychotic Symptoms in Bipolar Disorder Pedigrees

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12 December 2020

Association study of a functional catechol-O-methyltransferase gene polymorphism in Japanese schizophrenics

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12 December 2020

Preliminary evidence of an association between bipolar disorder in females and the catechol-O-methyltransferase gene

1 reference

12 December 2020

Continuity and discontinuity of affective disorders and schizophrenia. Results of a controlled family study

1 reference

12 December 2020

No association between catechol-O-methyltransferase (COMT) gene polymorphism and attention deficit hyperactivity disorder (ADHD) in an Irish sample

1 reference

12 December 2020

Executive dysfunctions as potential markers of familial vulnerability to bipolar disorder and schizophrenia

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

Catechol-O-methyltransferase: thermolabile enzyme in erythrocytes of subjects homozygous for allele for low activity

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

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12 December 2020

Identifiers

DOI

10.1186/1744-9081-1-19

1 reference

Dimensions Publication ID

1052817450

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1 reference

1 reference

PubMed publication ID

16232322

1 reference