The Val/Met functional polymorphism in COMT confers susceptibility to bipolar disorder: evidence from an association study and a meta-analysis (Q84175463)

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scientific article published on 04 July 2009

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English	The Val/Met functional polymorphism in COMT confers susceptibility to bipolar disorder: evidence from an association study and a meta-analysis	scientific article published on 04 July 2009

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scholarly article

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19578924 AND SRC:MED&resulttype=core&format=json

1 February 2020

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The Val/Met functional polymorphism in COMT confers susceptibility to bipolar disorder: evidence from an association study and a meta-analysis (English)

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1 February 2020

bipolar disorder

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inferred from title

1

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1 February 2020

author name string

Klaus Lindpaintner

2

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1 February 2020

Ronglin Che

3

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1 February 2020

Zangdong He

4

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1 February 2020

Peng Wang

5

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1 February 2020

Ping Yang

6

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1 February 2020

Guoyin Feng

7

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1 February 2020

Lin He

8

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1 February 2020

Yongyong Shi

9

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1 February 2020

publication date

4 July 2009

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1 February 2020

Journal of Neural Transmission

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1 February 2020

116

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1 February 2020

10

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1 February 2020

1193-1200

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1 February 2020

The catechol O-methyltransferase Val158Met polymorphism and herpes simplex virus type 1 infection are risk factors for cognitive impairment in bipolar disorder: additive gene-environmental effects in a complex human psychiatric disorder

1 reference

https://pubmed.ncbi.nlm.nih.gov/19578924

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Catechol-O-methyltransferase gene Val/Met functional polymorphism and risk of schizophrenia: a large-scale association study plus meta-analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/19578924

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association analysis of the catechol O-methyltransferase gene and bipolar affective disorder

1 reference

https://pubmed.ncbi.nlm.nih.gov/19578924

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Low activity allele of catechol-O-methyltransferase gene associated with rapid cycling bipolar disorder

1 reference

https://pubmed.ncbi.nlm.nih.gov/19578924

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

No evidence for an association of affective disorders with high- or low-activity allele of catechol-o-methyltransferase gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/19578924

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association studies of bipolar disorder.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19578924

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A navigator for human genome epidemiology

1 reference

https://pubmed.ncbi.nlm.nih.gov/19578924

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Meta-analysis of COMT val158met in panic disorder: ethnic heterogeneity and gender specificity

1 reference

https://pubmed.ncbi.nlm.nih.gov/19578924

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Meta-analysis of the association between the catecholamine-O-methyl-transferase gene and obsessive-compulsive disorder

1 reference

https://pubmed.ncbi.nlm.nih.gov/19578924

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association analysis of MAOA and COMT with neuroticism assessed by peers

1 reference

https://pubmed.ncbi.nlm.nih.gov/19578924

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Velo-cardio-facial syndrome: 30 Years of study

1 reference

https://pubmed.ncbi.nlm.nih.gov/19578924

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lack of association of catechol-O-methyltransferase (COMT) functional polymorphism in bipolar affective disorder

1 reference

https://pubmed.ncbi.nlm.nih.gov/19578924

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Meta-analysis in clinical trials

1 reference

https://pubmed.ncbi.nlm.nih.gov/19578924

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Impact of complex genetic variation in COMT on human brain function

1 reference

https://pubmed.ncbi.nlm.nih.gov/19578924

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Low activity allele of catechol-o-methyltransferase gene and Japanese unipolar depression

1 reference

https://pubmed.ncbi.nlm.nih.gov/19578924

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association between the COMT Val158Met polymorphism and propensity to anxiety in an Australian population-based longitudinal study of adolescent health

1 reference

https://pubmed.ncbi.nlm.nih.gov/19578924

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Differential association of the COMT Val158Met polymorphism with clinical phenotypes in schizophrenia and bipolar disorder

1 reference

https://pubmed.ncbi.nlm.nih.gov/19578924

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder

1 reference

https://pubmed.ncbi.nlm.nih.gov/19578924

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human catechol-O-methyltransferase haplotypes modulate protein expression by altering mRNA secondary structure.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19578924

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Catechol o-methyltransferase, serotonin transporter, and tryptophan hydroxylase gene polymorphisms in bipolar disorder patients with and without comorbid panic disorder

1 reference

https://pubmed.ncbi.nlm.nih.gov/19578924

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Development and validation of MIX: comprehensive free software for meta-analysis of causal research data

1 reference

https://pubmed.ncbi.nlm.nih.gov/19578924

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Functional analysis of genetic variation in catechol-O-methyltransferase (COMT): effects on mRNA, protein, and enzyme activity in postmortem human brain

1 reference

https://pubmed.ncbi.nlm.nih.gov/19578924

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association between catechol O-methyltransferase (COMT) haplotypes and severity of hyperactivity symptoms in adults

1 reference

https://pubmed.ncbi.nlm.nih.gov/19578924

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lack of association of the COMT (Val158/108 Met) gene and schizophrenia: a meta-analysis of case-control studies

1 reference

https://pubmed.ncbi.nlm.nih.gov/19578924

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

No allelic association or interaction of three known functional polymorphisms with bipolar disorder in a northern Swedish isolated population

1 reference

https://pubmed.ncbi.nlm.nih.gov/19578924

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

https://pubmed.ncbi.nlm.nih.gov/19578924

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Family-based association studies of bipolar disorder with candidate genes involved in dopamine neurotransmission: DBH, DAT1, COMT, DRD2, DRD3 and DRD5

1 reference

https://pubmed.ncbi.nlm.nih.gov/19578924

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Catechol-O-methyltransferase gene variants in mood disorders in the Italian population

1 reference

https://pubmed.ncbi.nlm.nih.gov/19578924

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ultradian rapid cycling in prepubertal and early adolescent bipolarity is not in transmission disequilibrium with val/met COMT alleles.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19578924

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

SHEsis, a powerful software platform for analyses of linkage disequilibrium, haplotype construction, and genetic association at polymorphism loci

1 reference

https://pubmed.ncbi.nlm.nih.gov/19578924

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/19578924

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/19578924

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/19578924

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/19578924

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multicentre Italian family-based association study on tyrosine hydroxylase, catechol-O-methyl transferase and Wolfram syndrome 1 polymorphisms in mood disorders

1 reference

https://pubmed.ncbi.nlm.nih.gov/19578924

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

COMT genotype increases risk for bipolar I disorder and influences neurocognitive performance

1 reference

https://pubmed.ncbi.nlm.nih.gov/19578924

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Bias in meta-analysis detected by a simple, graphical test

1 reference

https://pubmed.ncbi.nlm.nih.gov/19578924

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular genetics of bipolar disorder and depression.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19578924

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/19578924

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Bipolar 1 disorder is not associated with the RGS4, PRODH, COMT and GRK3 genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/19578924

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/19578924

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

COMT: a common susceptibility gene in bipolar disorder and schizophrenia.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19578924

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Family, twin, and adoption studies of bipolar disorder

1 reference

https://pubmed.ncbi.nlm.nih.gov/19578924

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

No association between bipolar disorder and alleles at a functional polymorphism in the COMT gene. Biomed European Bipolar Collaborative Group

1 reference

https://pubmed.ncbi.nlm.nih.gov/19578924

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00702-009-0260-7

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19578924 AND SRC:MED&resulttype=core&format=json

1 February 2020

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19578924 AND SRC:MED&resulttype=core&format=json

1 February 2020

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