(Q42928107)

11 November 2017

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

1 reference

11 November 2017

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7

1 reference

11 November 2017

Nicholas J Bray

1

0 references

Hywel Williams

1 reference

ORCID Public Data File 2021

author name string

Paul R Buckland

2

1 reference

11 November 2017

Nigel M Williams

3

1 reference

11 November 2017

Hywel J Williams

4

1 reference

11 November 2017

Nadine Norton

5

1 reference

11 November 2017

Michael J Owen

6

1 reference

11 November 2017

language of work or name

English

0 references

publication date

11 June 2003

1 reference

American Journal of Human Genetics

11 November 2017

1 reference

11 November 2017

73

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11 November 2017

1

1 reference

11 November 2017

152-161

1 reference

Enzymatic O-methylation of epinephrine and other catechols.

11 November 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180576

A highly significant association between a COMT haplotype and schizophrenia.

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180576

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

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180576

Association analysis of a functional catechol-o-methyltransferase gene polymorphism in schizophrenic patients in Taiwan

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180576

Search for schizophrenia susceptibility genes

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180576

Molecular definition of the 22q11 deletions in velo-cardio-facial syndrome

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180576

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

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180576

The significance of dopamine-receptor blockade for the mechanism of action of neuroleptic drugs

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180576

Soluble and particulate forms of rat catechol-O-methyltransferase distinguished by gel electrophoresis and immune fixation

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180576

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

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180576

Parental imprinting studied by allele-specific primer extension after PCR: paternal X chromosome-linked genes are transcribed prior to preferential paternal X chromosome inactivation

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180576

Detection of regulatory variation in mouse genes

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180576

Universal, robust, highly quantitative SNP allele frequency measurement in DNA pools.

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180576

Model-free analysis and permutation tests for allelic associations.

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180576

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

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180576

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

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180576

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

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180576

No evidence for allelic association between schizophrenia and a polymorphism determining high or low catechol O-methyltransferase activity

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180576

Allelic Variation in Human Gene Expression

3 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180576

Preferential transmission of the high activity allele of COMT in schizophrenia

1 December 2018

1 reference

https://pubmed.ncbi.nlm.nih.gov/12802784

12 December 2020

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/12802784

12 December 2020

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/12802784

12 December 2020

Cheap, accurate and rapid allele frequency estimation of single nucleotide polymorphisms by primer extension and DHPLC in DNA pools

1 reference

https://pubmed.ncbi.nlm.nih.gov/12802784

12 December 2020

Characterization of membrane-bound and soluble catechol-O-methyltransferase from human frontal cortex

1 reference

https://pubmed.ncbi.nlm.nih.gov/12802784

12 December 2020

Identifiers

DOI

10.1086/376578

1 reference

11 November 2017

1 reference

11 November 2017

PubMed publication ID

12802784

1 reference