No Association Between Functional Polymorphisms in COMT and MTHFR and Schizophrenia Risk in Korean Population (Q41568991)

3 October 2017

No Association Between Functional Polymorphisms in COMT and MTHFR and Schizophrenia Risk in Korean Population (English)

1 reference

3 October 2017

1 reference

Ho Jin Kang

1

1 reference

3 October 2017

Byeong Moo Choe

2

1 reference

3 October 2017

Seong Hwan Kim

3

1 reference

3 October 2017

Seung-Rak Son

4

1 reference

3 October 2017

Kyoung-Mu Lee

5

1 reference

3 October 2017

Byoung Gwon Kim

6

1 reference

3 October 2017

Young-Seoub Hong

7

1 reference

3 October 2017

language of work or name

1 reference

24 December 2010

1 reference

3 October 2017

Epidemiology and Health

1 reference

3 October 2017

32

1 reference

3 October 2017

e2010011

1 reference

Creative Commons Attribution-NonCommercial 3.0 Unported

3 October 2017

start time

24 December 2010

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

Methylenetetrahydrofolate reductase (MTHFR) genetic polymorphisms and psychiatric disorders: a HuGE review

1 reference

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Hypomethylation of MB-COMT promoter is a major risk factor for schizophrenia and bipolar disorder

6 June 2018

1 reference

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Homocysteine, methylenetetrahydrofolate reductase and risk of schizophrenia: a meta-analysis

6 June 2018

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

6 June 2018

1 reference

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COMT haplotypes suggest P2 promoter region relevance for schizophrenia.

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3013321

A highly significant association between a COMT haplotype and schizophrenia.

6 June 2018

1 reference

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A common mutation in the 5,10-methylenetetrahydrofolate reductase gene affects genomic DNA methylation through an interaction with folate status.

6 June 2018

1 reference

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

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3013321

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

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3013321

Schizophrenia: genes and environment

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3013321

A second common mutation in the methylenetetrahydrofolate reductase gene: an additional risk factor for neural-tube defects?

6 June 2018

1 reference

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Human methylenetetrahydrofolate reductase: isolation of cDNA, mapping and mutation identification

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3013321

A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase

6 June 2018

1 reference

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The Comprehensive Assessment of Symptoms and History (CASH). An instrument for assessing diagnosis and psychopathology.

6 June 2018

1 reference

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Meta-analysis of association between genetic variants in COMT and schizophrenia: an update

6 June 2018

1 reference

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Interactive effects of COMT Val108/158Met and MTHFR C677T on executive function in schizophrenia

19 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3013321

Effects of the methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism on executive function in schizophrenia.

19 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3013321

Impact of complex genetic variation in COMT on human brain function.

19 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3013321

C677T and A1298C methylenetetrahydrofolate reductase gene polymorphisms in schizophrenia, bipolar disorder and depression: a meta-analysis of genetic association studies.

19 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3013321

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

19 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3013321

A meta-analysis of the MTHFR C677T polymorphism and schizophrenia risk

19 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3013321

COMT Val(158)Met and BDNF C(270)T polymorphisms in schizophrenia: a case-control study.

19 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3013321

Multiple promoters of catechol-O-methyltransferase gene are selectively inactivated by CpG hypermethylation in endometrial cancer.

19 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3013321

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

19 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3013321

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

19 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3013321

Schizophrenia and functional polymorphisms in the MAOA and COMT genes: no evidence for association or epistasis.

19 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3013321

Screening for 22q11 deletions in a schizophrenia population.

19 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3013321

A second common variant in the methylenetetrahydrofolate reductase (MTHFR) gene and its relationship to MTHFR enzyme activity, homocysteine, and cardiovascular disease risk

19 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3013321

Catechol-O-methyltransferase Val158Met polymorphism in relation to aggressive schizophrenia in a Korean population

19 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3013321

Effects of the catechol-O-methyltransferase Val158Met polymorphism on executive function: a meta-analysis of the Wisconsin Card Sort Test in schizophrenia and healthy controls

4 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3013321

No associations exist between five functional polymorphisms in the catechol-O-methyltransferase gene and schizophrenia in a Japanese population

2 December 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21217836

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Association of the 3' region of COMT with schizophrenia in Taiwan

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21217836

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Catechol-O-methyltransferase Val-108/158-Met gene variants associated with performance on the Wisconsin Card Sorting Test

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21217836

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.4178/EPIH/E2010011

1 reference

3 October 2017

1 reference

3 October 2017

1 reference