(Q45115362)

English

Single-nucleotide polymorphisms in genes relating to homocysteine metabolism: how applicable are public SNP databases to a typical European population?

scientific article published in January 2005

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

9 December 2017

Single-nucleotide polymorphisms in genes relating to homocysteine metabolism: how applicable are public SNP databases to a typical European population? (English)

1 reference

Europe PubMed Central

PubMed publication ID

9 December 2017

single-nucleotide polymorphism

1 reference

based on heuristic

inferred from title

3

1 reference

Europe PubMed Central

PubMed publication ID

9 December 2017

author name string

Bohumila Janosíková

1

1 reference

Europe PubMed Central

PubMed publication ID

9 December 2017

Petra Zavadáková

2

1 reference

Europe PubMed Central

PubMed publication ID

9 December 2017

publication date

1 January 2005

1 reference

Europe PubMed Central

PubMed publication ID

9 December 2017

European Journal of Human Genetics

1 reference

Europe PubMed Central

PubMed publication ID

9 December 2017

13

1 reference

Europe PubMed Central

PubMed publication ID

9 December 2017

1

1 reference

Europe PubMed Central

PubMed publication ID

9 December 2017

86-95

1 reference

Europe PubMed Central

PubMed publication ID

9 December 2017

Data mining of public SNP databases for the selection of intragenic SNPs

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201282

21 January 2018

dbSNP: the NCBI database of genetic variation

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201282

21 January 2018

Data mining: Efficiency of using sequence databases for polymorphism discovery

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201282

21 January 2018

Single-nucleotide polymorphisms in the public domain: how useful are they?

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201282

21 January 2018

A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201282

21 January 2018

Quality and completeness of SNP databases

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201282

21 January 2018

Characterization of 458 single nucleotide polymorphisms of disease candidate genes in the Korean population

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201282

21 January 2018

Single-nucleotide polymorphisms in the interleukin-10 gene: differences in frequencies, linkage disequilibrium patterns, and haplotypes in three United States ethnic groups.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201282

21 January 2018

Cystathionine beta-synthase polymorphisms and hyperhomocysteinaemia: an association study

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201282

21 January 2018

Glutamate carboxypeptidase II: a polymorphism associated with lower levels of serum folate and hyperhomocysteinemia.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201282

21 January 2018

A Polymorphism, R653Q, in the Trifunctional Enzyme Methylenetetrahydrofolate Dehydrogenase/Methenyltetrahydrofolate Cyclohydrolase/Formyltetrahydrofolate Synthetase Is a Maternal Genetic Risk Factor for Neural Tube Defects

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201282

21 January 2018

Essential hypertension in adolescents: association with insulin resistance and with metabolism of homocysteine and vitamins.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201282

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201282

21 January 2018

Genetic polymorphisms of methylenetetrahydrofolate reductase (MTHFR) and methionine synthase reductase (MTRR) in ethnic populations in Texas; a report of a novel MTHFR polymorphic site, G1793A.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201282

21 January 2018

The methionine synthase reductase (MTRR) A66G polymorphism is a novel genetic determinant of plasma homocysteine concentrations

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201282

21 January 2018

Is mutated serine hydroxymethyltransferase (SHMT) involved in the etiology of neural tube defects?

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201282

21 January 2018

Genomic structure of human transcobalamin II: comparison to human intrinsic factor and transcobalamin I.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201282

21 January 2018

Polymorphism of human transcobalamin II: substitution of proline and/or glutamine residues by arginine

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201282

21 January 2018

Genetic variants of homocysteine metabolizing enzymes and the risk of coronary artery disease

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201282

21 January 2018

Investigating single nucleotide polymorphism (SNP) density in the human genome and its implications for molecular evolution

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201282

21 January 2018

Homocysteine and cardiovascular disease: cause or effect?

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201282

7 January 2021

based on heuristic

inferred from DOI database lookup

The controversy over homocysteine and cardiovascular risk

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201282

7 January 2021

based on heuristic

inferred from DOI database lookup

Allele frequency determination of publicly available cSNPs in the Korean population

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201282

7 January 2021

based on heuristic

inferred from DOI database lookup

Betaine-homocysteine methyltransferase (BHMT): genomic sequencing and relevance to hyperhomocysteinemia and vascular disease in humans

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201282

7 January 2021

based on heuristic

inferred from DOI database lookup

Genomic basis of cystathioninuria (MIM 219500) revealed by multiple mutations in cystathionine gamma-lyase (CTH).

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201282

7 January 2021

based on heuristic

inferred from DOI database lookup

A polymorphism (80G->A) in the reduced folate carrier gene and its associations with folate status and homocysteinemia

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201282

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1038/SJ.EJHG.5201282

1 reference

Europe PubMed Central

PubMed publication ID

9 December 2017

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

9 December 2017

ResearchGate publication ID

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