(Q80162829)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17436311%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

title

Large-scale population-based metabolic phenotyping of thirteen genetic polymorphisms related to one-carbon metabolism (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17436311%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

3

Per Magne Ueland

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17436311%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

4

Stein Emil Vollset

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17436311%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

5

Tom Grotmol

1 reference

29 December 2019

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17436311%20AND%20SRC:MED&resulttype=core&format=json

Ase Fredriksen

series ordinal

1

object named as

Ase Fredriksen

1 reference

29 December 2019

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17436311%20AND%20SRC:MED&resulttype=core&format=json

Jørn Schneede

series ordinal

6

object named as

Jørn Schneede

1 reference

29 December 2019

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17436311%20AND%20SRC:MED&resulttype=core&format=json

author name string

Klaus Meyer

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17436311%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

publication date

1 September 2007

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17436311%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17436311%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

volume

28

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17436311%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

issue

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17436311%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

page(s)

856-865

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17436311%20AND%20SRC:MED&resulttype=core&format=json

Single nucleotide polymorphisms in the transcobalamin gene: relationship with transcobalamin concentrations and risk for neural tube defects

29 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20522

7 January 2021

Influence of 699C-->T and 1080C-->T polymorphisms of the cystathionine beta-synthase gene on plasma homocysteine levels.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20522

7 January 2021

The influence of genetic and environmental factors on plasma homocysteine concentrations in a population at high risk for coronary artery disease

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20522

7 January 2021

Design, organization and management of a controlled population screening study for detection of colorectal neoplasia: attendance rates in the NORCCAP study (Norwegian Colorectal Cancer Prevention).

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20522

7 January 2021

Methylenetetrahydrofolate reductase (MTHFR) 677C>T and methionine synthase reductase (MTRR) 66A>G polymorphisms: association with serum homocysteine and angiographic coronary artery disease in the era of flour products fortified with folic acid

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20522

7 January 2021

Effects of 5' regulatory-region polymorphisms on paraoxonase-gene (PON1) expression

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20522

7 January 2021

5,10-Methylenetetrahydrofolate reductase 677C-->T and 1298A-->C mutations are genetic determinants of elevated homocysteine

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20522

7 January 2021

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/10.1002%2FHUMU.20522

7 January 2021

Influence of a methionine synthase (D919G) polymorphism on plasma homocysteine and folate levels and relation to risk of myocardial infarction

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20522

7 January 2021

Polymorphisms in the one-carbon metabolic pathway, plasma folate levels and colorectal cancer in a prospective study

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20522

7 January 2021

Linkage disequilibrium at the cystathionine β synthase (CBS) locus and the association between genetic variation at the CBS locus and plasma levels of homocysteine

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20522

7 January 2021

The effect of the C677T and A1298C polymorphisms in the methylenetetrahydrofolate reductase gene on homocysteine levels in elderly men and women from the British regional heart study

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20522

7 January 2021

Methionine metabolism in mammals

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20522

7 January 2021

Homocysteine: overview of biochemistry, molecular biology, and role in disease processes

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20522

7 January 2021

A common mutation A1298C in human methylenetetrahydrofolate reductase gene: association with plasma total homocysteine and folate concentrations

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20522

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20522

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20522

7 January 2021

Genetic determinants of plasma total homocysteine.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20522

7 January 2021

Association of MTRRA66G polymorphism (but not of MTHFR C677T and A1298C, MTRA2756G, TCN C776G) with homocysteine and coronary artery disease in the French population.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20522

7 January 2021

Methionine synthase D919G polymorphism is a significant but modest determinant of circulating homocysteine concentrations

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20522

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20522

7 January 2021

Molecular genetic analysis of the gene encoding the trifunctional enzyme MTHFD (methylenetetrahydrofolate-dehydrogenase, methenyltetrahydrofolate-cyclohydrolase, formyltetrahydrofolate synthetase) in patients with neural tube defects

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20522

7 January 2021

Determination of choline, betaine, and dimethylglycine in plasma by a high-throughput method based on normal-phase chromatography-tandem mass spectrometry

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20522

7 January 2021

Betaine and folate status as cooperative determinants of plasma homocysteine in humans

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20522

7 January 2021

The molecular basis of the human serum paraoxonase activity polymorphism.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20522

7 January 2021

Effect of heterozygosity for the methionine synthase 2756 A-->G mutation on the risk for recurrent cardiovascular events

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20522

7 January 2021

Relation between folate status, a common mutation in methylenetetrahydrofolate reductase, and plasma homocysteine concentrations.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20522

7 January 2021

Effects of polymorphisms of methionine synthase and methionine synthase reductase on total plasma homocysteine in the NHLBI Family Heart Study.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20522

7 January 2021

Genetic determinants of homocysteine thiolactonase activity in humans: implications for atherosclerosis.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20522

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20522

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20522

7 January 2021

5,10-Methylenetetrahydrofolate reductase polymorphisms and pharmacogenetics: a new role of single nucleotide polymorphisms in the folate metabolic pathway in human health and disease

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20522

7 January 2021

The 2756A>G variant in the gene encoding methionine synthase: its relation with plasma homocysteine levels and risk of coronary heart disease in a Dutch case-control study

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20522

7 January 2021

A common 844INS68 insertion variant in the cystathionine beta-synthase gene

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20522

7 January 2021

Genetic and nutritional factors contributing to hyperhomocysteinemia in young adults.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20522

7 January 2021

Plasma homocysteine, MTHFR C677T, CBS 844ins68bp, and MTHFD1 G1958A polymorphisms in spontaneous cervical artery dissections

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20522

7 January 2021

The human cystathionine beta-synthase (CBS) gene: complete sequence, alternative splicing, and polymorphisms

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20522

7 January 2021

Polymorphisms in the CBS gene associated with decreased risk of coronary artery disease and increased responsiveness to total homocysteine lowering by folic acid

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20522

7 January 2021

Detection of genotyping errors and pseudo-SNPs via deviations from Hardy-Weinberg equilibrium

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20522

7 January 2021

Human methionine synthase: cDNA cloning and identification of mutations in patients of the cblG complementation group of folate/cobalamin disorders

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20522

7 January 2021

Isolation and sequence analysis of variant forms of human transcobalamin II.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20522

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20522

7 January 2021

Methylenetetrahydrofolate reductase polymorphism, plasma folate, homocysteine, and risk of myocardial infarction in US physicians

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20522

7 January 2021

Transcobalamin polymorphism and serum holo-transcobalamin in relation to Alzheimer's disease.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20522

7 January 2021

Betaine concentration as a determinant of fasting total homocysteine concentrations and the effect of folic acid supplementation on betaine concentrations.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20522

7 January 2021

High-level multiplex genotyping of polymorphisms involved in folate or homocysteine metabolism by matrix-assisted laser desorption/ionization mass spectrometry

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20522

7 January 2021

Multianalyte quantification of vitamin B6 and B2 species in the nanomolar range in human plasma by liquid chromatography-tandem mass spectrometry

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20522

7 January 2021

Transcobalamin II 775G>C polymorphism and indices of vitamin B12 status in healthy older adults

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20522

7 January 2021

Microbiological assay for serum, plasma, and red cell folate using cryopreserved, microtiter plate method

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20522

7 January 2021

Folate and homocysteine interrelationships including genetics of the relevant enzymes

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20522

7 January 2021

Evaluation of genetic variants in the reduced folate carrier and in glutamate carboxypeptidase II for spina bifida risk

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20522

7 January 2021

Common variant in betaine-homocysteine methyltransferase (BHMT) and risk for spina bifida

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20522

7 January 2021

Polymorphism of the methionine synthase gene : association with homocysteine metabolism and late-onset vascular diseases in the Japanese population

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20522

7 January 2021

Transcobalamin codon 259 polymorphism in HT-29 and Caco-2 cells and in Caucasians: relation to transcobalamin and homocysteine concentration in blood

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20522

7 January 2021

World distribution of the T833C/844INS68 CBS in cis double mutation: a reliable anthropological marker

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20522

7 January 2021

Facts and recommendations about total homocysteine determinations: an expert opinion

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20522

7 January 2021

Genetic modulation of homocysteinemia

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20522

7 January 2021

Relation between plasma homocysteine concentration, the 844ins68 variant of the cystathionine beta-synthase gene, and pyridoxal-5'-phosphate concentration.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20522

7 January 2021

Polygenic influence on plasma homocysteine: association of two prevalent mutations, the 844ins68 of cystathionine beta-synthase and A(2756)G of methionine synthase, with lowered plasma homocysteine levels.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20522

7 January 2021

Biological and clinical implications of the MTHFR C677T polymorphism

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20522

7 January 2021

Functional inference of the methylenetetrahydrofolate reductase 677C > T and 1298A > C polymorphisms from a large-scale epidemiological study

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20522

7 January 2021

Sequence analysis of the coding region of human methionine synthase: relevance to hyperhomocysteinaemia in neural-tube defects and vascular disease

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20522

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20522

7 January 2021

Transcobalamin 776C->G polymorphism negatively affects vitamin B-12 metabolism

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20522

7 January 2021

Analysis of the transcobalamin II 776C>G (259P>R) single nucleotide polymorphism by denaturing HPLC in healthy elderly: associations with cobalamin, homocysteine and holo-transcobalamin II.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20522

7 January 2021

The 1298A-->C polymorphism in methylenetetrahydrofolate reductase (MTHFR): in vitro expression and association with homocysteine

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20522

7 January 2021

Investigations of a common genetic variant in betaine-homocysteine methyltransferase (BHMT) in coronary artery disease.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20522

7 January 2021

A common variant in methionine synthase reductase combined with low cobalamin (vitamin B12) increases risk for spina bifida

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20522

7 January 2021

Automated assay for the determination of methylmalonic acid, total homocysteine, and related amino acids in human serum or plasma by means of methylchloroformate derivatization and gas chromatography-mass spectrometry

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20522

7 January 2021

G80A reduced folate carrier SNP modulates cellular uptake of folate and affords protection against thrombosis via a non homocysteine related mechanism

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20522

7 January 2021

Identifiers

DOI

10.1002/HUMU.20522

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17436311%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

1 reference