(Q28284199)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16315005%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

title

Evaluation of a methylenetetrahydrofolate-dehydrogenase 1958G>A polymorphism for neural tube defect risk (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16315005%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

1 reference

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16315005%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

author name string

Patrizia De Marco

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16315005%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

Elisa Merello

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16315005%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

Maria Grazia Calevo

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16315005%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

Samantha Mascelli

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16315005%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

Alessandro Raso

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16315005%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

Armando Cama

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16315005%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

language of work or name

English

0 references

publication date

29 November 2005

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16315005%20AND%20SRC:MED&resulttype=core&format=json

Journal of Human Genetics

9 January 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16315005%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

volume

51

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16315005%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16315005%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

page(s)

98-103

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16315005%20AND%20SRC:MED&resulttype=core&format=json

5,10-Methylenetetrahydrofolate reductase gene variants and congenital anomalies: a HuGE review

9 January 2020

cites work

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS10038-005-0329-6

Transmission disequilibrium test (TDT) when only one parent is available: the 1-TDT.

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS10038-005-0329-6

Methylenetetrahydrofolate dehydrogenase-methenyltetrahydrofolate cyclohydrolase-formyltetrahydrofolate synthetase. A multifunctional protein from porcine liver

21 January 2018

1 reference

12 December 2020

Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM)

1 reference

12 December 2020

A unified approach to adjusting association tests for population admixture with arbitrary pedigree structure and arbitrary missing marker information.

1 reference

12 December 2020

Elevated rates of severe neural tube defects in a high-prevalence area in northern China.

1 reference

12 December 2020

Prevention of the First Occurrence of Neural-Tube Defects by Periconceptional Vitamin Supplementation

1 reference

12 December 2020

Differentiating between fetal and maternal genotypic effects, using the transmission test for linkage disequilibrium.

1 reference

12 December 2020

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

12 December 2020

Genetic studies in neural tube defects. NTD Collaborative Group

1 reference

12 December 2020

Primary structure of a human trifunctional enzyme. Isolation of a cDNA encoding methylenetetrahydrofolate dehydrogenase-methenyltetrahydrofolate cyclohydrolase-formyltetrahydrofolate synthetase

1 reference

12 December 2020

Genetics of neural tube defects.

1 reference

12 December 2020

Chromosomal localization of the gene for the human trifunctional enzyme, methylenetetrahydrofolate dehydrogenase-methenyltetrahydrofolate cyclohydrolase-formyltetrahydrofolate synthetase

1 reference

12 December 2020

Prevention of neural tube defects: results of the Medical Research Council Vitamin Study. MRC Vitamin Study Research Group

1 reference

12 December 2020

The thermolabile variant of methylenetetrahydrofolate reductase (MTHFR) is not a major risk factor for neural tube defect in American Caucasians. The NTD Collaborative Group

1 reference

12 December 2020

Human mitochondrial C1-tetrahydrofolate synthase: gene structure, tissue distribution of the mRNA, and immunolocalization in Chinese hamster ovary calls

1 reference

12 December 2020

The descriptive epidemiology of congenital defects at birth in Italy

1 reference

12 December 2020

Proportion of disease caused or prevented by a given exposure, trait or intervention

1 reference

12 December 2020

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

12 December 2020

Methylenetetrahydrofolate reductase and neural tube defects

1 reference

12 December 2020

NAD-dependent methylenetetrahydrofolate dehydrogenase is expressed by immortal cells

1 reference

12 December 2020

Screening of the C677T mutation on the methylenetetrahydrofolate reductase gene in French patients with neural tube defects

1 reference

12 December 2020

Genotype frequencies and linkage disequilibrium in the CEPH human diversity panel for variants in folate pathway genes MTHFR, MTHFD, MTRR, RFC1, and GCP2.

1 reference

12 December 2020

Folic acid: nutritional biochemistry, molecular biology, and role in disease processes

1 reference

12 December 2020