articleTop 10% cited
Genetic Predisposition to Hyperhomocysteinemia: Deficiency of Methylenetetrahydrofolate Reductase (MTHFR)
Thrombosis and Haemostasis · 1997 · Vol. 78(01) · pp. 523–526
Rima Rozen✉(Montreal Children's Hospital)
Folate and B Vitamins ResearchIron Metabolism and DisordersEsophageal and GI PathologyMethylenetetrahydrofolate reductaseHyperhomocysteinemiaMedicineHomocysteineGenetic predispositionGeneticsInternal medicineBiologyGenotypeGene
MeSH terms
Oxidoreductases Acting on CH-NH Group DonorsCardiovascular DiseasesHomocysteineHumansRisk FactorsGenetic VariationGenetic Predisposition to DiseaseMethylenetetrahydrofolate Reductase (NADPH2)
Citations
362
FWCI
11.04
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30
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99%
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Cited by
THE BRITISH JOURNAL OF NUTRITION
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5, 10-Methylenetetrahydrofolate Reductase Gene Variants and Congenital Anomalies: A HuGE Review
American Journal of Epidemiology · 2000 · 1,048 citations
Geographical and ethnic variation of the 677C>T allele of 5,10 methylenetetrahydrofolate reductase (<i>MTHFR</i>): findings from over 7000 newborns from 16 areas world wide
Journal of Medical Genetics · 2003 · 459 citations
References
A Quantitative Assessment of Plasma Homocysteine as a Risk Factor for Vascular Disease
JAMA · 1995 · 3,600 citations
Maternal hyperhomocysteinemia: A risk factor for neural-tube defects?
Metabolism · 1994 · 409 citations
A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase
Nature Genetics · 1995 · 5,697 citations
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