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Association of the Maternal MTHFR C677T Polymorphism with Susceptibility to Neural Tube Defects in Offsprings: Evidence from 25 Case-Control Studies

Overview of attention for article published in PLOS ONE, October 2012
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Title
Association of the Maternal MTHFR C677T Polymorphism with Susceptibility to Neural Tube Defects in Offsprings: Evidence from 25 Case-Control Studies
Published in
PLOS ONE, October 2012
DOI 10.1371/journal.pone.0041689
Pubmed ID
Authors

Lifeng Yan, Lin Zhao, Yan Long, Peng Zou, Guixiang Ji, Aihua Gu, Peng Zhao

Abstract

Methylenetetrahydrofolate reductase (MTHFR) is a critical enzyme in folate metabolism and is involved in DNA methylation, DNA synthesis, and DNA repair. In addition, it is a possible risk factor in neural tube defects (NTDs). The association of the C677T polymorphism in the MTHFR gene and NTD susceptibility has been widely demonstrated, but the results remain inconclusive. In this study, we performed a meta-analysis with 2429 cases and 3570 controls to investigate the effect of the MTHFR C677T polymorphism on NTDs.

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Mendeley readers

The data shown below were compiled from readership statistics for 114 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Spain 1 <1%
Unknown 113 99%

Demographic breakdown

Readers by professional status Count As %
Student > Bachelor 33 29%
Student > Master 22 19%
Student > Postgraduate 8 7%
Student > Ph. D. Student 8 7%
Student > Doctoral Student 7 6%
Other 23 20%
Unknown 13 11%
Readers by discipline Count As %
Medicine and Dentistry 32 28%
Biochemistry, Genetics and Molecular Biology 21 18%
Agricultural and Biological Sciences 20 18%
Nursing and Health Professions 8 7%
Neuroscience 5 4%
Other 11 10%
Unknown 17 15%