Literature DB >> 8596396

Is mutated MTHFR a risk factor for neural tube defects?

D L Posey, M J Khoury, J Mulinare, M J Adams, C Y Ou.   

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Year:  1996        PMID： 8596396

Source DB:  PubMed          Journal:  Lancet        ISSN： 0140-6736            Impact factor:   79.321


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  14 in total

Review 1.  Hyperhomocysteinaemia and associated disease.

Authors:  R C Bakker; D P Brandjes
Journal:  Pharm World Sci       Date:  1997-06

2.  Making the most of case-mother/control-mother studies.

Authors:  M Shi; D M Umbach; S H Vermeulen; C R Weinberg
Journal:  Am J Epidemiol       Date:  2008-07-23       Impact factor: 4.897

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

Authors:  L E Mitchell
Journal:  Am J Hum Genet       Date:  1997-04       Impact factor: 11.025

4.  Maternal genetic effects, exerted by genes involved in homocysteine remethylation, influence the risk of spina bifida.

Authors:  Marie-Therese Doolin; Sandrine Barbaux; Maeve McDonnell; Katy Hoess; Alexander S Whitehead; Laura E Mitchell
Journal:  Am J Hum Genet       Date:  2002-10-09       Impact factor: 11.025

5.  Folate deficiency causes uracil misincorporation into human DNA and chromosome breakage: implications for cancer and neuronal damage.

Authors:  B C Blount; M M Mack; C M Wehr; J T MacGregor; R A Hiatt; G Wang; S N Wickramasinghe; R B Everson; B N Ames
Journal:  Proc Natl Acad Sci U S A       Date:  1997-04-01       Impact factor: 11.205

6.  Variants in maternal COMT and MTHFR genes and risk of neural tube defects in offspring.

Authors:  Jufen Liu; Yali Zhang; Lei Jin; Guoxing Li; Linlin Wang; Yanping Bao; Yunting Fu; Zhiwen Li; Le Zhang; Rongwei Ye; Aiguo Ren
Journal:  Metab Brain Dis       Date:  2014-07-04       Impact factor: 3.584

7.  Translational upregulation of folate receptors is mediated by homocysteine via RNA-heterogeneous nuclear ribonucleoprotein E1 interactions.

Authors:  Aśok Antony; Ying-Sheng Tang; Rehana A Khan; Mangatt P Biju; Xiangli Xiao; Qing-Jun Li; Xin-Lai Sun; Hiremagalur N Jayaram; Sally P Stabler
Journal:  J Clin Invest       Date:  2004-01       Impact factor: 14.808

8.  Lack of association between folate receptor autoantibodies and conotruncal congenital heart defects.

Authors:  Laura B Lewandowski; Darshak Sanghavi
Journal:  Pediatr Cardiol       Date:  2012-08-23       Impact factor: 1.655

9.  A common mutation in the methylenetetrahydrofolate reductase gene is associated with an accumulation of formylated tetrahydrofolates in red blood cells.

Authors:  P J Bagley; J Selhub
Journal:  Proc Natl Acad Sci U S A       Date:  1998-10-27       Impact factor: 11.205

10.  118 SNPs of folate-related genes and risks of spina bifida and conotruncal heart defects.

Authors:  Gary M Shaw; Wei Lu; Huiping Zhu; Wei Yang; Farren B S Briggs; Suzan L Carmichael; Lisa F Barcellos; Edward J Lammer; Richard H Finnell
Journal:  BMC Med Genet       Date:  2009-06-03       Impact factor: 2.103
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