Literature DB >> 9718345

Heterogeneity in world distribution of the thermolabile C677T mutation in 5,10-methylenetetrahydrofolate reductase.

G Pepe, O Camacho Vanegas, B Giusti, T Brunelli, R Marcucci, M Attanasio, O Rickards, G F De Stefano, D Prisco, G F Gensini, R Abbate.   

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Year:  1998        PMID： 9718345      PMCID： PMC1377403          DOI： 10.1086/302015

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN： 0002-9297            Impact factor:   11.025


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  26 in total

1.  Spectrum of MTHFR gene SNPs C677T and A1298C: a study among 23 population groups of India.

Authors:  Kallur Nava Saraswathy; Mohammad Asghar; Ratika Samtani; Benrithung Murry; Prakash Ranjan Mondal; Pradeep Kumar Ghosh; Mohinder Pal Sachdeva
Journal:  Mol Biol Rep       Date:  2011-12-07       Impact factor: 2.316

2.  Environmental influence on the worldwide prevalence of a 776C->G variant in the transcobalamin gene (TCN2).

Authors:  Jean-Louis Guéant; Nicodème W Chabi; Rosa-Maria Guéant-Rodriguez; Osvaldo M Mutchinick; Renée Debard; Corinne Payet; Xiaohong Lu; Christian Villaume; Jean-Pierre Bronowicki; Edward V Quadros; Ambaliou Sanni; Emile Amouzou; Bing Xia; Min Chen; Guido Anello; Paolo Bosco; Corrado Romano; Heidy R Arrieta; Beatríz E Sánchez; Antonino Romano; Bernard Herbeth; Wafaa Anwar; Fares Namour
Journal:  J Med Genet       Date:  2007-01-12       Impact factor: 6.318

3.  Association of the methylenetetrahydrofolate reductase C677T polymorphism and fracture risk in Chinese postmenopausal women.

Authors:  Xiumei Hong; Yi-Hsiang Hsu; Henry Terwedow; Genfu Tang; Xue Liu; Shanqun Jiang; Xin Xu; Xiping Xu
Journal:  Bone       Date:  2006-12-15       Impact factor: 4.398

4.  Methylenetetrahydrofolate reductase (MTHFR) 677C>T gene polymorphism as a possible factor for reducing clinical severity of psoriasis.

Authors:  Ercan Karabacak; Ersin Aydin; Omer Ozcan; Bilal Dogan; Mustafa Gultepe; Alpaslan Cosar; Tuba Muftuoglu
Journal:  Int J Clin Exp Med       Date:  2014-03-15

5.  Methylenetetrahydrofolate reductase C677T polymorphism and susceptibility to epilepsy.

Authors:  Vandana Rai; Pradeep Kumar
Journal:  Neurol Sci       Date:  2018-09-28       Impact factor: 3.307

6.  The frequent 5,10-methylenetetrahydrofolate reductase C677T polymorphism is associated with a common haplotype in whites, Japanese, and Africans.

Authors:  Nurit Rosenberg; Mitsuru Murata; Yasuo Ikeda; Ohene Opare-Sem; Ariella Zivelin; Eli Geffen; Uri Seligsohn
Journal:  Am J Hum Genet       Date:  2002-01-04       Impact factor: 11.025

Review 7.  The search for genetic polymorphisms in the homocysteine/folate pathway that contribute to the etiology of human neural tube defects.

Authors:  Anne M Molloy; Lawrence C Brody; James L Mills; John M Scott; Peadar N Kirke
Journal:  Birth Defects Res A Clin Mol Teratol       Date:  2009-04

Review 8.  Association of methylenetetrahydrofolate reductase (MTHFR) gene C677T polymorphism with autism: evidence of genetic susceptibility.

Authors:  Vandana Rai
Journal:  Metab Brain Dis       Date:  2016-03-08       Impact factor: 3.584

Review 9.  Review on genetic variants and maternal smoking in the etiology of oral clefts and other birth defects.

Authors:  Min Shi; George L Wehby; Jeffrey C Murray
Journal:  Birth Defects Res C Embryo Today       Date:  2008-03

10.  Cleft lip and palate genetics and application in early embryological development.

Authors:  Wenli Yu; Maria Serrano; Symone San Miguel; L Bruno Ruest; Kathy K H Svoboda
Journal:  Indian J Plast Surg       Date:  2009-10
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