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The Journal of Maternal-Fetal & Neonatal Medicine Volume 24, 2011 - Issue 1
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Short Reports

The MTHFD1 c.1958 G>A polymorphism and recurrent spontaneous abortions

Tania O. CrişanDepartment of Medical Genetics, ‘Iuliu Haţieganu’ University of Medicine and Pharmacy, Cluj-Napoca, RomaniaCorrespondence[email protected]
,
Adrian TrifaDepartment of Medical Genetics, ‘Iuliu Haţieganu’ University of Medicine and Pharmacy, Cluj-Napoca, Romania
,
Marius FarcaşDepartment of Medical Genetics, ‘Iuliu Haţieganu’ University of Medicine and Pharmacy, Cluj-Napoca, Romania
,
Mariela MilitaruDepartment of Medical Genetics, ‘Iuliu Haţieganu’ University of Medicine and Pharmacy, Cluj-Napoca, Romania
,
Mihai NeteaDepartment of Medicine, Nijmegen University Centre for Infectious Diseases, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands
,
Ioan PopDepartment of Medical Genetics, ‘Iuliu Haţieganu’ University of Medicine and Pharmacy, Cluj-Napoca, Romania
&
Radu PoppDepartment of Medical Genetics, ‘Iuliu Haţieganu’ University of Medicine and Pharmacy, Cluj-Napoca, Romania
 show all
Pages 189-192 | Received 16 Nov 2009, Accepted 11 Feb 2010, Published online: 24 Mar 2010

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Shilpi Dasgupta, Aruna Meka & Battini Mohan Reddy. (2012) Genetic factors influencing recurrent pregnancy loss: lessons learnt from recent studies. Expert Review of Obstetrics & Gynecology 7:4, pages 363-378.
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Articles from other publishers (5)

Xue-Yun Qin, Si-Yao Ha, Lu Chen, Tao Zhang & Ming-Qing Li. (2023) Recent Advances in Folates and Autoantibodies against Folate Receptors in Early Pregnancy and Miscarriage. Nutrients 15:23, pages 4882.
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T.V. Zhilyaeva, O.M. Chekanina, G.V. Rukavishnikov, A.S. Blagonravova & G.E. Mazo. (2022) Methylenetetrahydrofolate dehydrogenase-1 (MTHFD1) 1958 G>A genetic polymorphism (rs2236225) is associated with lower schizophrenia risk: Preliminary study. Gene Reports 27, pages 101625.
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Fabio Coppedè. 2021. Molecular Nutrition: Mother and Infant. Molecular Nutrition: Mother and Infant 317 335 .
Jingjing Meng, Lei Han & Bo Zhuang. (2015) Association between MTHFD1 polymorphisms and neural tube defect susceptibility. Journal of the Neurological Sciences 348:1-2, pages 188-194.
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K.E. Christensen, L. Deng, K.Y. Leung, E. Arning, T. Bottiglieri, O.V. Malysheva, M.A. Caudill, N.I. Krupenko, N.D. Greene, L. Jerome-Majewska, R.E. MacKenzie & R. Rozen. (2013) A novel mouse model for genetic variation in 10-formyltetrahydrofolate synthetase exhibits disturbed purine synthesis with impacts on pregnancy and embryonic development. Human Molecular Genetics 22:18, pages 3705-3719.
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