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Results: 1 to 20 of 106

Similar articles for PubMed (Select 20664391)

1.

Maternal folate-related gene environment interactions and congenital heart defects.

Hobbs CA, Cleves MA, Karim MA, Zhao W, MacLeod SL.

Obstet Gynecol. 2010 Aug;116(2 Pt 1):316-22. doi: 10.1097/AOG.0b013e3181e80979.

2.
3.

Polymorphisms in genes related to folate and cobalamin metabolism and the associations with complex birth defects.

Brouns R, Ursem N, Lindemans J, Hop W, Pluijm S, Steegers E, Steegers-Theunissen R.

Prenat Diagn. 2008 Jun;28(6):485-93. doi: 10.1002/pd.2006.

PMID:
18435414
4.

Associations between maternal genotypes and metabolites implicated in congenital heart defects.

Chowdhury S, Hobbs CA, MacLeod SL, Cleves MA, Melnyk S, James SJ, Hu P, Erickson SW.

Mol Genet Metab. 2012 Nov;107(3):596-604. doi: 10.1016/j.ymgme.2012.09.022. Epub 2012 Sep 27.

5.

Association of SNPs in genes involved in folate metabolism with the risk of congenital heart disease.

Wang B, Liu M, Yan W, Mao J, Jiang D, Li H, Chen Y.

J Matern Fetal Neonatal Med. 2013 Dec;26(18):1768-77. doi: 10.3109/14767058.2013.799648. Epub 2013 Jun 10.

PMID:
23701284
6.

Investigations of single nucleotide polymorphisms in folate pathway genes in Chinese families with neural tube defects.

Liu J, Qi J, Yu X, Zhu J, Zhang L, Ning Q, Luo X.

J Neurol Sci. 2014 Feb 15;337(1-2):61-6. doi: 10.1016/j.jns.2013.11.017. Epub 2013 Nov 19.

PMID:
24326202
7.

Maternal MTHFR 677C>T is a risk factor for congenital heart defects: effect modification by periconceptional folate supplementation.

van Beynum IM, Kapusta L, den Heijer M, Vermeulen SH, Kouwenberg M, Daniëls O, Blom HJ.

Eur Heart J. 2006 Apr;27(8):981-7. Epub 2006 Mar 7.

8.

Methylenetetrahydrofolate reductase C677T and reduced folate carrier 80 G>A polymorphisms are associated with an increased risk of conotruncal heart defects.

Gong D, Gu H, Zhang Y, Gong J, Nie Y, Wang J, Zhang H, Liu R, Hu S, Zhang H.

Clin Chem Lab Med. 2012 Feb 4;50(8):1455-61. doi: 10.1515/cclm-2011-0759.

PMID:
22868813
9.

Maternal risk for Down syndrome is modulated by genes involved in folate metabolism.

Zampieri BL, Biselli JM, Goloni-Bertollo EM, Vannucchi H, Carvalho VM, Cordeiro JA, Pavarino EC.

Dis Markers. 2012;32(2):73-81. doi: 10.3233/DMA-2011-0869.

10.

Folate intake, methylenetetrahydrofolate reductase polymorphisms, and risk of esophageal cancer.

Zhao P, Lin F, Li Z, Lin B, Lin J, Luo R.

Asian Pac J Cancer Prev. 2011;12(8):2019-23.

11.

Evaluation of C677T and A1298C polymorphisms of the MTHFR gene as maternal risk factors for Down syndrome and congenital heart defects.

Brandalize AP, Bandinelli E, dos Santos PA, Roisenberg I, Schüler-Faccini L.

Am J Med Genet A. 2009 Oct;149A(10):2080-7. doi: 10.1002/ajmg.a.32989.

PMID:
19725133
12.

Maternal folate, alcohol and energy metabolism-related gene polymorphisms and the risk of recurrent pregnancy loss.

Sata F, Yamada H, Kishi R, Minakami H.

J Dev Orig Health Dis. 2012 Oct;3(5):327-32. doi: 10.1017/S2040174412000359.

PMID:
25102261
13.

[Study of correlationship between congenital heart disease and 5, 10-methylenetetra hydrofolate reductase gene's polymorphism or folacin intakes].

Li D, Jing XA, Wang HY, Ye WJ, Fan H.

Zhonghua Yu Fang Yi Xue Za Zhi. 2009 Aug;43(8):700-4. Chinese.

PMID:
20021850
14.

MTHFR C677T and A1298C gene polymorphisms and their relation to homocysteine level in Egyptian children with congenital heart diseases.

Zidan HE, Rezk NA, Mohammed D.

Gene. 2013 Oct 15;529(1):119-24. doi: 10.1016/j.gene.2013.07.053. Epub 2013 Aug 8.

PMID:
23933414
15.

Maternal one-carbon metabolism, MTHFR and TCN2 genotypes and neural tube defects in India.

Godbole K, Gayathri P, Ghule S, Sasirekha BV, Kanitkar-Damle A, Memane N, Suresh S, Sheth J, Chandak GR, Yajnik CS.

Birth Defects Res A Clin Mol Teratol. 2011 Sep;91(9):848-56. doi: 10.1002/bdra.20841. Epub 2011 Jul 18.

PMID:
21770021
16.

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

Shaw GM, Lu W, Zhu H, Yang W, Briggs FB, Carmichael SL, Barcellos LF, Lammer EJ, Finnell RH.

BMC Med Genet. 2009 Jun 3;10:49. doi: 10.1186/1471-2350-10-49.

17.

Common 894G>T single nucleotide polymorphism in the gene coding for endothelial nitric oxide synthase (eNOS) and risk of congenital heart defects.

van Beynum IM, Mooij C, Kapusta L, Heil S, den Heijer M, Blom HJ.

Clin Chem Lab Med. 2008;46(10):1369-75. doi: 10.1515/CCLM.2008.271.

PMID:
18844489
18.

Risk of congenital heart defects is influenced by genetic variation in folate metabolism.

Christensen KE, Zada YF, Rohlicek CV, Andelfinger GU, Michaud JL, Bigras JL, Richter A, Dubé MP, Rozen R.

Cardiol Young. 2013 Feb;23(1):89-98. doi: 10.1017/S1047951112000431. Epub 2012 Apr 5.

PMID:
22475273
19.

Polymorphisms of folate metabolic genes and susceptibility to bladder cancer: a case-control study.

Lin J, Spitz MR, Wang Y, Schabath MB, Gorlov IP, Hernandez LM, Pillow PC, Grossman HB, Wu X.

Carcinogenesis. 2004 Sep;25(9):1639-47. Epub 2004 Apr 29.

20.

Variants of folate metabolism genes and risk of left-sided cardiac defects.

Mitchell LE, Long J, Garbarini J, Paluru P, Goldmuntz E.

Birth Defects Res A Clin Mol Teratol. 2010 Jan;88(1):48-53. doi: 10.1002/bdra.20622.

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