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Items: 1 to 20 of 129

1.

Evaluation of 64 candidate single nucleotide polymorphisms as risk factors for neural tube defects in a large Irish study population.

Carter TC, Pangilinan F, Troendle JF, Molloy AM, VanderMeer J, Mitchell A, Kirke PN, Conley MR, Shane B, Scott JM, Brody LC, Mills JL.

Am J Med Genet A. 2011 Jan;155A(1):14-21. doi: 10.1002/ajmg.a.33755. Epub 2010 Dec 10.

2.

Heme oxygenase-1 promoter polymorphisms and risk of spina bifida.

Fujioka K, Yang W, Wallenstein MB, Zhao H, Wong RJ, Stevenson DK, Shaw GM.

Birth Defects Res A Clin Mol Teratol. 2015 Sep;103(9):741-6. doi: 10.1002/bdra.23343. Epub 2015 Jul 15.

PMID:
26173399
3.

Association between maternal COMT gene polymorphisms and fetal neural tube defects risk in a Chinese population.

Liu J, Wang L, Fu Y, Li Z, Zhang Y, Zhang L, Jin L, Ye R, Ren A.

Birth Defects Res A Clin Mol Teratol. 2014 Jan;100(1):22-9. doi: 10.1002/bdra.23208. Epub 2013 Dec 31.

PMID:
24382678
4.

DNA methylation aberrations rather than polymorphisms of FZD3 gene increase the risk of spina bifida in a high-risk region for neural tube defects.

Shangguan S, Wang L, Chang S, Lu X, Wang Z, Wu L, Wang J, Wang X, Guan Z, Bao Y, Zhao H, Zou J, Niu B, Zhang T.

Birth Defects Res A Clin Mol Teratol. 2015 Jan;103(1):37-44. doi: 10.1002/bdra.23285. Epub 2014 Aug 18.

PMID:
25131656
5.

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
6.

Association between maternal single nucleotide polymorphisms in genes regulating glucose metabolism and risk for neural tube defects in offspring.

Fu Y, Wang LL, Yi D, Jin L, Liu J, Zhang Y, Ren A.

Birth Defects Res A Clin Mol Teratol. 2015 Jun;103(6):471-8. doi: 10.1002/bdra.23332. Epub 2014 Nov 5.

PMID:
25369983
8.

The 19-bp deletion polymorphism in intron-1 of dihydrofolate reductase (DHFR) may decrease rather than increase risk for spina bifida in the Irish population.

Parle-McDermott A, Pangilinan F, Mills JL, Kirke PN, Gibney ER, Troendle J, O'Leary VB, Molloy AM, Conley M, Scott JM, Brody LC.

Am J Med Genet A. 2007 Jun 1;143A(11):1174-80.

PMID:
17486595
9.

Genes in glucose metabolism and association with spina bifida.

Davidson CM, Northrup H, King TM, Fletcher JM, Townsend I, Tyerman GH, Au KS.

Reprod Sci. 2008 Jan;15(1):51-8. doi: 10.1177/1933719107309590.

10.

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.

11.

Microsatellites proximal to leptin and leptin receptor as risk factors for spina bifida.

Shaw GM, Barber R, Todoroff K, Lammer EJ, Finnell RH.

Teratology. 2000 Mar;61(3):231-5.

PMID:
10661913
12.

The methionine synthase reductase 66A>G polymorphism is a maternal risk factor for spina bifida.

van der Linden IJ, den Heijer M, Afman LA, Gellekink H, Vermeulen SH, Kluijtmans LA, Blom HJ.

J Mol Med (Berl). 2006 Dec;84(12):1047-54. Epub 2006 Oct 6.

PMID:
17024475
13.

Evaluation of common genetic variants in 82 candidate genes as risk factors for neural tube defects.

Pangilinan F, Molloy AM, Mills JL, Troendle JF, Parle-McDermott A, Signore C, O'Leary VB, Chines P, Seay JM, Geiler-Samerotte K, Mitchell A, VanderMeer JE, Krebs KM, Sanchez A, Cornman-Homonoff J, Stone N, Conley M, Kirke PN, Shane B, Scott JM, Brody LC.

BMC Med Genet. 2012 Aug 2;13:62.

14.

Screening for new MTHFR polymorphisms and NTD risk.

O'Leary VB, Mills JL, Parle-McDermott A, Pangilinan F, Molloy AM, Cox C, Weiler A, Conley M, Kirke PN, Scott JM, Brody LC; Birth Defects Research Group.

Am J Med Genet A. 2005 Oct 1;138A(2):99-106.

PMID:
16145688
15.

Reduced folate carrier polymorphisms and neural tube defect risk.

O'leary VB, Pangilinan F, Cox C, Parle-McDermott A, Conley M, Molloy AM, Kirke PN, Mills JL, Brody LC, Scott JM; Members of the Birth Defects Research Group.

Mol Genet Metab. 2006 Apr;87(4):364-9. Epub 2005 Dec 15.

PMID:
16343969
16.
17.

The 894G>T variant in the endothelial nitric oxide synthase gene and spina bifida risk.

van der Linden IJ, Heil SG, den Heijer M, Blom HJ.

J Hum Genet. 2007;52(6):516-20. Epub 2007 May 4.

18.

Association between CFL1 gene polymorphisms and spina bifida risk in a California population.

Zhu H, Enaw JO, Ma C, Shaw GM, Lammer EJ, Finnell RH.

BMC Med Genet. 2007 Mar 12;8:12.

19.

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

Liu J, Zhang Y, Jin L, Li G, Wang L, Bao Y, Fu Y, Li Z, Zhang L, Ye R, Ren A.

Metab Brain Dis. 2015 Apr;30(2):507-13. doi: 10.1007/s11011-014-9582-8. Epub 2014 Jul 4. Erratum in: Metab Brain Dis. 2015 Apr;30(2):515-7.

PMID:
24990354
20.

Interaction of PDGFRA promoter haplotypes and maternal environmental exposures in the risk of spina bifida.

Toepoel M, Steegers-Theunissen RP, Ouborg NJ, Franke B, González-Zuloeta Ladd AM, Joosten PH, van Zoelen EJ.

Birth Defects Res A Clin Mol Teratol. 2009 Jul;85(7):629-36. doi: 10.1002/bdra.20574.

PMID:
19215021

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