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Results: 15

Cited In for PubMed (Select 12673279)


Replication and exploratory analysis of 24 candidate risk polymorphisms for neural tube defects.

Pangilinan F, Molloy AM, Mills JL, Troendle JF, Parle-McDermott A, Kay DM, Browne ML, McGrath EC, Abaan HO, Sutton M, Kirke PN, Caggana M, Shane B, Scott JM, Brody LC.

BMC Med Genet. 2014 Oct 8;15:102. doi: 10.1186/s12881-014-0102-9.


The association of idiopathic recurrent early pregnancy loss with polymorphisms in folic acid metabolism-related genes.

Cao Y, Zhang Z, Zheng Y, Yuan W, Wang J, Liang H, Chen J, Du J, Shen Y.

Genes Nutr. 2014 May;9(3):402. doi: 10.1007/s12263-014-0402-x. Epub 2014 Apr 12.


Folate-related gene variants in Irish families affected by neural tube defects.

Fisk Green R, Byrne J, Crider KS, Gallagher M, Koontz D, Berry RJ.

Front Genet. 2013 Nov 6;4:223. doi: 10.3389/fgene.2013.00223. eCollection 2013.


Neural tube defects, folic acid and methylation.

Imbard A, Benoist JF, Blom HJ.

Int J Environ Res Public Health. 2013 Sep 17;10(9):4352-89. doi: 10.3390/ijerph10094352. Review.


RFC - 1 Gene Polymorphism and the Risk of Down Syndrome in Romanian Population.

Neagos D, Cretu R, Tutulan-Cunita A, Stoian V, Bohiltea LC.

Maedica (Buchar). 2010 Dec;5(4):280-5.


Association of folate receptor (FOLR1, FOLR2, FOLR3) and reduced folate carrier (SLC19A1) genes with meningomyelocele.

O'Byrne MR, Au KS, Morrison AC, Lin JI, Fletcher JM, Ostermaier KK, Tyerman GH, Doebel S, Northrup H.

Birth Defects Res A Clin Mol Teratol. 2010 Aug;88(8):689-94. doi: 10.1002/bdra.20706.


Folic acid in early pregnancy: a public health success story.

Obican SG, Finnell RH, Mills JL, Shaw GM, Scialli AR.

FASEB J. 2010 Nov;24(11):4167-74. doi: 10.1096/fj.10-165084. Epub 2010 Jul 14.


Genetic and lifestyle variables associated with homocysteine concentrations and the distribution of folate derivatives in healthy premenopausal women.

Summers CM, Mitchell LE, Stanislawska-Sachadyn A, Baido SF, Blair IA, Von Feldt JM, Whitehead AS.

Birth Defects Res A Clin Mol Teratol. 2010 Aug;88(8):679-88. doi: 10.1002/bdra.20683.


Knockout of the folate transporter folt-1 causes germline and somatic defects in C. elegans.

Austin MU, Liau WS, Balamurugan K, Ashokkumar B, Said HM, LaMunyon CW.

BMC Dev Biol. 2010 May 4;10:46. doi: 10.1186/1471-213X-10-46.


Epidemiologic and genetic aspects of spina bifida and other neural tube defects.

Au KS, Ashley-Koch A, Northrup H.

Dev Disabil Res Rev. 2010;16(1):6-15. doi: 10.1002/ddrr.93. Review.


The reduced folate carrier (SLC19A1) c.80G>A polymorphism is associated with red cell folate concentrations among women.

Stanisławska-Sachadyn A, Mitchell LE, Woodside JV, Buckley PT, Kealey C, Young IS, Scott JM, Murray L, Boreham CA, McNulty H, Strain JJ, Whitehead AS.

Ann Hum Genet. 2009 Sep;73(Pt 5):484-91. doi: 10.1111/j.1469-1809.2009.00529.x. Epub 2009 Jul 28.


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.


Membrane transporters and folate homeostasis: intestinal absorption and transport into systemic compartments and tissues.

Zhao R, Matherly LH, Goldman ID.

Expert Rev Mol Med. 2009 Jan 28;11:e4. doi: 10.1017/S1462399409000969. Review.


Metabolic endophenotype and related genotypes are associated with oxidative stress in children with autism.

James SJ, Melnyk S, Jernigan S, Cleves MA, Halsted CH, Wong DH, Cutler P, Bock K, Boris M, Bradstreet JJ, Baker SM, Gaylor DW.

Am J Med Genet B Neuropsychiatr Genet. 2006 Dec 5;141B(8):947-56.

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