192 related articles for article (PubMed ID: 20047525)
1. Role of parental folate pathway single nucleotide polymorphisms in altering the susceptibility to neural tube defects in South India.
Naushad SM; Devi AR
J Perinat Med; 2010; 38(1):63-9. PubMed ID: 20047525
[TBL] [Abstract][Full Text] [Related]
2. Association of MTHFR C677T, MTHFR A1298C, and MTRR A66G Polymorphisms with Neural Tube Defects in Tunisian Parents.
Nasri K; Midani F; Kallel A; Ben Jemaa N; Aloui M; Boulares M; Lassoued M; Ben Halima M; Ben Wafi S; Soussi M; Mahjoubi I; Baara A; Ben Fradj MK; Omar S; Feki M; Jemaa R; Gaigi SS; Marrakchi R
Pathobiology; 2019; 86(4):190-200. PubMed ID: 31238314
[TBL] [Abstract][Full Text] [Related]
3. "Polymorphisms in folate metabolism genes as maternal risk factor for neural tube defects: an updated meta-analysis".
Yadav U; Kumar P; Yadav SK; Mishra OP; Rai V
Metab Brain Dis; 2015 Feb; 30(1):7-24. PubMed ID: 25005003
[TBL] [Abstract][Full Text] [Related]
4. Association of neural tube defects with maternal alterations and genetic polymorphisms in one-carbon metabolic pathway.
Cai CQ; Fang YL; Shu JB; Zhao LS; Zhang RP; Cao LR; Wang YZ; Zhi XF; Cui HL; Shi OY; Liu W
Ital J Pediatr; 2019 Mar; 45(1):37. PubMed ID: 30867013
[TBL] [Abstract][Full Text] [Related]
5. Variants c.677 C>T, c.1298 A>C in
Zhang Y; Zhan W; Du Q; Wu L; Ding H; Liu F; Yin A
Genet Test Mol Biomarkers; 2020 Nov; 24(11):717-722. PubMed ID: 33121283
[No Abstract] [Full Text] [Related]
6. Genetic and environmental influences on total plasma homocysteine and coronary artery disease (CAD) risk among South Indians.
Vinukonda G; Shaik Mohammad N; Md Nurul Jain J; Prasad Chintakindi K; Rama Devi Akella R
Clin Chim Acta; 2009 Jul; 405(1-2):127-31. PubMed ID: 19394322
[TBL] [Abstract][Full Text] [Related]
7. Association of FOLH1, DHFR, and MTHFR gene polymorphisms with susceptibility of Neural Tube Defects: A case control study from Eastern India.
Paul S; Sadhukhan S; Munian D; Bankura B; Das M
Birth Defects Res; 2018 Aug; 110(14):1129-1138. PubMed ID: 30120883
[TBL] [Abstract][Full Text] [Related]
8. Gene-gene interaction in folate-related genes and risk of neural tube defects in a UK population.
Relton CL; Wilding CS; Pearce MS; Laffling AJ; Jonas PA; Lynch SA; Tawn EJ; Burn J
J Med Genet; 2004 Apr; 41(4):256-60. PubMed ID: 15060097
[TBL] [Abstract][Full Text] [Related]
9. 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; 337(1-2):61-6. PubMed ID: 24326202
[TBL] [Abstract][Full Text] [Related]
10. 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. PubMed ID: 21770021
[TBL] [Abstract][Full Text] [Related]
11. Association of main folate metabolic pathway gene polymorphisms with neural tube defects in Han population of Northern China.
Fang Y; Zhang R; Zhi X; Zhao L; Cao L; Wang Y; Cai C
Childs Nerv Syst; 2018 Apr; 34(4):725-729. PubMed ID: 29392422
[TBL] [Abstract][Full Text] [Related]
12. 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. PubMed ID: 22475273
[TBL] [Abstract][Full Text] [Related]
13. Polymorphisms in genes involved in folate metabolism as maternal risk factors for Down syndrome.
Hobbs CA; Sherman SL; Yi P; Hopkins SE; Torfs CP; Hine RJ; Pogribna M; Rozen R; James SJ
Am J Hum Genet; 2000 Sep; 67(3):623-30. PubMed ID: 10930360
[TBL] [Abstract][Full Text] [Related]
14. The impact of folate pathway polymorphisms combined to nutritional deficiency as a maternal predisposition factor for Down syndrome.
Santos-Rebouças CB; Corrêa JC; Bonomo A; Fintelman-Rodrigues N; Moura KC; Rodrigues CS; Santos JM; Pimentel MM
Dis Markers; 2008; 25(3):149-57. PubMed ID: 19096127
[TBL] [Abstract][Full Text] [Related]
15. 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. PubMed ID: 17024475
[TBL] [Abstract][Full Text] [Related]
16. MTHFR 677C-->T and 1298A-->C polymorphisms: evaluation of maternal genotypic risk and association with level of neural tube defect.
Dalal A; Pradhan M; Tiwari D; Behari S; Singh U; Mallik GK; Das V; Agarwal S
Gynecol Obstet Invest; 2007; 63(3):146-50. PubMed ID: 17085942
[TBL] [Abstract][Full Text] [Related]
17. Polymorphisms in folate-related genes and risk of pediatric acute lymphoblastic leukemia.
de Jonge R; Tissing WJ; Hooijberg JH; Jansen G; Kaspers GJ; Lindemans J; Peters GJ; Pieters R
Blood; 2009 Mar; 113(10):2284-9. PubMed ID: 19020309
[TBL] [Abstract][Full Text] [Related]
18. [Folate gene polymorphism and the risk of Down syndrome pregnancies in young Chinese women].
Liao YP; Bao MS; Liu CQ; Liu H; Zhang D
Yi Chuan; 2010 May; 32(5):461-6. PubMed ID: 20466634
[TBL] [Abstract][Full Text] [Related]
19. [Case-control study on the association between four single nucleotide polymorphisms in folate metabolism way and the risk of congenital heart disease].
Duan S; Li G; Qiu F; Zhao L; Zhao M; Wang L; Feng Z; Ma X
Wei Sheng Yan Jiu; 2018 Jul; 47(4):536-542. PubMed ID: 30081977
[TBL] [Abstract][Full Text] [Related]
20. Folate levels and N(5),N(10)-methylenetetrahydrofolate reductase genotype (MTHFR) in mothers of offspring with neural tube defects: a case-control study.
Martínez de Villarreal LE; Delgado-Enciso I; Valdéz-Leal R; Ortíz-López R; Rojas-Martínez A; Limón-Benavides C; Sánchez-Peña MA; Ancer-Rodríguez J; Barrera-Saldaña HA; Villarreal-Pérez JZ
Arch Med Res; 2001; 32(4):277-82. PubMed ID: 11440783
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
