218 related articles for article (PubMed ID: 12730722)
1. Analysis of the MTHFR 1298A-->C and 677C-->T polymorphisms as risk factors for neural tube defects.
Parle-McDermott A; Mills JL; Kirke PN; O'Leary VB; Swanson DA; Pangilinan F; Conley M; Molloy AM; Cox C; Scott JM; Brody LC
J Hum Genet; 2003; 48(4):190-3. PubMed ID: 12730722
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Linkage disequilibrium of MTHFR genotypes 677C/T-1298A/C in the German population and association studies in probands with neural tube defects(NTD).
Stegmann K; Ziegler A; Ngo ET; Kohlschmidt N; Schröter B; Ermert A; Koch MC
Am J Med Genet; 1999 Nov; 87(1):23-9. PubMed ID: 10528242
[TBL] [Abstract][Full Text] [Related]
4. Variants in MTHFR gene and neural tube defects susceptibility in China.
Wang Y; Liu Y; Ji W; Qin H; Wu H; Xu D; Turtuohut T; Wang Z
Metab Brain Dis; 2015 Aug; 30(4):1017-26. PubMed ID: 25855017
[TBL] [Abstract][Full Text] [Related]
5. Analysis of MTHFR 1298A>C in addition to MTHFR 677C>T polymorphism as a risk factor for neural tube defects in the Turkish population.
Boduroğlu K; Alanay Y; Alikaşifoğlu M; Aktaş D; Tunçbilek E
Turk J Pediatr; 2005; 47(4):327-33. PubMed ID: 16363341
[TBL] [Abstract][Full Text] [Related]
6. [C677T polymorphism of the methylentetrahydrofolate reductase gene in mothers of children affected with neural tube defects].
Morales de Machín A; Méndez K; Solís E; Borjas de Borjas L; Bracho A; Hernández ML; Negrón A; Delgado W; Sánchez Y
Invest Clin; 2015 Sep; 56(3):284-95. PubMed ID: 26710543
[TBL] [Abstract][Full Text] [Related]
7. Impact of 5,10-methylenetetrahydrofolate reductase gene polymorphism on neural tube defects.
Harisha PN; Devi BI; Christopher R; Kruthika-Vinod TP
J Neurosurg Pediatr; 2010 Oct; 6(4):364-7. PubMed ID: 20887110
[TBL] [Abstract][Full Text] [Related]
8. Polymorphisms of 5,10-methylenetetrahydrofolate reductase and cystathionine beta-synthase genes as a risk factor for neural tube defects in Sétif, Algeria.
Houcher B; Bourouba R; Djabi F; Yilmaz E; Eğin Y; Akar N
Pediatr Neurosurg; 2009; 45(6):472-7. PubMed ID: 20160465
[TBL] [Abstract][Full Text] [Related]
9. 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;
Am J Med Genet A; 2005 Oct; 138A(2):99-106. PubMed ID: 16145688
[TBL] [Abstract][Full Text] [Related]
10. Metabolic effects and the methylenetetrahydrofolate reductase (MTHFR) polymorphism associated with neural tube defects in southern Brazil.
Félix TM; Leistner S; Giugliani R
Birth Defects Res A Clin Mol Teratol; 2004 Jul; 70(7):459-63. PubMed ID: 15259035
[TBL] [Abstract][Full Text] [Related]
11. MTHFR C677T polymorphism as a risk factor of neural tube defects in Malay: a case control study.
Hayati AR; Zainal AI; Tan GC; Ong LC; Khoo TB
Med J Malaysia; 2008 Dec; 63(5):379-83. PubMed ID: 19803295
[TBL] [Abstract][Full Text] [Related]
12. Interaction of folate and homocysteine pathway genotypes evaluated in susceptibility to neural tube defects (NTD) in a German population.
Richter B; Stegmann K; Röper B; Böddeker I; Ngo ET; Koch MC
J Hum Genet; 2001; 46(3):105-9. PubMed ID: 11310576
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Association of the maternal MTHFR C677T polymorphism with susceptibility to neural tube defects in offsprings: evidence from 25 case-control studies.
Yan L; Zhao L; Long Y; Zou P; Ji G; Gu A; Zhao P
PLoS One; 2012; 7(10):e41689. PubMed ID: 23056169
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. A1298C polymorphism of the MTHFR gene and neural tube defects in the state of Yucatan, Mexico.
Gonzalez-Herrera L; Castillo-Zapata I; Garcia-Escalante G; Pinto-Escalante D
Birth Defects Res A Clin Mol Teratol; 2007 Aug; 79(8):622-6. PubMed ID: 17621650
[TBL] [Abstract][Full Text] [Related]
17. Gene-gene interaction between the cystathionine beta-synthase 31 base pair variable number of tandem repeats and the methylenetetrahydrofolate reductase 677C > T polymorphism on homocysteine levels and risk for neural tube defects.
Afman LA; Lievers KJ; Kluijtmans LA; Trijbels FJ; Blom HJ
Mol Genet Metab; 2003 Mar; 78(3):211-5. PubMed ID: 12649066
[TBL] [Abstract][Full Text] [Related]
18. Reduced folate carrier polymorphism (80A-->G) and neural tube defects.
De Marco P; Calevo MG; Moroni A; Merello E; Raso A; Finnell RH; Zhu H; Andreussi L; Cama A; Capra V
Eur J Hum Genet; 2003 Mar; 11(3):245-52. PubMed ID: 12673279
[TBL] [Abstract][Full Text] [Related]
19. Association of
Li J; Feng D; He S; Yang H; Su Z; Ye H
J Obstet Gynaecol; 2022 Aug; 42(6):1811-1822. PubMed ID: 35282788
[TBL] [Abstract][Full Text] [Related]
20. Methylenetetrahydrofolate reductase gene polymorphisms c.677C/T and c.1298A/C are not associated with open angle glaucoma.
Mabuchi F; Tang S; Kashiwagi K; Yamagata Z; Iijima H; Tsukahara S
Mol Vis; 2006 Jul; 12():735-9. PubMed ID: 16862068
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
