These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
2. 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]
3. Methylenetetrahydrofolate reductase enzyme polymorphisms as maternal risk for Down syndrome among Turkish women. Boduroğlu K; Alanay Y; Koldan B; Tunçbilek E Am J Med Genet A; 2004 May; 127A(1):5-10. PubMed ID: 15103709 [TBL] [Abstract][Full Text] [Related]
4. The Frequency of the 677C>T and 1298A>C Polymorphisms in the Methylenetetrahydrofolate Reductase (MTHFR) Gene in the Population. Nefic H; Mackic-Djurovic M; Eminovic I Med Arch; 2018 Jun; 72(3):164-169. PubMed ID: 30061759 [TBL] [Abstract][Full Text] [Related]
5. MTHFR genetic polymorphism as a risk factor in Egyptian mothers with Down syndrome children. Meguid NA; Dardir AA; Khass M; Hossieny LE; Ezzat A; El Awady MK Dis Markers; 2008; 24(1):19-26. PubMed ID: 18057532 [TBL] [Abstract][Full Text] [Related]
6. Maternal polymorphisms 677C-T and 1298A-C of MTHFR, and 66A-G MTRR genes: is there any relationship between polymorphisms of the folate pathway, maternal homocysteine levels, and the risk for having a child with Down syndrome? Martínez-Frías ML; Pérez B; Desviat LR; Castro M; Leal F; Rodríguez L; Mansilla E; Martínez-Fernández ML; Bermejo E; Rodríguez-Pinilla E; Prieto D; Ugarte M; Am J Med Genet A; 2006 May; 140(9):987-97. PubMed ID: 16575899 [TBL] [Abstract][Full Text] [Related]
7. [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]
8. The roles of methylenetetrahydrofolate reductase 677C>T and 1298A>C polymorphisms in moyamoya disease patients. Park YS; Jeon YJ; Kim HS; Han IB; Choi JU; Kim DS; Kim NK Childs Nerv Syst; 2014 Oct; 30(10):1687-95. PubMed ID: 25098357 [TBL] [Abstract][Full Text] [Related]
9. Associations between 2 polymorphisms in the methylenetetrahydrofolate reductase gene and placental abruption. Ananth CV; Peltier MR; De Marco C; Elsasser DA; Getahun D; Rozen R; Smulian JC; Am J Obstet Gynecol; 2007 Oct; 197(4):385.e1-7. PubMed ID: 17904970 [TBL] [Abstract][Full Text] [Related]
10. Folate gene polymorphisms and the risk of Down syndrome pregnancies in young Italian women. Coppedè F; Marini G; Bargagna S; Stuppia L; Minichilli F; Fontana I; Colognato R; Astrea G; Palka G; Migliore L Am J Med Genet A; 2006 May; 140(10):1083-91. PubMed ID: 16596679 [TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. Genetic polymorphism of methylenetetrahydrofolate reductase is associated with insulin resistance in Egyptian women with polycystic ovary syndrome. Nsrallah AA; Abd-El Fatah AH; Ahmed HS J Gene Med; 2019 Apr; 21(4):e3076. PubMed ID: 30743312 [TBL] [Abstract][Full Text] [Related]
14. Association of MTHFR 677C>T, 1298A>C and MTR 2756A>G Polymorphisms with Risk of Retinoblastoma. Gohari M; Dastgheib S. A.; Jafari-Nedooshan J; Akbarian-Bafghi M. J.; Morovati-Sharifabad M; Mirjalili S. R.; Neamatzadeh H Klin Onkol; 2019; 32(5):375-379. PubMed ID: 31610671 [TBL] [Abstract][Full Text] [Related]
15. 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]
16. Prevalence of methylenetetrahydrofolate reductase 677T and 1298C alleles and folate status: a comparative study in Mexican, West African, and European populations. Guéant-Rodriguez RM; Guéant JL; Debard R; Thirion S; Hong LX; Bronowicki JP; Namour F; Chabi NW; Sanni A; Anello G; Bosco P; Romano C; Amouzou E; Arrieta HR; Sánchez BE; Romano A; Herbeth B; Guilland JC; Mutchinick OM Am J Clin Nutr; 2006 Mar; 83(3):701-7. PubMed ID: 16522920 [TBL] [Abstract][Full Text] [Related]
17. [The relationship between polymorphism of gene involved in folate metabolism, homocysteine level and risk of Down syndrome]. Wang W; Xie W; Wang Xy Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Oct; 24(5):533-7. PubMed ID: 17922421 [TBL] [Abstract][Full Text] [Related]
18. Maternal MTHFR genotype and haplotype predict deficits in early cognitive development in a lead-exposed birth cohort in Mexico City. Pilsner JR; Hu H; Wright RO; Kordas K; Ettinger AS; Sánchez BN; Cantonwine D; Lazarus AL; Cantoral A; Schnaas L; Téllez-Rojo MM; Hernández-Avila M Am J Clin Nutr; 2010 Jul; 92(1):226-34. PubMed ID: 20504979 [TBL] [Abstract][Full Text] [Related]
19. [Association of MTHFR and MTRR genes polymorphisms with non-disjunctions of chromosomes 18 and 21]. Guo Q; Wang H; Yang K; Zhang B; Li T; Liao S Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Jun; 32(3):395-9. PubMed ID: 26037359 [TBL] [Abstract][Full Text] [Related]
20. The maternal homocysteine pathway is influenced by riboflavin intake and MTHFR polymorphisms without affecting the risk of orofacial clefts in the offspring. Vujkovic M; Steegers EA; van Meurs J; Yazdanpanah N; van Rooij IA; Uitterlinden AG; Steegers-Theunissen RP Eur J Clin Nutr; 2010 Mar; 64(3):266-73. PubMed ID: 19935819 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]