151 related articles for article (PubMed ID: 16596679)
1. 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]
2. [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]
3. Polymorphisms in folate and homocysteine metabolizing genes and chromosome damage in mothers of Down syndrome children.
Coppedè F; Colognato R; Bonelli A; Astrea G; Bargagna S; Siciliano G; Migliore L
Am J Med Genet A; 2007 Sep; 143A(17):2006-15. PubMed ID: 17702010
[TBL] [Abstract][Full Text] [Related]
4. Analysis of seven maternal polymorphisms of genes involved in homocysteine/folate metabolism and risk of Down syndrome offspring.
Scala I; Granese B; Sellitto M; Salomè S; Sammartino A; Pepe A; Mastroiacovo P; Sebastio G; Andria G
Genet Med; 2006 Jul; 8(7):409-16. PubMed ID: 16845273
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. No association between common polymorphisms in genes of folate and homocysteine metabolism and the risk of Down's syndrome among French mothers.
Chango A; Fillon-Emery N; Mircher C; Bléhaut H; Lambert D; Herbeth B; James SJ; Réthoré MO; Nicolas JP
Br J Nutr; 2005 Aug; 94(2):166-9. PubMed ID: 16115349
[TBL] [Abstract][Full Text] [Related]
7. Impact of RFC1, MTHFR, and MTHFD1 polymorphism on unexplained pregnancy loss (UPL): comparative analysis of maternal and fetal components using mother-abortus paired samples.
Kim JY; Kim JW; Sung SR; Park JE; Shim SH; Cha DH
Eur J Obstet Gynecol Reprod Biol; 2018 Dec; 231():152-157. PubMed ID: 30388610
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. 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]
11. Evaluation of C677T and A1298C polymorphisms of the MTHFR gene as maternal risk factors for Down syndrome and congenital heart defects.
Brandalize AP; Bandinelli E; dos Santos PA; Roisenberg I; Schüler-Faccini L
Am J Med Genet A; 2009 Oct; 149A(10):2080-7. PubMed ID: 19725133
[TBL] [Abstract][Full Text] [Related]
12. Genetic polymorphisms involved in folate metabolism and elevated plasma concentrations of homocysteine: maternal risk factors for Down syndrome in Brazil.
Biselli JM; Goloni-Bertollo EM; Zampieri BL; Haddad R; Eberlin MN; Pavarino-Bertelli EC
Genet Mol Res; 2008 Jan; 7(1):33-42. PubMed ID: 18273817
[TBL] [Abstract][Full Text] [Related]
13.
Romero-Bolaño YM; Bobadilla-Morales L; Corona-Rivera A; Cuero-Quezada I; Santana-Hernández J; Peña-Padilla C; Brukman-Jiménez A; Orozco-Vela M; Navia-Espinoza N; Corona-Rivera JR
Genet Test Mol Biomarkers; 2024 Jun; 28(6):263-266. PubMed ID: 38717090
[No Abstract] [Full Text] [Related]
14. Association of maternal polymorphisms in folate metabolizing genes with chromosome damage and risk of Down syndrome offspring.
Coppedè F; Migheli F; Bargagna S; Siciliano G; Antonucci I; Stuppia L; Palka G; Migliore L
Neurosci Lett; 2009 Jan; 449(1):15-9. PubMed ID: 18983896
[TBL] [Abstract][Full Text] [Related]
15. Role of folate-homocysteine pathway gene polymorphisms and nutritional cofactors in Down syndrome: A triad study.
Sukla KK; Jaiswal SK; Rai AK; Mishra OP; Gupta V; Kumar A; Raman R
Hum Reprod; 2015 Aug; 30(8):1982-93. PubMed ID: 26040482
[TBL] [Abstract][Full Text] [Related]
16. Polymorphisms in genes involved in folate metabolism as risk factors for NTDs.
De Marco P; Calevo MG; Moroni A; Arata L; Merello E; Cama A; Finnell RH; Andreussi L; Capra V
Eur J Pediatr Surg; 2001 Dec; 11 Suppl 1():S14-7. PubMed ID: 11813127
[TBL] [Abstract][Full Text] [Related]
17. Methionine synthase (MTR) 2756 (A --> G) polymorphism, double heterozygosity methionine synthase 2756 AG/methionine synthase reductase (MTRR) 66 AG, and elevated homocysteinemia are three risk factors for having a child with Down syndrome.
Bosco P; Guéant-Rodriguez RM; Anello G; Barone C; Namour F; Caraci F; Romano A; Romano C; Guéant JL
Am J Med Genet A; 2003 Sep; 121A(3):219-24. PubMed ID: 12923861
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. The biochemical structure and function of methylenetetrahydrofolate reductase provide the rationale to interpret the epidemiological results on the risk for infants with Down syndrome.
Martínez-Frías ML
Am J Med Genet A; 2008 Jun; 146A(11):1477-82. PubMed ID: 18446861
[TBL] [Abstract][Full Text] [Related]
20. Association of COMT, MTHFR, and SLC19A1(RFC-1) polymorphisms with homocysteine blood levels and cognitive impairment in Parkinson's disease.
Białecka M; Kurzawski M; Roszmann A; Robowski P; Sitek EJ; Honczarenko K; Gorzkowska A; Budrewicz S; Mak M; Jarosz M; Gołąb-Janowska M; Koziorowska-Gawron E; Droździk M; Sławek J
Pharmacogenet Genomics; 2012 Oct; 22(10):716-24. PubMed ID: 22890010
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
