188 related articles for article (PubMed ID: 11857541)
1. Maternal periconceptional vitamin use, genetic variation of infant reduced folate carrier (A80G), and risk of spina bifida.
Shaw GM; Lammer EJ; Zhu H; Baker MW; Neri E; Finnell RH
Am J Med Genet; 2002 Feb; 108(1):1-6. PubMed ID: 11857541
[TBL] [Abstract][Full Text] [Related]
2. Genetic variation of infant reduced folate carrier (A80G) and risk of orofacial and conotruncal heart defects.
Shaw GM; Zhu H; Lammer EJ; Yang W; Finnell RH
Am J Epidemiol; 2003 Oct; 158(8):747-52. PubMed ID: 14561664
[TBL] [Abstract][Full Text] [Related]
3. Maternal vitamin use, genetic variation of infant methylenetetrahydrofolate reductase, and risk for spina bifida.
Shaw GM; Rozen R; Finnell RH; Wasserman CR; Lammer EJ
Am J Epidemiol; 1998 Jul; 148(1):30-7. PubMed ID: 9663401
[TBL] [Abstract][Full Text] [Related]
4. Evaluation of infant methylenetetrahydrofolate reductase genotype, maternal vitamin use, and risk of high versus low level spina bifida defects.
Volcik KA; Shaw GM; Lammer EJ; Zhu H; Finnell RH
Birth Defects Res A Clin Mol Teratol; 2003 Mar; 67(3):154-7. PubMed ID: 12797455
[TBL] [Abstract][Full Text] [Related]
5. Genetic variation of infant reduced folate carrier (A80G) and risk of orofacial defects and congenital heart defects in China.
Pei L; Zhu H; Zhu J; Ren A; Finnell RH; Li Z
Ann Epidemiol; 2006 May; 16(5):352-6. PubMed ID: 16019224
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Interaction between maternal periconceptional supplementation of folic acid and reduced folate carrier gene polymorphism of neural tube defects.
Pei LJ; Zhu HP; Li ZW; Zhang W; Ren AG; Zhu JH; Li Z
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Jun; 22(3):284-7. PubMed ID: 15952116
[TBL] [Abstract][Full Text] [Related]
8. [Epidemiological study on reduced folate carrier gene(RFC1 A80G) polymorphism and other risk factors of neural tube defects].
Pei LJ; Li ZW; Zhang W; Ren AG; Zhu HP; Hao L; Zhu JH; Li Z
Beijing Da Xue Xue Bao Yi Xue Ban; 2005 Aug; 37(4):341-5. PubMed ID: 16086047
[TBL] [Abstract][Full Text] [Related]
9. Spina bifida and other neural tube defects.
Northrup H; Volcik KA
Curr Probl Pediatr; 2000; 30(10):313-32. PubMed ID: 11147289
[TBL] [Abstract][Full Text] [Related]
10. Altered folate metabolism and disposition in mothers affected by a spina bifida pregnancy: influence of 677c --> t methylenetetrahydrofolate reductase and 2756a --> g methionine synthase genotypes.
Lucock M; Daskalakis I; Briggs D; Yates Z; Levene M
Mol Genet Metab; 2000 May; 70(1):27-44. PubMed ID: 10833329
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. The C677T mutation of the 5,10-methylenetetrahydrofolate reductase gene is a moderate risk factor for spina bifida in Italy.
de Franchis R; Buoninconti A; Mandato C; Pepe A; Sperandeo MP; Del Gado R; Capra V; Salvaggio E; Andria G; Mastroiacovo P
J Med Genet; 1998 Dec; 35(12):1009-13. PubMed ID: 9863598
[TBL] [Abstract][Full Text] [Related]
13. Spina bifida, folate metabolism, and dietary folate intake in a Northern Canadian aboriginal population.
Arbour L; Christensen B; Delormier T; Platt R; Gilfix B; Forbes P; Kovitch I; Morel J; Rozen R
Int J Circumpolar Health; 2002 Nov; 61(4):341-51. PubMed ID: 12546192
[TBL] [Abstract][Full Text] [Related]
14. [Study on reduced folate carrier gene (RFC1) polymorphism in the southern and northern Chinese population].
Pei LJ; Ren AG; Zhu HP; Hao L; Zhao WR; Li Z; Hou GW; Zhang BL; Jiang YY; Wu LM; Pan YJ; Zhang ML
Zhonghua Liu Xing Bing Xue Za Zhi; 2004 Jun; 25(6):499-502. PubMed ID: 15231126
[TBL] [Abstract][Full Text] [Related]
15. Evaluation of genetic variants in the reduced folate carrier and in glutamate carboxypeptidase II for spina bifida risk.
Morin I; Devlin AM; Leclerc D; Sabbaghian N; Halsted CH; Finnell R; Rozen R
Mol Genet Metab; 2003 Jul; 79(3):197-200. PubMed ID: 12855225
[TBL] [Abstract][Full Text] [Related]
16. Spina bifida and folate-related genes: a study of gene-gene interactions.
de Franchis R; Botto LD; Sebastio G; Ricci R; Iolascon A; Capra V; Andria G; Mastroiacovo P
Genet Med; 2002; 4(3):126-30. PubMed ID: 12180146
[TBL] [Abstract][Full Text] [Related]
17. Re: "Maternal vitamin use, genetic variation of infant methylenetetrahydrofolate reductase, and risk for spina bifida".
Botto LD; Mulinare J
Am J Epidemiol; 1999 Aug; 150(3):323-4. PubMed ID: 10430239
[No Abstract] [Full Text] [Related]
18. Genetic polymorphisms in methylenetetrahydrofolate reductase and methionine synthase, folate levels in red blood cells, and risk of neural tube defects.
Christensen B; Arbour L; Tran P; Leclerc D; Sabbaghian N; Platt R; Gilfix BM; Rosenblatt DS; Gravel RA; Forbes P; Rozen R
Am J Med Genet; 1999 May; 84(2):151-7. PubMed ID: 10323741
[TBL] [Abstract][Full Text] [Related]
19. Infant C677T mutation in MTHFR, maternal periconceptional vitamin use, and cleft lip.
Shaw GM; Rozen R; Finnell RH; Todoroff K; Lammer EJ
Am J Med Genet; 1998 Nov; 80(3):196-8. PubMed ID: 9843036
[TBL] [Abstract][Full Text] [Related]
20. CHKA and PCYT1A gene polymorphisms, choline intake and spina bifida risk in a California population.
Enaw JO; Zhu H; Yang W; Lu W; Shaw GM; Lammer EJ; Finnell RH
BMC Med; 2006 Dec; 4():36. PubMed ID: 17184542
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]