Finnell RH - Search Results

1

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. De Marco P, et al. Among authors: finnell rh. Eur J Hum Genet. 2003 Mar;11(3):245-52. doi: 10.1038/sj.ejhg.5200946. Eur J Hum Genet. 2003. PMID: 12673279

2

Investigation of folate pathway gene polymorphisms and the incidence of neural tube defects in a Texas hispanic population.

Barber R, Shalat S, Hendricks K, Joggerst B, Larsen R, Suarez L, Finnell R. Barber R, et al. Mol Genet Metab. 2000 May;70(1):45-52. doi: 10.1006/mgme.2000.2991. Mol Genet Metab. 2000. PMID: 10833330

3

Folate pathway gene alterations in patients with neural tube defects.

De Marco P, Moroni A, Merello E, de Franchis R, Andreussi L, Finnell RH, Barber RC, Cama A, Capra V. De Marco P, et al. Among authors: finnell rh. Am J Med Genet. 2000 Nov 27;95(3):216-23. doi: 10.1002/1096-8628(20001127)95:3<216::aid-ajmg6>3.0.co;2-f. Am J Med Genet. 2000. PMID: 11102926

4

A screen for mutations in human homologues of mice exencephaly genes Tfap2alpha and Msx2 in patients with neural tube defects.

Stegmann K, Boecker J, Richter B, Capra V, Finnell RH, Ngo ET, Strehl E, Ermert A, Koch MC. Stegmann K, et al. Among authors: finnell rh. Teratology. 2001 May;63(5):167-75. doi: 10.1002/tera.1031. Teratology. 2001. PMID: 11320527

5

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. De Marco P, et al. Among authors: finnell rh. Eur J Pediatr Surg. 2001 Dec;11 Suppl 1:S14-7. doi: 10.1055/s-2001-19739. Eur J Pediatr Surg. 2001. PMID: 11813127

6

Lack of association between ZIC2 and ZIC3 genes and the risk of neural tube defects (NTDs) in Hispanic populations.

Zhu H, Junker WM, Finnell RH, Brown S, Shaw GM, Lammer EJ, Canfield M, Hendricks K. Zhu H, et al. Among authors: finnell rh. Am J Med Genet A. 2003 Feb 1;116A(4):414-5. doi: 10.1002/ajmg.a.10032. Am J Med Genet A. 2003. PMID: 12522805 No abstract available.

7

Homocysteine remethylation enzyme polymorphisms and increased risks for neural tube defects.

Zhu H, Wicker NJ, Shaw GM, Lammer EJ, Hendricks K, Suarez L, Canfield M, Finnell RH. Zhu H, et al. Among authors: finnell rh. Mol Genet Metab. 2003 Mar;78(3):216-21. doi: 10.1016/s1096-7192(03)00008-8. Mol Genet Metab. 2003. PMID: 12649067

8

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. Volcik KA, et al. Among authors: finnell rh. Birth Defects Res A Clin Mol Teratol. 2003 Mar;67(3):154-7. doi: 10.1002/bdra.10008. Birth Defects Res A Clin Mol Teratol. 2003. PMID: 12797455

9

Risk factors for neural tube defects: associations between uncoupling protein 2 polymorphisms and spina bifida.

Volcik KA, Shaw GM, Zhu H, Lammer EJ, Finnell RH. Volcik KA, et al. Among authors: finnell rh. Birth Defects Res A Clin Mol Teratol. 2003 Mar;67(3):158-61. doi: 10.1002/bdra.10019. Birth Defects Res A Clin Mol Teratol. 2003. PMID: 12797456

10

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. Shaw GM, et al. Among authors: finnell rh. Am J Epidemiol. 2003 Oct 15;158(8):747-52. doi: 10.1093/aje/kwg189. Am J Epidemiol. 2003. PMID: 14561664

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