Finnell RH - Search Results

1

Apolipoprotein E and apolipoprotein B genotypes and risk for spina bifida.

Volcik KA, Zhu H, Shaw GM, Lammer EJ, Finnell RH. Volcik KA, et al. Among authors: finnell rh. Teratology. 2002 Nov;66(5):257-9. doi: 10.1002/tera.10097. Teratology. 2002. PMID: 12397634

2

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. Shaw GM, et al. Among authors: finnell rh. Am J Med Genet. 2002 Feb 15;108(1):1-6. doi: 10.1002/ajmg.10195. Am J Med Genet. 2002. PMID: 11857541

3

Apolipoprotein B and apolipoprotein E genotypes and sporadic holoprosencephaly.

Croen LA, Shaw GM, Barber RC, Baker MM, Finnell RH, Lammer EJ. Croen LA, et al. Among authors: finnell rh. Am J Med Genet. 2002 Feb 15;108(1):75-7. Am J Med Genet. 2002. PMID: 11857554 No abstract available.

4

Does prenatal screening for 5,10-methylenetetrahydrofolate reductase (MTHFR) mutations in high-risk neural tube defect pregnancies make sense?

Finnell RH, Shaw GM, Lammer EJ, Volcik KA. Finnell RH, et al. Genet Test. 2002 Spring;6(1):47-52. doi: 10.1089/109065702760093915. Genet Test. 2002. PMID: 12180076

5

Integration of DNA sample collection into a multi-site birth defects case-control study.

Rasmussen SA, Lammer EJ, Shaw GM, Finnell RH, McGehee RE Jr, Gallagher M, Romitti PA, Murray JC; National Birth Defects Prevention Study. Rasmussen SA, et al. Among authors: finnell rh. Teratology. 2002 Oct;66(4):177-84. doi: 10.1002/tera.10086. Teratology. 2002. PMID: 12353214

6

Importance of gene-environment interactions in the etiology of selected birth defects.

Zhu H, Kartiko S, Finnell RH. Zhu H, et al. Among authors: finnell rh. Clin Genet. 2009 May;75(5):409-23. doi: 10.1111/j.1399-0004.2009.01174.x. Clin Genet. 2009. PMID: 19459879 Review.

7

Biomarkers of exposure to combustion by-products in a human population in Shanxi, China.

Naufal Z, Zhiwen L, Zhu L, Zhou GD, McDonald T, He LY, Mitchell L, Ren A, Zhu H, Finnell R, Donnelly KC. Naufal Z, et al. J Expo Sci Environ Epidemiol. 2010 Jun;20(4):310-9. doi: 10.1038/jes.2009.19. Epub 2009 Mar 11. J Expo Sci Environ Epidemiol. 2010. PMID: 19277067

8

Study of MTHFR and MS polymorphisms as risk factors for NTD in the Italian population.

De Marco P, Calevo MG, Moroni A, Arata L, Merello E, Finnell RH, Zhu H, Andreussi L, Cama A, Capra V. De Marco P, et al. Among authors: finnell rh. J Hum Genet. 2002;47(6):319-24. doi: 10.1007/s100380200043. J Hum Genet. 2002. PMID: 12111380

9

Exome sequencing identifies variants in infants with sacral agenesis.

Pitsava G, Feldkamp ML, Pankratz N, Lane J, Kay DM, Conway KM, Hobbs C, Shaw GM, Reefhuis J, Jenkins MM, Almli LM, Moore C, Werler M, Browne ML, Cunniff C, Olshan AF, Pangilinan F, Brody LC, Sicko RJ, Finnell RH, Bamshad MJ, McGoldrick D, Nickerson DA, Mullikin JC, Romitti PA, Mills JL; UW Center for Mendelian Genomics, NISC Comparative Sequencing Program and the National Birth Defects Prevention Study. Pitsava G, et al. Among authors: finnell rh. Birth Defects Res. 2022 Apr;114(7):215-227. doi: 10.1002/bdr2.1987. Epub 2022 Mar 10. Birth Defects Res. 2022. PMID: 35274497 Free PMC article.

10

Cerebral folate deficiency with developmental delay, autism, and response to folinic acid.

Moretti P, Sahoo T, Hyland K, Bottiglieri T, Peters S, del Gaudio D, Roa B, Curry S, Zhu H, Finnell RH, Neul JL, Ramaekers VT, Blau N, Bacino CA, Miller G, Scaglia F. Moretti P, et al. Among authors: finnell rh. Neurology. 2005 Mar 22;64(6):1088-90. doi: 10.1212/01.WNL.0000154641.08211.B7. Neurology. 2005. PMID: 15781839

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