Shaw GM - Search Results

1

Defective sumoylation pathway directs congenital heart disease.

Wang J, Chen L, Wen S, Zhu H, Yu W, Moskowitz IP, Shaw GM, Finnell RH, Schwartz RJ. Wang J, et al. Among authors: shaw gm. Birth Defects Res A Clin Mol Teratol. 2011 Jun;91(6):468-76. doi: 10.1002/bdra.20816. Epub 2011 May 11. Birth Defects Res A Clin Mol Teratol. 2011. PMID: 21563299 Free PMC article.

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. 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: shaw gm. 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. Among authors: shaw gm. Genet Test. 2002 Spring;6(1):47-52. doi: 10.1089/109065702760093915. Genet Test. 2002. PMID: 12180076

5

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. Am J Epidemiol. 2003 Oct 15;158(8):747-52. doi: 10.1093/aje/kwg189. Am J Epidemiol. 2003. PMID: 14561664

6

Promoter haplotype combinations for the human PDGFRA gene are associated with risk of neural tube defects.

Zhu H, Wicker NJ, Volcik K, Zhang J, Shaw GM, Lammer EJ, Suarez L, Canfield M, Finnell RH. Zhu H, et al. Among authors: shaw gm. Mol Genet Metab. 2004 Feb;81(2):127-32. doi: 10.1016/j.ymgme.2003.11.003. Mol Genet Metab. 2004. PMID: 14741194

7

Associations between polymorphisms within the thymidylate synthase gene and spina bifida.

Volcik KA, Shaw GM, Zhu H, Lammer EJ, Laurent C, Finnell RH. Volcik KA, et al. Among authors: shaw gm. Birth Defects Res A Clin Mol Teratol. 2003 Nov;67(11):924-8. doi: 10.1002/bdra.10029. Birth Defects Res A Clin Mol Teratol. 2003. PMID: 14745930

8

Limb deficiency defects, MSX1, and exposure to tobacco smoke.

Carmichael SL, Shaw GM, Yang W, Lammer EJ, Zhu H, Finnell RH. Carmichael SL, et al. Among authors: shaw gm. Am J Med Genet A. 2004 Mar 15;125A(3):285-9. doi: 10.1002/ajmg.a.20517. Am J Med Genet A. 2004. PMID: 14994238

9

Evaluation of the Cited2 gene and risk for spina bifida and congenital heart defects.

Volcik KA, Zhu H, Finnell RH, Shaw GM, Canfield M, Lammer EJ. Volcik KA, et al. Among authors: shaw gm. Am J Med Genet A. 2004 Apr 30;126A(3):324-5. doi: 10.1002/ajmg.a.20578. Am J Med Genet A. 2004. PMID: 15054851 No abstract available.

10

Evaluation of the jumonji gene and risk for spina bifida and congenital heart defects.

Volcik KA, Zhu H, Finnell RH, Shaw GM, Canfield M, Lammer EJ. Volcik KA, et al. Among authors: shaw gm. Am J Med Genet A. 2004 Apr 15;126A(2):215-7. doi: 10.1002/ajmg.a.20574. Am J Med Genet A. 2004. PMID: 15057990 No abstract available.

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