Mitchell LE - Search Results

1

Mitchell LE, Adzick NS, Melchionne J, Pasquariello PS, Sutton LN, Whitehead AS. Mitchell LE, et al. Lancet. 2004 Nov 20-26;364(9448):1885-95. doi: 10.1016/S0140-6736(04)17445-X. Lancet. 2004. PMID: 15555669 Review.

2

Maternal genotype for the monocyte chemoattractant protein 1 A(-2518)G promoter polymorphism is associated with the risk of spina bifida in offspring.

Jensen LE, Etheredge AJ, Brown KS, Mitchell LE, Whitehead AS. Jensen LE, et al. Among authors: mitchell le. Am J Med Genet A. 2006 May 15;140(10):1114-8. doi: 10.1002/ajmg.a.31212. Am J Med Genet A. 2006. PMID: 16596675 No abstract available.

3

Loss of function polymorphisms in NAT1 protect against spina bifida.

Jensen LE, Hoess K, Mitchell LE, Whitehead AS. Jensen LE, et al. Among authors: mitchell le. Hum Genet. 2006 Aug;120(1):52-7. doi: 10.1007/s00439-006-0181-6. Epub 2006 May 6. Hum Genet. 2006. PMID: 16680433

4

Maternal genetic effects, exerted by genes involved in homocysteine remethylation, influence the risk of spina bifida.

Doolin MT, Barbaux S, McDonnell M, Hoess K, Whitehead AS, Mitchell LE. Doolin MT, et al. Among authors: mitchell le. Am J Hum Genet. 2002 Nov;71(5):1222-6. doi: 10.1086/344209. Epub 2002 Oct 9. Am J Hum Genet. 2002. PMID: 12375236 Free PMC article.

5

Evidence that the risk of spina bifida is influenced by genetic variation at the NOS3 locus.

Brown KS, Cook M, Hoess K, Whitehead AS, Mitchell LE. Brown KS, et al. Among authors: mitchell le. Birth Defects Res A Clin Mol Teratol. 2004 Mar;70(3):101-6. doi: 10.1002/bdra.20002. Birth Defects Res A Clin Mol Teratol. 2004. PMID: 15039923

6

A common ABCC2 promoter polymorphism is not a determinant of the risk of spina bifida.

Jensen LE, Wall AM, Cook M, Hoess K, Thorn CF, Whitehead AS, Mitchell LE. Jensen LE, et al. Among authors: mitchell le. Birth Defects Res A Clin Mol Teratol. 2004 Jun;70(6):396-9. doi: 10.1002/bdra.20023. Birth Defects Res A Clin Mol Teratol. 2004. PMID: 15211708

7

The human T locus and spina bifida risk.

Jensen LE, Barbaux S, Hoess K, Fraterman S, Whitehead AS, Mitchell LE. Jensen LE, et al. Among authors: mitchell le. Hum Genet. 2004 Nov;115(6):475-82. doi: 10.1007/s00439-004-1185-8. Epub 2004 Sep 24. Hum Genet. 2004. PMID: 15449172

8

The NAT1 C1095A polymorphism, maternal multivitamin use and smoking, and the risk of spina bifida.

Jensen LE, Hoess K, Whitehead AS, Mitchell LE. Jensen LE, et al. Among authors: mitchell le. Birth Defects Res A Clin Mol Teratol. 2005 Jul;73(7):512-6. doi: 10.1002/bdra.20143. Birth Defects Res A Clin Mol Teratol. 2005. PMID: 15959877

9

Folate and homocysteine phenotypes: Comparative findings using research and clinical laboratory data.

Mitchell LE, Morales M, Khartulyari S, Huang Y, Murphy K, Mei M, Von Feldt JM, Blair IA, Whitehead AS. Mitchell LE, et al. Clin Biochem. 2009 Aug;42(12):1275-81. doi: 10.1016/j.clinbiochem.2009.04.014. Epub 2009 May 8. Clin Biochem. 2009. PMID: 19427846 Free PMC article.

10

Spina Bifida Research Resource: study design and participant characteristics.

Mitchell LE. Mitchell LE. Birth Defects Res A Clin Mol Teratol. 2008 Oct;82(10):684-91. doi: 10.1002/bdra.20465. Birth Defects Res A Clin Mol Teratol. 2008. PMID: 18553493

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