Mitchell LE - Search Results

1

Genome-Wide Association Studies of Conotruncal Heart Defects with Normally Related Great Vessels in the United States.

Oluwafemi OO, Musfee FI, Mitchell LE, Goldmuntz E, Xie HM, Hakonarson H, Morrow BE, Guo T, Taylor DM, McDonald-McGinn DM, Emanuel BS, Agopian AJ. Oluwafemi OO, et al. Among authors: mitchell le. Genes (Basel). 2021 Jul 1;12(7):1030. doi: 10.3390/genes12071030. Genes (Basel). 2021. PMID: 34356046 Free PMC article.

2

Frequency of 22q11 deletions in patients with conotruncal defects.

Goldmuntz E, Clark BJ, Mitchell LE, Jawad AF, Cuneo BF, Reed L, McDonald-McGinn D, Chien P, Feuer J, Zackai EH, Emanuel BS, Driscoll DA. Goldmuntz E, et al. Among authors: mitchell le. J Am Coll Cardiol. 1998 Aug;32(2):492-8. doi: 10.1016/s0735-1097(98)00259-9. J Am Coll Cardiol. 1998. PMID: 9708481 Free article.

3

PCR assay for screening patients at risk for 22q11.2 deletion.

Driscoll DA, Emanuel BS, Mitchell LE, Budarf ML. Driscoll DA, et al. Among authors: mitchell le. Genet Test. 1997;1(2):109-13. doi: 10.1089/gte.1997.1.109. Genet Test. 1997. PMID: 10464634

4

Evaluation of potential modifiers of the palatal phenotype in the 22q11.2 deletion syndrome.

Driscoll DA, Boland T, Emanuel BS, Kirschner RE, LaRossa D, Manson J, McDonald-McGinn D, Randall P, Solot C, Zackai E, Mitchell LE. Driscoll DA, et al. Among authors: mitchell le. Cleft Palate Craniofac J. 2006 Jul;43(4):435-41. doi: 10.1597/05-070.1. Cleft Palate Craniofac J. 2006. PMID: 16854201 Free PMC article.

5

Evaluation of potential modifiers of the cardiac phenotype in the 22q11.2 deletion syndrome.

Goldmuntz E, Driscoll DA, Emanuel BS, McDonald-McGinn D, Mei M, Zackai E, Mitchell LE. Goldmuntz E, et al. Among authors: mitchell le. Birth Defects Res A Clin Mol Teratol. 2009 Feb;85(2):125-9. doi: 10.1002/bdra.20501. Birth Defects Res A Clin Mol Teratol. 2009. PMID: 18770859 Free PMC article.

6

Cumulative ligand activity of NODAL mutations and modifiers are linked to human heart defects and holoprosencephaly.

Roessler E, Pei W, Ouspenskaia MV, Karkera JD, Veléz JI, Banerjee-Basu S, Gibney G, Lupo PJ, Mitchell LE, Towbin JA, Bowers P, Belmont JW, Goldmuntz E, Baxevanis AD, Feldman B, Muenke M. Roessler E, et al. Among authors: mitchell le. Mol Genet Metab. 2009 Sep-Oct;98(1-2):225-34. doi: 10.1016/j.ymgme.2009.05.005. Epub 2009 May 27. Mol Genet Metab. 2009. PMID: 19553149 Free PMC article.

7

Descriptive epidemiology of nonsyndromic omphalocele in Texas, 1999-2004.

Agopian A, Marengo L, Mitchell LE. Agopian A, et al. Among authors: mitchell le. Am J Med Genet A. 2009 Oct;149A(10):2129-33. doi: 10.1002/ajmg.a.33000. Am J Med Genet A. 2009. PMID: 19760656

8

Variants of folate metabolism genes and risk of left-sided cardiac defects.

Mitchell LE, Long J, Garbarini J, Paluru P, Goldmuntz E. Mitchell LE, et al. Birth Defects Res A Clin Mol Teratol. 2010 Jan;88(1):48-53. doi: 10.1002/bdra.20622. Birth Defects Res A Clin Mol Teratol. 2010. PMID: 19777601 Free PMC article.

9

Variants of folate metabolism genes and the risk of conotruncal cardiac defects.

Goldmuntz E, Woyciechowski S, Renstrom D, Lupo PJ, Mitchell LE. Goldmuntz E, et al. Among authors: mitchell le. Circ Cardiovasc Genet. 2008 Dec;1(2):126-32. doi: 10.1161/CIRCGENETICS.108.796342. Epub 2008 Dec 9. Circ Cardiovasc Genet. 2008. PMID: 20031554 Free PMC article.

10

Gene-gene interactions in the folate metabolic pathway and the risk of conotruncal heart defects.

Lupo PJ, Goldmuntz E, Mitchell LE. Lupo PJ, et al. Among authors: mitchell le. J Biomed Biotechnol. 2010;2010:630940. doi: 10.1155/2010/630940. Epub 2010 Jan 12. J Biomed Biotechnol. 2010. PMID: 20111745 Free PMC article.

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