Ware SM - Search Results

1

Clinical spectrum, morbidity, and mortality in 113 pediatric patients with mitochondrial disease.

Scaglia F, Towbin JA, Craigen WJ, Belmont JW, Smith EO, Neish SR, Ware SM, Hunter JV, Fernbach SD, Vladutiu GD, Wong LJ, Vogel H. Scaglia F, et al. Among authors: ware sm. Pediatrics. 2004 Oct;114(4):925-31. doi: 10.1542/peds.2004-0718. Pediatrics. 2004. PMID: 15466086

2

A complex syndrome of left-right axis, central nervous system and axial skeleton defects in Zic3 mutant mice.

Purandare SM, Ware SM, Kwan KM, Gebbia M, Bassi MT, Deng JM, Vogel H, Behringer RR, Belmont JW, Casey B. Purandare SM, et al. Among authors: ware sm. Development. 2002 May;129(9):2293-302. doi: 10.1242/dev.129.9.2293. Development. 2002. PMID: 11959836

3

Identification and functional analysis of ZIC3 mutations in heterotaxy and related congenital heart defects.

Ware SM, Peng J, Zhu L, Fernbach S, Colicos S, Casey B, Towbin J, Belmont JW. Ware SM, et al. Am J Hum Genet. 2004 Jan;74(1):93-105. doi: 10.1086/380998. Epub 2003 Dec 16. Am J Hum Genet. 2004. PMID: 14681828 Free PMC article.

4

Molecular genetics of heterotaxy syndromes.

Belmont JW, Mohapatra B, Towbin JA, Ware SM. Belmont JW, et al. Among authors: ware sm. Curr Opin Cardiol. 2004 May;19(3):216-20. doi: 10.1097/00001573-200405000-00005. Curr Opin Cardiol. 2004. PMID: 15096953 Review.

5

Genetic predictors and remodeling of dilated cardiomyopathy in muscular dystrophy.

Jefferies JL, Eidem BW, Belmont JW, Craigen WJ, Ware SM, Fernbach SD, Neish SR, Smith EO, Towbin JA. Jefferies JL, et al. Among authors: ware sm. Circulation. 2005 Nov 1;112(18):2799-804. doi: 10.1161/CIRCULATIONAHA.104.528281. Epub 2005 Oct 24. Circulation. 2005. PMID: 16246949

6

Genetics of human heterotaxias.

Zhu L, Belmont JW, Ware SM. Zhu L, et al. Among authors: ware sm. Eur J Hum Genet. 2006 Jan;14(1):17-25. doi: 10.1038/sj.ejhg.5201506. Eur J Hum Genet. 2006. PMID: 16251896 Review.

7

Zic3 is critical for early embryonic patterning during gastrulation.

Ware SM, Harutyunyan KG, Belmont JW. Ware SM, et al. Dev Dyn. 2006 Mar;235(3):776-85. doi: 10.1002/dvdy.20668. Dev Dyn. 2006. PMID: 16397896 Free article.

8

Heart defects in X-linked heterotaxy: evidence for a genetic interaction of Zic3 with the nodal signaling pathway.

Ware SM, Harutyunyan KG, Belmont JW. Ware SM, et al. Dev Dyn. 2006 Jun;235(6):1631-7. doi: 10.1002/dvdy.20719. Dev Dyn. 2006. PMID: 16496285 Free article.

9

Identification and functional characterization of NODAL rare variants in heterotaxy and isolated cardiovascular malformations.

Mohapatra B, Casey B, Li H, Ho-Dawson T, Smith L, Fernbach SD, Molinari L, Niesh SR, Jefferies JL, Craigen WJ, Towbin JA, Belmont JW, Ware SM. Mohapatra B, et al. Among authors: ware sm. Hum Mol Genet. 2009 Mar 1;18(5):861-71. doi: 10.1093/hmg/ddn411. Epub 2008 Dec 8. Hum Mol Genet. 2009. PMID: 19064609 Free PMC article.

10

Infantile cardiomyopathy caused by a mutation in the overlapping region of mitochondrial ATPase 6 and 8 genes.

Ware SM, El-Hassan N, Kahler SG, Zhang Q, Ma YW, Miller E, Wong B, Spicer RL, Craigen WJ, Kozel BA, Grange DK, Wong LJ. Ware SM, et al. J Med Genet. 2009 May;46(5):308-14. doi: 10.1136/jmg.2008.063149. Epub 2009 Feb 2. J Med Genet. 2009. PMID: 19188198

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