Ware SM - Search Results

1

Novel Timothy syndrome mutation leading to increase in CACNA1C window current.

Boczek NJ, Miller EM, Ye D, Nesterenko VV, Tester DJ, Antzelevitch C, Czosek RJ, Ackerman MJ, Ware SM. Boczek NJ, et al. Among authors: ware sm. Heart Rhythm. 2015 Jan;12(1):211-9. doi: 10.1016/j.hrthm.2014.09.051. Epub 2014 Sep 28. Heart Rhythm. 2015. PMID: 25260352 Free PMC article.

2

Pediatric restrictive cardiomyopathy associated with a mutation in beta-myosin heavy chain.

Ware SM, Quinn ME, Ballard ET, Miller E, Uzark K, Spicer RL. Ware SM, et al. Clin Genet. 2008 Feb;73(2):165-70. doi: 10.1111/j.1399-0004.2007.00939.x. Epub 2007 Dec 12. Clin Genet. 2008. PMID: 18076673

3

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

4

High resolution SNP based microarray mapping of mosaic supernumerary marker chromosomes 13 and 17: delineating novel loci for apraxia.

Kogan JM, Miller E, Ware SM. Kogan JM, et al. Among authors: ware sm. Am J Med Genet A. 2009 May;149A(5):887-93. doi: 10.1002/ajmg.a.32750. Am J Med Genet A. 2009. PMID: 19353585

5

A mouse model of conduction system patterning abnormalities in heterotaxy syndrome.

Czosek RJ, Haaning A, Ware SM. Czosek RJ, et al. Among authors: ware sm. Pediatr Res. 2010 Oct;68(4):275-80. doi: 10.1203/PDR.0b013e3181ee0028. Pediatr Res. 2010. PMID: 20581739 Free PMC article.

6

Implications for genotype-phenotype predictions in Townes-Brocks syndrome: case report of a novel SALL1 deletion and review of the literature.

Miller EM, Hopkin R, Bao L, Ware SM. Miller EM, et al. Among authors: ware sm. Am J Med Genet A. 2012 Mar;158A(3):533-40. doi: 10.1002/ajmg.a.34426. Epub 2012 Feb 3. Am J Med Genet A. 2012. PMID: 22308078 Review.

7

Pediatric cardiomyopathy: importance of genetic and metabolic evaluation.

Kindel SJ, Miller EM, Gupta R, Cripe LH, Hinton RB, Spicer RL, Towbin JA, Ware SM. Kindel SJ, et al. Among authors: ware sm. J Card Fail. 2012 May;18(5):396-403. doi: 10.1016/j.cardfail.2012.01.017. Epub 2012 Mar 10. J Card Fail. 2012. PMID: 22555271 Free PMC article.

8

Uptake of cardiac screening and genetic testing among hypertrophic and dilated cardiomyopathy families.

Miller EM, Wang Y, Ware SM. Miller EM, et al. Among authors: ware sm. J Genet Couns. 2013 Apr;22(2):258-67. doi: 10.1007/s10897-012-9544-4. Epub 2012 Oct 10. J Genet Couns. 2013. PMID: 23054336

9

Genetic testing practices in infants with congenital heart disease.

Connor JA, Hinton RB, Miller EM, Sund KL, Ruschman JG, Ware SM. Connor JA, et al. Among authors: ware sm. Congenit Heart Dis. 2014 Mar-Apr;9(2):158-67. doi: 10.1111/chd.12112. Epub 2013 Jun 20. Congenit Heart Dis. 2014. PMID: 23782710

10

Provision of cardiovascular genetic counseling services: current practice and future directions.

Somers AE, Ware SM, Collins K, Jefferies JL, He H, Miller EM. Somers AE, et al. Among authors: ware sm. J Genet Couns. 2014 Dec;23(6):976-83. doi: 10.1007/s10897-014-9719-2. Epub 2014 May 1. J Genet Couns. 2014. PMID: 24788056

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