Ware SM - Search Results

1

A Multicenter Analysis of Abnormal Chromosomal Microarray Findings in Congenital Heart Disease.

Landis BJ, Helvaty LR, Geddes GC, Lin JI, Yatsenko SA, Lo CW, Border WL, Wechsler SB, Murali CN, Azamian MS, Lalani SR, Hinton RB, Garg V, McBride KL, Hodge JC, Ware SM. Landis BJ, et al. Among authors: ware sm. J Am Heart Assoc. 2023 Sep 19;12(18):e029340. doi: 10.1161/JAHA.123.029340. Epub 2023 Sep 8. J Am Heart Assoc. 2023. PMID: 37681527 Free PMC article.

2

Replacement of the aortic valve in a patient with mucolipidosis III.

Cripe LH, Ware SM, Hinton RB. Cripe LH, et al. Among authors: ware sm. Cardiol Young. 2009 Dec;19(6):641-3. doi: 10.1017/S1047951109991120. Epub 2009 Sep 24. Cardiol Young. 2009. PMID: 19775498

3

A fetus with hypertrophic cardiomyopathy, restrictive, and single-ventricle physiology, and a beta-myosin heavy chain mutation.

Hinton RB, Michelfelder EC, Marino BS, Bove KE, Ware SM. Hinton RB, et al. Among authors: ware sm. J Pediatr. 2010 Jul;157(1):164-6. doi: 10.1016/j.jpeds.2010.02.044. Epub 2010 Apr 14. J Pediatr. 2010. PMID: 20394946 Free PMC article.

4

SHROOM3 is a novel candidate for heterotaxy identified by whole exome sequencing.

Tariq M, Belmont JW, Lalani S, Smolarek T, Ware SM. Tariq M, et al. Among authors: ware sm. Genome Biol. 2011 Sep 21;12(9):R91. doi: 10.1186/gb-2011-12-9-r91. Genome Biol. 2011. PMID: 21936905 Free PMC article.

5

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.

6

Modifying Mendel: approaches for identification of susceptibility alleles for human cardiovascular malformations.

McBride KL, Ware SM. McBride KL, et al. Among authors: ware sm. Circ Cardiovasc Genet. 2012 Jun;5(3):274-6. doi: 10.1161/CIRCGENETICS.112.963579. Circ Cardiovasc Genet. 2012. PMID: 22715278 No abstract available.

7

Rare DNA copy number variants in cardiovascular malformations with extracardiac abnormalities.

Lalani SR, Shaw C, Wang X, Patel A, Patterson LW, Kolodziejska K, Szafranski P, Ou Z, Tian Q, Kang SH, Jinnah A, Ali S, Malik A, Hixson P, Potocki L, Lupski JR, Stankiewicz P, Bacino CA, Dawson B, Beaudet AL, Boricha FM, Whittaker R, Li C, Ware SM, Cheung SW, Penny DJ, Jefferies JL, Belmont JW. Lalani SR, et al. Among authors: ware sm. Eur J Hum Genet. 2013 Feb;21(2):173-81. doi: 10.1038/ejhg.2012.155. Epub 2012 Aug 29. Eur J Hum Genet. 2013. PMID: 22929023 Free PMC article.

8

Left ventricular noncompaction cardiomyopathy and aortopathy in a patient with recessive dystrophic epidermolysis bullosa.

Ryan TD, Ware SM, Lucky AW, Towbin JA, Jefferies JL, Hinton RB. Ryan TD, et al. Among authors: ware sm. Circ Heart Fail. 2012 Sep 1;5(5):e81-2. doi: 10.1161/CIRCHEARTFAILURE.112.969675. Circ Heart Fail. 2012. PMID: 22991407 No abstract available.

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

Twins with progressive thoracic aortic aneurysm, recurrent dissection and ACTA2 mutation.

Ware SM, Shikany A, Landis BJ, James JF, Hinton RB. Ware SM, et al. Pediatrics. 2014 Oct;134(4):e1218-23. doi: 10.1542/peds.2013-2503. Epub 2014 Sep 15. Pediatrics. 2014. PMID: 25225139

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