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Jill D. Siegfried

University of Miami

16

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1502

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Update 2011: Clinical and Genetic Issues in Familial Dilated Cardiomyopathy

2011 Journal of the American College of Cardiology
- Ray E. Hershberger
- Jill D. Siegfried
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Rare variant mutations identified in pediatric patients with dilated cardiomyopathy

2011 Progress in Pediatric Cardiology
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Assessment of LMNA Copy Number Variation in 58 Probands with Dilated Cardiomyopathy

2011 Clinical and Translational Science
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Functional Characterization of TNNC1 Rare Variants Identified in Dilated Cardiomyopathy

2011 Journal of Biological Chemistry
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Genome-wide studies of copy number variation and exome sequencing identify rare variants in BAG3 as a cause of dilated cardiomyopathy.

2011 American Journal of Human Genetics
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Coding sequence rare variants identified in MYBPC3, MYH6, TPM1, TNNC1, and TNNI3 from 312 patients with familial or idiopathic dilated cardiomyopathy.

2010 Circulation-cardiovascular Genetics
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Late Onset Sporadic Dilated Cardiomyopathy Caused by a Cardiac Troponin T Mutation

2010 Clinical and Translational Science
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Clinical and genetic issues in dilated cardiomyopathy: a review for genetics professionals.

2010 Genetics in Medicine
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Rare Variant Mutations in Pregnancy-Associated or Peripartum Cardiomyopathy

2010 Circulation
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Progress With Genetic Cardiomyopathies Screening, Counseling, and Testing in Dilated, Hypertrophic, and Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy

2009 Circulation-heart Failure
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Citations (178)