Siegfried JD - Search Results

1

Progress with genetic cardiomyopathies: screening, counseling, and testing in dilated, hypertrophic, and arrhythmogenic right ventricular dysplasia/cardiomyopathy.

Hershberger RE, Cowan J, Morales A, Siegfried JD. Hershberger RE, et al. Among authors: siegfried jd. Circ Heart Fail. 2009 May;2(3):253-61. doi: 10.1161/CIRCHEARTFAILURE.108.817346. Circ Heart Fail. 2009. PMID: 19808347 Free PMC article. Review.

2

Temporal relationship of conduction system disease and ventricular dysfunction in LMNA cardiomyopathy.

Brodt C, Siegfried JD, Hofmeyer M, Martel J, Rampersaud E, Li D, Morales A, Hershberger RE. Brodt C, et al. Among authors: siegfried jd. J Card Fail. 2013 Apr;19(4):233-9. doi: 10.1016/j.cardfail.2013.03.001. J Card Fail. 2013. PMID: 23582089 Free PMC article.

3

Return of genetic results in the familial dilated cardiomyopathy research project.

Siegfried JD, Morales A, Kushner JD, Burkett E, Cowan J, Mauro AC, Huggins GS, Li D, Norton N, Hershberger RE. Siegfried JD, et al. J Genet Couns. 2013 Apr;22(2):164-74. doi: 10.1007/s10897-012-9532-8. Epub 2012 Aug 11. J Genet Couns. 2013. PMID: 22886719 Free PMC article.

4

Assessment of LMNA copy number variation in 58 probands with dilated cardiomyopathy.

Norton N, Siegfried JD, Li D, Hershberger RE. Norton N, et al. Among authors: siegfried jd. Clin Transl Sci. 2011 Oct;4(5):351-2. doi: 10.1111/j.1752-8062.2011.00305.x. Clin Transl Sci. 2011. PMID: 22029807 Free PMC article.

5

Functional characterization of TNNC1 rare variants identified in dilated cardiomyopathy.

Pinto JR, Siegfried JD, Parvatiyar MS, Li D, Norton N, Jones MA, Liang J, Potter JD, Hershberger RE. Pinto JR, et al. Among authors: siegfried jd. J Biol Chem. 2011 Sep 30;286(39):34404-12. doi: 10.1074/jbc.M111.267211. Epub 2011 Aug 5. J Biol Chem. 2011. PMID: 21832052 Free PMC article.

6

Update 2011: clinical and genetic issues in familial dilated cardiomyopathy.

Hershberger RE, Siegfried JD. Hershberger RE, et al. Among authors: siegfried jd. J Am Coll Cardiol. 2011 Apr 19;57(16):1641-9. doi: 10.1016/j.jacc.2011.01.015. J Am Coll Cardiol. 2011. PMID: 21492761 Free PMC article. Review.

7

Rare variant mutations identified in pediatric patients with dilated cardiomyopathy.

Rampersaud E, Siegfried JD, Norton N, Li D, Martin E, Hershberger RE. Rampersaud E, et al. Among authors: siegfried jd. Prog Pediatr Cardiol. 2011 Jan 1;31(1):39-47. doi: 10.1016/j.ppedcard.2010.11.008. Prog Pediatr Cardiol. 2011. PMID: 21483645 Free PMC article.

8

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

Norton N, Li D, Rieder MJ, Siegfried JD, Rampersaud E, Züchner S, Mangos S, Gonzalez-Quintana J, Wang L, McGee S, Reiser J, Martin E, Nickerson DA, Hershberger RE. Norton N, et al. Among authors: siegfried jd. Am J Hum Genet. 2011 Mar 11;88(3):273-82. doi: 10.1016/j.ajhg.2011.01.016. Epub 2011 Feb 25. Am J Hum Genet. 2011. PMID: 21353195 Free PMC article.

9

SCN5A rare variants in familial dilated cardiomyopathy decrease peak sodium current depending on the common polymorphism H558R and common splice variant Q1077del.

Cheng J, Morales A, Siegfried JD, Li D, Norton N, Song J, Gonzalez-Quintana J, Makielski JC, Hershberger RE. Cheng J, et al. Among authors: siegfried jd. Clin Transl Sci. 2010 Dec;3(6):287-94. doi: 10.1111/j.1752-8062.2010.00249.x. Clin Transl Sci. 2010. PMID: 21167004 Free PMC article.

10

Late onset sporadic dilated cardiomyopathy caused by a cardiac troponin T mutation.

Morales A, Pinto JR, Siegfried JD, Li D, Norton N, Hofmeyer M, Vallin M, Morales AR, Potter JD, Hershberger RE. Morales A, et al. Among authors: siegfried jd. Clin Transl Sci. 2010 Oct;3(5):219-26. doi: 10.1111/j.1752-8062.2010.00228.x. Clin Transl Sci. 2010. PMID: 20973921 Free PMC article.

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