Li D - Search Results

1

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. Among authors: li d. 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.

2

Lamin A/C mutation analysis in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathy.

Parks SB, Kushner JD, Nauman D, Burgess D, Ludwigsen S, Peterson A, Li D, Jakobs P, Litt M, Porter CB, Rahko PS, Hershberger RE. Parks SB, et al. Among authors: li d. Am Heart J. 2008 Jul;156(1):161-9. doi: 10.1016/j.ahj.2008.01.026. Epub 2008 Mar 12. Am Heart J. 2008. PMID: 18585512 Free PMC article.

3

Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy.

Hershberger RE, Parks SB, Kushner JD, Li D, Ludwigsen S, Jakobs P, Nauman D, Burgess D, Partain J, Litt M. Hershberger RE, et al. Among authors: li d. Clin Transl Sci. 2008 May;1(1):21-6. doi: 10.1111/j.1752-8062.2008.00017.x. Clin Transl Sci. 2008. PMID: 19412328 Free PMC article.

4

Clinical and functional characterization of TNNT2 mutations identified in patients with dilated cardiomyopathy.

Hershberger RE, Pinto JR, Parks SB, Kushner JD, Li D, Ludwigsen S, Cowan J, Morales A, Parvatiyar MS, Potter JD. Hershberger RE, et al. Among authors: li d. Circ Cardiovasc Genet. 2009 Aug;2(4):306-13. doi: 10.1161/CIRCGENETICS.108.846733. Epub 2009 May 15. Circ Cardiovasc Genet. 2009. PMID: 20031601 Free PMC article.

5

Morphological analysis of 13 LMNA variants identified in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathy.

Cowan J, Li D, Gonzalez-Quintana J, Morales A, Hershberger RE. Cowan J, et al. Among authors: li d. Circ Cardiovasc Genet. 2010 Feb;3(1):6-14. doi: 10.1161/CIRCGENETICS.109.905422. Epub 2009 Nov 17. Circ Cardiovasc Genet. 2010. PMID: 20160190 Free PMC article.

6

Coding sequence rare variants identified in MYBPC3, MYH6, TPM1, TNNC1, and TNNI3 from 312 patients with familial or idiopathic dilated cardiomyopathy.

Hershberger RE, Norton N, Morales A, Li D, Siegfried JD, Gonzalez-Quintana J. Hershberger RE, et al. Among authors: li d. Circ Cardiovasc Genet. 2010 Apr;3(2):155-61. doi: 10.1161/CIRCGENETICS.109.912345. Epub 2010 Mar 9. Circ Cardiovasc Genet. 2010. PMID: 20215591 Free PMC article.

7

Rare variant mutations in pregnancy-associated or peripartum cardiomyopathy.

Morales A, Painter T, Li R, Siegfried JD, Li D, Norton N, Hershberger RE. Morales A, et al. Among authors: li d, li r. Circulation. 2010 May 25;121(20):2176-82. doi: 10.1161/CIRCULATIONAHA.109.931220. Epub 2010 May 10. Circulation. 2010. PMID: 20458009 Free PMC article.

8

Identification of novel mutations in RBM20 in patients with dilated cardiomyopathy.

Li D, Morales A, Gonzalez-Quintana J, Norton N, Siegfried JD, Hofmeyer M, Hershberger RE. Li D, et al. Clin Transl Sci. 2010 Jun;3(3):90-7. doi: 10.1111/j.1752-8062.2010.00198.x. Clin Transl Sci. 2010. PMID: 20590677 Free PMC article.

9

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: li d. 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.

10

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: li d. 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.

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