Cowan J - Search Results

1

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: cowan j. 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.

2

Family history: an essential tool for cardiovascular genetic medicine.

Morales A, Cowan J, Dagua J, Hershberger RE. Morales A, et al. Among authors: cowan j. Congest Heart Fail. 2008 Jan-Feb;14(1):37-45. doi: 10.1111/j.1751-7133.2008.08201.x. Congest Heart Fail. 2008. PMID: 18256568 Free article. Review.

3

The family history as a tool to identify patients at risk for dilated cardiomyopathy.

Nauman D, Morales A, Cowan J, Dagua J, Hershberger RE. Nauman D, et al. Among authors: cowan j. Prog Cardiovasc Nurs. 2008 Winter;23(1):41-4. doi: 10.1111/j.1751-7117.2008.08223.x. Prog Cardiovasc Nurs. 2008. PMID: 18326985 Review. No abstract available.

4

Genetic testing and genetic counseling in cardiovascular genetic medicine: overview and preliminary recommendations.

Cowan J, Morales A, Dagua J, Hershberger RE. Cowan J, et al. Congest Heart Fail. 2008 Mar-Apr;14(2):97-105. doi: 10.1111/j.1751-7133.2008.08217.x. Congest Heart Fail. 2008. PMID: 18401220 Free article. Review.

5

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: cowan j. 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.

6

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. 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.

7

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: cowan j. 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.

8

Is Left Ventricular Noncompaction a Trait, Phenotype, or Disease? The Evidence Points to Phenotype.

Hershberger RE, Morales A, Cowan J. Hershberger RE, et al. Among authors: cowan j. Circ Cardiovasc Genet. 2017 Dec;10(6):e001968. doi: 10.1161/CIRCGENETICS.117.001968. Circ Cardiovasc Genet. 2017. PMID: 29212902 No abstract available.

9

Multigenic Disease and Bilineal Inheritance in Dilated Cardiomyopathy Is Illustrated in Nonsegregating LMNA Pedigrees.

Cowan JR, Kinnamon DD, Morales A, Salyer L, Nickerson DA, Hershberger RE. Cowan JR, et al. Circ Genom Precis Med. 2018 Jul;11(7):e002038. doi: 10.1161/CIRCGEN.117.002038. Circ Genom Precis Med. 2018. PMID: 30012837 Free PMC article.

10

SOS1 Gain-of-Function Variants in Dilated Cardiomyopathy.

Cowan JR, Salyer L, Wright NT, Kinnamon DD, Amaya P, Jordan E, Bamshad MJ, Nickerson DA, Hershberger RE. Cowan JR, et al. Circ Genom Precis Med. 2020 Aug;13(4):e002892. doi: 10.1161/CIRCGEN.119.002892. Epub 2020 Jun 30. Circ Genom Precis Med. 2020. PMID: 32603605 Free PMC article.

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