PubRank

Ketty Schwartz

Author PubWeight™ 31.58‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Hypertrophic cardiomyopathy: distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy. Circulation 2003 5.85
2 Autologous skeletal myoblast transplantation for severe postinfarction left ventricular dysfunction. J Am Coll Cardiol 2003 4.91
3 Mouse model carrying H222P-Lmna mutation develops muscular dystrophy and dilated cardiomyopathy similar to human striated muscle laminopathies. Hum Mol Genet 2004 2.31
4 Skeletal myoblast transplantation in ischemic heart failure: long-term follow-up of the first phase I cohort of patients. Circulation 2006 1.63
5 Nuclear envelope alterations in fibroblasts from LGMD1B patients carrying nonsense Y259X heterozygous or homozygous mutation in lamin A/C gene. Exp Cell Res 2003 1.60
6 Identification of the genotypes causing hypertrophic cardiomyopathy in northern Sweden. J Mol Cell Cardiol 2003 1.48
7 Asymmetric septal hypertrophy in heterozygous cMyBP-C null mice. Cardiovasc Res 2004 1.39
8 Long-term efficacy of myoblast transplantation on regional structure and function after myocardial infarction. Circulation 2002 1.27
9 Nonsense-mediated mRNA decay and ubiquitin-proteasome system regulate cardiac myosin-binding protein C mutant levels in cardiomyopathic mice. Circ Res 2009 1.26
10 Novel deletions in MYH7 and MYBPC3 identified in Indian families with familial hypertrophic cardiomyopathy. J Mol Cell Cardiol 2003 1.04
11 Emery-Dreifuss muscular dystrophy. Eur J Hum Genet 2002 0.99
12 Structural analysis of four and half LIM protein-2 in dilated cardiomyopathy. Biochem Biophys Res Commun 2007 0.93
13 Biomolecular interactions between human recombinant beta-MyHC and cMyBP-Cs implicated in familial hypertrophic cardiomyopathy. Cardiovasc Res 2003 0.91
14 Distinction between two populations of islet-1-positive cells in hearts of different murine strains. Stem Cells Dev 2010 0.87
15 Polymorphisms of genes of the cardiac calcineurin pathway and cardiac hypertrophy. Eur J Hum Genet 2003 0.86
16 A new polymorphism in human calmodulin III gene promoter is a potential modifier gene for familial hypertrophic cardiomyopathy. Eur Heart J 2009 0.85
17 Apical left ventricular aneurysm without atrio-ventricular block due to a lamin A/C gene mutation. Eur J Heart Fail 2003 0.85
18 82nd ENMC international workshop, 5th international Emery-Dreifuss muscular dystrophy (EDMD) workshop, 1st Workshop of the MYO-CLUSTER project EUROMEN (European muscle envelope nucleopathies), 15-16 September 2000, Naarden, The Netherlands. Neuromuscul Disord 2002 0.84
19 Electrotransfer at MR imaging: tool for optimization of gene transfer protocols--feasibility study in mice. Radiology 2003 0.83
20 Diagnostic accuracy of a 2D left ventricle hypertrophy score for familial hypertrophic cardiomyopathy. Eur Heart J 2005 0.81
21 Genetics of familial cardiomyopathies and arrhythmias. Swiss Med Wkly 2002 0.79