Stephanie K. Mewborn

Disruption of nesprin-1 produces an Emery Dreifuss muscular dystrophy-like phenotype in mice

Megan J. Puckelwartz, Elizabeth R. Kessler, Yuan Zhang et al. · Human Molecular Genetics · 2008 · 190 citations · Full text

Mutation analysis of the DCX gene and genotype/phenotype correlation in subcortical band heterotopia

Naomichi Matsumoto, Richard J. Leventer, Julie A. Kuc et al. · European Journal of Human Genetics · 2001 · 160 citations · Full text

Genotype/phenotype Correlation, Subcortical Band Heterotopia, Neurogenomics +11

Nesprin-1 mutations in human and murine cardiomyopathy

Megan J. Puckelwartz, Eric Kessler, Gene Kim et al. · Journal of Molecular and Cellular Cardiology · 2009 · 142 citations

Nesprin-1 Mutations, Cardiomyopathy, Heart Failure +6

Altered Chromosomal Positioning, Compaction, and Gene Expression with a Lamin A/C Gene Mutation

Stephanie K. Mewborn, Megan J. Puckelwartz, Fida Abuisneineh et al. · PLoS ONE · 2010 · 114 citations · Full text

Sarcomere Mutations in Cardiomyopathy With Left Ventricular Hypertrabeculation

Lisa Dellefave, Peter Pytel, Stephanie K. Mewborn et al. · Circulation Cardiovascular Genetics · 2009 · 94 citations