Matthias Vorgerd

Nesprin-1 and -2 are involved in the pathogenesis of Emery–Dreifuss muscular dystrophy and are critical for nuclear envelope integrity

Qiuping Zhang, Cornelia Bethmann, Nathalie F. Worth et al. · Human Molecular Genetics · 2007 · 535 citations · Full text

Clinical and molecular genetic spectrum of autosomal dominant Emery-Dreifuss muscular dystrophy due to mutations of the lamin A/C gene

Gisèle Bonne, Eugenio Mercuri, Antoine Muchir et al. · Annals of Neurology · 2000 · 486 citations

Cardiac Muscle, Engineering, Genetics +23

A Mutation in the Dimerization Domain of Filamin C Causes a Novel Type of Autosomal Dominant Myofibrillar Myopathy

Matthias Vorgerd, Peter F. M. van der Ven, Vera Bruchertseifer et al. · The American Journal of Human Genetics · 2005 · 309 citations · Full text

Mendelian Disorder, Novel Type, Genetics +6

Oxidative stress in patients with Friedreich ataxia

Jörg B. Schulz, Thomas Dehmer, Lüdger Schöls et al. · Neurology · 2000 · 303 citations

Distinct muscle imaging patterns in myofibrillar myopathies

Dirk Fischer, Rudolf A. Kley, Katharina Strach et al. · Neurology · 2008 · 252 citations · Full text