Eva M. Wicklein

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 · 491 citations

Medicine, Genetics, Molecular Genetics +14

Nonsense Mutations in SMPX, Encoding a Protein Responsive to Physical Force, Result in X-Chromosomal Hearing Loss

Antje K. Huebner, Marta Gandía, Peter Frommolt et al. · The American Journal of Human Genetics · 2011 · 86 citations · Full text

Life Sciences, Genetics, Molecular Genetics +9

Molecular diagnosis of McArdle disease: Revised genomic structure of the myophosphorylase gene and identification of a novel mutation

Christian Kubisch, Eva M. Wicklein, Thomas J. Jentsch · Human Mutation · 1998 · 75 citations

Life Sciences, Genetics, Molecular Genetics +14

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 · 32 citations

Medicine, Genetics, Molecular Genetics +14

Prominent sensory ataxia in Guillain–Barré syndrome associated with IgG anti-GD1b antibody

Eva M. Wicklein, G. Pfeiffer, Nobuhiro Yuki et al. · Journal of the Neurological Sciences · 1997 · 29 citations

Life Sciences, Neurology, Neuroscience +14