J. M. Schröder

Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A

Stephan Züchner, Irina Mersiyanova, M. Muglia et al. · Nature Genetics · 2004 · 1.5K citations · Full text

Neurodegenerative Diseases, Molecular Neuroscience, Mitochondrial Function +9

Mutations in SIL1 cause Marinesco-Sjögren syndrome, a cerebellar ataxia with cataract and myopathy

Jan Senderek, Michael J. B. Krieger, Claudia Stendel et al. · Nature Genetics · 2005 · 248 citations

Mendelian Disorder, Ophthalmology, Genetic Disorder +5

Mutations in a Gene Encoding a Novel SH3/TPR Domain Protein Cause Autosomal Recessive Charcot-Marie-Tooth Type 4C Neuropathy

Jan Senderek, Carsten Bergmann, Claudia Stendel et al. · The American Journal of Human Genetics · 2003 · 210 citations · Full text

Neurodegenerative Diseases, Molecular Neuroscience, Mendelian Disorder +9

Localization of the α-chemokine SDF-1 and its receptor CXCR4 in idiopathic inflammatory myopathies

Boél De Paepe, J. M. Schröder, Jean‐Jacques Martin et al. · Neuromuscular Disorders · 2004 · 130 citations

Inflammation, Cytokine, α-Chemokine Sdf-1 +15

Occurrence and characterization of peripheral nerve involvement in neurofibromatosis type 2

A.D Sperfeld, Claudine Hein, J. M. Schröder et al. · Brain · 2002 · 128 citations · Full text