| Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A S Züchner, IV Mersiyanova, M Muglia, N Bissar-Tadmouri, J Rochelle, ... Nature genetics 36 (5), 449-451, 2004 | 1862 | 2004 |
| MFN2 mutation distribution and genotype/phenotype correlation in Charcot–Marie–Tooth type 2 K Verhoeven, KG Claeys, S Züchner, JM Schröder, J Weis, C Ceuterick, ... Brain 129 (8), 2093-2102, 2006 | 430 | 2006 |
| Mutations in SIL1 cause Marinesco-Sjögren syndrome, a cerebellar ataxia with cataract and myopathy J Senderek, M Krieger, C Stendel, C Bergmann, M Moser, ... Nature genetics 37 (12), 1312-1314, 2005 | 289 | 2005 |
| Mutations in a gene encoding a novel SH3/TPR domain protein cause autosomal recessive Charcot-Marie-Tooth type 4C neuropathy J Senderek, C Bergmann, C Stendel, J Kirfel, N Verpoorten, P De Jonghe, ... The American Journal of Human Genetics 73 (5), 1106-1119, 2003 | 243 | 2003 |
| Altered ratio between axon diameter and myelin sheath thickness in regenerated nerve fibers JM Schro Brain research 45 (1), 49-65, 1972 | 243 | 1972 |
| Mutations in the ganglioside‐induced differentiation‐associated protein‐1 (GDAP1) gene in intermediate type autosomal recessive Charcot–Marie–Tooth … J Senderek, C Bergmann, VT Ramaekers, E Nelis, GÈ Bernert, ... Brain 126 (3), 642-649, 2003 | 169 | 2003 |
| Occurrence and characterization of peripheral nerve involvement in neurofibromatosis type 2 AD Sperfeld, C Hein, JM Schröder, AC Ludolph, CO Hanemann Brain 125 (5), 996-1004, 2002 | 155 | 2002 |
| Differential expression of chemokines in inflammatory myopathies JL De Bleecker, B De Paepe, IE Vanwalleghem, JM Schröder Neurology 58 (12), 1779-1785, 2002 | 138 | 2002 |
| The role of Schwann cells in the formation of “onion bulbs” found in chronic neuropathies H deF. Webster, JM SchröDer, AK Asbury, RD Adams Journal of Neuropathology & Experimental Neurology 26 (2), 276-299, 1967 | 136 | 1967 |
| Pathologie der Muskulatur JM Schröder Springer-Verlag, 2013 | 133 | 2013 |
| Calcium potentials and tetrodotoxin-resistant sodium potentials in unmyelinated C fibres of biopsied human sural nerve S Quasthoff, J Grosskreutz, JM Schröder, U Schneider, P Grafe Neuroscience 69 (3), 955-965, 1995 | 128 | 1995 |
| Periaxin mutations cause a broad spectrum of demyelinating neuropathies H Takashima, CF Boerkoel, P De Jonghe, C Ceuterick, JJ Martin, T Voit, ... Annals of Neurology: Official Journal of the American Neurological …, 2002 | 127 | 2002 |
| Muscle biopsy substantiates long‐term MRI alterations one year after a single dose of botulinum toxin injected into the lateral gastrocnemius muscle of healthy volunteers AS Schroeder, B Ertl‐Wagner, S Britsch, JM Schröder, S Nikolin, J Weis, ... Movement disorders: official journal of the Movement Disorder Society 24 (10 …, 2009 | 125 | 2009 |
| The novel neurofilament light (NEFL) mutation Glu397Lys is associated with a clinically and morphologically heterogeneous type of Charcot-Marie-Tooth neuropathy S Züchner, M Vorgerd, E Sindern, JM Schröder Neuromuscular Disorders 14 (2), 147-157, 2004 | 116 | 2004 |
| Expression of calcium-binding proteins MRP8 and MRP14 in inflammatory muscle diseases S Seeliger, T Vogl, IH Engels, JM Schröder, C Sorg, C Sunderkötter, ... The American journal of pathology 163 (3), 947-956, 2003 | 108 | 2003 |
| Identification of the characteristic vascular changes in a sural nerve biopsy of a case with cerebral autosomal dominant arteriopathy with subcortical infarcts and … JM Schröder, B Sellhaus, J Jörg Acta neuropathologica 89, 116-121, 1995 | 106 | 1995 |
| The ultrastructural morphology of the muscle fiber in myotonic dystrophy JM Schröder, RD Adams Acta neuropathologica 10, 218-241, 1968 | 106 | 1968 |
| Changes of the ratio between myelin thickness and axon diameter in the human developing sural nerve JM Schröder, J Bohl, K Brodda Acta neuropathologica 43 (1), 169-178, 1978 | 101 | 1978 |
| Homozygous mutations in caveolin‐3 cause a severe form of rippling muscle disease C Kubisch, BGH Schoser, M Düring, RC Betz, HH Goebel, S Zahn, ... Annals of Neurology: Official Journal of the American Neurological …, 2003 | 93 | 2003 |
| X-linked dominant Charcot–Marie–Tooth neuropathy: clinical, electrophysiological, and morphological phenotype in four families with different connexin32 mutations J Senderek, B Hermanns, C Bergmann, B Boroojerdi, M Bajbouj, ... Journal of the neurological sciences 167 (2), 90-101, 1999 | 92 | 1999 |
Thomas VoitProfessor University College LondonVerified email at ucl.ac.uk
