Matthias Vorgerd - Concepedia

Author

Matthias Vorgerd

Also Known As

John Vissing, M Vorgerd, M. Vorgerd, Mark Tarnopolsky, Matthias Türk, Matthias Vorgerd, Peter Vollmann, Vorgerd, M., Vorgerd, Matthias

336

Publications

Citations

H-Index

170

Concepts

All Affiliations

Ruhr University Bochum BG University Hospital Bergmannsheil Bochum University of Bonn Ludwig-Maximilians-Universität München Friedrich Baur Stiftung

About

Matthias Vorgerd is an author at Ruhr University Bochum specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	37	59	4K
2	Health Sciences	13	14	686
3	Natural Sciences	3	3	227
4	Public Health	3	3	236
5	Engineering	2	2	512

Matthias Vorgerd

123

Publications

7.9K

Citations

H-Index

Page 1

	Year	Citations
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, Human Molecular Genetics	2007	535
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, Annals of Neurology Cardiac MuscleEngineeringGeneticsMolecular GeneticsCytoskeleton	2000	486
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, The American Journal of Human Genetics Mendelian DisorderNovel TypeGeneticsMolecular BiologyMolecular Genetics	2005	309
Oxidative stress in patients with Friedreich ataxia Jörg B. Schulz, Thomas Dehmer, Lüdger Schöls, Neurology	2000	303
Distinct muscle imaging patterns in myofibrillar myopathies Dirk Fischer, Rudolf A. Kley, Katharina Strach, Neurology	2008	252
Mutations in CAV3 cause mechanical hyperirritability of skeletal muscle in rippling muscle disease Regina C. Betz, Benedikt Schoser, Dagmar Kasper, Nature Genetics MechanobiologyMuscle FunctionMuscle InjurySkeletal MuscleMedicine	2001	210
De novo desmin-mutation N116S is associated with arrhythmogenic right ventricular cardiomyopathy Baerbel Klauke, Sabine Kossmann, Anna Gaertner, Human Molecular Genetics Heart FailureTerminal Heart FailureGeneticsGenetic EpidemiologyPathology	2010	186
Mitochondrial impairment in patients and asymptomatic mutation carriers of Huntington's disease Carsten Saft, Jochen Zange, Jürgen Andrich, Movement Disorders	2005	180
Safety and efficacy of avalglucosidase alfa versus alglucosidase alfa in patients with late-onset Pompe disease (COMET): a phase 3, randomised, multicentre trial Jordi Díaz‐Manera, Priya S. Kishnani, Hani Kushlaf, The Lancet Neurology Late-onset Pompe DiseaseAutoimmune DiseaseClinical Infectious DiseaseMedicinePhase 3	2021	169
Creatine Therapy in Myophosphorylase Deficiency (McArdle Disease) Matthias Vorgerd, Torsten Grehl, M. Jäger, Archives of Neurology	2000	150

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