Hans H. Goebel - Concepedia

Author

Hans H. Goebel

Johannes Gutenberg University Mainz ORCID

Also Known As

Barbara Goebel, Eberhard Barth, G GOEBEL, G Goebel, G. GOEBEL, G. Goebel, G.P Goebel, GEORG GOEBEL, Gavin Goebel, Georg Goebel

1.6K

Publications

46K

Citations

110

H-Index

197

Concepts

All Affiliations

Johannes Gutenberg University Mainz University of Göttingen University Medical Center of the Johannes Gutenberg University Mainz Charité - Universitätsmedizin Berlin Heidelberg University

About

Hans H. Goebel is an author at Johannes Gutenberg University Mainz specializing in medicine, pathology, and neuropathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	45	134	6.3K
2	Health Sciences	17	23	1.1K
3	Natural Sciences	7	7	271
4	Engineering	1	1	26
5	Public Health	1	1	32

Hans H. Goebel

189

Publications

9.4K

Citations

H-Index

Page 1

	Year	Citations
224th ENMC International Workshop: Yves Allenbach, Andrew L. Mammen, Olivier Benvéniste, Neuromuscular Disorders Enmc International WorkshopGlobal ChallengePerformance StudiesPreprint	2017	526
Mutations in the skeletal muscle α-actin gene in patients with actin myopathy and nemaline myopathy Kristen L. Nowak, Duangrurdee Wattanasirichaigoon, Hans H. Goebel, Nature Genetics Muscle PhysiologyMuscle FunctionHealth SciencesMuscle InjurySkeletal Muscle	1999	398
Neuronal loss and brain atrophy in mice lacking cathepsins B and L Ute Felbor, Benedikt M. Kessler, Walther Mothes, Proceedings of the National Academy of Sciences ApoptosisCell DeathSynaptic SignalingSocial SciencesNeuroinflammation	2002	335
Phenotype of arylsulfatase A-deficient mice: Relationship to human metachromatic leukodystrophy Paul Säftig, Dieter Hartmann, R. Coenen, Proceedings of the National Academy of Sciences Arylsulfatase APathologyExperimental PathologyNeuroinflammationInflammation	1996	250
Mutations in the β-tropomyosin (TPM2) gene – a rare cause of nemaline myopathy Kati Donner, Miina Ollikainen, Maaret Ridanpää, Neuromuscular Disorders Rare CauseMedicineMolecular BiologyPathologyCytoskeleton	2002	225
Desmin‐related myopathy with mallory body–like inclusions is caused by mutations of the selenoprotein N gene Ana Ferreiro, Chantal Ceuterick‐de Groote, Jared J. Marks, Annals of Neurology GeneticsSelenoprotein N GenePathologyMolecular GeneticsDisease Gene Identification	2004	194
Myo-, neuro-, gastrointestinal encephalopathy (MNGIE syndrome) due to partial deficiency of cytochrome-c-oxidase A. Bardosi, W. Creutzfeldt, S. DiMauro, Acta Neuropathologica Partial DeficiencyPhysiologyMngie SyndromeNutritional NeurosciencePathology	1987	175
Late infantile neuronal ceroid lipofuscinosis: Quantitative description of the clinical course in patients with <i>CLN2</i> mutations Robert Steinfeld, Peter Heim, Henning von Gregory, American Journal of Medical Genetics	2002	172
Secondary reduction in calpain 3 expression in patients with limb girdle muscular dystrophy type 2B and Miyoshi myopathy (primary dysferlinopathies) Louise V.B. Anderson, Ruth M Harrison, Robert Pogue, Neuromuscular Disorders Miyoshi MyopathyCalpain 3Skeletal MusclePhysiologySecondary Reduction	2000	163
The neuronal ceroid-lipofuscinoses: A historical introduction Matti Haltia, Hans H. Goebel Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease Neuro-oncologyEpendymaNeuroanatomyHistopathologyPathology	2012	146

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