Klaus-Dieter Gerbitz

Author

Also Known As

K D Gerbitz, K Gerbitz, K. -D. Gerbitz, K. D. Gerbitz, K. Gerbitz, K.- D. Gerbitz, K.-D. GERBITZ, K.-D. Gerbitz, K.D. Gerbitz, K.‐D. GERBITZ

Publications

3.3K

Citations

H-Index

125

Concepts

All Affiliations

München Klinik Schwabing Ludwig-Maximilians-Universität München Institute of Diabetes Research Friedrich Baur Stiftung Inserm

About

Klaus-Dieter Gerbitz is an author at München Klinik Schwabing specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	22	35	1.4K
2	Natural Sciences	9	9	361
3	Health Sciences	3	3	173
4	Public Health	1	1	38
5	Social Sciences	1	1	19

Klaus-Dieter Gerbitz

Publications

2.5K

Citations

H-Index

Page 1

	Year	Citations
Population Genetics and Disease Susceptibility: Characterization of Central European Haplogroups By mtDNA Gene Mutations, Correlation with D Loop Variants and Association With Disease Sabine Hofmann, Michaela Jaksch, Reimar Bezold, Human Molecular Genetics	1997	168
Loss-of-function mutations of SURF-1 are specifically associated with Leigh syndrome with cytochromec oxidase deficiency Valeria Tiranti, Michaela Jaksch, Sabine Hofmann, Annals of Neurology	1999	119
Genetic and structural characterization of the human mitochondrial inner membrane translocase 1 1Edited by J. Karn Matthias Bauer, Klaus Gempel, Andreas S. Reichert, Journal of Molecular Biology Membrane FusionStructural CharacterizationMitochondrial BiogenesisBiochemistryMitochondrial Function	1999	116
Role of the Deafness Dystonia Peptide 1 (DDP1) in Import of Human Tim23 into the Inner Membrane of Mitochondria Sabine Hofmann, Nicole Mühlenbein, Stefan A. Paschen, Journal of Biological Chemistry	2001	102
The C66W Mutation in the Deafness Dystonia Peptide 1 (DDP1) Affects the Formation of Functional DDP1·TIM13 Complexes in the Mitochondrial Intermembrane Space Sabine Hofmann, Nicole Mühlenbein, Walter Neupert, Journal of Biological Chemistry	2002	92
Novel mutations of mitochondrial complex I in pathologically proven Parkinson disease Siegfried Kösel, E. M. Grasbon-Frodl, Ulrike Mautsch, Neurogenetics Mitochondrial FunctionMedicineParkinson DiseaseGeneticsNovel Mutations	1998	85
The mitochondrial TIM22 preprotein translocase is highly conserved throughout the eukaryotic kingdom Matthias Bauer, Nicole Mühlenbein, Richard J. Smith, FEBS Letters	1999	84
Myoadenylate deaminase deficiency: Successful symptomatic therapy by high dose oral administration of ribose N. Zöllner, Sebastian Reiter, D. Pongratz, Journal of Molecular Medicine MedicinePathologyMyoadenylate Deaminase DeficiencyPharmacologySuccessful Symptomatic Therapy	1986	83
Homozygosity (E140K) in <i>SCO2</i> causes delayed infantile onset of cardiomyopathy and neuropathy Michaela Jaksch, Rita Horváth, Nina Horn, Neurology	2001	81
Mitochondria and diabetes. Genetic, biochemical, and clinical implications of the cellular energy circuit Klaus-Dieter Gerbitz, Klaus Gempel, D. Brdiczka Diabetes Clinical ImplicationsCellular Energy CircuitMitochondrial FunctionBiochemistryMitochondrial Dynamic	1996	81

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