Concepedia

Klaus-Dieter Gerbitz

KG

53

Publications

2.5K

Citations

32

H-Index

1969

Active since

Affiliations

München Klinik Schwabing(Current)

Ludwig-Maximilians-Universität München

Institute of Diabetes Research

Friedrich Baur Stiftung

Inserm

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

Top concepts

Publications per year

1969–2005

53

Publications

53

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 et al. · Human Molecular Genetics · 1997 · 168 citations · Full text

Loss-of-function mutations of SURF-1 are specifically associated with Leigh syndrome with cytochromec oxidase deficiency

Valeria Tiranti, Michaela Jaksch, Sabine Hofmann et al. · Annals of Neurology · 1999 · 119 citations

Genetic and structural characterization of the human mitochondrial inner membrane translocase 1 1Edited by J. Karn

Matthias Bauer, Klaus Gempel, Andreas S. Reichert et al. · Journal of Molecular Biology · 1999 · 116 citations

, , +12

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 et al. · Journal of Biological Chemistry · 2001 · 102 citations · Full text

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 et al. · Journal of Biological Chemistry · 2002 · 92 citations · Full text

Rows per page

1–5 of 53