Beate Leo‐Kottler
Bernstein Center for Computational Neuroscience Tübingen(DE)STZ eyetrial(DE)
Publications by Year
Research Areas
Mitochondrial Function and Pathology, ATP Synthase and ATPases Research, Retinal Development and Disorders, Metabolism and Genetic Disorders, Neutrophil, Myeloperoxidase and Oxidative Mechanisms
Most-Cited Works
- → OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28(2000)1,310 cited
- → Rare Primary Mitochondrial DNA Mutations and Probable Synergistic Variants in Leber’s Hereditary Optic Neuropathy(2012)106 cited
- → Sequence analysis of the complete mitochondrial genome in patients with Leber's hereditary optic neuropathy lacking the three most common pathogenic DNA mutations(2002)66 cited
- → Mutation Analysis of the ND6 Gene in Patients with Lebers Hereditary Optic Neuropathy(1997)61 cited
- → Genomic rearrangements in OPA1 are frequent in patients with autosomal dominant optic atrophy(2009)58 cited
- Segregation patterns and heteroplasmy prevalence in Leber's hereditary optic neuropathy.(2001)
- → OPA1, encoding a dynamin-related GTPase is mutated in autosomal dominant optic atrophy linked to chromosome 3q28