Rita Horváth
University of Queensland(AU)The University of Queensland(AU)University of Szeged(HU)University of Cambridge(GB)Cambridge School(PT)Nemours Children's Health System(US)Prince Charles Hospital(AU)Hungarian School Sport Federation(HU)
Publications by Year
Research Areas
Mitochondrial Function and Pathology, Metabolism and Genetic Disorders, ATP Synthase and ATPases Research, Hereditary Neurological Disorders, Genetic Neurodegenerative Diseases
Most-Cited Works
- → Prevalence of nuclear and mitochondrial DNA mutations related to adult mitochondrial disease(2015)927 cited
- → Multi-system neurological disease is common in patients with OPA1 mutations(2010)439 cited
- → Universal heteroplasmy of human mitochondrial DNA(2012)435 cited
- → Phenotypic spectrum associated with mutations of the mitochondrial polymerase gene(2006)398 cited
- → Use of Whole-Exome Sequencing to Determine the Genetic Basis of Multiple Mitochondrial Respiratory Chain Complex Deficiencies(2014)361 cited
- → Clinical Expression of Leber Hereditary Optic Neuropathy Is Affected by the Mitochondrial DNA–Haplogroup Background(2007)356 cited