Michaela Jaksch

Risk of developing a mitochondrial DNA deletion disorder

Patrick F. Chinnery, Salvatore DiMauro, Sara Shanske et al. · The Lancet · 2004 · 229 citations

Mitochondrial Biogenesis, Mitochondrial Function, Genetics +4

Mutations in SCO2 are associated with a distinct form of hypertrophic cardiomyopathy and cytochrome c oxidase deficiency

Michaela Jaksch · Human Molecular Genetics · 2000 · 225 citations

Mitochondrial Phosphate–Carrier Deficiency: A Novel Disorder of Oxidative Phosphorylation

Johannes A. Mayr, Olaf Merkel, Sepp D. Kohlwein et al. · The American Journal of Human Genetics · 2007 · 168 citations · Full text

Biochemistry, Mitochondrial Function, Natural Sciences +8

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

Neurologic phenotypes associated with <i>COL4A1</i> / <i>2</i> mutations

Sara Zagaglia, C. Selch, Jelena Radić Nišević et al. · Neurology · 2018 · 140 citations · Full text