Maike Stentenbach

Early-onset Parkinson disease caused by a mutation in CHCHD2 and mitochondrial dysfunction

Richard G. Lee, Maryam Sedghi, Mehri Salari et al. · Neurology Genetics · 2018 · 46 citations · Full text

The FASTK family proteins fine-tune mitochondrial RNA processing

Akira Ohkubo, Lindsey Van Haute, Danielle L. Rudler et al. · PLoS Genetics · 2021 · 40 citations · Full text

Functional Genomics, Engineering, Mitochondrial Function +14

Quantitative subcellular reconstruction reveals a lipid mediated inter-organelle biogenesis network

Richard G. Lee, Danielle L. Rudler, Samuel A. Raven et al. · Nature Cell Biology · 2023 · 38 citations · Full text

Quantitative Subcellular Reconstruction, Cell Organelle, Cytoskeleton +6

Deleterious variants in<i>CRLS1</i>lead to cardiolipin deficiency and cause an autosomal recessive multi-system mitochondrial disease

Richard G. Lee, Shanti Balasubramaniam, Maike Stentenbach et al. · Human Molecular Genetics · 2022 · 35 citations · Full text

Crls1 Variants, Genetics, Pathology +17

A common genetic variant of a mitochondrial RNA processing enzyme predisposes to insulin resistance

Giulia Rossetti, Judith A. Ermer, Maike Stentenbach et al. · Science Advances · 2021 · 14 citations · Full text