Thomas J. Nicholls

Loss-of-function mutations in MGME1 impair mtDNA replication and cause multisystemic mitochondrial disease

Cornelia Kornblum, Thomas J. Nicholls, Tobias B. Haack et al. · Nature Genetics · 2013 · 235 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15

Mutations in GTPBP3 Cause a Mitochondrial Translation Defect Associated with Hypertrophic Cardiomyopathy, Lactic Acidosis, and Encephalopathy

Robert Kopajtich, Thomas J. Nicholls, Joanna Rorbach et al. · The American Journal of Human Genetics · 2014 · 158 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

ELAC2 Mutations Cause a Mitochondrial RNA Processing Defect Associated with Hypertrophic Cardiomyopathy

Tobias B. Haack, Robert Kopajtich, Peter Freisinger et al. · The American Journal of Human Genetics · 2013 · 147 citations · Full text

Life Sciences, Genetics, Molecular Biology +17

Topoisomerase 3α Is Required for Decatenation and Segregation of Human mtDNA

Thomas J. Nicholls, Cristina A. Nadalutti, Elisa Motori et al. · Molecular Cell · 2017 · 133 citations · Full text

Life Sciences, Genetics, Molecular Biology +10

MRM2 and MRM3 are involved in biogenesis of the large subunit of the mitochondrial ribosome

Joanna Rorbach, Pierre Boesch, Payam A. Gammage et al. · Molecular Biology of the Cell · 2014 · 128 citations · Full text

Life Sciences, Biochemistry, Molecular Biology +17