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Nature Reviews. Neurology|July 3, 2013
New treatments for mitochondrial disease-no time to drop our standardsGerald Pfeffer, Rita Horvath, Thomas Klopstock, et al.Nature Cell Biology|January 17, 2018
Segregation of mitochondrial DNA heteroplasmy through a developmental genetic bottleneck in human embryosVasileios I Floros, Angela Pyle, Sabine Dietmann, et al.Nature Cell Biology|April 21, 2018
Author Correction: Segregation of mitochondrial DNA heteroplasmy through a developmental genetic bottleneck in human embryosVasileios I Floros, Angela Pyle, Sabine Dietmann, et al.Neurology|May 7, 2013
Two-stage association study and meta-analysis of mitochondrial DNA variants in Parkinson diseaseGavin Hudson, Mike Nalls, Jonathan R Evans, et al.Neurology|May 4, 2018
Multifocal demyelinating motor neuropathy and hamartoma syndrome associated with a de novo <i>PTEN</i> mutationBoglarka Bansagi, Vietxuan Phan, Mark R Baker, et al.Molecular Cell|January 2, 2018
Topoisomerase 3α Is Required for Decatenation and Segregation of Human mtDNAThomas J Nicholls, Cristina A Nadalutti, Elisa Motori, et al.Neurology|March 3, 2017
Genetic heterogeneity of motor neuropathiesBoglarka Bansagi, Helen Griffin, Roger G Whittaker, et al.Hepatology (Baltimore, Md.)|March 25, 2009
Locating the stem cell niche and tracing hepatocyte lineages in human liverTariq G Fellous, Shahriar Islam, Paul J Tadrous, et al.Brain : a Journal of Neurology|July 27, 2011
A randomized placebo-controlled trial of idebenone in Leber's hereditary optic neuropathyThomas Klopstock, Patrick Yu-Wai-Man, Konstantinos Dimitriadis, et al.Clinical Genetics|October 11, 2019
Identification of a novel heterozygous guanosine monophosphate reductase (GMPR) variant in a patient with a late-onset disorder of mitochondrial DNA maintenanceEwen W Sommerville, Ilaria Dalla Rosa, Masha M Rosenberg, et al.Pageof 37