Woranontee Weraarpachai

Mutation in TACO1, encoding a translational activator of COX I, results in cytochrome c oxidase deficiency and late-onset Leigh syndrome

Woranontee Weraarpachai, Hana Antonická, Florin Sasarman et al. · Nature Genetics · 2009 · 304 citations

Late-onset Leigh Syndrome, Mitochondrial Function, Genetic Disorder +8

MITRAC Links Mitochondrial Protein Translocation to Respiratory-Chain Assembly and Translational Regulation

David U. Mick, Sven Dennerlein, Heike Wiese et al. · Cell · 2012 · 251 citations · Full text

Respiratory-chain Assembly, Mitochondrial Function, Natural Sciences +8

A High-Density Human Mitochondrial Proximity Interaction Network

Hana Antonická, Zhen‐Yuan Lin, Alexandre Janer et al. · Cell Metabolism · 2020 · 197 citations · Full text

Engineering, Mitochondrial Function, Computational Biology +4

Mutations in C12orf65 in Patients with Encephalomyopathy and a Mitochondrial Translation Defect

Hana Antonická, Elsebet Østergaard, Florin Sasarman et al. · The American Journal of Human Genetics · 2010 · 159 citations · Full text

Mitochondrial Translation Defect, Mendelian Disorder, Mitochondrial Function +8

Mutations in C12orf62, a Factor that Couples COX I Synthesis with Cytochrome c Oxidase Assembly, Cause Fatal Neonatal Lactic Acidosis

Woranontee Weraarpachai, Florin Sasarman, Tamiko Nishimura et al. · The American Journal of Human Genetics · 2012 · 107 citations · Full text

Biochemistry, Natural Sciences, Pathology +9