Woranontee Weraarpachai, Ph.D.
Affiliations: | 2012 | Department of Human Genetics | McGill University, Montreal, QC, Canada |
Area:
Genetics, Molecular BiologyGoogle:
"Woranontee Weraarpachai"Parents
Sign in to add mentor| Eric A. Shoubridge | grad student | 2012 | McGill | |
| (Identification and characterization of novel genes involved in cytochrome c oxidase deficiencies.) | ||||
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Publications
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| Straub IR, Weraarpachai W, Shoubridge EA. (2021) Multi-OMICS study of a CHCHD10 variant causing ALS demonstrates metabolic rewiring and activation of endoplasmic reticulum and mitochondrial unfolded protein responses. Human Molecular Genetics. 30: 687-705 |
| Antonicka H, Lin ZY, Janer A, et al. (2020) A High-Density Human Mitochondrial Proximity Interaction Network. Cell Metabolism. 32: 479-497.e9 |
| Straub IR, Janer A, Weraarpachai W, et al. (2017) Loss of CHCHD10-CHCHD2 complexes required for respiration underlies the pathogenicity of a CHCHD10 mutation in ALS. Human Molecular Genetics |
| Mitsopoulos P, Lapohos O, Weraarpachai W, et al. (2017) Stomatin-like protein 2 deficiency results in impaired mitochondrial translation. Plos One. 12: e0179967 |
| La Piana R, Weraarpachai W, Ospina LH, et al. (2017) Identification and functional characterization of a novel MTFMT mutation associated with selective vulnerability of the visual pathway and a mild neurological phenotype. Neurogenetics |
| Sasarman F, Thiffault I, Weraarpachai W, et al. (2015) The 3' addition of CCA to mitochondrial tRNASer(AGY) is specifically impaired in patients with mutations in the tRNA nucleotidyl transferase TRNT1. Human Molecular Genetics. 24: 2841-7 |
| Ostergaard E, Weraarpachai W, Ravn K, et al. (2015) Mutations in COA3 cause isolated complex IV deficiency associated with neuropathy, exercise intolerance, obesity, and short stature. Journal of Medical Genetics. 52: 203-7 |
| Sasarman F, Nishimura T, Antonicka H, et al. (2015) Tissue-specific responses to the LRPPRC founder mutation in French Canadian Leigh Syndrome Human Molecular Genetics. 24: 480-491 |
| Leary SC, Antonicka H, Sasarman F, et al. (2013) Novel mutations in SCO1 as a cause of fatal infantile encephalopathy and lactic acidosis. Human Mutation. 34: 1366-70 |
| Mick DU, Dennerlein S, Wiese H, et al. (2012) MITRAC links mitochondrial protein translocation to respiratory-chain assembly and translational regulation. Cell. 151: 1528-41 |