Charles Morin

Identification of a gene causing human cytochrome <i>c</i> oxidase deficiency by integrative genomics

Vamsi K. Mootha, Kathleen A. Miller, Jakob Bunkenborg et al. · Proceedings of the National Academy of Sciences · 2003 · 570 citations

The role of the <i>LRPPRC</i> (leucine-rich pentatricopeptide repeat cassette) gene in cytochrome oxidase assembly: mutation causes lowered levels of COX (cytochrome <i>c</i> oxidase) I and COX III mRNA

Fenghao Xu, Charles Morin, Grant A. Mitchell et al. · Biochemical Journal · 2004 · 168 citations · Full text

Determinants of omalizumab dose–related efficacy in oral immunotherapy: Evidence from a cohort of 181 patients

Pauline Azzano, Maxime Paquin, Alexandra Langlois et al. · Journal of Allergy and Clinical Immunology · 2020 · 56 citations

Metronomic Therapy, Clinical Epidemiology, Immunology +5

A Genomewide Linkage-Disequilibrium Scan Localizes the Saguenay–Lac-Saint-Jean Cytochrome Oxidase Deficiency to 2p16

Nana Lee, Mark J. Daly, Terrye Delmonte et al. · The American Journal of Human Genetics · 2001 · 43 citations · Full text

Genetics, Biochemical Genetics, Molecular Biology +5

A founder mutation in the PEX6 gene is responsible for increased incidence of Zellweger syndrome in a French Canadian population

Sébastien Lévesque, Charles Morin, Simon‐Pierre Guay et al. · BMC Medical Genetics · 2012 · 41 citations · Full text