Charles Morin
Centre Intégré Universitaire de Santé et de Services Sociaux du Saguenay–Lac-Saint-Jean(CA)
Publications by Year
Research Areas
Mitochondrial Function and Pathology, Metabolism and Genetic Disorders, Skin and Cellular Biology Research, ATP Synthase and ATPases Research, Sleep and related disorders
Most-Cited Works
- → Identification of a gene causing human cytochrome c oxidase deficiency by integrative genomics(2003)570 cited
- → Meta-analysis identifies seven susceptibility loci involved in the atopic march(2015)174 cited
- → The role of the LRPPRC (leucine-rich pentatricopeptide repeat cassette) gene in cytochrome oxidase assembly: mutation causes lowered levels of COX (cytochrome c oxidase) I and COX III mRNA(2004)168 cited
- → Determinants of omalizumab dose–related efficacy in oral immunotherapy: Evidence from a cohort of 181 patients(2020)56 cited
- → A Genomewide Linkage-Disequilibrium Scan Localizes the Saguenay–Lac-Saint-Jean Cytochrome Oxidase Deficiency to 2p16(2001)43 cited
- → A founder mutation in the PEX6 gene is responsible for increased incidence of Zellweger syndrome in a French Canadian population(2012)41 cited
- → Stroke-like episodes in autosomal recessive cytochrome oxidase deficiency(1999)37 cited
- → The effect of short-term dimethylglycine treatment on oxygen consumption in cytochrome oxidase deficiency: A double-blind randomized crossover clinical trial(2003)34 cited
- → Genetic burden linked to founder effects in Saguenay–Lac-Saint-Jean illustrates the importance of genetic screening test availability(2021)33 cited
- → Mitochondrial Vulnerability and Increased Susceptibility to Nutrient-Induced Cytotoxicity in Fibroblasts from Leigh Syndrome French Canadian Patients(2015)30 cited