Jocelyne Mercier
Université du Québec à Montréal(CA)Centre Hospitalier Universitaire Sainte-Justine(CA)
Publications by Year
Research Areas
Genetic Neurodegenerative Diseases, Mitochondrial Function and Pathology, Adipose Tissue and Metabolism, Neurological diseases and metabolism, Liver Disease Diagnosis and Treatment
Most-Cited Works
- → ARSACS, a spastic ataxia common in northeastern Québec, is caused by mutations in a new gene encoding an 11.5-kb ORF(2000)434 cited
- → Phenotypic variability in friedreich ataxia: Role of the associated GAA triplet repeat expansion(1997)270 cited
- → A Missense Mutation (R565W) in Cirhin (FLJ14728) in North American Indian Childhood Cirrhosis(2002)118 cited
- → Location Score and Haplotype Analyses of the Locus for Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay, in Chromosome Region 13q11(1999)91 cited
- → Localization of a Recessive Gene for North American Indian Childhood Cirrhosis to Chromosome Region 16q22—and Identification of a Shared Haplotype(2000)43 cited
- → The impact of a short-term high-fat diet on mitochondrial respiration, reactive oxygen species production, and dynamics in oxidative and glycolytic skeletal muscles of young rats(2018)43 cited
- → A Short-Term High-Fat Diet Alters Glutathione Levels and IL-6 Gene Expression in Oxidative Skeletal Muscles of Young Rats(2019)39 cited
- → Altered Lipid Metabolism Impairs Skeletal Muscle Force in Young Rats Submitted to a Short-Term High-Fat Diet(2018)33 cited
- → Autosomal Recessive Spastic Ataxia of Charlevoix–Saguenay (ARSACS): High-Resolution Physical and Transcript Map of the Candidate Region in Chromosome Region 13q11(1999)32 cited
- → Friedreich ataxia in Acadian families from eastern Canada: Clinical diversity with conserved haplotypes(1996)25 cited