Yvon Trottier
Centre National de la Recherche Scientifique(FR)Inserm(FR)Institut de génétique et de biologie moléculaire et cellulaire(FR)
Publications by Year
Research Areas
Genetic Neurodegenerative Diseases, Mitochondrial Function and Pathology, Neurological disorders and treatments, Metabolism and Genetic Disorders, DNA Repair Mechanisms
Most-Cited Works
- → Exon 1 of the HD Gene with an Expanded CAG Repeat Is Sufficient to Cause a Progressive Neurological Phenotype in Transgenic Mice(1996)3,074 cited
- → Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeats(1996)851 cited
- → Intranuclear Inclusions of Expanded Polyglutamine Protein in Spinocerebellar Ataxia Type 3(1997)841 cited
- → Frataxin is Reduced in Friedreich Ataxia Patients and is Associated with Mitochondrial Membranes(1997)735 cited
- → Polyglutamine expansion as a pathological epitope in Huntington's disease and four dominant cerebellar ataxias(1995)653 cited
- Phenotypic Characterization of Individuals with 30–40 CAG Repeats in the Huntington Disease (HD) Gene Reveals HD Cases with 36 Repeats and Apparently Normal Elderly Individuals with 36–39 Repeats(1996)