Giovanni Stévanin
University of Verona(IT)Centre National de la Recherche Scientifique(FR)Centre National de la Recherche Scientifique(FR)Université de Bordeaux(FR)École Pratique des Hautes Études(FR)Université Paris Sciences et Lettres(FR)Sorbonne Université(FR)Institut de Neurosciences Cognitives et Intégratives d’Aquitaine(FR)Bordeaux Population Health(FR)Provincia Autonoma di Trento(IT)Sylvana Research(US)Institut du Cerveau(FR)
Publications by Year
Research Areas
Genetic Neurodegenerative Diseases, Mitochondrial Function and Pathology, Hereditary Neurological Disorders, Neurological diseases and metabolism, Neurogenetic and Muscular Disorders Research
Most-Cited Works
- → Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeats(1996)851 cited
- → Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion(1997)770 cited
- → Polyglutamine expansion as a pathological epitope in Huntington's disease and four dominant cerebellar ataxias(1995)653 cited
- → Exome Sequencing Links Corticospinal Motor Neuron Disease to Common Neurodegenerative Disorders(2014)537 cited
- → Senataxin, the ortholog of a yeast RNA helicase, is mutant in ataxia-ocular apraxia 2(2004)518 cited
- → Spinocerebellar ataxia 3 and machado‐joseph disease: Clinical, molecular, and neuropathological features(1996)446 cited