Claire Guissart
Inserm(FR)Université de Montpellier(FR)Centre Hospitalier Universitaire de Montpellier(FR)Centre Hospitalier Régional et Universitaire de Nancy(FR)Centre d’Investigation Clinique Innovation Technologique de Nancy(FR)Institut de Génétique Moléculaire de Montpellier(FR)Institute for Neurosciences of Montpellier(FR)Université de Nîmes(FR)
Publications by Year
Research Areas
Genetic Neurodegenerative Diseases, Mitochondrial Function and Pathology, Neurogenetic and Muscular Disorders Research, Amyotrophic Lateral Sclerosis Research, Prenatal Screening and Diagnostics
Most-Cited Works
- → Developmental Consequences of Defective ATG7-Mediated Autophagy in Humans(2021)189 cited
- → Dual Molecular Effects of Dominant RORA Mutations Cause Two Variants of Syndromic Intellectual Disability with Either Autism or Cerebellar Ataxia(2018)81 cited
- → Plasma oxysterols: biomarkers for diagnosis and treatment in spastic paraplegia type 5(2017)74 cited
- → Assessment of a Targeted Gene Panel for Identification of Genes Associated With Movement Disorders(2018)70 cited
- → Delayed‐onset Friedreich's ataxia revisited(2015)68 cited
- → Mutation of SLC9A1, encoding the major Na+/H+ exchanger, causes ataxia-deafness Lichtenstein-Knorr syndrome(2014)47 cited