Author
Centre National de la Recherche ScientifiqueORCID 0000-0001-6798-4567Unclaimed ORCID profile · follow to get notified of new preprints
3 papers
Recent·Most cited
Elsa Leitão, Amandine Santini, Benjamin Cogné…·Johanna Herwig
The paper identifies RNU2-2 variants as a frequent cause of neurodevelopmental disorders, both dominant and recessive, in a large cohort of individuals with rare disorders.
Mathieu Yèche, Antoine Collomb‐Clerc, Katia Lehongre…·Marie‐Laure Welter
This study identifies distinct roles of the cuneiform and pedunculopontine nuclei in gait initiation and freezing of gait in Parkinson's disease using local field potentials and biomechanical markers.
Violette Delforge, Giulia Coarelli, Eugénie Mutez…·Vincent Huin
The paper screens patients with parkinsonism for RFC1 gene expansions and finds that Parkinson's disease and multiple system atrophy can be gateways to RFC1-related disorders.