Search Results for author: Mathieu Barbier

Found 3 papers, 0 papers with code

Hierarchical Light Transformer Ensembles for Multimodal Trajectory Forecasting

no code implementations26 Mar 2024 Adrien Lafage, Mathieu Barbier, Gianni Franchi, David Filliat

Accurate trajectory forecasting is crucial for the performance of various systems, such as advanced driver-assistance systems and self-driving vehicles.

Motion Forecasting Trajectory Forecasting +1

Reply: Early-onset phenotype of bi-allelic GRN mutations

no code implementations20 Jan 2021 Vincent Huin, Mathieu Barbier, Alexandra Durr, Isabelle Le Ber

We would like to reply to Neuray et al. who report a series of five new patients from four unrelated families with bi-allelic mutations of GRN.

Homozygous GRN mutations: unexpected phenotypes and new insights into pathological and molecular mechanisms

no code implementations20 Nov 2020 Vincent Huin, Mathieu Barbier, Armand Bottani, Johannes Lobrinus, Fabienne Clot, Foudil Lamari, Laureen Chat, Benoît Rucheton, Frédérique Fluchère, Stéphane Auvin, Peter Myers, Antoinette Gelot, Agnès Camuzat, Catherine Caillaud, Ludmila Jornéa, Sylvie Forlani, Dario Saracino, Charles Duyckaerts, Alexis Brice, Alexandra Durr, Isabelle Le Ber

Homozygous mutations in the progranulin gene (GRN) are associated with neuronal ceroid lipofuscinosis 11 (CLN11), a rare lysosomal-storage disorder characterized by cerebellar ataxia, seizures, retinitis pigmentosa, and cognitive disorders, usually beginning between 13 and 25 years of age.

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