Stéphanie Millecamps
7PUBLICATIONS
31CO-AUTHORS
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Publications (7)
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|Aug 26, 2025
ALS/FTD-linked TBK1 deficiency in microglia induces an aged-like microglial signature and drives social recognition deficits in mice.Isadora Lenoel, Matthieu Ribon, Félicie Lorenc
|Mar 18, 2025
MAPT mutations in amyotrophic lateral sclerosis: clinical, neuropathological and functional insights.Sibylle De Bertier, Géraldine Lautrette, Maria-Del-Mar Amador
|Jan 20, 2023
Integrative genetic analysis illuminates ALS heritability and identifies risk genes.Salim Megat, Natalia Mora, Jason Sanogo
|May 28, 2022
The Amyotrophic Lateral Sclerosis M114T PFN1 Mutation Deregulates Alternative Autophagy Pathways and Mitochondrial Homeostasis.Elisa Teyssou, Laura Chartier, Delphine Roussel
|Dec 24, 2021
Phenoconversion from Spastic Paraplegia to ALS/FTD Associated with CYP7B1 Compound Heterozygous Mutations.Julian Theuriet, Antoine Pegat, Pascal Leblanc
|Mar 31, 2021
Impact of a frequent nearsplice SOD1 variant in amyotrophic lateral sclerosis: optimising SOD1 genetic screening for gene therapy opportunities.François Muratet, Elisa Teyssou, Aude Chiot
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Frequent Collaborators
2 joint publications
Séverine Boillée
2 joint publications
Erik Storkebaum
2 joint publications
Christoph Neuwirth
2 joint publications
Peter Munch Andersen
2 joint publications
Tobias Boeckers
2 joint publications
Alberto Catanese
2 joint publications
Jan H Veldink
2 joint publications
Markus Weber
2 joint publications
Natalia Mora
2 joint publications
Salim Megat
