Author

Nathalie Bonello‐Palot

Centre de Génétique Médicale de MarseilleORCID 0000-0002-8657-1271Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetics· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Organism:mouse· 2 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Approach:statistical model· 1

Frequent Co-Authors

Nathalie Bernard‐MarissaliD· 2 shared Nathalie Roëckel· 2 shared Shahram AttarianiD· 2 shared Valérie DelagueiD· 2 shared Zeinab HamzéiD· 2 shared Alessandro BertiniiD· 1 shared Alix de BecdelièvreiD· 1 shared Amandine Pauset· 1 shared

Activity by Year

2025-2025 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersNeuroscience

Nathalie Bernard‐MarissalORCID

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2 papers

Recent·Most cited

Gene therapy-mediated overexpression of wild-type MFN2 improves Charcot-Marie-Tooth disease type 2A

Marine Tessier, Zeinab Hamzé, Nathalie Bonello‐Palot, Nathalie Roëckel, Shahram Attarian, Marc Bartoli, Valérie Delague, Bernard Laurent Schneider, Nathalie Bernard‐Marissal

This study shows that overexpressing wild-type MFN2 via gene therapy improves CMT2A in mice, restoring ER-mitochondria contacts and motor function even after symptom onset.

bioRxiv · Oct 15, 2025 · PreprintNeuroscience

Bi-allelic mutations in KCTD11 cause a new form of autosomal recessive intermediate Charcot-Marie-Tooth disease

Jihane Gadacha, Zahraa Haidar, Nathalie Roëckel, Amandine Pauset, Christel Castro, Coralie Provost, Zeinab Hamzé, Camille Humbert, Karine Bertaux, Nicolas Lenfant, Marion Masingue, Alix de Becdelièvre, Marina Konyukh, Nathalie Bonello‐Palot, Anne‐Sophie Lia, , Valérie Delague

This paper identifies bi-allelic mutations in KCTD11 as a cause of autosomal recessive intermediate Charcot-Marie-Tooth disease and elucidates its role in myelin homeostasis through molecular mechanisms.

bioRxiv · Jun 30, 2025 · PreprintGenetics