Author

Charlotte Zaouter

Institut National de la Recherche Scientifique

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Developmental Biology· 1 Genetics· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Organism:zebrafish· 3 Approach:experimental assay· 2 Research Focus:cell type annotation· 1 Research Focus:drug response / drug discovery· 1 Assay:proteomics· 1 Assay:spatial transcriptomics· 1 Approach:statistical model· 1

Frequent Co-Authors

Shunmoogum A. PatteniD· 3 shared Nicolas PiloniD· 2 shared Antoine DufouriD· 1 shared Bettina M. WillieiD· 1 shared Carol X.‐Q. CheniD· 1 shared Daniel W YoungiD· 1 shared Éric SamarutiD· 1 shared Fanny NobilleauiD· 1 shared

Activity by Year

2024-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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3 shared papersNeuroscience

Shunmoogum A. PattenORCID

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Targeting calpastatin pharmacologically restores synaptic proteolysis and preserves motor neurons survival and function in C9orf72 ALS

Léa Lescouzères, Zoé Butti, Mathilde Chaineau, Daniel W Young, Zhipeng You, Michaël Nicouleau, Carol X.‐Q. Chen, Ghazal Haghi, Nathalia Aprahamian, Charlotte Zaouter, Antoine Dufour, Thomas M. Durcan, Shunmoogum A. Patten

This study shows that restoring calpastatin activity improves motor neuron function and survival in C9orf72 ALS models by enhancing synaptic proteolysis and NMJ integrity.

bioRxiv · May 11, 2026 · PreprintNeuroscience

RFC1 regulates the expansion of neural progenitors in the developing zebrafish cerebellum

Fanny Nobilleau, Sébastien Audet, Sanaa Turk, Charlotte Zaouter, Meijiang Liao, Nicolas Pilon, Martine Tétreault, Shunmoogum A. Patten, Éric Samarut

This study investigates RFC1's role in zebrafish cerebellar development, showing its necessity for neural progenitor genomic integrity and neurogenesis.

bioRxiv · Jun 28, 2024 · PreprintDevelopmental Biology

Abnormal craniofacial and spinal bone development with col2a1a depletion in a zebrafish model of CHARGE syndrome

Maximilian Breuer, Maximilian Rummler, Jaskaran Singh, Sabrina Maher, Charlotte Zaouter, Priyanka Jamadagni, Nicolas Pilon, Bettina M. Willie, Shunmoogum A. Patten

This study identifies skeletal abnormalities in chd7-/- zebrafish, linking col2a1a depletion to craniofacial and spinal bone development defects in CHARGE syndrome.

Journal of Bone and Mineral Research · Feb 4, 2024Peer-reviewedGenetics