Author

Benjamin Delprat

InsermORCID 0000-0002-2457-6923Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Neuroscience· 2

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 2 Organism:human· 2 Organism:mouse· 2 Assay:bulk RNA-seq· 1 Research Focus:cell type annotation· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Assay:proteomics· 1

Frequent Co-Authors

Chantal CazevieilleiD· 2 shared Élodie M. RichardiD· 2 shared Alberto DaneseiD· 1 shared Andrea Louise VincentiD· 1 shared Cansu de MuijnckiD· 1 shared Élodie ReboussiniD· 1 shared Hernán H. DiégueziD· 1 shared Jérôme Sarniguet· 1 shared

Activity by Year

2023-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 38 mutual co-author links

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2 shared papersNeuroscience

Chantal CazevieilleORCID

Mutual co-authors in cluster

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2 papers

Recent·Most cited

NeurosciencebioRxivPreprintOct 13, 2025

WFS1E864K in humans and mice causes Wolfram-like syndrome optic atrophy via early axonal mitochondrial dysfunction

Hernán H. Diéguez, Kevin Dubois, Élodie Reboussin…·Élodie M. Richard

DOI 10.1101/2025.10.13.682105

𝕏 PostBluesky

NeurosciencebioRxivPreprintNov 16, 2023

The Wolfram-like variant WFS1E864K destabilizes MAM and compromises autophagy and mitophagy in human and mice.

Simone Patergnani, Méghane S. Bataillard, Alberto Danese…·Élodie M. Richard

This study shows that the WFS1E864K variant reduces MAM integrity and disrupts autophagy and mitophagy in human and mouse models of Wolfram-like syndrome.

1 citation

𝕏 PostBluesky