Author

Maria Michielde van Genderen

University Medical Center UtrechtORCID 0000-0002-9286-8397Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Neuroscience· 1

Signature Assays, Organisms & Methods

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Assay:bulk RNA-seq· 1 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Organism:mouse· 1 Approach:statistical model· 1

Frequent Co-Authors

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

Activity by Year

2025-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperNeuroscience

Andrea Louise VincentORCID

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1 paper

Recent·Most cited

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

Hernán H. Diéguez, Kevin Dubois, Élodie Reboussin, Cansu de Muijnck, Jérôme Sarniguet, Chantal Cazevieille, Stacy L. Alves, Julie Dégardin, Valérie Fradot, Serge A. Picaud, Stéphane Melik Parsadaniantz, Maria Michielde van Genderen, Andrea Louise Vincent, Benjamin Delprat, Élodie M. Richard

bioRxiv · Oct 13, 2025 · PreprintNeuroscience