Author

Olivier Detante

InsermORCID 0000-0001-8761-3288Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

Anne Briançon‐MarjolletiD· 1 shared Antoine Boutin-ParadisiD· 1 shared Aurélien DelphiniD· 1 shared Bayan El Amine· 1 shared Benjamin LemassoniD· 1 shared Bérengère KoehliD· 1 shared Caroline Le Van KimiD· 1 shared Cédric VrignaudiD· 1 shared

Activity by Year

2022-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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1 shared paperNeuroscience

Anne Briançon‐MarjolletORCID

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2 papers

Recent·Most cited

NeurosciencebioRxivPreprintOct 22, 2025

Multimodal Characterization and Evolution of Malonate-induced Stroke Model: advanced MRI, Histology-Molecular Profiling

Bayan El Amine, Benjamin Lemasson, Aurélien Delphin…·Claire Rome

This paper characterizes the temporal evolution of ischemic injury in a rat model using MRI and molecular analysis, revealing changes in lesion volume, vascular function, inflammation, and angiogenesis.

1 citation

ratspatial transcriptomics

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Genetic & Genomic MedicinemedRxivPreprintMay 13, 2022

Lack of the human choline transporter-like protein CTL2 causes hearing impairment and a rare red blood cell phenotype

Bérengère Koehl, Cédric Vrignaud, Mahmoud Mikdar…·Thierry Peyrard

The paper identifies CTL2 deficiency in humans causing hearing loss, arterial aneurysms, and epilepsy, while showing normal platelet function and erythropoiesis.

DOI 10.1101/2022.05.13.22273920

humanDNA methylation

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