Author

Vincent Cantagrel

InsermORCID 0000-0002-5180-4848Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:human· 2 Assay:bulk RNA-seq· 1 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Assay:electronic health records· 1 Assay:metabolomics· 1 Approach:statistical model· 1

Frequent Co-Authors

Lydie BürgleniD· 2 shared Adolfo SaiardiiD· 1 shared Amaël Davakan· 1 shared Arnaud MonteiliD· 1 shared Arnold MünnichiD· 1 shared Bárbara Bruna Ribeiro Oliveira-MendesiD· 1 shared Catherine Fossoud· 1 shared Céline BanaliD· 1 shared

Activity by Year

2020-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 25 mutual co-author links

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2 shared papersNeuroscience

Lydie BürglenORCID

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2 papers

Recent·Most cited

NeuroscienceFrontiers in PharmacologyPeer-reviewedOct 2, 2025

Electrophysiological classification of CACNA1G gene variants associated with neurodevelopmental and neurological disorders

Amaël Davakan, Leoš Cmarko, Bárbara Bruna Ribeiro Oliveira-Mendes…·Philippe Lory

This study uses automated and manual patch-clamp techniques to analyze Cav3.1 channel variants, identifying gain- and loss-of-function properties linked to neurological disorders.

4 citations

humanelectronic health records

𝕏 PostBluesky

GeneticsNature CommunicationsPeer-reviewedNov 30, 2020

MINPP1 prevents intracellular accumulation of the cation chelator inositol hexakisphosphate and is mutated in Pontocerebellar Hypoplasia

Ekin Ucuncu, Karthyayani Rajamani, Miranda Wilson…·Vincent Cantagrel

This study identifies MINPP1 mutations as a cause of Pontocerebellar Hypoplasia, showing that MINPP1 deficiency leads to IP6 accumulation and cation chelation, disrupting brain development.

62 citationstop 2%

humanbulk RNA-seq

𝕏 PostBluesky