Author

Carlos Cardoso

InsermORCID 0000-0003-1914-9553Unclaimed 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· 3 Organism:mouse· 3 Approach:statistical model· 3 Research Focus:cell type annotation· 2 Research Focus:cell-cell communication· 2 Research Focus:differential expression· 2 Assay:electronic health records· 2 Research Focus:gene regulatory network inference· 2

Frequent Co-Authors

Alfonso RepresaiD· 4 shared Antoine de ChevignyiD· 2 shared Emilie Pallesi‐PocachardiD· 2 shared Françoise Watrin AiD· 2 shared Lucas SilvagnoliiD· 2 shared Rémi MathieuiD· 2 shared A. GélotiD· 1 shared Andreas BosioiD· 1 shared

Activity by Year

2020-2024 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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4 shared papersNeuroscience

Alfonso RepresaORCID

Mutual co-authors in cluster

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4 papers

Recent·Most cited

NeurosciencebioRxivPreprintSep 2, 2024

Inferring Ligand-Receptor Interactions between neuronal subtypes during mouse cortical development

Rémi Mathieu, Léa Corbières, Tangra Draia-Nicolau…·Antoine de Chevigny

The paper identifies ligand-receptor interactions between neuronal subtypes during mouse cortical development using single-cell transcriptomics and bioinformatic analysis.

1 citation

mousescRNA-seq

𝕏 PostBluesky

NeurosciencebioRxivPreprintDec 1, 2023

Pathogenic MTOR somatic variant causing focal cortical dysplasia drives hyperexcitability via overactivation of neuronal GluN2C NMDA receptors

Louison Pineau, Emmanuelle Buhler, Sarah Tarhini…·Nail Burnashev

This study shows that a somatic MTOR variant in FCD type II causes hyperexcitability through overactivation of GluN2C NMDA receptors in rat neurons.

1 citation

ratelectronic health records

𝕏 PostBluesky

NeurosciencebioRxivPreprintJun 6, 2023

Distinct subtypes of grey matter heterotopia show subtype-specific morpho-electric neuronal properties and dynamics of epileptiform activity in mice

Jean‐Christophe Vermoyal, Delphine Hardy, Lucas Goirand-Lopez…·Jean‐Bernard Manent

DOI 10.1101/2023.06.06.543853

mouseelectronic health records

𝕏 PostBluesky

NeurosciencebioRxivPreprintFeb 14, 2020

Disruption of the transcription factor NEUROD2 causes an autism syndrome via cell-autonomous defects in cortical projection neurons

Karen Runge, Rémi Mathieu, Stéphane Bugeon…·Antoine de Chevigny

This study identifies NEUROD2 mutations linked to ASD and intellectual disability, showing their role in cortical development and function through mouse models.

5 citations

mousebulk RNA-seq

𝕏 PostBluesky