Author

Antoine de Chevigny

InsermORCID 0000-0002-7413-0591Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Organism:mouse· 2 Approach:statistical model· 2 Research Focus:benchmarking· 1 Assay:bulk RNA-seq· 1 Research Focus:cell type annotation· 1 Research Focus:cell-cell communication· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1

Frequent Co-Authors

Alfonso RepresaiD· 2 shared Carlos CardosoiD· 2 shared Emilie Pallesi‐PocachardiD· 2 shared Rémi MathieuiD· 2 shared A. GélotiD· 1 shared Andreas BosioiD· 1 shared Annousha Devi GovindaniD· 1 shared Arie van HaeringeniD· 1 shared

Activity by Year

2020-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 40 mutual co-author links

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2 shared papersNeuroscience

Alfonso RepresaORCID

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2 papers

Recent·Most cited

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

Rémi Mathieu, Léa Corbières, Tangra Draia-Nicolau, Annousha Devi Govindan, Vianney Bensa, Emilie Pallesi‐Pocachard, Lucas Silvagnoli, Alfonso Represa, Carlos Cardoso, Ludovic Telley, Antoine de Chevigny

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

bioRxiv · Sep 2, 2024 · PreprintNeuroscience

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

Karen Runge, Rémi Mathieu, Stéphane Bugeon, Sahra Lafi, Corinne Beurrier, Surajit Sahu, Fabienne Schaller, Arthur Loubat, Léonard Hérault, Stéphane Gaillard, Mélanie Cahuc, Emilie Pallesi‐Pocachard, Aurélie Montheil, Andreas Bosio, Jill Anne Rosenfeld, , 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.

bioRxiv · Feb 14, 2020 · PreprintNeuroscience