Author

Carine Dalle

Centre National de la Recherche Scientifique

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetic & Genomic Medicine· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 2 Organism:human· 2 Research Focus:cell type annotation· 1 Approach:machine learning (classical)· 1 Assay:scRNA-seq· 1 Approach:statistical model· 1

Frequent Co-Authors

Agnès Rastetter· 1 shared Alexander P.A. StegmanniD· 1 shared Alma Kuechler· 1 shared Amélie PitoniD· 1 shared Bénédicte Duban‐Bedu· 1 shared Bénédicte GérardiD· 1 shared Bernhard HorsthemkeiD· 1 shared Boris KereniD· 1 shared

Activity by Year

2022-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Agnès Rastetter

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Mosaic human cortical organoids model mTOR-related focal cortical dysplasia through DEPDC5 loss-of-function

Marina Maletic, Sara Bizzotto, Théo Ribierre, Kenza Guerdoud, Corentin Raoux, Marion Doladilhe, Carine Dalle, Fabienne Picard, Stéphanie Baulac

This study uses mosaic DEPDC5 variants in human cortical organoids to model FCDII, showing increased mTOR activity and neuronal dysmorphology.

bioRxiv · Jun 25, 2025 · PreprintNeuroscience

Systematic analysis and prediction of genes associated with disorders on chromosome X

Elsa Leitão, Christopher Schröder, Ilaria Parenti, Carine Dalle, Agnès Rastetter, Theresa Kühnel, Alma Kuechler, Sabine Kaya, Bénédicte Gérard, Élise Schaefer, Caroline Nava, Nathalie Drouot, Camille Engel, Juliette Piard, Bénédicte Duban‐Bedu, , Christel Depienne

The paper systematically analyzes chrX genes to predict disease associations, identifying 235 genes likely involved in disorders and reporting damaging variants in CDK16 and TRPC5 in patients with intellectual disability or autism.

Nature Communications · Nov 2, 2022Peer-reviewedGenetic & Genomic Medicine