Author

Meghna Kannan

Centre National de la Recherche ScientifiqueORCID 0000-0002-0360-0015Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetics· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Research Focus:cell type annotation· 1 Research Focus:cell-cell communication· 1 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Organism:mouse· 1

Frequent Co-Authors

Binnaz YalciniD· 2 shared Stephan C. CollinsiD· 2 shared Ahlam A. Hamed· 1 shared Alexandre ReymondiD· 1 shared Anna Mikhaleva· 1 shared Bruno RinaldiiD· 1 shared Carlos M. A. GuardiaiD· 1 shared Charlotte Montillot· 1 shared

Activity by Year

2022-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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2 shared papersNeuroscience

Binnaz YalcinORCID

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2 papers

Recent·Most cited

NeuroscienceEMBO Molecular MedicinePeer-reviewedNov 28, 2024

Bi-allelic variants in WDR47 lead to neuronal loss causing a rare neurodevelopmental syndrome with corpus callosum dysgenesis in humans.

Efil Bayam, Peggy Tilly, Stephan C. Collins…·Juliette D. Godin

The paper identifies bi-allelic WDR47 variants as a cause of a neurodevelopmental syndrome with corpus callosum dysgenesis and associated neuroanatomical abnormalities.

2 citations

humanexperimental assay

𝕏 PostBluesky

GeneticsbioRxivPreprintJan 23, 2022

Dissecting the autism-associated 16p11.2 locus identifies multiple drivers in brain phenotypes and unveils a new role for the major vault protein

Perrine F. Kretz, Christel Wagner, Charlotte Montillot…·Binnaz Yalcin

The paper identifies multiple genes at the 16p11.2 locus contributing to brain size and neuroanatomical phenotypes in mice, with MVP as a key driver, and shows its interaction with ERK in regulating brain morphology and behavior.

2 citations

mouseexperimental assay

𝕏 PostBluesky