Author

Juliette D. Godin

Centre National de la Recherche ScientifiqueORCID 0000-0001-6559-1065Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Neuroscience· 2 Developmental Biology· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 4 Organism:mouse· 3 Assay:ATAC-seq· 1 Assay:bulk RNA-seq· 1 Assay:ChIP-seq· 1 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1

Frequent Co-Authors

Peggy TillyiD· 4 shared Bastien MorletiD· 2 shared José Rivera AlvareziD· 2 shared Noémie Schwaller· 2 shared Ahlam A. Hamed· 1 shared Aline DubosiD· 1 shared Anastasiya Petrova· 1 shared Anne-Cécile ReymanniD· 1 shared

Activity by Year

2023-2025 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 25 mutual co-author links

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4 shared papersNeuroscience

Peggy TillyORCID

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4 papers

Recent·Most cited

GenomicsNucleic Acids ResearchPeer-reviewedSep 5, 2025

Disrupted transcriptional networks regulated by CHD1L during neurodevelopment underlie the mirrored neuroanatomical and growth phenotypes of the 1q21.1 copy number variant

Marianne Victoria Lemée, Maria Nicla Loviglio, Tao Ye…·Christelle Golzio

The paper identifies CHD1L as a key regulator of neurodevelopmental processes, showing its role in shaping neuroanatomical and growth phenotypes linked to 1q21.1 copy number variants.

4 citations

zebrafishmouse

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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

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Developmental BiologybioRxivPreprintNov 9, 2023

Interneuron migration defects during corticogenesis contribute to Dyrk1a haploinsufficiency syndrome pathogenesis via actomyosin dynamics deregulations

María-Victoria Hinckelmann, Aline Dubos, Victorine Artot…·Yann Hérault

This study shows that Dyrk1a regulates interneuron migration via actomyosin dynamics, leading to cortical GABAergic system defects and phenotypes seen in DYRK1A-haploinsufficiency syndrome.

2 citations

mouseexperimental assay

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NeuroscienceCell ReportsPeer-reviewedJul 1, 2023

The kinesin Kif21b regulates radial migration of cortical projection neurons through a noncanonical function on actin cytoskeleton.

José Rivera Alvarez, Laure Asselin, Peggy Tilly…·Juliette D. Godin

This study identifies a noncanonical role of Kif21b in regulating actin cytoskeleton dynamics during radial migration of cortical projection neurons in mice.

12 citations

mouseexperimental assay

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