Juliette D Godin
5PUBLICATIONS
35CO-AUTHORS
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Publications (5)
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|Jul 09, 2025
Interneuron migration defects during corticogenesis contribute to Dyrk1a haploinsufficiency syndrome pathogenesis.Maria Victoria Hinckelmann, Aline Dubos, Victorine Artot
|Mar 22, 2025
ADAT3 variants disrupt the activity of the ADAT tRNA deaminase complex and impair neuronal migration.Jordi Del-Pozo-Rodriguez, Peggy Tilly, Romain Lecat
|Nov 28, 2024
Bi-allelic variants in WDR47 cause a complex neurodevelopmental syndrome.Efil Bayam, Peggy Tilly, Stephan C Collins
|May 17, 2020
Mutations in the KIF21B kinesin gene cause neurodevelopmental disorders through imbalanced canonical motor activity.Laure Asselin, José Rivera Alvarez, Solveig Heide
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Frequent Collaborators
2 joint publications
Christel Depienne
2 joint publications
Binnaz Yalcin
1 joint publications
José Rivera Alvarez
1 joint publications
Hélène Vitet
1 joint publications
Neil A Hanchard
1 joint publications
Kirsty McWalter
1 joint publications
Marjan M Weiss
1 joint publications
Frédéric Saudou
1 joint publications
Efil Bayam
1 joint publications
Stephan C Collins