Sébastien Moutton
20PUBLICATIONS
218CO-AUTHORS
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Publications (20)
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|Sep 22, 2025
Further phenotypical delineation of DLG3-related neurodevelopmental disorders.Marlène Malbos, Thierry Gautier, Amelle Shillington
|Sep 04, 2025
A large cohort study of prenatal exome sequencing redefines diagnosis in fetal corpus callosum anomalies.Delphine Héron, Anna Gerasimenko, Lisa Frugère
|Dec 31, 2024
RICTOR variants are associated with neurodevelopmental disorders.Raphael Carapito, Anne Molitor, Lisa Pavinato
|May 27, 2024
Expectations, needs and mid-term outcomes in people accessing to secondary findings from ES: 1st French mixed study (FIND Study).Eléonore Viora-Dupont, Françoise Robert, Aline Chassagne
|Mar 10, 2023
Mechanism of KMT5B haploinsufficiency in neurodevelopment in humans and mice.Sarah E Sheppard, Laura Bryant, Rochelle N Wickramasekara
|Feb 09, 2023
The clinical and genetic spectrum of autosomal-recessive TOR1A-related disorders.Afshin Saffari, Tracy Lau, Homa Tajsharghi
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Frequent Collaborators
8 joint publications
Ange-Line Bruel
8 joint publications
Antonio Vitobello
6 joint publications
Christophe Philippe
6 joint publications
Frédéric Tran-Mau-Them
5 joint publications
Laurence Faivre
5 joint publications
Christel Thauvin-Robinet
5 joint publications
Sophie Nambot
4 joint publications
Anne-Sophie Denommé-Pichon
3 joint publications
Caroline Racine
3 joint publications
Arthur Sorlin
