Frédéric Bilan
4PUBLICATIONS
51CO-AUTHORS
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Publications (4)
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|Jul 20, 2023
AGAP1-associated endolysosomal trafficking abnormalities link gene-environment interactions in neurodevelopmental disorders.Sara A Lewis, Somayeh Bakhtiari, Jacob Forstrom
|Sep 08, 2022
De Novo Missense Variants in SLC32A1 Cause a Developmental and Epileptic Encephalopathy Due to Impaired GABAergic Neurotransmission.Konrad Platzer, Heinrich Sticht, Caleb Bupp
|May 04, 2021
Missense and truncating variants in CHD5 in a dominant neurodevelopmental disorder with intellectual disability, behavioral disturbances, and epilepsy.Ilaria Parenti, Daphné Lehalle, Caroline Nava
|May 01, 2019
Identification of a Novel CHD7 Mutation in a <i>CHARGE</i> Syndrome Patient in Indonesia.Gara Samara Brajadenta, Agustini Utari, Sylvie Patri
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Frequent Collaborators
1 joint publications
Gara Samara Brajadenta
1 joint publications
Agustini Utari
1 joint publications
Sylvie Patri
1 joint publications
Sultana Muhammad Hussein Faradz
1 joint publications
Alain Kitzis
1 joint publications
Vincent Thoreau
1 joint publications
Ilaria Parenti
1 joint publications
Daphné Lehalle
1 joint publications
Caroline Nava
1 joint publications
Erin Torti
