Andrée Delahaye-Duriez
12PUBLICATIONS
139CO-AUTHORS
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Publications (12)
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|Jun 25, 2025
Comprehensive analysis of CNOT3-related neurodevelopmental disorders: phenotypic and genotypic characterization.Camille Engel, Michaela Rendek, Jessica Assoumani
|May 16, 2025
Dominant variants in major spliceosome U4 and U5 small nuclear RNA genes cause neurodevelopmental disorders through splicing disruption.Caroline Nava, Benjamin Cogne, Amandine Santini
|Oct 30, 2024
Monoallelic loss-of-function variants in GSK3B lead to autism and developmental delay.Senwei Tan, Qiumeng Zhang, Rui Zhan
|Jun 13, 2022
Dysfunction of AMPA receptor GluA3 is associated with aggressive behavior in human.Shi-Xiao Peng, Jingwen Pei, Berardo Rinaldi
|Nov 27, 2021
Impact of Fetal Growth Restriction on the Neonatal Microglial Proteome in the Rat.Manuela Zinni, Julien Pansiot, Marina Colella
|Dec 18, 2019
New evidence that biallelic loss of function in EEF1B2 gene leads to intellectual disability.Lise Larcher, Julien Buratti, Bénédicte Héron-Longe
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Frequent Collaborators
3 joint publications
Marlène Rio
3 joint publications
André Reis
3 joint publications
Julien Van-Gils
3 joint publications
Jonathan Levy
3 joint publications
Anne-Sophie Denommé-Pichon
2 joint publications
Caroline Racine
2 joint publications
Bert Callewaert
2 joint publications
Juliette Piard
2 joint publications
Pierre Blanc
2 joint publications
Camille Engel
