Andree Delahaye-Duriez

13PUBLICATIONS
149CO-AUTHORS
Developmental genetics (incl. sex determination)NeurogeneticsNeurology and neuromuscular diseasesGene expression (incl. microarray and other genome-wide approaches)Epigenetics (incl. genome methylation and epigenomics)
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Publications (13)

|Oct 06, 2026
Diagnostic pathways in developmental disorders: a decade-apart comparison of two multicenter cohorts (2012-2022).

|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

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Frequent Collaborators

3 joint publications

Julien Van-Gils

3 joint publications

David Genevieve

3 joint publications

Anne-Sophie Denommé-Pichon

3 joint publications

André Reis