Dévina C. Ung

Gene regulation by PAX6: Structural-functional correlations of missense mutants and transcriptional control of Trpm3/miR-204

A. Fiser, A. Cvekl, K. Khafizov, 2014, Molecular vision.

Developmental and Behavioral Phenotypes in a Mouse Model of DDX3X Syndrome

J. Buxbaum, J. Lerch, J. Ellegood, 2021, Biological Psychiatry.

GRID1/GluD1 homozygous variants linked to intellectual disability and spastic paraplegia impair mGlu1/5 receptor signaling and excitatory synapses

B. Lambolez, G. Stevanin, A. Toutain, 2022, medRxiv.

Whole genome sequencing identifies a de novo 2.1 Mb balanced paracentric inversion disrupting FOXP1 and leading to severe intellectual disability.

R. Redon, A. Toutain, A. Boland, 2018, Clinica chimica acta; international journal of clinical chemistry.

Study of Ubiquitin Pathway Genes in a French Population with Amyotrophic Lateral Sclerosis: Focus on HECW1 Encoding the E3 Ligase NEDL1

P. Vourc'h, C. Andres, P. Corcia, 2023, International journal of molecular sciences.

Contribution of the dihydropyrimidinase-like proteins family in synaptic physiology and in neurodevelopmental disorders

P. Vourc'h, F. Laumonnier, M. Jeanne, 2023, Frontiers in Neuroscience.