Dévina C. Ung

Ptchd1 deficiency induces excitatory synaptic and cognitive dysfunctions in mouse

Dévina C. Ung, Giovanni Iacono, Hamid Méziane et al. · Molecular Psychiatry · 2017 · 86 citations · Full text

Developmental and Behavioral Phenotypes in a Mouse Model of DDX3X Syndrome

Andrea Boitnott, Marta García-Forn, Dévina C. Ung et al. · Biological Psychiatry · 2021 · 40 citations · Full text

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

Qing Xie, Dévina C. Ung, K. Khafizov et al. · PubMed · 2014 · 22 citations · Full text

Haploinsufficiency of the HIRA gene located in the 22q11 deletion syndrome region is associated with abnormal neurodevelopment and impaired dendritic outgrowth

Médéric Jeanne, Marie‐Laure Vuillaume, Dévina C. Ung et al. · Human Genetics · 2021 · 18 citations · Full text

Developmental Biology, Brain Development, Medicine +10

Novel missense mutations in PTCHD1 alter its plasma membrane subcellular localization and cause intellectual disability and autism spectrum disorder

Judith Halewa, Sylviane Marouillat, Manon Dixneuf et al. · Human Mutation · 2021 · 15 citations · Full text

Neurodevelopmental Disorders, Signal Transduction, Ptchd1 Alter +13