| Ptchd1 deficiency induces excitatory synaptic and cognitive dysfunctions in mouse DC Ung, G Iacono, H Méziane, E Blanchard, MA Papon, M Selten, ... Molecular psychiatry 23 (5), 1356-1367, 2018 | 88 | 2018 |
| Developmental and behavioral phenotypes in a mouse model of DDX3X syndrome A Boitnott, M Garcia-Forn, DC Ung, K Niblo, D Mendonca, Y Park, ... Biological psychiatry 90 (11), 742-755, 2021 | 34 | 2021 |
| Gene regulation by PAX6: structural-functional correlations of missense mutants and transcriptional control of Trpm3/miR-204 Q Xie, D Ung, K Khafizov, A Fiser, A Cvekl Molecular vision 20, 270, 2014 | 26 | 2014 |
| Haploinsufficiency of the HIRA gene located in the 22q11 deletion syndrome region is associated with abnormal neurodevelopment and impaired dendritic outgrowth M Jeanne, ML Vuillaume, DC Ung, VE Vancollie, C Wagner, SC Collins, ... Human Genetics 140, 885-896, 2021 | 19 | 2021 |
| Contribution of the dihydropyrimidinase-like proteins family in synaptic physiology and in neurodevelopmental disorders F Desprez, DC Ung, P Vourc’h, M Jeanne, F Laumonnier Frontiers in Neuroscience 17, 1154446, 2023 | 16 | 2023 |
| Whole genome sequencing identifies a de novo 2.1 Mb balanced paracentric inversion disrupting FOXP1 and leading to severe intellectual disability ML Vuillaume, B Cogné, M Jeanne, A Boland, DC Ung, D Quinquis, ... Clinica Chimica Acta 485, 218-223, 2018 | 14 | 2018 |
| Novel missense mutations in PTCHD1 alter its plasma membrane subcellular localization and cause intellectual disability and autism spectrum disorder J Halewa, S Marouillat, M Dixneuf, RA Thépault, DC Ung, N Chatron, ... Human Mutation 42 (7), 848-861, 2021 | 10 | 2021 |
| GRID1/GluD1 homozygous variants linked to intellectual disability and spastic paraplegia impair mGlu1/5 receptor signaling and excitatory synapses DC Ung, N Pietrancosta, EB Badillo, B Raux, D Tapken, A Zlatanovic, ... Molecular Psychiatry, 1-11, 2024 | 2 | 2024 |
| Study of Ubiquitin Pathway Genes in a French Population with Amyotrophic Lateral Sclerosis: Focus on HECW1 Encoding the E3 Ligase NEDL1 S Haouari, CR Andres, D Lanznaster, S Marouillat, C Brulard, ... International Journal of Molecular Sciences 24 (2), 1268, 2023 | 2 | 2023 |
| Developmental and behavioral phenotypes in a new mouse model of DDX3X syndrome A Boitnott, DC Ung, M Garcia-Forn, K Niblo, D Mendonca, M Flores, ... bioRxiv, 2021.01. 22.427482, 2021 | 1 | 2021 |
| GRID1/GluD1 homozygous variants linked to intellectual disability and spastic paraplegia impair mGlu1/5 receptor signaling and excitatory synapses | | 2022 |
| Behavioral and Cellular Characterization of a New Mouse Model for DDX3X Syndrome M Garcia-Forn, A Boitnott, DC Ung, K Niblo, D Mendonca, M Flores, ... INSAR 2021, 2021 | | 2021 |
| Deciphering DDX3X Syndrome to Capture Determinants of Intellectual Disability D Ung, A Boitnott, D Mendonca, K Niblo, R Soto-Rifo, E Drapeau, ... Biological Psychiatry 87 (9), S378-S379, 2020 | | 2020 |
| Récepteurs synaptiques et troubles du neuro-développement: approches translationnelles pour la caractérisation fonctionnelle des gènes PTCHD1 et GRID1| Theses. fr D Ung Tours, 2017 | | 2017 |
| Understanding the Neurodevelopmental Bases of DDX3X Syndrome DC Ung, A Boitnott, D Mendonca, K Niblo, JD Buxbaum, E Drapeau, ... INSAR 2020 Virtual Meeting, 0 | | |
