  | Plumacker, F., Mouraux, C., & Depierreux, F. (07 February 2025). Paediatric movement disorders diagnostic procedure: a new algorithm defined in a Belgian tertiary care centre [Poster presentation]. Neurodevelopmental syndromes & movement disorders - International symposium, Barcelone, Spain.  Peer reviewed |
 | Mouraux, C., Aktan, D., & Depierreux, F. (07 February 2025). Entire deletion of THAP1 gene and its phenotype [Poster presentation]. Neurodevelopmental syndromes & movement disorders - International symposium, Barcelone, Spain. Peer reviewed |
 | Mouraux, C., Alkan, S., CABERG, J.-H., & Depierreux, F. (07 February 2025). Hemiplegic migraine genes also cause neurodevelopmental and movement disorders [Poster presentation]. Neurodevelopmental syndromes & movement disorders - International symposium, Barcelone, Spain. Peer reviewed |
 | Mouraux, C., Aktan, D., & Depierreux, F. (2025). Deletion of the THAP1 gene is responsible for typical DYT-THAP1. Movement Disorders Clinical Practice. doi:10.1002/mdc3.14350 Peer Reviewed verified by ORBi |
 | Mouraux, C., Alkan, S., CABERG, J.-H., & Depierreux, F. (2024). Association between CACNA1A and ATP1A2 variants are responsible for severe neurodevelopmental disorder. Neuropediatrics. doi:10.1055/a-2500-7729 Peer Reviewed verified by ORBi |
 | Depierreux, F., & Mouraux, C. (17 September 2024). L'Etude MDWGS: Mouvements Anormaux et Neurogénétique [Paper presentation]. GLEM de Neuropédiatrie, Liège, Belgium. |
 | Depierreux, F., Mouraux, C., Lagier, A., Parmentier, E., & Salado, A.-L. (03 June 2024). Dystonie génétique - à propos d'un cas au coeur d'une collaboration neuro-ORL [Paper presentation]. Grandes Cliniques Intégrées 2024, Liège, Belgium. |
Mouraux, C. (31 May 2024). MOV Panel and MDWGS - Genomic studies for the diagnosis of movement disorders [Paper presentation]. Réunion NGS, Liège, Belgium. |
 | Mouraux, C., FOUQUET, C., Artesi, M., Durkin, K., Dideberg, V., BULK, S., & Depierreux, F. (2024). Homozygous pathogenic MYH3 variant associated with arthrogryposis and lingual dystonia [Poster presentation]. BeSHG annual symposium 2024, Belgium. Editorial reviewed |
 | Mouraux, C., Dangouloff, T., Poleur, M., Mackels, L., Vanden Brande, L., Daron, A., Servais, L., Maertens de Noordhout, A., & DELSTANCHE, S. (2024). Epidemiological study and diagnostic approach analysis of Neuromuscular population of Neuromuscular Reference Center of Liege, Belgium [Poster presentation]. BeSHG annual symposium 2024, Belgium. Peer reviewed |
 | Mouraux, C., & Depierreux, F. (2023). Late Diagnosis of 18p Syndrome with Movement Disorders by Whole Exome Sequencing Read‐Depth Based Algorithm. Movement Disorders Clinical Practice. doi:10.1002/mdc3.13865 Peer Reviewed verified by ORBi |
  | Aragon-Gawinska, K., Mouraux, C., Dangouloff, T., & Servais, L. (29 June 2023). Spinal Muscular Atrophy Treatment in Patients Identified by Newborn Screening-A Systematic Review. Genes, 14 (7), 1377. doi:10.3390/genes14071377 Peer Reviewed verified by ORBi |
 | Dangouloff, T., MOURAUX, C., Piazzon, F., Mashhadizadeh, D., Hovhannesyan, K., Helou, L., Palmeira, L., Boemer, F., & Servais, L. (2023). Dépistage génétique néonatal universel de 126 maladies précoces et traitables : premiers résultats du projet Babydetect [Poster presentation]. 33e Séminaire de Génétique Clinique, Angers, France. Peer reviewed |
 | MOURAUX, C., Van Egroo, M., Chylinski, D., Narbutas, J., Phillips, C., Salmon, E., Maquet, P., Bastin, C., Collette, F.* , & Vandewalle, G.*. (2023). Effort during prolonged wakefulness is associated with performance to attentional and executive tasks but not with cortical excitability in late-middle-aged healthy individuals. Neuropsychology, 37 (1), 77-92. doi:10.1037/neu0000868 Peer Reviewed verified by ORBi* These authors have contributed equally to this work. |
 | Koshmanova, E., Muto, V., Chylinski, D., MOURAUX, C., Reyt, M., Grignard, M., Talwar, P., Lambot, E., Berthomier, C., Brandewinder, M., Mortazavi, N., Degueldre, C., Luxen, A., Salmon, E., Georges, M., Collette, F., Maquet, P., Van Someren, E., & Vandewalle, G. (10 November 2022). Genetic risk for insomnia is associated with objective sleep measures in young and healthy good sleepers. Neurobiology of Disease, 175, 105924. doi:10.1016/j.nbd.2022.105924 Peer Reviewed verified by ORBi Dataset: 10.1016/j.nbd.2022.105924 |
 | MOURAUX, C., & Depierreux, F. (21 October 2022). Late onset dystonia in 18p chromosome deletion [Paper presentation]. Belgian Society of Pediatric Neurology - Autumn Meeting: Movement Disorders, Bruxelles, Belgium. Peer reviewed |
 | Muto, V.* , Koshmanova, E.* , Ghaemmaghami Tabrizi, P.* , Jaspar, M., Meyer, C., Elansary, M., Van Egroo, M., Chylinski, D., Berthomier, C., Brandewinder, M., Mouraux, C., Schmidt, C., Hammad, G., Coppieters, W., Ahariz, N., Degueldre, C., Luxen, A., Salmon, E., Phillips, C., ... Vandewalle, G. (16 July 2021). Alzheimer’s disease genetic risk and sleep phenotypes: association with more slow-waves and daytime sleepiness. Sleep, 44 (1), 137. doi:10.1093/sleep/zsaa137 Peer Reviewed verified by ORBi* These authors have contributed equally to this work. |
Mouraux, C. (2020). L'effort comme variable sensible à l'extension d'éveil et son impact sur les performances cognitives [Master’s dissertation, ULiège - Université de Liège]. ORBi-University of Liège. https://orbi.uliege.be/handle/2268/302112 |
Van Egroo, M., Chylinski, D., Narbutas, J., Vandeleene, N., Grignard, M., Deantoni, M., Cardone, P., Muto, V., Schmidt, C., Koshmanova, E., Mouraux, C., Berthomier, C., Brandewinder, M., Collette, F., Bastin, C., Salmon, E., Maquet, P., Balteau, E., Phillips, C., & Vandewalle, G. (22 September 2020). Sleep slow waves generation and medial prefrontal microstructure in healthy older individuals [Paper presentation]. 25th Congress of the European Sleep Research Society. Peer reviewed |
