  | Depierreux, F., Aktan, D., & Mouraux, C. (15 January 2026). Le diagnostic des maladies rares du mouvement en 2026. Phénotypage, génomique, neuroimagerie : un triptyque. Revue Médicale de Liège, 81 (1), 33 - 43.  Editorial Reviewed verified by ORBi |
  | Aktan, D., Mouraux, C., & Depierreux, F. (28 November 2025). Rethinking dyspraxia diagnoses in children [Paper presentation]. Advances in pediatric neurogenetics: the future is today, Liège, Belgium. Peer reviewed |
 | Mouraux, C., FOUQUET, C., Durkin, K., Dideberg, V., Bulk, S., Aktan, D., Artesi, M., & Depierreux, F. (27 October 2025). Homozygous Pathogenic MYH3 Variants Associated With Arthrogryposis and Lingual Dystonia. Tremor and Other Hyperkinetic Movements, 15, 53. doi:10.5334/tohm.1079 Peer Reviewed verified by ORBi |
Coarelli, G., & Mouraux, C. (2025). AFG3L2-Related Neurologic Disorders. In M. P. Adam, J. Feldman, G. M. Mirzaa, R. A. Pagon, S. E. Wallace, ... A. Amemiya (Eds.), GeneReviews®. Seattle wa: University of Washington, Seattle. Editorial reviewed |
 | Mouraux, C., Dangouloff, T., Poleur, M., Mackels, L., Vanden Brande, L., Daron, A., Servais, L., Maertens de Noordhout, A., & DELSTANCHE, S. (29 August 2025). Epidemiological report and diagnostic approach used in the neuromuscular population of Liege, Belgium. Orphanet Journal of Rare Diseases, 20 (1), 464. doi:10.1186/s13023-025-03963-2 Peer Reviewed verified by ORBi |
 | Mouraux, C., Alkan, S., CABERG, J.-H., & Depierreux, F. (August 2025). Association between CACNA1A and ATP1A2 variants are responsible for severe neurodevelopmental disorder. Neuropediatrics, 56 (4), 265-268. doi:10.1055/a-2500-7729 Peer Reviewed verified by ORBi |
 | Mouraux, C. (10 July 2025). When movement disorders point to the chromosome : a delayed diagnostic story [Paper presentation]. MDS-ES School for Young Neurologists, Paris, France. |
 | Mouraux, C., Méreaux, J.-L., Davoine, C.-S., Guillot Noel, L., Brice, A., Durr, A., & Coarelli, G. (2025). Expanding the clinical spectrum of RAB3A: from cerebellar ataxia to spastic paraplegia. Brain: a Journal of Neurology. doi:10.1093/brain/awaf236 Peer Reviewed verified by ORBi |
 | Depierreux, F., & Mouraux, C. (05 June 2025). Investigations en Mouvements Anormaux: de la pertinence des techniques modernes - Maîtrise de Neurologie 2025 [Paper presentation]. Cours de Maîtrise de Neurologie de l'ULiège, juin 2025, Liège, Belgium. |
 | Mouraux, C., Méreaux, J.-L., Guillot Noël, L., Davoine, C.-S., Ewenczyk, C., Coutelier, M., Coarelli, G., & Durr, A. (24 May 2025). The missing heritability of SPG7: a part of the answer in the detection of copy number variant [Poster presentation]. European Human Genetics Conference 2025, Milan, Italy. Editorial reviewed |
 | 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 |
 | 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 |
 | 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 |
