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Mouraux Charlotte

GIGA Cancer - Human Genetics

Département des sciences biomédicales et précliniques > GIGA

Génétique humaine

See author's contact details
ORCID
0000-0001-9569-9229
Main Referenced Co-authors
Depierreux, Frédérique  (5)
Chylinski, Daphné  (4)
Collette, Fabienne  (4)
Maquet, Pierre  (4)
Salmon, Eric  (4)
Main Referenced Keywords
Neurogenetics (3); Dystonia (2); Genetics (2); Humans (2); Movement Disorders (2);
Main Referenced Unit & Research Centers
GIGA CRC In vivo Imaging - Rare Movement Disorders Research Group - ULiège [BE] (2)
GIGA CRC In vivo Imaging-Neuroimaging, data acquisition and processing - ULiège [BE] (1)
Main Referenced Disciplines
Neurology (7)
Genetics & genetic processes (4)
Laboratory medicine & medical technology (3)
Neurosciences & behavior (2)
Otolaryngology (1)

Publications (total 14)

The most downloaded
245 downloads
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 https://hdl.handle.net/2268/249719

The most cited

36 citations (OpenAlex)

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 https://hdl.handle.net/2268/316220

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., 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., 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., & 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

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