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JACMIN Maxime

Main Referenced Co-authors
CRAWFORD, Alexander Dettmar  (2)
de Kovel, Carolien G. F. (2)
Esguerra, Camila V. (2)
Helbig, Ingo (2)
Koeleman, Bobby P. C. (2)
Main Referenced Keywords
Behavior (1); Dravet syndrome (1); Drug (1); zebrafish (1);
Main Referenced Unit & Research Centers
Luxembourg Centre for Systems Biomedicine (LCSB): Chemical Biology (Crawford Group) (3)
Luxembourg Centre for Systems Biomedicine (LCSB): Bioinformatics Core (R. Schneider Group) (2)
Luxembourg Centre for Systems Biomedicine (LCSB): Experimental Neurobiology (Balling Group) (1)
Main Referenced Disciplines
Neurology (2)
Biotechnology (1)
Genetics & genetic processes (1)

Publications (total 3)

The most cited

169 citations (Scopus®)

Schubert, J., Siekierska, A., Langlois, M., May, P., Huneau, C., Becker, F., Muhle, H., Suls, A., Lemke, J. R., de Kovel, C. G. F., Thiele, H., Konrad, K., Kawalia, A., Toliat, M. R., Sander, T., Ruschendorf, F., Caliebe, A., Nagel, I., Kohl, B., ... Lerche, H. (02 November 2014). Mutations in STX1B, encoding a presynaptic protein, cause fever-associated epilepsy syndromes. Nature Genetics, 46 (12), 1327-32. doi:10.1038/ng.3130 https://hdl.handle.net/10993/18655

Jacmin, M. (2018). Zebrafish models of Dravet syndrome: discovery of antiseizure drug leads and analysis of behavioural comorbidities [Doctoral thesis, Unilu - University of Luxembourg]. ORBilu-University of Luxembourg. https://orbilu.uni.lu/handle/10993/37339

Galizia, E. C., Myers, C. T., Leu, C., de Kovel, C. G. F., Afrikanova, T., Cordero-Maldonado, M. L., Martins, T., Jacmin, M., Drury, S., Krishna Chinthapalli, V., Muhle, H., Pendziwiat, M., Sander, T., Ruppert, A.-K., Møller, R. S., Thiele, H., Krause, R., Schubert, J., Lehesjoki, A.-E., ... Sisodiya, S. M. (2015). CHD2 variants are a risk factor for photosensitivity in epilepsy. Brain: a Journal of Neurology. doi:10.1093/brain/awv052
Peer reviewed

Schubert, J., Siekierska, A., Langlois, M., May, P., Huneau, C., Becker, F., Muhle, H., Suls, A., Lemke, J. R., de Kovel, C. G. F., Thiele, H., Konrad, K., Kawalia, A., Toliat, M. R., Sander, T., Ruschendorf, F., Caliebe, A., Nagel, I., Kohl, B., ... Lerche, H. (02 November 2014). Mutations in STX1B, encoding a presynaptic protein, cause fever-associated epilepsy syndromes. Nature Genetics, 46 (12), 1327-32. doi:10.1038/ng.3130
Peer Reviewed verified by ORBi

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