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Rikke Steensbjerre Møller

20152024

Research activity per year

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Collaborations and top research areas from the last five years

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  • Sleep disturbances in SCN8A-related disorders

    Furia, F., Johannesen, K. M., Bonardi, C. M., Previtali, R., Aledo-Serrano, A., Mastrangelo, M., Favaro, J., Masnada, S., di Micco, V., Proietti, J., Veggiotti, P., Rubboli, G., Cantalupo, G., Olofsson, K., Møller, R. S. & Gardella, E., 3 Oct 2024, (E-pub ahead of print) In: Epilepsia open.

    Research output: Contribution to journal › Journal article › Research › peer-review

  • Genotype-phenotype correlations in SCN8A-related disorders reveal prognostic and therapeutic implications

    Johannesen, K. M., Liu, Y., Koko, M., Gjerulfsen, C. E., Sonnenberg, L., Schubert, J., Fenger, C. D., Eltokhi, A., Rannap, M., Koch, N. A., Lauxmann, S., Krüger, J., Kegele, J., Canafoglia, L., Franceschetti, S., Mayer, T., Rebstock, J., Zacher, P., Ruf, S. & Alber, M. & 108 others, Sterbova, K., Lassuthová, P., Vlckova, M., Lemke, J. R., Platzer, K., Krey, I., Heine, C., Wieczorek, D., Kroell-Seger, J., Lund, C., Klein, K. M., Billie Au, P. Y., Rho, J. M., Ho, A. W., Masnada, S., Veggiotti, P., Giordano, L., Accorsi, P., Hoei-Hansen, C. E., Striano, P., Zara, F., Verhelst, H., Verhoeven, J. S., van der Zwaag, B., Harder, A. V. E., Brilstra, E., Pendziwiat, M., Lebon, S., Vaccarezza, M., Minh Le, N., Christensen, J., Grønborg, S., Scherer, S. W., Howe, J., Fazeli, W., Howell, K. B., Leventer, R., Stutterd, C., Walsh, S., Gerard, M., Gerard, B., Matricardi, S., Bonardi, C. M., Sartori, S., Berger, A., Hoffman-Zacharska, D., Mastrangelo, M., Darra, F., Vøllo, A., Motazacker, M. M., Lakeman, P., Nizon, M., Betzler, C., Altuzarra, C., Caume, R., Roubertie, A., Gélisse, P., Marini, C., Guerrini, R., Bilan, F., Tibussek, D., Koch-Hogrebe, M., Perry, M. S., Ichikawa, S., Dadali, E., Sharkov, A., Mishina, I., Abramov, M., Kanivets, I., Korostelev, S., Kutsev, S., Wain, K. E., Eisenhauer, N., Wagner, M., Savatt, J. M., Müller-Schlüter, K., Bassan, H., Borovikov, A., Nassogne, M.-C., Destrée, A., Schoonjans, A.-S., Meuwissen, M., Buzatu, M., Jansen, A., Scalais, E., Srivastava, S., Tan, W.-H., Olson, H. E., Loddenkemper, T., Poduri, A., Helbig, K. L., Helbig, I., Fitzgerald, M. P., Goldberg, E. M., Roser, T., Borggraefe, I., Brünger, T., May, P., Lal, D., Lederer, D., Rubboli, G., Heyne, H. O., Lesca, G., Hedrich, U. B. S., Benda, J., Gardella, E., Lerche, H. & Møller, R. S., 14 Sept 2022, In: Brain. 145, 9, p. 2991-3009 19 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  • Incidence of Aicardi-Goutières syndrome and KCNT1-related epilepsy in Denmark

    Møller, R. S., Zhao, L., Shoaff, J. R., Duno, M., Andersen, B. N., Nguyen, V., Fang, T. C., Kupelian, V. & Thorén, R., Dec 2022, In: Molecular Genetics and Metabolism Reports. 33, 100924.

    Research output: Contribution to journal › Journal article › Research › peer-review

    1 Citation (Scopus)

  • L-Serine Treatment is Associated with Improvements in Behavior, EEG, and Seizure Frequency in Individuals with GRIN-Related Disorders Due to Null Variants

    Krey, I., von Spiczak, S., Johannesen, K. M., Hikel, C., Kurlemann, G., Muhle, H., Beysen, D., Dietel, T., Møller, R. S., Lemke, J. R. & Syrbe, S., Jan 2022, In: Neurotherapeutics. 19, 1, p. 334-341 8 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

    32 Citations (Scopus)

  • Trisomy 20p/monosomy 18p associated with congenital bilateral perisylvian syndrome

    Bonardi, C. M., Bayat, A., Madsen, C. G., Hammer, T. B., Reale, C., Gardella, E., Marjanovic, D., Beniczky, S., Møller, R. S. & Rubboli, G., Jun 2022, In: Epileptic disorders : international epilepsy journal with videotape. 24, 3, p. 577-582 6 p., 1423.

    Research output: Contribution to journal › Journal article › Research › peer-review

View all 24 research outputs