Rikke Steensbjerre Møller

Research activity per year

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20 Journal article
1 Letter
1 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
110 Citations (Scopus)
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
6 Citations (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
49 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
PURA-Related Developmental and Epileptic Encephalopathy: Phenotypic and Genotypic Spectrum
PURA study group, Dec 2021, In: Neurology. Genetics. 7, 6, p. e613 e613.
Research output: Contribution to journal › Journal article › Research › peer-review
35 Citations (Scopus)

Rikke Steensbjerre Møller

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Collaborations and top research areas from the last five years

Dive into details

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

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

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

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

PURA-Related Developmental and Epileptic Encephalopathy: Phenotypic and Genotypic Spectrum

Rikke Steensbjerre Møller

Fingerprint

Collaborations and top research areas from the last five years

Research output

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

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

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

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

PURA-Related Developmental and Epileptic Encephalopathy: Phenotypic and Genotypic Spectrum