Møller, R S & International League Against Epilepsy Consortium on Complex Epilepsies 2014, ' Genetic determinants of common epilepsies : a meta-analysis of genome-wide association studies ', Lancet Neurology, vol. 13, no. 9, pp. 893-903 . https://doi.org/10.1016/S1474-4422(14)70171-1
Larsen, J, Stubbings, V, Møller, R S & Hjalgrim, H 2014, ' Glukosetransporter 1-mangelsyndrom har et varieret klinisk billede ', Ugeskrift for Laeger, bind 176, nr. 24, V04130248, s. 2268-2271 . < http://ugeskriftet.dk/videnskab/glukosetransporter-1-mangelsyndrom-har-et-varieret-klinisk-billede >
Nature Genetics Nature Genetics, Nature Publishing Group, 2014, 46 (6), pp.640-645. ⟨10.1038/ng.2952⟩ Nava, C, Dalle, C, Rastetter, A, Striano, P, de Kovel, C G F, Nabbout, R, Cancès, C, Ville, D, Brilstra, E H, Gobbi, G, Raffo, E, Bouteiller, D, Marie, Y, Trouillard, O, Robbiano, A, Keren, B, Agher, D, Roze, E, Lesage, S, Nicolas, A, Brice, A, Baulac, M, Vogt, C, El Hajj, N, Schneider, E, Suls, A, Weckhuysen, S, Gormley, P, Lehesjoki, A-E, De Jonghe, P, Helbig, I, Baulac, S, Zara, F, Koeleman, B P C, Haaf, T, LeGuern, E, Depienne, C, EuroEPINOMICS RES Consortium & Møller, R S 2014, ' De novo mutations in HCN1 cause early infantile epileptic encephalopathy ', Nature Genetics, vol. 46, no. 6, pp. 640-645 . https://doi.org/10.1038/ng.2952 Nature genetics Nature Genetics, 2014, 46 (6), pp.640-645. ⟨10.1038/ng.2952⟩
Kjærsgaard Hansen, L, Ousager, L B, Møller, R S, Uldall, P V & Hjalgrim, H 2012, ' Genetisk udredning ved infantile spasmer ', Ugeskrift for Laeger, bind 174, nr. 17, s. 1152-1155 .
Nissen, K B, Søndergaard, C, Thelle, T & Møller, R S 2011, ' Mowat-Wilson-syndrom hos tre danske børn ', Ugeskrift for Laeger, bind 173, nr. 36, s. 2199-2200 .
Møller, R S & Hjalgrim, H 2011, ' Submikroskopiske kromosomforandringer disponerer til epilepsi ', Ugeskrift for Laeger, bind 173, nr. 16-17, s. 1201-4 .
Klitten, L L, Møller, R S, Nikanorova, M, Silahtaroglu, A, Hjalgrim, H & Tommerup, N 2011, ' A balanced translocation disrupts SYNGAP1 in a patient with intellectual disability, speech impairment, and epilepsy with myoclonic absences (EMA) ', Epilepsia, vol. 52, no. 12, pp. e190-e193 . https://doi.org/10.1111/j.1528-1167.2011.03304.x