Schormair, B., Zhao, C., Bell, S., Tilch, E., Salminen, A. V., Pütz, B., Dauvilliers, Y., Stefani, A., Hoegl, B., Poewe, W.,
Kemlink, D., Sonka, K., Bachmann, C. G., Paulus, W., Trenkwalder, C., Oertel, W. H., Hornyak, M., Teder-Laving, M., Metspalu,
A., Hadjigeorgiou, G. M., Polo, O., Fietze, I., Ross, O. A., Wszolek, Z., Butterworth, A. S., Soranzo, N., Ouwehand, W. H.,
Roberts, D. J., Danesh, J., Allen, R. P., Earley, C. J., Ondo, W. G., Xiong, L., Montplaisir, J., Gan-Or, Z., Perola, M.,
Vodicka, P., Dina, C., Franke, A., Tittmann, L., Stewart, A. F. R., Shah, S. H., Gieger, C., Peters, A., Rouleau, G. A., Berger,
K., Oexle, K., Di Angelantonio, E., Hinds, D. A., Müller-Myhsok, B., & Winkelmann, J. (2017).
Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European
ancestry: a meta-analysis. LANCET NEUROLOGY, 16(11),
898-907. doi:10.1016/S1474-4422(17)30327-7.