Schulte, E.C., Kousi, M., Tan, P.L., Tilch, E., Knauf, F., Lichtner, P., Trenkwalder, C., Högl, B., Frauscher, B., Berger, K., Fietze, I., Hornyak, M., Oertel, W.H., Bachmann, C.G., Zimprich, A., Peters, A., Gieger, C., Meitinger, T., Müller-Myhsok, B., Katsanis, N., Winkelmann, J. (2014) Targeted resequencing and systematic in vivo functional testing identifies rare variants in MEIS1 as significant contributors to restless legs syndrome. American journal of human genetics. 95:85-95

Schulte, E.C., Kousi, M., Tan, P.L., Tilch, E., Knauf, F., Lichtner, P., Trenkwalder, C., Högl, B., Frauscher, B., Berger, K., Fietze, I., Hornyak, M., Oertel, W.H., Bachmann, C.G., Zimprich, A., Peters, A., Gieger, C., Meitinger, T., Müller-Myhsok, B., Katsanis, N., Winkelmann, J. (2014) Targeted resequencing and systematic in vivo functional testing identifies rare variants in MEIS1 as significant contributors to restless legs syndrome. American journal of human genetics. 95:85-95