Papiol, S., M. Begemann, A. Rosenberger, H. Friedrichs, K. Ribbe, S. Grube, M. H. Schwab, H. Jahn, S. Gunkel, F. Benseler, K.-A. Nave and H. Ehrenreich: A phenotype-based genetic association study reveals the contribution of neuregulin1 gene variants to age of onset and positive symptom severity in schizophrenia. In: American Journal of Medical Genetics B: Neuropsychiatric Genetics 156 B, 3, 340-345 (2011).
Grube, S., M. F. Gerchen, B. Adamcio, L. A. Pardo, S. Martin, D. Malzahn, S. Papiol, M. Begemann, K. Ribbe, H. Friedrichs, K. A. Radyushkin, M. Müller, F. Benseler, J. Riggert, P. Falkai, H. Bickeböller, K.-A. Nave, N. Brose, W. Stühmer and H. Ehrenreich: A CAG repeat polymorphism of KCNN3 predicts SK3 channel function and cognitive performance in schizophrenia. In: EMBO Molecular Medicine 3, 6, 309-319 (2011).
Begemann, M., S. Grube, S. Papiol, D. Malzahn, H. Krampe, K. Ribbe, H. Friedrichs, K. A. Radyushkin, A. El-Kordi, F. Benseler, K. Hannke, S. Sperling, D. Schwerdtfeger, I. Thannhäuser, M. F. Gerchen, M. Ghorbani, S. Gutwinski, C. Hilmes, R. Leppert, A. Ronnenberg, J. Sowislo, S. Stawicki, M. Stödtke, C. Szuszies, K. Reim, J. Riggert, F. Eckstein, P. Falkai, H. Bickeböller, K.-A. Nave, N. Brose and H. Ehrenreich: Modification of cognitive performance in schizophrenia by complexin 2 gene polymorphisms. In: Archives in General Psychiatry 67, 9, 879-888 (2010).
doi: 10.1001/archgenpsychiatry.2010.107
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