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Journal Article
Koller, A. C., Strohmaier, J., Ludwig, K. U., Degenhardt, F. C., Wulff, M., Breuer, D., Winkler, L., Neukirch, F., Maaser, A., Forstner, A., Sivalingam, S., Reif, A., Ramirez, A., Maier, W., Rujescu, D., Giegling, I., Thiele, H., Nuernberg, P., Heilmann-Heimbach, S., Andlauer, T., Fischer, A., Jain, G., Kaurani, L., Klockmeier, K., Worf, K., Krumsiek, J., Wildenauer, D., Schwab, S., Rietschel, M., Noethen, M. M. and Degenhardt, F. (2018). Large family-based exome sequencing study provides new insight into schizophrenia. Eur. J. Hum. Genet., 26. S. 417 - 419. LONDON: NATURE PUBLISHING GROUP. ISSN 1476-5438
Papaemmanuil, E., Cazzola, M., Boultwood, J., Malcovati, L., Vyas, P., Bowen, D., Pellagatti, A., Wainscoat, J. S., Hellstrom-Lindberg, E., Gambacorti-Passerini, C., Godfrey, A. L., Rapado, I., Cvejic, A., Rance, R., McGee, C., Ellis, P., Mudie, L. J., Stephens, P. J., McLaren, S., Massie, C. E., Tarpey, P. S., Varela, I., Nik-Zainal, S., Davies, H. R., Shlien, A., Jones, D., Raine, K., Hinton, J., Butler, A. P., Teague, J. W., Baxter, E. J., Score, J., Galli, A., Della Porta, M. G., Travaglino, E., Groves, M., Tauro, S., Munshi, N. C., Anderson, K. C., El-Naggar, A., Fischer, A., Mustonen, V., Warren, A. J., Cross, N. C. P., Green, A. R., Futreal, P. A., Stratton, M. R. and Campbell, P. J. (2011). Somatic SF3B1 Mutation in Myelodysplasia with Ring Sideroblasts. N. Engl. J. Med., 365 (15). S. 1384 - 1396. WALTHAM: MASSACHUSETTS MEDICAL SOC. ISSN 1533-4406