Entries of Nürnberg, P. on the publication server

Thomalla, D., Beckmann, L. , Grimm, C. , Oliverio, M. , Meder, L., Herling, C. D., Nieper, P., Feldmann, T., Merkel, O., Lorsy, E., da Palma Guerreiro, A., von Jan, J., Kisis, I. , Wasserburger, E., Claasen, J., Faitschuk-Meyer, E., Altmüller, J., Nürnberg, P., Yang, T.-P., Lienhard, M., Herwig, R. , Kreuzer, K.-A., Pallasch, C. P. , Büttner, R., Schäfer, S. C., Hartley, J., Abken, H., Peifer, M., Kashkar, H., Knittel, G., Eichhorst, B., Ullrich, R. T., Herling, M., Reinhardt, H. C., Hallek, M. , Schweiger, M. R. and Frenzel, L. P. (2022) Deregulation and epigenetic modification of BCL2-family genes cause resistance to venetoclax in hematologic malignancies. Blood 140 (20), pp. 2113-2126. Fulltext not available.

Wagener, R., Seufert, J., Raimondi, F., Bens, S., Kleinheinz, K., Nagel, I., Altmueller, J., Thiele, H., Huebschmann, D., Kohler, Christian, Nürnberg, P., Au-Yeung, R., Burkhardt, B., Horn, H., Leoncini, L., Jaffe, E. S., Ott, G., Rymkiewicz, G. , Schlesner, M. , Russell, R. B. , Klapper, W. and Siebert, R. (2018) The mutational landscape of Burkitt-like lymphoma with 11q aberration is distinct from that of Burkitt lymphoma. Blood. Fulltext not available.

Nieuwenhuis, M. A., Siedlinski, M. , van den Berge, M., Granell, R., Li, X., Niens, M., van der Vlies, P., Altmüller, J., Nürnberg, P., Kerkhof, M., van Schayck, O. C., Riemersma, R. A., van der Molen, T., de Monchy, J. G., Bossé, Y., Sandford, A., Bruijnzeel-Koomen, C. A., Gerth van Wijk, R., ten Hacken, N. H., Timens, W., Boezen, H. M., Henderson, J., Kabesch, M., Vonk, J. M., Postma, D. S. and Koppelman, G. H. (2016) Combining genomewide association study and lung eQTL analysis provides evidence for novel genes associated with asthma. Allergy 71 (12), pp. 1712-1720. Fulltext not available.

Krumbiegel, M., Pasutto, F., Schlötzer-Schrehardt, U., Uebe, S., Zenkel, M., Mardin, C. Y., Weisschuh, N., Paoli, D., Gramer, E., Becker, C., Ekici, A. B., Weber, Bernhard H. F. , Nürnberg, P., Kruse, F. E. and Reis, A. (2011) Genome-wide association study with DNA pooling identifies variants at CNTNAP2 associated with pseudoexfoliation syndrome. European Journal of Human Genetics 19 (2), pp. 186-193. Fulltext not available.