Publications - Neurofibromatosis

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Elevated risk for MPNST in NF1 microdeletion patients. Raedt, T., Brems, H., Wolkenstein, P., Vidaud, D., Pilotti, S., Perrone, F., Mautner, V., Frahm, S., Sciot, R. and Legius, E. Am. J. Hum. Genet. 72:1288-1292, 2003. [paper] 

Genetic and cellular defects contributing to benign tumor formation in neurofibromatosis Type 1. Rutkowski, J., Wu, K., Gutmann, D., Boyer, P. and Legius, E. Hum. Mol. Genet. 9: 1059-1066, 2000. [abstract] 

Germline mutations in NF1 patients with malignancies. Wu, R., L›pez-Correa, C., Rutkowski, J., Baumbach, Glover, T. and Legius, E. Genes, Chromo. & Cancer, 26:376-380, 1999. [paper] 

Multiple mechanism of benign tumor formation in Neurofibromatosis Type 1. Rutkowski, J., Wu, K., Gutmann, D., Boyer, P. and Legius, E. Human Mol. Gen. 9:1059-1066, 2000. [paper] 

Ruffling membrane, stress fiber, cell spreading and proliferation abnormalities in human Schwannoma cells. Pelton, P., Sherman, L., Rizvi, T., Marchionni, M., Wood, P., Friedman, R. and Ratner, N. Oncogene 17: 2195-2209, 1998. [paper]