Publications

1.  Martín-Pardillos, A., Tsaalbi-Shtylik, A., Chen S., Lazare, S, van Os, R.P., Dethmers-Ausema, A., Borhan Fakouri, N. Bosshard, M., Aprigliano, R., van Loon, B., D.C.F., Hashimoto, K., Dingemanse-van der Spek, C., Moriya, M., Rasmussen, L.J., de Haan, G., Raaijmakers, M.H.G.P., and de Wind, N., (2017). Genomic and functional integrity of the hematopoietic system requires tolerance of oxidative DNA lesions. Blood 130, 1523-1534.

2. Tsaalbi-Shtylik, A., Ferrás, C., Pauw, B., Hendriks, G., Temviriyanukul, P., Carlée, L., Calléja, F., van Hees, S., Akagi, J.-I., Iwai, S., Hanaoka, F., Jansen, J. G., and de Wind, N. (2015). Excision of translesion synthesis errors orchestrates responses to helix-distorting DNA lesions. The Journal of Cell Biology 209, 33-46.

3. Tomas-Roca, L., Tsaalbi-Shtylik, A., Jansen, J. G., Singh, M. K., Epstein, J. A., Altunoglu, U., Verzijl, H., Soria, L., van Beusekom, E., Roscioli, T., Iqbal, Z., Gilissen, C., Hoischen, A., de Brouwer, A. P. M., Erasmus, C., Schubert, D., Brunner, H., Pérez Aytés, A., Marin, F., Aroca, P., Kayserili, H., Carta, A., de Wind, N.*, Padberg, G. W.*, and van Bokhoven, H.* (2015). De novo mutations in PLXND1 and REV3L cause Möbius syndrome. Nature communications 6, 7199. *Co-corresponding authors

4. Drost, M., Koppejan, H. and de Wind,N. (2013) Inactivation of DNA mismatch repair by variants of uncertain significance in the PMS2 gene. Human Mutation 34, 1477-1480.

5. Drost, M., Lützen, A., van Hees, S., Ferreira, D., Calléja, F., Zonneveld, J. B. M., Nielsen, F. C., Rasmussen, L. J., and de Wind, N. (2013). Genetic screens to identify pathogenic gene variants in the common cancer predisposition Lynch syndrome. Proc. Natl. Acad. Sci. U.S.A. 110, 9403-9408.