A novel deletion in the RPL5 gene in a Lebanese child with diamond blackfan anemia unresponsive to steroid treatment by Farah, R, Kamel, L, Roy, N, Proven, M, Wray, K, Roberts, I, Wlodarski, M

Impaired human hematopoiesis due to a cryptic intronic GATA1 splicing mutation by Abdulhay, N, Fiorini, C, Verboon, J, Ludwig, L, Ulirsch, J, Zieger, B, Lareau, C, Mi, X, Roy, A, Obeng, E, Erlacher, M, Gupta, N, Gabriel, S, Ebert, B, Niemeyer, C, Khoriaty, R, Ancliff, P, Gazda, H, Wlodarski, M, Sankaran, V

A ribosomopathy reveals decoding defective ribosomes driving human dysmorphism. by Paolini, N, Attwood, M, Sondalle, S, Vieira, C, van Adrichem, A, di Summa, F, O'Donohue, M, Gleizes, P, Rachuri, S, Briggs, J, Fischer, R, Ratcliffe, P, Wlodarski, M, Houtkooper, R, von Lindern, M, Kuijpers, T, Dinman, J, Baserga, S, Cockman, M, MacInnes, A

GFI1(36N) as a therapeutic and prognostic marker for myelodysplastic syndrome (MDS) by Botezatu, L, Michel, L, Makishima, H, Schroeder, T, Germing, U, Haas, R, van der Reijden, B, Marneth, A, Bergevoet, S, Jansen, J, Przychodzen, B, Wlodarski, M, Niemeyer, C, Platzbecker, U, Ehninger, G, Unnikrishnan, A, Beck, D, Pimanda, J, Hellström-Lindberg, E, Cazzola, M, Malcovati, L, Boultwood, J, Pellagatti, A, Papaemmanuil, E, Le Coutre, P, Kaeda, J, Opalka, B, Möröy, T, Dührsen, U, Maciejewski, J, Khandanpour, C