Identification of 2 DNA methylation subtypes of Waldenström macroglobulinemia with plasma and memory B-cell features by Roos-Weil, D, Giacopelli, B, Armand, M, Della-Valle, V, Ghamlouch, H, Decaudin, C, Metzner, M, Lu, J, Le Garff-Tavernier, M, Leblond, V, Vyas, P, Zenz, T, Nguyen-Khac, F, Bernard, OA, Oakes, CC

Presence of multiple recurrent mutations confers poor trial outcome of relapsed/refractory CLL. by Guièze, R, Robbe, P, Clifford, R, de Guibert, S, Pereira, B, Timbs, A, Dilhuydy, M, Cabes, M, Ysebaert, L, Burns, A, Nguyen-Khac, F, Davi, F, Véronèse, L, Combes, P, Le Garff-Tavernier, M, Leblond, V, Merle-Béral, H, Alsolami, R, Hamblin, A, Mason, J, Pettitt, A, Hillmen, P, Taylor, J, Knight, S, Tournilhac, O, Schuh, A

A recurrent activating missense mutation in Waldenström macroglobulinemia affects the DNA binding of the ETS transcription factor SPI1 and enhances proliferation by Roos-Weil, D, Decaudin, C, Armand, M, Della-Valle, V, Diop, M, Ghamlouch, H, Ropars, V, Herate, C, Lara, D, Durot, E, Haddad, R, Mylonas, E, Damm, F, Pflumio, F, Stoilova, B, Metzner, M, Elemento, O, Dessen, P, Camara-Clayette, V, Cosset, F, Verhoeyen, E, Leblond, V, Ribrag, V, Cornillet-Lefebvre, P, Rameau, P, Azar, N, Charlotte, F, Morel, P, Charbonnier, J, Vyas, P, Mercher, T, Aoufouchi, S, Droin, N, Guillouf, C, Nguyen-Khac, F, Bernard, O