PRPF8 defects cause missplicing in myeloid malignancies. by Kurtovic-Kozaric, A, Przychodzen, B, Singh, J, Konarska, M, Clemente, M, Otrock, Z, Nakashima, M, Hsi, E, Yoshida, K, Shiraishi, Y, Chiba, K, Tanaka, H, Miyano, S, Ogawa, S, Boultwood, J, Makishima, H, Maciejewski, J, Padgett, R

Recurrent genetic defects on chromosome 5q in myeloid neoplasms by Hosono, N, Makishima, H, Mahfouz, R, Przychodzen, B, Yoshida, K, Jerez, A, LaFramboise, T, Polprasert, C, Clemente, M, Shiraishi, Y, Chiba, K, Tanaka, H, Miyano, S, Sanada, M, Cui, E, Verma, A, McDevitt, M, List, A, Saunthararajah, Y, Sekeres, M, Boultwood, J, Ogawa, S, Maciejewski, J

Loss of heterozygosity in 7q myeloid disorders: clinical associations and genomic pathogenesis. by Jerez, A, Sugimoto, Y, Makishima, H, Verma, A, Jankowska, A, Przychodzen, B, Visconte, V, Tiu, R, O'Keefe, C, Mohamedali, A, Kulasekararaj, A, Pellagatti, A, McGraw, K, Muramatsu, H, Moliterno, A, Sekeres, M, McDevitt, M, Kojima, S, List, A, Boultwood, J, Mufti, G, Maciejewski, J

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