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Home > Organization > Divisions and Independent Research Units > Division of Cancer Evolution > Research Papers > 2013

2013

  1. Damm, F., Chesnais, V., Nagata, Y., Yoshida K., Scourzic, L., Okuno, Y., Itzykson, R., Sanada, M., Shiraishi, Y., Gelsi-Boyer, V., Renneville, A., Miyano, S., Mori, H., Shih, L. Y., Park, S., Dreyfus, F., Guerci-Bresler, A., Solary, E., Rose, C., Cheze, S., Prebet, T., Vey, N., Legentil, M., Duffourd, Y., de Botton, S., Preudhomme, C., Birnbaum, D., Bernard, O. A., Ogawa, S., Fontenay, M., Kosmider, O.: BCOR and BCORL1 mutations in myelodysplastic syndromes and related disorders. Blood, 122: 3169-3177 (2013).
  2. Gomez-Segui, I., Makishima, H., Jerez, A., Yoshida K., Przychodzen, B., Miyano, S., Shiraishi, Y., Husseinzadeh, H. D., Guinta, K., Clemente, M., Hosono, N., McDevitt, M. A., Moliterno, A. R., Sekeres, M. A., Ogawa, S., Maciejewski, J. P.: Novel recurrent mutations in the RAS-like GTP-binding gene RIT1 in myeloid malignancies. Leukemia, 27: 1943-1946 (2013).
  3. Hira, A., Yabe, H., Yoshida K., Okuno, Y., Shiraishi, Y., Chiba, K., Tanaka, H., Miyano, S., Nakamura, J., Kojima, S., Ogawa, S., Matsuo, K., Takata, M., Yabe, M.: Variant ALDH2 is associated with accelerated progression of bone marrow failure in Japanese Fanconi anemia patients. Blood, 122: 3206-3209 (2013).
  4. Kitamura, K., Yoshida K., Shiraishi, Y., Chiba, K., Tanaka, H., Furukawa, K., Miyano, S., Ogawa, S., Kunishima, S.: Normal neutrophil myosin IIA localization in an immunofluorescence analysis can rule out MYH9 disorders. J Thromb Haemost, 11: 2071-2073 (2013).
  5. Kon, A., Shih, L. Y., Minamino, M., Sanada, M., Shiraishi, Y., Nagata, Y., Yoshida K., Okuno, Y., Bando, M., Nakato, R., Ishikawa, S., Sato-Otsubo, A., Nagae, G., Nishimoto, A., Haferlach, C., Nowak, D., Sato, Y., Alpermann, T., Nagasaki, M., Shimamura, T., Tanaka, H., Chiba, K., Yamamoto, R., Yamaguchi, T., Otsu, M., Obara, N., Sakata-Yanagimoto, M., Nakamaki, T., Ishiyama, K., Nolte, F., Hofmann, W. K., Miyawaki, S., Chiba, S., Mori, H., Nakauchi, H., Koeffler, H. P., Aburatani, H., Haferlach, T., Shirahige, K., Miyano, S., Ogawa, S.: Recurrent mutations in multiple components of the cohesin complex in myeloid neoplasms. Nat Genet, 45: 1232-1237 (2013).
  6. Kunishima, S., Okuno, Y., Yoshida K., Shiraishi, Y., Sanada, M., Muramatsu, H., Chiba, K., Tanaka, H., Miyazaki, K., Sakai, M., Ohtake, M., Kobayashi, R., Iguchi, A., Niimi, G., Otsu, M., Takahashi, Y., Miyano, S., Saito, H., Kojima, S., Ogawa, S.: ACTN1 mutations cause congenital macrothrombocytopenia. Am J Hum Genet, 92: 431-438 (2013).
  7. Makishima, H., Yoshida K., Nguyen, N., Przychodzen, B., Sanada, M., Okuno, Y., Ng, K. P., Gudmundsson, K. O., Vishwakarma, B. A., Jerez, A., Gomez-Segui, I., Takahashi, M., Shiraishi, Y., Nagata, Y., Guinta, K., Mori, H., Sekeres, M. A., Chiba, K., Tanaka, H., Muramatsu, H., Sakaguchi, H., Paquette, R. L., McDevitt, M. A., Kojima, S., Saunthararajah, Y., Miyano, S., Shih, L. Y., Du, Y., Ogawa, S., Maciejewski, J. P.: Somatic SETBP1 mutations in myeloid malignancies. Nat Genet, 45: 942-946 (2013).
  8. Ohba, R., Furuyama, K., Yoshida K., Fujiwara, T., Fukuhara, N., Onishi, Y., Manabe, A., Ito, E., Ozawa, K., Kojima, S., Ogawa, S., Harigae, H.: Clinical and genetic characteristics of congenital sideroblastic anemia: comparison with myelodysplastic syndrome with ring sideroblast (MDS-RS). Ann Hematol, 92: 1-9 (2013).
  9. Saida, S., Watanabe, K., Sato-Otsubo, A., Terui, K., Yoshida K., Okuno, Y., Toki, T., Wang, R., Shiraishi, Y., Miyano, S., Kato, I., Morishima, T., Fujino, H., Umeda, K., Hiramatsu, H., Adachi, S., Ito, E., Ogawa, S., Ito, M., Nakahata, T., Heike, T.: Clonal selection in xenografted TAM recapitulates the evolutionary process of myeloid leukemia in Down syndrome. Blood, 121: 4377-4387 (2013).
  10. Sakaguchi, H., Okuno, Y., Muramatsu, H., Yoshida K., Shiraishi, Y., Takahashi, M., Kon, A., Sanada, M., Chiba, K., Tanaka, H., Makishima, H., Wang, X., Xu, Y., Doisaki, S., Hama, A., Nakanishi, K., Takahashi, Y., Yoshida, N., Maciejewski, J. P., Miyano, S., Ogawa, S., Kojima, S.: Exome sequencing identifies secondary mutations of SETBP1 and JAK3 in juvenile myelomonocytic leukemia. Nat Genet, 45: 937-941 (2013).
  11. Sato, Y., Yoshizato, T., Shiraishi, Y., Maekawa, S., Okuno, Y., Kamura, T., Shimamura, T., Sato-Otsubo, A., Nagae, G., Suzuki, H., Nagata, Y., Yoshida K., Kon, A., Suzuki, Y., Chiba, K., Tanaka, H., Niida, A., Fujimoto, A., Tsunoda, T., Morikawa, T., Maeda, D., Kume, H., Sugano, S., Fukayama, M., Aburatani, H., Sanada, M., Miyano, S., Homma, Y., Ogawa, S.: Integrated molecular analysis of clear-cell renal cell carcinoma. Nat Genet, 45: 860-867 (2013).
  12. Shiraishi, Y., Sato, Y., Chiba, K., Okuno, Y., Nagata, Y., Yoshida K., Shiba, N., Hayashi, Y., Kume, H., Homma, Y., Sanada, M., Ogawa, S., Miyano, S.: An empirical Bayesian framework for somatic mutation detection from cancer genome sequencing data. Nucleic Acids Res, 41: e89 (2013).
  13. Yoshida K., Sanada, M., Ogawa, S.: Deep sequencing in cancer research. Jpn J Clin Oncol, 43: 110-115 (2013).
  14. Yoshida K., Toki, T., Okuno, Y., Kanezaki, R., Shiraishi, Y., Sato-Otsubo, A., Sanada, M., Park, M. J., Terui, K., Suzuki, H., Kon, A., Nagata, Y., Sato, Y., Wang, R., Shiba, N., Chiba, K., Tanaka, H., Hama, A., Muramatsu, H., Hasegawa, D., Nakamura, K., Kanegane, H., Tsukamoto, K., Adachi, S., Kawakami, K., Kato, K., Nishimura, R., Izraeli, S., Hayashi, Y., Miyano, S., Kojima, S., Ito, E., Ogawa, S.: The landscape of somatic mutations in Down syndrome-related myeloid disorders. Nat Genet, 45: 1293-1299 (2013).
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