Deregulated intracellular signaling by mutated c-CBL in myeloid neoplasms

by Ogawa, S., Shih, L.-Y., Suzuki, T., Otsu, M., Nakauchi, H., Koeffler, H.P., Sanada, M.
Published 2016

A nonsense mutation of IDH1 in myelodysplastic syndromes and related disorders

by Yoshida, K., Sanada, M., Kato, M., Kawahata, R., Matsubara, A., Takita, J., Shih, L.-Y., Mori, H., Koeffler, H.P., Ogawa, S.
Published 2016

An unusual outbreak of hypoglycemia - A correction

by Shih, L.K., Cheng, L.C., Tan, B., Lim, C.C.T., Dalan, R., Gardner, D., Pratt, E., Lee, M., Kok, O.L.
Published 2016

Validation of the 18-gene classifier as a prognostic biomarker of distant metastasis in breast cancer

by Cheng, S.H.-C, Huang, T.-T, Cheng, Y.-H., Tan, T.B.K., Horng, C.-F., Wang, Y.A., Brian, N.S., Shih, L.-S., Yu, B.-L.
Published 2020

Identification of marker genes including RUNX3 (AML2) that discriminate between different myeloproliferative neoplasms and normal individuals

by Muller, C.I., Luong, Q.T., Jones, L.C., Desmond, J.C., Kawamata, N., Koeffler, H.P., Shih, L.-Y., Tcherniantchouk, O., Liu, Q., Ito, K., Osato, M., Ito, Y., Tefferi, A., de, Vos S.
Published 2012

Prevalence and prognostic impact of allelic imbalances associated with leukemic transformation of Philadelphia chromosome-negative myeloproliferative neoplasms

by Thoennissen, N.H., Krug, U.O., Lee, D.H.T., Kawamata, N., Iwanski, G.B., Lasho, T., Weiss, T., Nowak, D., Koren-Michowitz, M., Kato, M., Sanada, M., Shih, L.-Y., Nagler, A., Raynaud, S.D., Müller-Tidow, C., Mesa, R., Haferlach, T., Gilliland, D.G., Tefferi, A., Ogawa, S., Phillip Koeffler, H.
Published 2016

ASXL2 regulates hematopoiesis in mice and its deficiency promotes myeloid expansion

by Madan, V., Han, L., Hattori, N., Woon Teoh, W., Mayakonda, A., Sun, Q.-Y., Ding, L.-W., Mohd Nordin, H.B., Lim, S.L., Shyamsunder, P., Dakle, P., Sundaresan, J., Doan, N.B., Sanada, M., Sato-Otsubo, A., Meggendorfer, M., Yang, H., Said, J.W., Ogawa, S., Haferlach, T., Liang, D.-C., Shih, L.-Y., Nakamaki, T., Wang, Q.T., Koeffler, H.P.
Published 2021

Frequent pathway mutations of splicing machinery in myelodysplasia

by Yoshida, K., Sanada, M., Shiraishi, Y., Nowak, D., Nagata, Y., Yamamoto, R., Sato, Y., Sato-Otsubo, A., Kon, A., Nagasaki, M., Chalkidis, G., Suzuki, Y., Shiosaka, M., Kawahata, R., Yamaguchi, T., Otsu, M., Obara, N., Sakata-Yanagimoto, M., Ishiyama, K., Mori, H., Nolte, F., Hofmann, W.-K., Miyawaki, S., Sugano, S., Haferlach, C., Koeffler, H.P., Shih, L.-Y., Haferlach, T., Chiba, S., Nakauchi, H., Miyano, S., Ogawa, S.
Published 2016

Recurrent mutations in multiple components of the cohesin complex in myeloid neoplasms

by 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.
Published 2016

Consensus-based clinical practice recommendations for the examination and management of falls in patients with Parkinson's disease

by van der Marck M.A., Klok M.P., Okun M.S., Giladi N., Munneke M., Bloem B.R., Arney K., Browner N.M., Caunter M., Cianci H.J., Dunlop B., Eggert K., Fisher B., Hass C.J., Hunter C., Jabre M., Kraakevik J., Lyons K.E., Phibbs F., Scott B.L., Shih L., Tan E.-K., Tan L., Varanese S., Voss T., Ashburn A., Ballinger C., Bhatti M.T., Hausdorff J., Lindvall S., Morris M.E., Nieuwboer A., Schwalb J.M., Studenski S., Wood B.H.
Published 2018