| Landscape of genetic lesions in 944 patients with myelodysplastic syndromes T Haferlach, Y Nagata, V Grossmann, Y Okuno, U Bacher, G Nagae, ... Leukemia 28 (2), 241-247, 2014 | 1657 | 2014 |
| Integrated molecular analysis of clear-cell renal cell carcinoma Y Sato, T Yoshizato, Y Shiraishi, S Maekawa, Y Okuno, T Kamura, ... Nature genetics 45 (8), 860-867, 2013 | 1150 | 2013 |
| Somatic RHOA mutation in angioimmunoblastic T cell lymphoma M Sakata-Yanagimoto, T Enami, K Yoshida, Y Shiraishi, R Ishii, Y Miyake, ... Nature genetics 46 (2), 171-175, 2014 | 692 | 2014 |
| Somatic mutations and clonal hematopoiesis in aplastic anemia T Yoshizato, B Dumitriu, K Hosokawa, H Makishima, K Yoshida, ... New England Journal of Medicine 373 (1), 35-47, 2015 | 640 | 2015 |
| Genomic and molecular characterization of esophageal squamous cell carcinoma DC Lin, JJ Hao, Y Nagata, L Xu, L Shang, X Meng, Y Sato, Y Okuno, ... Nature genetics 46 (5), 467-473, 2014 | 625 | 2014 |
| Dynamics of clonal evolution in myelodysplastic syndromes H Makishima, T Yoshizato, K Yoshida, MA Sekeres, T Radivoyevitch, ... Nature genetics 49 (2), 204-212, 2017 | 429 | 2017 |
| Recurrent mutations in multiple components of the cohesin complex in myeloid neoplasms A Kon, LY Shih, M Minamino, M Sanada, Y Shiraishi, Y Nagata, ... Nature genetics 45 (10), 1232-1237, 2013 | 424 | 2013 |
| The landscape of somatic mutations in Down syndrome–related myeloid disorders K Yoshida, T Toki, Y Okuno, R Kanezaki, Y Shiraishi, A Sato-Otsubo, ... Nature genetics 45 (11), 1293-1299, 2013 | 401 | 2013 |
| Somatic SETBP1 mutations in myeloid malignancies H Makishima, K Yoshida, N Nguyen, B Przychodzen, M Sanada, Y Okuno, ... Nature genetics 45 (8), 942-946, 2013 | 281 | 2013 |
| Exome sequencing identifies secondary mutations of SETBP1 and JAK3 in juvenile myelomonocytic leukemia H Sakaguchi, Y Okuno, H Muramatsu, K Yoshida, Y Shiraishi, ... Nature genetics 45 (8), 937-941, 2013 | 247 | 2013 |
| ACTN1 mutations cause congenital macrothrombocytopenia S Kunishima, Y Okuno, K Yoshida, Y Shiraishi, M Sanada, H Muramatsu, ... The American Journal of Human Genetics 92 (3), 431-438, 2013 | 226 | 2013 |
| An empirical Bayesian framework for somatic mutation detection from cancer genome sequencing data Y Shiraishi, Y Sato, K Chiba, Y Okuno, Y Nagata, K Yoshida, N Shiba, ... Nucleic acids research 41 (7), e89-e89, 2013 | 221 | 2013 |
| BCOR and BCORL1 mutations in myelodysplastic syndromes and related disorders F Damm, V Chesnais, Y Nagata, K Yoshida, L Scourzic, Y Okuno, ... Blood, The Journal of the American Society of Hematology 122 (18), 3169-3177, 2013 | 220 | 2013 |
| Profiling of somatic mutations in acute myeloid leukemia with FLT3-ITD at diagnosis and relapse M Garg, Y Nagata, D Kanojia, A Mayakonda, K Yoshida, S Haridas Keloth, ... Blood, The Journal of the American Society of Hematology 126 (22), 2491-2501, 2015 | 219 | 2015 |
| Integrated genetic and epigenetic analysis defines novel molecular subgroups in rhabdomyosarcoma M Seki, R Nishimura, K Yoshida, T Shimamura, Y Shiraishi, Y Sato, ... Nature communications 6 (1), 7557, 2015 | 193 | 2015 |
| Variant ALDH2 is associated with accelerated progression of bone marrow failure in Japanese Fanconi anemia patients A Hira, H Yabe, K Yoshida, Y Okuno, Y Shiraishi, K Chiba, H Tanaka, ... Blood, The Journal of the American Society of Hematology 122 (18), 3206-3209, 2013 | 191 | 2013 |
| Defective Epstein–Barr virus in chronic active infection and haematological malignancy Y Okuno, T Murata, Y Sato, H Muramatsu, Y Ito, T Watanabe, T Okuno, ... Nature microbiology 4 (3), 404-413, 2019 | 167 | 2019 |
| Mutations in the gene encoding the E2 conjugating enzyme UBE2T cause Fanconi anemia A Hira, K Yoshida, K Sato, Y Okuno, Y Shiraishi, K Chiba, H Tanaka, ... The American Journal of Human Genetics 96 (6), 1001-1007, 2015 | 135 | 2015 |
| Identification of RET autophosphorylation sites by mass spectrometry Y Kawamoto, K Takeda, Y Okuno, Y Yamakawa, Y Ito, R Taguchi, M Kato, ... Journal of Biological Chemistry 279 (14), 14213-14224, 2004 | 126 | 2004 |
| Loss of function mutations in RPL27 and RPS27 identified by whole‐exome sequencing in Diamond‐Blackfan anaemia RN Wang, K Yoshida, T Toki, T Sawada, T Uechi, Y Okuno, ... British journal of haematology 168 (6), 854-864, 2015 | 124 | 2015 |
