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British Journal of Haematology|February 3, 2026
Identification of cellular hierarchy in paediatric acute myeloid leukaemia: The Japan Children's Cancer Group trial (JCCG AML-12)Tomoya Komori, Tomoko Kawai, Yusuke Okuno, et al.
Human Genetics|April 1, 2003
Polymorphisms in the MLL breakpoint cluster region (BCR)Deborah R Echlin-Bell, Lydia L Smith, Loretta Li, et al.
Leukemia|January 31, 2019
A germline HLTF mutation in familial MDS induces DNA damage accumulation through impaired PCNA polyubiquitinationKensuke Takaoka, Masahito Kawazu, Junji Koya, et al.
Nature Communications|August 28, 2014
Recurrent CDC25C mutations drive malignant transformation in FPD/AMLAkihide Yoshimi, Takashi Toya, Masahito Kawazu, et al.
Pediatric Blood & Cancer|December 6, 2023
High IL2RA/CD25 expression is a prognostic stem cell biomarker for pediatric acute myeloid leukemia without a core-binding factorTakahiro Aoki, Norio Shiba, Shinichi Tsujimoto, et al.
British Journal of Haematology|August 30, 2002
Risk-directed treatment of infant acute lymphoblastic leukaemia based on early assessment of MLL gene status: results of the Japan Infant Leukaemia Study (MLL96)Keiichi Isoyama, Mariko Eguchi, Shigeyoshi Hibi, et al.
Leukemia & Lymphoma|March 12, 2020
Nationwide epidemiological survey of familial myelodysplastic syndromes/acute myeloid leukemia in Japan: a multicenter retrospective studyKensuke Takaoka, Junji Koya, Akihide Yoshimi, et al.
British Journal of Haematology|July 14, 2021
Characteristics of genetic alterations of peripheral T-cell lymphoma in childhood including identification of novel fusion genes: the Japan Children's Cancer Group (JCCG)Kentaro Ohki, Nobutaka Kiyokawa, Satoru Watanabe, et al.
Pediatric Blood & Cancer|September 30, 2017
Genetic heterogeneity of uncharacterized childhood autoimmune diseases with lymphoproliferationMasatoshi Takagi, Akihiro Hoshino, Kenichi Yoshida, et al.
Genes, Chromosomes & Cancer|January 8, 2017
Prognostic impact of specific molecular profiles in pediatric acute megakaryoblastic leukemia in non-Down syndromeYusuke Hara, Norio Shiba, Kentaro Ohki, et al.
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