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Shunsuke Kimura
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Recurrent SPI1 (PU.1) fusions in high-risk pediatric T cell acute lymphoblastic leukemia
M Seki, S Kimura, T Isobe, K Yoshida, H Ueno, Y Nakajima-Takagi, ...
Nature genetics 49 (8), 1274-1281, 2017
1332017
Enhancer Hijacking Drives Oncogenic BCL11B Expression in Lineage-Ambiguous Stem Cell Leukemia
LE Montefiori, S Bendig, Z Gu, X Chen, P Pölönen, X Ma, A Murison, ...
Cancer discovery 11 (11), 2846-2867, 2021
962021
Biologic and therapeutic implications of genomic alterations in acute lymphoblastic leukemia
I Iacobucci, S Kimura, CG Mullighan
Journal of clinical medicine 10 (17), 3792, 2021
582021
Integrated multiomics analysis of hepatoblastoma unravels its heterogeneity and provides novel druggable targets
M Sekiguchi, M Seki, T Kawai, K Yoshida, M Yoshida, T Isobe, N Hoshino, ...
NPJ precision oncology 4 (1), 20, 2020
472020
Molecular markers in ALL: Clinical implications
S Kimura, CG Mullighan
Best Practice & Research Clinical Haematology 33 (3), 101193, 2020
402020
Landscape of driver mutations and their clinical impacts in pediatric B-cell precursor acute lymphoblastic leukemia
H Ueno, K Yoshida, Y Shiozawa, Y Nannya, Y Iijima-Yamashita, ...
Blood Advances 4 (20), 5165-5173, 2020
352020
NOTCH 1 pathway activating mutations and clonal evolution in pediatric T‐cell acute lymphoblastic leukemia
S Kimura, M Seki, K Yoshida, Y Shiraishi, M Akiyama, K Koh, T Imamura, ...
Cancer Science 110 (2), 784-794, 2019
322019
Enhancer retargeting of CDX2 and UBTF:: ATXN7L3 define a subtype of high-risk B-progenitor acute lymphoblastic leukemia
S Kimura, L Montefiori, I Iacobucci, Y Zhao, Q Gao, EM Paietta, ...
Blood, 2022
282022
Integrated molecular characterization of the lethal pediatric cancer pancreatoblastoma
T Isobe, M Seki, K Yoshida, M Sekiguchi, Y Shiozawa, Y Shiraishi, ...
Cancer Research 78 (4), 865-876, 2018
272018
Autosomal recessive complete STAT1 deficiency caused by compound heterozygous intronic mutations
S Sakata, M Tsumura, T Matsubayashi, S Karakawa, S Kimura, ...
International Immunology 32 (10), 663-671, 2020
262020
Human gain-of-function STAT1 mutation disturbs IL-17 immunity in mice
M Tamaura, N Satoh-Takayama, M Tsumura, T Sasaki, S Goda, ...
International immunology 32 (4), 259-272, 2020
252020
DNA methylation-based classification reveals difference between pediatric T-cell acute lymphoblastic leukemia and normal thymocytes
S Kimura, M Seki, T Kawai, H Goto, K Yoshida, T Isobe, M Sekiguchi, ...
Leukemia 34 (4), 1163-1168, 2020
172020
A Tumor Suppressor Enhancer of PTEN in T-cell Development and Leukemia
L Tottone, O Lancho, JW Loh, A Singh, S Kimura, J Roels, A Kuchmiy, ...
Blood cancer discovery 2 (1), 92-109, 2021
162021
Multi-omics analysis defines highly refractory RAS burdened immature subgroup of infant acute lymphoblastic leukemia
T Isobe, M Takagi, A Sato-Otsubo, A Nishimura, G Nagae, C Yamagishi, ...
Nature communications 13 (1), 4501, 2022
152022
CCL22 mutations drive natural killer cell lymphoproliferative disease by deregulating microenvironmental crosstalk
C Baer, S Kimura, MS Rana, AB Kleist, T Flerlage, DJ Feith, P Chockley, ...
Nature genetics 54 (5), 637-648, 2022
152022
Association of allele-specific methylation of the ASNS gene with asparaginase sensitivity and prognosis in T-ALL
K Akahane, S Kimura, K Miyake, A Watanabe, K Kagami, K Yoshimura, ...
Blood Advances 6 (1), 212-224, 2022
132022
Association of high-risk neuroblastoma classification based on expression profiles with differentiation and metabolism
S Kimura, M Sekiguchi, K Watanabe, M Hiwatarai, M Seki, K Yoshida, ...
PLoS One 16 (1), e0245526, 2021
122021
Comprehensive genetic analysis of pediatric germ cell tumors identifies potential drug targets
Y Kubota, M Seki, T Kawai, T Isobe, M Yoshida, M Sekiguchi, S Kimura, ...
Communications biology 3 (1), 544, 2020
122020
Association of aberrant ASNS imprinting with asparaginase sensitivity and chromosomal abnormality in childhood BCP-ALL
A Watanabe, K Miyake, J Nordlund, AC Syvänen, L van der Weyden, ...
Blood, The Journal of the American Society of Hematology 136 (20), 2319-2333, 2020
112020
Constitutional abnormalities of IDH1 combined with secondary mutations predispose a patient with Maffucci syndrome to acute lymphoblastic leukemia
S Hirabayashi, M Seki, D Hasegawa, M Kato, N Hyakuna, T Shuo, ...
Pediatric Blood & Cancer 64 (12), e26647, 2017
112017
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