Shinsuke Hirabayashi

发表

Prevalence, clinical characteristics, and prognosis of GATA2-related myelodysplastic syndromes in children and adolescents.

M. Wlodarski, J. Maciejewski, A. Yoshimi, 2016, Blood.

K. Okamura, K. Matsuda, M. Kubo, 2017, Haematologica.

Dasatinib and low‐intensity chemotherapy for Philadelphia chromosome‐positive acute lymphoblastic leukemia in a child with Down syndrome

N. Takahashi, N. Kiyokawa, M. Miura, 2019, Pediatric blood & cancer.

Duplication of ALK F1245 missense mutation due to acquired uniparental disomy associated with aggressive progression in a patient with relapsed neuroblastoma

S. Miyano, S. Ogawa, J. Takita, 2019, Oncology letters.

Mutational landscape in children with myelodysplastic syndromes is distinct from adults: specific somatic drivers and novel germline variants

M. Wlodarski, A. Yoshimi, I. Baumann, 2017, Leukemia.

Acquisition of monosomy 7 and a RUNX1 mutation in Pearson syndrome

S. Miyano, Y. Shiraishi, S. Ogawa, 2020, Pediatric blood & cancer.

Diagnostic Capability of Cerebrospinal Fluid-Placental Alkaline Phosphatase Value in Intracranial Germ Cell Tumor

K. Houkin, T. Hashimoto, Takashi Mori, 2020, Oncology.

Synonymous GATA2 mutations result in selective loss of mutated RNA and are common in patients with GATA2 deficiency

M. Boerries, H. Busch, E. Mejstrikova, 2020, Leukemia.

Heterogeneity of GATA2-related myeloid neoplasms

M. Wlodarski, C. Niemeyer, S. Hirabayashi, 2017, International Journal of Hematology.

Somatic Genetic and Epigenetic Architecture of Myelodysplastic Syndromes Arising from GATA2 Deficiency

J. Tchinda, E. Mejstrikova, O. Haas, 2015 .

Clonal Mutational Landscape of Childhood Myelodysplastic Syndromes

M. Wlodarski, J. Maciejewski, P. D. Paepe, 2015 .

Unexpected High Frequency of GATA2 Mutations in Children with Non-Familial MDS and Monosomy 7

M. Wlodarski, I. Baumann, C. Niemeyer, 2012 .

Clinical evolution, genetic landscape and trajectories of clonal hematopoiesis in SAMD9/SAMD9L syndromes

J. Tchinda, B. Burkhardt, A. Schulz, 2021, Nature Medicine.

Association of Unbalanced Translocation der(1;7) with Germline GATA2 Mutations.

J. Tchinda, S. Holland, C. Mecucci, 2021, Blood.

Role of GATA 2 in normal and malignant hematopoiesis

M. Wlodarski, C. Niemeyer, S. Hirabayashi, 2017 .

Spliceosomal gene aberrations are rare, coexist with oncogenic mutations, and are unlikely to exert a driver effect in childhood MDS and JMML.

Franco Locatelli, Michael Heuser, Seishi Ogawa, 2012, Blood.

Clinical and Molecular Heterogeneity of RTEL1 Deficiency

U. Pannicke, K. Schwarz, S. Ehl, 2017, Front. Immunol..

Clinical characteristics and treatment outcome in 65 cases with refractory cytopenia of childhood defined according to the WHO 2008 classification

A. Yoshimi, T. Nakahata, S. Kojima, 2014, British journal of haematology.

Prognostic impact of FLT3-ITD, NPM1 mutation and CEBPA bZIP domain mutation in cytogenetically normal acute myeloid leukemia: a Hokkaido Leukemia Net study

Y. Kakinoki, T. Nagashima, A. Mori, 2023, International Journal of Hematology.

High‐grade neuroepithelial tumor with BCL6 corepressor‐alteration presenting pathological and radiological calcification: A case report

A. Manabe, S. Nobusawa, Hiroaki Motegi, 2021, Pathology international.

Constitutional abnormalities of IDH1 combined with secondary mutations predispose a patient with Maffucci syndrome to acute lymphoblastic leukemia

S. Miyano, Y. Shiraishi, K. Chiba, 2017, Pediatric blood & cancer.

Clinical and molecular characteristics of MEF2D fusion-positive B-cell precursor acute lymphoblastic leukemia in childhood, including a novel translocation resulting in MEF2D-HNRNPH1 gene fusion

K. Okamura, K. Matsuda, Y. Hayashi, 2018, Haematologica.

Integrated Analysis of Epigenetic and Genetic Changes During MDS Progression Reveals the Tight Association of Epigenetic Changes with Genetic Selection

M. Rehli, D. Nowak, W. Hofmann, 2017 .

Vaginal Transmission of Cancer from Mothers with Cervical Cancer to Infants.

N. Yanaihara, A. Okamoto, T. Kohno, 2021, The New England journal of medicine.

Clinical characteristics and outcomes of B-ALL with ZNF384 rearrangements: a retrospective analysis by the Ponte di Legno Childhood ALL Working Group

M. Loh, C. Pui, C. Mullighan, 2021, Leukemia.

A left ventricular noncompaction in a patient with long QT syndrome caused by a KCNQ1 mutation: a case report

W. Shimizu, N. Sumitomo, I. Kusakawa, 2012, Heart and Vessels.

Acute megakaryoblastic leukemia with acquired trisomy 21 and GATA1 mutations in phenotypically normal children

Kenichi Yoshida, T. Toki, E. Ito, 2015, European Journal of Pediatrics.

The ex vivo production of ammonia predicts l-asparaginase biological activity in children with acute lymphoblastic leukemia

Kenichi Yoshida, A. Manabe, A. Ohara, 2009, International journal of hematology.

Clinical characteristics and outcomes of B-cell precursor ALL with MEF2D rearrangements: a retrospective study by the Ponte di Legno Childhood ALL Working Group

M. Loh, C. Pui, C. Mullighan, 2022, Leukemia.

Notable therapeutic response in a patient with systemic juvenile xanthogranuloma with KIF5B‐ALK fusion

A. Manabe, I. Kinoshita, Hiroaki Motegi, 2021, Pediatric blood & cancer.

Clinical features of complex karyotype in newly diagnosed acute myeloid leukemia

Y. Kakinoki, T. Kondo, A. Mori, 2022, International Journal of Hematology.

Clinical utility of target capture‐based panel sequencing in hematological malignancies: A multicenter feasibility study

K. Karube, Y. Shiraishi, S. Ogawa, 2020, Cancer science.

Bortezomib combined with standard induction chemotherapy in Japanese children with refractory acute lymphoblastic leukemia

T. Ariga, A. Manabe, H. Tada, 2017, International Journal of Hematology.