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Journal Articles

Branching Trajectories and Diversification of Clonal Escape in Aplastic Anemia Revealed By Single-Cell Genomics

Masanori Yoshida, Paula Arnold, Carmelo Gurnari, Charnise Goodings, Shinsuke Hirabayashi, Miriam Erlacher, Jaroslaw P. Maciejewski, Charlotte Marie Niemeyer, Marcin W Wlodarski

Blood (2023) 142 (Supplement 1): 705.

https://doi.org/10.1182/blood-2023-186205

Published: 2023

Journal Articles

Severe Congenital Neutropenia-Type 5: Impaired T Cell Proliferation, Aberrant Th1 Cytokine Production, Abnormal Megakaryocytes, and Impaired Platelet Granule Formation in a Patient with VPS45 Deficiency Caused By Uniparental Isodisomy

Masahiro Ueki, Shinsuke Hirabayashi, Daichi Sajiki, Masataka Hasegawa, Yukayo Terashita, Hiroki Ohata, Manabu Wakamatsu, Shunichiro Takezaki, Yuko Cho, Kazuhiko Nakabayashi, Hideki Muramatsu, Takahiro Yamada, Yoshiyuki Takahashi, Atsushi Manabe

Blood (2023) 142 (Supplement 1): 5382.

https://doi.org/10.1182/blood-2023-183059

Published: 2023

Journal Articles

Genetic Mutation and Outcome of Venetoclax-Based Therapy in Newly Diagnosed AML in the Real World: Hokkaido Leukemia Net Study

Blood (2023) 142 (Supplement 1): 1470.

https://doi.org/10.1182/blood-2023-173909

Published: 2023

Journal Articles

Prognostic Impact of CEBPA bZIP Domain Mutation in Cytogenetically Normal Acute Myeloid Leukemia

Blood (2022) 140 (Supplement 1): 8950–8951.

https://doi.org/10.1182/blood-2022-158653

Published: 2022

Journal Articles

Better Prognosis of Dominant-Negative Type of IKZF1 Deletion in BCR-ABL- positive Adult B-Cell Acute Lymphoblastic Leukemia

Blood (2022) 140 (Supplement 1): 9207–9208.

https://doi.org/10.1182/blood-2022-157881

Published: 2022

Journal Articles

Clinical Features of Complex Karyotype in Newly Diagnosed Acute Myeloid Leukemia

Blood (2022) 140 (Supplement 1): 3210–3211.

https://doi.org/10.1182/blood-2022-157874

Published: 2022

Journal Articles

Association of unbalanced translocation der(1;7) with germline GATA2 mutations

Blood (2021) 138 (23): 2441–2445.

https://doi.org/10.1182/blood.2021012781

Published: 2021

Includes: Supplemental data

Journal Articles

Heterozygous NUDT15 Gene Polymorphism Would Not Associate with the Severity of 6-Mercaptopurine Side Effects in Early Intensification Therapy for Childhood Acute Lymphoblastic Leukemia

Jimei Zhao, Masahiro Ueki, Saori Sawai, Minako Sugiyama, Yukayo Terashita, Shinsuke Hirabayashi, Yuko Cho, Yoichi Tanaka, Atsushi Manabe

Blood (2021) 138 (Supplement 1): 1240.

https://doi.org/10.1182/blood-2021-147230

Published: 2021

Journal Articles

Acute Lymphoblastic Leukemia with Zinc-Finger Protein 384 (ZNF384)-Related Rearrangements: A Retrospective Analysis from the Ponte Di Legno Childhood ALL Working Group

Blood (2019) 134 (Supplement_1): 652.

https://doi.org/10.1182/blood-2019-123236

Published: 2019

Journal Articles

Systematic Assessment of GATA2 Genetic Variation Reveals the Presence of Novel Disease-Causing Synonymous Exonic Mutations

Blood (2017) 130 (Supplement 1): 2449.

https://doi.org/10.1182/blood.V130.Suppl_1.2449.2449

Published: 2017

Journal Articles

Genetic Abnormalities and Prognosis in Pediatric B-Precursor Acute Lymphoblastic Leukemia without Conventional Genetic Abnormalities; Tokyo Children's Cancer Study Group

Kenro Ohki, MD PhD, Shinsuke Hirabayashi, MD, Akinori Yaguchi, Akinori Yaguchi, Kazuki Terada, MD, Jun Ohkubo, PhD MD, Norio Shiba, MD PhD, Motohiro Kato, MD PhD, Takashi Fukushima, MD PhD, Katsuyoshi Koh, MD PhD, Hayashi Yasuhide, MD PhD, Atsushi Manabe, MD PhD, Akira Ohara, MD PhD, Nobutaka Kiyokawa, MD PhD

Blood (2016) 128 (22): 4079.

https://doi.org/10.1182/blood.V128.22.4079.4079

Published: 2016

Journal Articles

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

Blood (2016) 127 (11): 1387–1397.

https://doi.org/10.1182/blood-2015-09-669937

Published: 2016

Includes: Supplemental data

Journal Articles

Clonal Mutational Landscape of Childhood Myelodysplastic Syndromes

Blood (2015) 126 (23): 1662.

https://doi.org/10.1182/blood.V126.23.1662.1662

Published: 2015

Journal Articles

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

Victor Bengt Pastor Loyola, MSc, Shinsuke Hirabayashi, MD, Sandra Pohl, PhD, Emilia J Kozyra, MSc, Albert Catala, MD, Barbara De Moerloose, MD PhD, Michael Dworzak, MD, Henrik Hasle, MD, Riccardo Masetti, MD, Markus Schmugge, MD, Owen Smith, Jan Starý, MD, Marek Ussowicz, MD, Marry M. van den Heuvel-Eibrink, MD PhD, Ester Mejstrikova, MD PhD, Ulrich Salzer, MD, Michael Lübbert, MD, Daniel Heudobler, MD, David Betts, MD, Jose Cervera, MD, Gudrun Göhring, MD, Oskar A. Haas, Olga Haus, MD, Kyra Michalova, PhD DSc, Francesco Pasquali, MD, Joelle Tchinda, MD, Nadine van Roy, MD, Brigitte Schlegelberger, MD Prof., H. Berna Beverloo, PhD, Peter Noellke, MSc, Ayami Yoshimi, MD, Franco Locatelli, Prof, MD PhD, Brigitte Strahm, MD, Jaroslaw P. Maciejewski, MD PhD, Michael Rehli, PhD, Charlotte M Niemeyer, Prof, MD, Marcin W Wlodarski, MD

Blood (2015) 126 (23): 299.

https://doi.org/10.1182/blood.V126.23.299.299

Published: 2015

Journal Articles

Hematopoietic Stem Cell Transplantation for Patients with Refractory Cytopenia of Childhood

Daisuke Hasegawa, Shinsuke Hirabayashi, Shizuka Watanabe, PharmD, Yuji Zaike, Masahiro Tsuchida, MD PhD, Atsuko Masunaga, Ayami Yoshimi, MD PhD, Asahito Hama, MD PhD, Seiji Kojima, MD PhD, Masafumi Ito, MD PhD, Tatsutoshi Nakahata, MD PhD, Atsushi Manabe, MD PhD

Blood (2014) 124 (21): 4646.

https://doi.org/10.1182/blood.V124.21.4646.4646

Published: 2014

Journal Articles

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

Blood (2012) 120 (21): 1699.

https://doi.org/10.1182/blood.V120.21.1699.1699

Published: 2012

Journal Articles

Characteristics of Diamond Blackfan Anemia Patients with Unknown Genetic Defect

Tamas Farkas, Joerg Meerpohl, Shinsuke Hirabayashi, Alyson MacInnes, Gunda Ruzaike, Paul Essers, Sandra Urbaniak, Jessica Moetter, Friedrich Kapp, Alexandra Fischer, Charlotte M Niemeyer, Marcin W Wlodarski

Blood (2012) 120 (21): 1267.

https://doi.org/10.1182/blood.V120.21.1267.1267

Published: 2012

Journal Articles

Recurrent 6pLOH Is the Most Common Somatic Lesion in Refractory Cytopenia of Childhood and Occurs Very Infrequently in Severe Aplastic Anemia

Marcin W Wlodarski, Shinsuke Hirabayashi, Brigitte Strahm, Sandra Urbaniak, Brigitte Schlegelberger, Ingrid Furlan, Alexandra Fischer, Wilfried Truckenmüller, Ayami Yoshimi-Noellke, Peter Noellke, Irith Baumann, Charlotte M Niemeyer

Blood (2012) 120 (21): 644.

https://doi.org/10.1182/blood.V120.21.644.644

Published: 2012

Journal Articles

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

Blood (2012) 119 (11): e96–e99.

https://doi.org/10.1182/blood-2011-12-395087

Published: 2012

Journal Articles

Analysis of Ribosomal Protein Genes Associated with Diamond Blackfan Anemia (DBA) In German DBA Patients and Their Relatives

Jessica Moetter, Ph.D., Mutlu Kartal, M.D., Joerg Meerpohl, M.D., Alexandra Fischer, Thorsten Simon, Prof. Dr., Sandra Urbaniak, Shinsuke Hirabayashi, Friedrich Kapp, M.D., Peter Noellke, MPH, Christian Kratz, MD, Charlotte M Niemeyer, Marcin W. Wlodarski, M.D.

Blood (2011) 118 (21): 729.

https://doi.org/10.1182/blood.V118.21.729.729

Published: 2011

NARROW

Branching Trajectories and Diversification of Clonal Escape in Aplastic Anemia Revealed By Single-Cell Genomics

Severe Congenital Neutropenia-Type 5: Impaired T Cell Proliferation, Aberrant Th1 Cytokine Production, Abnormal Megakaryocytes, and Impaired Platelet Granule Formation in a Patient with VPS45 Deficiency Caused By Uniparental Isodisomy

Genetic Mutation and Outcome of Venetoclax-Based Therapy in Newly Diagnosed AML in the Real World: Hokkaido Leukemia Net Study

Prognostic Impact of CEBPA bZIP Domain Mutation in Cytogenetically Normal Acute Myeloid Leukemia

Better Prognosis of Dominant-Negative Type of IKZF1 Deletion in BCR-ABL- positive Adult B-Cell Acute Lymphoblastic Leukemia

Clinical Features of Complex Karyotype in Newly Diagnosed Acute Myeloid Leukemia

Association of unbalanced translocation der(1;7) with germline GATA2 mutations

Heterozygous NUDT15 Gene Polymorphism Would Not Associate with the Severity of 6-Mercaptopurine Side Effects in Early Intensification Therapy for Childhood Acute Lymphoblastic Leukemia

Acute Lymphoblastic Leukemia with Zinc-Finger Protein 384 (ZNF384)-Related Rearrangements: A Retrospective Analysis from the Ponte Di Legno Childhood ALL Working Group

Systematic Assessment of GATA2 Genetic Variation Reveals the Presence of Novel Disease-Causing Synonymous Exonic Mutations

Genetic Abnormalities and Prognosis in Pediatric B-Precursor Acute Lymphoblastic Leukemia without Conventional Genetic Abnormalities; Tokyo Children's Cancer Study Group

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

Clonal Mutational Landscape of Childhood Myelodysplastic Syndromes

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

Hematopoietic Stem Cell Transplantation for Patients with Refractory Cytopenia of Childhood

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

Characteristics of Diamond Blackfan Anemia Patients with Unknown Genetic Defect

Recurrent 6pLOH Is the Most Common Somatic Lesion in Refractory Cytopenia of Childhood and Occurs Very Infrequently in Severe Aplastic Anemia

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

Analysis of Ribosomal Protein Genes Associated with Diamond Blackfan Anemia (DBA) In German DBA Patients and Their Relatives

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American Society of Hematology

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American Society of Hematology

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