Hirabayashi Shinsuke 平林真介

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HIRABAYASHI Shinsuke 平林真介

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Researcher Number	50769635
Other IDs
Affiliation (Current)	2025: 北海道大学, 大学病院, 助教
Affiliation (based on the past Project Information) *help	2020 – 2023: 北海道大学, 大学病院, 助教 2019: 北海道大学, 大学病院, 特任助教 2016 – 2018: 聖路加国際大学, 聖路加国際病院, 常勤嘱託
Review Section/Research Field	Principal Investigator Basic Section 54010:Hematology and medical oncology-related / Hematology Except Principal Investigator Basic Section 54010:Hematology and medical oncology-related
Keywords	Principal Investigator MDS / Cancer predisposition / 遺伝性素因 / 骨髄異形成症候群 / 先天性素因 / 癌 / ゲノム / Pearson syndrome / ALL / Maffucci syndrome / Ｒａｒｅ　ｓｙｎｄｒｏｍｅ / 造血器腫瘍 / 希少症候群 … More Except Principal Investigator … More FLT3-ITD / 急性骨髄性白血病 / NUP98::NSD1 Less

NUP98::NSD1白血病の治療抵抗性の解明と新規治療法の開発
- Principal Investigator
  
  松川敏大
- Project Period (FY)
  2023 – 2025
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 54010:Hematology and medical oncology-related
- Research Institution
  Hokkaido University
小児・AYA世代におけるMDSの発生機序と治療戦略の解明Principal Investigator
- Principal Investigator
  
  平林真介
- Project Period (FY)
  2021 – 2024
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 54010:Hematology and medical oncology-related
- Research Institution
  Hokkaido University
Analysis of germline predisposition and clinical features of childhood and AYA myelodysplastic syndromePrincipal Investigator
- Principal Investigator
  
  Hirabayashi Shinsuke
- Project Period (FY)
  2018 – 2022
- Research Category
  
  Grant-in-Aid for Early-Career Scientists
- Review Section
  
  Basic Section 54010:Hematology and medical oncology-related
- Research Institution
  Hokkaido University
  St. Luke's International University
Research for mechanism of hematological malignancies in rare syndrome in childrenPrincipal Investigator
- Principal Investigator
  
  HIRABAYASHI Shinsuke
- Project Period (FY)
  2016 – 2018
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Hematology
- Research Institution
  St. Luke's International University

All 2023 2022 2021 2020 2019 2018 2017 2016

All Journal Article Presentation Book

[Book] 血液フロンティア　2016年11月号2016
- Author(s)
  平林真介
- Publisher
  医薬ジャーナル社
- Data Source
  KAKENHI-PROJECT-16K21376
[Journal Article] Clinical features of complex karyotype in newly diagnosed acute myeloid leukemia2023
- Author(s)
  Yoshida S, Onozawa, M, Hirabayashi S
- Journal Title
  
  Int J Hematol.
  
  Volume: 117 Issue: 4 Pages: 544-552
- DOI
  10.1007/s12185-022-03522-6
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21K08361
[Journal Article] Hematopoietic cell transplantation for hematological malignancies in Bloom syndrome2023
- Author(s)
  Nishiyama Yohei、Hirabayashi Shinsuke et al.
- Journal Title
  
  Pediatric Blood & Cancer
  
  Volume: 70 Issue: 11
- DOI
  10.1002/pbc.30655
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21K08361, KAKENHI-PROJECT-22K07887, KAKENHI-PROJECT-21K07746
[Journal Article] Association of unbalanced translocation der(1;7) with germline GATA2 mutations2021
- Author(s)
  Kozyra EJ, Hirabayashi S, Onozawa M, Wlodarski MW
- Journal Title
  
  Blood
  
  Volume: 138 Issue: 23 Pages: 2441-2445
- DOI
  10.1182/blood.2021012781
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21K08361
[Journal Article] Clinical evolution, genetic landscape and trajectories of clonal hematopoiesis in SAMD9/SAMD9L syndromes2021
- Author(s)
  Sahoo SS,Hirabayashi S, Wlodarski MW.
- Journal Title
  
  Nat Med .
  
  Volume: 27 Issue: 10 Pages: 1806-1817
- DOI
  10.1038/s41591-021-01511-6
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K16128
[Journal Article] Acquisition of monosomy 7 and a RUNX1 mutation in Pearson syndrome2020
- Author(s)
  Nishimura Akira、Hirabayashi Shinsuke、Hasegawa Daisuke、Yoshida Kenichi、Shiraishi Yuichi、Ashiarai Miho、Hosoya Yosuke、Fujiwara Tohru、Harigae Hideo、Miyano Satoru、Ogawa Seishi、Manabe Atsushi
- Journal Title
  
  Pediatric Blood & Cancer
  
  Volume: 68 Issue: 2
- DOI
  10.1002/pbc.28799
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-18K08314, KAKENHI-PROJECT-18K16128, KAKENHI-PROJECT-19H05656
[Journal Article] 遺伝性造血器腫瘍2020
- Author(s)
  平林真介、真部淳
- Journal Title
  
  日本臨床
  
  Volume: 78 Pages: 146-151
- Data Source
  KAKENHI-PROJECT-18K16128
[Journal Article] Synonymous GATA2 mutations result in selective loss of mutated RNA and are common in patients with GATA2 deficiency2020
- Author(s)
  Kozyra EJ, Hirabayashi S, Wlodarski MW
- Journal Title
  
  Leukemia
  
  Volume: 34 Issue: 10 Pages: 2673-2687
- DOI
  10.1038/s41375-020-0899-5
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K16128
[Journal Article] Dasatinib and low-intensity chemotherapy for Philadelphia chromosome-positive acute lymphoblastic leukemia in a child with Down syndrome2019
- Author(s)
  Hirabayashi Shinsuke、Hasegawa Daisuke、Yamamoto Kaoru、Nishimura Akira、Hosoya Yosuke、Shuo Takuya、Kiyokawa Nobutaka、Miura Masatomo、Takahashi Naoto、Manabe Atsushi
- Journal Title
  
  Pediatric Blood & Cancer
  
  Volume: 66 Issue: 5
- DOI
  10.1002/pbc.27612
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-16K21376
[Journal Article] Childhood cancer and familial tumors2019
- Author(s)
  平林真介、真部淳
- Journal Title
  
  JOURNAL OF FAMILIAL TUMORS
  
  Volume: 19 Issue: 1 Pages: 28-31
- DOI
  10.18976/jsft.19.1_28
- NAID
  130007708930
- ISSN
  1346-1052, 2189-6674
- Language
  Japanese
- Open Access
- Data Source
  KAKENHI-PROJECT-18K16128
[Journal Article] <i>TP53</i> mutations and hematological malignancies2018
- Author(s)
  平林真介、鈴木美慧、真部淳
- Journal Title
  
  Rinsho Ketsueki
  
  Volume: 59 Issue: 11 Pages: 2468-2474
- DOI
  10.11406/rinketsu.59.2468
- NAID
  130007528449
- ISSN
  0485-1439, 1882-0824
- Language
  Japanese
- Data Source
  KAKENHI-PROJECT-18K16128, KAKENHI-PROJECT-16K21376
[Journal Article] Constitutional abnormalities of IDH1 combined with secondary mutations predispose a patient with Maffucci syndrome to acute lymphoblastic leukemia2017
- Author(s)
  Hirabayashi Shinsuke、Seki Masafumi、Hasegawa Daisuke、Kato Motohiro、Hyakuna Nobuyuki、Shuo Takuya、Kimura Shunsuke、Yoshida Kenichi、Kataoka Keisuke、Fujii Yoichi、Shiraishi Yuichi、Chiba Kenichi、Tanaka Hiroko、Kiyokawa Nobutaka、Miyano Satoru、Ogawa Seishi、Takita Junko、Manabe Atsushi
- Journal Title
  
  Pediatric Blood & Cancer
  
  Volume: 64 Issue: 12
- DOI
  10.1002/pbc.26647
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K21376, KAKENHI-PLANNED-15H05909, KAKENHI-PROJECT-17H04224, KAKENHI-PROJECT-16K15533
[Journal Article] Familial hematological malignancies2017
- Author(s)
  平林真介、真部淳
- Journal Title
  
  Rinsho Ketsueki
  
  Volume: 58 Issue: 10 Pages: 1878-1883
- DOI
  10.11406/rinketsu.58.1878
- NAID
  130006132670
- ISSN
  0485-1439, 1882-0824
- Language
  Japanese
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-16K21376
[Journal Article] Heterogeneity of GATA2-related myeloid neoplasms2017
- Author(s)
  Hirabayashi Shinsuke、Wlodarski Marcin W.、Kozyra Emilia、Niemeyer Charlotte M.
- Journal Title
  
  International Journal of Hematology
  
  Volume: 106 Issue: 2 Pages: 175-182
- DOI
  10.1007/s12185-017-2285-2
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-16K21376
[Presentation] Analysis of GATA2 and RUNX1 mutations in young AML or MDS with trisomy 82022
- Author(s)
  宮下直樹、小野澤真弘、平林真介
- Organizer
  第84回日本血液学会学術集会
- Data Source
  KAKENHI-PROJECT-21K08361
[Presentation] 小児におけるGATA2異常：最新知識の整理2022
- Author(s)
  平林真介
- Organizer
  第26回小児ＭＤＳ治療研究会
- Data Source
  KAKENHI-PROJECT-18K16128
[Presentation] 遺伝性素因とMDS/白血病2021
- Author(s)
  平林真介
- Organizer
  第83回日本血液学会学術集会
- Data Source
  KAKENHI-PROJECT-21K08361
[Presentation] 小児の骨髄異形成症候群2020
- Author(s)
  平林真介
- Organizer
  小児血液・がん学会北海道セミナー
- Data Source
  KAKENHI-PROJECT-18K16128
[Presentation] 遺伝性骨髄不全症候群オーバービュー2020
- Author(s)
  平林真介
- Organizer
  小児血液・がん学会
- Data Source
  KAKENHI-PROJECT-18K16128
[Presentation] 小児造血器腫瘍におけるクリニカルシーケンスの実行可能性に関する研究2019
- Author(s)
  平林真介　他
- Organizer
  第81回日本血液学会
- Data Source
  KAKENHI-PROJECT-18K16128
[Presentation] MDS-predisposing syndromes; オーバービューと最近の話題2018
- Author(s)
  平林　真介
- Organizer
  小児MDS治療研究会
- Data Source
  KAKENHI-PROJECT-16K21376
[Presentation] MDS-predisposing syndromes; オーバービューと最近の話題2018
- Author(s)
  平林　真介
- Organizer
  小児MDS治療研究会
- Data Source
  KAKENHI-PROJECT-18K16128
[Presentation] ダサチニブ併用による低減集中化学療法を用いたダウン症候群に伴ったPh+急性リンパ性白血病2017
- Author(s)
  平林　真介
- Organizer
  第79回日本血液学会学術集会
- Data Source
  KAKENHI-PROJECT-16K21376
[Presentation] モノソミー7を伴いクローン進化を来たしたPearson症候群2017
- Author(s)
  平林　真介
- Organizer
  第79回日本血液学会学術集会
- Data Source
  KAKENHI-PROJECT-16K21376
[Presentation] IDH1 and KRAS mutations are involved in acute lymphoblastic leukemia in Maffucci syndrome.2017
- Author(s)
  Shinsuke Hirabayashi
- Organizer
  49th Congress of the International Society of Paediatric Oncology, Washington, USA
- Data Source
  KAKENHI-PROJECT-16K21376
[Presentation] IDH1 and KRAS mutations are involved in acute lymphoblastic leukemia in Maffucci syndrome2016
- Author(s)
  平林真介
- Organizer
  第78回日本血液学会学術集会
- Place of Presentation
  横浜市　パシフィコ横浜
- Year and Date
  2016-10-14
- Data Source
  KAKENHI-PROJECT-16K21376

1. 真部淳 (20292849)

# of Collaborated Projects: 2 results

# of Collaborated Products: 2 results
2. 小野澤真弘 (70455632)

# of Collaborated Projects: 2 results

# of Collaborated Products: 3 results
3. 鳴海覚志 (40365317)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
4. 三谷絹子 (50251244)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
5. 松川敏大 (20963169)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
6. 藤原亨

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results

Hirabayashi Shinsuke 平林 真介

HIRABAYASHI Shinsuke 平林 真介

Research Projects

Research Products

Co-Researchers

NUP98::NSD1白血病の治療抵抗性の解明と新規治療法の開発

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

小児・AYA世代におけるMDSの発生機序と治療戦略の解明Principal Investigator

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

Analysis of germline predisposition and clinical features of childhood and AYA myelodysplastic syndromePrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

Research for mechanism of hematological malignancies in rare syndrome in childrenPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

[Book] 血液フロンティア 2016年11月号2016

Author(s)

Publisher

Data Source

[Journal Article] Clinical features of complex karyotype in newly diagnosed acute myeloid leukemia2023

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Hematopoietic cell transplantation for hematological malignancies in Bloom syndrome2023

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Association of unbalanced translocation der(1;7) with germline GATA2 mutations2021

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Clinical evolution, genetic landscape and trajectories of clonal hematopoiesis in SAMD9/SAMD9L syndromes2021

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Acquisition of monosomy 7 and a RUNX1 mutation in Pearson syndrome2020

Author(s)

Journal Title

DOI

Data Source

[Journal Article] 遺伝性造血器腫瘍2020

Author(s)

Journal Title

Data Source

[Journal Article] Synonymous GATA2 mutations result in selective loss of mutated RNA and are common in patients with GATA2 deficiency2020

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Dasatinib and low-intensity chemotherapy for Philadelphia chromosome-positive acute lymphoblastic leukemia in a child with Down syndrome2019

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Childhood cancer and familial tumors2019

Author(s)

Journal Title

DOI

NAID

ISSN

Language

Data Source

Hirabayashi Shinsuke 平林真介

HIRABAYASHI Shinsuke 平林真介

[Book] 血液フロンティア　2016年11月号2016