Rchr
J-GLOBAL ID：201801020816091151   Update date: May. 16, 2024

Akagawa Hiroyuki

アカガワ ヒロユキ | Akagawa Hiroyuki
Affiliation and department：
Tokyo Women's Medical University

About Tokyo Women's Medical University


Research field  (1)： Neurosurgery
Research theme for competitive and other funds  (19)：
  • 2023 - 2026 特発性頚部内頚動脈攣縮症の遺伝子改変モデルラットを用いた病態解明研究
  • 2021 - 2024 リアルタイムPCRを用いた術中迅速遺伝子診断による新たな神経膠腫手術戦略の確立
  • 2021 - 2024 システマチックアプローチによるMonogenic diabetes発症機序の解明
  • 2019 - 2022 もやもや症候群の基礎疾患遺伝子群に対するターゲット遺伝子シーケンシング
  • 2018 - 2022 Analysis of rare variants in RNF213 in patients of cerebral aneurysm
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Papers (68)：
  • Satoshi Tanaka, Hiroyuki Akagawa, Kenkou Azuma, Sayaka Higuchi, Atsushi Ujiie, Koshi Hashimoto, Naoko Iwasaki. High prevalence of copy number variations in the Japanese participants with suspected MODY. Clinical Genetics. 2024
  • Tadashi Inoue, Ryuta Takase, Keiko Uchida, Kazuki Kodo, Kenji Suda, Yoriko Watanabe, Koh-Ichiro Yoshiura, Masaya Kunimatsu, Reina Ishizaki, Kenko Azuma, et al. Correction: The c.1617del variant of TMEM260 is identified as the most frequent single gene determinant for Japanese patients with a specific type of congenital heart disease. Journal of human genetics. 2024. 69. 5. 223-223
  • Ayako Chida-Nagai, Hiroyuki Akagawa, Saori Sawai, Yue-Jiao Ma, Satoshi Yakuwa, Jun Muneuchi, Kazushi Yasuda, Hirokuni Yamazawa, Toshiyuki Yamamoto, Emi Takakuwa, et al. Identification of Prostaglandin I2 Synthase Rare Variants in Patients With Williams Syndrome and Severe Peripheral Pulmonary Stenosis. Journal of the American Heart Association. 2024. e032872
  • Tadashi Inoue, Ryuta Takase, Keiko Uchida, Kazuki Kodo, Kenji Suda, Yoriko Watanabe, Koh-Ichiro Yoshiura, Masaya Kunimatsu, Reina Ishizaki, Kenko Azuma, et al. The c.1617del variant of TMEM260 is identified as the most frequent single gene determinant for Japanese patients with a specific type of congenital heart disease. Journal of human genetics. 2024
  • Yusuke Ushio, Hiroshi Kataoka, Hiroyuki Akagawa, Masayo Sato, Shun Manabe, Keiko Kawachi, Shiho Makabe, Taro Akihisa, Momoko Seki, Atsuko Teraoka, et al. Factors associated with early-onset intracranial aneurysms in patients with autosomal dominant polycystic kidney disease. Journal of nephrology. 2024
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MISC (73)：
  • 赤川 浩之. 遺伝医学アップデート 基礎医学から臨床現場まで 脳動脈瘤の感受性遺伝子の解析. 東京女子医科大学雑誌. 2023. 93. 2. 49-56
  • 稲次基希, THIPARPA Thamamongood, 原祥子, 石嶋希美, 田中洋次, 赤川浩之, 成相直, 前原健寿. Three cases of moyamoya disease who had vestibulobasilar stenoocclusive lesion. 小児の脳神経(Web). 2023. 48. 2
  • 原 祥子, 成相 直, 矢藤 優一, タンマモングッド・ティプアーパー, 赤川 浩之, 糟谷 英俊, 前原 健寿. RNF213 p.R4810K変異遺伝子変異と小児もやもや病の臨床像. 小児の脳神経. 2021. 46. 2. 199-199
  • Thyroid Autoantibodies and Genotype of RNF213 in Moyamoya Disease. 2020
  • 山本 圭子, 今泉 太一, 赤川 浩之, 菅野 仁, 山本 俊至. 選択的IgG2低下を示し中耳炎を反復したZBTB20のde novo変異によるPrimrose症候群の1例(Primrose syndrome caused by ZBTB20 mutation with recurrent otitis media and IgG2 deficiency). 脳と発達. 2020. 52. Suppl. S306-S306
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Lectures and oral presentations  (3)：
  • もやもや病の感受性遺伝子
    (ICSVD2024 International Seminar of Cerebrovascular Disease 2024)
  • ゲノム解析におけるウエブツール・データベースの利用法
    (第7回ゲノム医学研究会講演会 2024)
  • Exome sequencing identified CCER2 as a novel candidate gene for Moyamoya disease
    (5th International Moyamoya Meeting (IMM2018) 2018)
Awards (2)：
  • 2007/10 - 日本脳神経外科学会 学会奨励賞 血管障害
  • 2003/10 - 第62回日本脳神経外科学会総会 優秀演題賞
Association Membership(s) (3)：
THE JAPAN SOCIETY OF HUMAN GENETICS ,  THE JAPAN STROKE SOCIETY ,  The Japan Neurosurgical Society
※ Researcher’s information displayed in J-GLOBAL is based on the information registered in researchmap. For details, see here.

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