Rchr
J-GLOBAL ID:200901048932710758   Update date: Apr. 14, 2024

Yamagata Takanori

ヤマガタ タカノリ | Yamagata Takanori
Affiliation and department:
Job title: Professor
Research field  (3): Fetal medicine/Pediatrics ,  Medical biochemistry ,  Neuroscience - general
Research keywords  (6): developmental disorder ,  pediatric neurology ,  neuroscience ,  human genetics ,  pediatrics ,  New Science in General
Research theme for competitive and other funds  (20):
  • 2019 - 2023 Development of treatment for autism spectrum disorder relating with oxytocin and miRNA
  • 2016 - 2019 Genetic analysis for autism spectrum disorder and intellectual disability focusing on synaptic network abnormality
  • 2013 - 2016 Genetic and molecular analyses of causative genes for autism-spectrum disorders
  • 2012 - 2016 Comprehensive analyses of causative genes for intellectual disability and autism-spectrum disorders
  • 2006 - 2008 candidate gene analysis for autism focusing on the epigenetic mechanism
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Papers (328):
  • Akihiko Miyauchi, Chika Watanabe, Naoya Yamada, Eriko F Jimbo, Mizuki Kobayashi, Natsumi Ohishi, Atsuko Nagayoshi, Shiho Aoki, Yoshihito Kishita, Akira Ohtake, et al. Apomorphine is a potent inhibitor of ferroptosis independent of dopaminergic receptors. Scientific reports. 2024. 14. 1. 4820-4820
  • Ayumi Matsumoto, Shintaro Kano, Natsumi Kobayashi, Mitsuru Matsuki, Rieko Furukawa, Hirokazu Yamagishi, Hiroki Yoshinari, Waka Nakata, Hiroko Wakabayashi, Hidetoshi Tsuda, et al. Unfavorable switching of skewed X chromosome inactivation leads to Menkes disease in a female infant. Scientific reports. 2024. 14. 1. 440-440
  • Ayaka Ikeda, Yoko Hakuno, Kosuke Asada, Takahiro Ikeda, Takanori Yamagata, Masahiro Hirai. Development of emotion comprehension in children with autism spectrum disorder and Williams syndrome. Autism research : official journal of the International Society for Autism Research. 2023
  • 瀬戸 翔太, 北村 薫, 三谷 忠宏, 橋口 万里奈, 浅井 眞穂, 門田 行史, 村松 一洋, 小坂 仁, 山形 崇倫, 田島 敏広. グアンファシン過量内服による臨床像について. 栃木県医学会々誌. 2023. 53. 10-10
  • Koyuru Kurane, Keizo Wakae, Hirokazu Yamagishi, Yuta Kawahara, Marika Ono, Daisuke Tamura, Kaito Furuya, Naoyuki Taga, Mitsuru Matsuki, Takanori Yamagata, et al. The first case of hemorrhagic shock and encephalopathy syndrome with fulminant hypercytokinemia associated with pediatric COVID-19. Brain and Development. 2023
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MISC (187):
  • Takahiro Ikeda, Akari Inoue, Masako Nagashima-Kawada, Tatsuya Tokuda, Takanori Yamagata, Ippeita Dan, Yukifumi Monden. Neural Bases of Executive Function in ADHD Children as Assessed Using fNIRS. Frontiers in Clinical Drug Research - CNS and Neurological Disorders. 2022. 10. 188-225
  • 松本歩, 津田英利, 池田尚広, 宮内彰彦, 橋口万里奈, 門田行史, 轡田行信, 渡邊和寿, 村松一洋, 小坂仁, et al. 難治性てんかん,光,音過敏を呈したDNM1L変異の1歳男児例. 日本人類遺伝学会大会プログラム・抄録集. 2022. 67th (CD-ROM)
  • 田中大輔, 池田尚広, 橋口万里奈, 松本歩, 門田行史, 村松一洋, 小坂仁, 山形崇倫. シトリン欠損症合併SCN8A変異例におけるphenytoinの有効性と乳児期早期胆道酵素上昇作用. 脳と発達. 2022. 54. 1
  • 倉田和美, 柳橋達彦, 門田行史, 池田尚宏, 山形崇倫, 阿部隆明. 2年間体重が増えずに発症した摂食障害患児の治療経過~児童精神科と小児科との治療連携と役割分担~. 日本小児科学会雑誌. 2022. 126. 5
  • 石垣景子, 石垣景子, 石垣景子, 中川栄二, 中川栄二, 山形崇倫, 青木吉嗣, 横井貴之. 神経筋疾患の最新の遺伝子治療を考える. 脳と発達. 2022. 54. 2
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Education (2):
  • - 1986 Gifu University School of Medicine Medical Course
  • - 1986 Gifu University Faculty of Medicine
Professional career (1):
  • (BLANK) (Jichi Medical University)
Work history (5):
  • 2011/05 - 現在 Department of Pediatrics, Jichi Medical University Professor
  • 1997/11 - 2000/03 Departement of Molecular and Human Genetics research fellow
  • 1997 - 2000 Research Associate, Department of Molecular
  • Medicine, USA
  • and Human Genetics, Baylor College of
Association Membership(s) (13):
American society of gene and cell therapy ,  Japanese society of gene and cell therapy ,  Japanese Society for Mass-screening ,  Japanese Society for Neuroinfectious Diseases ,  JAPANESE SOCIETY OF NEUROLOGY ,  The Japan Society of Pediatric Genetics ,  日本ADHD学会 ,  JAPANESE SOCIETY FOR INHERITED METABOLIC DISEASES ,  The American Society of Human Gevetics ,  The Japan Epilepsy Society ,  THE JAPAN SOCIETY OF HUMAN GENETICS ,  THE JAPANESE SOCIETY OF CHILD NEUROLOGY ,  JAPAN PEDIATRIC SOCIETY
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