Rchr
J-GLOBAL ID:200901066999967077   Update date: Aug. 31, 2020

Inoue Ken

イノウエ ケン | Inoue Ken
Affiliation and department:
Job title: Head
Research field  (3): Medical biochemistry ,  Systems genomics ,  Genomics
Research keywords  (4): hypomyelinating leukodystrophy ,  neurogenetics ,  myelin ,  human genome
Research theme for competitive and other funds  (3):
  • 1998 - 2010 Human inherited diseases caused by SOX10 mutations
  • 1995 - 2010 Molecular genetics of Pelizaeus Merzbacher disease
  • 2004 - 2009 Physiological roles of non-sense mediated mRNA decay
Papers (78):
  • Kenshiro Tabata, Aritoshi Iida, Eri Takeshita, Eiji Nakagawa, Noriko Sato, Masayuki Sasaki, Ken Inoue, Yu-Ichi Goto. A novel pathogenic NFIX variant in a Malan syndrome patient associated with hindbrain overcrowding. Journal of the neurological sciences. 2020. 412. 116758-116758
  • Hadia Hijazi, Fernanda S Coelho, Claudia Gonzaga-Jauregui, Laura Bernardini, Soe S Mar, Melanie A Manning, Andrea Hanson-Kahn, SakkuBai Naidu, Siddharth Srivastava, Jennifer A Lee, Julie R Jones, Michael J Friez, Thomas Alberico, Barbara Torres, Ping Fang, Sau Wai Cheung, Xiaofei Song, Angelique Davis-Williams, Carly Jornlin, Patricia A Wight, Pankaj Patyal, Jennifer Taube, Andrea Poretti, Ken Inoue, Feng Zhang, Davut Pehlivan, Claudia M B Carvalho, Grace M Hobson, James R Lupski. Xq22 deletions and correlation with distinct neurological disease traits in females: Further evidence for a contiguous gene syndrome. Human mutation. 2020. 41. 1. 150-168
  • Ayaka Hirasawa-Inoue, Eri Takeshita, Yuko Shimizu-Motohashi, Akihiko Ishiyama, Takashi Saito, Hirofumi Komaki, Eiji Nakagawa, Kenji Sugai, Ken Inoue, Yu-Ichi Goto, Masayuki Sasaki. Static Leukoencephalopathy Associated with 17p13.3 Microdeletion Syndrome: A Case Report. Neuropediatrics. 2019. 50. 6. 387-390
  • Aritoshi Iida, Kyoko Takano, Eri Takeshita, Chihiro Abe-Hatano, Shinichi Hirabayashi, Yuji Inaba, Shunichi Kosugi, Yoichiro Kamatani, Yukihide Momozawa, Michiaki Kubo, Eiji Nakagawa, Ken Inoue, Yu-Ichi Goto. A novel PAK3 pathogenic variant identified in two siblings from a Japanese family with X-linked intellectual disability: case report and review of the literature. Cold Spring Harbor molecular case studies. 2019. 5. 6
  • Kouga T, Koizume S, Aoki S, Jimbo E, Yamagata T, Inoue K, Osaka H. Drug screening for Pelizaeus-Merzbacher disease by quantifying the total levels and membrane localization of PLP1. Molecular genetics and metabolism reports. 2019. 20. 100474
more...
MISC (43):
  • 平澤 絢香, 竹下 絵里, 本橋 裕子, 石山 昭彦, 齋藤 貴志, 小牧 宏文, 中川 栄二, 須貝 研司, 井上 健, 後藤 雄一, 佐々木 征行. 大脳白質異常、多発奇形からアレイCGHで診断した17p13.3微細欠失症候群の1例. 脳と発達. 2018. 50. 5. 372-372
  • 井上 健, 黒澤 健司, 才津 浩智, 山本 俊至, 小坂 仁, 高梨 潤一. 先天性大脳白質形成不全症の診断サポートのためのコンサルテーションボード. 脳と発達. 2018. 50. Suppl. S302-S302
  • 植松 有里佳, 植松 貢, 佐藤 亮, 井上 健, 呉 繁夫. 線維芽細胞から神経細胞へのdirect conversionによる疾患原因遺伝子変異の機能解析. 脳と発達. 2018. 50. Suppl. S346-S346
  • 小坂 仁, 井上 健, 久保田 雅也, 黒澤 健司, 才津 浩智, 佐々木 征行, 高梨 潤一, 松井 大, 三重野 牧子, 山本 俊至, 吉田 誠克. 遺伝性白質疾患の診断・治療・研究システムの構築. 脳と発達. 2017. 49. Suppl. S208-S208
  • Leo Gotoh, Ken Inoue, Guy Heiman, Sara Mora, Kiran Maski, Janet S. Soul, Miriam Bloom, Sarah H. Evans, Yu-ichi Goto, Ljubica Caldovic, Grace M. Hobson, Adeline Vanderver. GJC2 promoter mutations causing Pelizaeus-Merzbacher-like disease (vol 111, pg 393, 2014). MOLECULAR GENETICS AND METABOLISM. 2016. 119. 3. 113-113
more...
Books (1):
  • Inoue K, Lupski JR. Mendelian, Non-mendelian, multigenetic and complex traits. In: Rosenberg RN, Prusiner SB, DiMauro S, Barchi RL, Nestler EJ, eds. The Molecular Basis of Neurological and Psychiatric Disease. Third edition.
    Butter Heinemann. Philadelphia, PA.
Works (2):
  • Human Inherited diseases caused by SOX10 mutations
    2004 - 2010
  • Molecular Genetics of Pelizaeus-Merzbacher disease
    2004 - 2010
Education (3):
  • 1990 - 1994 Yokohama City University Graduate Graduate School of Medicine
  • - 1994 Yokohama City University Graduate School, Division of Medicine psychiatry
  • Yokohama City University School of Medicine Medicine
Professional career (2):
  • Ph.D. (Yokohama City University(Japan))
  • M.D. (Yokohama City University(Japan))
Work history (8):
  • 2004 - 現在 Division chief. National Institute of Neuroscience,
  • 2002 - 2004 Assistant Professor. Baylor College of Medicine,
  • 1997 - 2002 Post doc. Baylor College of Medicine,
  • 1992 - 1993 Post doc. Univ. California, San Diego
  • National Center of Neurology and Psychiatry
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Association Membership(s) (2):
American Society of Human Genetics ,  Japan Society of Human Genetics
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