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SASAKI Masayuki  佐々木 柾行

ORCIDConnect your ORCID iD *help
Researcher Number 60235273
Other IDs
Affiliation (based on the past Project Information) *help 2016: 国立精神・神経医療研究センター病院, 小児神経診療部, 部長
2012: 国立精神, 神経医療研究センター病院, 部長
Review Section/Research Field
Except Principal Investigator
Radiation science / Pediatrics
Keywords
Except Principal Investigator
SPECT / 限局性皮質異型性 / 画像統計解析 / PET / MR / epilepsy / DTI / MRI / 画像解析 / てんかん … More / シーケンサー / 精神発達 / 比較 / レット症候群 / 双子 / 神経疾患 / 自閉症 / エピゲノム / エピジェネティクス / 次世代シーケンサー / 双生児 / 精神発達障害 / 遺伝子 / ゲノム Less
  • Research Projects

    (2 results)
  • Research Products

    (5 results)
  • Co-Researchers

    (5 People)
  •  Multifaced imaging analysis in patients with intractable epilepsy: a study for surgical treatment approach

    • Principal Investigator
      Sato Noriko
    • Project Period (FY)
      2013 – 2016
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Radiation science
    • Research Institution
      National Center of Neurology and Psychiatry
  •  Comparison of genomic and epigenomicexpression in monozygotic twins using next-generation sequencing.

    • Principal Investigator
      KUBOTA Takeo
    • Project Period (FY)
      2011 – 2012
    • Research Category
      Grant-in-Aid for Challenging Exploratory Research
    • Research Field
      Pediatrics
    • Research Institution
      University of Yamanashi

All 2016 2013 2012

All Journal Article Presentation

  • [Journal Article] Comparison of genomic and epigenomic expression in monozygotic twins discordant for Rett syndrome2013

    • Author(s)
      Miyake K,Yang C,Minakuchi Y, OhoriK,Soutome M,HirasawaT,KazukiY, Adachi N,Suzuki S, Itoh M, Goto Y, Andoh T, KurosawaH, OshimuraM, SasakiM, Toyoda A, Kubota T
    • Journal Title

      PLoS ONE

      Volume: (印刷中)

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23659519
  • [Journal Article] Spread of X-chromosome inactivation into chromosome 15 is associated with Prader-Willi syndrome phenotype in a boy with a t(X;15)(p21.1;q11.2) translocation.2012

    • Author(s)
      Sakazume S, et al.
    • Journal Title

      Hum Genet

      Volume: 131 Issue: 1 Pages: 121-130

    • DOI

      10.1007/s00439-011-1051-4

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23390272, KAKENHI-PROJECT-23659519
  • [Journal Article] Spread of X-chromosome inactivation into chromosome 15 is associated with Prader-Willi syndrome phenotype in a boy with a t(X;15)(p21.1;q11.2) translocation.2012

    • Author(s)
      Sakazume S, Ohashi H, Sasaki Y, Harada N, Nakanishi K, Sato H, Emi M, Endoh K, Sohma R, Kido Y, Nagai T, Kubota T.
    • Journal Title

      Hum Genet

      Volume: 131 Pages: 121-130

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23659519
  • [Presentation] 難治てんかんで発症した Rosette-forming glioneuronal tumor の1例2016

    • Author(s)
      住友典子,中川栄二,石山昭彦,竹下絵里,本橋裕子,齋藤貴志,小牧宏文,須貝研司,高橋章夫,大槻泰介,佐藤典子,澁谷誠,齊藤祐子,佐々木征行
    • Organizer
      多摩神経懇話会
    • Place of Presentation
      東京
    • Year and Date
      2016-06-16
    • Data Source
      KAKENHI-PROJECT-25461865
  • [Presentation] 2型ICF症候群の原因遺伝子候補ZBTB24の機能解析.2012

    • Author(s)
      新田洋久、久保田健夫、古庄知己、高橋浩士、佐々木裕之.
    • Organizer
      日本人類遺伝学会第57回大会
    • Place of Presentation
      京王プラザホテル(東京都)
    • Data Source
      KAKENHI-PROJECT-23659519
  • 1.  KUBOTA Takeo (70293511)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 3 results
  • 2.  TOYODA Atsushi (10267495)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 1 results
  • 3.  Sato Noriko (10322017)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 1 results
  • 4.  SONE Daichi
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 5.  KIMURA Yukio
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results

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