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Nagata Eiko  永田 絵子

Researcher Number 90535569
Other IDs
  • ORCIDhttps://orcid.org/0000-0002-0353-8565
Affiliation (based on the past Project Information) *help 2018 – 2019: 浜松医科大学, 医学部附属病院, 特任講師
2017: 浜松医科大学, 医学部, 特任助教
2016: 浜松医科大学, 医学部附属病院, 特任助教
2015: 浜松医科大学, 医学部附属病院, 助教
2014: 浜松医科大学, 医学部, 特任研究員
Review Section/Research Field
Principal Investigator
Pediatrics
Keywords
Principal Investigator
臨床遺伝学 / 遺伝子解析 / 先天異常 / ゲノム / 遺伝学 / ヒトゲノム解析 / 希少疾患 / 整形外科学 / 先天奇形 / 小児科学 / 人類遺伝学 / 原因遺伝子 / 裂手裂足症
  • Research Projects

    (2 results)
  • Research Products

    (7 results)
  • Co-Researchers

    (5 People)
  •  Elucidating the mechanisms that causes SHFMPrincipal Investigator

    • Principal Investigator
      NAGATA EIKO
    • Project Period (FY)
      2016 – 2019
    • Research Category
      Grant-in-Aid for Young Scientists (B)
    • Research Field
      Pediatrics
    • Research Institution
      Hamamatsu University School of Medicine
  •  Genetic mechanism of split-hand/foot malformation with or without long bone deficiencyPrincipal Investigator

    • Principal Investigator
      Nagata Eiko
    • Project Period (FY)
      2013 – 2016
    • Research Category
      Grant-in-Aid for Young Scientists (B)
    • Research Field
      Pediatrics
    • Research Institution
      Hamamatsu University School of Medicine

All 2019 2016 2015 2014 Other

All Journal Article Presentation

  • [Journal Article] Comprehensive clinical and molecular studies in split-hand/foot malformation: identification of two plausible candidate genes (LRP6 and UBA2)2019

    • Author(s)
      Yamoto Kaori、Saitsu Hirotomo、Nishimura Gen、Kosaki Rika、Takayama Shinichiro、Haga Nobuhiko、Tonoki Hidefumi、Okumura Akihisa、Horii Emiko、Okamoto Nobuhiko、Suzumura Hiroshi、Ikegawa Shiro、Kato Fumiko、Fujisawa Yasuko、Nagata Eiko、Takada Shuji、Fukami Maki、Ogata Tsutomu
    • Journal Title

      European Journal of Human Genetics

      Volume: 27 Issue: 12 Pages: 1845-1857

    • DOI

      10.1038/s41431-019-0473-7

    • Peer Reviewed / Open Access / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-18K07890, KAKENHI-PLANNED-17H06428, KAKENHI-PROJECT-17H04204, KAKENHI-PROJECT-16K21079
  • [Journal Article] Femoral-tibial-digital malformations in a boy with the Japanese founder triplication of BHLHA9.2015

    • Author(s)
      Nagata E, Haga N, Fujisawa Y, Fukami M, Nishimura G, Ogata T.
    • Journal Title

      Am J Med Genet A

      Volume: 167 Issue: 12 Pages: 3226-3228

    • DOI

      10.1002/ajmg.a.37290

    • Peer Reviewed / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-26461524, KAKENHI-PROJECT-26870255, KAKENHI-PROJECT-25253023
  • [Journal Article] Japanese founder duplications/triplications involving BHLHA9 are associated with split-hand/foot malformation with or without long bone deficiency and Gollop-Wolfgang complex.2014

    • Author(s)
      Nagata E, Kano H, Kato F, Yamaguchi R, Nakashima S, Takayama S, Kosaki R, Tonoki H, Mizuno S, Watanabe S, Yoshiura KI, Kosho T, Hasegawa T, Kimizuka M, Suzuki A, Shimizu K, Ohashi H, Haga N, Numabe H, Horii E, Nagai T, Yoshihashi H, Nishimura G, Toda T, et al.
    • Journal Title

      Orphanet J Rare Dis

      Volume: 9 Issue: 1 Pages: 125-125

    • DOI

      10.1186/s13023-014-0125-5

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PLANNED-22129006, KAKENHI-PLANNED-22132004, KAKENHI-PROJECT-22227002, KAKENHI-PROJECT-25253023, KAKENHI-PROJECT-26253057, KAKENHI-PROJECT-26870255
  • [Presentation] 若手シンポジウム2016

    • Author(s)
      永田絵子
    • Organizer
      日本小児遺伝学術集会
    • Place of Presentation
      東京
    • Year and Date
      2016-12-09
    • Invited
    • Data Source
      KAKENHI-PROJECT-26870255
  • [Presentation] 若手シンポジウム2016

    • Author(s)
      永田絵子
    • Organizer
      日本小児遺伝学会学術集会
    • Place of Presentation
      東京
    • Year and Date
      2016-12-09
    • Invited
    • Data Source
      KAKENHI-PROJECT-16K21079
  • [Presentation] HOXDクラスターを含む2q31領域ヘテロ欠失と外陰部・四肢形成不全2015

    • Author(s)
      永田絵子
    • Organizer
      第49回日本小児内分泌学会学術集会
    • Place of Presentation
      タワーホール船堀
    • Year and Date
      2015-10-08
    • Data Source
      KAKENHI-PROJECT-26870255
  • [Presentation] BHLHA9を含む約200 kbの同一領域の日本人創始者コピー数増加は四肢形成不全発症の顕著な感受性因子である

    • Author(s)
      永田絵子
    • Organizer
      日本小児内分泌学会
    • Place of Presentation
      アクトシティ浜松
    • Year and Date
      2014-09-25 – 2014-09-27
    • Data Source
      KAKENHI-PROJECT-26870255
  • 1.  Fukami Maki (40265872)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 2.  Ogata Tsutomu (40169173)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 3.  藤澤 泰子
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 4.  戸田 達史
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 5.  奥村 彰久
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results

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