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2009 Fiscal Year Final Research Report

Study for establishment of genome medical research supporting system

Research Project

  • PDF
Project/Area Number 17019003
Research Category

Grant-in-Aid for Scientific Research on Priority Areas

Allocation TypeSingle-year Grants
Review Section Biological Sciences
Research InstitutionChiba University

Principal Investigator

HATA Akira  Chiba University, 大学院・医学研究院, 教授 (00244541)

Co-Investigator(Kenkyū-buntansha) KUBOTA Motoo  千葉大学, 医学部附属病院, 助手 (10225211)
ISHII Takuma  千葉大学, 大学院・医学研究院, 助手 (70312452)
Project Period (FY) 2005 – 2009
Keywordsゲノム / 研究支援 / インフォームド・コンセント
Research Abstract

The aim of this study is to find out what kind of supporting system to recruit samples for genome medical research is most effective, convenient, and ethical in Japan. For common diseases, support personnel for informed consent procedures are reveled to be the most demanding. We decided to establish genome research coordinator accreditation system. Now we have the system based on the Japanese Human Genetic Society, and a significant number of coordinators have been certified. For rare diseases, nation-wide network of certified medical geneticists was constructed.

  • Research Products

    (8 results)

All 2009 2008 Other

All Journal Article (5 results) Book (1 results) Remarks (2 results)

  • [Journal Article] International web-based survey of informed consent procedures in genetic epidemiological studies: towards the establishment of a research coordinator accrefitation system.2009

    • Author(s)
      Yamamoto M, Funamizu M, Muto K, Hata A.
    • Journal Title

      J Hum Genet. 54

      Pages: 713-720

  • [Journal Article] CD14 and IL4R gene polymorphisms modify the effect of day care attendance on serum IgE levels.2009

    • Author(s)
      Suzuki Y, Hattori S, Mashimo Y, Funamizu M, Kohno Y, Okamoto Y, Hata A, Shimojo N.
    • Journal Title

      J Allergy Clin Immunol. 123

      Pages: 1408-1411

  • [Journal Article] Susceptibility loci for intracranial aneurysm in European and Japanese populations.2008

    • Author(s)
      Bilguvar K, Yasuno K, Niemela M,Ruigrok YM, von Und Zu Fraunberg M, vanDuijn CM, van den Berg LH, Mane S,Mason CE, Choi M, Gaal E, Bayri Y, KolbL, Arlier Z, Ravuri S, Ronkainen A,Tajima A, Laakso A, Hata A, Kasuya H,Koivisto T, Rinne J, Ohman J, BretelerMM, Wijmenga C, State MW, Rinkel GJ,Hernesniemi J, Jaaskelainen JE,Palotie A, Inoue I, Lifton RP, GunelM.
    • Journal Title

      Nature Genet 40

      Pages: 1472-1477

  • [Journal Article] Heterozygous Deletion at 14q22. 1-q22. 3 including the BMP4 gene in a Patient with Psychomotor Retardation, Congenital Corneal Opacity and Feet Polysyndactyly.2008

    • Author(s)
      Hayashi S, Okamoto N, Yoshio Makita Y, Hata A, Imoto I, Inazawa J.
    • Journal Title

      Am J Med Genet. 146A

      Pages: 2905-2910

  • [Journal Article] The CASK gene harbored in a deletion detected by array-CGH as a potential candidate for a gene causative of X-linked dominant mental retardation.2008

    • Author(s)
      Hayashi S, Mizuno S, Migita O, Okuyama T, Makita Y, Hata A, Imoto I, Inazawa J.
    • Journal Title

      Am J Med Genet. 146A

      Pages: 2145-2151

  • [Book] アレイCGH診断活用ガイドブック-知っておきたい染色体微細構造異常症-稲澤譲治(羽田明編)2008

    • Author(s)
      蒔田芳男
    • Total Pages
      239
    • Publisher
      医薬ジャーナル社
  • [Remarks]

    • URL

      http://www.genome-sci.jp/kumomaku/

  • [Remarks]

    • URL

      http://jshg.jp/qualifications/gmrc.html

URL: 

Published: 2011-06-18   Modified: 2016-04-21  

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