Biomedical research such as iPS cell research and genome research is dramatically advancing. However, in translating this research development into clinical settings, it is important not only to promote science but also to take into account its social implication. We would like to deliver the benefits of this science promotion to society under ethical, legal and social considerations. In this process, through discussion with various international and domestic stakeholders, we hope to value the diversity and breadth of these stakeholders’ perspectives.
Please contact me if you’re interested in working together.
Email: jusaku.minari*cira.kyoto-u.ac.jp（Please change* to @）
2005 B.S., Faculty of Environmental Engineering The University of Kitakyushu
2006 M.S., Graduate School of Environmental Engineering The University of Kitakyushu
2010 Ph.D., Graduate School of Environmental Engineering The University of Kitakyushu
2010 Postdoctoral Researcher, Institute for Research in Humanities Kyoto University
2013 Assistant Professor, Biomedical Ethics and Public Policy Graduate School of
Medicine Osaka University
2015 Deputy Director, Department of Research Infrastructure Japan Agency for
Medical Research and Development (AMED)
2016 Assistant Professor, Biomedical Ethics and Public Policy Graduate School of
Medicine Osaka University
2017 Project Associate Professor, Uehiro Research Division for
iPS Cell Ethics Center of iPS Cell Research and Application
- 2019 - Present
Collaboration with HeLEX (Faculty of Law, the University of Oxford)
- 2018 - Present
Committee Member of the Governmental Ethical Guidelines
(Human Genome Research, and General Medical Research)
- 2017 - Present
JST* Program Advisor (Future Society & AI)
- 2016 - Present
AMED Program Officer (Genome Research)
- 2016 - 2018
AMED** Program Officer (ELSI on Genome Research)
*JST: Japan Science and Technology Agency
**AMED: Japan Agency for Medical Research and Development
- M. Prictor, MA. Lewis, AJ. Newson, M. Haas, S. Baba, H. Kim, M. Kokado, J. Minari, F. Molnár-Gábor, B. Yamamoto, J. Kaye and HJA. Teare. Dynamic consent: an evaluation and reporting framework. Journal of Empirical Research on Human Research Ethics, Vol. 15, 2020.
- A. Hibino, G. Yoshizawa and J. Minari. Meaning of ambiguity: a Japanese survey on synthetic biology and genome editing. Frontiers in Sociology, 4:81, 2019.
- Y. Hishiyama, J. Minari and N Suganuma. The survey of public perception and general knowledge of genomic research and medicine in Japan conducted by the Japan Agency for Medical Research and Development. Journal of Human Genetics, Vol. 64, pp 397-407, 2019.
- J. Minari. Ethical, social and policy considerations for realizing genomic medicine. BIO Clinica, Vol. 33, pp 63-66, 2018 (in Japanese).
- J. Minari. “Genomic medicine,” in Bioethics: inheritance and development. ed. M. Maruyama (Kawashima Shoten, 2018) (in Japanese).
- J. Minari, K. B. Brothers and M. Morrison. Tensions in ethics and policy created by National Precision Medicine Programs. Human Genomics (Opinion Article) , 12:22, 2018.
- J. Minari, O. Kato, M. Sakurai and A. Saito. The novel approach of AMED in realizing genomic medicine: the process of achieving the AMED data sharing policy. Idenshi Igaku MOOK, Vol. 33, pp 168-172, 2018 (in Japanese).
- J. Kaye, S. F. Terry, E. Juengst, S. Coy, J. R. Harris, D. Chalmers, E. S. Dove, I. Budin-Ljosne, C. Adebamowo, E. Ogbe, L. Bezuidenhout, M. Morrison, J. T. Minion, M. J. Murtagh, J. Minari, H. Teare, R. Isasi, K. Kato, E. Rial-Sebbag, P. Marshall, B. Koenig and A. Cambon-Thomsen. Including all voices in international data-sharing governance. Human Genomics (Opinion Article) , 12:13, 2018.
- J. Minari. Island lessons: inheritance, solidarity, creativity (Considerations of islands, science and technologies and art). Islands, Vol. 253, pp 56-59, 2018 (in Japanese).
- J. Minari and G. Yoshizawa. Ethics policy and public engagement in biomedical research on genomic information. Journal of Medicine, Life and Ethics, Society, Vol. 14, pp 52-60, 2017 (in Japanese).
- V. Coathup, H. Teare, J. Minari, G. Yoshizawa, J. Kaye, M. Takahashi and K. Kato. Using digital technologies to engage with medical research: views of myotonic dystrophy patients in Japan. BMC Medical Ethics, 17:51, 2016.
- D. Chalmers, D. Nicol, J. Kaye, J. Bell, A. V. Campbell, C. W. Ho, K. Kato, J. Minari, C. H. Ho, C. Mitchell, F. Molnár-Gábor, M. Otlowski, D. Thiel, S. M. Fullerton and T. Whitton. Has the biobank bubble burst? Withstanding the challenges for sustainable biobanking in the digital era. BMC Medical Ethics (Review) , 17:39, 2016.
- J. Minari. Genomic data sharing in the personal genome era: data sharing policy and ethical considerations. Journal of Medicine, Life and Ethics, Society, Vol. 12, pp 105-114, 2015 (in Japanese).
- J. Minari, H. Teare, C. Mitchell, J. Kaye and K. Kato. The emerging need for family-centric initiatives for obtaining consent in personal genome research. Genome Medicine (Comment) , 6:118, 2014.
- J. Minari, D. Chalmers and K. Kato. Return of genetic research results: the Japanese experience and its implications for the international debate. SCRIPTed (Analysis) , Vol. 11, pp 180-192, 2014.
- G. Yoshizawa, C. W. Ho, W. Zhu, C. Hu, Y. Syukriani, I. Lee, H. Kim, D. F. Tsai, J. Minari and K. Kato. ELSI practices in genomic research in East Asia: implications for research collaboration and public participation. Genome Medicine (Review) , 6:39, 2014.
- J. Minari, T. Shirai and K. Kato. Ethical considerations of research policy for personal genome analysis: the approach of the Genome Science Project in Japan. Life Sciences, Society and Policy, 10:4, 2014.
- J. Minari and K. Kato. Research governance in the personal genome era. Medicine and Drug Journal, Vol. 50, pp 55-58, 2014 (in Japanese).