Framework and Practical Guidance for the Ethical Use of Electronic Methods for Communication With Participants in Medical Research

by Atsushi Kogetsu, Kazuto Kato
Published 2022-04-01

Authentication of Patients and Participants in Health Information Exchange and Consent for Medical Research: A Key Step for Privacy Protection, Respect for Autonomy, and Trustworth...

by Atsushi Kogetsu, Soichi Ogishima, Kazuto Kato
Published 2018-06-01

Why does it take so long for rare disease patients to get an accurate diagnosis?-A qualitative investigation of patient experiences of hereditary angioedema.

by Moeko Isono, Minori Kokado, Kazuto Kato
Published 2022-01-01

Mouse model: what do Japanese life sciences researchers mean by this term?

by Kae Takahashi, Jin Higashijima, Kazuto Kato
Published 2009-01-01

Analysis of Japanese newspaper articles on genetic modification

by Ryuma Shineha, Aiko Hibino, Kazuto Kato
Published 2008-06-01

Access, autonomy, and affordability: ethical and human rights issues surrounding multigene panel testing for cancer in Japan and Switzerland

by Kate Nakasato, Carlotta Manz, Kazuto Kato
Published 2024-01-01

Why does it take so long for rare disease patients to get an accurate diagnosis?—A qualitative investigation of patient experiences of hereditary angioedema

by Moeko Isono, Minori Kokado, Kazuto Kato
Published 2022-01-01

Evaluating standards for ‘serious’ disease for preimplantation genetic testing: a multi-case study on regulatory frameworks in Japan, the UK, and Western Australia

by Kate Nakasato, Beverley Anne Yamamoto, Kazuto Kato
Published 2022-05-01

Patient involvement in priority-setting for medical research: A mini review of initiatives in the rare disease field

by Amelia Katirai, Atsushi Kogetsu, Kazuto Kato, Beverley Yamamoto
Published 2022-07-01

Institutional and Social Issues Surrounding Genetic Counselors in Japan: Current Challenges and Implications for the Global Community

by Yayoi Aizawa, Atsushi Watanabe, Atsushi Watanabe, Kazuto Kato
Published 2021-04-01

Perspectives on artificial intelligence in healthcare from a Patient and Public Involvement Panel in Japan: an exploratory study

by Amelia Katirai, Beverley Anne Yamamoto, Atsushi Kogetsu, Kazuto Kato
Published 2023-09-01

Public attitudes in Japan toward participation in whole genome sequencing studies

by Taketoshi Okita, Noriko Ohashi, Daijiro Kabata, Ayumi Shintani, Kazuto Kato
Published 2018-04-01

Machine Learning and Ethics in Plastic Surgery

by Jungen Koimizu, MD, Toshiaki Numajiri, MD, PhD, Kazuto Kato, PhD
Published 2019-03-01

Social and Communicative Functions of Informed Consent Forms in East Asia and Beyond

by Go Yoshizawa, Teguh H. Sasongko, Teguh H. Sasongko, Chih-Hsing Ho, Kazuto Kato
Published 2017-07-01

Genetic discrimination: introducing the Asian perspective to the debate

by Hannah Kim, Calvin W. L. Ho, Chih-Hsing Ho, P. S. Athira, Kazuto Kato, Leonardo De Castro, Hui Kang, Richard Huxtable, Hub Zwart, Jonathan Ives, Ilhak Lee, Yann Joly, So Yoon Kim
Published 2021-07-01

The practice of active patient involvement in rare disease research using ICT: experiences and lessons from the RUDY JAPAN project

by Nao Hamakawa, Atsushi Kogetsu, Moeko Isono, Chisato Yamasaki, Shirou Manabe, Toshihiro Takeda, Kazumasa Iwamoto, Tomoya Kubota, Joe Barrett, Nathanael Gray, Alison Turner, Harriet Teare, Yukie Imamura, Beverley Anne Yamamoto, Jane Kaye, Michihiro Hide, Masanori P. Takahashi, Yasushi Matsumura, Muhammad Kassim Javaid, Kazuto Kato
Published 2021-02-01

Including all voices in international data-sharing governance

by Jane Kaye, Sharon F. Terry, Eric Juengst, Sarah Coy, Jennifer R. Harris, Don Chalmers, Edward S. Dove, Isabelle Budin-Ljøsne, Clement Adebamowo, Emilomo Ogbe, Louise Bezuidenhout, Michael Morrison, Joel T. Minion, Madeleine J. Murtagh, Jusaku Minari, Harriet Teare, Rosario Isasi, Kazuto Kato, Emmanuelle Rial-Sebbag, Patricia Marshall, Barbara Koenig, Anne Cambon-Thomsen
Published 2018-03-01

Engaged genomic science produces better and fairer outcomes: an engagement framework for engaging and involving participants, patients and publics in genomics research and healthca...

by Joel T. Minion, Richard Milne, Stephanie Mulrine, Mogomotsi Matshaba, Rosalyn Ryan, Christine Patch, Fiona Maleady-Crowe, Jantina de Vries, Judit Kumuthini, Anna Middleton, William Viney, Madeleine J. Murtagh, Mavis Machirori, Mwenza T. Blell, Clara L. Gaff, Edward S. Dove, Megan Doerr, Jillian Hastings Ward, Audrey Duncanson, Calvin W. L. Ho, Rachele Hendricks-Sturrup, Yann Joly, Amber Johns, Keiko Katsui, Kazuto Kato
Published 2021-11-01

Key challenges in bringing CRISPR-mediated somatic cell therapy into the clinic

by Dianne Nicol, Lisa Eckstein, Michael Morrison, Jacob S. Sherkow, Margaret Otlowski, Tess Whitton, Tania Bubela, Kathryn P. Burdon, Don Chalmers, Sarah Chan, Jac Charlesworth, Christine Critchley, Merlin Crossley, Sheryl de Lacey, Joanne L. Dickinson, Alex W. Hewitt, Joanne Kamens, Kazuto Kato, Erika Kleiderman, Satoshi Kodama, John Liddicoat, David A. Mackey, Ainsley J. Newson, Jane Nielsen, Jennifer K. Wagner, Rebekah E. McWhirter
Published 2017-09-01

Reflections on the cost of "low-cost" whole genome sequencing: framing the health policy debate.

by Timothy Caulfield, Jim Evans, Amy McGuire, Christopher McCabe, Tania Bubela, Robert Cook-Deegan, Jennifer Fishman, Stuart Hogarth, Fiona A Miller, Vardit Ravitsky, Barbara Biesecker, Pascal Borry, Mildred K Cho, June C Carroll, Holly Etchegary, Yann Joly, Kazuto Kato, Sandra Soo-Jin Lee, Karen Rothenberg, Pamela Sankar, Michael J Szego, Pilar Ossorio, Daryl Pullman, Francois Rousseau, Wendy J Ungar, Brenda Wilson
Published 2013-11-01