Saori Watanabe, Kaori Muto, Hideki Yui, et al. Awareness and perceptions of patient and public involvement in rare disease research in Japan: the role of patient advocacy groups and family members. Research Involvement and Engagement, 12(1), 2026.
doi:10.1186/s40900-026-00955-9
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Barnes M, Bledsoe M, Kusunose M, Lawlor R, Morrin H, Schmid A. International Ethical Principles for Banking and Secondary Research Use of Human Biospecimens and Associated Data: The Seattle Principles. Journal of Law, Medicine & Ethics. Published online 2026:1-9.
doi:10.1017/jme.2026.10252
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Kirby, E., Bernier, A., Guigó, R., Kusunose M., et al. Data sharing ethics toolkit: The Human Cell Atlas. Nature Communications 15, 9901, 2024
https://doi.org/10.1038/s41467-024-54300-3
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Sato, M., Muto, K., Momozawa, Y. et al. (Not So) Lost in Translation: Considering the GA4GH Diversity in Datasets Policy in the Japanese Context. Asian Bioethics Review 2024
https://doi.org/10.1007/s41649-024-00305-5
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Yukitaka Kiya, Hideki Yui, Kaori Muto, et al. Attitudes of patients with IVF/ICSI toward human embryo in vitro culture beyond 14 days. Regenerative Therapy 26, 2024
https://doi.org/10.1016/j.reth.2024.09.005
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RIKEN Center for Integrative Medical SciencesLaboratory for Biomedical Ethics and Co-design