•  215
    Special issue on the emergence of analytic philosophy in East Asia
    with Yarran Hominh, Dien Ho, Yi Jiang, Joe Y. F. Lau, Ting-An lin, Nikolaj Jang L. Pedersen, Yeollim Bae, Jungkyun Kim, Youngsung Kim, and Seong Soo Park
    Apa Studies on Asian and Asian American Philosophers and Philosophies 23 (2). 2024.
    This paper summarizes the evolution of analytic philosophy in Taiwan, examines its impact within and beyond academia, and discusses the future of the discipline. The roots of modern philosophy in Taiwan can be traced back to the Japanese colonial era, and analytic philosophy was introduced to the country in the late 1940s when many intellectuals in China moved to Taiwan. However, massive curbs were imposed on philosophy during Chiang Kai-shek’s dictatorship, and the discipline began to thrive ag…Read more
  • New Studies in Japanese Aesthetics (edited book)
    Lexington Books. forthcoming.
  •  27
    New Essays in Japanese Aesthetics (edited book)
    Lexington Books. 2017.
    This collection begins with an engaging historical overview of Japanese aesthetics and offers contemporary multidisciplinary and interdisciplinary perspectives on the artistic and aesthetic traditions of Japan and the central themes in Japanese art and aesthetics.
  •  27
    Of the Rights and Best Interests of Future Generations
    with Erika Kleiderman and Bartha Maria Knoppers
    American Journal of Bioethics 20 (8): 38-40. 2020.
    Volume 20, Issue 8, August 2020, Page 38-40.
  •  42
    Model consent clauses for rare disease research
    with Jack Goldblatt, Rosario Isasi, Marlene Jagut, Anneliene Hechtelt Jonker, Petra Kaufmann, Laetitia Ouillade, Fruszina Molnar-Gabor, Mahsa Shabani, Eric Sid, Anne Marie Tassé, Durhane Wong-Rieger, and Bartha Maria Knoppers
    BMC Medical Ethics 20 (1): 1-7. 2019.
    Rare Disease research has seen tremendous advancements over the last decades, with the development of new technologies, various global collaborative efforts and improved data sharing. To maximize the impact of and to further build on these developments, there is a need for model consent clauses for rare diseases research, in order to improve data interoperability, to meet the informational needs of participants, and to ensure proper ethical and legal use of data sources and participants’ overall…Read more
  •  7
    The Caring State? On Rural Welfare Governance in Post-reform Vietnam and China
    with Meixuan Chen
    Ethics and Social Welfare 11 (3): 230-247. 2017.
  •  21
    Beyond the Global Care Chain: Boundaries, Institutions and Ethics of Care
    with Roberta Zavoretti and Joan Tronto
    Ethics and Social Welfare 11 (3): 199-212. 2017.