Equitable Participation in Biobanks: The Risks and Benefits of a “Dynamic Consent” Approach by Megan Prictor, Harriet J. A. Teare, Harriet J. A. Teare, Jane Kaye, Jane Kaye

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Regulating human stem cell research and therapy in low- and middle-income countries: Malaysian perspectives by Mohammad Firdaus Bin Abdul Aziz, Michael Morrison, Jane Kaye

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Making the most of the waiting room: Electronic patient engagement, a mixed methods study by Victoria Coathup, Teresa Finlay, Harriet JA Teare, Jane Kaye, Matthew South, Fiona E Watt, Raashid Luqmani

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Public Health Genomics (PHG) and Public Participation: Points to Consider by Catherine Heeney, Denise Avard, Jane Kaye, Lucie M. Bucci, Michael M. Burgess, Tarik Sabry, Yanick Farmer

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Preferences of the Public for Sharing Health Data: Discrete Choice Experiment by Jennifer Viberg Johansson, Heidi Beate Bentzen, Nisha Shah, Eik Haraldsdóttir, Guðbjörg Andrea Jónsdóttir, Jane Kaye, Deborah Mascalzoni, Jorien Veldwijk

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Health Data Linkage for Public Interest Research in the UK: Key Obstacles and Solutions by Miranda Jane Mourby, James Doidge, Kerina H Jones, Ruth Gilbert, Stergios Aidinlis, Hannah Smith, Jessica Bell, Peter Dutey-Magni, Jane Kaye

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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

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Public Preferences for Digital Health Data Sharing: Discrete Choice Experiment Study in 12 European Countries by Roberta Biasiotto, Jennifer Viberg Johansson, Melaku Birhanu Alemu, Virginia Romano, Heidi Beate Bentzen, Jane Kaye, Mirko Ancillotti, Johanna Maria Catharina Blom, Gauthier Chassang, Dara Hallinan, Guðbjörg Andrea Jónsdóttir, Aníbal Monasterio Astobiza, Emmanuelle Rial-Sebbag, David Rodríguez-Arias, Nisha Shah, Lea Skovgaard, Ciara Staunton, Katharina Tschigg, Jorien Veldwijk, Deborah Mascalzoni

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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

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Research ethics recommendations for whole-genome research: consensus statement. by Timothy Caulfield, Amy L McGuire, Mildred Cho, Janet A Buchanan, Michael M Burgess, Ursula Danilczyk, Christina M Diaz, Kelly Fryer-Edwards, Shane K Green, Marc A Hodosh, Eric T Juengst, Jane Kaye, Laurence Kedes, Bartha Maria Knoppers, Trudo Lemmens, Eric M Meslin, Juli Murphy, Robert L Nussbaum, Margaret Otlowski, Daryl Pullman, Peter N Ray, Jeremy Sugarman, Michael Timmons

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