Landscape of pediatric cancer treatment refusal and abandonment in the US: A qualitative study by Daniel J. Benedetti, Daniel J. Benedetti, Catherine M. Hammack-Aviran, Carolyn Diehl, Laura M. Beskow

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Forensic mental health professionals’ perceptions of their dual loyalty conflict: findings from a qualitative study by Helene Merkt, Sophie Haesen, Ariel Eytan, Elmar Habermeyer, Marcelo F. Aebi, Bernice Elger, Tenzin Wangmo

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A case for preference-sensitive decision timelines to aid shared decision-making in intensive care: need and possible application by Beatrix Göcking, Sophie Gloeckler, Andrea Ferrario, Andrea Ferrario, Giovanna Brandi, Andrea Glässel, Andrea Glässel, Nikola Biller-Andorno

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Factors of influenza vaccine inoculation and non-inoculation behavior of community-dwelling residents in Japan: Suggestions for vaccine policy and public health ethics after COVID-... by Mayuko T. Komada, Jung Su Lee, Etsuko Watanabe, Eisuke Nakazawa, Katsumi Mori, Akira Akabayashi

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Australian Public Perspectives on Genomic Newborn Screening: Risks, Benefits, and Preferences for Implementation by Fiona Lynch, Stephanie Best, Clara Gaff, Lilian Downie, Alison D. Archibald, Christopher Gyngell, Ilias Goranitis, Riccarda Peters, Julian Savulescu, Sebastian Lunke, Zornitza Stark, Danya F. Vears

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Editorial: Approaches for Severe and Persistent Mental Illness by Anna Lisa Westermair, Anna Lisa Westermair, Scott A. Irwin, Ulrich Schweiger, Manuel Trachsel, Manuel Trachsel

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eHealth interventions for psychiatry in Switzerland and Russia: a comparative study by Olga Chivilgina, Bernice S. Elger, Bernice S. Elger, Ilya Fedotov, Fabrice Jotterand, Fabrice Jotterand

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The Meaning and Importance of Genetic Relatedness: Fertility Preservation Decision Making Among Israeli Adolescent Cancer Survivors and Their Parents by Dorit Barlevy, Bernice S Elger, Tenzin Wangmo, Shifra Ash, Vardit Ravitsky

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Individual Experiences with Being Pushed to Limits and Variables That Influence the Strength to Which These Are Felt: A Cross-Sectional Survey Study by Eisuke Nakazawa, Katsumi Mori, Akira Akabayashi

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Do Papers with Japanese Authors Have a Different Number of Authors? A Follow-Up Study after 25 Years and Implication for Other Countries by Akira Akabayashi, Eisuke Nakazawa, Katsumi Mori

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Why genomics researchers are sometimes morally required to hunt for secondary findings by Julian J. Koplin, Julian Savulescu, Danya F. Vears

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Enhancing evidence-informed policymaking in medicine and healthcare: stakeholder involvement in the Commons Project for rare diseases in Japan by Atsushi Kogetsu, Moeko Isono, Tatsuki Aikyo, Junichi Furuta, Dai Goto, Nao Hamakawa, Michihiro Hide, Risa Hori, Noriko Ikeda, Keiko Inoi, Naomi Kawagoe, Tomoya Kubota, Shirou Manabe, Yasushi Matsumura, Koji Matsuyama, Tomoko Nakai, Ikuko Nakao, Yuki Saito, Midori Senoo, Masanori P. Takahashi, Toshihiro Takeda, Megumi Takei, Katsuto Tamai, Akio Tanaka, Yasuhiro Torashima, Yuya Tsuchida, Chisato Yamasaki, Beverley Anne Yamamoto, Kazuto Kato

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Editorial: Assisted dying in persons with mental illness by Manuel Trachsel, Manuel Trachsel, Manuel Trachsel, Anna Lisa Westermair, Anna Lisa Westermair, Anna Lisa Westermair, Marc Graf, Christian G. Huber

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Stay fit or get bit – ethical issues in sharing health data with insurers’ apps by Andrea Martani, David Shaw, Bernice Simone Elger

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Rapid Genomic Testing in Intensive Care: Health Professionals’ Perspectives on Ethical Challenges by Katie Arkell, Christopher Gyngell, Zornitza Stark, Danya F. Vears

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Motivation and training needs of prison healthcare professionals: findings from a qualitative study by Benjamin Jeker, David Shaw, Nicolas Lagnaux, Tenzin Wangmo, Bernice S. Elger

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P639: Large-scale genome reanalysis of 159 individuals affected by undiagnosed genetic diseases from the Stanford Center for Undiagnosed Diseases by Hector Mendez, Devon Bonner, Chloe Reuter, Jennefer Kohler, Shruti Marwaha, Laurens van de Wiel, Elijah Kravets, Charlotte Ostrow, Raquel Alvarez, Sara Emami, Meghan Halley, Holly Tabor, Suha Bachir, Jonathan Bernstein, Matthew Wheeler

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V.R. POTTER’S GLOBAL BIOETHICS by DIEGO CARLOS ZANELLA, ANOR SGANZERLA, LEOCIR PESSINI

“…Bioethics was born in the United States and there developed a conception that reduced it to a vision of biomedical ethics. In response to this reductionism, the father of bioethics, V. …”
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From the principles of genomic data sharing to the practices of data access committees by Mahsa Shabani, Bartha Maria Knoppers, Pascal Borry

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Enduring uncertainties. Medical accounts on caring for young people with variations of sex characteristics by Nina Reber, Eva De Clercq

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