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Nature Medicine|August 8, 2019
Genetic testing, insurance discrimination and medical research: what the United States can learn from peer countriesJean-Christophe Bélisle-Pipon, Effy Vayena, Robert C Green, et al.
Lancet (London, England)|February 6, 2026
The paradox of trust in health care in the age of social mediaMarcello Ienca, Celine Gounder, Ezekiel J Emanuel
Neuron|January 19, 2018
From Healthcare to Warfare and Reverse: How Should We Regulate Dual-Use Neurotechnology?Marcello Ienca, Fabrice Jotterand, Bernice S Elger
BMJ Open|August 26, 2022
Public preferences towards data management and governance in Swiss biobanks: results from a nationwide surveyCaroline Brall, Claudia Berlin, Marcel Zwahlen, et al.
Plos One|April 1, 2021
Public willingness to participate in personalized health research and biobanking: A large-scale Swiss surveyCaroline Brall, Claudia Berlin, Marcel Zwahlen, et al.
Bjpsych Open|March 27, 2026
When forensic psychiatry clashes with jurisdiction: nemesis and challenges of a patient suffering from glioblastomaAmbra D'Imperio, Didier Delessert, Marcello Ienca, et al.
NPJ Digital Medicine|August 8, 2025
Ethical gaps in closed-loop neurotechnology: a scoping reviewLea Haag, Georg Starke, Markus Ploner, et al.
JMIR Research Protocols|November 30, 2018
User Perspectives of a Web-Based Data-Sharing Platform (Open Humans) on Ethical Oversight in Participant-Led Research: Protocol for a Quantitative StudyMarta Fadda, Anna Jobin, Alessandro Blasimme, et al.
Plos One|January 11, 2023
Expectations and attitudes towards medical artificial intelligence: A qualitative study in the field of strokeJulia Amann, Effy Vayena, Kelly E Ormond, et al.
BMC Geriatrics|July 3, 2021
Digital health interventions for healthy ageing: a qualitative user evaluation and ethical assessmentMarcello Ienca, Christophe Schneble, Reto W Kressig, et al.
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