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Pediatric Transplantation|June 21, 2019
Should minors and young adults qualify as potential live kidney donors? The views of international transplant professionalsKristof Thys, Pascal Borry, Paul Schotsmans, et al.BMC Medical Ethics|September 19, 2021
Polygenic risk scoring of human embryos: a qualitative study of media coverageTiny Pagnaer, Maria Siermann, Pascal Borry, et al.Drug Testing and Analysis|March 11, 2018
Do athletes have a right to access data in their Athlete Biological Passport?Thijs Devriendt, Davit Chokoshvili, Maddalena Favaretto, et al.Trends in Genetics : TIG|April 21, 2018
Forensic Epigenetic Age Estimation and Beyond: Ethical and Legal ConsiderationsMahsa Shabani, Pascal Borry, Inge Smeers, et al.Accountability in Research|November 9, 2023
Governance of research and product improvement studies in consumer mental health apps. Interviews with researchers and app developersKamiel Verbeke, Charu Jain, Ambra Shpendi, et al.Plos One|March 24, 2018
The author who wasn't there? Fairness and attribution in publications following access to population biobanksErika Kleiderman, Amy Pack, Pascal Borry, et al.Human Genetics|June 28, 2011
Closure of population biobanks and direct-to-consumer genetic testing companiesMa'n H Zawati, Pascal Borry, Heidi Carmen HowardMedicine, Health Care, and Philosophy|August 18, 2015
"You hoped we would sleep walk into accepting the collection of our data": controversies surrounding the UK care.data scheme and their wider relevance for biomedical researchSigrid Sterckx, Vojin Rakic, Julian Cockbain, et al.Journal of Empirical Research on Human Research Ethics : JERHRE|May 23, 2019
The Use of Samples Originating From Doping Control Procedures for Research Purposes: A Qualitative StudyThijs Devriendt, Amicia Phillips, Mahsa Shabani, et al.Plos One|July 1, 2025
Vulnerability in research ethics: A systematic review of policy guidelines and documentsAsia Grigis, Giorgia Beretta, Pascal Borry, et al.Pageof 35