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Genome Medicine|May 24, 2013
Survey of European clinical geneticists on awareness, experiences and attitudes towards direct-to-consumer genetic testingHeidi Carmen Howard, Pascal BorryJournal of Gynecology Obstetrics and Human Reproduction|January 14, 2026
Understanding of trisomy 21 prenatal screening among pregnant women in France: a cross-sectional study in light of 2019 guidelinesClément Wulveryck, Eva Van Steijvoort, Nicolas Sananès, et al.Trends in Genetics : TIG|November 15, 2017
Raw Genomic Data: Storage, Access, and SharingMahsa Shabani, Danya Vears, Pascal BorryEuropean Journal of Human Genetics : EJHG|August 25, 2016
Who should have access to genomic data and how should they be held accountable? Perspectives of Data Access Committee members and expertsMahsa Shabani, Adrian Thorogood, Pascal BorryAJOB Empirical Bioethics|February 11, 2020
Ethics Review in Anti-Doping Research: Experiences of StakeholdersThijs Devriendt, Virginia Sanchini, Pascal BorryAccountability in Research|August 29, 2022
Appropriate inclusion of adult research participants with intellectual disability: an in-depth review of guidelines and policy statementsKlara Meierer, Pascal Borry, Virginia SanchiniJournal of Medical Internet Research|January 13, 2022
Credit and Recognition for Contributions to Data-Sharing Platforms Among Cohort Holders and Platform Developers in Europe: Interview StudyThijs Devriendt, Pascal Borry, Mahsa ShabaniPlos One|July 2, 2021
Factors that influence data sharing through data sharing platforms: A qualitative study on the views and experiences of cohort holders and platform developersThijs Devriendt, Pascal Borry, Mahsa ShabaniAccountability in Research|November 16, 2017
Research ethics review for the use of anonymized samples and data: A systematic review of normative documentsAmicia Phillips, Pascal Borry, Mahsa ShabaniJournal of Evaluation in Clinical Practice|May 26, 2006
Evidence-based medicine and its role in ethical decision-makingPascal Borry, Paul Schotsmans, Kris DierickxPageof 20