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European Journal of Pediatrics|September 9, 2018
Renal Replacement Therapy in children with severe developmental disability: guiding questions for decision-makingLore Willem, Noël Knops, Djalila Mekahli, et al.Frontiers in Medicine|October 27, 2022
Challenges related to data protection in clinical research before and during the COVID-19 pandemic: An exploratory studyTeodora Lalova-Spinks, Evelien De Sutter, Peggy Valcke, et al.European Journal of Human Genetics : EJHG|June 21, 2012
Developing a policy for paediatric biobanks: principles for good practiceKristien Hens, Carla E Van El, Pascal Borry, et al.IRB|August 9, 2018
Recontacting Pediatric Research Participants for Consent When They Reach the Age of MajorityBartha Maria Knoppers, Karine Sénécal, Joanne Boisjoli, et al.Journal of Medical Ethics|March 3, 2023
Sport-related concussion research agenda beyond medical science: culture, ethics, science, policyMike McNamee, Lynley C Anderson, Pascal Borry, et al.European Journal of Human Genetics : EJHG|June 15, 2023
Reconciling the biomedical data commons and the GDPR: three lessons from the EUCAN ELSI collaboratoryAlexander Bernier, Fruzsina Molnár-Gábor, Bartha M Knoppers, et al.European Journal of Human Genetics : EJHG|October 13, 2017
Responsible implementation of expanded carrier screeningLidewij Henneman, Pascal Borry, Davit Chokoshvili, et al.European Journal of Human Genetics : EJHG|March 17, 2016
Responsible implementation of expanded carrier screeningLidewij Henneman, Pascal Borry, Davit Chokoshvili, et al.BMC Genomics|November 9, 2015
Crowdsourced direct-to-consumer genomic analysis of a family quartetManuel Corpas, Willy Valdivia-Granda, Nazareth Torres, et al.European Journal of Human Genetics : EJHG|September 25, 2014
Points to consider for prioritizing clinical genetic testing services: a European consensus process oriented at accountability for reasonablenessFranziska Severin, Pascal Borry, Martina C Cornel, et al.Pageof 20