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Accountability in Research|June 3, 2024
Truthfulness as the basis for ethical safeguards in deceptive research: An interview study with researchersKamiel Verbeke, Jan Piasecki, Dieter Baeyens, et al.AJOB Empirical Bioethics|October 5, 2020
Old Challenges or New Issues? Genetic Health Professionals' Experiences Obtaining Informed Consent in Diagnostic Genomic SequencingDanya F Vears, Pascal Borry, Julian Savulescu, et al.Journal of Community Genetics|September 1, 2017
Readability of informed consent forms for whole-exome and whole-genome sequencingEmilia Niemiec, Danya F Vears, Pascal Borry, et al.Familial Cancer|March 29, 2024
Clinician perspectives on policy approaches to genetic risk disclosure in familiesAmicia Phillips, Danya F Vears, Ine Van Hoyweghen, et al.Plos One|November 20, 2020
Crowdfunding for complementary and alternative medicine: What are cancer patients seeking?Jeremy Snyder, Marco Zenone, Timothy CaulfieldBiopreservation and Biobanking|May 22, 2014
Biobanking, consent, and control: a survey of Albertans on key research ethics issuesTimothy Caulfield, Christen Rachul, Erin NelsonGenetics in Medicine : Official Journal of the American College of Medical Genetics|March 28, 2022
A review of normative documents on preimplantation genetic testing: Recommendations for PGT-PMaria Siermann, Olga Tšuiko, Joris Robert Vermeesch, et al.Expert Review of Molecular Diagnostics|December 22, 2012
Why do participants enroll in population biobank studies? A systematic literature reviewHélène Nobile, Eric Vermeulen, Kristof Thys, et al.Journal of Obstetric, Gynecologic, and Neonatal Nursing : JOGNN|November 23, 2016
Attitudes of European Geneticists Regarding Expanded Carrier ScreeningSandra Janssens, Davit Chokoshvili, Danya Vears, et al.Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|May 7, 2016
Controversies with Kalydeco: Newspaper coverage in Canada and the United States of the cystic fibrosis "wonder drug"Christen Rachul, Maeghan Toews, Timothy CaulfieldPageof 35