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Critical Reviews in Clinical Laboratory Sciences|January 31, 2017
Unsolved challenges in pediatric whole-exome sequencing: A literature analysisGabrielle Bertier, Karine Sénécal, Pascal Borry, et al.Journal of Community Genetics|October 12, 2012
The challenge of implementing genetic tests with clinical utility while avoiding unsound applicationsMartina C Cornel, Carla G van El, Pascal BorryHuman Mutation|September 21, 2016
Content Analysis of Informed Consent for Whole Genome Sequencing Offered by Direct-to-Consumer Genetic Testing CompaniesEmilia Niemiec, Pascal Borry, Wim Pinxten, et al.BMC Health Services Research|February 22, 2023
Informing a European guidance framework on electronic informed consent in clinical research: a qualitative studyEvelien De Sutter, Pascal Borry, Isabelle Huys, et al.BMC Medical Ethics|August 1, 2021
Personalized and long-term electronic informed consent in clinical research: stakeholder viewsEvelien De Sutter, Pascal Borry, David Geerts, et al.Science Translational Medicine|March 28, 2014
Whole-genome sequencing in newborn screening programsBartha M Knoppers, Karine Sénécal, Pascal Borry, et al.Trials|July 10, 2026
Vulnerability, protection and fairness: ethical and regulatory limits in small-N gene therapy trialsMargaux Reckelbus, Eva Van Steijvoort, Isabelle Huys, et al.Expert Review of Molecular Diagnostics|November 12, 2019
How does carrier status for recessive disorders influence reproductive decisions? A systematic review of the literatureJeffrey Cannon, Eva Van Steijvoort, Pascal Borry, et al.European Journal of Human Genetics : EJHG|November 4, 2005
Carrier testing in minors: a systematic review of guidelines and position papersPascal Borry, Jean-Pierre Fryns, Paul Schotsmans, et al.Familial Cancer|June 3, 2009
Health-related direct-to-consumer genetic testing: a review of companies' policies with regard to genetic testing in minorsPascal Borry, Heidi C Howard, Karine Sénécal, et al.Pageof 35