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Patient Education and Counseling|July 29, 2022
Exploring informed choice in preconception reproductive genetic carrier screening by using a modified Multidimensional Measure of Informed ChoiceEva Van Steijvoort, Hilde Peeters, Hilde Vandecruys, et al.
European Journal of Human Genetics : EJHG|July 30, 2015
Attitudes of cystic fibrosis patients and parents toward carrier screening and related reproductive issuesSandra Janssens, Davit Chokoshvilli, Carmen Binst, et al.
Digital Health|January 25, 2024
Personalized and longitudinal electronic informed consent in clinical trials: How to move the needle?Evelien De Sutter, Liese Barbier, Pascal Borry, et al.
Digital Health|October 6, 2023
Crowdsourcing smartphone data for biomedical research: Ethical and legal questionsMichael Lang, Kyle McKibbin, Mahsa Shabani, et al.
Personalized Medicine|May 12, 2018
Participants' decision to enroll in cohort studies with biobanks: quantitative insights from two German studiesHélène Nobile, Pascal Borry, Tobias Pischon, et al.
European Journal of Human Genetics : EJHG|June 16, 2016
Legal approaches regarding health-care decisions involving minors: implications for next-generation sequencingKarine Sénécal, Kristof Thys, Danya F Vears, et al.
European Journal of Human Genetics : EJHG|February 14, 2023
Experiences of nonpregnant couples after receiving reproductive genetic carrier screening results in BelgiumEva Van Steijvoort, Hilde Peeters, Hilde Vandecruys, et al.
Reproductive Biomedicine Online|July 18, 2024
Perspectives of preimplantation genetic testing patients in Belgium on the ethics of polygenic embryo screeningMaria Siermann, Joris R Vermeesch, Taneli Raivio, et al.
European Journal of Human Genetics : EJHG|January 26, 2024
Should non-invasive prenatal testing (NIPT) be used for fetal sex determination? Perspectives and experiences of healthcare professionalsZoë Claesen-Bengtson, Hilary Bowman-Smart, Eline Vermeersch, et al.
Sociology of Health & Illness|October 3, 2022
Navigating the uncertainties of next-generation sequencing in the genetics clinicJanneke M L Kuiper, Pascal Borry, Danya F Vears, et al.
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