Coming of age of personalized medicine: challenges ahead

von Borry, Pascal
Veröffentlicht 2009

Challenges of web-based personal genomic data sharing

von Shabani, Mahsa, Borry, Pascal
Veröffentlicht in Life Sci Soc Policy (2015)

Rules for processing genetic data for research purposes in view of the new EU General Data Protection Regulation

von Shabani, Mahsa, Borry, Pascal
Veröffentlicht in Eur J Hum Genet (2017)

Is there a doctor in the house?: The presence of physicians in the direct-to-consumer genetic testing context

von Howard, Heidi Carmen, Borry, Pascal
Veröffentlicht 2011

To ban or not to ban?: Clinical geneticists' views on the regulation of direct-to-consumer genetic testing

von Howard, Heidi Carmen, Borry, Pascal
Veröffentlicht 2012

To ban or not to ban?: Clinical geneticists' views on the regulation of direct-to-consumer genetic testing

von Howard, Heidi Carmen, Borry, Pascal
Veröffentlicht 2012

Survey of European clinical geneticists on awareness, experiences and attitudes towards direct-to-consumer genetic testing

von Howard, Heidi Carmen, Borry, Pascal
Veröffentlicht 2013

How international is bioethics? A quantitative retrospective study

von Borry, Pascal, Schotsmans, Paul, Dierickx, Kris
Veröffentlicht 2006

Who should have access to genomic data and how should they be held accountable? Perspectives of Data Access Committee members and experts

von Shabani, Mahsa, Thorogood, Adrian, Borry, Pascal
Veröffentlicht in Eur J Hum Genet (2016)

Third party interpretation of raw genetic data: an ethical exploration

von Badalato, Lauren, Kalokairinou, Louiza, Borry, Pascal
Veröffentlicht in Eur J Hum Genet (2017)

Data sharing platforms and the academic evaluation system

von Devriendt, Thijs, Shabani, Mahsa, Borry, Pascal
Veröffentlicht in EMBO Rep (2020)

Factors that influence data sharing through data sharing platforms: A qualitative study on the views and experiences of cohort holders and platform developers

von Devriendt, Thijs, Borry, Pascal, Shabani, Mahsa
Veröffentlicht in PLoS One (2021)

Users’ motivations to purchase direct-to-consumer genome-wide testing: an exploratory study of personal stories

von Su, Yeyang, Howard, Heidi C., Borry, Pascal
Veröffentlicht 2011

Are the kids really all right? Direct-to-consumer genetic testing in children: are company policies clashing with professional norms?

von Howard, Heidi Carmen, Avard, Denise, Borry, Pascal
Veröffentlicht 2011

From the principles of genomic data sharing to the practices of data access committees

von Shabani, Mahsa, Knoppers, Bartha Maria, Borry, Pascal
Veröffentlicht in EMBO Mol Med (2015)

Blurring lines

von Howard, Heidi C, Knoppers, Bartha Maria, Borry, Pascal
Veröffentlicht 2010

Where are you going, where have you been: a recent history of the direct-to-consumer genetic testing market

von Borry, Pascal, Cornel, Martina C., Howard, Heidi C.
Veröffentlicht 2010

“You hoped we would sleep walk into accepting the collection of our data”: controversies surrounding the UK care.data scheme and their wider relevance for biomedical research

von Sterckx, Sigrid, Rakic, Vojin, Cockbain, Julian, Borry, Pascal
Veröffentlicht in Med Health Care Philos (2015)

The challenge of implementing genetic tests with clinical utility while avoiding unsound applications

von Cornel, Martina C., van El, Carla G., Borry, Pascal
Veröffentlicht 2012

The author who wasn’t there? Fairness and attribution in publications following access to population biobanks

von Kleiderman, Erika, Pack, Amy, Borry, Pascal, Zawati, Ma’n
Veröffentlicht in PLoS One (2018)