Coming of age of personalized medicine: challenges ahead

par Borry, Pascal
Publié 2009

Challenges of web-based personal genomic data sharing

par Shabani, Mahsa, Borry, Pascal
Publié dans Life Sci Soc Policy (2015)

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

par Shabani, Mahsa, Borry, Pascal
Publié dans Eur J Hum Genet (2017)

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

par Howard, Heidi Carmen, Borry, Pascal
Publié 2011

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

par Howard, Heidi Carmen, Borry, Pascal
Publié 2012

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

par Howard, Heidi Carmen, Borry, Pascal
Publié 2012

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

par Howard, Heidi Carmen, Borry, Pascal
Publié 2013

How international is bioethics? A quantitative retrospective study

par Borry, Pascal, Schotsmans, Paul, Dierickx, Kris
Publié 2006

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

par Shabani, Mahsa, Thorogood, Adrian, Borry, Pascal
Publié dans Eur J Hum Genet (2016)

Third party interpretation of raw genetic data: an ethical exploration

par Badalato, Lauren, Kalokairinou, Louiza, Borry, Pascal
Publié dans Eur J Hum Genet (2017)

Data sharing platforms and the academic evaluation system

par Devriendt, Thijs, Shabani, Mahsa, Borry, Pascal
Publié dans 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

par Devriendt, Thijs, Borry, Pascal, Shabani, Mahsa
Publié dans PLoS One (2021)

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

par Su, Yeyang, Howard, Heidi C., Borry, Pascal
Publié 2011

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

par Howard, Heidi Carmen, Avard, Denise, Borry, Pascal
Publié 2011

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

par Shabani, Mahsa, Knoppers, Bartha Maria, Borry, Pascal
Publié dans EMBO Mol Med (2015)

Blurring lines

par Howard, Heidi C, Knoppers, Bartha Maria, Borry, Pascal
Publié 2010

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

par Borry, Pascal, Cornel, Martina C., Howard, Heidi C.
Publié 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

par Sterckx, Sigrid, Rakic, Vojin, Cockbain, Julian, Borry, Pascal
Publié dans Med Health Care Philos (2015)

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

par Cornel, Martina C., van El, Carla G., Borry, Pascal
Publié 2012

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

par Kleiderman, Erika, Pack, Amy, Borry, Pascal, Zawati, Ma’n
Publié dans PLoS One (2018)