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  1. 1
    Genetic testing in asymptomatic minors: recommendations of the European Society of Human Genetics

    Genetic testing in asymptomatic minors: recommendations of the European Society of Human Genetics por Pascal Borry

    Publicado em 2009
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  2. 2
    Statement of the ESHG on direct-to-consumer genetic testing for health-related purposes

    Statement of the ESHG on direct-to-consumer genetic testing for health-related purposes por Pascal Borry

    Publicado em 2010
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  3. 3
    Is there a doctor in the house?

    Is there a doctor in the house? por Heidi Howard, Pascal Borry

    Publicado em 2011
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  4. 4
    Rules for processing genetic data for research purposes in view of the new EU General Data Protection Regulation

    Rules for processing genetic data for research purposes in view of the new EU General Data Protection Regulation por Mahsa Shabani, Pascal Borry

    Publicado em 2017
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  5. 5
    THE BIRTH OF THE EMPIRICAL TURN IN BIOETHICS

    THE BIRTH OF THE EMPIRICAL TURN IN BIOETHICS por Pascal Borry, Paul Schotsmans, Kris Dierickx

    Publicado em 2005
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  6. 6
    Users’ motivations to purchase direct-to-consumer genome-wide testing: an exploratory study of personal stories

    Users’ motivations to purchase direct-to-consumer genome-wide testing: an exploratory study of personal stories por Yeyang Su, Heidi Howard, Pascal Borry

    Publicado em 2011
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  7. 7
    What is the role of empirical research in bioethical reflection and decision-making? An ethical analysis

    What is the role of empirical research in bioethical reflection and decision-making? An ethical analysis por Pascal Borry, Paul Schotsmans, Kris Dierickx

    Publicado em 2004
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  8. 8
    Empirical research in bioethical journals. A quantitative analysis

    Empirical research in bioethical journals. A quantitative analysis por Pascal Borry, Paul Schotsmans, Kris Dierickx

    Publicado em 2006
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  9. 9
    Third party interpretation of raw genetic data: an ethical exploration

    Third party interpretation of raw genetic data: an ethical exploration por Lauren Badalato, Louiza Kalokairinou, Pascal Borry

    Publicado em 2017
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  10. 10
    ‘NOBODY TOSSES A DWARF!’ THE RELATION BETWEEN THE EMPIRICAL AND THE NORMATIVE REEXAMINED

    ‘NOBODY TOSSES A DWARF!’ THE RELATION BETWEEN THE EMPIRICAL AND THE NORMATIVE REEXAMINED por Carlo Leget, Pascal Borry, Raymond De Vries

    Publicado em 2009
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  11. 11
    Where are you going, where have you been: a recent history of the direct-to-consumer genetic testing market

    Where are you going, where have you been: a recent history of the direct-to-consumer genetic testing market por Pascal Borry, Martina C. Cornel, Heidi Howard

    Publicado em 2010
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  12. 12
    From the principles of genomic data sharing to the practices of data access committees

    From the principles of genomic data sharing to the practices of data access committees por Mahsa Shabani, Bartha Maria Knoppers, Pascal Borry

    Publicado em 2015
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  13. 13
    Expanded carrier screening for monogenic disorders: where are we now?

    Expanded carrier screening for monogenic disorders: where are we now? por Davit Chokoshvili, Danya F. Vears, Pascal Borry

    Publicado em 2017
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  14. 14
    Reporting practices for variants of uncertain significance from next generation sequencing technologies

    Reporting practices for variants of uncertain significance from next generation sequencing technologies por Danya F. Vears, Karine Sénécal, Pascal Borry

    Publicado em 2017
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  15. 15
    “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

    “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 por Sigrid Sterckx, Vojin Rakić, Julian Cockbain, Pascal Borry

    Publicado em 2015
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  16. 16
    Carrier testing in minors: a systematic review of guidelines and position papers

    Carrier testing in minors: a systematic review of guidelines and position papers por Pascal Borry, Jean‐Pierre Fryns, Paul Schotsmans, Kris Dierickx

    Publicado em 2005
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  17. 17
    Analysis of VUS reporting, variant reinterpretation and recontact policies in clinical genomic sequencing consent forms

    Analysis of VUS reporting, variant reinterpretation and recontact policies in clinical genomic sequencing consent forms por Danya F. Vears, Emilia Niemiec, Heidi Howard, Pascal Borry

    Publicado em 2018
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  18. 18
    Minors and Informed Consent: A Comparative Approach

    Minors and Informed Consent: A Comparative Approach por L Stultiens, Kris Dierickx, Herman Nys, Tom Goffin, Pascal Borry

    Publicado em 2007
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  19. 19
    Controlled Access under Review: Improving the Governance of Genomic Data Access

    Controlled Access under Review: Improving the Governance of Genomic Data Access por Mahsa Shabani, Stephanie O. M. Dyke, Yann Joly, Pascal Borry

    Publicado em 2015
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  20. 20
    Presymptomatic and predictive genetic testing in minors: a systematic review of guidelines and position papers

    Presymptomatic and predictive genetic testing in minors: a systematic review of guidelines and position papers por Pascal Borry, L Stultiens, Herman Nys, J‐J Cassiman, Kris Dierickx

    Publicado em 2006
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