Ohcanbohtosat - Pascal Borry

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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 Dahkki Pascal Borry

    Almmustuhtton 2009
    Viečča ollesdeavstta Viečča ollesdeavstta
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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 Dahkki Pascal Borry

    Almmustuhtton 2010
    Viečča ollesdeavstta Viečča ollesdeavstta
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  3. 3
    Is there a doctor in the house?

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

    Almmustuhtton 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 Dahkki Mahsa Shabani, Pascal Borry

    Almmustuhtton 2017
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  5. 5
    THE BIRTH OF THE EMPIRICAL TURN IN BIOETHICS

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

    Almmustuhtton 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 Dahkki Yeyang Su, Heidi Howard, Pascal Borry

    Almmustuhtton 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 Dahkki Pascal Borry, Paul Schotsmans, Kris Dierickx

    Almmustuhtton 2004
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  8. 8
    Empirical research in bioethical journals. A quantitative analysis

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

    Almmustuhtton 2006
    Viečča ollesdeavstta Viečča ollesdeavstta
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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 Dahkki Lauren Badalato, Louiza Kalokairinou, Pascal Borry

    Almmustuhtton 2017
    Viečča ollesdeavstta Viečča ollesdeavstta
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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 Dahkki Carlo Leget, Pascal Borry, Raymond De Vries

    Almmustuhtton 2009
    Viečča ollesdeavstta Viečča ollesdeavstta
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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 Dahkki Pascal Borry, Martina C. Cornel, Heidi Howard

    Almmustuhtton 2010
    Viečča ollesdeavstta Viečča ollesdeavstta
    Artigo
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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 Dahkki Mahsa Shabani, Bartha Maria Knoppers, Pascal Borry

    Almmustuhtton 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? Dahkki Davit Chokoshvili, Danya F. Vears, Pascal Borry

    Almmustuhtton 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 Dahkki Danya F. Vears, Karine Sénécal, Pascal Borry

    Almmustuhtton 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 Dahkki Sigrid Sterckx, Vojin Rakić, Julian Cockbain, Pascal Borry

    Almmustuhtton 2015
    Viečča ollesdeavstta Viečča ollesdeavstta
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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 Dahkki Pascal Borry, Jean‐Pierre Fryns, Paul Schotsmans, Kris Dierickx

    Almmustuhtton 2005
    Viečča ollesdeavstta Viečča ollesdeavstta
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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 Dahkki Danya F. Vears, Emilia Niemiec, Heidi Howard, Pascal Borry

    Almmustuhtton 2018
    Viečča ollesdeavstta Viečča ollesdeavstta
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  18. 18
    Minors and Informed Consent: A Comparative Approach

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

    Almmustuhtton 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 Dahkki Mahsa Shabani, Stephanie O. M. Dyke, Yann Joly, Pascal Borry

    Almmustuhtton 2015
    Viečča ollesdeavstta Viečča ollesdeavstta
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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 Dahkki Pascal Borry, L Stultiens, Herman Nys, J‐J Cassiman, Kris Dierickx

    Almmustuhtton 2006
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