Lista de obras - Graeme T. Laurie - Dominio Público Uruguay

"DNA theft": new crime in the UK.

artículo científico publicado en 2003

A qualitative study of participants' views on re-consent in a longitudinal biobank

artículo científico publicado en 2017

An Ethics Framework for Big Data in Health and Research

scholarly article by Vicki Xafis et al published September 2019 in Asian Bioethics Review

Asian Bioethics Review Enters a New Era

artículo científico publicado en 2020

Balancing open source stem cell science with commercialization

artículo científico publicado en 2011

Better to hesitate at the threshold of compulsion: PKU testing and the concept of family autonomy in Eire.

artículo científico publicado en 2002

Beyond regulatory compression: confronting the liminal spaces of health research regulation

artículo científico publicado en 2016

Bidding farewell to 2020: what lessons have we learned and what can bioethics continue to teach us?

artículo científico publicado en 2020

Biomedicine, self and society: An agenda for collaboration and engagement

scholarly article by Martyn Pickersgill published in January 2019

CHALLENGING MEDICAL-LEGAL NORMS: THE ROLE OF AUTONOMY, CONFIDENTIALITY, AND PRIVACY IN PROTECTING INDIVIDUAL AND FAMILIAL GROUP RIGHTS IN GENETIC INFORMATION

artículo científico publicado en 2001

COMMENTARY

Charting Regulatory Stewardship in Health Research: Making the Invisible Visible.

artículo científico publicado en 2018

Clarifying how to deploy the public interest criterion in consent waivers for health data and tissue research

scientific article published on 20 March 2020

Co-production and Managing Uncertainty in Health Research Regulation: A Delphi Study

scientific article published on 31 August 2019

Cross-Sectoral Big Data: The Application of an Ethics Framework for Big Data in Health and Research

artículo científico publicado en 2019

Data Safe Havens and Trust: Toward a Common Understanding of Trusted Research Platforms for Governing Secure and Ethical Health Research

artículo científico publicado en 2016

Delivering a Practical Framework for Ethical Decision-Making Involving Big Data in Health and Research

scholarly article by Graeme Laurie & E. Shyong Tai published September 2019 in Asian Bioethics Review

Delivering proportionate governance in the era of eHealth: Making linkage and privacy work together

artículo científico publicado en 2013

Developments in medical law in the United Kingdom in 2005 and 2006.

artículo científico publicado en 2006

Editorial comment on Y M Barilan's ‘Is the clock ticking for the terminally ill patients in Israel?'.

artículo científico publicado en 2004

Enacting Bioethics

artículo científico publicado en 2020

Evidence of support for biobanking practices.

artículo científico publicado en 2008

Fail to Prepare and you Prepare to Fail: the Human Rights Consequences of the UK Government's Inaction during the COVID-19 Pandemic

artículo científico publicado en 2020

Familial genetic risks: how can we better navigate patient confidentiality and appropriate risk disclosure to relatives?

artículo científico publicado en 2019

Genetic databases: assessing the benefits and the impact on human and patient rights--a WHO report

artículo científico publicado en 2004

Genetics and patients' rights: where are the limits?

artículo científico publicado en 2000

Governing risk, engaging publics and engendering trust: New horizons for law and social science?

article by S. H. E. Harmon et al published 15 January 2013 in Science and Public Policy

How do we make sense of chaos? Navigating health research regulation through the liminality of the Brexit process

article

In defence of ignorance: genetic information and the right not to know

artículo científico publicado en 1999

Learning lessons and making differences: the European Association of Health Law conference 2009.

artículo científico publicado en 2010

Liminality and the Limits of Law in Health Research Regulation: What are we Missing in the Spaces in-Between?

artículo científico publicado en 2016

Memories of Ken Mason

artículo científico publicado en 2017

On moving targets and magic bullets: Can the UK lead the way with responsible data linkage for health research?

artículo científico publicado en 2015

Patents, morality and DNA: should there be intellectual property protection of the Human Genome Project?

Protecting and promoting privacy in an uncertain world: further defences of ignorance and the right not to know

scientific article published on 01 June 2000

Recognizing the Right Not to Know: Conceptual, Professional, and Legal Implications

artículo científico publicado en 2014

Reconfiguring Social Value in Health Research Through the Lens of Liminality

scientific article published on February 2017

Reflexive governance in biobanking: on the value of policy led approaches and the need to recognise the limits of law ⬇️

artículo científico publicado el 16 de julio de 2011

Respecting Autonomy Over Time: Policy and Empirical Evidence on Re-Consent in Longitudinal Biomedical Research

artículo científico publicado en 2016

Rhetoric or reality: what is the legal status of the consent form in health-related research?

artículo científico publicado en 2012

Role of the UK Biobank Ethics and Governance Council

artículo científico publicado en 2009

Susceptibility genes and neurological disorders: learning the right lessons from the human genome project.

artículo científico publicado en 2000

Sustaining Bioethical Contributions in Times of Crisis and Change

artículo científico publicado en 2020

Tackling community concerns about commercialisation and genetic research: A modest interdisciplinary proposal

artículo científico publicado en 2007

The European Association Of Health Law: addressing unmet needs in policy, practice and research

article

The other side of the coin: Harm due to the non-use of health-related data.

artículo científico publicado en 2016

The social licence for research: why care.data ran into trouble

artículo científico publicado en 2015

The social sciences, humanities, and health

article

The stem cell research environment: a patchwork of patchworks

artículo científico publicado en 2009

Towards Principles-Based Approaches to Governance of Health-related Research using Personal Data

artículo científico publicado en 2013

When Can the Child Speak for Herself? The Limits of Parental Consent in Data Protection Law for Health Research.

artículo científico publicado en 2017

Lista de obras de Graeme T. Laurie

"DNA theft": new crime in the UK.

A qualitative study of participants' views on re-consent in a longitudinal biobank

An Ethics Framework for Big Data in Health and Research

Asian Bioethics Review Enters a New Era

Balancing open source stem cell science with commercialization

Better to hesitate at the threshold of compulsion: PKU testing and the concept of family autonomy in Eire.

Beyond regulatory compression: confronting the liminal spaces of health research regulation

Bidding farewell to 2020: what lessons have we learned and what can bioethics continue to teach us?

Biomedicine, self and society: An agenda for collaboration and engagement

CHALLENGING MEDICAL-LEGAL NORMS: THE ROLE OF AUTONOMY, CONFIDENTIALITY, AND PRIVACY IN PROTECTING INDIVIDUAL AND FAMILIAL GROUP RIGHTS IN GENETIC INFORMATION

COMMENTARY

COMMENTARY

Charting Regulatory Stewardship in Health Research: Making the Invisible Visible.

Clarifying how to deploy the public interest criterion in consent waivers for health data and tissue research

Co-production and Managing Uncertainty in Health Research Regulation: A Delphi Study

Cross-Sectoral Big Data: The Application of an Ethics Framework for Big Data in Health and Research

Data Safe Havens and Trust: Toward a Common Understanding of Trusted Research Platforms for Governing Secure and Ethical Health Research

Delivering a Practical Framework for Ethical Decision-Making Involving Big Data in Health and Research

Delivering proportionate governance in the era of eHealth: Making linkage and privacy work together

Developments in medical law in the United Kingdom in 2005 and 2006.

Editorial comment on Y M Barilan's ‘Is the clock ticking for the terminally ill patients in Israel?'.

Enacting Bioethics

Evidence of support for biobanking practices.

Fail to Prepare and you Prepare to Fail: the Human Rights Consequences of the UK Government's Inaction during the COVID-19 Pandemic

Familial genetic risks: how can we better navigate patient confidentiality and appropriate risk disclosure to relatives?

Genetic databases: assessing the benefits and the impact on human and patient rights--a WHO report

Genetics and patients' rights: where are the limits?

Governing risk, engaging publics and engendering trust: New horizons for law and social science?

How do we make sense of chaos? Navigating health research regulation through the liminality of the Brexit process

In defence of ignorance: genetic information and the right not to know

Learning lessons and making differences: the European Association of Health Law conference 2009.

Liminality and the Limits of Law in Health Research Regulation: What are we Missing in the Spaces in-Between?

Memories of Ken Mason

On moving targets and magic bullets: Can the UK lead the way with responsible data linkage for health research?

Patents, morality and DNA: should there be intellectual property protection of the Human Genome Project?

Protecting and promoting privacy in an uncertain world: further defences of ignorance and the right not to know

Recognizing the Right Not to Know: Conceptual, Professional, and Legal Implications

Reconfiguring Social Value in Health Research Through the Lens of Liminality

Reflexive governance in biobanking: on the value of policy led approaches and the need to recognise the limits of law ⬇️

Respecting Autonomy Over Time: Policy and Empirical Evidence on Re-Consent in Longitudinal Biomedical Research

Rhetoric or reality: what is the legal status of the consent form in health-related research?

Role of the UK Biobank Ethics and Governance Council

Susceptibility genes and neurological disorders: learning the right lessons from the human genome project.

Sustaining Bioethical Contributions in Times of Crisis and Change

Tackling community concerns about commercialisation and genetic research: A modest interdisciplinary proposal

The European Association Of Health Law: addressing unmet needs in policy, practice and research

The other side of the coin: Harm due to the non-use of health-related data.

The social licence for research: why care.data ran into trouble

The social sciences, humanities, and health

The stem cell research environment: a patchwork of patchworks

Towards Principles-Based Approaches to Governance of Health-related Research using Personal Data

When Can the Child Speak for Herself? The Limits of Parental Consent in Data Protection Law for Health Research.