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Evaluation of Nine Consensus Indices in Delphi Foresight Research and Their Dependency on Delphi Survey Characteristics: A Simulation Study and Debate on Delphi Design and Interpretation

PloS one, 2015-08, Vol.10 (8), p.e0135162-e0135162

2015

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Psychiatric Illness and Clinical Negligence: When Can “Secondary Victims” Successfully Claim for Damages? Recent Developments from the United Kingdom

Journal of bioethical inquiry, 2024-06, Vol.21 (2), p.217-224

Dove, Edward S.

2024

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Data sharing in the post-genomic world: the experience of the International Cancer Genome Consortium (ICGC) Data Access Compliance Office (DACO)

PLoS computational biology, 2012, Vol.8 (7), p.e1002549-e1002549

2012

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Biobanks, Data Sharing, and the Drive for a Global Privacy Governance Framework

The Journal of law, medicine & ethics, 2015-12, Vol.43 (4), p.675-689

Dove, Edward S.

2015

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Regulatory Stewardship of Health Research : Navigating Participant Protection and Research Promotion

Dove, Edward S

1, 2020

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Requiring a Single IRB for Cooperative Research in the Revised Common Rule: What Lessons Can Be Learned from the UK and Elsewhere?

The Journal of law, medicine & ethics, 2019-06, Vol.47 (2), p.264-282

Dove, Edward S.

2019

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A Delphi Technology Foresight Study: Mapping Social Construction of Scientific Evidence on Metagenomics Tests for Water Safety

PloS one, 2015-06, Vol.10 (6), p.e0129706-e0129706

2015

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Beyond individualism: Is there a place for relational autonomy in clinical practice and research?

Clinical ethics, 2017-09, Vol.12 (3), p.150-165

2017

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Raising standards for global data-sharing

Science (American Association for the Advancement of Science), 2021-01, Vol.371 (6525), p.133-134

2021

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Confidentiality, public interest, and the human right to science: when can confidential information be used for the benefit of the wider community?

Journal of law and the biosciences, 2023-01, Vol.10 (1), p.lsad013-lsad013

Dove, Edward S

2023

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Should consent for data processing be privileged in health research? A comparative legal analysis

International data privacy law, 2020-05, Vol.10 (2), p.117-131

2020

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

Journal of medical ethics, 2019-08, Vol.45 (8), p.504-507

2019

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A qualitative interview study to determine barriers and facilitators of implementing automated decision support tools for genomic data access

BMC medical ethics, 2024-05, Vol.25 (1), p.51-51, Article 51

2024

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Achieving Procedural Parity in Managing Access to Genomic and Related Health Data: A Global Survey of Data Access Committee Members

Biopreservation and biobanking, 2024-04, Vol.22 (2), p.123-129

2024

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A human rights approach to an international code of conduct for genomic and clinical data sharing

Human genetics, 2014-07, Vol.133 (7), p.895-903

2014

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Automating Justice: An Ethical Responsibility of Computational Bioethics

American journal of bioethics, 2022-07, Vol.22 (7), p.30-33

2022

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To What Extent Does the EU General Data Protection Regulation (GDPR) Apply to Citizen Scientist-Led Health Research with Mobile Devices?

The Journal of law, medicine & ethics, 2020-03, Vol.48 (1_suppl), p.187-195

2020

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Ethics review of big data research: What should stay and what should be reformed?

BMC medical ethics, 2021-04, Vol.22 (1), p.51-51, Article 51

2021

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Leveraging Algorithms to Improve Decision-Making Workflows for Genomic Data Access and Management

Biopreservation and biobanking, 2022-10, Vol.20 (5), p.429-435

2022

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Genomic cloud computing: legal and ethical points to consider

European journal of human genetics : EJHG, 2015-10, Vol.23 (10), p.1271-1278

2015

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International Charter of principles for sharing bio-specimens and data

European journal of human genetics : EJHG, 2015-06, Vol.23 (6), p.721-728

2015

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Signalling Standards for Progress: Bridging the Divide Between a Valid Consent to Use Patient Data Under Data Protection Law and the Common Law Duty of Confidentiality

Medical law review, 2021-10, Vol.29 (3), p.411-445

2021

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Review of Calvin Wai-Loon Ho, Juridification in Bioethics: Governance of Human Pluripotent Cell Research

American journal of bioethics, 2017-11, Vol.17 (11), p.W12-W13

Dove, Edward S

2017

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"Data makes the story come to life:" understanding the ethical and legal implications of Big Data research involving ethnic minority healthcare workers in the United Kingdom-a qualitative study

BMC medical ethics, 2022-12, Vol.23 (1), p.136-136, Article 136

2022

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The epiknowledge of socially responsible innovation

EMBO reports, 2014-05, Vol.15 (5), p.462-463

2014

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Evaluation of Nine Consensus Indices in Delphi Foresight Research and Their Dependency on Delphi Survey Characteristics: A Simulation Study and Debate on Delphi Design and Interpretation

Psychiatric Illness and Clinical Negligence: When Can “Secondary Victims” Successfully Claim for Damages? Recent Developments from the United Kingdom

Data sharing in the post-genomic world: the experience of the International Cancer Genome Consortium (ICGC) Data Access Compliance Office (DACO)

Biobanks, Data Sharing, and the Drive for a Global Privacy Governance Framework

Regulatory Stewardship of Health Research : Navigating Participant Protection and Research Promotion

Requiring a Single IRB for Cooperative Research in the Revised Common Rule: What Lessons Can Be Learned from the UK and Elsewhere?

A Delphi Technology Foresight Study: Mapping Social Construction of Scientific Evidence on Metagenomics Tests for Water Safety

Beyond individualism: Is there a place for relational autonomy in clinical practice and research?

Raising standards for global data-sharing

Confidentiality, public interest, and the human right to science: when can confidential information be used for the benefit of the wider community?

Should consent for data processing be privileged in health research? A comparative legal analysis

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

A qualitative interview study to determine barriers and facilitators of implementing automated decision support tools for genomic data access

Achieving Procedural Parity in Managing Access to Genomic and Related Health Data: A Global Survey of Data Access Committee Members

A human rights approach to an international code of conduct for genomic and clinical data sharing

Automating Justice: An Ethical Responsibility of Computational Bioethics

To What Extent Does the EU General Data Protection Regulation (GDPR) Apply to Citizen Scientist-Led Health Research with Mobile Devices?

Ethics review of big data research: What should stay and what should be reformed?

Leveraging Algorithms to Improve Decision-Making Workflows for Genomic Data Access and Management

Genomic cloud computing: legal and ethical points to consider

International Charter of principles for sharing bio-specimens and data

Signalling Standards for Progress: Bridging the Divide Between a Valid Consent to Use Patient Data Under Data Protection Law and the Common Law Duty of Confidentiality

Review of Calvin Wai-Loon Ho, Juridification in Bioethics: Governance of Human Pluripotent Cell Research

"Data makes the story come to life:" understanding the ethical and legal implications of Big Data research involving ethnic minority healthcare workers in the United Kingdom-a qualitative study

The epiknowledge of socially responsible innovation

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