Boddington, Paula.
باولا بودينغتون
بودينغتون، باولا
VIAF ID: 237538271 (Personal)
Permalink: http://viaf.org/viaf/237538271
Preferred Forms
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- 100 1 _ ‡a Boddington, Paula
- 100 1 _ ‡a Boddington, Paula
- 100 1 _ ‡a Boddington, Paula
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- 100 1 _ ‡a Boddington, Paula
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- 100 0 _ ‡a باولا بودينغتون
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4xx's: Alternate Name Forms (4)
Works
Title | Sources |
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Adolescent Carrier Testing in Practice: The Impact of Legal Rulings and Problems with “Gillick Competence” | |
AI Ethics : A Textbook | |
Assessing the privacy risks of data sharing in genomics | |
Autonomy and Its Limits: The View from Genomics | |
Big Data, Small Talk: Lessons from the Ethical Practices of Interpersonal Communication for the Management of Biomedical Big Data | |
Bioethics and Social Reality - Edited by Matti Häyry, Tuija Takala and Peter Herrisone-Kelly | |
The canary in the coal mine: Continence care for people with dementia in acute hospital wards as a crisis of dehumanization. | |
The causation of disease - the practical and ethical consequences of competing explanations. | |
Commentary 1. 'Telling the truth about genomics': hype and hope | |
Communicating about haemophilia within the family: the importance of context and of experience. | |
Communicating genetic information in the family: enriching the debate through the notion of integrity | |
Consent Forms in Genomics: The Difference between Law and Practice | |
Data sharing in genomics--re-shaping scientific practice | |
Dietary choices, health, and freedom: hidden fats, hidden choices, hidden constraints | |
EPSRC Principles of Robotics: commentary on safety, robots as products, and responsibility | |
Ethical challenges in genomics research, c2012: | |
Ethical implications of the use of whole genome methods in medical research | |
The ethics and regulation of direct-to-consumer genetic testing | |
The “Ethics Job” | |
Heart disease and social inequality: ethical issues in the aetiology, prevention and treatment of heart disease. | |
Identifiability, Genomics and UK Data Protection Law | |
The Issue of Women’s Philosophy | |
It's only teeth--limits to genetic testing? A response to Aldred, Crawford, Savarirayan, and Savulescu | |
The Limits of Medical Paternalism | |
Measuring quality of life in theory and in practice: a dialogue between philosophical and psychological approaches. | |
Neuroethics and the Critical Appraisal of Our Moral Intuitions: A New Kid on an Old Block | |
Organ Donation After Death - Should I Decide, or Should My Family? | |
Organ donation and ethics — could Australia accept the Spanish model of organ donation? | |
Ownership of Biomedical Information in Biobanks | |
The Path Forward for DNA Data | |
Planning for translational research in genomics | |
Policy Recommendations for Carrier Testing and Predictive Testing in Childhood: A Distinction That Makes a Real Difference | |
Preimplantation genetic diagnosis for familial hypercholesterolaemia: a commentary on the recent HFEA decision | |
Presentation of the clothed self on the hospital ward: an ethnographic account of perceptual attention and implications for the personhood of people living with dementia | |
Public access to genome-wide data: five views on balancing research with privacy and protection | |
Repeating history: use and abuse of research findings and the misrepresentation of responsibility for health conditions. | |
Reply to Anstötz: what we can learn from people with learning difficulties. | |
Responsibilities of Researchers in Genetics | |
Rethinking the problems of adherence to medications | |
The rhetorical construction of ethical positions: policy recommendations for nontherapeutic genetic testing in childhood | |
Self-Deception | |
The Social and Institutional Setting of Ethics | |
Starting Analysis in Ethics: A Practical Guide | |
The Status of Morality | |
Theoretical and practical issues in the definition of health: insights from Aboriginal Australia. | |
Towards a code of ethics for artificial intelligence | |
What Ethics Is, What It Is Not, and How We Are Going to Proceed | |
Who are the mentally handicapped? | |
Working up policy: the use of specific disease exemplars in formulating general principles governing childhood genetic testing |