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• Members
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• Research
  • Genetics
    • Governing Genetic Databases
    • Procardis: Ethical issues in the translation of genomic research on coronary artery disease into clinical practice.
    • The impact of human gene patents on translational research in genetics
    • Research and Clinical Practice
    • The Genethics Club: an ethnography of ethics in clinical genetics practice
    • Oxford Genetics Knowledge Park
    • The Oxford Bioethics Network
  • Global Public Health and Epidemiology
    • The concept of social value in developing countries
    • The impact of genetic risk in UK Pakistani families
    • The use of patient records in e-science research in medicine
    • MalariaGEN overview
    • Ethical challenges in the release and publication of ethnicity-related research results (MalariaGEN)
    • The roles of ethics in effective global genomics research networks (MalariaGEN)
    • Agenda Setting Social Science and Ethics Workshop 2007 (MalariaGEN)
    • Consent in genomic research in malaria (MalariaGEN)
  • Clinical Ethics
    • UK Clinical Ethics Network Project
  • Mental Health and Neuroscience
    • Neuroscience and moral decision-making
    • Competence and treatment decision-making in Anorexia Nervosa
    • Ethical issues for the carers of people with Alzheimer's
    • Survey of psychiatrists regarding decision-making in anorexia nervosa
    • Ethical issues in the use of MRI imaging in newborn infants with birth asphyxia
  • Research Archive
    • Genetics Archive
    • Clinical Ethics Archive
• Research Staff
  • Michael Parker
  • Carolyn April
  • Susan Barrington
  • Paula Boddington
  • Lindsey Brown
  • Susan Bull
  • Andrew Cooper
  • Sue Gibbons
  • Naomi Hawkins
  • Catherine Heeney
  • Don Hill
  • Tony Hope
  • Jane Kaye
  • Geoffrey Lairumbi
  • Vicki Marsh
  • Alison Shaw
  • Anne Slowther
  • Jacinta Tan
  • Jantina de Vries
  • Dominic Wilkinson
  • Visting Researchers
  • Ethox Fellows
  • Former Staff Members
• Education
  • Teaching Materials
    • course aims, objectives and resources
    • session one (year 4): introductory Lecture
    • session two (year 4): confidentiality and introduction to medical law
    • session three (year 4): consent
    • session four (year 4): ethical and legal issues at the end of life
    • session five (year 4): genetic testing
    • session six (year 4): medical research with human participants
    • year four assessment
    • session seven (year 5): treating patients without consent
    • session eight (year 5): pregnancy
  • Courses and Workshops
  • Doing Postgraduate Research at Ethox
  • PFGS Event 2008
• Clinical Ethics Support
  • UK Clinical Ethics Network
  • Provision of ethics support to health professionals and clinical ethics committees
  • Clinical Ethics Education
  • The Genethics Club
• Ethox Photo Archive
• Bibliography
  • Governing Genetic Databases: Collection, Storage and Use
  • Genetic testing without consent: the implications of the new Human Tissue Act 2004
  • End of Life Decision-Making in Neonatal Care
  • Do we need a uniform regulatory system for biobanks across Europe?
  • Safeguards for research using large scale DNA collections
  • The Class Action in Common Law Legal Systems: A Comparative Perspective by Rachael P Mulheron
  • Governing Genetic Databases: Challenges Facing Research Regulation and Practice
  • Governance of Population Genetic Databases: A Comparative Analysis of Legal Regulation in Estonia, Iceland, Sweden and the UK
  • Police access to DNA samples and information
  • Lessons from European Population Genetic Databases: Comparing the law in Iceland, Sweden, Estonia and the UK
  • Implications of data protection legislation for family history.
  • Ethical Review of Research into Rare Genetic Disorders
  • Genetic Information: A Joint Account?
  • Are UK Genetic Databases Governed Adequately? A Comparative Legal Analysis
  • The Best Possible Child
  • Medical Ethics and Law: The Core Curriculum
  • Medical Ethics: A Very Short Introduction
  • Competence to refuse treatment in anorexia nervosa
  • Ethical problems before conception
  • Health care need: three interpretations
  • Valid Consent for Genomic Epidemiology in Developing Countries
  • Influenza in the Neonatal Intesive Care Unit
  • Is it in the Best Interests of an Intellectually Disabled Infant to Die?
  • Death in the Neonatal Intensive Care Unit: Changing Patterns of End of Life Care Over Two Decades
  • Awake Upper Airway Obstruction in Cerebral Palsy
  • Selling Organs and Souls: Should the State Prohibit 'Demeaning' Practices?
  • Communicating about haemophilia within the family: the importance of context and experience
  • Trouble with biocitizenship: duties, responsibilities, identity
  • Working up policy: the use of specific disease exemplars in formulating general principles governing childhood genetic testing
  • Policy recommendations for carrier testing and predictive testing in childhood: a distinction that makes a real difference
  • Returning to the Alder Hey Report and its reporting: addressing confusions and improving inquiries
  • Ethnography/Ethics
  • Informed Consent in a Changing Environment
• Contact Us
  • Contact Information
• About Ethox
  • What is Ethox?
  • The Ethox Foundation
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