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Participatory action research: considerations for ethical review

Social science & medicine (1982), 2005-05, Vol.60 (10), p.2333-2340

2005

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Modifying Photovoice for community-based participatory Indigenous research

Social science & medicine (1982), 2008-03, Vol.66 (6), p.1393-1405

2008

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Proposing modesty for informed consent

Social science & medicine (1982), 2007-12, Vol.65 (11), p.2284-2295

Burgess, Michael M.

2007

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From consent to institutions: Designing adaptive governance for genomic biobanks

Social science & medicine (1982), 2011-08, Vol.73 (3), p.367-374

2011

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Ethics and the ethnography of medical research in Africa

Social science & medicine (1982), 2008-09, Vol.67 (5), p.685-695

2008

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Incorporating intersectionality theory into population health research methodology: Challenges and the potential to advance health equity

Social science & medicine (1982), 2014-06, Vol.110, p.10-17

Bauer, Greta R.

2014

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From “our world” to the “real world”: Exploring the views and behaviour of policy-influential Australian public health researchers

Social science & medicine (1982), 2011-04, Vol.72 (7), p.1047-1055

2011

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Informative inducement: Study payment as a signal of risk

Social science & medicine (1982), 2010-02, Vol.70 (3), p.455-464

2010

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Understanding and representing ‘place’ in health research: A relational approach

Social science & medicine (1982), 2007-11, Vol.65 (9), p.1825-1838

2007

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Community researchers conducting health disparities research: Ethical and other insights from fieldwork journaling

Social science & medicine (1982), 2011-07, Vol.73 (1), p.145-152

2011

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Methodological and ethical issues in Internet-mediated research in the field of health: An integrated review of the literature

Social science & medicine (1982), 2007-08, Vol.65 (4), p.782-791

Whitehead, Lisa Claire

2007

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Competent children? Minors’ consent to health care treatment and research

Social science & medicine (1982), 2007-12, Vol.65 (11), p.2272-2283

Alderson, Priscilla

2007

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Conflicting notions of research ethics the mutually challenging traditions of social scientists and medical researchers

Social science & medicine (1982), 2005-10, Vol.61 (8), p.1741-1749

2005

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Variation in the interpretation of scientific integrity in community-based participatory health research

Social science & medicine (1982), 2013-11, Vol.97, p.134-142

2013

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A changing landscape for advance directives in dementia research

Social science & medicine (1982), 2010-02, Vol.70 (4), p.623-630

Pierce, Robin

2010

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Informed consent, anticipatory regulation and ethnographic practice

Social science & medicine (1982), 2007-12, Vol.65 (11), p.2223-2234

2007

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Beyond “misunderstanding”: Written information and decisions about taking part in a genetic epidemiology study

Social science & medicine (1982), 2007-12, Vol.65 (11), p.2212-2222

2007

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Ethics is for human subjects too: Participant perspectives on responsibility in health research

Social science & medicine (1982), 2013-12, Vol.98, p.224-231

2013

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Assessing the quality of democratic deliberation: A case study of public deliberation on the ethics of surrogate consent for research

Social science & medicine (1982), 2010-06, Vol.70 (12), p.1896-1903

2010

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Risk perception and decision processes underlying informed consent to research participation

Social science & medicine (1982), 2007-11, Vol.65 (10), p.2105-2115

2007

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Should “acculturation” be a variable in health research? A critical review of research on US Hispanics

Social science & medicine (1982), 2004-09, Vol.59 (5), p.973-986

2004

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Promoting research participation: Why not advertise altruism?

Social science & medicine (1982), 2008-04, Vol.66 (7), p.1451-1456

2008

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Bereaved parents’ experience of research participation

Social science & medicine (1982), 2004, Vol.58 (2), p.391-400

Dyregrov, Kari

2004

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Standardization as situation-specific achievement: Regulatory diversity and the production of value in intercontinental collaborations in stem cell medicine

Social science & medicine (1982), 2014-12, Vol.122, p.72-80

Rosemann, Achim

2014

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Supporting knowledge translation through collaborative translational research initiatives: ‘Bridging’ versus ‘blurring’ boundary-spanning approaches in the UK CLAHRC initiative

Social science & medicine (1982), 2014-04, Vol.106, p.119-127

2014

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Participatory action research: considerations for ethical review

Modifying Photovoice for community-based participatory Indigenous research

Proposing modesty for informed consent

From consent to institutions: Designing adaptive governance for genomic biobanks

Ethics and the ethnography of medical research in Africa

Incorporating intersectionality theory into population health research methodology: Challenges and the potential to advance health equity

From “our world” to the “real world”: Exploring the views and behaviour of policy-influential Australian public health researchers

Informative inducement: Study payment as a signal of risk

Understanding and representing ‘place’ in health research: A relational approach

Community researchers conducting health disparities research: Ethical and other insights from fieldwork journaling

Methodological and ethical issues in Internet-mediated research in the field of health: An integrated review of the literature

Competent children? Minors’ consent to health care treatment and research

Conflicting notions of research ethics the mutually challenging traditions of social scientists and medical researchers

Variation in the interpretation of scientific integrity in community-based participatory health research

A changing landscape for advance directives in dementia research

Informed consent, anticipatory regulation and ethnographic practice

Beyond “misunderstanding”: Written information and decisions about taking part in a genetic epidemiology study

Ethics is for human subjects too: Participant perspectives on responsibility in health research

Assessing the quality of democratic deliberation: A case study of public deliberation on the ethics of surrogate consent for research

Risk perception and decision processes underlying informed consent to research participation

Should “acculturation” be a variable in health research? A critical review of research on US Hispanics

Promoting research participation: Why not advertise altruism?

Bereaved parents’ experience of research participation

Standardization as situation-specific achievement: Regulatory diversity and the production of value in intercontinental collaborations in stem cell medicine

Supporting knowledge translation through collaborative translational research initiatives: ‘Bridging’ versus ‘blurring’ boundary-spanning approaches in the UK CLAHRC initiative

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