List of works - Fiona Miller

'Your true and proper gender': the Barr body as a good enough science of sex.

scientific article

A Concurrent Analysis of Three Institutions that Transform Health Technology-Based Ventures: Economic Policy, Capital Investment, and Market Approval

article

A secondary benefit: the reproductive impact of carrier results from newborn screening for cystic fibrosis

scientific article published on 8 September 2016

CANADIAN PIONEERS: Remembering Norma Ford Walker

article

Carrier detection and clinical uncertainty: the case for public health ethics

article

Citizen expectations of 'academic entrepreneurship' in health research: public science, practical benefit

scientific article published on 14 May 2014

Confronting the "gray zones" of technology assessment: evaluating genetic testing services for public insurance coverage in Canada

scientific article published on 01 January 2003

Contending visions in the evolution of genetic medicine: the case of cancer genetic services in Ontario, Canada

scientific article published on 23 April 2008

Decision-making about inherited cancer risk: exploring dimensions of genetic responsibility

scientific article published on 18 March 2009

Do canadian researchers and the lay public prioritize biomedical research outcomes equally? A choice experiment

scientific article published on April 2013

Does a duty of disclosure foster special treatment of genetic research participants?

scientific article published on 17 May 2013

Early economic evaluation of emerging health technologies: protocol of a systematic review

scientific article

Economic considerations for health insurance coverage of emerging genetic tests

scientific article published on January 2003

Ethics in Canadian health technology assessment: a descriptive review

scientific article published on October 2009

Examining the ethical and social issues of health technology design through the public appraisal of prospective scenarios: a study protocol describing a multimedia-based deliberative method

scientific article

Expectations and values about expanded newborn screening: a public engagement study

scientific article published on February 2013

Gene patents—more evidence needed, but policymakers must act

article

Genomic testing in cancer: patient knowledge, attitudes, and expectations

scientific article published on 24 June 2014

Half a Century of Wilson & Jungner: Reflections on the Governance of Population Screening

scientific article published on 06 July 2020

Health-care providers' views on pursuing reproductive benefit through newborn screening: the case of sickle cell disorders.

scientific article published on 9 November 2011

Horizon 2020 and the need to reinvent health technology development

scientific article published on 25 October 2013

How do values shape technology design? An exploration of what makes the pursuit of health and wealth legitimate in academic spin-offs

article by Pascale Lehoux et al published June 2014 in Sociology of Health and Illness

Imagining value, imagining users: academic technology transfer for health innovation

scientific article

Incorporating documents into qualitative nursing research

scientific article

Insulin pump use and discontinuation in children and teens: a population-based cohort study in Ontario, Canada

scientific article published on 8 January 2016

Leveraging the “living laboratory”: On the emergence of the entrepreneurial hospital ⬇️

scientific article published on 05 May 2012

Managing sickle cell carrier results generated through newborn screening in Ontario: a precedent-setting policy story

scientific article published on 20 October 2016

Measuring clinical utility in the context of genetic testing: a scoping review

scientific article published on 21 October 2020

Not so simple: a quasi-experimental study of how researchers adjudicate genetic research results

scientific article

One thing leads to another: the cascade of obligations when researchers report genetic research results to study participants ⬇️

scientific article published on February 15, 2012

Parents' perspectives on participating in genetic research in autism

scientific article published on March 2013

Parents' preferences for drug treatments in juvenile idiopathic arthritis: a discrete choice experiment

scientific article published in September 2012

Postal survey of physicians and laboratories: practices and perceptions of molecular oncology testing

scientific article

Public involvement and health research system governance: a qualitative study

article

Public involvement in health research systems: a governance framework

article

Public views on participating in newborn screening using genome sequencing

scientific article

Questioning the consensus: managing carrier status results generated by newborn screening

article

Rebalancing health systems toward community-based care: The role of subsectoral politics

article

Reconsidering reproductive benefit through newborn screening: a systematic review of guidelines on preconception, prenatal and newborn screening

scientific article

Redefining disease? The nosologic implications of molecular genetic knowledge

scientific article

Reflections on the cost of "low-cost" whole genome sequencing: framing the health policy debate

scientific article (publication date: November 2013)

Reframing norms: boundary maintenance and partial accommodations in the work of academic technology transfer

Reply to Ross' commentary: Reproductive benefit through newborn screening: preferences, policy and ethics ⬇️

scientific article published on February 29, 2012

Ruling in and ruling out: Implications of molecular genetic diagnoses for disease classification

scientific article published on 14 June 2005

Scientists and policy-makers at work: listening to epistemic conversations in a genetics science network

article

Testing personalized medicine: patient and physician expectations of next-generation genomic sequencing in late-stage cancer care

scientific article published on 17 July 2013

The Helix in the Labyrinth: Do We Need Genetic Health Services and Policy Research?

article

The expansion of newborn screening: is reproductive benefit an appropriate pursuit?

The importance of being marginal: Norma Ford Walker and a Canadian school of medical genetics

scientific article published in August 2002

Understanding sickle cell carrier status identified through newborn screening: a qualitative study.

scientific article

Understanding the new human genetics: a review of scientific editorials.

scientific article

Vulnerability of the medical product supply chain: the wake-up call of COVID-19

scientific article published on 02 November 2020

What Place Ethics?

What does it mean to trust a health system? A qualitative study of Canadian health care values

scientific article

What is a meaningful result? Disclosing the results of genomic research in autism to research participants

scientific article published on 17 March 2010

When research seems like clinical care: a qualitative study of the communication of individual cancer genetic research results

scientific article

List of works by Fiona Miller

'Your true and proper gender': the Barr body as a good enough science of sex.

A Concurrent Analysis of Three Institutions that Transform Health Technology-Based Ventures: Economic Policy, Capital Investment, and Market Approval

A secondary benefit: the reproductive impact of carrier results from newborn screening for cystic fibrosis

CANADIAN PIONEERS: Remembering Norma Ford Walker

Carrier detection and clinical uncertainty: the case for public health ethics

Citizen expectations of 'academic entrepreneurship' in health research: public science, practical benefit

Confronting the "gray zones" of technology assessment: evaluating genetic testing services for public insurance coverage in Canada

Contending visions in the evolution of genetic medicine: the case of cancer genetic services in Ontario, Canada

Decision-making about inherited cancer risk: exploring dimensions of genetic responsibility

Do canadian researchers and the lay public prioritize biomedical research outcomes equally? A choice experiment

Does a duty of disclosure foster special treatment of genetic research participants?

Early economic evaluation of emerging health technologies: protocol of a systematic review

Economic considerations for health insurance coverage of emerging genetic tests

Ethics in Canadian health technology assessment: a descriptive review

Examining the ethical and social issues of health technology design through the public appraisal of prospective scenarios: a study protocol describing a multimedia-based deliberative method

Expectations and values about expanded newborn screening: a public engagement study

Gene patents—more evidence needed, but policymakers must act

Genomic testing in cancer: patient knowledge, attitudes, and expectations

Half a Century of Wilson & Jungner: Reflections on the Governance of Population Screening

Health-care providers' views on pursuing reproductive benefit through newborn screening: the case of sickle cell disorders.

Horizon 2020 and the need to reinvent health technology development

How do values shape technology design? An exploration of what makes the pursuit of health and wealth legitimate in academic spin-offs

Imagining value, imagining users: academic technology transfer for health innovation

Incorporating documents into qualitative nursing research

Insulin pump use and discontinuation in children and teens: a population-based cohort study in Ontario, Canada

Leveraging the “living laboratory”: On the emergence of the entrepreneurial hospital ⬇️

Managing sickle cell carrier results generated through newborn screening in Ontario: a precedent-setting policy story

Measuring clinical utility in the context of genetic testing: a scoping review

Not so simple: a quasi-experimental study of how researchers adjudicate genetic research results

One thing leads to another: the cascade of obligations when researchers report genetic research results to study participants ⬇️

Parents' perspectives on participating in genetic research in autism

Parents' preferences for drug treatments in juvenile idiopathic arthritis: a discrete choice experiment

Postal survey of physicians and laboratories: practices and perceptions of molecular oncology testing

Public involvement and health research system governance: a qualitative study

Public involvement in health research systems: a governance framework

Public views on participating in newborn screening using genome sequencing

Questioning the consensus: managing carrier status results generated by newborn screening

Rebalancing health systems toward community-based care: The role of subsectoral politics

Reconsidering reproductive benefit through newborn screening: a systematic review of guidelines on preconception, prenatal and newborn screening

Redefining disease? The nosologic implications of molecular genetic knowledge

Reflections on the cost of "low-cost" whole genome sequencing: framing the health policy debate

Reframing norms: boundary maintenance and partial accommodations in the work of academic technology transfer

Reply to Ross' commentary: Reproductive benefit through newborn screening: preferences, policy and ethics ⬇️

Ruling in and ruling out: Implications of molecular genetic diagnoses for disease classification

Scientists and policy-makers at work: listening to epistemic conversations in a genetics science network

Testing personalized medicine: patient and physician expectations of next-generation genomic sequencing in late-stage cancer care

The Helix in the Labyrinth: Do We Need Genetic Health Services and Policy Research?

The expansion of newborn screening: is reproductive benefit an appropriate pursuit?

The importance of being marginal: Norma Ford Walker and a Canadian school of medical genetics

Understanding sickle cell carrier status identified through newborn screening: a qualitative study.

Understanding the new human genetics: a review of scientific editorials.

Vulnerability of the medical product supply chain: the wake-up call of COVID-19

What Place Ethics?

What does it mean to trust a health system? A qualitative study of Canadian health care values

What is a meaningful result? Disclosing the results of genomic research in autism to research participants

When research seems like clinical care: a qualitative study of the communication of individual cancer genetic research results