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List of works by Eline M Bunnik

A Model for Communication About Longshot Treatments in the Context of Early Access to Unapproved, Investigational Drugs.

scientific article published in January 2018

A tiered-layered-staged model for informed consent in personal genome testing ⬇️

scientific article published on November 21, 2012

Amniocentesis is still the best option for advanced genomic testing in case of fetal malformations

scientific article published on 17 November 2017

At, with and beyond risk: expectations of living with the possibility of future dementia.

scientific article published on 16 April 2018

Choosing between Higher and Lower Resolution Microarrays: do Pregnant Women Have Sufficient Knowledge to Make Informed Choices Consistent with their Attitude?

scientific article published on 4 July 2017

Do genomic tests enhance autonomy?

scientific article

Ethical Considerations in Screening for Rapid Eye Movement Sleep Behavior Disorder in the General Population

scientific article published on 15 September 2020

Ethical Issues in Research and Development of Epigenome-wide Technologies

scientific article published on 13 April 2020

Ethical Issues in the Beauty Salon: The Development of National Ethics Guidelines for Aestheticians in the Netherlands

scientific article published on 01 January 2018

Ethical Issues in the Development of Readiness Cohorts in Alzheimer's Disease Research

scientific article

Ethical framework for the detection, management and communication of incidental findings in imaging studies, building on an interview study of researchers' practices and perspectives

scientific article

Ethics of routine: a critical analysis of the concept of 'routinisation' in prenatal screening.

scientific article

How Attitudes Research Contributes to Overoptimistic Expectations of Personal Genome Testing

journal article; published in The American Journal of Bioethics in 2009

Implementing non-invasive prenatal testing (NIPT) in the Netherlands: An interview study exploring opinions about and experiences with societal pressure, reimbursement, and an expanding scope

scientific article published on 11 November 2019

Incidental findings in population imaging revisited

scientific article published on 9 February 2016

Informed Consent in Direct‐to‐Consumer Personal Genome Testing: The Outline of A Model between Specific and Generic Consent ⬇️

scientific article published on November 8, 2012

Informed consent practices for exome sequencing: An interview study with clinical geneticists in the Netherlands

scientific article published on 12 February 2022

Let Us Not Take the Ethics Out of Innovative Practice: A Case Against Institutional Review

scientific article published on 01 June 2019

Limits to the scope of non-invasive prenatal testing (NIPT): an analysis of the international ethical framework for prenatal screening and an interview study with Dutch professionals

scientific article published on 19 October 2018

Little to lose and no other options: Ethical issues in efforts to facilitate expanded access to investigational drugs

scientific article published on 18 June 2018

Mainstreaming informed consent for genomic sequencing: A call for action

scientific article published on 27 March 2021

On the personal utility of Alzheimer's disease-related biomarker testing in the research context

scientific article published on 28 August 2018

Personal genome testing: test characteristics to clarify the discourse on ethical, legal and societal issues

scientific article

Personal utility in genomic testing: is there such a thing?

scientific article published on 28 May 2014

Perspectives on Communicating Biomarker-Based Assessments of Alzheimer's Disease to Cognitively Healthy Individuals.

scientific article published in January 2018

Physicians Must Discuss Potential Long-Term Risks of Fecal Microbiota Transplantation to Ensure Informed Consent

scientific article published in May 2017

Physicians’ Perspectives on Ethical Issues Regarding Expensive Anti-Cancer Treatments: A Qualitative Study

scientific article published in 2022

Psychological, behavioral and social effects of disclosing Alzheimer's disease biomarkers to research participants: a systematic review.

scientific article

Response to Open Peer Commentaries on Toward a Framework for Assessing Privacy Risks in Multi-Omic Research and Databases

scientific article published in 2022

Response to letter entitled: Re: Mainstreaming informed consent for genomic sequencing: A call for action

scientific article published on 12 August 2021

Rethinking counselling in prenatal screening: An ethical analysis of informed consent in the context of non-invasive prenatal testing (NIPT)

scientific article published on 04 July 2020

Scanning the body, sequencing the genome: Dealing with unsolicited findings

scientific article published on 4 October 2017

Should pregnant women be charged for non-invasive prenatal screening? Implications for reproductive autonomy and equal access

scientific article published on 16 September 2019

The changing landscape of expanded access to investigational drugs for patients with unmet medical needs: ethical implications

scientific article published on 21 February 2017

The new genetics and informed consent: differentiating choice to preserve autonomy

scientific article published on 30 May 2013

The role of disease characteristics in the ethical debate on personal genome testing

scientific article

Uninformed consent in nutrigenomic research

scientific article published on 10 May 2017

What do patients with unmet medical needs want? A qualitative study of patients' views and experiences with expanded access to unapproved, investigational treatments in the Netherlands

scientific article published on 09 November 2019

Why not order direct-to-consumer genetic testing for your children?

scientific article published on 15 December 2010

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