Lista de obras - Eline M Bunnik - Dominio Público Uruguay

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

artículo científico publicado en 2018

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

artículo científico publicado en 2012

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

artículo científico publicado en 2017

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

artículo científico publicado en 2018

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

artículo científico publicado en 2017

Do genomic tests enhance autonomy?

artículo científico publicado en 2014

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

artículo científico publicado en 2020

Ethical Issues in Research and Development of Epigenome-wide Technologies

artículo científico publicado en 2020

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

artículo científico publicado en 2018

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

artículo científico publicado en 2017

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

artículo científico publicado en 2017

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

artículo científico publicado en 2018

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

artículo científico publicado en 2019

Incidental findings in population imaging revisited

artículo científico publicado en 2016

Informed consent in direct-to-consumer personal genome testing: the outline of a model between specific and generic consent.

artículo científico publicado en 2012

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

artículo científico publicado en 2022

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

artículo científico publicado en 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

artículo científico publicado en 2018

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

artículo científico publicado en 2018

Mainstreaming informed consent for genomic sequencing: A call for action

artículo científico publicado en 2021

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

artículo científico publicado en 2018

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

artículo científico publicado en 2011

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

artículo científico publicado en 2014

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

artículo científico publicado en 2018

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

artículo científico publicado en 2017

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

artículo científico publicado en 2022

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

artículo científico publicado en 2016

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

artículo científico publicado en 2022

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

artículo científico publicado en 2021

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

artículo científico publicado en 2020

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

artículo científico publicado en 2017

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

artículo científico publicado en 2019

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

artículo científico publicado en 2017

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

artículo científico publicado en 2013

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

artículo científico publicado en 2012

Uninformed consent in nutrigenomic research

artículo científico publicado en 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?

artículo científico publicado en 2010

Lista de obras de Eline M Bunnik

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

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

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

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

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

Do genomic tests enhance autonomy?

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

Ethical Issues in Research and Development of Epigenome-wide Technologies

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

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

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

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

How Attitudes Research Contributes to Overoptimistic Expectations of Personal Genome Testing

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

Incidental findings in population imaging revisited

Informed consent in direct-to-consumer personal genome testing: the outline of a model between specific and generic consent.

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

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

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

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

Mainstreaming informed consent for genomic sequencing: A call for action

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Uninformed consent in nutrigenomic research

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

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