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The Fetus as a Patient: A Contested Concept and its Normative Implications

1, 2018

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Opportunistic genomic screening. Recommendations of the European Society of Human Genetics

European journal of human genetics : EJHG, 2021-03, Vol.29 (3), p.365-377

2021

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Stakeholder views on opportunistic genomic screening in the Netherlands: a qualitative study

European journal of human genetics : EJHG, 2021-06, Vol.29 (6), p.949-956

2021

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Mainstreaming informed consent for genomic sequencing: A call for action

European journal of cancer (1990), 2021-05, Vol.148, p.405-410

2021

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Responsible implementation of expanded carrier screening

European journal of human genetics : EJHG, 2016-06, Vol.24 (6), p.e1-e12

2016

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Debate ethics of embryo models from stem cells

Nature (London), 2018-12, Vol.564 (7735), p.183-185

2018

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Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening

European journal of human genetics : EJHG, 2015-03, Vol.23 (11), p.1438-1450

2015

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The 'thousand-dollar genome': an ethical exploration

European journal of human genetics : EJHG, 2013-06, Vol.21 Suppl 1 (S1), p.S6-S26

2013

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Balancing Ethical Pros and Cons of Stem Cell Derived Gametes

Annals of biomedical engineering, 2017-07, Vol.45 (7), p.1620-1632

2017

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Modelling human embryogenesis: embryo-like structures spark ethical and policy debate

Human reproduction update, 2020-11, Vol.26 (6), p.779-798

2020

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Advantages of expanded universal carrier screening: what is at stake?

European journal of human genetics : EJHG, 2016-01, Vol.25 (1), p.17-21

2016

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Parents, their children, whole exome sequencing and unsolicited findings: growing towards the child's future autonomy

European journal of human genetics : EJHG, 2021-06, Vol.29 (6), p.911-919

2021

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Attitudes of pregnant women and male partners towards non-invasive prenatal testing and widening the scope of prenatal screening

European journal of human genetics : EJHG, 2014-12, Vol.22 (12), p.1345-1350

2014

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Societal implications of expanded universal carrier screening: a scoping review

European journal of human genetics : EJHG, 2023-01, Vol.31 (1), p.55-72

2023

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The closer the knit, the tighter the fit: conceptual and ethical issues of human embryo modelling

Reproductive biomedicine online, 2021-12, Vol.43 (6), p.1123-1125

2021

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Response to letter entitled: Re: Mainstreaming informed consent for genomic sequencing: A call for action: Discussing opt-out options during informed consent discussions in mainstream settings

European journal of cancer (1990), 2021-09, Vol.155, p.310-312

2021

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Factors for successful implementation of population-based expanded carrier screening: learning from existing initiatives

European journal of public health, 2017-04, Vol.27 (2), p.372-377

2017

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Uncertain futures and unsolicited findings in pediatric genomic sequencing: guidelines for return of results in cases of developmental delay

BMC medical ethics, 2023-11, Vol.24 (1), p.1-98, Article 98

2023

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Anonymity 2.0: direct-to-consumer genetic testing and donor conception

Fertility and sterility, 2014-03, Vol.101 (3), p.630-632

2014

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Reflecting on Earlier Experiences with Unsolicited Findings: Points to Consider for Next-Generation Sequencing and Informed Consent in Diagnostics

Human mutation, 2013-10, Vol.34 (10), p.1322-1328

2013

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Dynamics and ethics of comprehensive preimplantation genetic testing: a review of the challenges

Human reproduction update, 2013-07, Vol.19 (4), p.366-375

2013

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What Do Parents of Children with Down Syndrome Think about Non-Invasive Prenatal Testing (NIPT)?

Journal of genetic counseling, 2017-06, Vol.26 (3), p.522-531

2017

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Situating trade-offs: Stakeholder perspectives on overtreatment versus missed diagnosis in transition to Xpert MTB/RIF Ultra in Kenya and Swaziland

PloS one, 2020-02, Vol.15 (2), p.e0228669-e0228669

2020

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NIPT-based screening for Down syndrome and beyond: what do pregnant women think?

Prenatal diagnosis, 2015-06, Vol.35 (6), p.598-604

2015

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Advances in prenatal screening: the ethical dimension

Nature reviews. Genetics, 2011-09, Vol.12 (9), p.657

2011

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The Fetus as a Patient: A Contested Concept and its Normative Implications

Opportunistic genomic screening. Recommendations of the European Society of Human Genetics

Stakeholder views on opportunistic genomic screening in the Netherlands: a qualitative study

Mainstreaming informed consent for genomic sequencing: A call for action

Responsible implementation of expanded carrier screening

Debate ethics of embryo models from stem cells

Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening

The 'thousand-dollar genome': an ethical exploration

Balancing Ethical Pros and Cons of Stem Cell Derived Gametes

Modelling human embryogenesis: embryo-like structures spark ethical and policy debate

Advantages of expanded universal carrier screening: what is at stake?

Parents, their children, whole exome sequencing and unsolicited findings: growing towards the child's future autonomy

Attitudes of pregnant women and male partners towards non-invasive prenatal testing and widening the scope of prenatal screening

Societal implications of expanded universal carrier screening: a scoping review

The closer the knit, the tighter the fit: conceptual and ethical issues of human embryo modelling

Response to letter entitled: Re: Mainstreaming informed consent for genomic sequencing: A call for action: Discussing opt-out options during informed consent discussions in mainstream settings

Factors for successful implementation of population-based expanded carrier screening: learning from existing initiatives

Uncertain futures and unsolicited findings in pediatric genomic sequencing: guidelines for return of results in cases of developmental delay

Anonymity 2.0: direct-to-consumer genetic testing and donor conception

Reflecting on Earlier Experiences with Unsolicited Findings: Points to Consider for Next-Generation Sequencing and Informed Consent in Diagnostics

Dynamics and ethics of comprehensive preimplantation genetic testing: a review of the challenges

What Do Parents of Children with Down Syndrome Think about Non-Invasive Prenatal Testing (NIPT)?

Situating trade-offs: Stakeholder perspectives on overtreatment versus missed diagnosis in transition to Xpert MTB/RIF Ultra in Kenya and Swaziland

NIPT-based screening for Down syndrome and beyond: what do pregnant women think?

Advances in prenatal screening: the ethical dimension

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