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Will the EU Medical Device Regulation help to improve the safety and performance of medical AI devices?

Digital health, 2022, Vol.8, p.20552076221089079-20552076221089079

Niemiec, Emilia

2022

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Willingness to donate genomic and other medical data: results from Germany

European journal of human genetics : EJHG, 2020-08, Vol.28 (8), p.1000-1009

2020

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Analysis of VUS reporting, variant reinterpretation and recontact policies in clinical genomic sequencing consent forms

European journal of human genetics : EJHG, 2018-12, Vol.26 (12), p.1743-1751

2018

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Ethical issues related to research on genome editing in human embryos

Computational and structural biotechnology journal, 2020-01, Vol.18, p.887-896

2020

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Trust in genomic data sharing among members of the general public in the UK, USA, Canada and Australia

Human genetics, 2019-12, Vol.138 (11-12), p.1237-1246

2019

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COVID-19 and misinformation: Is censorship of social media a remedy to the spread of medical misinformation?

EMBO reports, 2020-11, Vol.21 (11), p.e51420-e51420

Niemiec, Emilia

2020

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Communicating genetic information to family members: analysis of consent forms for diagnostic genomic sequencing

European journal of human genetics : EJHG, 2020-09, Vol.28 (9), p.1160-1167

2020

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Members of the public in the USA, UK, Canada and Australia expressing genetic exceptionalism say they are more willing to donate genomic data

European journal of human genetics : EJHG, 2020-04, Vol.28 (4), p.424-434

2020

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Reply to Bronstein and Vinogradov

EMBO reports, 2021-03, Vol.22 (3), p.e52500-n/a

Niemiec, Emilia

2021

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COVID‐19 and misinformation

EMBO reports, 2020-11, Vol.21 (11), p.n/a

Niemiec, Emilia

2020

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Attitudes of publics who are unwilling to donate DNA data for research

European journal of medical genetics, 2019-05, Vol.62 (5), p.316-323

2019

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Transparency, consent and trust in the use of customers' data by an online genetic testing company: an Exploratory survey among 23andMe users

New genetics and society, 2020-10, Vol.39 (4), p.459-482

2020

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A cautionary tale about the adoption of medical AI in Sweden

Nature machine intelligence, 2023-01, Vol.5 (1), p.5-7

Niemiec, Emilia

2023

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'Your DNA, Your Say': global survey gathering attitudes toward genomics: design, delivery and methods

Personalized medicine, 2018-07, Vol.15 (4), p.311-318

2018

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Engage egg donors in editing debate

Nature (London), 2019-11, Vol.575 (7781), p.51-51

2019

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Include egg donors in CRISPR gene-editing debate

Nature (London), 2019-11, Vol.575 (7781), p.51-51

2019

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Ethical issues in consumer genome sequencing: Use of consumers' samples and data

Applied & translational genomics, 2016-03, Vol.8, p.23-30

2016

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Germline Genome Editing Research: What Are Gamete Donors (Not) Informed About in Consent Forms?

CRISPR journal, 2020-02, Vol.3 (1), p.52-63

2020

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Proteomic and transcriptomic experiments reveal an essential role of RNA degradosome complexes in shaping the transcriptome of Mycobacterium tuberculosis

Nucleic acids research, 2019-06, Vol.47 (11), p.5892-5905

2019

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Current ethical and legal issues in health-related direct-to-consumer genetic testing

Personalized medicine, 2017-09, Vol.14 (5), p.433-445

2017

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Content Analysis of Informed Consent for Whole Genome Sequencing Offered by Direct-to-Consumer Genetic Testing Companies

Human mutation, 2016-12, Vol.37 (12), p.1248-1256

2016

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Global Public Perceptions of Genomic Data Sharing: What Shapes the Willingness to Donate DNA and Health Data?

American journal of human genetics, 2020-10, Vol.107 (4), p.743-752

2020

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How do consent forms for diagnostic high‐throughput sequencing address unsolicited and secondary findings? A content analysis

Clinical genetics, 2018-10, Vol.94 (3-4), p.321-329

2018

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Content Analysis of Informed Consent for Whole Genome Sequencing Offered by Direct-to-Consumer Genetic Testing Companies: HUMAN MUTATION

Human mutation, 2016-12, Vol.37 (12), p.1248-1256

2016

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Plant nonsense-mediated mRNA decay is controlled by different autoregulatory circuits and can be induced by an EJC-like complex

Nucleic acids research, 2013-07, Vol.41 (13), p.6715-6728

2013

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Will the EU Medical Device Regulation help to improve the safety and performance of medical AI devices?

Willingness to donate genomic and other medical data: results from Germany

Analysis of VUS reporting, variant reinterpretation and recontact policies in clinical genomic sequencing consent forms

Ethical issues related to research on genome editing in human embryos

Trust in genomic data sharing among members of the general public in the UK, USA, Canada and Australia

COVID-19 and misinformation: Is censorship of social media a remedy to the spread of medical misinformation?

Communicating genetic information to family members: analysis of consent forms for diagnostic genomic sequencing

Members of the public in the USA, UK, Canada and Australia expressing genetic exceptionalism say they are more willing to donate genomic data

Reply to Bronstein and Vinogradov

COVID‐19 and misinformation

Attitudes of publics who are unwilling to donate DNA data for research

Transparency, consent and trust in the use of customers' data by an online genetic testing company: an Exploratory survey among 23andMe users

A cautionary tale about the adoption of medical AI in Sweden

'Your DNA, Your Say': global survey gathering attitudes toward genomics: design, delivery and methods

Engage egg donors in editing debate

Include egg donors in CRISPR gene-editing debate

Ethical issues in consumer genome sequencing: Use of consumers' samples and data

Germline Genome Editing Research: What Are Gamete Donors (Not) Informed About in Consent Forms?

Proteomic and transcriptomic experiments reveal an essential role of RNA degradosome complexes in shaping the transcriptome of Mycobacterium tuberculosis

Current ethical and legal issues in health-related direct-to-consumer genetic testing

Content Analysis of Informed Consent for Whole Genome Sequencing Offered by Direct-to-Consumer Genetic Testing Companies

Global Public Perceptions of Genomic Data Sharing: What Shapes the Willingness to Donate DNA and Health Data?

How do consent forms for diagnostic high‐throughput sequencing address unsolicited and secondary findings? A content analysis

Content Analysis of Informed Consent for Whole Genome Sequencing Offered by Direct-to-Consumer Genetic Testing Companies: HUMAN MUTATION

Plant nonsense-mediated mRNA decay is controlled by different autoregulatory circuits and can be induced by an EJC-like complex

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