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Stockpiling Basic Medical Equipment for Public Health Emergencies and “The-Right-Thing-To-Do.” Charting the Ethical Territory

International journal of public health, 2022-05, Vol.67, p.1604679-1604679

Martani, Andrea

2022

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Comment on: Research projects in human genetics in Switzerland: analysis of research protocols submitted to cantonal ethics committees in 2018

Swiss medical weekly, 2021-06, Vol.151 (2526), p.w20521

Martani, Andrea

2021

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"I'm not your grandpa": Experiences of advanced age fathers raising their teenage children in Belgium, an interpretative phenomenological analysis

PloS one, 2024-08, Vol.19 (8), p.e0309448

2024

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Data protection and biomedical research in Switzerland: setting the record straight

Swiss medical weekly, 2020-09, Vol.150 (3536), p.w20332

2020

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Structural racism in precision medicine: leaving no one behind

BMC medical ethics, 2020-02, Vol.21 (1), p.17-17, Article 17

2020

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Factors influencing harmonized health data collection, sharing and linkage in Denmark and Switzerland: A systematic review

PloS one, 2019-12, Vol.14 (12), p.e0226015

2019

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Stay fit or get bit - ethical issues in sharing health data with insurers' apps

Swiss medical weekly, 2019-06, Vol.149, p.w20089

2019

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Digital pills: a scoping review of the empirical literature and analysis of the ethical aspects

BMC medical ethics, 2020-01, Vol.21 (1), p.3-3, Article 3

2020

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Individual notions of fair data sharing from the perspectives of Swiss stakeholders

BMC health services research, 2021-09, Vol.21 (1), p.1-1007, Article 1007

2021

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'It’s not something you can take in your hands'. Swiss experts’ perspectives on health data ownership: an interview-based study

BMJ open, 2021-04, Vol.11 (4), p.e045717

2021

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Fiona Kelly, Deborah Dempsey and Adrienne Byrt (eds), Donor-Linked Family in the Digital Age: Relatedness and Regulation

Medical law review, 2024-07

Martani, Andrea

2024

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Megatrends in Healthcare: Review for the Swiss National Science Foundation's National Research Programme 74 (NRP74) "Smarter Health Care"

Public health reviews, 2022-03, Vol.43, p.1604434

2022

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Health in data space: Formative and experiential dimensions of cross-border health data sharing

Big data & society, 2024-03, Vol.11 (1)

2024

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Changing the regulation of human germline genome editing: what does a truly broad societal debate entail?

Law, innovation and technology, 2024-09, p.1-28

Martani, Andrea

2024

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Regulating the Secondary Use of Data for Research: Arguments Against Genetic Exceptionalism

Frontiers in genetics, 2019-12, Vol.10, p.1254-1254

2019

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Emerging Health Care Leaders: Lessons From a Novel Leadership and Community-Building Program

Public health reviews, 2024, Vol.45, p.1606794-1606794

2024

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Precision Public Health and Structural Racism in the United States: Promoting Health Equity in the COVID-19 Pandemic Response

JMIR public health and surveillance, 2022-03, Vol.8 (3), p.e33277-e33277

2022

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Systemic Fairness for Sharing Health Data: Perspectives From Swiss Stakeholders

Frontiers in public health, 2021-05, Vol.9, p.669463-669463

2021

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Evolution or Revolution? Recommendations to Improve the Swiss Health Data Framework

Frontiers in public health, 2021-05, Vol.9, p.668386-668386

2021

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Right to Try and Physician Assisted Suicide: Similar or Different?

Studia Universitatis Babeş-Bolyai. Bioethica, 2021-09, Vol.66 (Special Issue), p.122-122

Martani, Andrea

2021

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Sensing the (digital) pulse. Future steps for improving the secondary use of data for research in Switzerland

Digital health, 2023-01, Vol.9, p.20552076231169826-20552076231169826

2023

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Der Aufbau einer neuen Generation von Führungskräften für das Schweizer Gesundheitswesen

Primary and hospital care (Deutsche Ausg. Internet), 2023-10

2023

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RE: “I Think It’s Been Met With a Shrug:” Oncologists’ Views Toward and Experiences With Right-to-Try

JNCI : Journal of the National Cancer Institute, 2021-03, Vol.113 (3), p.338-339

2021

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Against age limits for men in reproductive care

Medicine, health care, and philosophy, 2024-09, Vol.27 (3), p.299-307

2024

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Personal responsibility for health: the impact of digitalisation

Journal of medical law and ethics, 2019-12, Vol.7 (3), p.241-258

2019

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Stockpiling Basic Medical Equipment for Public Health Emergencies and “The-Right-Thing-To-Do.” Charting the Ethical Territory

Comment on: Research projects in human genetics in Switzerland: analysis of research protocols submitted to cantonal ethics committees in 2018

"I'm not your grandpa": Experiences of advanced age fathers raising their teenage children in Belgium, an interpretative phenomenological analysis

Data protection and biomedical research in Switzerland: setting the record straight

Structural racism in precision medicine: leaving no one behind

Factors influencing harmonized health data collection, sharing and linkage in Denmark and Switzerland: A systematic review

Stay fit or get bit - ethical issues in sharing health data with insurers' apps

Digital pills: a scoping review of the empirical literature and analysis of the ethical aspects

Individual notions of fair data sharing from the perspectives of Swiss stakeholders

'It’s not something you can take in your hands'. Swiss experts’ perspectives on health data ownership: an interview-based study

Fiona Kelly, Deborah Dempsey and Adrienne Byrt (eds), Donor-Linked Family in the Digital Age: Relatedness and Regulation

Megatrends in Healthcare: Review for the Swiss National Science Foundation's National Research Programme 74 (NRP74) "Smarter Health Care"

Health in data space: Formative and experiential dimensions of cross-border health data sharing

Changing the regulation of human germline genome editing: what does a truly broad societal debate entail?

Regulating the Secondary Use of Data for Research: Arguments Against Genetic Exceptionalism

Emerging Health Care Leaders: Lessons From a Novel Leadership and Community-Building Program

Precision Public Health and Structural Racism in the United States: Promoting Health Equity in the COVID-19 Pandemic Response

Systemic Fairness for Sharing Health Data: Perspectives From Swiss Stakeholders

Evolution or Revolution? Recommendations to Improve the Swiss Health Data Framework

Right to Try and Physician Assisted Suicide: Similar or Different?

Sensing the (digital) pulse. Future steps for improving the secondary use of data for research in Switzerland

Der Aufbau einer neuen Generation von Führungskräften für das Schweizer Gesundheitswesen

RE: “I Think It’s Been Met With a Shrug:” Oncologists’ Views Toward and Experiences With Right-to-Try

Against age limits for men in reproductive care

Personal responsibility for health: the impact of digitalisation

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