Effy Vayena

Q: What Schools Are Affiliated With Effy Vayena

Effy Vayena is affiliated with the following schools: ETH Zurich, University of Zurich

Effy Vayena's AcademicInfluence.com Rankings

Effy Vayena

Philosophy

#6867

World Rank

#9978

Historical Rank

Bioethics

#58

World Rank

#58

Historical Rank

philosophy Degrees

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Philosophy

Effy Vayena's Degrees

PhD Bioethics University of Zurich

Why Is Effy Vayena Influential?

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According to Wikipedia, Eftychia Vayena is a Greek and Swiss bioethicist. Since 2017 she has held the position of chair of bioethics at the Swiss Institute of Technology in Zurich, ETH Zurich. She is an elected member of the Swiss Academy of Medical Sciences.

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Effy Vayena's Published Works

Number of citations in a given year to any of this author's works

Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

The global landscape of AI ethics guidelines (2019) (891)
AI4People—An Ethical Framework for a Good AI Society: Opportunities, Risks, Principles, and Recommendations (2018) (787)
Artificial Intelligence: the global landscape of ethics guidelines (2019) (577)
On the responsible use of digital data to tackle the COVID-19 pandemic (2020) (357)
Current Practices and Controversies in Assisted Reproduction (2002) (344)
Machine learning in medicine: Addressing ethical challenges (2018) (305)
Explainability for artificial intelligence in healthcare: a multidisciplinary perspective (2020) (268)
Ethical Challenges of Big Data in Public Health (2015) (235)
Digital tools against COVID-19: taxonomy, ethical challenges, and navigation aid (2020) (167)
Current practices and controversies in assisted reproduction : report of a meeting on "Medical, Ethical and Social Aspects of Assisted Reproduction" held at WHO headquarters in Geneva, Switzerland, 17-21 September 2001 (2002) (143)
Use of Modern Contraception by the Poor Is Falling Behind (2007) (132)
Considerations for ethics review of big data health research: A scoping review (2018) (130)
Adapting Standards: Ethical Oversight of Participant-Led Health Research (2013) (107)
Policy implications of big data in the health sector (2017) (90)
Health Research with Big Data: Time for Systemic Oversight (2018) (86)
Shaping parents: impact of contrasting professional counseling on parents' decision making for children with disorders of sex development. (2013) (85)
Early Evidence of Effectiveness of Digital Contact Tracing for SARS-CoV-2 in Switzerland (2020) (83)
Biomedical Big Data: New Models of Control Over Access, Use and Governance (2017) (76)
Elements of Trust in Digital Health Systems: Scoping Review (2018) (75)
Research led by participants: a new social contract for a new kind of research (2015) (73)
Digital health: meeting the ethical and policy challenges. (2018) (73)
Between Openness and Privacy in Genomics (2016) (69)
Assisted reproductive technology in developing countries: why should we care? (2002) (68)
Experiences of Early Users of Direct-to-Consumer Genomics in Switzerland: An Exploratory Study (2012) (58)
Direct-to-consumer genomics on the scales of autonomy (2014) (55)
Open sharing of genomic data: Who does it and why? (2017) (53)
A research agenda for digital proximity tracing apps. (2020) (52)
The ethics of participant-led biomedical research (2013) (51)
Digital contact-tracing during the Covid-19 pandemic: an analysis of newspaper coverage in Germany, Austria, and Switzerland (2020) (51)
“We the Scientists”: a Human Right to Citizen Science (2015) (50)
Data Sharing For Precision Medicine: Policy Lessons And Future Directions. (2018) (49)
Assisted reproductive technologies in developing countries: are we caring yet? (2009) (49)
Ethical issues in health research with novel online sources. (2012) (48)
Caught in the Web: Informed Consent for Online Health Research (2013) (47)
Key challenges for next‐generation pharmacogenomics (2014) (46)
What's next for COVID-19 apps? Governance and oversight (2020) (45)
“Strictly Biomedical? Sketching the Ethics of the Big Data Ecosystem in Biomedicine” (2016) (43)
Development of the mHealth App Trustworthiness checklist (2019) (43)
Digital tools against COVID-19: Framing the ethical challenges and how to address them (2020) (39)
Big Data and Dementia: Charting the Route Ahead for Research, Ethics, and Policy (2018) (38)
Ready to put metadata on the post-2015 development agenda? Linking data publications to responsible innovation and science diplomacy. (2014) (37)
Becoming partners, retaining autonomy: ethical considerations on the development of precision medicine (2016) (37)
Genetic testing, insurance discrimination and medical research: what the United States can learn from peer countries (2019) (36)
Beyond the clinic: 'direct-to-consumer' genomic profiling services and pharmacogenomics. (2013) (35)
Opinion: Learning as we go: Lessons from the publication of Facebook’s social-computing research (2014) (34)
Digital Contact Tracing Against COVID-19 in Europe: Current Features and Ongoing Developments (2021) (34)
Playing a Part in Research? University Students' Attitudes to Direct-To-Consumer Genomics (2014) (33)
Revolutionizing Medical Data Sharing Using Advanced Privacy-Enhancing Technologies: Technical, Legal, and Ethical Synthesis (2020) (33)
Improving the Measurement of Scientific Success by Reporting a Self-Citation Index (2017) (33)
From principles to practice: benchmarking government guidance on health apps. (2019) (32)
The dynamics of big data and human rights: the case of scientific research (2016) (31)
Sharing benefits in international health research (2007) (29)
Genetic incidental findings: autonomy regained? (2013) (29)
Test Pricing and Reimbursement in Genomic Medicine: Towards a General Strategy (2016) (28)
Democratizing Health Research Through Data Cooperatives (2018) (28)
What Is Trust? Ethics and Risk Governance in Precision Medicine and Predictive Analytics (2017) (26)
Big Data, Health Law, and Bioethics (2018) (25)
A Harm-Reduction Framework for Algorithmic Fairness (2018) (25)
Elements of a new ethical framework for big data research (2016) (25)
Is there a duty to participate in digital epidemiology? (2018) (23)
Children’s rights in pediatrics (2010) (23)
Bridging genomics research between developed and developing countries: the Genomic Medicine Alliance. (2014) (21)
Big Data, precision medicine and private insurance: A delicate balancing act (2019) (21)
Future-proofing biobanks’ governance (2020) (21)
Public willingness to participate in personalized health research and biobanking: A large-scale Swiss survey (2021) (20)
“Tailored-to-You”: Public Engagement and the Political Legitimation of Precision Medicine (2017) (20)
Key Ethical Challenges in the European Medical Information Framework (2018) (20)
The Ethics of AI in Biomedical Research, Patient Care, and Public Health (2019) (20)
The next step in the patient revolution: patients initiating and leading research (2014) (20)
Qualitative analysis of visual risk communication on twitter during the Covid-19 pandemic (2021) (20)
New ethical challenges of digital technologies, machine learning and artificial intelligence in public health: a call for papers (2019) (17)
Ethics review of big data research: What should stay and what should be reformed? (2021) (17)
Data protection and ethics requirements for multisite research with health data: a comparative examination of legislative governance frameworks and the role of data protection technologies† (2020) (17)
Attitudes towards personal genomics among older Swiss adults: An exploratory study (2016) (16)
Balancing risks and benefits of artificial intelligence in the health sector (2020) (16)
Odon device for instrumental vaginal deliveries: results of a medical device pilot clinical study (2018) (15)
A Code of Ethics for Ethicists: What Would Pierre Bourdieu Say? “Do Not Misuse Social Capital in the Age of Consortia Ethics” (2015) (15)
An Appeal to the Global Health Community for a Tripartite Innovation: An "Essential Diagnostics List," "Health in All Policies," and "See-Through 21(st) Century Science and Ethics". (2015) (15)
Public involvement in the governance of population-level biomedical research: unresolved questions and future directions (2020) (15)
Value from health data: European opportunity to catalyse progress in digital health (2021) (15)
Odon device for instrumental vaginal deliveries: results of a medical device pilot clinical study (2018) (15)
The challenge of personal genomics in Germany (2013) (14)
Guidelines on biobanks: emerging consensus and unresolved controversies (2005) (13)
The place of human rights and the common good in global health policy (2016) (13)
Personal Genomics in Greece: An Overview of Available Direct-to-Consumer Genomic Services and the Relevant Legal Framework (2014) (12)
Towards a Governance Framework for Brain Data (2021) (12)
Combining the best interest standard with shared decision-making in paediatrics—introducing the shared optimum approach based on a qualitative study (2020) (12)
Heritable Human Genome Editing: The Public Engagement Imperative. (2020) (11)
Feasibility and safety study of a new device (Odón device) for assisted vaginal deliveries: study protocol (2013) (11)
Big Data, Biomedical Research, and Ethics Review: New Challenges for IRBs (2020) (11)
Digital bioethics: introducing new methods for the study of bioethical issues (2021) (11)
Balancing ethical criteria for the recruitment of gamete donors (2012) (11)
Getting human rights right in global health policy (2015) (11)
Informed Consent and the Disclosure of Clinical Results to Research Participants (2017) (11)
Assisted Reproduction in Developing Countries: The Debate at a Turning Point (2009) (11)
Assessing Public Opinion on CRISPR-Cas9: Combining Crowdsourcing and Deep Learning (2020) (11)
Genes wide open: Data sharing and the social gradient of genomic privacy (2018) (11)
The Mobile Health App Trustworthiness Checklist: Usability Assessment (2020) (11)
Children’s rights in pediatric (2011) (10)
Regulating Genomics: Time for a Broader Vision (2013) (10)
AD HOC COMMITTEE ON ARTIFICIAL INTELLIGENCE (CAHAI) (2020) (9)
Benefits, Challenges and Contributors to Success for National eHealth Systems Implementation: A Scoping Review (2021) (9)
Project Categories to Guide Institutional Oversight of Responsible Conduct of Scientists Leading Citizen Science in the United States (2019) (9)
Bernard Lerer: recipient of the 2014 inaugural Werner Kalow Responsible Innovation Prize in Global Omics and Personalized Medicine (Pacific Rim Association for Clinical Pharmacogenetics). (2014) (8)
The Promising Revolution of Participant-Led Research in Rare Neurological Diseases; Potential Benefits and Pitfalls (2015) (7)
Dual use in the 21st century: emerging risks and global governance. (2018) (7)
Potential for diagnosis of infectious disease from the 100,000 Genomes Project Metagenomic Dataset: Recommendations for reporting results (2019) (7)
“Hunting Down My Son’s Killer”: New Roles of Patients in Treatment Discovery and Ethical Uncertainty (2020) (6)
Direct-to-Consumer Neurotechnology: What Is It and What Is It for? (2019) (6)
Navigating the Ethics of Big Data in Public Health (2019) (6)
Precision global health: a roadmap for augmented action (2020) (6)
Philanthropy on trial: can the rich rescue shelved compounds? (2017) (5)
Ethical Issues with Using Internet of Things Devices in Citizen Science Research: A Scoping Review (2020) (5)
Digital Medicine and Ethics: Rooting for Evidence (2018) (5)
Mobile apps for travel medicine and ethical considerations: A systematic review. (2021) (5)
A Systemic Approach to the Oversight of Machine Learning Clinical Translation (2022) (4)
Student’s Knowledge and Attitude Towards Direct-To-Consumer Genetic Tests (2015) (4)
Public engagement with health data governance: the role of visuality (2021) (4)
Just Global Health: Integrating Human Rights and Common Goods (2015) (4)
The Challenges of Big Data for Research Ethics Committees: A Qualitative Swiss Study (2021) (4)
How the General Data Protection Regulation changes the rules for scientific research: Study (2019) (3)
Reproductive Donation: Challenges in intra-family donation (2012) (3)
Towards Adaptive Governance in Big Data Health Research: Implementing Regulatory Principles (2019) (3)
Combining Crowdsourcing and Deep Learning to Assess Public Opinion on CRISPR-Cas9 (2019) (3)
O607 THE ODÓN DEVICE. A NEW SIMPLE INSTRUMENT FOR ASSISTED VAGINAL DELIVERY (2012) (3)
Sharing benefits in international health researchy building as an example of an indirect collective benefit (2007) (3)
Rosalyn Yalow, Nobel Laureate: Her Life and Work in Medicine: Her Life and Work in Medicine (2002) (2)
Public Health and Human Rights. (2016) (2)
The Genomic Medicine Alliance: A global effort to facilitate the introduction of genomics into healthcare in developing nations (2018) (2)
Ethical requirements for responsible research with hacked data (2021) (2)
Autonomous surgical robotic systems and the liability dilemma (2022) (2)
Towards Adaptive Governance in Big Data Health Research (2021) (2)
Visualizing an Ethics Framework: A Method to Create Interactive Knowledge Visualizations From Health Policy Documents (2020) (2)
The Ethics of AI in Biomedical Research, Patient Care and Public Health (2019) (1)
Assessing the Governance of Digital Contact Tracing in Response to COVID-19: Results of a Multi-National Study (2022) (1)
The Regulation of Human Germline Genome Modification in Switzerland (2020) (1)
In the shadow of privacy: Overlooked ethical concerns in COVID-19 digital epidemiology (2022) (1)
Reporting Genetic Findings to Individual Research Participants: Guidelines From the Swiss Personalized Health Network (2020) (1)
Big Data, Health Law, and Bioethics: Introduction (Cambridge University Press, 2018) (2018) (1)
[Personal genomics: are we debating the right Issues?]. (2012) (1)
Covid-19 on Twitter: an analysis of risk communication with visuals (2021) (1)
Genetic testing, insurance discrimination and medical research: what the United States can learn from peer countries (2019) (1)
Expectations and attitudes towards medical artificial intelligence: A qualitative study in the field of stroke (2023) (1)
Reproductive Donation: Reproductive donation (2012) (1)
Ethics guidelines in Citizen Science (2020) (1)
Beyond high hopes: A scoping review of the 2019–2021 scientific discourse on machine learning in medical imaging (2023) (1)
Just Global Health (2020) (1)
Medical Students Knowledge and Attitude Towards Direct-To-Consumer Genetic Tests (2022) (1)
Assessing Public Opinion on CRISPR-Cas9: Combining Crowdsourcing and Deep Learning (Preprint) (2020) (0)
The regulation of human germline genome modification in France (2020) (0)
Becoming partners, retaining autonomy: ethical considerations on the development of precision medicine (2016) (0)
Is it ethical to use hacked data in scientific research? (2021) (0)
Protecting health privacy in the world of Big Data (2018) (0)
Stuck in translation: Stakeholder perspectives on impediments to responsible digital health (2023) (0)
The Mobile Health App Trustworthiness Checklist: Usability Assessment (Preprint) (2019) (0)
The global landscape of AI ethics guidelines (2019) (0)
Reproductive donation: global perspectives and cultural diversity (2019) (0)
Contents Vol. 17, 2014 (2014) (0)
The place of human rights and the common good in global health policy (2016) (0)
Decentralised clinical trials: ethical opportunities and challenges (2023) (0)
Revolutionizing Medical Data Sharing Using Advanced Privacy-Enhancing Technologies: Technical, Legal, and Ethical Synthesis (Preprint) (2020) (0)
How Interactive Visualizations Compare to Ethical Frameworks as Stand-Alone Ethics Learning Tools for Health Researchers and Professionals. (2023) (0)
Big Data and Artificial Intelligence for Global Health (2021) (0)
Challenges in intra-family donation (2019) (0)
International Organizations and the Global Governance of AI in Health (2023) (0)
Is there a duty to participate in digital epidemiology? (2018) (0)
Big Data (2019) (0)
Review: Rosalyn Yalow, Nobel Laureate: Her Life and Work in Medicine (2002) (0)
On the responsible use of digital data to tackle the COVID-19 pandemic (2020) (0)
Scientific papers: can the internet play a role in reducing the global burden of infertility? (2002) (0)
Ethics Oversight of Participant Led Medical Research: Problems and Prospects (2013) (0)
Health data privacy through homomorphic encryption and distributed ledger computing: an ethical-legal qualitative expert assessment study (2022) (0)
Choices and dilemmas in the new reproductive technologies. (2001) (0)
Democratizing Health Research Through Data Cooperatives (2018) (0)
When Reproductive Freedom Encounters Medical Responsibility (2018) (0)
“We the Scientists”: a Human Right to Citizen Science (2015) (0)
"Personalized health" : report to discuss options and frame for a new Swiss initiative (2014) (0)
Key Ethical Challenges in the European Medical Information Framework (2018) (0)
Understanding Global Challenges of Rapidly Developing Technologies: Digital Methods for Empirical Bioethics (2021) (0)
Contents Vol. 19, 2016 (2017) (0)
Public preferences towards data management and governance in Swiss biobanks: results from a nationwide survey (2022) (0)
User Perspectives of a Web-Based Data-Sharing Platform (Open Humans) on Ethical Oversight in Participant-Led Research: Protocol for a Quantitative Study (2018) (0)
Contents Vol. 15, 2012 (2012) (0)
Unlock Digital Health Promotion in LMICs to Benefit the Youth (2023) (0)
Public engagement with health data governance: the role of visuality (2021) (0)
Whose Health Record? A Comparison of Patient Rights Under National Electronic Health Record (Nehr) Regulations in Europe and Asia-Pacific Jurisdictions (2020) (0)
Future-proofing biobanks’ governance (2020) (0)
How Private Individuals Maintain Privacy and Govern Their Own Health Data Cooperative (2021) (0)
Self-citations and academic assessments: putting data before the carrot (2017) (0)

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What Schools Are Affiliated With Effy Vayena?

Effy Vayena is affiliated with the following schools:

Effy Vayena's Academic­Influence.com Rankings