Crossref Citations
This article has been cited by the following publications. This list is generated based on data provided by
Crossref.
Wolf, Susan M.
Clayton, Ellen Wright
and
Lawrenz, Frances
2018.
The Past, Present, and Future of Informed Consent in Research and Translational Medicine.
Journal of Law, Medicine & Ethics,
Vol. 46,
Issue. 1,
p.
7.
Vayena, Effy
Blasimme, Alessandro
and
Cohen, I. Glenn
2018.
Machine learning in medicine: Addressing ethical challenges.
PLOS Medicine,
Vol. 15,
Issue. 11,
p.
e1002689.
Ienca, Marcello
Ferretti, Agata
Hurst, Samia
Puhan, Milo
Lovis, Christian
Vayena, Effy
and
Biemba, Godfrey
2018.
Considerations for ethics review of big data health research: A scoping review.
PLOS ONE,
Vol. 13,
Issue. 10,
p.
e0204937.
Haeusermann, Tobias
Fadda, Marta
Blasimme, Alessandro
Tzovaras, Bastian Greshake
and
Vayena, Effy
2018.
Genes wide open: Data sharing and the social gradient of genomic privacy.
AJOB Empirical Bioethics,
Vol. 9,
Issue. 4,
p.
207.
Blasimme, Alessandro
Fadda, Marta
Schneider, Manuel
and
Vayena, Effy
2018.
Data Sharing For Precision Medicine: Policy Lessons And Future Directions.
Health Affairs,
Vol. 37,
Issue. 5,
p.
702.
Kostkova, Patty
2018.
Disease surveillance data sharing for public health: the next ethical frontiers.
Life Sciences, Society and Policy,
Vol. 14,
Issue. 1,
Adjekum, Afua
Blasimme, Alessandro
and
Vayena, Effy
2018.
Elements of Trust in Digital Health Systems: Scoping Review.
Journal of Medical Internet Research,
Vol. 20,
Issue. 12,
p.
e11254.
Cohen, I. Glenn
and
Mello, Michelle M.
2019.
Big Data, Big Tech, and Protecting Patient Privacy.
JAMA,
Vol. 322,
Issue. 12,
p.
1141.
McLennan, Stuart
2019.
The ethical oversight of learning health care activities in Switzerland: a qualitative study.
International Journal for Quality in Health Care,
Dankar, Fida K.
Gergely, Marton
and
Dankar, Samar K.
2019.
Informed Consent in Biomedical Research.
Computational and Structural Biotechnology Journal,
Vol. 17,
Issue. ,
p.
463.
Nickel, Philip J.
2019.
The Ethics of Medical Data Donation.
Vol. 137,
Issue. ,
p.
55.
Dankar, Fida K.
Gergely, Marton
Malin, Bradley
Badji, Radja
Dankar, Samar K.
and
Shuaib, Khaled
2020.
Dynamic-informed consent: A potential solution for ethical dilemmas in population sequencing initiatives.
Computational and Structural Biotechnology Journal,
Vol. 18,
Issue. ,
p.
913.
Blasimme, Alessandro
Brall, Caroline
and
Vayena, Effy
2020.
Reporting Genetic Findings to Individual Research Participants: Guidelines From the Swiss Personalized Health Network.
Frontiers in Genetics,
Vol. 11,
Issue. ,
Bu, Daniel D.
Liu, Shelley H.
Liu, Bian
and
Li, Yan
2020.
Achieving Value in Population Health Big Data.
Journal of General Internal Medicine,
Vol. 35,
Issue. 11,
p.
3342.
Allam, Zaheer
2020.
Surveying the Covid-19 Pandemic and its Implications.
p.
89.
Blasimme, Alessandro
and
Vayena, Effy
2020.
What's next for COVID-19 apps? Governance and oversight.
Science,
Vol. 370,
Issue. 6518,
p.
760.
Char, Danton S.
Abràmoff, Michael D.
and
Feudtner, Chris
2020.
Identifying Ethical Considerations for Machine Learning Healthcare Applications.
The American Journal of Bioethics,
Vol. 20,
Issue. 11,
p.
7.
Urban, Alexander
2020.
“…This Has to Do With My Identity. And I Don't Want to Make it Totally Transparent.” Identity Relevance in the Attitudes of Affected People and Laypersons to the Handling of High-Throughput Genomic Data.
Frontiers in Sociology,
Vol. 5,
Issue. ,
Gille, Felix
Vayena, Effy
and
Blasimme, Alessandro
2020.
Future-proofing biobanks’ governance.
European Journal of Human Genetics,
Vol. 28,
Issue. 8,
p.
989.
Harlow, John
Weibel, Nadir
Al Kotob, Rasheed
Chan, Vincent
Bloss, Cinnamon
Linares-Orozco, Rubi
Takemoto, Michelle
and
Nebeker, Camille
2020.
Using Participatory Design to Inform the Connected and Open Research Ethics (CORE) Commons.
Science and Engineering Ethics,
Vol. 26,
Issue. 1,
p.
183.