Crossref Citations
This article has been cited by the following publications. This list is generated based on data provided by
Crossref.
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.
Kostkova, Patty
2018.
Disease surveillance data sharing for public health: the next ethical frontiers.
Life Sciences, Society and Policy,
Vol. 14,
Issue. 1,
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.
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.
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.
Nickel, Philip J.
2019.
The Ethics of Medical Data Donation.
Vol. 137,
Issue. ,
p.
55.
Cohen, I. Glenn
and
Mello, Michelle M.
2019.
Big Data, Big Tech, and Protecting Patient Privacy.
JAMA,
Vol. 322,
Issue. 12,
p.
1141.
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.
McLennan, Stuart
2019.
The ethical oversight of learning health care activities in Switzerland: a qualitative study.
International Journal for Quality in Health Care,
O'Leary, Colin P.
and
Cavender, Matthew A.
2020.
Emerging opportunities to harness real world data: An introduction to data sources, concepts, and applications.
Diabetes, Obesity and Metabolism,
Vol. 22,
Issue. S3,
p.
3.
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.
Blasimme, Alessandro
and
Vayena, Effy
2020.
What's next for COVID-19 apps? Governance and oversight.
Science,
Vol. 370,
Issue. 6518,
p.
760.
Schneble, Christophe Olivier
Elger, Bernice Simone
and
Shaw, David Martin
2020.
All Our Data Will Be Health Data One Day: The Need for Universal Data Protection and Comprehensive Consent.
Journal of Medical Internet Research,
Vol. 22,
Issue. 5,
p.
e16879.
Allam, Zaheer
2020.
Surveying the Covid-19 Pandemic and its Implications.
p.
89.
Ienca, Marcello
and
Vayena, Effy
2020.
“Hunting Down My Son’s Killer”: New Roles of Patients in Treatment Discovery and Ethical Uncertainty.
Journal of Bioethical Inquiry,
Vol. 17,
Issue. 1,
p.
37.
Gille, Felix
Vayena, Effy
and
Blasimme, Alessandro
2020.
Future-proofing biobanks’ governance.
European Journal of Human Genetics,
Vol. 28,
Issue. 8,
p.
989.
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.
Lysaght, Tamra
Ballantyne, Angela
Xafis, Vicki
Ong, Serene
Schaefer, Gerald Owen
Ling, Jeffrey Min Than
Newson, Ainsley J.
Khor, Ing Wei
and
Tai, E. Shyong
2020.
“Who is watching the watchdog?”: ethical perspectives of sharing health-related data for precision medicine in Singapore.
BMC Medical Ethics,
Vol. 21,
Issue. 1,