BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

149 related articles for article (PubMed ID: 31423602)

  • 1. Resisting big data exploitations in public healthcare: free riding or distributive justice?
    Vezyridis P; Timmons S
    Sociol Health Illn; 2019 Nov; 41(8):1585-1599. PubMed ID: 31423602
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Kenyan health stakeholder views on individual consent, general notification and governance processes for the re-use of hospital inpatient data to support learning on healthcare systems.
    Mbuthia D; Molyneux S; Njue M; Mwalukore S; Marsh V
    BMC Med Ethics; 2019 Jan; 20(1):3. PubMed ID: 30621693
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Adjusting the focus: A public health ethics approach to data research.
    Ballantyne A
    Bioethics; 2019 Mar; 33(3):357-366. PubMed ID: 30667080
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Investigating the Extent to Which Patients Should Control Access to Patient Records for Research: A Deliberative Process Using Citizens' Juries.
    Tully MP; Bozentko K; Clement S; Hunn A; Hassan L; Norris R; Oswald M; Peek N
    J Med Internet Res; 2018 Mar; 20(3):e112. PubMed ID: 29592847
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Ethical aspects of digital health from a justice point of view.
    Brall C; Schröder-Bäck P; Maeckelberghe E
    Eur J Public Health; 2019 Oct; 29(Supplement_3):18-22. PubMed ID: 31738439
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Big Data and Health Research-The Governance Challenges in a Mixed Data Economy.
    Holm S; Ploug T
    J Bioeth Inq; 2017 Dec; 14(4):515-525. PubMed ID: 28980135
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 'Kindling the fire' of NHS patient data exploitations: The care.data controversy in news media discourses.
    Vezyridis P
    Soc Sci Med; 2024 May; 348():116824. PubMed ID: 38598987
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Challenges arising when seeking broad consent for health research data sharing: a qualitative study of perspectives in Thailand.
    Cheah PY; Jatupornpimol N; Hanboonkunupakarn B; Khirikoekkong N; Jittamala P; Pukrittayakamee S; Day NPJ; Parker M; Bull S
    BMC Med Ethics; 2018 Nov; 19(1):86. PubMed ID: 30404642
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A qualitative study of big data and the opioid epidemic: recommendations for data governance.
    Evans EA; Delorme E; Cyr K; Goldstein DM
    BMC Med Ethics; 2020 Oct; 21(1):101. PubMed ID: 33087123
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Public good, personal privacy: a citizens' deliberation about using medical information for pharmacoepidemiological research.
    Parkin L; Paul C
    J Epidemiol Community Health; 2011 Feb; 65(2):150-6. PubMed ID: 19948532
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Patient Perspectives About Decisions to Share Medical Data and Biospecimens for Research.
    Kim J; Kim H; Bell E; Bath T; Paul P; Pham A; Jiang X; Zheng K; Ohno-Machado L
    JAMA Netw Open; 2019 Aug; 2(8):e199550. PubMed ID: 31433479
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Dissenting from care.data: an analysis of opt-out forms.
    Vezyridis P; Timmons S
    J Med Ethics; 2016 Dec; 42(12):792-796. PubMed ID: 27884968
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Informed consent in the context of pharmacogenomic research: ethical considerations.
    Howard HC; Joly Y; Avard D; Laplante N; Phillips M; Tardif JC
    Pharmacogenomics J; 2011 Jun; 11(3):155-61. PubMed ID: 21445091
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The Ethics in Synthetics: Statistics in the Service of Ethics and Law in Health-Related Research in Big Data from Multiple Sources.
    Bassan S; Harel O
    J Law Health; 2018; 31(1):87-117. PubMed ID: 30889335
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Better governance, better access: practising responsible data sharing in the METADAC governance infrastructure.
    Murtagh MJ; Blell MT; Butters OW; Cowley L; Dove ES; Goodman A; Griggs RL; Hall A; Hallowell N; Kumari M; Mangino M; Maughan B; Mills MC; Minion JT; Murphy T; Prior G; Suderman M; Ring SM; Rogers NT; Roberts SJ; Van der Straeten C; Viney W; Wiltshire D; Wong A; Walker N; Burton PR
    Hum Genomics; 2018 Apr; 12(1):24. PubMed ID: 29695297
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Balancing Benefits and Risks of Immortal Data: Participants' Views of Open Consent in the Personal Genome Project.
    Zarate OA; Brody JG; Brown P; Ramirez-Andreotta MD; Perovich L; Matz J
    Hastings Cent Rep; 2016; 46(1):36-45. PubMed ID: 26678513
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Donor's support tool: Enabling informed secondary use of patient's biomaterial and personal data.
    Kondylakis H; Koumakis L; Hänold S; Nwankwo I; Forgó N; Marias K; Tsiknakis M; Graf N
    Int J Med Inform; 2017 Jan; 97():282-292. PubMed ID: 27919386
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Informed consent: A study of patients with life-threatening illnesses.
    Busquets M; Caïs J
    Nurs Ethics; 2017 Jun; 24(4):430-440. PubMed ID: 26659024
    [TBL] [Abstract][Full Text] [Related]  

  • 19. "You cannot collect data using your own resources and put It on open access": Perspectives from Africa about public health data-sharing.
    Anane-Sarpong E; Wangmo T; Ward CL; Sankoh O; Tanner M; Elger BS
    Dev World Bioeth; 2018 Dec; 18(4):394-405. PubMed ID: 28745008
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [The origin of informed consent].
    Mallardi V
    Acta Otorhinolaryngol Ital; 2005 Oct; 25(5):312-27. PubMed ID: 16602332
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.