| scholarly article | Q13442814 |
| P356 | DOI | 10.1080/15265161.2013.768864 |
| P698 | PubMed publication ID | 23514395 |
| P50 | author | John Ioannidis | Q6251482 |
| P2860 | cites work | Potential etiologic and functional implications of genome-wide association loci for human diseases and traits | Q22066284 |
| Developing a simplified consent form for biobanking | Q33719347 | ||
| The importance of potential studies that have not existed and registration of observational data sets | Q34370321 | ||
| Challenges in creating an opt-in biobank with a registrar-based consent process and a commercial EHR. | Q36364595 | ||
| Written informed consent and selection bias in observational studies using medical records: systematic review | Q37403302 | ||
| Risk factors and interventions with statistically significant tiny effects | Q44196482 | ||
| Does consent bias research? | Q45627963 | ||
| Differentiating and evaluating common good and public good: making implicit assumptions explicit in the contexts of consent and duty to participate. | Q45950925 | ||
| Consent and research governance in biobanks: evidence from focus groups with medical researchers | Q48425377 | ||
| Privacy, consent, and the electronic mental health record: The Person vs. the System. | Q50772008 | ||
| Electronic consent channels: preserving patient privacy without handcuffing researchers | Q57190375 | ||
| P433 | issue | 4 | |
| P921 | main subject | informed consent | Q764527 |
| big data | Q858810 | ||
| data ethics | Q45933174 | ||
| P1104 | number of pages | 3 | |
| P304 | page(s) | 40-42 | |
| P577 | publication date | 2013-01-01 | |
| P1433 | published in | American Journal of Bioethics | Q4744234 |
| P1476 | title | Informed consent, big data, and the oxymoron of research that is not research | |
| P478 | volume | 13 |
| Q88488256 | All our data will be health data one day: the need for universal data protection and comprehensive consent |
| Q44430670 | An unbiased response to the open peer commentaries on "does consent bias research?". |
| Q47173407 | Big Data in Public Health: Terminology, Machine Learning, and Privacy. |
| Q57778638 | Big data analytics in E-commerce: a systematic review and agenda for future research |
| Q28602477 | Big data are coming to psychiatry: a general introduction |
| Q31042693 | Consent and confidentiality in the light of recent demands for data sharing |
| Q42617729 | Data sharing: Don't compromise on informed consent |
| Q73121811 | Ethical Dimensions of Dynamic Consent in Data-Intense Biomedical Research—Paradigm Shift, or Red Herring? |
| Q36315748 | Ethics and Epistemology in Big Data Research |
| Q35211265 | How electronic clinical data can improve health technology assessment |
| Q64054698 | Informed Consent in Biomedical Research |
| Q24289150 | Lost in Translation (LiT): IUPHAR Review 6 |
| Q36698437 | Participant views on consent in cancer genetics research: preparing for the precision medicine era. |
| Q92264420 | Participatory Disease Surveillance Systems: Ethical Framework |
| Q58206373 | Personal Data Management with the Databox |
| Q31046490 | Routinely collected data and comparative effectiveness evidence: promises and limitations |
| Q28608552 | Sweat, Skepticism, and Uncharted Territory: A Qualitative Study of Opinions on Data Sharing Among Public Health Researchers and Research Participants in Mumbai, India |
| Q30957260 | The Ethics of Big Data: Current and Foreseeable Issues in Biomedical Contexts. |
| Q89876282 | What is your definition of Big Data? Researchers' understanding of the phenomenon of the decade |
| Q56034273 | Where are human subjects in Big Data research? The emerging ethics divide |
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