| scholarly article | Q13442814 |
| P50 | author | Barbara A Koenig | Q46003128 |
| P2860 | cites work | Is informed consent broken? | Q27009211 |
| The Mayo Clinic Biobank: a building block for individualized medicine | Q34648736 | ||
| Fixing research subjects protection in the United States: moving beyond consent | Q43550488 | ||
| From consent to institutions: designing adaptive governance for genomic biobanks | Q56776803 | ||
| P433 | issue | 4 | |
| P921 | main subject | informed consent | Q764527 |
| P304 | page(s) | 33-34 | |
| P577 | publication date | 2014-07-01 | |
| P1433 | published in | Hastings Center Report | Q5680291 |
| P1476 | title | Have we asked too much of consent? | |
| P478 | volume | 44 |
| Q38879425 | A strategic stakeholder approach for addressing further analysis requests in whole genome sequencing research |
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| Q42096376 | Beyond individualism: Is there a place for relational autonomy in clinical practice and research? |
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| Q55458665 | Capacity, Vulnerability, and Informed Consent for Research. |
| Q34526631 | Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine |
| Q45951505 | Consent, ethics and genetic biobanks: the case of the Athlome project. |
| Q37190670 | Did I Tell You That? Ethical Issues Related to Using Computational Methods to Discover Non-Disclosed Patient Characteristics |
| Q47547185 | Effect of deliberation on the public's attitudes toward consent policies for biobank research. |
| Q30985209 | Ethical Issues in Big Data Health Research: Currents in Contemporary Bioethics |
| Q38681963 | Ethically sustainable governance in the biobanking of eggs and embryos for research |
| Q40374517 | Every participant is a PI. Citizen science and participatory governance in population studies |
| Q37497641 | From "Personalized" to "Precision" Medicine: The Ethical and Social Implications of Rhetorical Reform in Genomic Medicine |
| Q93147980 | Genomic Data-Sharing Practices |
| Q56888569 | Grudging Trust and the Limits of Trustworthy Biorepository Curation |
| Q90399971 | Health Research with Big Data: Time for Systemic Oversight |
| Q38633533 | Healthcare professionals' and patients' perspectives on consent to clinical genetic testing: moving towards a more relational approach. |
| Q27007763 | If you build it, they will come: unintended future uses of organised health data collections |
| Q64054698 | Informed Consent in Biomedical Research |
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| Q37354569 | Lessons from HeLa Cells: The Ethics and Policy of Biospecimens |
| Q36275964 | National survey and community advisory board development for a bipolar disorder biobank |
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| Q36433723 | Privacy and confidentiality in pragmatic clinical trials |
| Q47631267 | Start me up: ways to encourage sharing of genomic information with research participants |
| Q47765271 | The Precision Medicine Nation |
| Q94484113 | The ethics of genetic testing for kidney diseases |
| Q57823480 | The “We” in the “Me” |
| Q37516194 | Thinking ethical and regulatory frameworks in medicine from the perspective of solidarity on both sides of the Atlantic |
| Q104795288 | Toward better governance of human genomic data |
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