| scholarly article | Q13442814 |
| P356 | DOI | 10.1017/S096318011100048X |
| P698 | PubMed publication ID | 22152457 |
| P50 | author | Gert Helgesson | Q47360037 |
| P2093 | author name string | Gert Helgesson | |
| P2860 | cites work | Coding and consent: moral challenges of the database project in Iceland. | Q34323542 |
| Potential harms, anonymization, and the right to withdraw consent to biobank research | Q34429768 | ||
| Trends in ethical and legal frameworks for the use of human biobanks | Q34658049 | ||
| Ethical, legal, and social implications of biobanks for genetics research | Q34763998 | ||
| Consent and anonymization in research involving biobanks: differing terms and norms present serious barriers to an international framework | Q34766838 | ||
| Broadening consent--and diluting ethics? | Q34933645 | ||
| Biobanking: international norms | Q36150035 | ||
| Should donors be allowed to give broad consent to future biobank research? | Q36410751 | ||
| A prospective study of the relationship between prediagnostic human papillomavirus seropositivity and HPV DNA in subsequent cervical carcinomas | Q36645918 | ||
| "Broad" consent, exceptions to consent and the question of using biological samples for research purposes different from the initial collection purpose. | Q39935993 | ||
| Quantitative aspects of informed consent: considering the dose response curve when estimating quantity of information | Q42017976 | ||
| Human tissue bank regulations | Q48089074 | ||
| Navigating an ethical patchwork--human gene banks | Q48139225 | ||
| The consent problem within DNA biobanks. | Q52855245 | ||
| Bypassing consent for research on biological material. | Q53131362 | ||
| P433 | issue | 1 | |
| P921 | main subject | informed consent | Q764527 |
| broad consent | Q108920204 | ||
| P304 | page(s) | 40-50 | |
| P577 | publication date | 2012-01-01 | |
| P1433 | published in | Cambridge Quarterly of Healthcare Ethics | Q5025503 |
| P1476 | title | In defense of broad consent | |
| P478 | volume | 21 |
| Q45934134 | Big Data and Health Research-The Governance Challenges in a Mixed Data Economy. |
| Q31020801 | Big Data in medical research and EU data protection law: challenges to the consent or anonymise approach |
| Q28662280 | Biobanking: The Melding of Research with Clinical Care |
| Q45934130 | Biomedical Big Data: New Models of Control Over Access, Use and Governance. |
| Q58287393 | Broad Consent and the Implantation of Predictive Brain Technologies |
| Q90727485 | Broad consent for biobanks is best - provided it is also deep |
| Q38072659 | Broad consent versus dynamic consent in biobank research: is passive participation an ethical problem? |
| Q90525375 | Clarifying how to deploy the public interest criterion in consent waivers for health data and tissue research |
| Q59808463 | Consent requirements for research with human tissue: Swiss ethics committee members disagree |
| Q44556717 | Demystifying biobanks |
| Q38623422 | Eliciting meta consent for future secondary research use of health data using a smartphone application - a proof of concept study in the Danish population |
| Q57640341 | Ethics in genetic counselling |
| Q90399971 | Health Research with Big Data: Time for Systemic Oversight |
| Q39238864 | Informed consent, and an ethico-legal framework for paediatric observational research and biobanking: the experience of an Italian birth cohort study |
| Q37354569 | Lessons from HeLa Cells: The Ethics and Policy of Biospecimens |
| Q41419890 | Managing Human Tissue Transfer Across National Boundaries - An Approach from an Institution in South Africa |
| Q28654959 | Newspaper coverage of biobanks |
| Q38262805 | Next generation sequencing: considering the ethics |
| Q36251826 | No regrets: Young adult patients in psychiatry report positive reactions to biobank participation |
| Q36698437 | Participant views on consent in cancer genetics research: preparing for the precision medicine era. |
| Q92264420 | Participatory Disease Surveillance Systems: Ethical Framework |
| Q34193448 | Re-contacting participants for inclusion in the database of Genotypes and Phenotypes (dbGaP): Findings from three case-control studies of lung cancer |
| Q37586101 | Relevant Information and Informed Consent in Research: In Defense of the Subjective Standard of Disclosure. |
| Q30825512 | Seeking consent for research with indigenous communities: a systematic review |
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