| scholarly article | Q13442814 |
| P50 | author | Bartha Knoppers | Q2885924 |
| P2860 | cites work | Resolving individuals contributing trace amounts of DNA to highly complex mixtures using high-density SNP genotyping microarrays | Q21092481 |
| Data sharing in genomics--re-shaping scientific practice | Q24550016 | ||
| From genetic privacy to open consent | Q24550752 | ||
| Prepublication data sharing | Q26283296 | ||
| Using lifetime risk estimates in personal genomic profiles: estimation of uncertainty | Q28392540 | ||
| Public access to genome-wide data: five views on balancing research with privacy and protection | Q28751338 | ||
| Size matters: just how big is BIG?: Quantifying realistic sample size requirements for human genome epidemiology | Q28755468 | ||
| Data storage and DNA banking for biomedical research: technical, social and ethical issues | Q30882730 | ||
| Genomics and policymaking: from static models to complex systems? | Q37404576 | ||
| Research 2.0: social networking and direct-to-consumer (DTC) genomics | Q42642327 | ||
| Evaluation of genetic tests for susceptibility to common complex diseases: why, when and how? | Q56780467 | ||
| Personal Genome Testing: Do You Know What You Are Buying? | Q57238664 | ||
| Personal genomics: information can be harmful | Q82426335 | ||
| 'Principled' personalized medicine? | Q88759229 | ||
| P433 | issue | 6 | |
| P921 | main subject | genomics | Q222046 |
| informed consent | Q764527 | ||
| P304 | page(s) | 416-419 | |
| P577 | publication date | 2010-05-07 | |
| P1433 | published in | EMBO Reports | Q5323356 |
| P1476 | title | Consent to 'personal' genomics and privacy. Direct-to-consumer genetic tests and population genome research challenge traditional notions of privacy and consent | |
| P478 | volume | 11 |
| Q28711804 | 'Sifting the significance from the data' - the impact of high-throughput genomic technologies on human genetics and health care |
| Q28596875 | Addressing Benefits, Risks and Consent in Next Generation Sequencing Studies |
| Q48627080 | Biobanks and the phantom public |
| Q57730176 | CCMG statement on direct-to-consumer genetic testing* |
| Q64102258 | Direct-to-Consumer Genetic Testing's Red Herring: "Genetic Ancestry" and Personalized Medicine |
| Q82470351 | Direct-to-consumer genetic testing: driving choice? |
| Q34313389 | From protection of privacy to control of data streams: a focus group study on biobanks in the information society |
| Q28601541 | Identifiability and privacy in pluripotent stem cell research |
| Q37742635 | Precision medicine driven by cancer systems biology |
| Q51455341 | Protecting posted genes: social networking and the limits of GINA. |
| Q30529892 | Publics and biobanks: Pan-European diversity and the challenge of responsible innovation |
| Q90168491 | Rethinking the ethical principles of genomic medicine services |
| Q28603135 | Samples and data accessibility in research biobanks: an explorative survey |
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