| P50 | author | Bartha Knoppers | Q2885924 |
| | Adrian Thorogood | Q40164567 |
| | Yann Joly | Q46004599 |
| P2093 | author name string | Anthoula Lazaris | |
| | Ayat Salman | |
| | Peter Metrakos | |
| | Tommy Nilsson | |
| P2860 | cites work | Return of individual research results and incidental findings: facing the challenges of translational science | Q27026989 |
| | Whole-genome sequencing in health care: recommendations of the European Society of Human Genetics | Q30391601 |
| | Disclosure of individual genetic data to research participants: the debate reconsidered | Q33781801 |
| | Managing incidental findings and research results in genomic research involving biobanks and archived data sets | Q34205284 |
| | Principles of human subjects protections applied in an opt-out, de-identified biobank | Q34788719 |
| | Ethical and practical guidelines for reporting genetic research results to study participants: updated guidelines from a National Heart, Lung, and Blood Institute working group | Q34960621 |
| | Offering individual genetic research results: context matters | Q35106928 |
| | Practical implementation issues and challenges for biobanks in the return of individual research results | Q36073696 |
| | Managing incidental findings in human subjects research: analysis and recommendations | Q36954360 |
| | Empirical analysis of current approaches to incidental findings | Q36962832 |
| | Point-counterpoint. Patient autonomy and incidental findings in clinical genomics | Q37040336 |
| | How do researchers manage genetic results in practice? The experience of the multinational Colon Cancer Family Registry | Q37639436 |
| | Considerations and costs of disclosing study findings to research participants | Q37644176 |
| | Reporting results from whole-genome and whole-exome sequencing in clinical practice: a proposal for Canada? | Q38147064 |
| | Anticipate and communicate: Ethical management of incidental and secondary findings in the clinical, research, and direct-to-consumer contexts (December 2013 report of the Presidential Commission for the Study of Bioethical Issues). | Q38242504 |
| | Population studies: return of research results and incidental findings Policy Statement | Q39588665 |
| | The Babel of genetic data terminology. | Q45936245 |
| | Disclosure of individual research results in clinico-genomic trials: challenges, classification and criteria for decision-making | Q46086451 |
| | Return of research results: general principles and international perspectives | Q48545504 |
| | Deploying whole genome sequencing in clinical practice and public health: meeting the challenge one bin at a time | Q57785176 |
| P433 | issue | 1 | |
| P921 | main subject | incidental finding | Q228172 |
| P304 | page(s) | 88 | |
| P577 | publication date | 2014-12-23 | |
| P1433 | published in | BMC Medical Ethics | Q15762173 |
| P1476 | title | An implementation framework for the feedback of individual research results and incidental findings in research | |
| P478 | volume | 15 | |