scholarly article | Q13442814 |
P6179 | Dimensions Publication ID | 1033201839 |
P356 | DOI | 10.1186/S13073-014-0118-Y |
P932 | PMC publication ID | 4295276 |
P698 | PubMed publication ID | 25593596 |
P5875 | ResearchGate publication ID | 270961972 |
P50 | author | Kazuto Kato | Q89617150 |
Jane Kaye | Q46001602 | ||
Harriet Teare | Q57053485 | ||
P2093 | author name string | Colin Mitchell | |
Jusaku Minari | |||
P2860 | cites work | Research ethics and the challenge of whole-genome sequencing | Q24550756 |
From patients to partners: participant-centric initiatives in biomedical research | Q27016065 | ||
Dynamic consent: a patient interface for twenty-first century research networks | Q28654606 | ||
Return of genomic results to research participants: the floor, the ceiling, and the choices in between | Q34000877 | ||
Informed consent in genomics and genetic research | Q35551797 | ||
No small matter: qualitatively distinct challenges of pediatric genomic studies | Q35617378 | ||
Human genetic research: emerging trends in ethics | Q35998786 | ||
Family consent, communication, and advance directives for cancer disclosure: a Japanese case and discussion | Q36688575 | ||
Policy uncertainty, sequencing, and cell lines | Q37079488 | ||
P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
P6216 | copyright status | copyrighted | Q50423863 |
P433 | issue | 12 | |
P921 | main subject | informed consent | Q764527 |
P304 | page(s) | 118 | |
P577 | publication date | 2014-12-17 | |
P1433 | published in | Genome Medicine | Q15816848 |
P1476 | title | The emerging need for family-centric initiatives for obtaining consent in personal genome research | |
P478 | volume | 6 |
Q42599863 | "Not Tied Up Neatly with a Bow": Professionals' Challenging Cases in Informed Consent for Genomic Sequencing |
Q26772241 | Between Openness and Privacy in Genomics |
Q58763025 | Equitable Participation in Biobanks: The Risks and Benefits of a "Dynamic Consent" Approach |
Q37354569 | Lessons from HeLa Cells: The Ethics and Policy of Biospecimens |
Q36828474 | Participants and Study Decliners' Perspectives About the Risks of Participating in a Clinical Trial of Whole Genome Sequencing |
Q38642050 | Social and Communicative Functions of Informed Consent Forms in East Asia and Beyond. |
Q52318815 | Tensions in ethics and policy created by National Precision Medicine Programs. |
Q36110612 | Using digital technologies to engage with medical research: views of myotonic dystrophy patients in Japan |
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