Experiences and attitudes of genome investigators regarding return of individual genetic test results.
about
Attitudes towards the sharing of genetic information with at-risk relatives: results of a quantitative surveyPotential research participants support the return of raw sequence data.Can I be sued for that? Liability risk and the disclosure of clinically significant genetic research findingsReturn of results: ethical and legal distinctions between research and clinical care.Models of consent to return of incidental findings in genomic researchLiving laboratory: whole-genome sequencing as a learning healthcare enterprise.Researchers' views on informed consent for return of secondary results in genomic research.Expectation versus Reality: The Impact of Utility on Emotional Outcomes after Returning Individualized Genetic Research Results in Pediatric Rare Disease Research, a Qualitative Interview Study.Returning a Research Participant's Genomic Results to Relatives: Perspectives from Managers of Two Distinct Research Biobanks.Attitudes of nearly 7000 health professionals, genomic researchers and publics toward the return of incidental results from sequencing research.When Participants in Genomic Research Grow Up: Contact and Consent at the Age of MajorityOncologists' and cancer patients' views on whole-exome sequencing and incidental findings: results from the CanSeq studyAdolescent perspectives on the return of individual results in genomic addiction research.Parental attitudes, values, and beliefs toward the return of results from exome sequencing in children.Processes and factors involved in decisions regarding return of incidental genomic findings in research.Disclosure of incidental findings in cancer genomic research: investigators' perceptions on obligations and barriers.Return of individual genomic research results: what do consent forms tell participants?Public's Views toward Return of Secondary Results in Genomic Sequencing: It's (Almost) All about the Choice.Is there concordance in attitudes and beliefs between parents and scientists about autism spectrum disorder?Genomic information and a person's right not to know: A closer look at variations in hypothetical informational preferences in a German sample.Improved ethical guidance for the return of results from psychiatric genomics research
P2860
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P2860
Experiences and attitudes of genome investigators regarding return of individual genetic test results.
description
2013 nî lūn-bûn
@nan
2013 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
name
Experiences and attitudes of g ...... dividual genetic test results.
@ast
Experiences and attitudes of g ...... dividual genetic test results.
@en
Experiences and attitudes of g ...... dividual genetic test results.
@nl
type
label
Experiences and attitudes of g ...... dividual genetic test results.
@ast
Experiences and attitudes of g ...... dividual genetic test results.
@en
Experiences and attitudes of g ...... dividual genetic test results.
@nl
prefLabel
Experiences and attitudes of g ...... dividual genetic test results.
@ast
Experiences and attitudes of g ...... dividual genetic test results.
@en
Experiences and attitudes of g ...... dividual genetic test results.
@nl
P2093
P2860
P356
P1433
P1476
Experiences and attitudes of g ...... dividual genetic test results.
@en
P2093
Debra S Morley
Jill Oliver Robinson
Rachel B Ramoni
Sharon E Plon
P2860
P2888
P304
P356
10.1038/GIM.2013.58
P407
P577
2013-05-02T00:00:00Z