4.1 Article

PARENT PERSPECTIVES ON PEDIATRIC GENETIC RESEARCH AND IMPLICATIONS FOR GENOTYPE-DRIVEN RESEARCH RECRUITMENT

出版社

SAGE PUBLICATIONS INC
DOI: 10.1525/jer.2011.6.4.41

关键词

informed consent; recruitment; risk; benefit; genotype-driven; autism; diabetes; ethics

资金

  1. NIH-NHGRI [RC-HG005787]
  2. NIH-NCRR [1UL1 RR 025014-05]

向作者/读者索取更多资源

AS GENETIC RESEARCH IS INCREASINGLY conducted in children, it is important to understand how parents make decisions about enrolling their children and what they think about receiving their children's genetic research results. We conducted semi-structured phone interviews with 23 parents of children enrolled in genetic studies of autism or diabetes. Qualitative thematic analysis focused on two important components of genetic research and genotype-driven recruitment: participation in genetic research and return of results. Our findings suggest that parents' preferences and perspectives may be specific to their child's disease and the needs of the family as a whole. Assessing the expectations of target research populations will be beneficial for developing best practices for pediatric genetic research, return of results, and genotype-driven recruitment.

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