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Participant-Partners in Genetic Research: An Exome Study with Families of Children with Unexplained Medical Conditions.

Sara Huston KatsanisMollie A MinearAzita SadeghpourHeidi CopeYezmin PerillaRobert M Cook-Deegannull nullNicholas KatsanisErica E DavisMisha Angrist
Published in: Journal of participatory medicine (2018)
Most participants chose partnership, including its rights and potential burdens; however, active engagement in study activities remained the exception. Not surprisingly, the overwhelming majority of participants-both partners and traditional-expected to receive all genetic information resulting from the research study.
Keyphrases
  • healthcare
  • copy number
  • gene expression
  • risk assessment
  • hepatitis c virus
  • health information
  • hiv infected