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Secondary Findings in Genomic Research

Häftad, Engelska, 2020

2 099 kr

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Secondary Findings in Genomic Research offers a single, highly accessible resource on interpreting, managing and disclosing secondary findings in genomic research. With chapters written by experts in the field, this book is the first to concisely explain the ethical and practical issues raised by secondary genomics findings for a multi and interdisciplinary audience of genomic researchers, translational scientists, clinicians, medical students, genetic counselors, ethicists, legal experts and law students, public policy specialists and regulators.

Contributors from Europe, North America, and Asia effectively synthesize perspectives from a spectrum of different scientific, societal, and global contexts, and offer pragmatic approaches to a range of topics, including oversight, governance and policy surrounding secondary genomic results, criteria for identifying results for return, communication and consent, stakeholders' attitudes and perspectives, disclosing results, and clinical, patient-centered protocols.



  • Thoroughly addresses the scientific, ethical, practical and clinical issues raised by secondary findings resulting from genomic research, including active debate and challenges in the field
  • Provides researchers, clinicians, regulators, and stakeholders with a holistic, interdisciplinary approach to interpreting, managing and disclosing secondary findings
  • Brings together expert analysis from scholars across Europe, North America, and Asia representing a wide variety of scientific and societal contexts

Produktinformation

  • Utgivningsdatum2020-03-04
  • Mått191 x 235 x 13 mm
  • Vikt430 g
  • FormatHäftad
  • SpråkEngelska
  • SerieTranslational and Applied Genomics
  • Antal sidor244
  • FörlagElsevier Science
  • ISBN9780128165492

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