Readability of informed consent forms for whole-exome and whole-genome sequencing

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From Genomics & Health Impact Scan Database

This database includes published scientific literature on evidence-based translation of genomic discoveries into improved health care and disease prevention that have a potential impact on population health.

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• Readability of informed consent forms for whole-exome and whole-genome sequencing.  
  Niemiec Emilia et al. Journal of community genetics 2017 Aug
• Health-Related Genetic Direct-to-Consumer Tests in the German Setting: The Available Offer and the Potential Implications for a Solidarily Financed Health-Care System.  
  Plöthner Marika et al. Public health genomics 2017 Jun
• Anticipating the Ethical Challenges of Psychiatric Genetic Testing.  
  Appelbaum Paul S et al. Current psychiatry reports 2017 Jul 19(7) 39
• Is It Desirable that I Must Disclose My Genetic Data to Swiss Private Medical Insurances?  
  Bräm Corina et al. Public health genomics 2016 Aug
• A Web-Based Platform for Educating Researchers About Bioethics and Biobanking.  
  Sehovic Ivana et al. J Cancer Educ 2015 Mar 17.

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