When you have a serious hereditary disease, who has a right to know

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Last Posted: Jul 13, 2018

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• When you have a serious hereditary disease, who has a right to know  
  S Raviv, Mosaic, Wellcome, July 11, 2018
• Bringing Us Closer to Understanding Health and Disease at an Individual Level  
  E Ramos. ASHG Blog, July 2018
• Changes to the Employers' Use of Genetic Information and Non-discrimination for Health Insurance in the USA: Implications for Australians.  
  Bilkey Gemma A et al. Frontiers in public health 2018 6183
• The right to know one's genetic origins and cross-border medically assisted reproduction.  
  Ravitsky Vardit et al. Israel journal of health policy research 2017 63
• The UK National DNA Database: Implementation of the Protection of Freedoms Act 2012.  
  Amankwaa Aaron Opoku et al. Forensic science international 2018 Mar 284117-128
• Celebrating Our Nation’s Birth and What It Means for All of Us  
  F Collins, NIH Director's Blog, July 3, 2018
• Creating a data resource: what will it take to build a medical information commons?  
  Deverka Patricia A et al. Genome medicine 2017 Sep 9(1) 84
• Potentials and Challenges of the Health Data Cooperative Model.  
  van Roessel Ilse et al. Public health genomics 2018 Jun 1-11
• Science Wants Your Data  
  MK Baker, Five Thirty Eight, June 25, 2018
• Sociogenetic Risks - Ancestry DNA Testing, Third-Party Identity, and Protection of Privacy.  
  May Thomas et al. The New England journal of medicine 2018 Jun

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