4.8 Editorial Material

Roadmap for a precision-medicine initiative in the Nordic region

Journal

NATURE GENETICS
Volume 51, Issue 6, Pages 924-930

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/s41588-019-0391-1

Keywords

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Funding

  1. Norwegian Research Council [223273]
  2. NordForsk
  3. Swedish Research Council
  4. European Research Council [AdG 293574]
  5. Research Council of Norway [240413]
  6. Helse Vest (PERSON-MED-DIA)
  7. Stiftelsen Kristian Gerhard Jebsen (Center for Diabetes Research)
  8. Novo Nordisk Fonden
  9. Bergen Research Foundation
  10. [ERC-2015-CoG_ NASCENT_681742]

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The Nordic region, comprising primarily Denmark, Estonia, Finland, Iceland, Norway and Sweden, has many of the necessary characteristics for being at the forefront of genome-based precision medicine. These include egalitarian and universal healthcare, expertly curated patient and population registries, biobanks, large population-based prospective cohorts linked to registries and biobanks, and a widely embraced sense of social responsibility that motivates public engagement in biomedical research. However, genome-based precision medicine can be achieved only through coordinated action involving all actors in the healthcare sector. Now is an opportune time to organize scientists in the Nordic region, together with other stakeholders including patient representatives, governments, pharmaceutical companies, academic institutions and funding agencies, to initiate a Nordic Precision Medicine Initiative. We present a roadmap for how this organization can be created. The Initiative should facilitate research, clinical trials and knowledge transfer to meet regional and global health challenges.

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