The Nordic countries as a cohort for pharmacoepidemiological research.

By K. Furu, B. Wettermark, M. Andersen, J. Martikainen, A. Almarsdóttir, H. Sørensen. Basic & Clinical Pharmacology & Toxicology, 2010

601 citations recorded by the source corpus.

Subfields: Cardiology and Cardiovascular Medicine, Geriatrics and Gerontology, Psychiatry and Mental health

View Paper: https://www.semanticscholar.org/paper/80e8de766fde221c9dca3e049c0c2406e79dfbae

How researchers see this paper

The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.

1. M. Schmidt
2. H. Sørensen
3. Wei-Qi Wei
4. J. Hallas
5. Joshua Charles Denny
6. Helle Wallach Kildemoes
7. H. Toft Sørensen
8. L. Pedersen

Citations in the corpus

• Extracting research-quality phenotypes from electronic health records to support precision medicine (2015, background): “These biobanks contain health information from 25 million inhabitants, including 4 million DNA samples, 100,000 malignant neoplasm samples [67] and 17 million users’ prescription data [68].”
• The Danish Civil Registration System as a tool in epidemiology (2014, background): “makes it possible to combine nationwide registers from several countries to create Nordic cohorts [14–16], or to make cross-national comparisons of drug utilization [15] or”
• The Danish National Prescription Registry (2011, background): “The Danish National Prescription Registry is one of the few individual-level prescription registers that cover an entire nation [2].”