ArticleNature genetics2019
Roadmap for a precision-medicine initiative in the Nordic region.
Abstract readLetter
In one paragraph
Article in Nature genetics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.
0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
–field-weighted citation impact
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
12 citing papers in PubMed.
- An AI-Health infrastructure for the Nordic region: technical foundations, data assets, and a roadmap for deployment.Nature medicine · 2026Article
- Nordic AI-Health: a unique opportunity for discovery and clinical impact.The Lancet regional health. Europe · 2026Article
- User journeys in cross-European secondary use of health data: insights ahead of the European Health Data Space.European journal of public health · 2025Article
- Harnessing Pharmacomultiomics for Precision Medicine in Diabetes: A Comprehensive Review.Biomedicines · 2025Review
- Interdisciplinary Research in Iran VII: The Convergence of Biology and Artificial Intelligence.Journal of medical signals and sensors · 2025Article
- How Real-World Data Can Facilitate the Development of Precision Medicine Treatment in Psychiatry.Biological psychiatry · 2024Review
- Polygenic liability for antipsychotic dosage and polypharmacy - a real-world registry and biobank study.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2024Article
- A topic-based hierarchical publish/subscribe messaging middleware for COVID-19 detection in X-ray image and its metadata.Soft computing · 2023Article
- Public R&D Projects-Based Investment and Collaboration Framework for an Overarching South Korean National Strategy of Personalized Medicine.International journal of environmental research and public health · 2022Article
- The genetic structure of Norway.European journal of human genetics : EJHG · 2021Article
- The Need for Precision Medicine to be Applied to Diabetes.Journal of diabetes science and technology · 2020Article
- Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
31 authors.
Pål Rasmus NjølstadCenter for Diabetes Research, Department of Clinical Science, University of Bergen, Bergen, Norway. pal.njolstad@uib.no.ORCID http://orcid.org/0000-0003-0304-6728
Ole Andreas AndreassenNORMENT Centre, Division of Mental Health and Addiction, Oslo University Hospital, Oslo, Norway.ORCID http://orcid.org/0000-0002-4461-3568
Søren BrunakDisease Systems Biology, Novo Nordisk Foundation Center for Protein Research, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Anders D BørglumDepartment of Biomedicine, Aarhus University, Aarhus, Denmark.ORCID http://orcid.org/0000-0001-8627-7219
Joakim DillnerDepartment of Laboratory Medicine, Karolinska Institutet, Stockholm, Sweden.
Tõnu EskoThe Estonian Genome Center, University of Tartu, Tartu, Estonia.ORCID http://orcid.org/0000-0003-1982-6569
Paul W FranksGenetic and Molecular Epidemiology Unit, Lund University Diabetes Centre, Lund University, Malmö, Sweden.
Nelson FreimerSemel Institute for Neuroscience and Human Behavior, Los Angeles, CA, USA.ORCID http://orcid.org/0000-0003-3586-6587
Leif GroopGenetic and Molecular Epidemiology Unit, Lund University Diabetes Centre, Lund University, Malmö, Sweden.ORCID http://orcid.org/0000-0002-0187-3263
Hakon HeimerSchool of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
David M HougaardDepartment for Congenital Disorders, Statens Serum Institut, Copenhagen, Denmark.ORCID http://orcid.org/0000-0001-5928-3517
Eivind HovigDepartment of Tumor Biology, Institute for Cancer Research, Oslo University Hospital, Oslo, Norway.ORCID http://orcid.org/0000-0002-9103-1077
Kristian HveemK.G. Jebsen Center for Genetic Epidemiology, Department of Public Health, Norwegian University of Science and Technology, Trondheim, Norway.
Anu JalankoGenomics and Biomarkers Unit, National Institute for Health and Welfare, Helsinki, Finland.
Jaakko KaprioFIMM Institute for Molecular Medicine Finland, University of Helsinki, Helsinki, Finland.ORCID http://orcid.org/0000-0002-3716-2455
Gun Peggy KnudsenNorwegian Institute of Public Health, Oslo, Norway.
Mads MelbyeDepartment of Epidemiology Research, Statens Serum Institut, Copenhagen, Denmark.ORCID http://orcid.org/0000-0001-8264-6785
Andres MetspaluThe Estonian Genome Center, University of Tartu, Tartu, Estonia.
Preben Bo MortensenNational Centre for Register-Based Research, Department of Economics and Business Economics, Aarhus University, Aarhus, Denmark.
Juni PalmgrenDepartment of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.ORCID http://orcid.org/0000-0002-9031-8615
Aarno PalotieMedical and Population Genetics Program, Broad Institute of Harvard and MIT, Cambridge, MA, USA.
Wenche ReedDepartment of Research, Innovation and Education, Oslo University Hospital, Oslo, Norway.
Hreinn StefánssondeCODE Genetics, Reykjavik, Iceland.ORCID http://orcid.org/0000-0002-9331-6666
Nathan O StitzielCardiovascular Division, Department of Medicine, Washington University, Saint Louis, MO, USA.
Patrick F SullivanDepartment of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.
Unnur ThorsteinsdóttirCardiovascular Division, Department of Medicine, Washington University, Saint Louis, MO, USA.
Marc VaudelCenter for Diabetes Research, Department of Clinical Science, University of Bergen, Bergen, Norway.
Eero VuorioDepartment of Medical Biochemistry and Genetics, University of Turku, Turku, Finland.
Thomas WergeDepartment for Congenital Disorders, Statens Serum Institut, Copenhagen, Denmark.ORCID http://orcid.org/0000-0003-1829-0766
Camilla StoltenbergGenomics and Biomarkers Unit, National Institute for Health and Welfare, Helsinki, Finland.
Kári StefánssondeCODE Genetics, Reykjavik, Iceland.ORCID http://orcid.org/0000-0003-1676-864X
Funding
No grant is acknowledged in the PubMed record.
Abstract
PubMed holds no abstract for this paper.
Indexed as
Access to InformationDatabases, FactualGenetic Association StudiesGenomicsHealth Plan ImplementationHealth Services AccessibilityHumansPrecision MedicineScandinavian and Nordic CountriesWeb Browser
Identifiers
PMID
30988515What OpenQuestion holds
Textmetadata
Read underepoch 390
Registered trials
None linked
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.