Kāri Stefánsson
Impact in
- Genetics top 0.1%
- Genetic Associations and Epidemiology
- Genetic Mapping and Diversity in Plants and Animals
- Genetic diversity and population structure
- Genetic and phenotypic traits in livestock
- Forensic and Genetic Research
- Genomic variations and chromosomal abnormalities
- Developmental Neuroscience top 0.5%
- Neurogenesis and neuroplasticity mechanisms
Papers in
- Genetics 84
- Genetic Associations and Epidemiology 37
- Genomics and Rare Diseases 16
- Genomic variations and chromosomal abnormalities 14
- Genetic diversity and population structure 14
- Forensic and Genetic Research 13
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- Cell Adhesion Molecules Research 15
- Co-authors
- Jeffrey R. GulcherAugustine KongDaníel F. GuðbjartssonRobert L. WollmannAgnar HelgasonMichael L. FriggeGísli MássonHreinn Stefánsson
- Journals
- Nature Genetics (23 papers)The American Journal of Human Genetics (14 papers)Nature Communications (9 papers)European Journal of Human Genetics (8 papers)PLoS Genetics (7 papers)
- Partner nations
- IcelandUnited StatesUnited Kingdom
In The Last Decade
Kāri Stefánsson
240 papers receiving 17.2k citations
Hit Papers
Peers
Comparison fields: 5 of 193
- Genetics 6.1k
- Developmental Neuroscience 722
- Immunology and Allergy 650
- Molecular Biology 6.5k
- Neurology 1.4k
Countries citing papers authored by Kāri Stefánsson
This map shows the geographic impact of Kāri Stefánsson's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Kāri Stefánsson with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Kāri Stefánsson more than expected).
Fields of papers citing papers by Kāri Stefánsson
This network shows the impact of papers produced by Kāri Stefánsson. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Kāri Stefánsson. The network helps show where Kāri Stefánsson may publish in the future.
Co-authors
The 25 scholars most cited alongside Kāri Stefánsson, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2024 | 17 | |
| 2 | 2024 | 1 | |
| 3 | 2024 | 3 | |
| 4 | 2024 | 1 | |
| 5 | 2023 | 5 | |
| 6 | 2023 | 4 | |
| 7 | 2023 | 1 | |
| 8 | 2023 | 1 | |
| 9 | 2022 | 6 | |
| 10 | 2020 | 56 | |
| 11 | 2019 | 8 | |
| 12 | 2019 | 20 | |
| 13 | 2019 | 30 | |
| 14 | 2019 | 83 | |
| 15 | 2018 | 50 | |
| 16 | 2017 | 113 | |
| 17 | 2017 | 38 | |
| 18 | 2016 | 52 | |
| 19 | 2016 | 29 | |
| 20 | 2004 | 6 |
About Kāri Stefánsson
Kāri Stefánsson is a scholar working on Genetics, Immunology and Allergy, Developmental Neuroscience, Molecular Biology and Rheumatology, having authored 246 papers that have together received 17.8k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (37 papers), Genomics and Rare Diseases (16 papers), Cell Adhesion Molecules Research (15 papers), Monoclonal and Polyclonal Antibodies Research (15 papers), Genomic variations and chromosomal abnormalities (14 papers), Glycosylation and Glycoproteins Research (14 papers), Genetic diversity and population structure (14 papers) and Forensic and Genetic Research (13 papers). The work is most often cited by research in Genetics (6.1k citations), Developmental Neuroscience (722 citations), Immunology and Allergy (650 citations), Molecular Biology (6.5k citations) and Neurology (1.4k citations). Kāri Stefánsson has collaborated with scholars based in Iceland, United States and United Kingdom. Frequent co-authors include Jeffrey R. Gulcher, Augustine Kong, Daníel F. Guðbjartsson, Robert L. Wollmann, Agnar Helgason, Michael L. Frigge, Gísli Másson, Hreinn Stefánsson, Unnur Þorsteinsdóttir and Guðmar Þorleifsson. Their work appears in journals such as Nature Genetics, The American Journal of Human Genetics, Nature Communications, European Journal of Human Genetics and PLoS Genetics.
Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.