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
- Forensic and Genetic Research
- Genetic and phenotypic traits in livestock
- Genomic variations and chromosomal abnormalities
- Developmental Neuroscience top 0.5%
- Neurogenesis and neuroplasticity mechanisms
Papers in
-
- Glycosylation and Glycoproteins Research 14
- Genetics 78
- Genetic Associations and Epidemiology 34
- Genetic diversity and population structure 14
- Genomics and Rare Diseases 14
- Genomic variations and chromosomal abnormalities 13
- Forensic and Genetic Research 13
- Co-authors
- Jeffrey R. Gulcher (62 shared papers)Augustine Kong (52 shared papers)Daníel F. Guðbjartsson (65 shared papers)Robert L. Wollmann (9 shared papers)Agnar Helgason (43 shared papers)Michael L. Frigge (25 shared papers)Gísli Másson (26 shared papers)Unnur Þorsteinsdóttir (49 shared papers)
- Journals
- Nature Genetics (22 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
239 papers receiving 17.2k citations
Kāri Stefánsson's Hit Papers
Peers
Comparison fields: 5 of 188
- Genetics 5.5k
- Developmental Neuroscience 698
- Immunology and Allergy 604
- Neurology 1.3k
- Neurology 671
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
Showing the 20 most-cited of 245 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | A high-resolution recombination map of the human genome Hit paper breakdown → | 2002 | 1304 |
| 2 | The nature of nurture: Effects of parental genotypes Hit paper breakdown → | 2018 | 530 |
| 3 | Common Sequence Variants in the LOXL1 Gene Confer Susceptibility to Exfoliation Glaucoma Hit paper breakdown → | 2007 | 482 |
| 4 | 2003 | 430 | |
| 5 | 2010 | 411 | |
| 6 | S-100 protein in soft-tissue tumors derived from Schwann cells and melanocytes. | 1982 | 297 |
| 7 | 2008 | 256 | |
| 8 | Interferon-gamma-induced oligodendrocyte cell death: implications for the pathogenesis of multiple sclerosis. | 1995 | 250 |
| 9 | 2010 | 245 | |
| 10 | 1982 | 243 | |
| 11 | 2019 | 239 | |
| 12 | 2012 | 238 | |
| 13 | 2008 | 233 | |
| 14 | 1995 | 232 | |
| 15 | 2004 | 207 | |
| 16 | 2000 | 206 | |
| 17 | 2006 | 205 | |
| 18 | 2004 | 202 | |
| 19 | 2003 | 196 | |
| 20 | 2002 | 194 |
About Kāri Stefánsson
Kāri Stefánsson is a scholar working on Molecular Biology, Genetics, Immunology, Radiology, Nuclear Medicine and Imaging and Physiology, having authored 245 papers that have together received 17.7k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (34 papers), Monoclonal and Polyclonal Antibodies Research (15 papers), Glycosylation and Glycoproteins Research (14 papers), Cell Adhesion Molecules Research (14 papers), Genetic diversity and population structure (14 papers), Genomics and Rare Diseases (14 papers), Genomic variations and chromosomal abnormalities (13 papers) and Forensic and Genetic Research (13 papers). The work is most often cited by research in Genetics (5.5k citations), Developmental Neuroscience (698 citations), Immunology and Allergy (604 citations), Neurology (1.3k citations) and Neurology (671 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, Unnur Þorsteinsdóttir, Hreinn Stefánsson 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.