Hreinn Stefánsson
- Genetics top 0.5%
- Genomic variations and chromosomal abnormalities 13
- Genetics and Neurodevelopmental Disorders 13
- Genetic Associations and Epidemiology 10
- Genomics and Rare Diseases 8
- Neurology top 1%
- Parkinson's Disease Mechanisms and Treatments 5
- Neurology top 2%
- Parkinson's Disease Mechanisms and Treatments 5
- Cognitive Neuroscience top 2%
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- Migraine and Headache Studies 9
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- Photosynthetic Processes and Mechanisms 8
- Congenital heart defects research 7
- Co-authors
- Kāri StefánssonJeffrey R. GulcherAugustine KongDaníel F. GuðbjartssonValgerður SteinthórsdóttirMichael L. FriggeRagnheiður FossdalAgnar Helgason
- Journals
- Science (2 papers)New England Journal of Medicine (1 paper)Proceedings of the National Academy of Sciences (2 papers)
- Partner nations
- IcelandUnited StatesDenmark
In The Last Decade
Hreinn Stefánsson
98 papers receiving 7.3k citations
Hit Papers
Peers
Comparison fields: 5 of 176
- Genetics 2.9k
- Neurology 968
- Neurology 492
- Cellular and Molecular Neuroscience 976
- Cognitive Neuroscience 998
Countries citing papers authored by Hreinn Stefánsson
This map shows the geographic impact of Hreinn 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 Hreinn Stefánsson with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Hreinn Stefánsson more than expected).
Fields of papers citing papers by Hreinn Stefánsson
This network shows the impact of papers produced by Hreinn 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 Hreinn Stefánsson. The network helps show where Hreinn Stefánsson may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Hreinn 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 | 3 | |
| 2 | 2024 | 1 | |
| 3 | 2024 | 2 | |
| 4 | 2023 | 3 | |
| 5 | 2022 | 7 | |
| 6 | 2021 | 14 | |
| 7 | 2021 | 23 | |
| 8 | 2020 | 1 | |
| 9 | 2019 | 30 | |
| 10 | 2017 | 42 | |
| 11 | 2017 | 23 | |
| 12 | 2015 | 12 | |
| 13 | 2014 | 4 | |
| 14 | 2013 | 56 | |
| 15 | 2011 | 8 | |
| 16 | 2008 | 50 | |
| 17 | 1998 | 82 | |
| 18 | 1997 | 5 | |
| 19 | 1995 | 13 | |
| 20 | 1989 | 8 |
About Hreinn Stefánsson
Hreinn Stefánsson is a scholar working on Genetics, Psychiatry and Mental health and Neurology, having authored 98 papers that have together received 7.5k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (13 papers), Genetics and Neurodevelopmental Disorders (13 papers), Genetic Associations and Epidemiology (10 papers), Migraine and Headache Studies (9 papers), Genomics and Rare Diseases (8 papers), Photosynthetic Processes and Mechanisms (8 papers), Congenital heart defects research (7 papers) and Parkinson's Disease Mechanisms and Treatments (5 papers). The work is most often cited by research in Genetics (2.9k citations), Neurology (968 citations) and Neurology (492 citations). Hreinn Stefánsson has collaborated with scholars based in Iceland, United States and Denmark. Frequent co-authors include Kāri Stefánsson, Jeffrey R. Gulcher, Augustine Kong, Daníel F. Guðbjartsson, Valgerður Steinthórsdóttir, Michael L. Frigge, Ragnheiður Fossdal, Agnar Helgason, Unnur Þorsteinsdóttir and Andrés Ingason. Their work appears in journals such as Science, New England Journal of Medicine and Proceedings of the National Academy of Sciences.
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.