Jonathan Rosand
Impact in
- Genetics top 10%
- Genetic Associations and Epidemiology
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- Atrial Fibrillation Management and Outcomes
- Cardiac electrophysiology and arrhythmias
Papers in
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- Folate and B Vitamins Research 2
- Moyamoya disease diagnosis and treatment 1
- Genetics 4
- Genetic Associations and Epidemiology 3
- Co-authors
- David Krishna Menon (1 shared paper)James F. Meschia (2 shared papers)Hugh Stephen Markus (1 shared paper)Steven J. Kittner (1 shared paper)Braxton D. Mitchell (1 shared paper)Ioana Cotlarciuc (1 shared paper)Martin Dichgans (1 shared paper)Guillaume Paré (1 shared paper)
- Journals
- Stroke (2 papers)The Lancet Neurology (1 paper)JAMA Network Open (1 paper)Frontiers in Neurology (1 paper)Nature Genetics (1 paper)
- Partner nations
- United StatesUnited KingdomSweden
In The Last Decade
Jonathan Rosand
12 papers receiving 1.1k citations
Jonathan Rosand's Hit Papers
Peers
Comparison fields: 5 of 85
- Genetics 291
- Cardiology and Cardiovascular Medicine 207
- Hematology 82
- Neurology 58
- Internal Medicine 21
Countries citing papers authored by Jonathan Rosand
This map shows the geographic impact of Jonathan Rosand'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 Jonathan Rosand with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jonathan Rosand more than expected).
Fields of papers citing papers by Jonathan Rosand
This network shows the impact of papers produced by Jonathan Rosand. 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 Jonathan Rosand. The network helps show where Jonathan Rosand may publish in the future.
Co-authors
The 24 scholars most cited alongside Jonathan Rosand, 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 | Stroke genetics informs drug discovery and risk prediction across ancestries Hit paper breakdown → | 2022 | 355 |
| 2 | 2017 | 266 | |
| 3 | 2018 | 180 | |
| 4 | 2021 | 132 | |
| 5 | 2019 | 120 | |
| 6 | 2014 | 31 | |
| 7 | 2021 | 17 | |
| 8 | 2021 | 10 | |
| 9 | 2000 | 3 | |
| 10 | 2022 | 2 | |
| 11 | 2007 | 2 | |
| 12 | 2009 | 1 |
About Jonathan Rosand
Jonathan Rosand is a scholar working on Rheumatology, Genetics, Immunology and Allergy, Pulmonary and Respiratory Medicine and Epidemiology, having authored 12 papers that have together received 1.1k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (3 papers), Folate and B Vitamins Research (2 papers), Acute Ischemic Stroke Management (2 papers), Cerebrovascular and Carotid Artery Diseases (2 papers), Cell Adhesion Molecules Research (1 paper), Lipoproteins and Cardiovascular Health (1 paper), Moyamoya disease diagnosis and treatment (1 paper) and Bioinformatics and Genomic Networks (1 paper). The work is most often cited by research in Genetics (291 citations), Cardiology and Cardiovascular Medicine (207 citations), Hematology (82 citations), Neurology (58 citations) and Internal Medicine (21 citations). Jonathan Rosand has collaborated with scholars based in United States, United Kingdom and Sweden. Frequent co-authors include David Krishna Menon, James F. Meschia, Hugh Stephen Markus, Steven J. Kittner, Braxton D. Mitchell, Ioana Cotlarciuc, Martin Dichgans, Guillaume Paré, Bradford B. Worrall and Myriam Fornage. Their work appears in journals such as Stroke, The Lancet Neurology, JAMA Network Open, Frontiers in Neurology and Nature 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.