Steve Bevan
Impact in
Papers in
- Co-authors
- Hugh Stephen Markus (34 shared papers)Richard S. Houlston (25 shared papers)Ian P.M. Tomlinson (6 shared papers)Lauri A. Aaltonen (4 shared papers)Martin Dichgans (14 shared papers)Heikki Järvinen (2 shared papers)Pertti Sistonen (1 shared paper)Robert W. Summers (1 shared paper)
- Journals
- Stroke (32 papers)Neurology (11 papers)Nature Genetics (7 papers)British Journal of Cancer (4 papers)Journal of Medical Genetics (4 papers)
- Partner nations
- United KingdomUnited StatesGermany
In The Last Decade
Steve Bevan
121 papers receiving 12.4k citations
Steve Bevan's Hit Papers
Peers
Comparison fields: 5 of 141
- Genetics 4.7k
- Neurology 1.1k
- Epidemiology 1.8k
- Pathology and Forensic Medicine 925
- Psychiatry and Mental health 967
Countries citing papers authored by Steve Bevan
This map shows the geographic impact of Steve Bevan'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 Steve Bevan with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Steve Bevan more than expected).
Fields of papers citing papers by Steve Bevan
This network shows the impact of papers produced by Steve Bevan. 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 Steve Bevan. The network helps show where Steve Bevan may publish in the future.
Co-authors
The 25 scholars most cited alongside Steve Bevan, 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 125 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Analysis of shared heritability in common disorders of the brain Hit paper breakdown → | 2018 | 1477 |
| 2 | Germline mutations in FH predispose to dominantly inherited uterine fibroids, skin leiomyomata and papillary renal cell cancer Hit paper breakdown → | 2002 | 1300 |
| 3 | Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes Hit paper breakdown → | 2018 | 1221 |
| 4 | Mutations in the SMAD4/DPC4 Gene in Juvenile Polyposis Hit paper breakdown → | 1998 | 738 |
| 5 | 2009 | 400 | |
| 6 | 2012 | 400 | |
| 7 | Stroke genetics informs drug discovery and risk prediction across ancestries Hit paper breakdown → | 2022 | 372 |
| 8 | 2012 | 355 | |
| 9 | The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals Hit paper breakdown → | 2016 | 335 |
| 10 | 2012 | 323 | |
| 11 | 2013 | 282 | |
| 12 | 2008 | 242 | |
| 13 | 2015 | 222 | |
| 14 | 2009 | 178 | |
| 15 | 2011 | 177 | |
| 16 | 1999 | 163 | |
| 17 | 2016 | 155 | |
| 18 | 2012 | 143 | |
| 19 | 2016 | 142 | |
| 20 | 2012 | 128 |
About Steve Bevan
Steve Bevan is a scholar working on Genetics, Neurology, Epidemiology, Cardiology and Cardiovascular Medicine and Gastroenterology, having authored 125 papers that have together received 13k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (63 papers), Acute Ischemic Stroke Management (19 papers), Cerebrovascular and genetic disorders (17 papers), Genetic factors in colorectal cancer (10 papers), Cardiovascular Health and Disease Prevention (10 papers), Celiac Disease Research and Management (7 papers), Blood Coagulation and Thrombosis Mechanisms (6 papers) and Atherosclerosis and Cardiovascular Diseases (5 papers). The work is most often cited by research in Genetics (4.7k citations), Neurology (1.1k citations), Epidemiology (1.8k citations), Pathology and Forensic Medicine (925 citations) and Psychiatry and Mental health (967 citations). Steve Bevan has collaborated with scholars based in United Kingdom, United States and Germany. Frequent co-authors include Hugh Stephen Markus, Richard S. Houlston, Ian P.M. Tomlinson, Lauri A. Aaltonen, Martin Dichgans, Heikki Järvinen, Pertti Sistonen, Robert W. Summers, James R. Howe and John C. Ringold. Their work appears in journals such as Stroke, Neurology, Nature Genetics, British Journal of Cancer and Journal of Medical 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.