Robert Swingler
Impact in
Papers in
- Co-authors
- Orla Hardiman (9 shared papers)D. A. S. Compston (11 shared papers)Adriano Chiò (7 shared papers)Giancarlo Logroscino (7 shared papers)Ettore Beghi (7 shared papers)Douglas Mitchell (5 shared papers)Shuna Colville (15 shared papers)Bryan Traynor (1 shared paper)
- Journals
- Journal of Neurology Neurosurgery & Psychiatry (14 papers)Journal of Neurology (6 papers)Neurology (3 papers)Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration (2 papers)Human Molecular Genetics (2 papers)
- Partner nations
- United KingdomUnited StatesIreland
In The Last Decade
Robert Swingler
63 papers receiving 4.5k citations
Robert Swingler's Hit Papers
Peers
Comparison fields: 5 of 129
- Neurology 3.1k
- Genetics 1.6k
- Neurology 652
- Pathology and Forensic Medicine 880
- Cellular and Molecular Neuroscience 361
Countries citing papers authored by Robert Swingler
This map shows the geographic impact of Robert Swingler'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 Robert Swingler with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Robert Swingler more than expected).
Fields of papers citing papers by Robert Swingler
This network shows the impact of papers produced by Robert Swingler. 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 Robert Swingler. The network helps show where Robert Swingler may publish in the future.
Co-authors
The 25 scholars most cited alongside Robert Swingler, 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 64 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Prognostic factors in ALS: A critical review Hit paper breakdown → | 2009 | 766 |
| 2 | ANG mutations segregate with familial and 'sporadic' amyotrophic lateral sclerosis Hit paper breakdown → | 2006 | 518 |
| 3 | 2007 | 324 | |
| 4 | 1999 | 245 | |
| 5 | 2006 | 164 | |
| 6 | 1999 | 163 | |
| 7 | 2018 | 160 | |
| 8 | 2015 | 135 | |
| 9 | 2008 | 108 | |
| 10 | 2010 | 106 | |
| 11 | 2008 | 105 | |
| 12 | 2010 | 99 | |
| 13 | 1993 | 98 | |
| 14 | 1996 | 93 | |
| 15 | 2015 | 92 | |
| 16 | 2017 | 85 | |
| 17 | 1993 | 83 | |
| 18 | 2007 | 79 | |
| 19 | The morbidity of multiple sclerosis. | 1992 | 77 |
| 20 | 1988 | 72 |
About Robert Swingler
Robert Swingler is a scholar working on Neurology, Genetics, Pathology and Forensic Medicine, Molecular Biology and Neurology, having authored 64 papers that have together received 4.7k indexed citations. Recurring topics across this work include Amyotrophic Lateral Sclerosis Research (37 papers), Neurogenetic and Muscular Disorders Research (19 papers), Parkinson's Disease Mechanisms and Treatments (13 papers), Multiple Sclerosis Research Studies (12 papers), Neurological diseases and metabolism (9 papers), Prion Diseases and Protein Misfolding (7 papers), Systemic Sclerosis and Related Diseases (7 papers) and Systemic Lupus Erythematosus Research (4 papers). The work is most often cited by research in Neurology (3.1k citations), Genetics (1.6k citations), Neurology (652 citations), Pathology and Forensic Medicine (880 citations) and Cellular and Molecular Neuroscience (361 citations). Robert Swingler has collaborated with scholars based in United Kingdom, United States and Ireland. Frequent co-authors include Orla Hardiman, D. A. S. Compston, Adriano Chiò, Giancarlo Logroscino, Ettore Beghi, Douglas Mitchell, Shuna Colville, Bryan Traynor, Bryan J. Traynor and Siddharthan Chandran. Their work appears in journals such as Journal of Neurology Neurosurgery & Psychiatry, Journal of Neurology, Neurology, Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration and Human Molecular 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.