Amanda Singleton
Impact in
- Neurology top 2%
- Parkinson's Disease Mechanisms and Treatments
- Neurological disorders and treatments
- Neurological diseases and metabolism
- Botulinum Toxin and Related Neurological Disorders
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- Genetic Neurodegenerative Diseases
- Nuclear Receptors and Signaling
Papers in
- Neurology 13
- Parkinson's Disease Mechanisms and Treatments 11
- Neurological disorders and treatments 6
- Neurological diseases and metabolism 3
- Botulinum Toxin and Related Neurological Disorders 2
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- Genetic Neurodegenerative Diseases 8
- Co-authors
- John Hardy (10 shared papers)Katrina Gwinn (11 shared papers)Andrew B. Singleton (8 shared papers)Anthony Crawley (4 shared papers)Melissa Hanson (6 shared papers)Matthew James Farrer (3 shared papers)Stephen Hague (2 shared papers)William K. Seltzer (2 shared papers)
- Journals
- Movement Disorders (4 papers)Parkinsonism & Related Disorders (2 papers)Neurology (2 papers)Human Molecular Genetics (2 papers)American Journal of Medical Genetics Part C Seminars in Medical Genetics (1 paper)
- Partner nations
- United StatesUnited KingdomVenezuela
In The Last Decade
Amanda Singleton
21 papers receiving 1.3k citations
Peers
Comparison fields: 5 of 88
- Neurology 775
- Cellular and Molecular Neuroscience 579
- Neurology 218
- Physiology 247
- Genetics 146
Countries citing papers authored by Amanda Singleton
This map shows the geographic impact of Amanda Singleton'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 Amanda Singleton with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Amanda Singleton more than expected).
Fields of papers citing papers by Amanda Singleton
This network shows the impact of papers produced by Amanda Singleton. 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 Amanda Singleton. The network helps show where Amanda Singleton may publish in the future.
Co-authors
The 25 scholars most cited alongside Amanda Singleton, 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 21 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2003 | 207 | |
| 2 | 2000 | 169 | |
| 3 | 2004 | 115 | |
| 4 | 2004 | 107 | |
| 5 | 2004 | 83 | |
| 6 | 2002 | 77 | |
| 7 | 2011 | 69 | |
| 8 | 2003 | 61 | |
| 9 | 2004 | 59 | |
| 10 | 2011 | 56 | |
| 11 | 2010 | 54 | |
| 12 | 2018 | 44 | |
| 13 | 2005 | 39 | |
| 14 | 2018 | 37 | |
| 15 | 2011 | 35 | |
| 16 | 2004 | 31 | |
| 17 | 2003 | 22 | |
| 18 | 2018 | 17 | |
| 19 | 2004 | 14 | |
| 20 | 2003 | 13 |
About Amanda Singleton
Amanda Singleton is a scholar working on Neurology, Cellular and Molecular Neuroscience, Neurology, Physiology and Genetics, having authored 21 papers that have together received 1.3k indexed citations. Recurring topics across this work include Parkinson's Disease Mechanisms and Treatments (11 papers), Genetic Neurodegenerative Diseases (8 papers), Neurological disorders and treatments (6 papers), Neurological diseases and metabolism (3 papers), Botulinum Toxin and Related Neurological Disorders (2 papers), BRCA gene mutations in cancer (2 papers), Mitochondrial Function and Pathology (2 papers) and Alzheimer's disease research and treatments (2 papers). The work is most often cited by research in Neurology (775 citations), Cellular and Molecular Neuroscience (579 citations), Neurology (218 citations), Physiology (247 citations) and Genetics (146 citations). Amanda Singleton has collaborated with scholars based in United States, United Kingdom and Venezuela. Frequent co-authors include John Hardy, Katrina Gwinn, Andrew B. Singleton, Anthony Crawley, Melissa Hanson, Matthew James Farrer, Stephen Hague, William K. Seltzer, Cheryl Waters and Roberto Weiser. Their work appears in journals such as Movement Disorders, Parkinsonism & Related Disorders, Neurology, Human Molecular Genetics and American Journal of Medical Genetics Part C Seminars in 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.