Amanda Singleton

1.6k total citations
17 papers, 985 citations indexed

About

Amanda Singleton is a scholar working on Neurology, Cellular and Molecular Neuroscience and Physiology. According to data from OpenAlex, Amanda Singleton has authored 17 papers receiving a total of 985 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Neurology, 7 papers in Cellular and Molecular Neuroscience and 5 papers in Physiology. Recurrent topics in Amanda Singleton's work include Parkinson's Disease Mechanisms and Treatments (10 papers), Neurological disorders and treatments (6 papers) and Genetic Neurodegenerative Diseases (6 papers). Amanda Singleton is often cited by papers focused on Parkinson's Disease Mechanisms and Treatments (10 papers), Neurological disorders and treatments (6 papers) and Genetic Neurodegenerative Diseases (6 papers). Amanda Singleton collaborates with scholars based in United States, Venezuela and Canada. Amanda Singleton's co-authors include John Hardy, Andrew Singleton, Katrina Gwinn, Anthony Crawley, Melissa Hanson, Matthew J. Farrer, Stephen Hague, William Seltzer, Roberto Weiser and Marisol Gallardo and has published in prestigious journals such as Brain, Neurology and Annals of Neurology.

In The Last Decade

Amanda Singleton

17 papers receiving 960 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Amanda Singleton United States 14 666 490 290 202 170 17 985
Nataša Dragašević Serbia 19 690 1.0× 478 1.0× 229 0.8× 99 0.5× 165 1.0× 47 1.2k
Barbara Jasińska‐Myga Poland 15 540 0.8× 202 0.4× 138 0.5× 182 0.9× 124 0.7× 29 710
N. Gouider‐Khouja Tunisia 16 496 0.7× 271 0.6× 236 0.8× 98 0.5× 167 1.0× 47 879
Yi‐Min Sun China 18 477 0.7× 225 0.5× 246 0.8× 307 1.5× 127 0.7× 73 919
Y Mizuno Japan 11 593 0.9× 356 0.7× 154 0.5× 102 0.5× 201 1.2× 35 740
Elena Lorenzo Spain 13 403 0.6× 179 0.4× 234 0.8× 185 0.9× 237 1.4× 20 741
Kari J. Strain United States 10 476 0.7× 375 0.8× 277 1.0× 115 0.6× 188 1.1× 10 883
Hiroshi Kurisaki Japan 15 358 0.5× 490 1.0× 525 1.8× 71 0.4× 84 0.5× 37 876
Lasse Pihlstrøm Norway 18 549 0.8× 284 0.6× 310 1.1× 222 1.1× 229 1.3× 49 904
Giselle Prunell Uruguay 14 618 0.9× 230 0.5× 309 1.1× 62 0.3× 150 0.9× 22 1.0k

Countries citing papers authored by Amanda Singleton

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Amanda Singleton

This figure shows the co-authorship network connecting the top 25 collaborators of Amanda Singleton. A scholar is included among the top collaborators of Amanda Singleton based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Amanda Singleton. Amanda Singleton is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

17 of 17 papers shown
1.
McWalter, Kirsty, Megan T. Cho, Rachel Nusbaum, et al.. (2018). Genetic counseling in industry settings: Opportunities in the era of precision health. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 178(1). 46–53. 16 indexed citations
2.
Singleton, Amanda & John Hardy. (2011). A generalizable hypothesis for the genetic architecture of disease: pleomorphic risk loci. Human Molecular Genetics. 20(R2). R158–R162. 55 indexed citations
3.
Singleton, Amanda, et al.. (2011). Informed Choice in Direct‐to‐Consumer Genetic Testing (DTCGT) Websites: A Content Analysis of Benefits, Risks, and Limitations. Journal of Genetic Counseling. 21(3). 433–439. 48 indexed citations
4.
Peckham, Elizabeth, Ejaz A. Shamim, Roneil G. Malkani, et al.. (2010). Clinical features of patients with blepharospasm: a report of 240 patients. European Journal of Neurology. 18(3). 382–386. 47 indexed citations
5.
Simón‐Sánchez, Javier, Melissa Hanson, Amanda Singleton, et al.. (2005). Analysis of SCA-2 and SCA-3 repeats in Parkinsonism: Evidence of SCA-2 expansion in a family with autosomal dominant Parkinson's disease. Neuroscience Letters. 382(1-2). 191–194. 32 indexed citations
6.
Hanson, Melissa, Melissa Honour, Amanda Singleton, et al.. (2004). Analysis of familial and sporadic restless legs syndrome in age of onset, gender, and severity features. Journal of Neurology. 251(11). 1398–1401. 27 indexed citations
7.
Evidente, Virgilio Gerald H., Jose Luis Hernández‐Davó, Filipinas F. Natividad, et al.. (2004). Smell testing is abnormal in ‘lubag’ or X-linked dystonia-parkinsonism: a pilot study. Parkinsonism & Related Disorders. 10(7). 407–410. 12 indexed citations
8.
Furtado, Sarah, Haydeh Payami, Paul J. Lockhart, et al.. (2004). Profile of families with parkinsonism‐predominant spinocerebellar ataxia type 2 (SCA2). Movement Disorders. 19(6). 622–629. 86 indexed citations
9.
Singleton, Amanda. (2004). The law of mass action applied to neurodegenerative disease: a hypothesis concerning the etiology and pathogenesis of complex diseases. Human Molecular Genetics. 13(90001). 123R–126. 69 indexed citations
10.
Singleton, Amanda, Katrina Gwinn, Sheng‐Ting Li, et al.. (2004). Association between cardiac denervation and parkinsonism caused by α‐synuclein gene triplication. Brain. 127(4). 768–772. 104 indexed citations
11.
Bruno, Michiko Kimura, Bernard Ravina, Gaëtan Garraux, et al.. (2003). Exercise‐induced dystonia as a preceding symptom of familial Parkinson's disease. Movement Disorders. 19(2). 228–230. 18 indexed citations
12.
Hernández, Dena, Melissa Hanson, Amanda Singleton, et al.. (2003). Mutation at the SCA17 locus is not a common cause of parkinsonism. Parkinsonism & Related Disorders. 9(6). 317–320. 11 indexed citations
13.
Hague, Stephen, Ekaterina Rogaeva, Dena G. Hernandez, et al.. (2003). Early‐onset Parkinson's disease caused by a compound heterozygous DJ‐1 mutation. Annals of Neurology. 54(2). 271–274. 190 indexed citations
14.
Kaufmann, Horacio, et al.. (2003). Primary hyperhidrosis. Clinical Autonomic Research. 13(2). 96–98. 55 indexed citations
15.
Gwinn, Katrina & Amanda Singleton. (2002). Familial Lewy Body Diseases. Journal of Geriatric Psychiatry and Neurology. 15(4). 217–223. 4 indexed citations
16.
Payami, Haydeh, John G. Nutt, S. Gancher, et al.. (2002). SCA2 may present as levodopa‐responsive parkinsonism. Movement Disorders. 18(4). 425–429. 66 indexed citations
17.
Chen, Jake Y., H.-C. Liu, Tzu‐Yu Liu, et al.. (2000). Spinocerebellar ataxia type 2 with parkinsonism in ethnic Chinese. Neurology. 55(6). 800–805. 145 indexed citations

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.

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