Amanda Singleton

1.6k citations

17 papers · 985 indexed · h-index 14

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
Cellular and Molecular Neuroscience top 5%
- Genetic Neurodegenerative Diseases
- Nuclear Receptors and Signaling

Papers in

Neurology 12
- Parkinson's Disease Mechanisms and Treatments 10
- Neurological disorders and treatments 6
- Neurological diseases and metabolism 3
- Botulinum Toxin and Related Neurological Disorders 2
Cellular and Molecular Neuroscience 7
- Genetic Neurodegenerative Diseases 6

Co-authors: John Hardy Katrina Gwinn Andrew Singleton Anthony Crawley Melissa Hanson Matthew J. Farrer Stephen Hague William Seltzer
Journals: Movement Disorders (3 papers)Human Molecular Genetics (2 papers)Parkinsonism & Related Disorders (2 papers)Clinical Autonomic Research (1 paper)European Journal of Neurology (1 paper)
Partner nations: United States Venezuela Canada

In The Last Decade

Amanda Singleton

17 papers receiving 960 citations

Peers

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

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.

Border = papers with Amanda Singleton Line = papers co-authored together Amanda Singleton links everyone, so they are left out of the graph.

All Works

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17 of 17 papers shown

#	Work
1	Genetic counseling in industry settings: Opportunities in the era of precision health American Journal of Medical Genetics Part C Seminars in Medical Genetics ·Kirsty McWalter, Megan T. Cho, Norio Higashi, Rachel Nusbaum, Courtney Sebold, Gavin Young, Rachel Klein, Bethany Friedman, Rebecca Willaert, Amanda Singleton, Nancy Steadman, Elizabeth Butler, Jane Juusola	2018	16
2	A generalizable hypothesis for the genetic architecture of disease: pleomorphic risk loci Human Molecular Genetics ·Amanda Singleton, John Hardy	2011	55
3	Informed Choice in Direct‐to‐Consumer Genetic Testing (DTCGT) Websites: A Content Analysis of Benefits, Risks, and Limitations Journal of Genetic Counseling ·Amanda Singleton, Lori H. Erby, Anthony Levasseur, Kimberly A. Kaphingst	2011	48
4	Clinical features of patients with blepharospasm: a report of 240 patients European Journal of Neurology ·Elizabeth Peckham, Carolina Monteiro da Silva, Ejaz A. Shamim, Michelle Battles, Stewart Lamb Cromar, Roneil G. Malkani, Mark Stacy, Nanoukon Chimène, Anthony Crawley, Amanda Singleton, Mark Hallett	2010	47
5	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 ·Javier Simón‐Sánchez, Melissa Hanson, Amanda Singleton, Dena G. Hernandez, Aideen McInerney‐Leo, Robert Nussbaum, John S. Werner, Marisol Gallardo, Roberto Weiser, Katrina Gwinn, Andrew B. Singleton, Jordi Clarimón	2005	32
6	Analysis of familial and sporadic restless legs syndrome in age of onset, gender, and severity features Journal of Neurology ·Melissa Hanson, Melissa Honour, Amanda Singleton, Anthony Crawley, Andrew Singleton, John Hardy, Katrina Gwinn	2004	27
7	Profile of families with parkinsonism‐predominant spinocerebellar ataxia type 2 (SCA2) Movement Disorders ·Sarah Furtado, Haydeh Payami, Paul J. Lockhart, Melissa Hanson, John G. Nutt, F CondÃ©, Amanda Singleton, J. D. Bower, Bonita Ford, Thomas D. Bird, Raúl de la Fuente‐Fernández, Yoshio Tsuboi, Mary Lou Klimek, Oksana Suchowersky, John Hardy, Donald B. Calne, Zbigniew K. Wszołek, Matthew J. Farrer, Katrina Gwinn, A. Jon Stoessl	2004	86
8	Smell testing is abnormal in ‘lubag’ or X-linked dystonia-parkinsonism: a pilot study Parkinsonism & Related Disorders ·Virgilio Gerald H. Evidente, Y. Yuan, Jose Luis Hernández‐Davó, Filipinas F. Natividad, Joel Advincula, Katrina Gwinn, John Hardy, Amanda Singleton, Andrew Singleton	2004	12
9	The law of mass action applied to neurodegenerative disease: a hypothesis concerning the etiology and pathogenesis of complex diseases Human Molecular Genetics ·Amanda Singleton	2004	69
10	Association between cardiac denervation and parkinsonism caused by α‐synuclein gene triplication Brain ·Amanda Singleton, Katrina Gwinn, Ali Hammoudi, Sheng‐Ting Li, Courtney Holmes, Raghuveer Dendi, John Hardy, Andrew Singleton, Anthony Crawley, David S. Goldstein	2004	104
11	Mutation at the SCA17 locus is not a common cause of parkinsonism Parkinsonism & Related Disorders ·Dena Hernández, Melissa Hanson, Amanda Singleton, Katrina Gwinn, Hanbiao Liu, Bernard Ravina, Dana Doheny, Marisol Gallardo, Roberto Weiser, John Hardy, Andrew Singleton	2003	11
12	Exercise‐induced dystonia as a preceding symptom of familial Parkinson's disease Movement Disorders ·Michiko Kimura Bruno, Bernard Ravina, Gaëtan Garraux, Mark Hallett, Louis J. Ptáček, Amanda Singleton, Janel Johnson, Andrew Singleton, Melissa Hanson, Elaine Considine, Katrina Gwinn	2003	18
13	Early‐onset Parkinson's disease caused by a compound heterozygous DJ‐1 mutation Annals of Neurology ·Stephen Hague, Ekaterina Rogaeva, Dena G. Hernandez, Noah Doucette, Amanda Singleton, Melissa Hanson, Janel Johnson, Roberto Weiser, Marisol Gallardo, Bernard Ravina, Katrina Gwinn, Anthony Crawley, Peter St George‐Hyslop, Anthony E. Lang, Peter Heutink, Vincenzo Bonifati, John Hardy, Andrew Singleton	2003	190
14	Primary hyperhidrosis Clinical Autonomic Research ·Horacio Kaufmann, Daniela Saadia, Charlene Polin, Stephen Hague, Amanda Singleton, Andrew Singleton	2003	55
15	SCA2 may present as levodopa‐responsive parkinsonism Movement Disorders ·Haydeh Payami, John G. Nutt, S. Gancher, Thomas D. Bird, U Vinay, William Seltzer, Jennifer Hussey, Paul J. Lockhart, Katrina Gwinn, Amanda Singleton, Andrew Singleton, John Hardy, Matthew J. Farrer	2002	66
16	Familial Lewy Body Diseases Journal of Geriatric Psychiatry and Neurology ·Katrina Gwinn, Amanda Singleton	2002	4
17	Spinocerebellar ataxia type 2 with parkinsonism in ethnic Chinese Neurology ·(unknown), Jake Y. Chen, H.-C. Liu, Tzu‐Yu Liu, Michael A. Boss, William Seltzer, Sugiura Akinori, Amanda Singleton, Walter J. Koroshetz, Cheryl Waters, John Hardy, Matthew J. Farrer	2000	145

About Amanda Singleton

Amanda Singleton is a scholar working on Neurology, Cellular and Molecular Neuroscience, Neurology, Sensory Systems and Physiology, having authored 17 papers that have together received 985 indexed citations. Recurring topics across this work include Parkinson's Disease Mechanisms and Treatments (10 papers), Neurological disorders and treatments (6 papers), Genetic Neurodegenerative Diseases (6 papers), Neurological diseases and metabolism (3 papers), Mitochondrial Function and Pathology (3 papers), Genomics and Rare Diseases (2 papers), Botulinum Toxin and Related Neurological Disorders (2 papers) and BRCA gene mutations in cancer (2 papers). The work is most often cited by research in Neurology (666 citations), Cellular and Molecular Neuroscience (490 citations), Neurology (170 citations), Physiology (202 citations) and Molecular Biology (290 citations). Amanda Singleton has collaborated with scholars based in United States, Venezuela and Canada. Frequent co-authors include John Hardy, Katrina Gwinn, Andrew Singleton, Anthony Crawley, Melissa Hanson, Matthew J. Farrer, Stephen Hague, William Seltzer, Marisol Gallardo and Roberto Weiser. Their work appears in journals such as Movement Disorders, Human Molecular Genetics, Parkinsonism & Related Disorders, Clinical Autonomic Research and European Journal of Neurology.

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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