Amanda Singleton

1.6k citations
17 papers · 1.1k · h-index 14

Impact in

  • Neurology top 2%
    • Parkinson's Disease Mechanisms and Treatments
    • Neurological disorders and treatments
    • Neurological diseases and metabolism
    • Genetic Neurodegenerative Diseases
    • Nuclear Receptors and Signaling

Papers in

Amanda Singleton

17 papers receiving 1.0k citations

Peers

Amanda Singleton
Comparison fields: 5 of 81
  • Neurology 649
  • Cellular and Molecular Neuroscience 505
  • Neurology 186
  • Physiology 205
  • Molecular Biology 276
Replace Audrey Strongosky with:
Audrey Strongosky United States
N. Gouider‐Khouja Tunisia
Elena Lorenzo Spain
J. Hagenah Germany
Barbara Jasińska‐Myga Poland
Patrizia Spadafora Italy
H. Sauer Germany
Y Mizuno Japan
Charles Duyckaerts France
Nataša Dragašević Serbia
Amanda Singleton relative to Audrey Strongosky United States Audrey Strongosky's profile →
Citations per field
00.5×1.5×
Audrey Strongosky · 1×
Citations per year

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-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.

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

All Works

17 of 17 papers shown
#Work
1 2003203
2 2000156
3 2004117
4 200495
5 200476
6 200272
7 200358
8 201157
9 201051
10 201148
11 200535
12 200429
13 200321
14 201818
15 200413
16 200312
17 20029

About Amanda Singleton

Amanda Singleton is a scholar working on Neurology, Cellular and Molecular Neuroscience, Physiology, Molecular Biology and Neurology, having authored 17 papers that have together received 1.1k indexed citations. Recurring topics across this work include Parkinson's Disease Mechanisms and Treatments (9 papers), Genetic Neurodegenerative Diseases (6 papers), Neurological disorders and treatments (5 papers), Neurological diseases and metabolism (3 papers), Alzheimer's disease research and treatments (2 papers), Genomics and Rare Diseases (2 papers), BRCA gene mutations in cancer (2 papers) and Mitochondrial Function and Pathology (2 papers). The work is most often cited by research in Neurology (649 citations), Cellular and Molecular Neuroscience (505 citations), Neurology (186 citations), Physiology (205 citations) and Molecular Biology (276 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, Roberto Weiser and Marisol Gallardo. 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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