Suran Nethisinghe

580 total citations
15 papers, 295 citations indexed

About

Suran Nethisinghe is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Neurology. According to data from OpenAlex, Suran Nethisinghe has authored 15 papers receiving a total of 295 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Cellular and Molecular Neuroscience, 14 papers in Molecular Biology and 5 papers in Neurology. Recurrent topics in Suran Nethisinghe's work include Genetic Neurodegenerative Diseases (15 papers), Mitochondrial Function and Pathology (9 papers) and Muscle Physiology and Disorders (4 papers). Suran Nethisinghe is often cited by papers focused on Genetic Neurodegenerative Diseases (15 papers), Mitochondrial Function and Pathology (9 papers) and Muscle Physiology and Disorders (4 papers). Suran Nethisinghe collaborates with scholars based in United Kingdom, Italy and Netherlands. Suran Nethisinghe's co-authors include Paola Giunti, J. Paul Chapple, Lisa E. L. Romano, Teisha Y. Bradshaw, Sally Pemble, Mary G. Sweeney, Nicholas Wood, Mary B. Davis, Rosella Abeti and Sascha Vermeer and has published in prestigious journals such as Nature Medicine, Brain and International Journal of Molecular Sciences.

In The Last Decade

Suran Nethisinghe

15 papers receiving 293 citations

Peers

Suran Nethisinghe

CMN

NEURO

Álex Pérez United States

Lauren M. Watson United Kingdom

Ruxu Zhang China

Ayami Nakanishi Japan

Niklas Schwarz Germany

Miren Zulaica Spain

Sriram Jayabal Canada

Margaret Maronski United States

Xavier Sánchez‐Sáez Spain

Lauren R. Moore United States

Álex Pérez United States

Suran Nethisinghe

165 ×0.7

99 ×0.5

CMN

50 ×0.8

NEURO

18 ×0.5

NEURO

50 ×1.8

Citations per year, relative to Suran Nethisinghe Suran Nethisinghe (= 1×) peers Álex Pérez

Countries citing papers authored by Suran Nethisinghe

Since Specialization

Citations

This map shows the geographic impact of Suran Nethisinghe'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 Suran Nethisinghe with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Suran Nethisinghe more than expected).

Fields of papers citing papers by Suran Nethisinghe

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Suran Nethisinghe. 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 Suran Nethisinghe. The network helps show where Suran Nethisinghe may publish in the future.

Co-authorship network of co-authors of Suran Nethisinghe

This figure shows the co-authorship network connecting the top 25 collaborators of Suran Nethisinghe. A scholar is included among the top collaborators of Suran Nethisinghe 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 Suran Nethisinghe. Suran Nethisinghe is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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15 of 15 papers shown

Scarabino, Daniela, Liana Veneziano, Suran Nethisinghe, et al.. (2024). Unusual Age‐Dependent Behavior of Leukocytes Telomere Length in Friedreich's Ataxia. Movement Disorders. 39(11). 2058–2066. 2 indexed citations

Nethisinghe, Suran, Valeria Ricotti, Thomas Voit, et al.. (2023). A wearable motion capture suit and machine learning predict disease progression in Friedreich’s ataxia. Nature Medicine. 29(1). 86–94. 36 indexed citations

Scarabino, Daniela, Liana Veneziano, Alessia Fiore, et al.. (2022). Leukocyte Telomere Length Variability as a Potential Biomarker in Patients with PolyQ Diseases. Antioxidants. 11(8). 1436–1436. 4 indexed citations

Romano, Lisa E. L., Wen Yih Aw, T. V. Novoselova, et al.. (2022). Multi-omic profiling reveals the ataxia protein sacsin is required for integrin trafficking and synaptic organization. Cell Reports. 41(5). 111580–111580. 8 indexed citations

Nethisinghe, Suran, Robyn Labrum, James M. Polke, et al.. (2021). Interruptions of the FXN GAA Repeat Tract Delay the Age at Onset of Friedreich’s Ataxia in a Location Dependent Manner. International Journal of Molecular Sciences. 22(14). 7507–7507. 12 indexed citations

Nethisinghe, Suran, et al.. (2021). Hsp90 Inhibition: A Promising Therapeutic Approach for ARSACS. International Journal of Molecular Sciences. 22(21). 11722–11722. 3 indexed citations

Nethisinghe, Suran, Sally Pemble, Mary G. Sweeney, et al.. (2018). PolyQ Tract Toxicity in SCA1 is Length Dependent in the Absence of CAG Repeat Interruption. Frontiers in Cellular Neuroscience. 12. 200–200. 16 indexed citations

Cagnoli, Claudia, Alessandro Brussino, Cecilia Mancini, et al.. (2018). Spinocerebellar Ataxia Tethering PCR. Journal of Molecular Diagnostics. 20(3). 289–297. 15 indexed citations

Parkinson, Michael, Lisa M. Clayton, Suran Nethisinghe, et al.. (2018). Optical coherence tomography in autosomal recessive spastic ataxia of Charlevoix-Saguenay. Brain. 141(4). 989–999. 38 indexed citations

10.

Larivière, Roxanne, Teisha Y. Bradshaw, Nicolas Sgarioto, et al.. (2017). Altered organization of the intermediate filament cytoskeleton and relocalization of proteostasis modulators in cells lacking the ataxia protein sacsin. Human Molecular Genetics. 26(16). 3130–3143. 45 indexed citations

11.

Bradshaw, Teisha Y., Lisa E. L. Romano, Suran Nethisinghe, et al.. (2016). A reduction in Drp1-mediated fission compromises mitochondrial health in autosomal recessive spastic ataxia of Charlevoix Saguenay. Human Molecular Genetics. 25(15). 3232–3244. 45 indexed citations

12.

Menon, Rajesh P., Suran Nethisinghe, Serena Faggiano, et al.. (2013). The Role of Interruptions in polyQ in the Pathology of SCA1. PLoS Genetics. 9(7). e1003648–e1003648. 55 indexed citations

13.

Fratta, Pietro, Toby Collins, Sally Pemble, et al.. (2013). Sequencing analysis of the spinal bulbar muscular atrophy CAG expansion reveals absence of repeat interruptions. Neurobiology of Aging. 35(2). 443.e1–443.e3. 11 indexed citations

14.

Giunti, Paola, Suran Nethisinghe, Lisa M. Clayton, et al.. (2012). 002 Detecting retinal changes in autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) using optical coherence tomography (OCT). Journal of Neurology Neurosurgery & Psychiatry. 83(3). e1.163–e1. 1 indexed citations

15.

Nethisinghe, Suran, Lisa M. Clayton, Sascha Vermeer, et al.. (2011). Retinal Imaging in Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay. Neuro-Ophthalmology. 35(4). 197–201. 4 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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