Rajith de Silva

1.5k total citations
29 papers, 687 citations indexed

About

Rajith de Silva is a scholar working on Neurology, Molecular Biology and Neurology. According to data from OpenAlex, Rajith de Silva has authored 29 papers receiving a total of 687 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Neurology, 11 papers in Molecular Biology and 9 papers in Neurology. Recurrent topics in Rajith de Silva's work include Neurological diseases and metabolism (8 papers), Prion Diseases and Protein Misfolding (6 papers) and Mitochondrial Function and Pathology (4 papers). Rajith de Silva is often cited by papers focused on Neurological diseases and metabolism (8 papers), Prion Diseases and Protein Misfolding (6 papers) and Mitochondrial Function and Pathology (4 papers). Rajith de Silva collaborates with scholars based in United Kingdom, United States and France. Rajith de Silva's co-authors include Hani T. S. Benamer, Robert Will, Thomas Esmonde, Julie Greenfield, Otto Windl, Richard Lathe, Paola Giunti, Maureen Dempster, Julie Vallortigara and Anthea Springbett and has published in prestigious journals such as The Lancet, Journal of Clinical Epidemiology and Movement Disorders.

In The Last Decade

Rajith de Silva

28 papers receiving 672 citations

Peers

Rajith de Silva

NEURO

CMN

Jessica Shaw United States

Mar O’Callaghan Spain

Inês Carrilho Portugal

Anna Krasnianski Germany

Maria Teresa Dotti Italy

Janina Gburek‐Augustat Germany

Dan Z. Milikovsky Israel

Inês Marques-Morgado Portugal

Pierre Labauge France

R. Kálmánchey Hungary

Jessica Shaw United States

Rajith de Silva

257 ×0.5

175 ×0.9

NEURO

39 ×0.2

NEURO

234 ×1.8

CMN

9 ×0.1

Citations per year, relative to Rajith de Silva Rajith de Silva (= 1×) peers Jessica Shaw

Countries citing papers authored by Rajith de Silva

Since Specialization

Citations

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

Fields of papers citing papers by Rajith de Silva

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Rajith de Silva. 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 Rajith de Silva. The network helps show where Rajith de Silva may publish in the future.

Co-authorship network of co-authors of Rajith de Silva

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

All Works

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20 of 20 papers shown

Silva, Rajith de, et al.. (2024). A Systematic Review of the Spectrum and Prevalence of Non-motor Symptoms in Multiple System Atrophy. The Cerebellum. 23(4). 1642–1650. 1 indexed citations

Cauldwell, Matthew, Pooja Dassan, Dominic Paviour, et al.. (2021). Maternal and fetal outcomes in women with cerebrovascular malformations in pregnancy: A multicentre retrospective cohort study. BJOG An International Journal of Obstetrics & Gynaecology. 129(7). 1151–1157. 1 indexed citations

Silva, Rajith de, et al.. (2019). Guidelines on the diagnosis and management of the progressive ataxias. Orphanet Journal of Rare Diseases. 14(1). 51–51. 49 indexed citations

Silva, Rajith de, et al.. (2019). Diagnosis and management of progressive ataxia in adults. Practical Neurology. 19(3). 196–207. 55 indexed citations

Appleton, Jason P., Andreea Ilinca, Arne Lindgren, et al.. (2015). Improving the likelihood of neurology patients being examined using patient feedback. BMJ Quality Improvement Reports. 4(1). u209610.w4063–u209610.w4063. 2 indexed citations

Clark, Camilla N., Laura Downey, Hannah L. Golden, et al.. (2014). “The Mind Is Its Own Place”: Amelioration of Claustrophobia in Semantic Dementia. Behavioural Neurology. 2014. 1–5. 3 indexed citations

Παπαθανασίου, Αθανάσιος, et al.. (2014). Reversible cerebral vasoconstriction syndrome as a cause of thunderclap headache: a retrospective case series study. The American Journal of Emergency Medicine. 33(6). 859.e3–859.e6. 3 indexed citations

Benamer, Hani T. S. & Rajith de Silva. (2010). <i>LRRK2</i> G2019S in the North African Population: A Review. European Neurology. 63(6). 321–325. 45 indexed citations

Kartsounis, L. D. & Rajith de Silva. (2010). Unusual amnesia in a patient with VGKC-Ab limbic encephalitis: A case study. Cortex. 47(4). 451–459. 14 indexed citations

10.

Benamer, Hani T. S., et al.. (2008). Parkinson's disease in Arabs: A systematic review. Movement Disorders. 23(9). 1205–1210. 30 indexed citations

11.

Harrower, Timothy, Joanna D. Stewart, Gavin Hudson, et al.. (2008). POLG1 Mutations Manifesting as Autosomal Recessive Axonal Charcot-Marie-Tooth Disease. Archives of Neurology. 65(1). 133–6. 33 indexed citations

12.

Silva, Rajith de, et al.. (2007). De Clerambault’s Syndrome (Erotomania) As a Presenting Feature of Fronto‐Temporal Dementia and Motor Neurone Disease (FTD‐MND). Behavioural Neurology. 18(3). 193–195. 14 indexed citations

13.

Blakely, Emma L., et al.. (2005). LHON/MELAS overlap syndrome associated with a mitochondrial MTND1 gene mutation. European Journal of Human Genetics. 13(5). 623–627. 79 indexed citations

14.

Silva, Rajith de. (2002). Neuroanatomical Basis of Clinical Neurology. Journal of the Royal Society of Medicine. 95(6). 321–322. 1 indexed citations

15.

Lange, Robert P.J. de, et al.. (2000). Detection of complement factor B in the cerebrospinal fluid of patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy disease using two-dimensional gel electrophoresis and mass spectrometry. Neuroscience Letters. 282(3). 149–152. 20 indexed citations

16.

Windl, Otto, Maureen Dempster, J. Peter Estibeiro, et al.. (1996). Genetic basis of Creutzfeldt-Jakob disease in the United Kingdom: a systematic analysis of predisposing mutations and allelic variation in the PRNP gene. Human Genetics. 98(3). 259–264. 164 indexed citations

17.

Silva, Rajith de, Alain Créange, M Parant, et al.. (1996). Pooled plasma derivatives and Creutzfeldt-Jakob disease. The Lancet. 347(9006). 967–967. 4 indexed citations

18.

Pickering‐Brown, Stuart, David Mann, F. Owen, et al.. (1995). Allelic variations in apolipoprotein E and prion protein genotype related to plaque formation and age of onset in sporadic Creutzfeldt-Jakob disease. Neuroscience Letters. 187(2). 127–129. 23 indexed citations

19.

Silva, Rajith de, James W. Ironside, Linda McCardle, et al.. (1994). Neuropathological phenotype and ‘prion protein’ genotype correlation in sporadic Creutzfeldt-Jakob disease. Neuroscience Letters. 179(1-2). 50–52. 28 indexed citations

20.

Angus, Brian, Rajith de Silva, Rosemarie Davidson, & I Bone. (1994). A family with adult-onset cerebral adrenoleucodystrophy. Journal of Neurology. 241(8). 497–499. 11 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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