Christopher Troedson

1.2k total citations
29 papers, 524 citations indexed

About

Christopher Troedson is a scholar working on Molecular Biology, Epidemiology and Neurology. According to data from OpenAlex, Christopher Troedson has authored 29 papers receiving a total of 524 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 8 papers in Epidemiology and 6 papers in Neurology. Recurrent topics in Christopher Troedson's work include Acute Ischemic Stroke Management (5 papers), Mitochondrial Function and Pathology (4 papers) and Genetic Neurodegenerative Diseases (4 papers). Christopher Troedson is often cited by papers focused on Acute Ischemic Stroke Management (5 papers), Mitochondrial Function and Pathology (4 papers) and Genetic Neurodegenerative Diseases (4 papers). Christopher Troedson collaborates with scholars based in Australia, France and United Kingdom. Christopher Troedson's co-authors include Russell C. Dale, Richard Webster, Deepak Gill, Manoj P. Menezes, Sachin Gupta, Meredith Wilson, Sekhar Pillai, Robert Ouvrier, Harry Singh and Kasia Kozlowska and has published in prestigious journals such as SHILAP Revista de lepidopterología, American Journal of Neuroradiology and Developmental Medicine & Child Neurology.

In The Last Decade

Christopher Troedson

28 papers receiving 514 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Christopher Troedson Australia 13 147 136 125 97 96 29 524
Gabriel Chow United Kingdom 12 261 1.8× 131 1.0× 93 0.7× 40 0.4× 98 1.0× 34 650
Faruk İncecik Türkiye 14 89 0.6× 149 1.1× 69 0.6× 184 1.9× 21 0.2× 86 587
Madoka Kajimoto Japan 12 70 0.5× 130 1.0× 121 1.0× 96 1.0× 40 0.4× 24 491
Rahul Singh United Kingdom 9 98 0.7× 81 0.6× 33 0.3× 46 0.5× 55 0.6× 15 265
James B Lilleker United Kingdom 20 281 1.9× 292 2.1× 656 5.2× 72 0.7× 106 1.1× 77 1.1k
Harold Moses United States 12 79 0.5× 176 1.3× 85 0.7× 45 0.5× 18 0.2× 19 492
Michael Karenfort Germany 13 86 0.6× 430 3.2× 36 0.3× 132 1.4× 15 0.2× 32 828
Nobuko Yamashita Japan 14 100 0.7× 174 1.3× 120 1.0× 16 0.2× 25 0.3× 34 599
David Callen Canada 8 56 0.4× 290 2.1× 34 0.3× 36 0.4× 35 0.4× 13 541
Lokesh Lingappa India 10 132 0.9× 65 0.5× 46 0.4× 43 0.4× 17 0.2× 44 366

Countries citing papers authored by Christopher Troedson

Since Specialization
Citations

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

Fields of papers citing papers by Christopher Troedson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Christopher Troedson

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

All Works

20 of 20 papers shown
1.
Bhatia, Kartik, Nomazulu Dlamini, Sachin Gupta, et al.. (2024). Relationship Between Baseline Infarct and Clinical Outcome in Pediatric Large‐Vessel Occlusion Ischemic Stroke. SHILAP Revista de lepidopterología. 4(5). e001357–e001357.
2.
Bhatia, Kartik, Sachin Gupta, Richard Webster, et al.. (2024). Mechanical Thrombectomy for Pediatric Arterial Ischemic Stroke from Acute M2 Occlusion. American Journal of Neuroradiology. 45(5). 588–591. 1 indexed citations
3.
Bhatia, Kartik, Robert Goetti, Richard Webster, et al.. (2023). Association Between Thrombectomy and Functional Outcomes in Pediatric Patients With Acute Ischemic Stroke From Large Vessel Occlusion. JAMA Neurology. 80(9). 910–910. 17 indexed citations
4.
Dale, Russell C., Terrence Thomas, Shrujna Patel, et al.. (2023). CSF neopterin and quinolinic acid are biomarkers of neuroinflammation and neurotoxicity in FIRES and other infection‐triggered encephalopathy syndromes. Annals of Clinical and Translational Neurology. 10(8). 1417–1432. 13 indexed citations
5.
D’Souza, Stephanie, Elizabeth H Barnes, Sachin Gupta, et al.. (2022). Predictors of longitudinal seizure outcomes after epilepsy surgery in childhood. Epilepsy & Behavior Reports. 19. 100561–100561. 5 indexed citations
6.
Bhatia, Kartik, Robert Goetti, Richard Webster, et al.. (2022). Incidence and Natural History of Pediatric Large Vessel Occlusion Stroke. JAMA Neurology. 79(5). 488–488. 24 indexed citations
7.
Jones, Hannah, Gladys Ho, Velda X. Han, et al.. (2021). Autosomal dominant ADAR c.3019G>A (p.(G1007R)) variant is an important mimic of hereditary spastic paraplegia and cerebral palsy. Brain and Development. 44(2). 153–160. 7 indexed citations
8.
Peters, Greg B., Simone Ardern‐Holmes, Richard Webster, et al.. (2019). Yield of comparative genomic hybridization microarray in pediatric neurology practice. Neurology Genetics. 5(6). e367–e367. 3 indexed citations
9.
Kothur, Kavitha, Katherine Holman, Elizabeth Farnsworth, et al.. (2018). Diagnostic yield of targeted massively parallel sequencing in children with epileptic encephalopathy. Seizure. 59. 132–140. 55 indexed citations
10.
Medley, Tanya L., Tyson L. Ware, Michael Cheung, et al.. (2018). Australian Clinical Consensus Guideline: The diagnosis and acute management of childhood stroke. International Journal of Stroke. 14(1). 94–106. 61 indexed citations
11.
Sevin, Caroline, Christine í Dali, Roberto Giugliani, et al.. (2017). Intrathecal delivery of recombinant human arylsulfatase A in children with late-infantile metachromatic leukodystrophy: an update following extended treatment. Molecular Genetics and Metabolism. 120(1-2). S121–S121. 4 indexed citations
12.
Tantsis, Esther, Deepak Gill, Lyn R. Griffiths, et al.. (2016). Eye movement disorders are an early manifestation of CACNA1A mutations in children. 2 indexed citations
13.
Tantsis, Esther, Deepak Gill, Lyn R. Griffiths, et al.. (2016). Eye movement disorders are an early manifestation of CACNA1A mutations in children. Developmental Medicine & Child Neurology. 58(6). 639–644. 51 indexed citations
14.
Grigg, John, et al.. (2015). A negative waveform in the scotopic response in a patient with phosphoglycerate kinase deficiency: a visual electrophysiology report. Documenta Ophthalmologica. 131(3). 215–220. 1 indexed citations
15.
Britton, Philip N, Christopher Troedson, Richard Webster, et al.. (2015). Mild encephalopathy with reversible splenial lesion: An important differential of encephalitis. European Journal of Paediatric Neurology. 19(3). 377–382. 66 indexed citations
16.
Troedson, Christopher, Melanie Wong, Meredith Wilson, et al.. (2013). Systemic lupus erythematosus due to C1q deficiency with progressive encephalopathy, intracranial calcification and acquired moyamoya cerebral vasculopathy. Lupus. 22(6). 639–643. 31 indexed citations
17.
Kesson, Alison, et al.. (2012). Echovirus 19 associated with a case of acute flaccid paralysis. Journal of Paediatrics and Child Health. 49(3). E239–42. 5 indexed citations
18.
Suleiman, Jehan, Tanja Brenner, Deepak Gill, et al.. (2011). Immune-mediated steroid-responsive epileptic spasms and epileptic encephalopathy associated with VGKC-complex antibodies. Developmental Medicine & Child Neurology. 53(11). 1058–1060. 32 indexed citations
19.
Compton, Alison G., Christopher Troedson, Meredith Wilson, et al.. (2010). Application of oligonucleotide array CGH in the detection of a large intragenic deletion in POLG associated with Alpers Syndrome. Mitochondrion. 11(1). 104–107. 11 indexed citations
20.
Dale, Russell C., et al.. (2010). A prospective study of acute movement disorders in children. Developmental Medicine & Child Neurology. 52(8). 739–748. 44 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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