Katrina Reardon

1.9k total citations
37 papers, 1.2k citations indexed

About

Katrina Reardon is a scholar working on Neurology, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Katrina Reardon has authored 37 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Neurology, 12 papers in Molecular Biology and 6 papers in Cognitive Neuroscience. Recurrent topics in Katrina Reardon's work include Parkinson's Disease Mechanisms and Treatments (8 papers), Neurological disorders and treatments (8 papers) and Muscle Physiology and Disorders (6 papers). Katrina Reardon is often cited by papers focused on Parkinson's Disease Mechanisms and Treatments (8 papers), Neurological disorders and treatments (8 papers) and Muscle Physiology and Disorders (6 papers). Katrina Reardon collaborates with scholars based in Australia, United States and United Kingdom. Katrina Reardon's co-authors include Edward Byrne, Peter Choong, Peter Kempster, Robert M. I. Kapsa, Malcolm Horne, Siew Yeen Chai, Xenia Dennett, Mary P. Galea, Benjamin Clissold and Justin O’Day and has published in prestigious journals such as Neurology, Brain Research and European Heart Journal.

In The Last Decade

Katrina Reardon

37 papers receiving 1.1k citations

Peers

Katrina Reardon

NEURO

CCM

PHYSI

CMN

Amilton Antunes Barreira Brazil

Wim H.J.P. Linssen Netherlands

Fabrizio Rinaldi Italy

Kiyoharu Inoue Japan

Dominic G. O’Donovan United Kingdom

Margaret Burnett Canada

Philip Jardine United Kingdom

Sabrina W. Yum United States

Genjiro Hirose Japan

Antonella Pini Italy

Amilton Antunes Barreira Brazil

Katrina Reardon

481 ×1.1

512 ×1.4

NEURO

171 ×0.9

CCM

186 ×1.0

PHYSI

339 ×2.0

CMN

Citations per year, relative to Katrina Reardon Katrina Reardon (= 1×) peers Amilton Antunes Barreira

Countries citing papers authored by Katrina Reardon

Since Specialization

Citations

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

Fields of papers citing papers by Katrina Reardon

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Katrina Reardon

This figure shows the co-authorship network connecting the top 25 collaborators of Katrina Reardon. A scholar is included among the top collaborators of Katrina Reardon 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 Katrina Reardon. Katrina Reardon 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

Ross, Laura, et al.. (2023). Muscle biopsy practices in the evaluation of neuromuscular disease: A systematic literature review. Neuropathology and Applied Neurobiology. 49(1). e12888–e12888. 8 indexed citations

Halliday, Amy J., et al.. (2022). 2373 Anti-LGI1 associated myopathy in setting of neuromuscular hyperexcitability syndrome. Abstracts. A48.3–A49. 1 indexed citations

Yeh, Wei Zhen, Penny McKelvie, Steven Collins, et al.. (2020). Lymphoma, a great imitator in neurology. Journal of Clinical Neuroscience. 73. 308–310. 2 indexed citations

Ding, Catherine, Jane Alty, Benjamin Clissold, et al.. (2018). Inferring the long duration response to levodopa in Parkinson’s disease. Parkinsonism & Related Disorders. 60. 133–137. 10 indexed citations

Andrews, Sophie C., et al.. (2017). Multimodal emotion processing deficits are present in amyotrophic lateral sclerosis.. Neuropsychology. 31(3). 304–310. 14 indexed citations

McKelvie, Penelope, Katrina Reardon, Katherine Bond, et al.. (2013). A further patient with parasitic myositis due to Haycocknema perplexum, a rare entity. Journal of Clinical Neuroscience. 20(7). 1019–1022. 12 indexed citations

Lindell, Annukka K., et al.. (2013). Exploring sarcasm detection in amyotrophic lateral sclerosis using ecologically valid measures. Frontiers in Human Neuroscience. 7. 178–178. 33 indexed citations

Alty, Jane, et al.. (2009). Longitudinal study of the levodopa motor response in Parkinson's disease: Relationship between cognitive decline and motor function. Movement Disorders. 24(16). 2337–2343. 11 indexed citations

Marotta, Rosetta, et al.. (2009). Association of the MELAS m.3243A>G mutation with myositis and the superiority of urine over muscle, blood and hair for mutation detection. Journal of Clinical Neuroscience. 16(9). 1223–1225. 13 indexed citations

10.

Villemagne, Victor L., Catriona McLean, Katrina Reardon, et al.. (2009). 11C-PiB PET studies in typical sporadic Creutzfeldt-Jakob disease. Journal of Neurology Neurosurgery & Psychiatry. 80(9). 998–1001. 50 indexed citations

11.

Clissold, Benjamin, et al.. (2006). Longitudinal study of the motor response to levodopa in Parkinson's disease. Movement Disorders. 21(12). 2116–2121. 48 indexed citations

12.

Paine, Mark, et al.. (2003). Immunotherapy of Ocular Myasthenia Gravis Reduces Conversion to Generalized Myasthenia Gravis. Journal of Neuro-Ophthalmology. 23(4). 251–255. 74 indexed citations

13.

Reardon, Katrina, et al.. (2002). Motor response to levodopa and the evolution of motor fluctuations in the first decade of treatment of Parkinson's disease. Movement Disorders. 17(6). 1227–1234. 56 indexed citations

14.

Quigley, Anita, et al.. (2001). A Novel Clinical Phenotype of Myopathy, Sensorimotor Neuropathy, Infertility, and Hypogonadism With Multiple Mitochondrial DNA Deletions. Journal of Clinical Neuromuscular Disease. 3(2). 77–82. 6 indexed citations

15.

Kilpatrick, Trevor J., et al.. (2001). Leukaemia inhibitory factor abrogates Paclitaxel-induced axonal atrophy in the Wistar rat. Brain Research. 911(2). 163–167. 19 indexed citations

16.

Reardon, Katrina, Robert M. I. Kapsa, Andrew J. Kornberg, et al.. (2000). Increased levels of leukemia inhibitory factor mRNA in muscular dystrophy and human muscle trauma. Muscle & Nerve. 23(6). 962–966. 11 indexed citations

17.

Reardon, Katrina, et al.. (2000). The angiotensin converting enzyme (ACE) inhibitor, perindopril, modifies the clinical features of Parkinson's disease. Australian and New Zealand Journal of Medicine. 30(1). 48–53. 92 indexed citations

18.

Reardon, Katrina, et al.. (1999). Evolution of motor fluctuations in Parkinson's disease: A longitudinal study over 6 years. Movement Disorders. 14(4). 605–611. 38 indexed citations

19.

Reardon, Katrina, et al.. (1999). How long should a routine EEG be?. Journal of Clinical Neuroscience. 6(6). 492–493. 11 indexed citations

20.

Goldman, Jonathan H., Krishna Prasad, Patrick J. Keeling, et al.. (1996). QT dispersion and RR variations on 12-lead ECGs in patients with congestive heart failure secondary to idiopathic dilated cardiomyopathy. European Heart Journal. 17(2). 258–263. 77 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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