Tom Webb

2.4k total citations
32 papers, 888 citations indexed

About

Tom Webb is a scholar working on Molecular Biology, Surgery and Anesthesiology and Pain Medicine. According to data from OpenAlex, Tom Webb has authored 32 papers receiving a total of 888 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 9 papers in Surgery and 7 papers in Anesthesiology and Pain Medicine. Recurrent topics in Tom Webb's work include Prion Diseases and Protein Misfolding (10 papers), Nausea and vomiting management (8 papers) and Anesthesia and Pain Management (8 papers). Tom Webb is often cited by papers focused on Prion Diseases and Protein Misfolding (10 papers), Nausea and vomiting management (8 papers) and Anesthesia and Pain Management (8 papers). Tom Webb collaborates with scholars based in United Kingdom, United States and Australia. Tom Webb's co-authors include Jun Tang, Ronald H. Wender, Paul F. White, Alexander Sloninsky, Robert Kariger, Robert Naruse, John Collinge, Simon Mead, Peter Rudge and Manxu Zhao and has published in prestigious journals such as Brain, Neurology and The Lancet Neurology.

In The Last Decade

Tom Webb

27 papers receiving 849 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Tom Webb United Kingdom 12 361 286 276 206 131 32 888
Per Nellgård Sweden 15 147 0.4× 52 0.2× 176 0.6× 31 0.2× 35 0.3× 22 670
Atsushi Kohjitani Japan 16 110 0.3× 285 1.0× 246 0.9× 12 0.1× 102 0.8× 52 747
Chingmuh Lee United States 17 184 0.5× 447 1.6× 235 0.9× 10 0.0× 117 0.9× 55 818
Xinning Mi China 13 114 0.3× 37 0.1× 30 0.1× 137 0.7× 43 0.3× 29 579
Thorsten Okulla Germany 6 137 0.4× 37 0.1× 24 0.1× 347 1.7× 15 0.1× 8 780
Yohei Fujimoto Japan 14 84 0.2× 98 0.3× 238 0.9× 72 0.3× 123 0.9× 35 625
James T Houston United States 11 95 0.3× 229 0.8× 124 0.4× 31 0.2× 51 0.4× 28 519
Matthias Paul Germany 14 113 0.3× 286 1.0× 250 0.9× 5 0.0× 138 1.1× 20 629
E Vincenti Italy 12 147 0.4× 116 0.4× 61 0.2× 7 0.0× 30 0.2× 44 539

Countries citing papers authored by Tom Webb

Since Specialization
Citations

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

Fields of papers citing papers by Tom Webb

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tom Webb

This figure shows the co-authorship network connecting the top 25 collaborators of Tom Webb. A scholar is included among the top collaborators of Tom Webb 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 Tom Webb. Tom Webb 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.
Huang, Wei‐Lieh, et al.. (2025). The Impact of Anhedonia on the Disease Burden of Major Depressive Disorder in the Asia–Pacific Region: A Cross‐Sectional Real‐World Study. Neuropsychopharmacology Reports. 45(1). e70007–e70007. 1 indexed citations
2.
Saga, Yosuke, et al.. (2025). Humanistic burden and medical care patterns of real-world patients with myasthenia gravis in Japan. Frontiers in Neurology. 16. 1673297–1673297.
4.
Webb, Tom, et al.. (2019). Reversible cerebral vasoconstriction syndrome after sudden caffeine withdrawal. British Journal of Hospital Medicine. 80(12). 730–731. 2 indexed citations
5.
Ceccarelli, Daniela, David Hargroves, Ibrahim Balogun, & Tom Webb. (2017). Hypertensive encephalopathy mimicking cerebral vasculitis with pontine oedema, cerebellar white matter lesions and multiple cerebral infarctions. BMJ Case Reports. 2017. bcr–2016.
6.
Carswell, Christopher, Suvankar Pal, Rebecca Macfarlane, et al.. (2012). Video Rating in Neurodegenerative Disease Clinical Trials: The Experience of PRION-1. Dementia and Geriatric Cognitive Disorders Extra. 2(1). 286–297. 5 indexed citations
7.
Hyare, Harpreet, Simon Mead, Peter Rudge, et al.. (2011). Distinct neuropsychological profiles correspond to distribution of cortical thinning in inherited prion disease caused by insertional mutation. Journal of Neurology Neurosurgery & Psychiatry. 83(1). 109–114. 11 indexed citations
8.
White, Paul F., Jun Tang, Ronald H. Wender, et al.. (2010). The Effects of Oral Ibuprofen and Celecoxib in Preventing Pain, Improving Recovery Outcomes and Patient Satisfaction After Ambulatory Surgery. Anesthesia & Analgesia. 112(2). 323–329. 44 indexed citations
9.
Hyare, Harpreet, S. Wroe, Tom Webb, et al.. (2010). Magnetization transfer ratio may be a surrogate of spongiform change in human prion diseases. Brain. 133(10). 3058–3068. 6 indexed citations
10.
White, Paul F., Jun Tang, Ronald H. Wender, et al.. (2009). Desflurane Versus Sevoflurane for Maintenance of Outpatient Anesthesia: The Effect on Early Versus Late Recovery and Perioperative Coughing. Anesthesia & Analgesia. 109(2). 387–393. 91 indexed citations
11.
Collinge, John, Michele Gorham, Fleur Hudson, et al.. (2009). Safety and efficacy of quinacrine in human prion disease (PRION-1 study): a patient-preference trial. The Lancet Neurology. 8(4). 334–344. 184 indexed citations
12.
Isaacs, Adrian M., Caroline Powell, Tom Webb, et al.. (2008). Lack of TAR‐DNA binding protein‐43 (TDP‐43) pathology in human prion diseases. Neuropathology and Applied Neurobiology. 34(4). 446–456. 22 indexed citations
13.
Webb, Tom, John C. Whittaker, John Collinge, & Simon Mead. (2008). Age of onset and death in inherited prion disease are heritable. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 150B(4). 496–501. 9 indexed citations
14.
Mead, Simon, Mark Poulter, James Uphill, et al.. (2008). Genetic risk factors for variant Creutzfeldt–Jakob disease: a genome-wide association study. The Lancet Neurology. 8(1). 57–66. 105 indexed citations
15.
White, Paul F., Jun Tang, Dajun Song, et al.. (2006). Transdermal Scopolamine: An Alternative to Ondansetron and Droperidol for the Prevention of Postoperative and Postdischarge Emetic Symptoms. Anesthesia & Analgesia. 104(1). 92–96. 44 indexed citations
16.
Tang, Jun, Xiaoguang Chen, Paul F. White, et al.. (2003). Antiemetic Prophylaxis for Office-based Surgery. Anesthesiology. 98(2). 293–298. 24 indexed citations
17.
Tang, Jun, Shitong Li, Paul F. White, et al.. (2002). Effect of Parecoxib, A Novel Intravenous Cyclooxygenase Type-2 Inhibitor, on the Postoperative Opioid Requirement and Quality of Pain Control. Anesthesiology. 96(6). 1305–1309. 95 indexed citations
18.
Chen, Xiao‐Guang, Jun Tang, Paul F. White, et al.. (2001). The Effect of Timing of Dolasetron Administration on its Efficacy as a Prophylactic Antiemetic in the Ambulatory Setting. Anesthesia & Analgesia. 93(4). 906–911. 19 indexed citations
19.
Chen, Xiao‐Guang, Manxu Zhao, Paul F. White, et al.. (2001). The Recovery of Cognitive Function After General Anesthesia in Elderly Patients: A Comparison of Desflurane and Sevoflurane. Anesthesia & Analgesia. 93(6). 1489–1494. 117 indexed citations
20.
Zhou, Tian, Margarita Coloma, Paul F. White, et al.. (2000). Spontaneous Recovery Profile of Rapacuronium During Desflurane, Sevoflurane, or Propofol Anesthesia for Outpatient Laparoscopy. Anesthesia & Analgesia. 91(3). 596–600. 7 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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