Richard Rees

1.3k total citations
26 papers, 970 citations indexed

About

Richard Rees is a scholar working on Nature and Landscape Conservation, Cellular and Molecular Neuroscience and Physiology. According to data from OpenAlex, Richard Rees has authored 26 papers receiving a total of 970 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Nature and Landscape Conservation, 8 papers in Cellular and Molecular Neuroscience and 6 papers in Physiology. Recurrent topics in Richard Rees's work include Ichthyology and Marine Biology (9 papers), Neuropeptides and Animal Physiology (7 papers) and Pain Mechanisms and Treatments (6 papers). Richard Rees is often cited by papers focused on Ichthyology and Marine Biology (9 papers), Neuropeptides and Animal Physiology (7 papers) and Pain Mechanisms and Treatments (6 papers). Richard Rees collaborates with scholars based in United Kingdom, Maldives and Finland. Richard Rees's co-authors include Mika Hukkanen, Stafford L. Lightman, Michael S. Harbuz, Seppo Santavirta, D. A. Brewerton, D.J.A. Eckland, D. S. Jessop, Satyabrata Kar, S. J. Gibson and Yrjö T. Konttinen and has published in prestigious journals such as Scientific Reports, Endocrinology and CHEST Journal.

In The Last Decade

Richard Rees

25 papers receiving 944 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Richard Rees United Kingdom 17 325 294 194 143 125 26 970
Robert M. Santer United Kingdom 17 331 1.0× 267 0.9× 32 0.2× 186 1.3× 85 0.7× 38 899
Johan Ruud Sweden 14 82 0.3× 440 1.5× 76 0.4× 338 2.4× 60 0.5× 21 1.4k
Mardi S. Byerly United States 18 162 0.5× 466 1.6× 16 0.1× 347 2.4× 83 0.7× 25 1.3k
B. J. Gannon Australia 23 303 0.9× 213 0.7× 19 0.1× 311 2.2× 50 0.4× 47 1.3k
Satoshi Hane United States 18 53 0.2× 151 0.5× 89 0.5× 235 1.6× 75 0.6× 26 1.2k
Graham C. Parker United States 20 138 0.4× 125 0.4× 20 0.1× 385 2.7× 29 0.2× 65 1.2k
Ji-Zeng Du China 20 63 0.2× 170 0.6× 216 1.1× 239 1.7× 88 0.7× 52 1.1k
Takeo Machida Japan 15 132 0.4× 64 0.2× 52 0.3× 231 1.6× 17 0.1× 46 624
Bettina Müller Germany 17 235 0.7× 58 0.2× 27 0.1× 244 1.7× 22 0.2× 47 738
Sara R. Chiocchio Argentina 20 290 0.9× 133 0.5× 130 0.7× 206 1.4× 8 0.1× 43 1.2k

Countries citing papers authored by Richard Rees

Since Specialization
Citations

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

Fields of papers citing papers by Richard Rees

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Richard Rees

This figure shows the co-authorship network connecting the top 25 collaborators of Richard Rees. A scholar is included among the top collaborators of Richard Rees 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 Richard Rees. Richard Rees 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.
Stewart, Joshua D., et al.. (2021). The impact of injury on apparent survival of whale sharks (Rhincodon typus) in South Ari Atoll Marine Protected Area, Maldives. Scientific Reports. 11(1). 937–937. 17 indexed citations
2.
Lanfredi, Caterina, Arianna Azzellino, Alessandra Savini, et al.. (2021). Analysis of the temporal and spatial variability of whale shark (Rhincodon typus) aggregation in the South Ari Marine Protected Area, Maldives, Indian Ocean. The European Zoological Journal. 88(1). 684–697. 4 indexed citations
3.
Stewart, Bryce D., et al.. (2021). Anthropogenic injury and site fidelity in Maldivian whale sharks (Rhincodon typus). Aquatic Conservation Marine and Freshwater Ecosystems. 31(6). 1429–1442. 9 indexed citations
4.
Figueiredo, Joana, et al.. (2018). Comparing length-measurement methods and estimating growth parameters of free-swimming whale sharks (Rhincodon typus) near the South Ari Atoll, Maldives. Marine and Freshwater Research. 69(10). 1487–1495. 23 indexed citations
5.
Stewart, Bryce D., et al.. (2018). Does bathymetry drive coastal whale shark (Rhincodon typus)aggregations?. PeerJ. 6. e4904–e4904. 19 indexed citations
7.
Donati, Giulia, et al.. (2016). New insights into the South Ari atoll whale shark, Rhincodon typus, aggregation. 3 indexed citations
8.
Hogarth, Maxine, Lewis L. Judd, C. J. Mathias, et al.. (2002). Cardiovascular autonomic function in systemic lupus erythematosus. Lupus. 11(5). 308–312. 16 indexed citations
9.
Konttinen, Yrjö T., Pertti Kemppinen, Mika Hukkanen, et al.. (1994). Peripheral and spinal neural mechanisms in arthritis, with particular reference to treatment of inflammation and pain. Arthritis & Rheumatism. 37(7). 965–982. 107 indexed citations
10.
Kar, Satyabrata, Richard Rees, & Rémi Quirion. (1994). Altered Calcitonin Gene‐related Peptide, Substance P and Enkephalin Immunoreactivities and Receptor Binding Sites in the Dorsal Spinal Cord of the Polyarthritic Rat. European Journal of Neuroscience. 6(3). 345–354. 42 indexed citations
11.
McCormack, David G., Richard Rees, David Crawley, Peter J. Barnes, & Timothy W. Evans. (1993). Sensory neuropeptides and hypoxic pulmonary vasoconstriction in the rat.. Thorax. 48(5). 554–557. 8 indexed citations
12.
Harbuz, Michael S., Richard Rees, & Stafford L. Lightman. (1993). HPA axis responses to acute stress and adrenalectomy during adjuvant-induced arthritis in the rat. American Journal of Physiology-Regulatory, Integrative and Comparative Physiology. 264(1). R179–R185. 54 indexed citations
14.
Konttinen, Yrjö T., Mika Hukkanen, Richard Rees, et al.. (1992). Relationship between Neuropeptide lmmuno reactive Nerves and Inflammatory Cells in Adjuvant Arthritic Rats. Scandinavian Journal of Rheumatology. 21(2). 55–59. 25 indexed citations
15.
Hukkanen, Mika, Yrjö T. Konttinen, Richard Rees, et al.. (1992). Innervation of bone from healthy and arthritic rats by substance P and calcitonin gene related peptide containing sensory fibers.. PubMed. 19(8). 1252–9. 81 indexed citations
17.
Hukkanen, Mika, et al.. (1991). Regional distribution of mast cells and peptide containing nerves in normal and adjuvant arthritic rat synovium.. PubMed. 18(2). 177–83. 52 indexed citations
18.
Kar, Satyabrata, S.J. Gibson, W.G.Z.O. Jura, et al.. (1989). Marked changes of calcitonin gene-related peptide (CGRP), substance P and enkephalin occur in the spinal cord and dorsal root ganglia of rats with adjuvant arthritis. Regulatory Peptides. 26(1). 76–76. 2 indexed citations
19.
Konttinen, Y. T., Mats Grönblad, Mika Hukkanen, et al.. (1989). Pain fibers in osteoarthritis: A review. Seminars in Arthritis and Rheumatism. 18(4). 35–40. 13 indexed citations
20.
Rees, Richard, J. Dixey, Stafford L. Lightman, & D. A. Brewerton. (1989). The influence of unilateral sciatic nerve section on the course of adjuvant arthritis in rats. 54. 2 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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