Anthony J. Hayes

7.7k total citations · 2 hit papers
114 papers, 6.1k citations indexed

About

Anthony J. Hayes is a scholar working on Cell Biology, Molecular Biology and Rheumatology. According to data from OpenAlex, Anthony J. Hayes has authored 114 papers receiving a total of 6.1k indexed citations (citations by other indexed papers that have themselves been cited), including 41 papers in Cell Biology, 36 papers in Molecular Biology and 28 papers in Rheumatology. Recurrent topics in Anthony J. Hayes's work include Proteoglycans and glycosaminoglycans research (38 papers), Osteoarthritis Treatment and Mechanisms (26 papers) and Connective tissue disorders research (18 papers). Anthony J. Hayes is often cited by papers focused on Proteoglycans and glycosaminoglycans research (38 papers), Osteoarthritis Treatment and Mechanisms (26 papers) and Connective tissue disorders research (18 papers). Anthony J. Hayes collaborates with scholars based in United Kingdom, Australia and United States. Anthony J. Hayes's co-authors include David Field, R. F. Hess, James Melrose, David Lloyd, Bruce Caterson, James R. Ralphs, Owen J. Sansom, Karen R. Reed, Alan R. Clarke and Douglas J. Winton and has published in prestigious journals such as Journal of Biological Chemistry, Genes & Development and The Journal of Immunology.

In The Last Decade

Anthony J. Hayes

112 papers receiving 6.0k citations

Hit Papers

Contour integration by th... 1993 2026 2004 2015 1993 2004 400 800 1.2k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Anthony J. Hayes United Kingdom 40 1.7k 1.1k 857 832 784 114 6.1k
Peter G. Smith United States 47 3.0k 1.8× 407 0.4× 408 0.5× 232 0.3× 1.1k 1.4× 250 7.9k
Takashi Yamane Japan 40 2.7k 1.6× 275 0.2× 575 0.7× 191 0.2× 588 0.8× 377 8.1k
Hong Yi China 60 6.1k 3.6× 505 0.5× 834 1.0× 136 0.2× 844 1.1× 280 12.4k
Koji Yamashita Japan 48 3.6k 2.1× 212 0.2× 499 0.6× 197 0.2× 454 0.6× 277 8.2k
Makoto Iwata Japan 45 2.1k 1.2× 607 0.5× 202 0.2× 205 0.2× 427 0.5× 463 11.3k
Do Young ‍Kim South Korea 44 1.9k 1.1× 133 0.1× 399 0.5× 482 0.6× 473 0.6× 336 6.7k
Fulvio Magni Italy 38 2.8k 1.7× 604 0.5× 429 0.5× 132 0.2× 470 0.6× 284 6.8k
Paolo Fortina United States 47 4.7k 2.8× 293 0.3× 594 0.7× 212 0.3× 1.4k 1.8× 208 9.2k
Ian D. Duncan United States 52 4.8k 2.8× 218 0.2× 629 0.7× 224 0.3× 494 0.6× 243 11.9k
Alfonso Baldi Italy 55 5.0k 2.9× 200 0.2× 809 0.9× 385 0.5× 2.7k 3.4× 398 12.1k

Countries citing papers authored by Anthony J. Hayes

Since Specialization
Citations

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

Fields of papers citing papers by Anthony J. Hayes

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Anthony J. Hayes. 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 Anthony J. Hayes. The network helps show where Anthony J. Hayes may publish in the future.

Co-authorship network of co-authors of Anthony J. Hayes

This figure shows the co-authorship network connecting the top 25 collaborators of Anthony J. Hayes. A scholar is included among the top collaborators of Anthony J. Hayes 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 Anthony J. Hayes. Anthony J. Hayes 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
3.
Hayes, Anthony J. & James Melrose. (2021). 3D distribution of perlecan within intervertebral disc chondrons suggests novel regulatory roles for this multifunctional modular heparan sulphate proteoglycan. European Cells and Materials. 41. 73–89. 15 indexed citations
4.
Hayes, Anthony J., Clare Hughes, Susan M. Smith, et al.. (2016). The CS Sulfation Motifs 4C3, 7D4, 3B3[−]; and Perlecan Identify Stem Cell Populations and Their Niches, Activated Progenitor Cells and Transitional Areas of Tissue Development in the Fetal Human Elbow. Stem Cells and Development. 25(11). 836–847. 24 indexed citations
5.
Millet, Coralie, Catrin F. Williams, Anthony J. Hayes, et al.. (2013). Mitochondria-derived organelles in the diplomonad fish parasite Spironucleus vortens. Experimental Parasitology. 135(2). 262–273. 13 indexed citations
6.
Hayes, Anthony J., et al.. (2013). Expression of glycosaminoglycan epitopes during zebrafish skeletogenesis. Developmental Dynamics. 242(6). 778–789. 8 indexed citations
7.
Melrose, James, Susan M. Smith, Clare Hughes, et al.. (2012). Chondroitin sulphate and heparan sulphate sulphation motifs and their proteoglycans are involved in articular cartilage formation during human foetal knee joint development. Histochemistry and Cell Biology. 138(3). 461–475. 43 indexed citations
8.
Hayes, Anthony J., Susan M. Smith, & James Melrose. (2012). Comparative immunolocalisation of fibrillin-1 and perlecan in the human foetal, and HS-deficient hspg2 exon 3 null mutant mouse intervertebral disc. Histochemistry and Cell Biology. 139(1). 1–11. 17 indexed citations
9.
Hooper, Samuel J., Steven L. Percival, Katja E. Hill, et al.. (2012). The visualisation and speed of kill of wound isolates on a silver alginate dressing. International Wound Journal. 9(6). 633–642. 21 indexed citations
10.
Li, Siyuan, Anthony J. Hayes, Bruce Caterson, & Clare Hughes. (2012). The effect of beta-xylosides on the chondrogenic differentiation of mesenchymal stem cells. Histochemistry and Cell Biology. 139(1). 59–74. 7 indexed citations
11.
Thorp‐Greenwood, Flora L., Vanesa Fernández‐Moreira, Coralie Millet, et al.. (2011). A ‘Sleeping Trojan Horse’ which transports metal ions into cells, localises in nucleoli, and has potential for bimodal fluorescence/PET imaging. Chemical Communications. 47(11). 3096–3096. 42 indexed citations
12.
Nowell, Mari A., Anwen S. Williams, Jürgen Scheller, et al.. (2009). Therapeutic Targeting of IL-6 Trans Signaling Counteracts STAT3 Control of Experimental Inflammatory Arthritis. The Journal of Immunology. 182(1). 613–622. 175 indexed citations
13.
Hayes, Anthony J., et al.. (2007). Chondroitin Sulfate Sulfation Motifs as Putative Biomarkers for Isolation of Articular Cartilage Progenitor Cells. Journal of Histochemistry & Cytochemistry. 56(2). 125–138. 83 indexed citations
14.
Blain, Emma J., Sophie Gilbert, Anthony J. Hayes, & Victor C. Duance. (2006). Disassembly of the vimentin cytoskeleton disrupts articular cartilage chondrocyte homeostasis. Matrix Biology. 25(7). 398–408. 68 indexed citations
15.
Hayes, Anthony J.. (2001). Extracellular matrix in development of the intervertebral disc. Matrix Biology. 20(2). 107–121. 179 indexed citations
16.
Kingdom, Frederick A. A., Anthony J. Hayes, & David Field. (2001). Sensitivity to contrast histogram differences in synthetic wavelet-textures. Vision Research. 41(5). 585–598. 38 indexed citations
17.
Hayes, Anthony J., Michael Benjamin, & James R. Ralphs. (1999). Role of actin stress fibres in the development of the intervertebral disc: Cytoskeletal control of extracellular matrix assembly. Developmental Dynamics. 215(3). 179–189. 6 indexed citations
18.
Hayes, Anthony J., et al.. (1999). Role of actin stress fibres in the development of the intervertebral disc: Cytoskeletal control of extracellular matrix assembly. Developmental Dynamics. 215(3). 179–189. 87 indexed citations
19.
Lloyd, David, Katie L. Thomas, Anthony J. Hayes, et al.. (1998). Micro-ecology of peat: minimally invasive analysis using confocal laser scanning microscopy, membrane inlet mass spectrometry and PCR amplification of methanogen-specific gene sequences. FEMS Microbiology Ecology. 25(2). 179–188. 18 indexed citations
20.
Lloyd, David & Anthony J. Hayes. (1995). Vigour, vitality and viability of microorganisms. FEMS Microbiology Letters. 133(1-2). 1–7. 127 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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