George Bou–Gharios

8.6k total citations · 1 hit paper
158 papers, 6.6k citations indexed

About

George Bou–Gharios is a scholar working on Molecular Biology, Genetics and Rheumatology. According to data from OpenAlex, George Bou–Gharios has authored 158 papers receiving a total of 6.6k indexed citations (citations by other indexed papers that have themselves been cited), including 90 papers in Molecular Biology, 24 papers in Genetics and 21 papers in Rheumatology. Recurrent topics in George Bou–Gharios's work include Connective Tissue Growth Factor Research (20 papers), Osteoarthritis Treatment and Mechanisms (19 papers) and Connective tissue disorders research (17 papers). George Bou–Gharios is often cited by papers focused on Connective Tissue Growth Factor Research (20 papers), Osteoarthritis Treatment and Mechanisms (19 papers) and Connective tissue disorders research (17 papers). George Bou–Gharios collaborates with scholars based in United Kingdom, United States and Japan. George Bou–Gharios's co-authors include Terence A. Partridge, David Abraham, Carol M. Black, Shiwen Xu, Christopher P. Denton, Andrew Leask, Qi Long Lu, Elisabetta Renzoni, David Abraham and Jeremy D. Pearson and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Journal of Biological Chemistry.

In The Last Decade

George Bou–Gharios

156 papers receiving 6.5k citations

Hit Papers

Systemic delivery of anti... 2004 2026 2011 2018 2004 100 200 300

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
George Bou–Gharios United Kingdom 44 3.4k 995 927 842 834 158 6.6k
Hitoshi Okochi Japan 36 3.1k 0.9× 1.2k 1.3× 474 0.5× 722 0.9× 1.1k 1.3× 108 6.3k
Lucy Liaw United States 52 4.9k 1.4× 927 0.9× 1.0k 1.1× 556 0.7× 365 0.4× 136 9.8k
Slobodan Vukičević Croatia 51 4.0k 1.2× 1.7k 1.7× 475 0.5× 560 0.7× 1.1k 1.3× 181 9.2k
Riitta Herva Finland 39 3.4k 1.0× 872 0.9× 1.3k 1.4× 393 0.5× 622 0.7× 124 6.6k
Beate Eckes Germany 50 2.2k 0.6× 605 0.6× 641 0.7× 895 1.1× 311 0.4× 117 7.1k
Franck Verrecchia France 40 3.4k 1.0× 600 0.6× 919 1.0× 749 0.9× 373 0.4× 99 6.2k
Hans-Peter Gerber United States 13 4.7k 1.4× 924 0.9× 988 1.1× 346 0.4× 591 0.7× 16 8.9k
Gaetano Magro Italy 39 1.5k 0.4× 978 1.0× 1.0k 1.1× 792 0.9× 310 0.4× 300 5.7k
Serena Zacchigna Italy 42 4.3k 1.3× 1.4k 1.4× 577 0.6× 273 0.3× 497 0.6× 112 7.2k
Setsuro Komiya Japan 50 3.0k 0.9× 2.0k 2.0× 1.1k 1.2× 1.5k 1.8× 412 0.5× 272 8.8k

Countries citing papers authored by George Bou–Gharios

Since Specialization
Citations

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

Fields of papers citing papers by George Bou–Gharios

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by George Bou–Gharios. 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 George Bou–Gharios. The network helps show where George Bou–Gharios may publish in the future.

Co-authorship network of co-authors of George Bou–Gharios

This figure shows the co-authorship network connecting the top 25 collaborators of George Bou–Gharios. A scholar is included among the top collaborators of George Bou–Gharios 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 George Bou–Gharios. George Bou–Gharios 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.
Lunn, Sharna, David A. Turner, Ke Liu, et al.. (2025). Skeletal progenitor LRP1 deficiency causes severe and persistent skeletal defects with Wnt pathway dysregulation. Bone Research. 13(1). 17–17. 2 indexed citations
2.
Ooi, Kazuhiro, Kazuhiro Yamamoto, Yutaka Kobayashi, et al.. (2025). Temporomandibular joint degeneration arises spontaneously in STR/ort mice and is prevented by targeted aggrecanase inhibition. Osteoarthritis and Cartilage Open. 7(2). 100599–100599. 1 indexed citations
3.
Norman, Brendan P., Hazel Sutherland, Peter J. Wilson, et al.. (2024). Hepatobiliary circulation and dominant urinary excretion of homogentisic acid in a mouse model of alkaptonuria. Journal of Inherited Metabolic Disease. 47(4). 664–673.
4.
Vincent, Krista M., et al.. (2024). Cancer-associated Fibroblast–specific Expression of the Matricellular Protein CCN1 Coordinates Neovascularization and Stroma Deposition in Melanoma Metastasis. Cancer Research Communications. 4(2). 556–570. 13 indexed citations
5.
Ranganath, L., Milad Khedr, Anna M. Milan, et al.. (2023). Increased prevalence of Parkinson's disease in alkaptonuria. JIMD Reports. 64(4). 282–292. 3 indexed citations
6.
Ooi, Nicola, Brendan P. Norman, James A. Gallagher, et al.. (2023). Evaluation of Homogentisic Acid, a Prospective Antibacterial Agent Highlighted by the Suitability of Nitisinone in Alkaptonuria 2 (SONIA 2) Clinical Trial. Cells. 12(13). 1683–1683. 1 indexed citations
7.
Quan, Taihao, Wei Xia, Tianyuan He, et al.. (2023). Matrix Metalloproteinase-1 Expression in Fibroblasts Accelerates Dermal Aging and Promotes Papilloma Development in Mouse Skin. Journal of Investigative Dermatology. 143(9). 1700–1707.e1. 22 indexed citations
8.
Marcélis, Lionel, Georges Casimir, Philippe Goyens, et al.. (2023). Hereditary Tyrosinemia Type 1 Mice under Continuous Nitisinone Treatment Display Remnants of an Uncorrected Liver Disease Phenotype. Genes. 14(3). 693–693. 3 indexed citations
9.
Bou–Gharios, George, Peter Clegg, Riaz Akhtar, et al.. (2022). Collagen (I) homotrimer potentiates the osteogenesis imperfecta (oim) mutant allele and reduces survival in male mice. Disease Models & Mechanisms. 15(9). 7 indexed citations
10.
Yamamoto, Kazuhiro, Carsten Scavenius, Ida B. Thøgersen, et al.. (2022). A top-down approach to uncover the hidden ligandome of low-density lipoprotein receptor-related protein 1 in cartilage. Matrix Biology. 112. 190–218. 14 indexed citations
11.
Kanakis, Ioannis, Peter Milner, Andrew Leask, et al.. (2020). Post-traumatic osteoarthritis development is not modified by postnatal chondrocyte deletion of Ccn2. Disease Models & Mechanisms. 13(7). 5 indexed citations
12.
Quan, Taihao, Yaping Xiang, Yingchun Liu, et al.. (2020). Dermal Fibroblast CCN1 Expression in Mice Recapitulates Human Skin Dermal Aging. Journal of Investigative Dermatology. 141(4). 1007–1016. 14 indexed citations
13.
Yamamoto, Kazuhiro, D. Wilkinson, & George Bou–Gharios. (2020). Targeting Dysregulation of Metalloproteinase Activity in Osteoarthritis. Calcified Tissue International. 109(3). 277–290. 39 indexed citations
14.
Kanakis, Ioannis, Ke Liu, B. Poulet, et al.. (2018). Targeted Inhibition of Aggrecanases Prevents Articular Cartilage Degradation and Augments Bone Mass in the STR/Ort Mouse Model of Spontaneous Osteoarthritis. Arthritis & Rheumatology. 71(4). 571–582. 11 indexed citations
15.
Moschidou, Dafni, Michelangelo Corcelli, Jacques Behmoaras, et al.. (2016). Human Chorionic Stem Cells: Podocyte Differentiation and Potential for the Treatment of Alport Syndrome. Stem Cells and Development. 25(5). 395–404. 16 indexed citations
16.
Fragiadaki, Maria, George Bou–Gharios, Terence Cook, et al.. (2012). Hyperglycemia Causes Renal Cell Damage via CCN2-Induced Activation of the TrkA Receptor. Diabetes. 61(9). 2280–2288. 22 indexed citations
17.
Xu, Shiwen, Laura Kennedy, Daphne Pala, et al.. (2006). CCN2 Is Necessary for Adhesive Responses to Transforming Growth Factor-β1 in Embryonic Fibroblasts. Journal of Biological Chemistry. 281(16). 10715–10726. 136 indexed citations
18.
Russo, Francesco Paolo, Malcolm Alison, Brian Bigger, et al.. (2006). The Bone Marrow Functionally Contributes to Liver Fibrosis. Gastroenterology. 130(6). 1807–1821. 371 indexed citations
19.
Chen, Yunliang, Shiwen Xu, Laura Kennedy, et al.. (2005). Matrix Contraction by Dermal Fibroblasts Requires Transforming Growth Factor-β/Activin-Linked Kinase 5, Heparan Sulfate-Containing Proteoglycans, and MEK/ERK. American Journal Of Pathology. 167(6). 1699–1711. 119 indexed citations
20.
Xu, Shiwen, Yunliang Chen, Christopher P. Denton, et al.. (2004). Endothelin-1 Promotes Myofibroblast Induction through the ETA Receptor via a rac/Phosphoinositide 3-Kinase/Akt-dependent Pathway and Is Essential for the Enhanced Contractile Phenotype of Fibrotic Fibroblasts. Molecular Biology of the Cell. 15(6). 2707–2719. 287 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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