Christopher Price

1.9k total citations
44 papers, 1.5k citations indexed

About

Christopher Price is a scholar working on Rheumatology, Biomedical Engineering and Surgery. According to data from OpenAlex, Christopher Price has authored 44 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Rheumatology, 21 papers in Biomedical Engineering and 13 papers in Surgery. Recurrent topics in Christopher Price's work include Osteoarthritis Treatment and Mechanisms (21 papers), Lower Extremity Biomechanics and Pathologies (18 papers) and Knee injuries and reconstruction techniques (12 papers). Christopher Price is often cited by papers focused on Osteoarthritis Treatment and Mechanisms (21 papers), Lower Extremity Biomechanics and Pathologies (18 papers) and Knee injuries and reconstruction techniques (12 papers). Christopher Price collaborates with scholars based in United States, China and United Kingdom. Christopher Price's co-authors include Liyun Wang, Xiaozhou Zhou, David L. Burris, Wen Li, Karl J. Jepsen, Axel C. Moore, Xiaohan Lai, Jun Pan, Bin Wang and Catherine B. Kirn‐Safran and has published in prestigious journals such as Proceedings of the National Academy of Sciences, PLoS ONE and Journal of Bone and Mineral Research.

In The Last Decade

Christopher Price

43 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Christopher Price United States 23 537 475 463 326 325 44 1.5k
C.M. Semeins Netherlands 18 592 1.1× 264 0.6× 475 1.0× 258 0.8× 329 1.0× 25 1.4k
Behzâd Javaheri United Kingdom 19 516 1.0× 212 0.4× 426 0.9× 172 0.5× 211 0.6× 54 1.2k
Gary Gibson United States 16 711 1.3× 449 0.9× 420 0.9× 221 0.7× 133 0.4× 27 1.5k
Stéphane Pallu France 21 475 0.9× 324 0.7× 300 0.6× 212 0.7× 509 1.6× 47 1.7k
Natasha Case United States 24 942 1.8× 341 0.7× 345 0.7× 276 0.8× 326 1.0× 31 2.0k
Yuko Mikuni‐Takagaki Japan 26 932 1.7× 389 0.8× 578 1.2× 241 0.7× 633 1.9× 59 2.2k
Massimo Marenzana United Kingdom 17 340 0.6× 205 0.4× 331 0.7× 223 0.7× 217 0.7× 31 1.1k
Padmaja Tummala United States 18 1.0k 1.9× 281 0.6× 377 0.8× 392 1.2× 355 1.1× 28 2.2k
Stephen D. Thorpe United Kingdom 28 568 1.1× 672 1.4× 154 0.3× 482 1.5× 558 1.7× 50 2.2k
Astrid Liedert Germany 25 864 1.6× 180 0.4× 446 1.0× 469 1.4× 412 1.3× 47 2.0k

Countries citing papers authored by Christopher Price

Since Specialization
Citations

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

Fields of papers citing papers by Christopher Price

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Christopher Price

This figure shows the co-authorship network connecting the top 25 collaborators of Christopher Price. A scholar is included among the top collaborators of Christopher Price 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 Christopher Price. Christopher Price 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.
Bhattacharjee, Arnab, et al.. (2025). Elevated Contact Stresses Compromise Activity-Mediated Cartilage Rehydration but not Lubrication. Annals of Biomedical Engineering. 53(7). 1672–1688. 1 indexed citations
2.
Burris, David L., et al.. (2024). Enzymatic digestion does not compromise sliding-mediated cartilage lubrication. Acta Biomaterialia. 178. 196–207. 8 indexed citations
3.
Moore, Axel C., et al.. (2021). The modes and competing rates of cartilage fluid loss and recovery. Acta Biomaterialia. 138. 390–397. 17 indexed citations
4.
Gilbert, Rachel M., et al.. (2021). Targeted Gq-GPCR activation drives ER-dependent calcium oscillations in chondrocytes. Cell Calcium. 94. 102363–102363. 8 indexed citations
5.
Ortved, Kyla F., et al.. (2021). Comparative tribology II–Measurable biphasic tissue properties have predictable impacts on cartilage rehydration and lubricity. Acta Biomaterialia. 138. 375–389. 17 indexed citations
6.
Ortved, Kyla F., et al.. (2021). Articular Cartilage Friction, Strain, and Viability Under Physiological to Pathological Benchtop Sliding Conditions. Cellular and Molecular Bioengineering. 14(4). 349–363. 11 indexed citations
7.
Moore, Axel C., et al.. (2020). Range-of-motion affects cartilage fluid load support: functional implications for prolonged inactivity. Osteoarthritis and Cartilage. 29(1). 134–142. 6 indexed citations
8.
Burris, David L., et al.. (2019). Effects of mechanical injury on the tribological rehydration and lubrication of articular cartilage. Journal of the mechanical behavior of biomedical materials. 101. 103422–103422. 28 indexed citations
9.
Moore, Axel C., et al.. (2017). Sliding enhances fluid and solute transport into buried articular cartilage contacts. Osteoarthritis and Cartilage. 25(12). 2100–2107. 48 indexed citations
10.
Price, Christopher, et al.. (2016). Seeing through Musculoskeletal Tissues: Improving In Situ Imaging of Bone and the Lacunar Canalicular System through Optical Clearing. PLoS ONE. 11(3). e0150268–e0150268. 42 indexed citations
11.
Locke, Ryan C., et al.. (2016). Early, focal changes in cartilage cellularity and structure following surgically induced meniscal destabilization in the mouse. Journal of Orthopaedic Research®. 35(3). 537–547. 23 indexed citations
12.
13.
Liu, Chao, Wen Li, Xiaoyu Gu, et al.. (2015). Bone's responses to mechanical loading are impaired in type 1 diabetes. Bone. 81. 152–160. 50 indexed citations
14.
Lai, Xiaohan, Christopher Price, X. Lucas Lu, & Liyun Wang. (2014). Imaging and quantifying solute transport across periosteum: Implications for muscle–bone crosstalk. Bone. 66. 82–89. 23 indexed citations
15.
Bonnevie, Edward D., et al.. (2012). Functional characterization of normal and degraded bovine meniscus: Rate-dependent indentation and friction studies. Bone. 51(2). 232–240. 27 indexed citations
16.
Pan, Jun, Bin Wang, Wen Li, et al.. (2011). Elevated cross-talk between subchondral bone and cartilage in osteoarthritic joints. Bone. 51(2). 212–217. 131 indexed citations
17.
Price, Christopher, Wen Li, John E. Novotny, & Liyun Wang. (2009). An in‐situ fluorescence‐based optical extensometry system for imaging mechanically loaded bone. Journal of Orthopaedic Research®. 28(6). 805–811. 14 indexed citations
18.
Jepsen, Karl J., Bin Hu, Steven M. Tommasini, et al.. (2008). Phenotypic integration of skeletal traits during growth buffers genetic variants affecting the slenderness of femora in inbred mouse strains. Mammalian Genome. 20(1). 21–33. 37 indexed citations
19.
Jepsen, Karl J., Bin Hu, Steven M. Tommasini, et al.. (2007). Genetic randomization reveals functional relationships among morphologic and tissue-quality traits that contribute to bone strength and fragility. Mammalian Genome. 18(6-7). 492–507. 65 indexed citations
20.
Wang, Yinong, Yalai Bai, Christopher Price, et al.. (2001). Combination of Electroporation and DNA/Dendrimer Complexes Enhances Gene Transfer into Murine Cardiac Transplants. American Journal of Transplantation. 1(4). 334–338. 25 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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