Matthew J. Hilton

6.8k total citations · 1 hit paper
88 papers, 5.3k citations indexed

About

Matthew J. Hilton is a scholar working on Molecular Biology, Rheumatology and Surgery. According to data from OpenAlex, Matthew J. Hilton has authored 88 papers receiving a total of 5.3k indexed citations (citations by other indexed papers that have themselves been cited), including 45 papers in Molecular Biology, 40 papers in Rheumatology and 17 papers in Surgery. Recurrent topics in Matthew J. Hilton's work include Osteoarthritis Treatment and Mechanisms (34 papers), Developmental Biology and Gene Regulation (13 papers) and Bone Metabolism and Diseases (13 papers). Matthew J. Hilton is often cited by papers focused on Osteoarthritis Treatment and Mechanisms (34 papers), Developmental Biology and Gene Regulation (13 papers) and Bone Metabolism and Diseases (13 papers). Matthew J. Hilton collaborates with scholars based in United States, China and Japan. Matthew J. Hilton's co-authors include Fanxin Long, Xiaolin Tu, Regis J. O’Keefe, Michael J. Zuscik, Anthony J. Mirando, Hongliang Hu, Ximei Wu, David M. Ornitz, Di Chen and Kai Yu and has published in prestigious journals such as Cell, Journal of Biological Chemistry and Journal of Clinical Investigation.

In The Last Decade

Matthew J. Hilton

86 papers receiving 5.2k citations

Hit Papers

Sequential roles of Hedgehog and Wnt signaling in osteobl... 2004 2026 2011 2018 2004 100 200 300 400 500

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Matthew J. Hilton United States 37 3.2k 1.4k 854 698 665 88 5.3k
T. Michael Underhill Canada 44 2.9k 0.9× 1.0k 0.7× 611 0.7× 748 1.1× 505 0.8× 108 5.1k
Shinsuke Ohba Japan 41 3.9k 1.2× 1.3k 1.0× 978 1.1× 732 1.0× 925 1.4× 135 6.5k
Mei Wan United States 45 3.8k 1.2× 1.4k 1.0× 1.4k 1.7× 727 1.0× 794 1.2× 127 6.9k
Hicham Drissi United States 49 4.2k 1.3× 1.9k 1.4× 1.4k 1.6× 1.1k 1.6× 910 1.4× 177 7.0k
Ling Qin United States 39 2.1k 0.7× 1.1k 0.8× 1.4k 1.6× 601 0.9× 479 0.7× 131 4.5k
Jennifer J. Westendorf United States 49 4.9k 1.5× 916 0.7× 1.6k 1.9× 626 0.9× 961 1.4× 141 7.5k
Kazuhisa Nakashima Japan 30 4.6k 1.4× 1.6k 1.2× 1.5k 1.7× 572 0.8× 918 1.4× 77 6.9k
Amy D. Bradshaw United States 41 1.7k 0.5× 1.7k 1.3× 791 0.9× 833 1.2× 569 0.9× 93 5.2k
Thomas A. Owen United States 38 3.6k 1.1× 1.4k 1.1× 1.1k 1.3× 578 0.8× 409 0.6× 78 6.6k
Masahiro Iwamoto United States 42 2.7k 0.8× 2.8k 2.1× 568 0.7× 719 1.0× 570 0.9× 99 5.7k

Countries citing papers authored by Matthew J. Hilton

Since Specialization
Citations

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

Fields of papers citing papers by Matthew J. Hilton

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Matthew J. Hilton

This figure shows the co-authorship network connecting the top 25 collaborators of Matthew J. Hilton. A scholar is included among the top collaborators of Matthew J. Hilton 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 Matthew J. Hilton. Matthew J. Hilton 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.
2.
Hoque, Jiaul, Vijitha Puviindran, Hunter Newman, et al.. (2023). Radiation-induced bone loss in mice is ameliorated by inhibition of HIF-2α in skeletal progenitor cells. Science Translational Medicine. 15(724). eabo5217–eabo5217. 3 indexed citations
3.
Rampersad, Rishi R., Amanda M. Eudy, Yinshi Ren, et al.. (2023). Aged G Protein-Coupled Receptor Kinase 3 (Grk3)-Deficient Mice Exhibit Enhanced Osteoclastogenesis and Develop Bone Lesions Analogous to Human Paget’s Disease of Bone. Cells. 12(7). 981–981. 1 indexed citations
4.
Bokshan, Steven L., et al.. (2023). Risk factors for intracellular fatty accumulation in rotator cuff muscle: a histologic analysis. Journal of Shoulder and Elbow Surgery. 33(4). e215–e222. 2 indexed citations
5.
Mirando, Anthony J., Douglas Rouse, Purushothama Rao Tata, et al.. (2022). Identification of distinct non-myogenic skeletal-muscle-resident mesenchymal cell populations. Cell Reports. 39(6). 110785–110785. 35 indexed citations
6.
Liao, Yihan, Yinshi Ren, Xin Luo, et al.. (2022). Interleukin-6 signaling mediates cartilage degradation and pain in posttraumatic osteoarthritis in a sex-specific manner. Science Signaling. 15(744). eabn7082–eabn7082. 69 indexed citations
7.
Wang, Kaiyuan, Christopher R. Donnelly, Changyu Jiang, et al.. (2021). STING suppresses bone cancer pain via immune and neuronal modulation. Nature Communications. 12(1). 4558–4558. 91 indexed citations
8.
Sharma, Deepika, et al.. (2021). HES1 is a novel downstream modifier of the SHH-GLI3 Axis in the development of preaxial polydactyly. PLoS Genetics. 17(12). e1009982–e1009982. 5 indexed citations
9.
Karner, Courtney M., et al.. (2021). Hypoxia depletes contaminating CD45+ hematopoietic cells from murine bone marrow stromal cell (BMSC) cultures: Methods for BMSC culture purification. Stem Cell Research. 53. 102317–102317. 3 indexed citations
10.
Lee, Chang‐Lung, Dadong Zhang, Alexander B. Sibley, et al.. (2021). Whole-Exome Sequencing of Radiation-Induced Thymic Lymphoma in Mouse Models Identifies Notch1 Activation as a Driver of p53 Wild-Type Lymphoma. Cancer Research. 81(14). 3777–3790. 12 indexed citations
11.
Wang, Kaiyuan, Yun Gu, Yihan Liao, et al.. (2020). PD-1 blockade inhibits osteoclast formation and murine bone cancer pain. Journal of Clinical Investigation. 130(7). 3603–3620. 131 indexed citations
12.
Tsushima, Hidetoshi, Yuning J. Tang, Vijitha Puviindran, et al.. (2018). Intracellular biosynthesis of lipids and cholesterol by Scap and Insig in mesenchymal cells regulates long bone growth and chondrocyte homeostasis. Development. 145(13). 21 indexed citations
13.
Kohn, Anat, et al.. (2016). HES factors regulate specific aspects of chondrogenesis and chondrocyte hypertrophy during cartilage development. Journal of Cell Science. 129(11). 2145–2155. 22 indexed citations
14.
Mirando, Anthony J., et al.. (2015). A dual role for notch signaling in joint cartilage maintenance and osteoarthritis. Osteoarthritis and Cartilage. 23. A64–A64. 3 indexed citations
15.
Jones, Kevin B., Maurizio Pacifici, & Matthew J. Hilton. (2014). Multiple hereditary exostoses (MHE): elucidating the pathogenesis of a rare skeletal disorder through interdisciplinary research. Connective Tissue Research. 55(2). 80–88. 18 indexed citations
16.
Wang, Cuicui, Jie Shen, Kiminori Yukata, et al.. (2014). Transient gamma-secretase inhibition accelerates and enhances fracture repair likely via Notch signaling modulation. Bone. 73. 77–89. 21 indexed citations
17.
Hilton, Matthew J.. (2014). Skeletal development and repair : methods and protocols. Humana Press eBooks. 14 indexed citations
18.
Dong, Yufeng, Anat Kohn, Tasuku Honjo, et al.. (2010). RBPjκ-dependent Notch signaling regulates mesenchymal progenitor cell proliferation and differentiation during skeletal development. Development. 137(9). 1461–1471. 149 indexed citations
19.
Christopher, Matthew, Fulu Liu, Matthew J. Hilton, Fanxin Long, & Daniel C. Link. (2009). Suppression of CXCL12 production by bone marrow osteoblasts is a common and critical pathway for cytokine-induced mobilization. Blood. 114(7). 1331–1339. 172 indexed citations
20.
Hu, Hongliang, Matthew J. Hilton, Xiaolin Tu, et al.. (2004). Sequential roles of Hedgehog and Wnt signaling in osteoblast development. Development. 132(1). 49–60. 536 indexed citations breakdown →

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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026