Matthew Spite

8.6k total citations · 3 hit papers
65 papers, 6.5k citations indexed

About

Matthew Spite is a scholar working on Nutrition and Dietetics, Biochemistry and Immunology. According to data from OpenAlex, Matthew Spite has authored 65 papers receiving a total of 6.5k indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Nutrition and Dietetics, 19 papers in Biochemistry and 19 papers in Immunology. Recurrent topics in Matthew Spite's work include Fatty Acid Research and Health (30 papers), Eicosanoids and Hypertension Pharmacology (16 papers) and Adipokines, Inflammation, and Metabolic Diseases (14 papers). Matthew Spite is often cited by papers focused on Fatty Acid Research and Health (30 papers), Eicosanoids and Hypertension Pharmacology (16 papers) and Adipokines, Inflammation, and Metabolic Diseases (14 papers). Matthew Spite collaborates with scholars based in United States, Australia and Hungary. Matthew Spite's co-authors include Charles N. Serhan, Brian E. Sansbury, Jason Hellmann, Aruni Bhatnagar, Rong Yang, Gabrielle Fredman, Yunan Tang, Michael J. Zhang, Joan Clària and Lucy V. Norling and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Matthew Spite

64 papers receiving 6.3k citations

Hit Papers

Maresins: novel macrophage mediators with potent antiinfl... 2008 2026 2014 2020 2008 2009 2016 200 400 600

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Matthew Spite United States 42 2.5k 2.0k 1.7k 1.5k 1.2k 65 6.5k
Romain A. Colas United States 46 2.8k 1.1× 1.7k 0.8× 1.7k 1.0× 1.8k 1.2× 777 0.7× 91 6.4k
Gabrielle Fredman United States 36 2.2k 0.9× 2.6k 1.3× 1.8k 1.1× 1.4k 0.9× 644 0.6× 60 6.4k
Song Hong United States 38 5.6k 2.3× 2.1k 1.0× 2.4k 1.4× 3.6k 2.3× 1.1k 1.0× 66 9.6k
Karsten Gronert United States 42 4.9k 2.0× 2.8k 1.4× 3.1k 1.8× 3.3k 2.1× 1.4k 1.2× 92 10.7k
Da Young Oh United States 31 1.1k 0.5× 1.0k 0.5× 2.0k 1.1× 560 0.4× 1.9k 1.7× 43 5.8k
Saswata Talukdar United States 32 1.2k 0.5× 1.0k 0.5× 3.2k 1.8× 693 0.4× 2.3k 1.9× 48 7.3k
Alyssa H. Hasty United States 54 907 0.4× 1.7k 0.8× 3.3k 1.9× 955 0.6× 2.6k 2.2× 135 9.4k
Paul C. Norris United States 30 1.2k 0.5× 960 0.5× 1.2k 0.7× 1.1k 0.7× 423 0.4× 46 3.6k
Takayoshi Suganami Japan 54 1.1k 0.4× 1.2k 0.6× 3.0k 1.7× 436 0.3× 2.5k 2.2× 121 9.6k
Hang Shi United States 44 802 0.3× 1.6k 0.8× 3.2k 1.9× 611 0.4× 3.6k 3.1× 103 9.4k

Countries citing papers authored by Matthew Spite

Since Specialization
Citations

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

Fields of papers citing papers by Matthew Spite

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Matthew Spite

This figure shows the co-authorship network connecting the top 25 collaborators of Matthew Spite. A scholar is included among the top collaborators of Matthew Spite 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 Spite. Matthew Spite 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.
Zheng, Jing‐Juan, Nolan L. Boyd, Brian E. Sansbury, et al.. (2025). Exercise-Stimulated Resolvin Biosynthesis in the Adipose Tissue Is Abrogated by High-Fat Diet–Induced Adrenergic Deficiency. Arteriosclerosis Thrombosis and Vascular Biology. 45(7). 1090–1110.
2.
Chen, Mian, et al.. (2024). Dynamic changes in proresolving lipid mediators and their receptors following acute vascular injury in male rats. Physiological Reports. 12(15). e16178–e16178. 3 indexed citations
3.
Berrueta, Lisbeth, Daniel Martı́n, Rebecca Thompson, et al.. (2023). Effect of stretching on inflammation in a subcutaneous carrageenan mouse model analyzed at single‐cell resolution. Journal of Cellular Physiology. 238(12). 2778–2793. 4 indexed citations
4.
Reeves, Andrew R., Brian E. Sansbury, Meixia Pan, et al.. (2021). Myeloid-Specific Deficiency of Long-Chain Acyl CoA Synthetase 4 Reduces Inflammation by Remodeling Phospholipids and Reducing Production of Arachidonic Acid–Derived Proinflammatory Lipid Mediators. The Journal of Immunology. 207(11). 2744–2753. 18 indexed citations
5.
Marinello, Michael, Brian E. Sansbury, Sudeshna Sadhu, et al.. (2021). Resolvin D1 Enhances Necroptotic Cell Clearance Through Promoting Macrophage Fatty Acid Oxidation and Oxidative Phosphorylation. Arteriosclerosis Thrombosis and Vascular Biology. 41(3). 1062–1075. 56 indexed citations
6.
Sansbury, Brian E., Xiaofeng Li, Blenda Wong, et al.. (2021). PCTR1 Enhances Repair and Bacterial Clearance in Skin Wounds. American Journal Of Pathology. 191(6). 1049–1063. 12 indexed citations
7.
Sadhu, Sudeshna, Brian E. Sansbury, Michael Marinello, et al.. (2021). Radiation-Induced Macrophage Senescence Impairs Resolution Programs and Drives Cardiovascular Inflammation. The Journal of Immunology. 207(7). 1812–1823. 28 indexed citations
8.
Heffron, Sean, Ada Weinstock, Bianca Scolaro, et al.. (2020). Platelet‐conditioned media induces an anti‐inflammatory macrophage phenotype through EP4. Journal of Thrombosis and Haemostasis. 19(2). 562–573. 19 indexed citations
9.
Ramirez, Joel L., Warren J. Gasper, Greg J. Zahner, et al.. (2019). Fish Oil Increases Specialized Pro-resolving Lipid Mediators in PAD (The OMEGA-PAD II Trial). Journal of Surgical Research. 238. 164–174. 47 indexed citations
10.
Gerlach, Brennan D., Michael Marinello, Brian E. Sansbury, et al.. (2019). Resolvin D1 promotes the targeting and clearance of necroptotic cells. Cell Death and Differentiation. 27(2). 525–539. 100 indexed citations
11.
Hellmann, Jason, Brian E. Sansbury, Blenda Wong, et al.. (2018). Biosynthesis of D-Series Resolvins in Skin Provides Insights into their Role in Tissue Repair. Journal of Investigative Dermatology. 138(9). 2051–2060. 63 indexed citations
12.
Colby, Jennifer K., Raja-Elie E. Abdulnour, Ho Pan Sham, et al.. (2016). Resolvin D3 and Aspirin-Triggered Resolvin D3 Are Protective for Injured Epithelia. American Journal Of Pathology. 186(7). 1801–1813. 48 indexed citations
13.
Varga, Tamás, Rémi Mounier, Andreas Patsalos, et al.. (2016). Macrophage PPARγ, a Lipid Activated Transcription Factor Controls the Growth Factor GDF3 and Skeletal Muscle Regeneration. Immunity. 45(5). 1038–1051. 138 indexed citations
14.
Hellmann, Jason, Yunan Tang, Michael J. Zhang, et al.. (2015). Atf3 negatively regulates Ptgs2/Cox2 expression during acute inflammation. Prostaglandins & Other Lipid Mediators. 116-117. 49–56. 52 indexed citations
15.
Spite, Matthew. (2013). Deciphering the role of n-3 polyunsaturated fatty acid-derived lipid mediators in health and disease. Proceedings of The Nutrition Society. 72(4). 441–450. 18 indexed citations
16.
Spite, Matthew, Joan Clària, & Charles N. Serhan. (2013). Resolvins, Specialized Proresolving Lipid Mediators, and Their Potential Roles in Metabolic Diseases. Cell Metabolism. 19(1). 21–36. 354 indexed citations
17.
Sansbury, Brian E., Timothy D. Cummins, Yunan Tang, et al.. (2012). Overexpression of Endothelial Nitric Oxide Synthase Prevents Diet-Induced Obesity and Regulates Adipocyte Phenotype. Circulation Research. 111(9). 1176–1189. 122 indexed citations
18.
Hellmann, Jason, Yunan Tang, & Matthew Spite. (2012). Proresolving lipid mediators and diabetic wound healing. Current Opinion in Endocrinology Diabetes and Obesity. 19(2). 104–108. 33 indexed citations
19.
Ho, Karen J., Matthew Spite, Christopher Owens, et al.. (2010). Aspirin-Triggered Lipoxin and Resolvin E1 Modulate Vascular Smooth Muscle Phenotype and Correlate with Peripheral Atherosclerosis. American Journal Of Pathology. 177(4). 2116–2123. 173 indexed citations
20.
Srivastava, Sanjay, Matthew Spite, John O. Trent, et al.. (2004). Aldose Reductase-catalyzed Reduction of Aldehyde Phospholipids. Journal of Biological Chemistry. 279(51). 53395–53406. 59 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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