Joseph B. Long

5.2k total citations
134 papers, 4.1k citations indexed

About

Joseph B. Long is a scholar working on Neurology, Epidemiology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Joseph B. Long has authored 134 papers receiving a total of 4.1k indexed citations (citations by other indexed papers that have themselves been cited), including 56 papers in Neurology, 55 papers in Epidemiology and 47 papers in Cellular and Molecular Neuroscience. Recurrent topics in Joseph B. Long's work include Traumatic Brain Injury and Neurovascular Disturbances (54 papers), Traumatic Brain Injury Research (53 papers) and Neuropeptides and Animal Physiology (25 papers). Joseph B. Long is often cited by papers focused on Traumatic Brain Injury and Neurovascular Disturbances (54 papers), Traumatic Brain Injury Research (53 papers) and Neuropeptides and Animal Physiology (25 papers). Joseph B. Long collaborates with scholars based in United States, Poland and Japan. Joseph B. Long's co-authors include John W. Holaday, Frank C. Tortella, William C. Mobley, Denes V. Agoston, Alaa Kamnaksh, Richard B. Rothman, Erzsébet Kövesdi, Peethambaran Arun, Richard A. Bauman and Victor Bykov and has published in prestigious journals such as Science, Neuron and SHILAP Revista de lepidopterología.

In The Last Decade

Joseph B. Long

127 papers receiving 3.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Joseph B. Long United States 37 1.6k 1.5k 1.3k 1.3k 701 134 4.1k
Alexander G. Rabchevsky United States 42 1.3k 0.8× 907 0.6× 1.6k 1.3× 507 0.4× 588 0.8× 78 5.3k
Matthias Spranger Germany 30 1.0k 0.7× 980 0.7× 905 0.7× 735 0.6× 717 1.0× 70 4.1k
Andreas Bender Germany 34 1.1k 0.7× 1.8k 1.2× 1.7k 1.3× 1.2k 1.0× 532 0.8× 96 4.5k
Niklas Marklund Sweden 40 862 0.5× 3.2k 2.2× 1.5k 1.1× 1.8k 1.5× 358 0.5× 166 5.5k
Pál Barzó Hungary 26 1.2k 0.8× 1.4k 1.0× 847 0.7× 787 0.6× 153 0.2× 114 3.3k
Marjorie R. Grafe United States 45 1.0k 0.7× 835 0.6× 985 0.8× 638 0.5× 779 1.1× 134 5.9k
José A. Rafols United States 39 1.3k 0.8× 1.1k 0.8× 1.5k 1.2× 648 0.5× 601 0.9× 85 4.7k
Stuart W. Hoffman United States 30 660 0.4× 1.6k 1.1× 1.2k 0.9× 883 0.7× 244 0.3× 44 3.9k
Jonathan Coles United Kingdom 45 691 0.4× 3.3k 2.2× 680 0.5× 1.6k 1.3× 395 0.6× 95 4.6k
J. T. Povlishock United States 33 808 0.5× 3.3k 2.2× 1.4k 1.1× 2.2k 1.7× 444 0.6× 53 5.0k

Countries citing papers authored by Joseph B. Long

Since Specialization
Citations

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

Fields of papers citing papers by Joseph B. Long

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Joseph B. Long. 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 Joseph B. Long. The network helps show where Joseph B. Long may publish in the future.

Co-authorship network of co-authors of Joseph B. Long

This figure shows the co-authorship network connecting the top 25 collaborators of Joseph B. Long. A scholar is included among the top collaborators of Joseph B. Long 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 Joseph B. Long. Joseph B. Long 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
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Govindarajulu, Manoj, et al.. (2025). Longitudinal Dysregulation of Adiponectin and Leptin Following Blast-Induced Polytrauma in a Rat Model. International Journal of Molecular Sciences. 26(14). 6860–6860.
3.
Govindarajulu, Manoj, et al.. (2025). Temporal Dynamics of Retinal Inflammation Following Blast Exposure in a Ferret Model. Neurotrauma Reports. 6(1). 283–290.
4.
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Rhind, Shawn G., Maria Y. Shiu, Catherine Tenn, et al.. (2025). Repetitive Low-Level Blast Exposure Alters Circulating Myeloperoxidase, Matrix Metalloproteinases, and Neurovascular Endothelial Molecules in Experienced Military Breachers. International Journal of Molecular Sciences. 26(5). 1808–1808. 2 indexed citations
6.
Wilder, Donna M., Raina Kumar, George Dimitrov, et al.. (2024). microRNA Profile Changes in Brain, Cerebrospinal Fluid, and Blood Following Low-Level Repeated Blast Exposure in a Rat Model. Journal of Neurotrauma. 42(17-18). 1654–1661. 1 indexed citations
7.
Wang, Ying, Yanling Wei, Ming Ren, et al.. (2024). Blast Exposure Alters Synaptic Connectivity in the Mouse Auditory Cortex. Journal of Neurotrauma. 41(11-12). 1438–1449.
8.
Sajja, Venkata Siva Sai Sujith, et al.. (2023). Comparison of Biomechanical Outcome Measures From Characteristically Different Blast Simulators and the Influence of Exposure Location. Military Medicine. 188(Supplement_6). 288–294. 3 indexed citations
9.
Govindarajulu, Manoj, Donna M. Wilder, Christina R. LaValle, et al.. (2023). Upregulation of multiple toll-like receptors in ferret brain after blast exposure: Potential targets for treatment. Neuroscience Letters. 810. 137364–137364. 5 indexed citations
10.
Arun, Peethambaran, et al.. (2023). Repeated Mild Concussive Events Heighten the Vulnerability of Brain to Blast Exposure. Journal of Neurotrauma. 41(7-8). 1000–1004. 2 indexed citations
11.
Arun, Peethambaran, et al.. (2021). Phosphorylated Neurofilament Heavy Chain in the Cerebrospinal Fluid Is a Suitable Biomarker of Acute and Chronic Blast-Induced Traumatic Brain Injury. Journal of Neurotrauma. 38(20). 2801–2810. 4 indexed citations
12.
Anderson, Laura M., et al.. (2021). The Neurobehavioral Effects of Buprenorphine and Meloxicam on a Blast-Induced Traumatic Brain Injury Model in the Rat. Frontiers in Neurology. 12. 746370–746370. 7 indexed citations
13.
Arun, Peethambaran, Donna M. Wilder, Venkata Siva Sai Sujith Sajja, et al.. (2019). Long-Term Effects of Blast Exposure: A Functional Study in Rats Using an Advanced Blast Simulator. Journal of Neurotrauma. 37(4). 647–655. 41 indexed citations
14.
Wang, Ying, Peethambaran Arun, Yanling Wei, et al.. (2014). Repeated Blast Exposures Cause Brain DNA Fragmentation in Mice. Journal of Neurotrauma. 31(5). 498–504. 25 indexed citations
15.
Wang, Ying, Yanling Wei, Samuel Oguntayo, et al.. (2011). Tightly Coupled Repetitive Blast-Induced Traumatic Brain Injury: Development and Characterization in Mice. Journal of Neurotrauma. 28(10). 2171–2183. 98 indexed citations
16.
Long, Joseph B., et al.. (2009). Blast Overpressure in Rats: Recreating a Battlefield Injury in the Laboratory. Journal of Neurotrauma. 26(6). 827–840. 284 indexed citations
17.
Kochanek, Patrick M., Richard A. Bauman, Joseph B. Long, C. Edward Dixon, & Larry W. Jenkins. (2009). A Critical Problem Begging for New Insight and New Therapies. Journal of Neurotrauma. 26(6). 813–814. 14 indexed citations
18.
Rothman, Richard B., Joseph B. Long, Victor Bykov, et al.. (1991). Upregulation of the opioid receptor complex by the chronic administration of morphine: A biochemical marker related to the development of tolerance and dependence. Peptides. 12(1). 151–160. 54 indexed citations
19.
Long, Joseph B., et al.. (1989). Arginine8-vasopressin reduces spinal cord blood flow after spinal subarachnoid injection in rats.. Journal of Pharmacology and Experimental Therapeutics. 249(2). 499–506. 6 indexed citations
20.
Long, Joseph B., Alberto Martinez‐Arizala, J.M. Petras, & John W. Holaday. (1986). Endogenous Opioids in Spinal Cord Injury: A Critical Evaluation. PubMed. 3(4). 295–315. 17 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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