Ronald L. Hayes

25.3k total citations · 3 hit papers
314 papers, 19.8k citations indexed

About

Ronald L. Hayes is a scholar working on Neurology, Molecular Biology and Epidemiology. According to data from OpenAlex, Ronald L. Hayes has authored 314 papers receiving a total of 19.8k indexed citations (citations by other indexed papers that have themselves been cited), including 187 papers in Neurology, 141 papers in Molecular Biology and 108 papers in Epidemiology. Recurrent topics in Ronald L. Hayes's work include Traumatic Brain Injury and Neurovascular Disturbances (176 papers), Traumatic Brain Injury Research (82 papers) and S100 Proteins and Annexins (68 papers). Ronald L. Hayes is often cited by papers focused on Traumatic Brain Injury and Neurovascular Disturbances (176 papers), Traumatic Brain Injury Research (82 papers) and S100 Proteins and Annexins (68 papers). Ronald L. Hayes collaborates with scholars based in United States, Italy and Austria. Ronald L. Hayes's co-authors include Kevin Wang, Guy L. Clifton, David J. Mayer, Bruce G. Lyeth, C. Edward Dixon, Donald D. Price, Robert J. Hamm, Larry W. Jenkins, G. Bruce Pike and Xiurong Zhao and has published in prestigious journals such as Science, Circulation and Analytical Chemistry.

In The Last Decade

Ronald L. Hayes

311 papers receiving 19.2k citations

Hit Papers

A controlled cortical imp... 1978 2026 1994 2010 1991 1987 1978 250 500 750

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ronald L. Hayes United States 82 10.8k 7.8k 6.6k 4.3k 3.5k 314 19.8k
W. Dalton Dietrich United States 90 10.5k 1.0× 9.0k 1.2× 5.3k 0.8× 6.2k 1.4× 3.6k 1.0× 420 32.0k
Ann C. McKee United States 70 10.8k 1.0× 5.1k 0.6× 8.4k 1.3× 2.9k 0.7× 5.0k 1.4× 236 22.3k
David A. Hovda United States 77 12.2k 1.1× 4.0k 0.5× 9.2k 1.4× 2.8k 0.6× 1.3k 0.4× 214 19.2k
John T. Povlishock United States 59 7.6k 0.7× 3.7k 0.5× 5.2k 0.8× 1.8k 0.4× 671 0.2× 132 11.5k
Linda J. Noble‐Haeusslein United States 57 4.2k 0.4× 4.5k 0.6× 2.6k 0.4× 2.7k 0.6× 1.1k 0.3× 132 13.5k
Esther Shohami Israel 64 4.3k 0.4× 5.0k 0.6× 2.4k 0.4× 3.0k 0.7× 2.1k 0.6× 238 14.7k
Patrick G. Sullivan United States 66 4.0k 0.4× 6.3k 0.8× 2.3k 0.3× 2.3k 0.5× 3.1k 0.9× 183 12.9k
Kathryn E. Saatman United States 57 5.2k 0.5× 3.3k 0.4× 3.4k 0.5× 1.5k 0.4× 927 0.3× 132 9.1k
C. Edward Dixon United States 56 6.0k 0.6× 3.6k 0.5× 3.8k 0.6× 1.4k 0.3× 638 0.2× 154 10.0k
Robert Vink Australia 55 5.6k 0.5× 3.5k 0.5× 3.1k 0.5× 2.0k 0.5× 910 0.3× 210 10.9k

Countries citing papers authored by Ronald L. Hayes

Since Specialization
Citations

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

Fields of papers citing papers by Ronald L. Hayes

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ronald L. Hayes. 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 Ronald L. Hayes. The network helps show where Ronald L. Hayes may publish in the future.

Co-authorship network of co-authors of Ronald L. Hayes

This figure shows the co-authorship network connecting the top 25 collaborators of Ronald L. Hayes. A scholar is included among the top collaborators of Ronald L. Hayes 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 Ronald L. Hayes. Ronald L. Hayes 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.
Schully, Kevin L., Melissa K. Gregory, Joost Brandsma, et al.. (2024). Retrospective Analysis of Blood Biomarkers of Neurological Injury in Human Cases of Viral Infection and Bacterial Sepsis. The Journal of Infectious Diseases. 231(3). 805–815.
2.
Chen, Hui, Victoria Y. Ding, Guangming Zhu, et al.. (2022). Association between Blood and Computed Tomographic Imaging Biomarkers in a Cohort of Mild Traumatic Brain Injury Patients. Journal of Neurotrauma. 39(19-20). 1329–1338. 7 indexed citations
3.
Osier, Nicole Danielle, Helen M. Bramlett, Deborah A. Shear, et al.. (2021). Kollidon VA64 Treatment in Traumatic Brain Injury: Operation Brain Trauma Therapy. Journal of Neurotrauma. 38(17). 2454–2472. 4 indexed citations
4.
Jha, Ruchira M., Stefania Mondello, Helen M. Bramlett, et al.. (2020). Glibenclamide Treatment in Traumatic Brain Injury: Operation Brain Trauma Therapy. Journal of Neurotrauma. 38(5). 628–645. 19 indexed citations
5.
Glushakova, Olena, Cesar V. Borlongan, Alex B. Valadka, et al.. (2017). Role of Caspase-3-Mediated Apoptosis in Chronic Caspase-3-Cleaved Tau Accumulation and Blood–Brain Barrier Damage in the Corpus Callosum after Traumatic Brain Injury in Rats. Journal of Neurotrauma. 35(1). 157–173. 72 indexed citations
6.
Glushakova, Olena, et al.. (2015). Acute Temporal Profiles of Serum Levels of UCH-L1 and GFAP and Relationships to Neuronal and Astroglial Pathology following Traumatic Brain Injury in Rats. Journal of Neurotrauma. 32(16). 1179–1189. 51 indexed citations
7.
Tóth, Arnold, Ilona M. Schmalfuss, Shelley C. Heaton, et al.. (2015). Lateral Ventricle Volume Asymmetry Predicts Midline Shift in Severe Traumatic Brain Injury. Journal of Neurotrauma. 32(17). 1307–1311. 9 indexed citations
9.
Papa, Linda, Salvatore Silvestri, Gretchen M. Brophy, et al.. (2014). GFAP Out-Performs S100β in Detecting Traumatic Intracranial Lesions on Computed Tomography in Trauma Patients with Mild Traumatic Brain Injury and Those with Extracranial Lesions. Journal of Neurotrauma. 31(22). 1815–1822. 140 indexed citations
10.
Brophy, Gretchen M., Stefania Mondello, Linda Papa, et al.. (2011). Biokinetic Analysis of Ubiquitin C-Terminal Hydrolase-L1 (UCH-L1) in Severe Traumatic Brain Injury Patient Biofluids. Journal of Neurotrauma. 28(6). 861–870. 164 indexed citations
11.
Mondello, Stefania, Andreas Jeromin, Jackson Streeter, et al.. (2011). Abstract 13492: Glial Fibrillary Acidic Protein, a Sensitive and Specific Marker in Serum for the Identification of Intracerebral Hemorrhage in Acute Stroke Patients: Results of Improved Assay Performance. Circulation. 124. 1 indexed citations
12.
Svetlov, Stanislav I., Stephen F. Larner, Daniel Kirk, et al.. (2009). Biomarkers of Blast-Induced Neurotrauma: Profiling Molecular and Cellular Mechanisms of Blast Brain Injury. Journal of Neurotrauma. 26(6). 913–921. 72 indexed citations
13.
Mazzeo, Anna Teresa, Gretchen M. Brophy, Charlotte Gilman, et al.. (2009). Safety and Tolerability of Cyclosporin A in Severe Traumatic Brain Injury Patients: Results from a Prospective Randomized Trial. Journal of Neurotrauma. 26(12). 2195–2206. 78 indexed citations
14.
Sadasivan, Shankar, William A. Dunn, Ronald L. Hayes, & Kevin Wang. (2008). Changes in autophagy proteins in a rat model of controlled cortical impact induced brain injury. Biochemical and Biophysical Research Communications. 373(4). 478–481. 47 indexed citations
15.
Crawford, Fiona, Scott Ferguson, Venkatarajan S. Mathura, et al.. (2007). Genomic analysis of response to traumatic brain injury in a mouse model of Alzheimer's disease (APPsw). Brain Research. 1185. 45–58. 15 indexed citations
16.
Svetlov, Stanislav I., Monika W. Oli, David P. Foley, et al.. (2006). Identification and preliminary validation of novel biomarkers of acute hepatic ischaemia/reperfusion injury using dual-platform proteomic/degradomic approaches. Biomarkers. 11(4). 355–369. 34 indexed citations
17.
Svetlov, Stanislav I., Т Н Игнатова, Kevin Wang, et al.. (2004). Lysophosphatidic Acid Induces Clonal Generation of Mouse Neurospheres via Proliferation of Sca-1- and AC133-Positive Neural Progenitors. Stem Cells and Development. 13(6). 685–693. 36 indexed citations
18.
Posmantur, Rand, A. Kampfl, William C. Taft, et al.. (1996). Diminished Microtubule-Associated Protein 2 (MAP2) Immunoreactivity following Cortical Impact Brain Injury. Journal of Neurotrauma. 13(3). 125–137. 75 indexed citations
19.
Miller, Leonard P., Bruce G. Lyeth, Larry W. Jenkins, et al.. (1990). Excitatory amino acid receptor subtype binding following traumatic brain injury. Brain Research. 526(1). 103–107. 116 indexed citations
20.
Hayes, Ronald L., Y. Katayama, Larry W. Jenkins, et al.. (1988). Regional Rates of Glucose Utilization in the Cat Following Concussive Head Injury. Journal of Neurotrauma. 5(2). 121–137. 48 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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