David F. Tate
About
David F. Tate is a scholar working on Epidemiology, Neurology and Emergency Medicine.
According to data from OpenAlex, David F. Tate has authored 145 papers receiving a total of 5.4k indexed citations (citations by other indexed papers that have themselves been cited), including 66 papers in Epidemiology, 40 papers in Neurology and 38 papers in Emergency Medicine. Recurrent topics in David F. Tate's work include Traumatic Brain Injury Research (59 papers), Traumatic Brain Injury and Neurovascular Disturbances (40 papers) and Cardiac Arrest and Resuscitation (28 papers). David F. Tate is often cited by papers focused on Traumatic Brain Injury Research (59 papers), Traumatic Brain Injury and Neurovascular Disturbances (40 papers) and Cardiac Arrest and Resuscitation (28 papers). David F. Tate collaborates with scholars based in United States, Australia and United Kingdom. David F. Tate's co-authors include Robert Paul, Ronald A. Cohen, John Gunstad, Evian Gordon, Erin D. Bigler, Mary Beth Spitznagel, Angela L. Jefferson, Adam M. Brickman, Erin D. Bigler and Karin F. Hoth and has published in prestigious journals such as PLoS ONE, NeuroImage and Neurology.
In The Last Decade
David F. Tate
141 papers receiving 5.3k citations
Hit Papers
Peers — A (Enhanced Table)
Peers by citation overlap · career bar shows stage (early→late) cites · hero ref
| Name | h | Career | Trend | Papers | Cites | |||||
|---|---|---|---|---|---|---|---|---|---|---|
| David F. Tate United States | 42 | 1.4k | 1.2k | 1.0k | 984 | 867 | 145 | 5.4k | ||
| Amy J. Jak United States | 41 | 1.2k 0.9× | 1.9k 1.6× | 2.9k 2.8× | 714 0.7× | 785 0.9× | 144 | 5.9k | ||
| Nancy D. Chiaravalloti United States | 50 | 1.3k 0.9× | 1.7k 1.4× | 1.6k 1.6× | 2.0k 2.0× | 530 0.6× | 220 | 8.6k | ||
| David J. Schretlen United States | 54 | 1.9k 1.3× | 3.2k 2.8× | 3.0k 2.9× | 1.5k 1.5× | 1.0k 1.2× | 166 | 10.1k | ||
| Sandra B. Chapman United States | 42 | 2.5k 1.7× | 2.2k 1.9× | 1.4k 1.4× | 844 0.9× | 326 0.4× | 149 | 5.9k | ||
| Lisa Delano‐Wood United States | 43 | 1.1k 0.8× | 1.6k 1.4× | 3.5k 3.5× | 857 0.9× | 934 1.1× | 154 | 6.4k | ||
| Molly E. Zimmerman United States | 46 | 1.3k 0.9× | 2.0k 1.7× | 3.1k 3.1× | 1.0k 1.0× | 1.2k 1.4× | 130 | 7.2k | ||
| David B. Arciniegas United States | 43 | 2.4k 1.6× | 971 0.8× | 1.1k 1.1× | 2.2k 2.2× | 364 0.4× | 154 | 5.4k | ||
| Ola A. Selnes United States | 59 | 1.5k 1.0× | 1.9k 1.7× | 2.0k 2.0× | 763 0.8× | 483 0.6× | 146 | 12.2k | ||
| Susanna Hinkka‐Yli‐Salomäki Finland | 38 | 571 0.4× | 1.1k 0.9× | 899 0.9× | 636 0.6× | 274 0.3× | 112 | 4.8k | ||
| Ronald M. Lazar United States | 51 | 1.9k 1.3× | 2.0k 1.8× | 1.1k 1.1× | 1.7k 1.8× | 712 0.8× | 144 | 8.5k |
Countries citing papers authored by David F. Tate
Since
Specialization
Citations
This map shows the geographic impact of David F. Tate'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 David F. Tate with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites David F. Tate more than expected).
Fields of papers citing papers by David F. Tate
Since
Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences
This network shows the impact of papers produced by David F. Tate. 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 David F. Tate. The network helps show where David F. Tate may publish in the future.
Co-authorship network of co-authors of David F. Tate
This figure shows the co-authorship network connecting the top 25 collaborators of David F. Tate. A scholar is included among the top collaborators of David F. Tate 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 David F. Tate. David F. Tate is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
1.
Wade, Benjamin, David F. Tate, Eamonn Kennedy, et al.. (2023). Microstructural Organization of Distributed White Matter Associated With Fine Motor Control in US Service Members With Mild Traumatic Brain Injury. Journal of Neurotrauma. 41(1-2). 32–40.
2.
Kennedy, Eamonn, Erin D. Bouldin, Samin Panahi, et al.. (2023). Phenotyping Depression After Mild Traumatic Brain Injury: Evaluating the Impact of Multiple Injury, Gender, and Injury Context. Journal of Neurotrauma. 41(7-8). 924–933.
3.
Tate, David F., Emily L. Dennis, Hannah M. Lindsey, & Elisabeth A. Wilde. (2023). Harmonization of neuropsychological and other clinical endpoints: Pitfalls and possibilities.. Neuropsychology. 37(3). 233–236.
4.
Merkley, Tricia L., Carrie Esopenko, Robert M. Bilder, et al.. (2022). Challenges and opportunities for harmonization of cross-cultural neuropsychological data.. Neuropsychology. 37(3). 237–246.
5.
Esopenko, Carrie, J. Scott Parrott, Tricia L. Merkley, et al.. (2022). Discriminating Mild Traumatic Brain Injury and Posttraumatic Stress Disorder Using Latent Neuroimaging and Neuropsychological Profiles in Active-Duty Military Service Members. Journal of Head Trauma Rehabilitation. 38(4). E254–E266.
6.
Kennedy, Jan E., Douglas B. Cooper, Glenn Curtiss, et al.. (2022). Research Letter: Long-Term Outcomes Following Cognitive Rehabilitation for Mild Traumatic Brain Injury: A 5-Year Follow-Up of a Cohort From the SCORE Randomized Clinical Trial. Journal of Head Trauma Rehabilitation. 37(6). 390–395.
7.
Fino, Peter C., Leland E. Dibble, Elisabeth A. Wilde, et al.. (2022). Sensory Phenotypes for Balance Dysfunction After Mild Traumatic Brain Injury. Neurology. 99(5). e521–e535.
8.
Esopenko, Carrie, J. Scott Parrott, Tricia L. Merkley, et al.. (2022). Latent Neuropsychological Profiles to Discriminate Mild Traumatic Brain Injury and Posttraumatic Stress Disorder in Active-Duty Service Members. Journal of Head Trauma Rehabilitation. 37(6). E438–E448.
9.
Allen, Mark D., Dana Waltzman, Kelly Sarmiento, et al.. (2020). Neuroimaging in Pediatric Patients with Mild Traumatic Brain Injury: Relating the Current 2018 Centers for Disease Control Guideline and the Potential of Advanced Neuroimaging Modalities for Research and Clinical Biomarker Development. Journal of Neurotrauma. 38(1). 44–52.
10.
Bouldin, Erin D., Alicia A. Swan, Rocío Norman, et al.. (2020). Health Phenotypes and Neurobehavioral Symptom Severity Among Post-9/11 Veterans With Mild Traumatic Brain Injury: A Chronic Effects of Neurotrauma Consortium Study. Journal of Head Trauma Rehabilitation. 36(1). 10–19.
11.
Cooper, Douglas B., Glenn Curtiss, Patrick Armistead‐Jehle, et al.. (2018). Neuropsychological Performance and Subjective Symptom Reporting in Military Service Members With a History of Multiple Concussions: Comparison With a Single Concussion, Posttraumatic Stress Disorder, and Orthopedic Trauma. Journal of Head Trauma Rehabilitation. 33(2). 81–90.
12.
Bolzenius, Jacob, Carmen Vélez, Jeffrey D. Lewis, et al.. (2018). Diffusion Imaging Findings in US Service Members With Mild Traumatic Brain Injury and Posttraumatic Stress Disorder. Journal of Head Trauma Rehabilitation. 33(6). 393–402.
13.
Bolzenius, Jacob, Benjamin Wade, Carmen Vélez, et al.. (2018). Relationships Between Subcortical Shape Measures and Subjective Symptom Reporting in US Service Members With Mild Traumatic Brain Injury. Journal of Head Trauma Rehabilitation. 33(2). 113–122.
14.
Cooper, Douglas B., Amy O. Bowles, Jan E. Kennedy, et al.. (2016). Cognitive Rehabilitation for Military Service Members With Mild Traumatic Brain Injury: A Randomized Clinical Trial. Journal of Head Trauma Rehabilitation. 32(3). E1–E15.
15.
Koerte, Inga K., Alexander Lin, Marc Muehlmann, et al.. (2015). A Review of Neuroimaging Findings in Repetitive Brain Trauma. Brain Pathology. 25(3). 318–349.
16.
Hua, Xue, Christina P. Boyle, Jaroslaw Harezlak, et al.. (2013). Disrupted cerebral metabolite levels and lower nadir CD4 + counts are linked to brain volume deficits in 210 HIV-infected patients on stable treatmentpatients on stable treatment. NeuroImage Clinical. 3. 132–142.
17.
Tate, David F., et al.. (2011). The Role of Medical Imaging in Defining CNS Abnormalities Associated with HIV-Infection and Opportunistic Infections. Neurotherapeutics. 8(1). 103–116.
18.
Paul, Robert, Snigdha Vallabhaneni, N. Kumarasamy, et al.. (2006). Neurocognitive consequences of HIV in southern India: A preliminary study of clade C virus. Journal of the International Neuropsychological Society. 12(3). 424–430.
19.
Tate, David F., Robert Paul, Timothy Flanigan, et al.. (2003). The Impact of Apathy and Depression on Quality of Life in Patients Infected with HIV. AIDS Patient Care and STDs. 17(3). 115–120.
20.
Bigler, Erin D. & David F. Tate. (2001). Brain Volume, Intracranial Volume, and Dementia. Investigative Radiology. 36(9). 539–546.
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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