Joseph L. Cheatwood

1.1k total citations
29 papers, 820 citations indexed

About

Joseph L. Cheatwood is a scholar working on Cellular and Molecular Neuroscience, Cognitive Neuroscience and Neurology. According to data from OpenAlex, Joseph L. Cheatwood has authored 29 papers receiving a total of 820 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Cellular and Molecular Neuroscience, 9 papers in Cognitive Neuroscience and 8 papers in Neurology. Recurrent topics in Joseph L. Cheatwood's work include Nerve injury and regeneration (5 papers), Memory and Neural Mechanisms (5 papers) and Neuroscience and Neuropharmacology Research (4 papers). Joseph L. Cheatwood is often cited by papers focused on Nerve injury and regeneration (5 papers), Memory and Neural Mechanisms (5 papers) and Neuroscience and Neuropharmacology Research (4 papers). Joseph L. Cheatwood collaborates with scholars based in United States, Switzerland and Canada. Joseph L. Cheatwood's co-authors include Gwendolyn L. Kartje, Roger L. Reep, James V. Corwin, April J. Emerick, Martin E. Schwab, Elliott R. Jacobson, Lara K. Maxwell, Shih‐Yen Tsai, Douglas G. Wallace and Bryan Kolb and has published in prestigious journals such as The Journal of Comparative Neurology, Stroke and Brain Research.

In The Last Decade

Joseph L. Cheatwood

29 papers receiving 801 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 L. Cheatwood United States 15 361 232 202 119 114 29 820
Ravi Tolwani United States 17 315 0.9× 72 0.3× 97 0.5× 149 1.3× 384 3.4× 33 1.1k
Krzysztof Turlejski Poland 18 466 1.3× 365 1.6× 132 0.7× 233 2.0× 260 2.3× 67 1.1k
Liliane Astic France 22 893 2.5× 416 1.8× 85 0.4× 153 1.3× 182 1.6× 45 2.0k
Catherine A. Smith United States 17 191 0.5× 302 1.3× 295 1.5× 94 0.8× 314 2.8× 26 1.5k
Erin MacDonald Canada 10 231 0.6× 174 0.8× 198 1.0× 15 0.1× 71 0.6× 16 723
Denis Combes France 17 397 1.1× 250 1.1× 103 0.5× 35 0.3× 103 0.9× 28 720
George Székely Hungary 14 193 0.5× 210 0.9× 81 0.4× 41 0.3× 145 1.3× 25 634
David E. Strochlic United States 9 445 1.2× 236 1.0× 211 1.0× 26 0.2× 605 5.3× 9 2.2k
N. Corvaja Italy 16 304 0.8× 99 0.4× 372 1.8× 39 0.3× 236 2.1× 33 842
Carla Lucini Italy 16 457 1.3× 30 0.1× 54 0.3× 300 2.5× 203 1.8× 81 899

Countries citing papers authored by Joseph L. Cheatwood

Since Specialization
Citations

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

Fields of papers citing papers by Joseph L. Cheatwood

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Joseph L. Cheatwood

This figure shows the co-authorship network connecting the top 25 collaborators of Joseph L. Cheatwood. A scholar is included among the top collaborators of Joseph L. Cheatwood 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 L. Cheatwood. Joseph L. Cheatwood 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
2.
Whishaw, Ian Q., et al.. (2023). Impairments and compensation in string-pulling after middle cerebral artery occlusion in the rat. Behavioural Brain Research. 450. 114469–114469. 3 indexed citations
3.
Knapp, Austen, Dustie N. Butteiger, William J. Banz, et al.. (2021). Effects of Dietary Soy Protein Isolate Versus Isoflavones Alone on Poststroke Skilled Ladder Rung Walking and Cortical mRNA Expression Differ in Adult Male Rats. Journal of Medicinal Food. 25(2). 158–165. 6 indexed citations
4.
Cheatwood, Joseph L., et al.. (2017). Unilateral lesions of the dorsocentral striatum (DCS) disrupt spatial and temporal characteristics of food protection behavior. Brain Structure and Function. 222(6). 2697–2710. 3 indexed citations
6.
Winter, Shawn S., et al.. (2016). The medial frontal cortex contributes to but does not organize rat exploratory behavior. Neuroscience. 336. 1–11. 10 indexed citations
7.
Davis, Matthew, et al.. (2015). Rhox8 Ablation in the Sertoli Cells Using a Tissue-Specific RNAi Approach Results in Impaired Male Fertility in Mice1. Biology of Reproduction. 93(1). 8–8. 23 indexed citations
8.
Cheatwood, Joseph L., et al.. (2015). Cholinergic deafferentation of the hippocampus causes non-temporally graded retrograde amnesia in an odor discrimination task. Behavioural Brain Research. 299. 97–104. 8 indexed citations
9.
Knapp, Austen, et al.. (2013). Subcutaneous daidzein administration enhances recovery of skilled ladder rung walking performance following stroke in rats. Behavioural Brain Research. 256. 428–431. 25 indexed citations
10.
Winter, Shawn S., et al.. (2012). Infusion of GAT1-saporin into the medial septum/vertical limb of the diagonal band disrupts self-movement cue processing and spares mnemonic function. Brain Structure and Function. 218(5). 1099–1114. 15 indexed citations
11.
Farrer, Robert G., et al.. (2010). Dendritic Spine Alterations in Neocortical Pyramidal Neurons following Postnatal Neuronal Nogo-A Knockdown. Developmental Neuroscience. 32(4). 313–320. 14 indexed citations
12.
Reep, Roger L., et al.. (2008). Quantification of synaptic density in corticostriatal projections from rat medial agranular cortex. Brain Research. 1233. 27–34. 6 indexed citations
13.
Cheatwood, Joseph L., April J. Emerick, & Gwendolyn L. Kartje. (2008). Neuronal Plasticity and Functional Recovery After Ischemic Stroke. Topics in Stroke Rehabilitation. 15(1). 42–50. 49 indexed citations
15.
Brenneman, Miranda M., Sebastian Wagner, Joseph L. Cheatwood, et al.. (2007). Nogo-A inhibition induces recovery from neglect in rats. Behavioural Brain Research. 187(2). 262–272. 18 indexed citations
16.
Tsai, Shih‐Yen, Tiffanie Markus, Ellen M. Andrews, et al.. (2007). Intrathecal treatment with anti-Nogo-A antibody improves functional recovery in adult rats after stroke. Experimental Brain Research. 182(2). 261–266. 53 indexed citations
17.
Tsai, Shih‐Yen, Joseph L. Cheatwood, Melanie R. Bollnow, et al.. (2005). Dendritic Plasticity in the Adult Rat Following Middle Cerebral Artery Occlusion and Nogo-A Neutralization. Cerebral Cortex. 16(4). 529–536. 101 indexed citations
18.
Cheatwood, Joseph L., James V. Corwin, & Roger L. Reep. (2005). Overlap and interdigitation of cortical and thalamic afferents to dorsocentral striatum in the rat. Brain Research. 1036(1-2). 90–100. 31 indexed citations
19.
Reep, Roger L., James V. Corwin, Joseph L. Cheatwood, et al.. (2004). A rodent model for investigating the neurobiology of contralateral neglect.. PubMed. 17(4). 191–4. 30 indexed citations
20.
Cheatwood, Joseph L., Roger L. Reep, & James V. Corwin. (2003). The associative striatum: cortical and thalamic projections to the dorsocentral striatum in rats. Brain Research. 968(1). 1–14. 51 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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