Pantelis Tsoulfas

5.9k total citations
62 papers, 4.7k citations indexed

About

Pantelis Tsoulfas is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Developmental Neuroscience. According to data from OpenAlex, Pantelis Tsoulfas has authored 62 papers receiving a total of 4.7k indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Cellular and Molecular Neuroscience, 33 papers in Molecular Biology and 24 papers in Developmental Neuroscience. Recurrent topics in Pantelis Tsoulfas's work include Nerve injury and regeneration (33 papers), Neurogenesis and neuroplasticity mechanisms (24 papers) and Spinal Cord Injury Research (11 papers). Pantelis Tsoulfas is often cited by papers focused on Nerve injury and regeneration (33 papers), Neurogenesis and neuroplasticity mechanisms (24 papers) and Spinal Cord Injury Research (11 papers). Pantelis Tsoulfas collaborates with scholars based in United States, Italy and Japan. Pantelis Tsoulfas's co-authors include Luis F. Parada, Lino Tessarollo, Scott R. Whittemore, Winston Walters, Kai Zinn, Jae K. Lee, Leonard G. Presta, Kevin K. Park, Dan Soppet and Roman Urfer and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Pantelis Tsoulfas

60 papers receiving 4.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Pantelis Tsoulfas United States 38 2.6k 2.1k 1.6k 790 512 62 4.7k
Clas B. Johansson Sweden 19 1.6k 0.6× 2.1k 1.0× 2.5k 1.5× 406 0.5× 812 1.6× 22 4.4k
Takuya Shimazaki Japan 32 1.4k 0.6× 2.7k 1.3× 2.0k 1.2× 451 0.6× 768 1.5× 61 5.1k
Bernard Rogister Belgium 40 1.7k 0.6× 2.2k 1.1× 1.3k 0.8× 433 0.5× 1.2k 2.3× 138 5.3k
Christian Göritz Sweden 22 2.0k 0.8× 2.1k 1.0× 1.9k 1.2× 731 0.9× 474 0.9× 30 5.2k
Jasodhara Ray United States 26 2.2k 0.9× 2.8k 1.4× 3.1k 1.9× 321 0.4× 556 1.1× 36 5.3k
Cynthia Wetmore United States 37 2.6k 1.0× 2.5k 1.2× 1.6k 1.0× 286 0.4× 1.1k 2.1× 86 5.6k
Shuxin Li United States 25 2.5k 1.0× 1.1k 0.6× 1.3k 0.8× 1.2k 1.5× 181 0.4× 48 3.7k
David Prevette United States 42 3.4k 1.3× 2.8k 1.3× 1.8k 1.1× 495 0.6× 837 1.6× 61 5.9k
Ann M. Turnley Australia 37 1.6k 0.6× 1.6k 0.8× 1.4k 0.8× 360 0.5× 227 0.4× 86 4.3k

Countries citing papers authored by Pantelis Tsoulfas

Since Specialization
Citations

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

Fields of papers citing papers by Pantelis Tsoulfas

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Pantelis Tsoulfas

This figure shows the co-authorship network connecting the top 25 collaborators of Pantelis Tsoulfas. A scholar is included among the top collaborators of Pantelis Tsoulfas 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 Pantelis Tsoulfas. Pantelis Tsoulfas 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.
Dvoryanchikov, Gennady, et al.. (2022). Selectively Imaging Cranial Sensory Ganglion Neurons Using AAV-PHP.S. eNeuro. 9(3). ENEURO.0373–21.2022. 6 indexed citations
2.
Milich, Lindsay M., James S. Choi, Susana R. Cerqueira, et al.. (2021). Single-cell analysis of the cellular heterogeneity and interactions in the injured mouse spinal cord. The Journal of Experimental Medicine. 218(8). 171 indexed citations
3.
Blackmore, Murray G., et al.. (2021). Widening spinal injury research to consider all supraspinal cell types: Why we must and how we can. Experimental Neurology. 346. 113862–113862. 6 indexed citations
4.
Campbell, Benjamin C., Elisa M. Nabel, Mitchell H. Murdock, et al.. (2020). mGreenLantern: a bright monomeric fluorescent protein with rapid expression and cell filling properties for neuronal imaging. Proceedings of the National Academy of Sciences. 117(48). 30710–30721. 93 indexed citations
5.
Bray, Eric R., et al.. (2017). 3D Visualization of Individual Regenerating Retinal Ganglion Cell Axons Reveals Surprisingly Complex Growth Paths. eNeuro. 4(4). ENEURO.0093–17.2017. 37 indexed citations
6.
Soderblom, Cynthia, Do-Hun Lee, Andrea J. Santamaría, et al.. (2015). 3D Imaging of Axons in Transparent Spinal Cords from Rodents and Nonhuman Primates. eNeuro. 2(2). ENEURO.0001–15.2015. 54 indexed citations
8.
Kitay, Brandon M., Ryan McCormack, Yunfang Wang, Pantelis Tsoulfas, & R. Grace Zhai. (2013). Mislocalization of neuronal mitochondria reveals regulation of Wallerian degeneration and NMNAT/WLDS-mediated axon protection independent of axonal mitochondria. Human Molecular Genetics. 22(8). 1601–1614. 57 indexed citations
9.
Kumagai, Gentaro, Pantelis Tsoulfas, Satoshi Toh, et al.. (2013). Genetically modified mesenchymal stem cells (MSCs) promote axonal regeneration and prevent hypersensitivity after spinal cord injury. Experimental Neurology. 248. 369–380. 62 indexed citations
10.
Enomoto, Mitsuhiro, Mary Bartlett Bunge, & Pantelis Tsoulfas. (2013). A multifunctional neurotrophin with reduced affinity to p75NTR enhances transplanted Schwann cell survival and axon growth after spinal cord injury. Experimental Neurology. 248. 170–182. 50 indexed citations
11.
Rotundo, Richard L., et al.. (2008). Assembly and regulation of acetylcholinesterase at the vertebrate neuromuscular junction. Chemico-Biological Interactions. 175(1-3). 26–29. 22 indexed citations
12.
Abdellatif, Ahmed, Richard Benton, Russell M. Howard, et al.. (2006). Gene delivery to the spinal cord: Comparison between lentiviral, adenoviral, and retroviral vector delivery systems. Journal of Neuroscience Research. 84(3). 553–567. 52 indexed citations
13.
Cao, Qilin, Xiao‐Ming Xu, William H. DeVries, et al.. (2005). Functional Recovery in Traumatic Spinal Cord Injury after Transplantation of Multineurotrophin-Expressing Glial-Restricted Precursor Cells. Journal of Neuroscience. 25(30). 6947–6957. 233 indexed citations
14.
Enzmann, Gaby, Richard Benton, John P. Woock, et al.. (2005). Consequences of noggin expression by neural stem, glial, and neuronal precursor cells engrafted into the injured spinal cord. Experimental Neurology. 195(2). 293–304. 59 indexed citations
15.
Lin, Michelle I., et al.. (2000). Trk C Receptor Signaling Regulates Cardiac Myocyte Proliferation during Early Heart Development in Vivo. Developmental Biology. 226(2). 180–191. 47 indexed citations
16.
Panchision, David M., Patricia A. Martin‐DeLeon, Takao Takeshima, et al.. (1998). An Immortalized, Type-1 Astrocyte of Mescencephalic Origin Source of a Dopaminergic Neurotrophic Factor. Journal of Molecular Neuroscience. 11(3). 209–222. 26 indexed citations
17.
Tessarollo, Lino, Pantelis Tsoulfas, Michael J. Donovan, et al.. (1997). Targeted deletion of all isoforms of the trkC gene suggests the use of alternate receptors by its ligand neurotrophin-3 in neuronal development and implicates trkC in normal cardiogenesis. Proceedings of the National Academy of Sciences. 94(26). 14776–14781. 170 indexed citations
18.
Tsoulfas, Pantelis, Robert M. Stephens, David R. Kaplan, & Luis F. Parada. (1996). TrkC Isoforms with Inserts in the Kinase Domain Show Impaired Signaling Responses. Journal of Biological Chemistry. 271(10). 5691–5697. 65 indexed citations
19.
Tessarollo, Lino, Pantelis Tsoulfas, Dionisio Martín‐Zanca, et al.. (1993). trkC, a receptor for neurotrophin-3, is widely expressed in the developing nervous system and in non-neuronal tissues. Development. 118(2). 463–475. 259 indexed citations
20.
Buvoli, Massimo, Giuseppe Biamonti, Pantelis Tsoulfas, et al.. (1988). cDNA cloning of human hnRNP protein Al reveals the existence of multiple mRNA isoforms. Nucleic Acids Research. 16(9). 3751–3770. 105 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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