Yelena Pressman

908 total citations
13 papers, 739 citations indexed

About

Yelena Pressman is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Developmental Neuroscience. According to data from OpenAlex, Yelena Pressman has authored 13 papers receiving a total of 739 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Cellular and Molecular Neuroscience, 5 papers in Molecular Biology and 4 papers in Developmental Neuroscience. Recurrent topics in Yelena Pressman's work include Nerve injury and regeneration (9 papers), Extracellular vesicles in disease (4 papers) and Neurogenesis and neuroplasticity mechanisms (4 papers). Yelena Pressman is often cited by papers focused on Nerve injury and regeneration (9 papers), Extracellular vesicles in disease (4 papers) and Neurogenesis and neuroplasticity mechanisms (4 papers). Yelena Pressman collaborates with scholars based in United States, China and France. Yelena Pressman's co-authors include Mary Bartlett Bunge, Patrick M. Wood, Damien D. Pearse, Raisa Puzis, Francisco C. Pereira, Brandon M. Kitay, Bas Blits, Kevin Golden, Andre R. Sanchez and Christian Andrade and has published in prestigious journals such as Journal of Neuroscience, PLoS ONE and Glia.

In The Last Decade

Yelena Pressman

12 papers receiving 734 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Yelena Pressman United States	7	609	355	312	141	122	13	739
Laura J. Smithson Canada	10	445 0.7×	237 0.7×	316 1.0×	190 1.3×	213 1.7×	19	806
Miranda W. Richter Canada	7	624 1.0×	452 1.3×	290 0.9×	115 0.8×	137 1.1×	7	747
Nicolas Guérout France	15	312 0.5×	236 0.7×	156 0.5×	155 1.1×	81 0.7×	29	632
Andre R. Sanchez United States	6	408 0.7×	204 0.6×	354 1.1×	74 0.5×	111 0.9×	7	568
Joseph S. Sparling Canada	9	693 1.1×	500 1.4×	656 2.1×	266 1.9×	340 2.8×	10	1.2k
Bogdan Czapiga Poland	10	333 0.5×	171 0.5×	192 0.6×	110 0.8×	144 1.2×	27	609
Eric A. Huebner United States	7	519 0.9×	269 0.8×	126 0.4×	263 1.9×	33 0.3×	8	799
Armin Buss Germany	12	742 1.2×	471 1.3×	317 1.0×	261 1.9×	50 0.4×	12	1.1k
Angela R. Filous United States	8	545 0.9×	313 0.9×	306 1.0×	225 1.6×	71 0.6×	11	924
Fernando X. Cuascut United States	8	544 0.9×	268 0.8×	303 1.0×	327 2.3×	91 0.7×	13	948

Countries citing papers authored by Yelena Pressman

Since Specialization

Citations

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

Fields of papers citing papers by Yelena Pressman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yelena Pressman

This figure shows the co-authorship network connecting the top 25 collaborators of Yelena Pressman. A scholar is included among the top collaborators of Yelena Pressman 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 Yelena Pressman. Yelena Pressman is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

13 of 13 papers shown

Khan, Aisha, Júlia Teixeira Oliveira, Yee‐Shuan Lee, et al.. (2025). Human Schwann Cell-Derived Extracellular Vesicle Isolation, Bioactivity Assessment, and Omics Characterization. International Journal of Nanomedicine. Volume 20. 4123–4144. 6 indexed citations

Pressman, Yelena, Juliana Sanchez‐Molano, Nadine Kerr, et al.. (2025). Human Schwann cell exosome treatment attenuates secondary injury mechanisms, histopathological consequences, and behavioral deficits after traumatic brain injury. Neurotherapeutics. 22(3). e00555–e00555. 5 indexed citations

Khan, Aisha, Yelena Pressman, Francisco J. Sánchez, et al.. (2025). Comparison of cellular-based therapies following a long-segmental peripheral nerve defect in a rat model. PLoS ONE. 20(1). e0313292–e0313292.

Nishimura, Kengo, Juliana Sanchez‐Molano, Nadine Kerr, et al.. (2024). Beneficial Effects of Human Schwann Cell-Derived Exosomes in Mitigating Secondary Damage After Penetrating Ballistic-Like Brain Injury. Journal of Neurotrauma. 41(21-22). 2395–2412. 9 indexed citations

Khan, Aisha, et al.. (2024). Assessing Survival, Distribution, and Optimal Loading Technique of Schwann Cell–Derived Exosomes Into Second-generation Axon Guidance Channels. Military Medicine. 189(Supplement_3). 63–66. 2 indexed citations

Wang, Shuo, et al.. (2023). A scaffold containing zinc oxide for Schwann cell-mediated axon growth. Journal of Neural Engineering. 20(6). 66009–66009. 4 indexed citations

Paudyal, Suraj, Yiqun Zhou, Keenan J. Mintz, et al.. (2022). DFMO Carbon Dots for Treatment of Neuroblastoma and Bioimaging. ACS Applied Bio Materials. 5(7). 3300–3309. 5 indexed citations

Puhl, Devan L., Anthony R. D’Amato, Dmitri V. Zagorevski, et al.. (2020). Aligned Fingolimod-Releasing Electrospun Fibers Increase Dorsal Root Ganglia Neurite Extension and Decrease Schwann Cell Expression of Promyelinating Factors. Frontiers in Bioengineering and Biotechnology. 8. 937–937. 13 indexed citations

Kanno, Haruo, Yelena Pressman, Alison Moody, et al.. (2014). Combination of Engineered Schwann Cell Grafts to Secrete Neurotrophin and Chondroitinase Promotes Axonal Regeneration and Locomotion after Spinal Cord Injury. Journal of Neuroscience. 34(5). 1838–1855. 134 indexed citations

10.

Zhang, Liqun, Zhengwen Ma, George M. Smith, et al.. (2009). GDNF‐enhanced axonal regeneration and myelination following spinal cord injury is mediated by primary effects on neurons. Glia. 57(11). 1178–1191. 133 indexed citations

11.

Pearse, Damien D., Andre R. Sanchez, Francisco C. Pereira, et al.. (2007). Transplantation of Schwann cells and/or olfactory ensheathing glia into the contused spinal cord: Survival, migration, axon association, and functional recovery. Glia. 55(9). 976–1000. 246 indexed citations

12.

Grimpe, Barbara, Yelena Pressman, Mary Bartlett Bunge, & Jerry Silver. (2004). The role of proteoglycans in Schwann cell/astrocyte interactions and in regeneration failure at PNS/CNS interfaces. Molecular and Cellular Neuroscience. 28(1). 18–29. 82 indexed citations

13.

Plant, Giles W., Paul F. Currier, Margaret L. Bates, et al.. (2002). Purified Adult Ensheathing Glia Fail to Myelinate Axons under Culture Conditions that Enable Schwann Cells to Form Myelin. Journal of Neuroscience. 22(14). 6083–6091. 100 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.

Explore authors with similar magnitude of impact