Aurora Lopez‐Rosas

2.0k total citations · 1 hit paper
24 papers, 1.5k citations indexed

About

Aurora Lopez‐Rosas is a scholar working on Immunology, Physiology and Cell Biology. According to data from OpenAlex, Aurora Lopez‐Rosas has authored 24 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Immunology, 8 papers in Physiology and 7 papers in Cell Biology. Recurrent topics in Aurora Lopez‐Rosas's work include Immune cells in cancer (11 papers), Lysosomal Storage Disorders Research (8 papers) and Cellular transport and secretion (5 papers). Aurora Lopez‐Rosas is often cited by papers focused on Immune cells in cancer (11 papers), Lysosomal Storage Disorders Research (8 papers) and Cellular transport and secretion (5 papers). Aurora Lopez‐Rosas collaborates with scholars based in United States, Italy and Sweden. Aurora Lopez‐Rosas's co-authors include Maria I. Givogri, Ernesto R. Bongarzone, Yu Han, Aida Rashidi, Jason Miska, Maciej S. Lesniak, Peng Zhang, Catalina Lee-Chang, Richard B. van Breemen and Ludovico Cantuti‐Castelvetri and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Nature Communications.

In The Last Decade

Aurora Lopez‐Rosas

23 papers receiving 1.5k citations

Hit Papers

STING agonist-loaded, CD4... 2023 2026 2024 2023 40 80 120

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Aurora Lopez‐Rosas United States 19 536 527 502 276 265 24 1.5k
Laura J. Lewis‐Tuffin United States 19 757 1.4× 181 0.3× 183 0.4× 326 1.2× 160 0.6× 23 1.5k
Stéphane C. Boutet United States 18 1.3k 2.3× 317 0.6× 153 0.3× 135 0.5× 171 0.6× 28 1.9k
Jillian Haight Canada 14 792 1.5× 535 1.0× 90 0.2× 225 0.8× 125 0.5× 20 1.6k
Tracy L. Hagemann United States 26 1.1k 2.1× 628 1.2× 134 0.3× 90 0.3× 458 1.7× 48 2.1k
Stefano Regis Italy 22 1.2k 2.2× 271 0.5× 521 1.0× 185 0.7× 317 1.2× 57 1.9k
Raymond K. Tong United States 12 1.1k 2.0× 200 0.4× 161 0.3× 582 2.1× 175 0.7× 15 1.7k
Karin Golan Israel 16 567 1.1× 435 0.8× 146 0.3× 184 0.7× 82 0.3× 30 1.4k
A.K.M. Ghulam Muhammad United States 18 1000 1.9× 517 1.0× 225 0.4× 303 1.1× 52 0.2× 35 2.1k
Mariko Kobayashi Japan 15 763 1.4× 417 0.8× 109 0.2× 273 1.0× 243 0.9× 33 1.9k
Siddhartha S. Mitra United States 23 960 1.8× 921 1.7× 106 0.2× 613 2.2× 103 0.4× 52 2.5k

Countries citing papers authored by Aurora Lopez‐Rosas

Since Specialization
Citations

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

Fields of papers citing papers by Aurora Lopez‐Rosas

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Aurora Lopez‐Rosas. 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 Aurora Lopez‐Rosas. The network helps show where Aurora Lopez‐Rosas may publish in the future.

Co-authorship network of co-authors of Aurora Lopez‐Rosas

This figure shows the co-authorship network connecting the top 25 collaborators of Aurora Lopez‐Rosas. A scholar is included among the top collaborators of Aurora Lopez‐Rosas 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 Aurora Lopez‐Rosas. Aurora Lopez‐Rosas 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.
Zhang, Peng, Aida Rashidi, Junfei Zhao, et al.. (2023). STING agonist-loaded, CD47/PD-L1-targeting nanoparticles potentiate antitumor immunity and radiotherapy for glioblastoma. Nature Communications. 14(1). 1610–1610. 139 indexed citations breakdown →
2.
Lopez‐Rosas, Aurora, et al.. (2023). IMMU-06. THE ROLE OF BRAIN TUMOR MICROENVIRONMENT ON T CELL TELOMERE SHORTENING. Neuro-Oncology. 25(Supplement_5). v142–v142.
3.
Miska, Jason, Aida Rashidi, Catalina Lee-Chang, et al.. (2021). Polyamines drive myeloid cell survival by buffering intracellular pH to promote immunosuppression in glioblastoma. Science Advances. 7(8). 75 indexed citations
4.
Hou, David, Brandyn Castro, Aida Rashidi, et al.. (2021). IMMU-36. B CELL-VACCINE ELICITS LONG TERM IMMUNITY AGAINST GLIOBLASTOMA VIA ACTIVATION AND DIFFERENTIATION OF TUMOR-SPECIFIC CD8+ MEMORY T CELLS. Neuro-Oncology. 23(Supplement_6). vi100–vi100. 1 indexed citations
5.
Lee-Chang, Catalina, Jason Miska, David Hou, et al.. (2020). Activation of 4-1BBL+ B cells with CD40 agonism and IFNγ elicits potent immunity against glioblastoma. The Journal of Experimental Medicine. 218(1). 49 indexed citations
6.
Lee-Chang, Catalina, Aida Rashidi, Jason Miska, et al.. (2019). Myeloid-Derived Suppressive Cells Promote B cell–Mediated Immunosuppression via Transfer of PD-L1 in Glioblastoma. Cancer Immunology Research. 7(12). 1928–1943. 120 indexed citations
7.
Miska, Jason, Catalina Lee-Chang, Aida Rashidi, et al.. (2019). HIF-1α Is a Metabolic Switch between Glycolytic-Driven Migration and Oxidative Phosphorylation-Driven Immunosuppression of Tregs in Glioblastoma. Cell Reports. 27(1). 226–237.e4. 230 indexed citations
8.
Rashidi, Aida, Jason Miska, Catalina Lee-Chang, et al.. (2019). GCN2 is essential for CD8+ T cell survival and function in murine models of malignant glioma. Cancer Immunology Immunotherapy. 69(1). 81–94. 40 indexed citations
9.
Wu, Congyu, Megan E. Muroski, Jason Miska, et al.. (2018). Repolarization of myeloid derived suppressor cells via magnetic nanoparticles to promote radiotherapy for glioma treatment. Nanomedicine Nanotechnology Biology and Medicine. 16. 126–137. 45 indexed citations
10.
Rashidi, Aida, Jason Miska, Catalina Lee-Chang, et al.. (2018). IMMU-06. ABSENCE OF THE AMINO ACID STRESS-SENSOR GCN2 REDUCES SUPPRESSIVE EFFECTS OF MDSCs IN GLIOMA. Neuro-Oncology. 20(suppl_6). vi122–vi122. 1 indexed citations
11.
Panek, Wojciech K., Katarzyna C. Pituch, Jason Miska, et al.. (2018). Local Application of Autologous Platelet-Rich Fibrin Patch (PRF-P) Suppresses Regulatory T Cell Recruitment in a Murine Glioma Model. Molecular Neurobiology. 56(7). 5032–5040. 18 indexed citations
12.
Muroski, Megan E., Jason Miska, Alan L. Chang, et al.. (2017). Fatty Acid Uptake in T Cell Subsets Using a Quantum Dot Fatty Acid Conjugate. Scientific Reports. 7(1). 5790–5790. 26 indexed citations
13.
Cantuti‐Castelvetri, Ludovico, Michael S. Marshall, Ludovic D’Auria, et al.. (2015). Mechanism of Neuromuscular Dysfunction in Krabbe Disease. Journal of Neuroscience. 35(4). 1606–1616. 28 indexed citations
14.
Pituch, Katarzyna C., Ana Lis Moyano, Aurora Lopez‐Rosas, et al.. (2015). Dysfunction of Platelet-derived Growth Factor Receptor α (PDGFRα) Represses the Production of Oligodendrocytes from Arylsulfatase A-deficient Multipotential Neural Precursor Cells. Journal of Biological Chemistry. 290(11). 7040–7053. 37 indexed citations
15.
Moyano, Ana Lis, Guannan Li, Aurora Lopez‐Rosas, et al.. (2014). Distribution of C16:0, C18:0, C24:1, and C24:0 sulfatides in central nervous system lipid rafts by quantitative ultra-high-pressure liquid chromatography tandem mass spectrometry. Analytical Biochemistry. 467. 31–39. 26 indexed citations
16.
Cantuti‐Castelvetri, Ludovico, Maria I. Givogri, Audrey Hébert, et al.. (2013). The Sphingolipid Psychosine Inhibits Fast Axonal Transport in Krabbe Disease by Activation of GSK3  and Deregulation of Molecular Motors. Journal of Neuroscience. 33(24). 10048–10056. 76 indexed citations
17.
Cantuti‐Castelvetri, Ludovico, et al.. (2012). Psychosine induces the dephosphorylation of neurofilaments by deregulation of PP1 and PP2A phosphatases. Neurobiology of Disease. 46(2). 325–335. 43 indexed citations
18.
Cantuti‐Castelvetri, Ludovico, Maria I. Givogri, Hongling Zhu, et al.. (2011). Axonopathy is a compounding factor in the pathogenesis of Krabbe disease. Acta Neuropathologica. 122(1). 35–48. 81 indexed citations
19.
Givogri, Maria I., Aurora Lopez‐Rosas, Hongmei Cao, et al.. (2009). Psychosine Accumulates in Membrane Microdomains in the Brain of Krabbe Patients, Disrupting the Raft Architecture. Journal of Neuroscience. 29(19). 6068–6077. 138 indexed citations
20.
Galbiati, Francesca, Veronica Basso, Ludovico Cantuti‐Castelvetri, et al.. (2007). Autonomic Denervation of Lymphoid Organs Leads to Epigenetic Immune Atrophy in a Mouse Model of Krabbe Disease. Journal of Neuroscience. 27(50). 13730–13738. 50 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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