Marı́a Pertusa

1.1k total citations
22 papers, 765 citations indexed

About

Marı́a Pertusa is a scholar working on Sensory Systems, Cellular and Molecular Neuroscience and Molecular Biology. According to data from OpenAlex, Marı́a Pertusa has authored 22 papers receiving a total of 765 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Sensory Systems, 13 papers in Cellular and Molecular Neuroscience and 7 papers in Molecular Biology. Recurrent topics in Marı́a Pertusa's work include Ion Channels and Receptors (14 papers), Neurobiology and Insect Physiology Research (8 papers) and Biochemical Analysis and Sensing Techniques (7 papers). Marı́a Pertusa is often cited by papers focused on Ion Channels and Receptors (14 papers), Neurobiology and Insect Physiology Research (8 papers) and Biochemical Analysis and Sensing Techniques (7 papers). Marı́a Pertusa collaborates with scholars based in Chile, Spain and France. Marı́a Pertusa's co-authors include Félix Viana, Rodolfo Madrid, Rosa Cristòfol, Coral Sanfeliu, Cruz Morenilla‐Palao, Eduard Rodrı́guez-Farré, Hugo Cabedo, Víctor Meseguer, Alejandro González and Carlos Belmonte and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Neuroscience and Pain.

In The Last Decade

Marı́a Pertusa

21 papers receiving 748 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Marı́a Pertusa Chile 15 305 305 255 203 123 22 765
Angélica Zepeda Mexico 19 309 1.0× 212 0.7× 372 1.5× 113 0.6× 118 1.0× 41 1.1k
Benito Ordaz Mexico 18 296 1.0× 175 0.6× 293 1.1× 231 1.1× 90 0.7× 31 781
Daniela Hirnet Germany 14 348 1.1× 462 1.5× 322 1.3× 78 0.4× 155 1.3× 23 863
Suya Sun China 15 442 1.4× 137 0.4× 396 1.6× 329 1.6× 95 0.8× 23 916
Axel Preuss Switzerland 7 195 0.6× 384 1.3× 268 1.1× 112 0.6× 115 0.9× 7 897
Michelle D. Amaral United States 13 360 1.2× 181 0.6× 326 1.3× 67 0.3× 30 0.2× 16 732
Ekaterina Pchitskaya Russia 10 528 1.7× 177 0.6× 462 1.8× 420 2.1× 132 1.1× 23 1.1k
Nima Dolatabadi United States 14 273 0.9× 128 0.4× 458 1.8× 247 1.2× 117 1.0× 15 881
Irena Vertkin Israel 9 369 1.2× 47 0.2× 294 1.2× 229 1.1× 104 0.8× 12 792
Wayne Chadwick United States 19 310 1.0× 53 0.2× 510 2.0× 220 1.1× 61 0.5× 31 1.0k

Countries citing papers authored by Marı́a Pertusa

Since Specialization
Citations

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

Fields of papers citing papers by Marı́a Pertusa

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marı́a Pertusa

This figure shows the co-authorship network connecting the top 25 collaborators of Marı́a Pertusa. A scholar is included among the top collaborators of Marı́a Pertusa 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 Marı́a Pertusa. Marı́a Pertusa 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.
Piña, Ricardo, Gonzalo Ugarte, Richard M. Pino, et al.. (2024). A functional unbalance of TRPM8 and Kv1 channels underlies orofacial cold allodynia induced by peripheral nerve damage. Frontiers in Pharmacology. 15. 1484387–1484387.
2.
Pertusa, Marı́a, et al.. (2023). Molecular determinants of TRPM8 function: key clues for a cool modulation. Frontiers in Pharmacology. 14. 1213337–1213337. 9 indexed citations
3.
Hwang, Ji Yeon, Jorge Fernández‐Trillo, Kang‐Sik Park, et al.. (2021). Constitutive Phosphorylation as a Key Regulator of TRPM8 Channel Function. Journal of Neuroscience. 41(41). 8475–8493. 14 indexed citations
4.
Cornejo, Víctor Hugo, et al.. (2020). Non-conventional Axonal Organelles Control TRPM8 Ion Channel Trafficking and Peripheral Cold Sensing. Cell Reports. 30(13). 4505–4517.e5. 18 indexed citations
5.
Pertusa, Marı́a, et al.. (2018). Non-invasive Neurite Mechanics in Differentiated PC12 Cells. Frontiers in Cellular Neuroscience. 12. 194–194. 6 indexed citations
6.
Pertusa, Marı́a, et al.. (2018). Critical role of the pore domain in the cold response of TRPM8 channels identified by ortholog functional comparison. Journal of Biological Chemistry. 293(32). 12454–12471. 27 indexed citations
7.
González, Alejandro, Gonzalo Ugarte, Ricardo Piña, et al.. (2017). Role of the Excitability Brake Potassium Current IKDin Cold Allodynia Induced by Chronic Peripheral Nerve Injury. Journal of Neuroscience. 37(12). 3109–3126. 38 indexed citations
8.
González, Alejandro, Gonzalo Ugarte, Ricardo Piña, et al.. (2017). IKD Current in Cold Transduction and Damage-Triggered Cold Hypersensitivity. Advances in experimental medicine and biology. 1015. 265–277. 5 indexed citations
9.
Rozas, Pablo, Ricardo Piña, Anita Terse, et al.. (2016). Targeted overexpression of tumor necrosis factor-α increases cyclin-dependent kinase 5 activity and TRPV1-dependent Ca2+ influx in trigeminal neurons. Pain. 157(6). 1346–1362. 43 indexed citations
10.
Betz, Timo, et al.. (2015). Time-resolved neurite mechanics by thermal fluctuation assessments. Physical Biology. 12(6). 66020–66020. 10 indexed citations
11.
Madrid, Rodolfo & Marı́a Pertusa. (2014). Intimacies and Physiological Role of the Polymodal Cold-Sensitive Ion Channel TRPM8. Current topics in membranes. 74. 293–324. 19 indexed citations
12.
Pertusa, Marı́a, et al.. (2014). Bidirectional Modulation of Thermal and Chemical Sensitivity of TRPM8 Channels by the Initial Region of the N-terminal Domain. Journal of Biological Chemistry. 289(32). 21828–21843. 25 indexed citations
13.
Pertusa, Marı́a, Rodolfo Madrid, Cruz Morenilla‐Palao, Carlos Belmonte, & Félix Viana. (2012). N-Glycosylation of TRPM8 Ion Channels Modulates Temperature Sensitivity of Cold Thermoreceptor Neurons. Journal of Biological Chemistry. 287(22). 18218–18229. 59 indexed citations
14.
Morenilla‐Palao, Cruz, Marı́a Pertusa, Víctor Meseguer, Hugo Cabedo, & Félix Viana. (2009). Lipid Raft Segregation Modulates TRPM8 Channel Activity. Journal of Biological Chemistry. 284(14). 9215–9224. 105 indexed citations
15.
Pertusa, Marı́a, et al.. (2007). Transcriptional Control of Cholesterol Biosynthesis in Schwann Cells by Axonal Neuregulin 1. Journal of Biological Chemistry. 282(39). 28768–28778. 32 indexed citations
16.
Pertusa, Marı́a, Albert Adell, T. Rodrigo, et al.. (2007). Expression of GDNF transgene in astrocytes improves cognitive deficits in aged rats. Neurobiology of Aging. 29(9). 1366–1379. 93 indexed citations
17.
Pertusa, Marı́a, et al.. (2007). Astrocytes aged in vitro show a decreased neuroprotective capacity. Journal of Neurochemistry. 101(3). 794–805. 135 indexed citations
18.
Sebastià, Jordi, Marı́a Pertusa, David Vı́lchez, et al.. (2006). Carboxyl-terminal fragment of amyloid precursor protein and hydrogen peroxide induce neuronal cell death through different pathways. Journal of Neural Transmission. 113(12). 1837–1845. 12 indexed citations
19.
20.
Sebastià, Jordi, Rosa Cristòfol, Marı́a Pertusa, et al.. (2004). Down's syndrome astrocytes have greater antioxidant capacity than euploid astrocytes. European Journal of Neuroscience. 20(9). 2355–2366. 25 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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