Natalia Murataeva

575 total citations
17 papers, 450 citations indexed

About

Natalia Murataeva is a scholar working on Pharmacology, Cognitive Neuroscience and Endocrine and Autonomic Systems. According to data from OpenAlex, Natalia Murataeva has authored 17 papers receiving a total of 450 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Pharmacology, 9 papers in Cognitive Neuroscience and 6 papers in Endocrine and Autonomic Systems. Recurrent topics in Natalia Murataeva's work include Cannabis and Cannabinoid Research (16 papers), Sleep and Wakefulness Research (9 papers) and Neuroscience of respiration and sleep (4 papers). Natalia Murataeva is often cited by papers focused on Cannabis and Cannabinoid Research (16 papers), Sleep and Wakefulness Research (9 papers) and Neuroscience of respiration and sleep (4 papers). Natalia Murataeva collaborates with scholars based in United States, Taiwan and Canada. Natalia Murataeva's co-authors include Alex Straiker, Ken Mackie, Heather B. Bradshaw, Amey Dhopeshwarkar, Sally Miller, Emma Leishman, Jim Wager‐Miller, Sherry Shu‐Jung Hu, Daniel J. Morgan and Brian J. Davis and has published in prestigious journals such as Scientific Reports, Journal of Pharmacology and Experimental Therapeutics and British Journal of Pharmacology.

In The Last Decade

Natalia Murataeva

14 papers receiving 449 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Natalia Murataeva United States 12 372 146 99 71 53 17 450
Ben Cravatt United States 5 389 1.0× 269 1.8× 98 1.0× 51 0.7× 41 0.8× 7 494
Anna-Maria Szczesniak Canada 15 392 1.1× 166 1.1× 100 1.0× 65 0.9× 82 1.5× 18 503
Enrico Mazzarella Italy 7 413 1.1× 182 1.2× 95 1.0× 44 0.6× 73 1.4× 8 527
Ana Cabranes Spain 8 411 1.1× 260 1.8× 82 0.8× 34 0.5× 40 0.8× 9 482
Linda Console‐Bram United States 10 375 1.0× 247 1.7× 65 0.7× 48 0.7× 170 3.2× 13 563
Francisco Espejo‐Porras Spain 12 335 0.9× 168 1.2× 56 0.6× 25 0.4× 85 1.6× 12 467
Camille Soubrane United Kingdom 4 266 0.7× 188 1.3× 61 0.6× 21 0.3× 65 1.2× 5 406
Lawrence C. Blume United States 7 342 0.9× 267 1.8× 74 0.7× 32 0.5× 101 1.9× 8 420
Valentina Vozella United States 12 179 0.5× 140 1.0× 44 0.4× 37 0.5× 95 1.8× 24 411
Cristina Palomo‐Garo Spain 8 562 1.5× 400 2.7× 120 1.2× 32 0.5× 55 1.0× 8 671

Countries citing papers authored by Natalia Murataeva

Since Specialization
Citations

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

Fields of papers citing papers by Natalia Murataeva

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Natalia Murataeva

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

All Works

17 of 17 papers shown
1.
Murataeva, Natalia, Emma Leishman, Jim Wager‐Miller, et al.. (2025). Acetaminophen inhibits diacylglycerol lipase synthesis of 2-arachidonoyl glycerol: Implications for nociception. Cell Reports Medicine. 6(6). 102139–102139. 1 indexed citations
2.
Murataeva, Natalia, Wenwen Du, Ruth A. Ross, et al.. (2024). CB1 Receptor Negative Allosteric Modulators as a Potential Tool to Reverse Cannabinoid Toxicity. Molecules. 29(8). 1881–1881. 2 indexed citations
3.
Murataeva, Natalia, et al.. (2024). Cannabinoid regulation of sex-dependent murine odorant-stimulated salivation. Scientific Reports. 14(1). 26720–26720.
4.
Murataeva, Natalia, et al.. (2024). Murine vaginal secretory responses to a male volatile chemical messenger. Scientific Reports. 14(1). 27707–27707.
5.
Murataeva, Natalia, et al.. (2024). A Sex-Dependent Cannabinoid CB1 Receptor Role in Circadian Tearing of the Mouse. Investigative Ophthalmology & Visual Science. 65(14). 10–10.
6.
Murataeva, Natalia, et al.. (2020). THC Regulates Tearing via Cannabinoid CB1 Receptors. Investigative Ophthalmology & Visual Science. 61(10). 48–48. 16 indexed citations
7.
Murataeva, Natalia, Sally Miller, Amey Dhopeshwarkar, et al.. (2019). Cannabinoid CB2R receptors are upregulated with corneal injury and regulate the course of corneal wound healing. Experimental Eye Research. 182. 74–84. 26 indexed citations
8.
Murataeva, Natalia, Xavier Taylor, Amey Dhopeshwarkar, et al.. (2019). Evidence for a GPR18 Role in Chemotaxis, Proliferation, and the Course of Wound Closure in the Cornea. Cornea. 38(7). 905–913. 16 indexed citations
9.
Murataeva, Natalia, Anna-Maria Szczesniak, Emma Leishman, et al.. (2018). Revisiting cannabinoid receptor 2 expression and function in murine retina. Neuropharmacology. 141. 21–31. 18 indexed citations
10.
Dhopeshwarkar, Amey, Natalia Murataeva, A. Makriyannis, Alex Straiker, & Ken Mackie. (2016). Two Janus Cannabinoids That Are Both CB2 Agonists and CB1 Antagonists. Journal of Pharmacology and Experimental Therapeutics. 360(2). 300–311. 23 indexed citations
11.
Murataeva, Natalia, et al.. (2016). Where’s my entourage? The curious case of 2-oleoylglycerol, 2-linolenoylglycerol, and 2-palmitoylglycerol. Pharmacological Research. 110. 173–180. 28 indexed citations
12.
Miller, Sally, Emma Leishman, Sherry Shu‐Jung Hu, et al.. (2016). Harnessing the Endocannabinoid 2-Arachidonoylglycerol to Lower Intraocular Pressure in a Murine Model. Investigative Ophthalmology & Visual Science. 57(7). 3287–3287. 26 indexed citations
13.
Miller, Sally, Emma Leishman, Natalia Murataeva, et al.. (2016). Evidence for a GPR18 Role in Diurnal Regulation of Intraocular Pressure. Investigative Ophthalmology & Visual Science. 57(14). 6419–6419. 37 indexed citations
14.
Murataeva, Natalia, Shimin Li, Sally Miller, et al.. (2015). Cannabinoid-Induced Chemotaxis in Bovine Corneal Epithelial Cells. Investigative Ophthalmology & Visual Science. 56(5). 3304–3304. 23 indexed citations
15.
Murataeva, Natalia, Alex Straiker, & Ken Mackie. (2013). Parsing the players: 2‐arachidonoylglycerol synthesis and degradation in theCNS. British Journal of Pharmacology. 171(6). 1379–1391. 182 indexed citations
16.
Murataeva, Natalia, Ken Mackie, & Alex Straiker. (2012). The CB2-preferring agonist JWH015 also potently and efficaciously activates CB1 in autaptic hippocampal neurons. Pharmacological Research. 66(5). 437–442. 24 indexed citations
17.
Morgan, Daniel J., Charles Müller, Natalia Murataeva, Brian J. Davis, & Ken Mackie. (2011). Δ9‐Tetrahydrocannabinol (Δ9‐THC) attenuates mouse sperm motility and male fecundity. British Journal of Pharmacology. 165(8). 2575–2583. 28 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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