Natalia Suntsova

1.6k total citations
26 papers, 1.3k citations indexed

About

Natalia Suntsova is a scholar working on Cognitive Neuroscience, Endocrine and Autonomic Systems and Experimental and Cognitive Psychology. According to data from OpenAlex, Natalia Suntsova has authored 26 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Cognitive Neuroscience, 15 papers in Endocrine and Autonomic Systems and 11 papers in Experimental and Cognitive Psychology. Recurrent topics in Natalia Suntsova's work include Sleep and Wakefulness Research (24 papers), Circadian rhythm and melatonin (13 papers) and Sleep and related disorders (11 papers). Natalia Suntsova is often cited by papers focused on Sleep and Wakefulness Research (24 papers), Circadian rhythm and melatonin (13 papers) and Sleep and related disorders (11 papers). Natalia Suntsova collaborates with scholars based in United States, Russia and Georgia. Natalia Suntsova's co-authors include Dennis McGinty, Rubén Guzmán-Marı́n, Ronald Szymusiak, Ronald Szymusiak, Melvi Methippara, Tariq Bashir, Md. Noor Alam, Sunil Kumar, Hui Gong and Noor Alam and has published in prestigious journals such as Journal of Neuroscience, The Journal of Physiology and Journal of Neurophysiology.

In The Last Decade

Natalia Suntsova

24 papers receiving 1.2k 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 Suntsova United States 15 1.0k 642 473 327 239 26 1.3k
Rubén Guzmán-Marı́n United States 16 1.0k 1.0× 654 1.0× 495 1.0× 370 1.1× 222 0.9× 19 1.3k
Melvi Methippara United States 12 650 0.6× 427 0.7× 339 0.7× 202 0.6× 102 0.4× 13 824
Yan‐Jia Luo China 17 659 0.6× 312 0.5× 190 0.4× 399 1.2× 148 0.6× 25 1.1k
Stéphanie Maret Switzerland 9 872 0.8× 544 0.8× 497 1.1× 288 0.9× 46 0.2× 10 1.1k
Shingo Soya Japan 14 555 0.5× 444 0.7× 278 0.6× 246 0.8× 49 0.2× 25 967
Teresa L. Steininger United States 19 1.4k 1.3× 1.2k 1.9× 601 1.3× 928 2.8× 114 0.5× 37 2.3k
Aaron B. Nelson United States 14 640 0.6× 218 0.3× 217 0.5× 451 1.4× 85 0.4× 22 1.1k
Loris L. Ferrari United States 16 1.0k 1.0× 787 1.2× 336 0.7× 512 1.6× 44 0.2× 20 1.4k
Heinrich S. Gompf United States 16 487 0.5× 495 0.8× 209 0.4× 502 1.5× 41 0.2× 24 1.1k
Raquel Yustos United Kingdom 15 732 0.7× 524 0.8× 236 0.5× 426 1.3× 66 0.3× 18 1.1k

Countries citing papers authored by Natalia Suntsova

Since Specialization
Citations

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

Fields of papers citing papers by Natalia Suntsova

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Natalia Suntsova

This figure shows the co-authorship network connecting the top 25 collaborators of Natalia Suntsova. A scholar is included among the top collaborators of Natalia Suntsova 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 Suntsova. Natalia Suntsova 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
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Gvilia, Irma, Natalia Suntsova, А. А. Костин, et al.. (2016). The role of adenosine in the maturation of sleep homeostasis in rats. Journal of Neurophysiology. 117(1). 327–335. 14 indexed citations
4.
Gvilia, Irma, Natalia Suntsova, Sunil Kumar, Dennis McGinty, & Ronald Szymusiak. (2015). Suppression of preoptic sleep-regulatory neuronal activity during corticotropin-releasing factor-induced sleep disturbance. American Journal of Physiology-Regulatory, Integrative and Comparative Physiology. 309(9). R1092–R1100. 7 indexed citations
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Methippara, Melvi, et al.. (2010). Hippocampal adult neurogenesis is enhanced by chronic eszopiclone treatment in rats. Journal of Sleep Research. 19(3). 384–393. 13 indexed citations
7.
Alam, Md. Noor, et al.. (2010). GABAergic regulation of the perifornical–lateral hypothalamic neurons during non-rapid eye movement sleep in rats. Neuroscience. 167(3). 920–928. 13 indexed citations
8.
Suntsova, Natalia, Sunil Kumar, Rubén Guzmán-Marı́n, et al.. (2009). A role for the preoptic sleep-promoting system in absence epilepsy. Neurobiology of Disease. 36(1). 126–141. 22 indexed citations
9.
Guzmán-Marı́n, Rubén, et al.. (2007). Hippocampal neurogenesis is reduced by sleep fragmentation in the adult rat. Neuroscience. 148(1). 325–333. 100 indexed citations
10.
Guzmán-Marı́n, Rubén, Natalia Suntsova, Tariq Bashir, Ronald Szymusiak, & Dennis McGinty. (2007). Cell proliferation in the dentate gyrus of the adult rat fluctuates with the light–dark cycle. Neuroscience Letters. 422(3). 198–201. 30 indexed citations
11.
Guzmán-Marı́n, Rubén, Zhe Ying, Natalia Suntsova, et al.. (2006). Suppression of hippocampal plasticity‐related gene expression by sleep deprivation in rats. The Journal of Physiology. 575(3). 807–819. 164 indexed citations
12.
Guzmán-Marı́n, Rubén, et al.. (2005). Sleep deprivation suppresses neurogenesis in the adult hippocampus of rats. European Journal of Neuroscience. 22(8). 2111–2116. 165 indexed citations
13.
Alam, Md. Noor, Sunil Kumar, Tariq Bashir, et al.. (2004). GABA‐mediated control of hypocretin‐ but not melanin‐concentrating hormone‐immunoreactive neurones during sleep in rats. The Journal of Physiology. 563(2). 569–582. 103 indexed citations
14.
Guzmán-Marı́n, Rubén, et al.. (2003). Sleep Deprivation Reduces Proliferation of Cells in the Dentate Gyrus of the Hippocampus in Rats. The Journal of Physiology. 549(2). 563–571. 160 indexed citations
15.
Suntsova, Natalia, et al.. (2003). The Role of the Medial Preoptic Area of the Hypothalamus in Organizing the Paradoxical Phase of Sleep. Neuroscience and Behavioral Physiology. 34(1). 29–35. 5 indexed citations
16.
Suntsova, Natalia, et al.. (2003). Dynamics of Neuron Activity in the Lateral Preoptic Area of the Hypothalamus during the Sleep–Waking Cycle. Neuroscience and Behavioral Physiology. 33(7). 651–658. 10 indexed citations
17.
Suntsova, Natalia, Ronald Szymusiak, Noor Alam, Rubén Guzmán-Marı́n, & Dennis McGinty. (2002). Sleep‐waking discharge patterns of median preoptic nucleus neurons in rats. The Journal of Physiology. 543(2). 665–677. 136 indexed citations
18.
Suntsova, Natalia, et al.. (2000). The role of the posterior hypothalamus in controlling the paradoxical phase of sleep. Neuroscience and Behavioral Physiology. 30(2). 161–167. 14 indexed citations
19.
Suntsova, Natalia, et al.. (1998). [The role of the posterior hypothalamus in the regulation of paradoxical sleep].. PubMed. 84(11). 1165–73. 3 indexed citations
20.
Suntsova, Natalia, et al.. (1997). Direct activating effect of the lateral preoptic region of the hypothalamus on the synchronizing system of the thalamus. Neuroscience and Behavioral Physiology. 27(4). 347–352. 4 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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