Alexey Brazhe

2.5k total citations
65 papers, 1.8k citations indexed

About

Alexey Brazhe is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Alexey Brazhe has authored 65 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 37 papers in Cellular and Molecular Neuroscience, 23 papers in Molecular Biology and 21 papers in Cognitive Neuroscience. Recurrent topics in Alexey Brazhe's work include Neuroscience and Neuropharmacology Research (30 papers), Neural dynamics and brain function (15 papers) and Neuroinflammation and Neurodegeneration Mechanisms (10 papers). Alexey Brazhe is often cited by papers focused on Neuroscience and Neuropharmacology Research (30 papers), Neural dynamics and brain function (15 papers) and Neuroinflammation and Neurodegeneration Mechanisms (10 papers). Alexey Brazhe collaborates with scholars based in Russia, Denmark and United Kingdom. Alexey Brazhe's co-authors include Olga Sosnovtseva, Nadezda A. Brazhe, Alexey Semyanov, Г. В. Максимов, Martin Lauritzen, Dmitry E. Postnov, Alexei Verkhratsky, Alexander Popov, Barbara Lykke Lind and E. Yu. Parshina and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Physical Review Letters and Nature Communications.

In The Last Decade

Alexey Brazhe

63 papers receiving 1.8k citations

Peers

Alexey Brazhe

CMN

NEURO

PHYSI

Karl A. Kasischke United States

André Zeug Germany

Jakub Włodarczyk Poland

Steven S. Hou United States

Maja Puchades Norway

Marc Dhénain France

Jesse Skoch United States

Silvia Mangia United States

Marcello D’Ascenzo Italy

Eduard Korkotian Israel

Karl A. Kasischke United States

Alexey Brazhe

822 ×1.2

CMN

361 ×0.7

NEURO

878 ×2.0

250 ×0.7

333 ×1.0

PHYSI

Citations per year, relative to Alexey Brazhe Alexey Brazhe (= 1×) peers Karl A. Kasischke

Countries citing papers authored by Alexey Brazhe

Since Specialization

Citations

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

Fields of papers citing papers by Alexey Brazhe

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alexey Brazhe

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

All Works

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20 of 20 papers shown

Popov, Alexander, Nadezda A. Brazhe, Konstantin S. Yashin, et al.. (2023). Mitochondrial malfunction and atrophy of astrocytes in the aged human cerebral cortex. Nature Communications. 14(1). 8380–8380. 51 indexed citations

Brazhe, Alexey, et al.. (2023). Dissociation Between Neuronal and Astrocytic Calcium Activity in Response to Locomotion in Mice. Function. 4(4). zqad019–zqad019. 16 indexed citations

Brazhe, Alexey, et al.. (2023). Computational Model of Noradrenaline Modulation of Astrocyte Responses to Synaptic Activity. Mathematics. 11(3). 628–628. 5 indexed citations

Popov, Alexander, Alexey Brazhe, Li Li, et al.. (2021). Astrocyte dystrophy in ageing brain parallels impaired synaptic plasticity. Aging Cell. 20(3). e13334–e13334. 104 indexed citations

Marina, Nephtalı́, Isabel N. Christie, Alla Korsak, et al.. (2020). Astrocytes monitor cerebral perfusion and control systemic circulation to maintain brain blood flow. Nature Communications. 11(1). 131–131. 146 indexed citations

McCauley, John P., Alioscka A. Sousa, Rose M. De Guzman, et al.. (2020). Circadian Modulation of Neurons and Astrocytes Controls Synaptic Plasticity in Hippocampal Area CA1. Cell Reports. 33(2). 108255–108255. 50 indexed citations

Popov, Alexander, Maxim L. Bychkov, Alexey Brazhe, et al.. (2020). Caloric restriction triggers morphofunctional remodeling of astrocytes and enhances synaptic plasticity in the mouse hippocampus. Cell Death and Disease. 11(3). 208–208. 49 indexed citations

Brazhe, Nadezda A., E. Yu. Parshina, Igor Medyanik, et al.. (2019). Distinguishing between tumor, infiltrated and normal cortex regions in glioma patients with Raman spectroscopy. Glia. 67. 1 indexed citations

Nielsen, Reena Murmu, Jonas C. Fordsmann, Changsi Cai, et al.. (2019). Sensory Stimulation-Induced Astrocytic Calcium Signaling in Electrically Silent Ischemic Penumbra. Frontiers in Aging Neuroscience. 11. 223–223. 3 indexed citations

10.

Brazhe, Alexey, et al.. (2018). Astrocytic Coverage of Dendritic Spines, Dendritic Shafts, and Axonal Boutons in Hippocampal Neuropil. Frontiers in Cellular Neuroscience. 12. 248–248. 76 indexed citations

11.

Brazhe, Alexey. (2018). Shearlet-based measures of entropy and complexity for two-dimensional patterns. Physical review. E. 97(6). 61301–61301. 13 indexed citations

12.

Brazhe, Alexey, Barbara Lykke Lind, Claus Mathiesen, et al.. (2014). GABA_AReceptor-Mediated Bidirectional Control of Synaptic Activity, Intracellular Ca²⁺, Cerebral Blood Flow, and Oxygen Consumption in Mouse Somatosensory Cortex In Vivo. Cerebral Cortex. 25(9). 2594–2609. 19 indexed citations

13.

Kutuzov, Nikolay, et al.. (2014). Orientational Ordering of Carotenoids in Myelin Membranes Resolved by Polarized Raman Microspectroscopy. Biophysical Journal. 107(4). 891–900. 10 indexed citations

14.

Lind, Barbara Lykke, et al.. (2013). Rapid stimulus-evoked astrocyte Ca ²⁺ elevations and hemodynamic responses in mouse somatosensory cortex in vivo. Proceedings of the National Academy of Sciences. 110(48). E4678–87. 140 indexed citations

15.

Brazhe, Alexey, Claus Mathiesen, & Martin Lauritzen. (2012). Multiscale vision model highlights spontaneous glial calcium waves recorded by 2-photon imaging in brain tissue. NeuroImage. 68. 192–202. 6 indexed citations

16.

Mathiesen, Claus, K Caesar, K Thomsen, et al.. (2011). Activity-dependent Increases in Local Oxygen Consumption Correlate with Postsynaptic Currents in the Mouse CerebellumIn Vivo. Journal of Neuroscience. 31(50). 18327–18337. 35 indexed citations

17.

Brazhe, Nadezda A., Alexey Brazhe, Olga Sosnovtseva, & Salim Abdali. (2009). Novel chiroptical analysis of hemoglobin by surface enhanced resonance Raman optical activity spectroscopy. Chirality. 21(1E). E307–12. 9 indexed citations

18.

Brazhe, Nadezda A., Salim Abdali, Alexey Brazhe, et al.. (2009). New Insight into Erythrocyte through In Vivo Surface-Enhanced Raman Spectroscopy. Biophysical Journal. 97(12). 3206–3214. 90 indexed citations

19.

Postnov, Dmitry E., et al.. (2008). Giant Glial Cell: New Insight Through Mechanism-Based Modeling. Journal of Biological Physics. 34(3-4). 441–457. 17 indexed citations

20.

Brazhe, Alexey, Nadezda A. Brazhe, Г. В. Максимов, et al.. (2008). Phase-modulation laser interference microscopy: an advance in cell imaging and dynamics study. Journal of Biomedical Optics. 13(3). 34004–34004. 17 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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