Venu Narayanan

622 total citations
15 papers, 449 citations indexed

About

Venu Narayanan is a scholar working on Molecular Biology, Pathology and Forensic Medicine and Cellular and Molecular Neuroscience. According to data from OpenAlex, Venu Narayanan has authored 15 papers receiving a total of 449 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 6 papers in Pathology and Forensic Medicine and 6 papers in Cellular and Molecular Neuroscience. Recurrent topics in Venu Narayanan's work include Multiple Sclerosis Research Studies (6 papers), Neuroscience and Neuropharmacology Research (5 papers) and Neuroinflammation and Neurodegeneration Mechanisms (4 papers). Venu Narayanan is often cited by papers focused on Multiple Sclerosis Research Studies (6 papers), Neuroscience and Neuropharmacology Research (5 papers) and Neuroinflammation and Neurodegeneration Mechanisms (4 papers). Venu Narayanan collaborates with scholars based in Germany, United States and Argentina. Venu Narayanan's co-authors include Hans‐Christian Pape, Thomas Seidenbecher, Jörg Lesting, Friederike Jansen, Sven G. Meuth, Norbert Sachser, Rebecca S. Heiming, Thomas Budde, Heinz Wiendl and Patrick Meuth and has published in prestigious journals such as Proceedings of the National Academy of Sciences, PLoS ONE and Cerebral Cortex.

In The Last Decade

Venu Narayanan

15 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
Venu Narayanan Germany 12 194 160 136 81 64 15 449
Valentina Durante Italy 8 115 0.6× 90 0.6× 115 0.8× 120 1.5× 28 0.4× 10 371
Frances Colyer United Kingdom 9 198 1.0× 79 0.5× 94 0.7× 119 1.5× 95 1.5× 11 434
Steven W. Gonzales United States 11 260 1.3× 126 0.8× 138 1.0× 49 0.6× 81 1.3× 25 509
Nadège Morisot United States 14 422 2.2× 128 0.8× 242 1.8× 37 0.5× 45 0.7× 23 583
Marilena Griguoli Italy 15 334 1.7× 201 1.3× 207 1.5× 56 0.7× 16 0.3× 23 531
Eisuke Haneda Japan 8 270 1.4× 71 0.4× 138 1.0× 110 1.4× 79 1.2× 10 478
Raymond B. Berry United States 10 260 1.3× 156 1.0× 260 1.9× 74 0.9× 45 0.7× 11 514
Dayna M. Hayes United States 10 225 1.2× 68 0.4× 104 0.8× 203 2.5× 70 1.1× 12 505
Olga Barca‐Mayo Spain 13 126 0.6× 92 0.6× 208 1.5× 69 0.9× 21 0.3× 25 652
Kyungdeok Kim South Korea 14 187 1.0× 139 0.9× 166 1.2× 81 1.0× 20 0.3× 24 493

Countries citing papers authored by Venu Narayanan

Since Specialization
Citations

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

Fields of papers citing papers by Venu Narayanan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Venu Narayanan

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

All Works

15 of 15 papers shown
1.
Bierhansl, Laura, Venu Narayanan, Andre Dik, et al.. (2024). Neuronal Mitochondrial Calcium Uniporter (MCU) Deficiency Is Neuroprotective in Hyperexcitability by Modulation of Metabolic Pathways and ROS Balance. Molecular Neurobiology. 61(11). 9529–9538. 8 indexed citations
2.
Bierhansl, Laura, Christina B. Schroeter, Venu Narayanan, et al.. (2023). NOX4-derived ROS are neuroprotective by balancing intracellular calcium stores. Cellular and Molecular Life Sciences. 80(5). 127–127. 13 indexed citations
3.
Börsch, Anna‐Lena, Xiaolin Li, Hanna Gerwien, et al.. (2021). Bcl6 controls meningeal Th17–B cell interaction in murine neuroinflammation. Proceedings of the National Academy of Sciences. 118(36). 22 indexed citations
4.
Chaudhary, Rahul, Stefanie Albrecht, Manuela Cerina, et al.. (2021). Modulation of pacemaker channel function in a model of thalamocortical hyperexcitability by demyelination and cytokines. Cerebral Cortex. 32(20). 4397–4421. 9 indexed citations
5.
Cerina, Manuela, Muthuraman Muthuraman, Nabin Koirala, et al.. (2020). Myelination- and immune-mediated MR-based brain network correlates. Journal of Neuroinflammation. 17(1). 186–186. 12 indexed citations
6.
Hundehege, Petra, Manuela Cerina, Susann Pankratz, et al.. (2019). The next-generation sphingosine-1 receptor modulator BAF312 (siponimod) improves cortical network functionality in focal autoimmune encephalomyelitis. Neural Regeneration Research. 14(11). 1950–1950. 26 indexed citations
7.
Zobeiri, Mehrnoush, Rahul Chaudhary, Anne Blaich, et al.. (2019). The Hyperpolarization-Activated HCN4 Channel is Important for Proper Maintenance of Oscillatory Activity in the Thalamocortical System. Cerebral Cortex. 29(5). 2291–2304. 47 indexed citations
8.
Albrecht, Stefanie, Venu Narayanan, Laura Starost, et al.. (2019). The K2P‐channel TASK1 affects Oligodendroglial differentiation but not myelin restoration. Glia. 67(5). 870–883. 5 indexed citations
9.
Cerina, Manuela, Venu Narayanan, Patrick Meuth, et al.. (2018). Protective potential of dimethyl fumarate in a mouse model of thalamocortical demyelination. Brain Structure and Function. 223(7). 3091–3106. 18 indexed citations
10.
Narayanan, Venu, Manuela Cerina, Kerstin Göbel, et al.. (2018). Impairment of frequency-specific responses associated with altered electrical activity patterns in auditory thalamus following focal and general demyelination. Experimental Neurology. 309. 54–66. 16 indexed citations
11.
Göbel, Kerstin, Susann Pankratz, Alexander M. Herrmann, et al.. (2018). Plasma kallikrein modulates immune cell trafficking during neuroinflammation via PAR2 and bradykinin release. Proceedings of the National Academy of Sciences. 116(1). 271–276. 43 indexed citations
12.
Zobeiri, Mehrnoush, Rahul Chaudhary, Annika Lüttjohann, et al.. (2017). Modulation of thalamocortical oscillations by TRIP8b, an auxiliary subunit for HCN channels. Brain Structure and Function. 223(3). 1537–1564. 31 indexed citations
13.
Cerina, Manuela, Venu Narayanan, Kerstin Göbel, et al.. (2016). The quality of cortical network function recovery depends on localization and degree of axonal demyelination. Brain Behavior and Immunity. 59. 103–117. 27 indexed citations
14.
Lesting, Jörg, et al.. (2013). Directional Theta Coherence in Prefrontal Cortical to Amygdalo-Hippocampal Pathways Signals Fear Extinction. PLoS ONE. 8(10). e77707–e77707. 78 indexed citations
15.
Narayanan, Venu, Rebecca S. Heiming, Friederike Jansen, et al.. (2011). Social Defeat: Impact on Fear Extinction and Amygdala-Prefrontal Cortical Theta Synchrony in 5-HTT Deficient Mice. PLoS ONE. 6(7). e22600–e22600. 94 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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