Louis S. Premkumar

6.2k total citations · 2 hit papers
73 papers, 5.0k citations indexed

About

Louis S. Premkumar is a scholar working on Molecular Biology, Sensory Systems and Physiology. According to data from OpenAlex, Louis S. Premkumar has authored 73 papers receiving a total of 5.0k indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Molecular Biology, 34 papers in Sensory Systems and 33 papers in Physiology. Recurrent topics in Louis S. Premkumar's work include Ion Channels and Receptors (34 papers), Pain Mechanisms and Treatments (29 papers) and Ion channel regulation and function (28 papers). Louis S. Premkumar is often cited by papers focused on Ion Channels and Receptors (34 papers), Pain Mechanisms and Treatments (29 papers) and Ion channel regulation and function (28 papers). Louis S. Premkumar collaborates with scholars based in United States, Australia and India. Louis S. Premkumar's co-authors include Gerard P. Ahern, Manish Raisinghani, Parul Sikand, Mahendra Bishnoi, Anthony Auerbach, Peter W. Gage, Nobuki Nakanishi, Stuart A. Lipton, Mary E. Pauza and Shuang-Quan Yu and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Neuron.

In The Last Decade

Louis S. Premkumar

73 papers receiving 4.9k citations

Hit Papers

Induction of vanilloid receptor channel activity by prote... 2000 2026 2008 2017 2000 2002 200 400 600

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Louis S. Premkumar United States 36 2.3k 2.1k 1.8k 1.7k 396 73 5.0k
Gerard P. Ahern United States 35 1.3k 0.6× 1.8k 0.9× 1.9k 1.0× 1.4k 0.9× 475 1.2× 57 4.8k
Martin J. Gunthorpe United Kingdom 32 2.4k 1.0× 2.1k 1.0× 4.0k 2.2× 2.5k 1.5× 814 2.1× 46 6.9k
Alex Harper United Kingdom 11 2.8k 1.2× 2.7k 1.3× 1.1k 0.6× 1.2k 0.7× 199 0.5× 18 4.7k
Christopher D. Benham United Kingdom 48 3.5k 1.5× 4.7k 2.3× 3.5k 1.9× 1.7k 1.0× 971 2.5× 92 9.1k
Iain F. James United Kingdom 27 2.0k 0.9× 1.8k 0.9× 1.0k 0.6× 1.2k 0.8× 175 0.4× 35 3.8k
Narender R. Gavva United States 33 888 0.4× 898 0.4× 2.4k 1.3× 1.5k 0.9× 385 1.0× 54 3.8k
Marc Freichel Germany 54 2.4k 1.1× 3.9k 1.9× 4.2k 2.3× 1.0k 0.6× 1.4k 3.4× 145 8.2k
Adrian D. Bonev United States 45 2.7k 1.2× 5.4k 2.6× 1.2k 0.7× 2.5k 1.5× 258 0.7× 90 8.5k
T. B. Bolton United Kingdom 46 3.5k 1.5× 6.1k 2.9× 1.3k 0.7× 1.8k 1.1× 232 0.6× 147 8.3k
Neil V. Marrion United Kingdom 41 3.8k 1.7× 5.5k 2.7× 530 0.3× 1.1k 0.7× 247 0.6× 74 9.1k

Countries citing papers authored by Louis S. Premkumar

Since Specialization
Citations

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

Fields of papers citing papers by Louis S. Premkumar

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Louis S. Premkumar. 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 Louis S. Premkumar. The network helps show where Louis S. Premkumar may publish in the future.

Co-authorship network of co-authors of Louis S. Premkumar

This figure shows the co-authorship network connecting the top 25 collaborators of Louis S. Premkumar. A scholar is included among the top collaborators of Louis S. Premkumar 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 Louis S. Premkumar. Louis S. Premkumar 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.
Sharma, Aarushi, et al.. (2018). CLCA2 is a positive regulator of store-operated calcium entry and TMEM16A. PLoS ONE. 13(5). e0196512–e0196512. 29 indexed citations
2.
Samineni, Vijay K., Louis S. Premkumar, & Carl L. Faingold. (2017). Neuropathic pain-induced enhancement of spontaneous and pain-evoked neuronal activity in the periaqueductal gray that is attenuated by gabapentin. Pain. 158(7). 1241–1253. 41 indexed citations
3.
Evans, M. Steven, et al.. (2012). Sumatriptan Inhibits TRPV1 Channels in Trigeminal Neurons. Headache The Journal of Head and Face Pain. 52(5). 773–784. 47 indexed citations
4.
Premkumar, Louis S., et al.. (2012). TRP channels and analgesia. Life Sciences. 92(8-9). 415–424. 99 indexed citations
5.
Cao, De-Shou, et al.. (2012). Expression of Transient Receptor Potential Ankyrin 1 (TRPA1) and Its Role in Insulin Release from Rat Pancreatic Beta Cells. PLoS ONE. 7(5). e38005–e38005. 106 indexed citations
6.
Bishnoi, Mahendra, et al.. (2011). Preservation of Acute Pain and Efferent Functions Following Intrathecal Resiniferatoxin-Induced Analgesia in Rats. Journal of Pain. 12(9). 991–1003. 33 indexed citations
7.
Walia, Vijay, Ming Ding, Sumit Kumar, et al.. (2009). hCLCA2 Is a p53-Inducible Inhibitor of Breast Cancer Cell Proliferation. Cancer Research. 69(16). 6624–6632. 53 indexed citations
8.
Premkumar, Louis S. & Parul Sikand. (2008). TRPV1: A Target for Next Generation Analgesics. Current Neuropharmacology. 6(2). 151–163. 94 indexed citations
9.
Sikand, Parul & Louis S. Premkumar. (2007). Potentiation of glutamatergic synaptic transmission by protein kinase C‐mediated sensitization of TRPV1 at the first sensory synapse. The Journal of Physiology. 581(2). 631–647. 109 indexed citations
10.
11.
Raisinghani, Manish, et al.. (2005). Activation of transient receptor potential vanilloid 1 (TRPV1) by resiniferatoxin. The Journal of Physiology. 567(3). 771–786. 112 indexed citations
12.
Premkumar, Louis S., et al.. (2005). Downregulation of Transient Receptor Potential Melastatin 8 by Protein Kinase C-Mediated Dephosphorylation. Journal of Neuroscience. 25(49). 11322–11329. 128 indexed citations
13.
Raisinghani, Manish, et al.. (2004). Direct Interaction of Adenosine with the TRPV1 Channel Protein. Journal of Neuroscience. 24(14). 3663–3671. 73 indexed citations
14.
Premkumar, Louis S., et al.. (2003). Functional impairment of TRPV1 in diabetic peripheral neuropathy. 3819. 1 indexed citations
15.
Das, Saumya, Y. Sasaki, Thomas Rothe, et al.. (1998). Increased NMDA current and spine density in mice lacking the NMDA receptor subunit NR3A. Nature. 393(6683). 377–381. 471 indexed citations
16.
Premkumar, Louis S., Feng Qin, & Anthony Auerbach. (1997). Subconductance States of a Mutant NMDA Receptor Channel Kinetics, Calcium, and Voltage Dependence . The Journal of General Physiology. 109(2). 181–189. 46 indexed citations
17.
Premkumar, Louis S. & Anthony Auerbach. (1996). Identification of a High Affinity Divalent Cation Binding Site near the Entrance of the NMDA Receptor Channel. Neuron. 16(4). 869–880. 90 indexed citations
18.
Premkumar, Louis S., et al.. (1996). Ion Channels Formed by NB, an Influenza B Virus Protein. The Journal of Membrane Biology. 150(2). 127–132. 67 indexed citations
19.
Premkumar, Louis S., Shin‐Ho Chung, & Peter W. Gage. (1990). GABA-induced potassium channels in cultured neurons. Proceedings of the Royal Society B Biological Sciences. 241(1301). 153–158. 33 indexed citations
20.
Chung, Shin‐Ho, J.B. Moore, L. Xia, Louis S. Premkumar, & Peter W. Gage. (1990). Characterization of single channel currents using digital signal processing techniques based on Hidden Markov Models. Philosophical Transactions of the Royal Society B Biological Sciences. 329(1254). 265–285. 148 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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