Vikas Arige

566 total citations
23 papers, 367 citations indexed

About

Vikas Arige is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Physiology. According to data from OpenAlex, Vikas Arige has authored 23 papers receiving a total of 367 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 7 papers in Cellular and Molecular Neuroscience and 7 papers in Physiology. Recurrent topics in Vikas Arige's work include Ion channel regulation and function (9 papers), Calcium signaling and nucleotide metabolism (7 papers) and Protein Kinase Regulation and GTPase Signaling (6 papers). Vikas Arige is often cited by papers focused on Ion channel regulation and function (9 papers), Calcium signaling and nucleotide metabolism (7 papers) and Protein Kinase Regulation and GTPase Signaling (6 papers). Vikas Arige collaborates with scholars based in United States, India and United Kingdom. Vikas Arige's co-authors include David I. Yule, Larry E. Wagner, Ryan E. Yoast, Scott M. Emrich, Mohamed Trebak, Guizhen Fan, Mariah R. Baker, Ping Xin, James Sneyd and Nadine Hempel and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Nature Communications.

In The Last Decade

Vikas Arige

20 papers receiving 366 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Vikas Arige United States 12 208 99 73 73 46 23 367
Baixia Hao Hong Kong 10 211 1.0× 80 0.8× 51 0.7× 108 1.5× 50 1.1× 13 432
Anne‐Sophie Borowiec France 15 300 1.4× 269 2.7× 141 1.9× 40 0.5× 44 1.0× 16 587
Krishna Samanta India 12 358 1.7× 150 1.5× 124 1.7× 44 0.6× 115 2.5× 25 555
Alexandre Bokhobza France 10 252 1.2× 273 2.8× 93 1.3× 39 0.5× 16 0.3× 13 480
Pierre Rybarczyk France 8 199 1.0× 157 1.6× 33 0.5× 33 0.5× 26 0.6× 13 435
Chun-Yin Lo Hong Kong 8 174 0.8× 121 1.2× 32 0.4× 23 0.3× 15 0.3× 10 334
Lu Sun China 12 261 1.3× 227 2.3× 130 1.8× 23 0.3× 36 0.8× 22 508
Maylis Raphaël France 8 309 1.5× 289 2.9× 79 1.1× 48 0.7× 82 1.8× 8 537
Jonathan E. Pottle United States 4 254 1.2× 128 1.3× 61 0.8× 29 0.4× 12 0.3× 5 341
A. Freek Weidema Netherlands 10 400 1.9× 204 2.1× 126 1.7× 100 1.4× 77 1.7× 14 612

Countries citing papers authored by Vikas Arige

Since Specialization
Citations

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

Fields of papers citing papers by Vikas Arige

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Vikas Arige

This figure shows the co-authorship network connecting the top 25 collaborators of Vikas Arige. A scholar is included among the top collaborators of Vikas Arige 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 Vikas Arige. Vikas Arige 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.
Arige, Vikas, Larry E. Wagner, Sundeep Malik, et al.. (2025). Functional investigation of a putative calcium-binding site involved in the inhibition of inositol 1,4,5-trisphosphate receptor activity. Journal of Biological Chemistry. 301(3). 108302–108302.
2.
Arige, Vikas, David M. MacLean, & David I. Yule. (2024). Inositol 1,4,5-Trisphosphate Receptor Mutations Associated with Human Disease: Insights into Receptor Function and Dysfunction. Annual Review of Physiology. 87(1). 201–228. 3 indexed citations
3.
Arige, Vikas & David I. Yule. (2024). PIP2 primes IP3 receptor activity: It takes at least three IP3s to open!. Cell Calcium. 124. 102970–102970.
4.
Baker, Mariah R., Guizhen Fan, Vikas Arige, David I. Yule, & Irina I. Serysheva. (2023). Understanding IP3R channels: From structural underpinnings to ligand-dependent conformational landscape. Cell Calcium. 114. 102770–102770. 13 indexed citations
6.
Yuan, Yu, Vikas Arige, Ryo� Saito, et al.. (2023). Two-pore channel-2 and inositol trisphosphate receptors coordinate Ca2+ signals between lysosomes and the endoplasmic reticulum. Cell Reports. 43(1). 113628–113628. 18 indexed citations
7.
Arige, Vikas, Larry E. Wagner, Sundeep Malik, et al.. (2022). Functional determination of calcium-binding sites required for the activation of inositol 1,4,5-trisphosphate receptors. Proceedings of the National Academy of Sciences. 119(39). e2209267119–e2209267119. 28 indexed citations
8.
Fan, Guizhen, Mariah R. Baker, Vikas Arige, et al.. (2022). Conformational motions and ligand-binding underlying gating and regulation in IP3R channel. Nature Communications. 13(1). 6942–6942. 29 indexed citations
9.
Yuan, Yu, Taufiq Rahman, Stephen R. Bolsover, et al.. (2022). Segregated cation flux by TPC2 biases Ca2+ signaling through lysosomes. Nature Communications. 13(1). 4481–4481. 20 indexed citations
10.
Arige, Vikas, Julika Neumann, Sundeep Malik, et al.. (2022). Missense mutations in inositol 1,4,5-trisphosphate receptor type 3 result in leaky Ca2+ channels and activation of store-operated Ca2+ entry. iScience. 25(12). 105523–105523. 7 indexed citations
11.
Arige, Vikas & David I. Yule. (2022). Spatial and temporal crosstalk between the cAMP and Ca2+ signaling systems. Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1869(9). 119293–119293. 12 indexed citations
12.
Arige, Vikas, et al.. (2021). CREB regulates the expression of type 1 inositol 1,4,5-trisphosphate receptors. Journal of Cell Science. 134(20). 9 indexed citations
13.
Emrich, Scott M., Ryan E. Yoast, Ping Xin, et al.. (2021). Omnitemporal choreographies of all five STIM/Orai and IP3Rs underlie the complexity of mammalian Ca2+ signaling. Cell Reports. 34(9). 108760–108760. 70 indexed citations
14.
Arige, Vikas, et al.. (2021). An evolutionarily-conserved promoter allele governs HMG-CoA reductase expression in spontaneously hypertensive rat. Journal of Molecular and Cellular Cardiology. 158. 140–152. 3 indexed citations
15.
Yoast, Ryan E., Scott M. Emrich, Xuexin Zhang, et al.. (2021). The Mitochondrial Ca2+ uniporter is a central regulator of interorganellar Ca2+ transfer and NFAT activation. Journal of Biological Chemistry. 297(4). 101174–101174. 38 indexed citations
16.
17.
Arige, Vikas & David I. Yule. (2020). Pivotal role of type-1 inositol 1,4,5-trisphosphate receptor for glucagon-induced gluconeogenesis. Cell Calcium. 90. 102243–102243. 2 indexed citations
18.
Ponrasu, Thangavel, et al.. (2019). Design and evaluation of Konjac glucomannan-based bioactive interpenetrating network (IPN) scaffolds for engineering vascularized bone tissues. International Journal of Biological Macromolecules. 143. 30–40. 38 indexed citations
19.
Arige, Vikas, et al.. (2019). Regulation of Monoamine Oxidase B Gene Expression: Key Roles for Transcription Factors Sp1, Egr1 and CREB, and microRNAs miR-300 and miR-1224. Journal of Molecular Biology. 431(6). 1127–1147. 11 indexed citations
20.
Arige, Vikas, et al.. (2016). Functional promoter polymorphisms direct the expression of cystathionine gamma-lyase gene in mouse models of essential hypertension. Journal of Molecular and Cellular Cardiology. 102. 61–73. 7 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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