Leonidas Tsiokas

6.1k total citations · 2 hit papers
49 papers, 4.7k citations indexed

About

Leonidas Tsiokas is a scholar working on Molecular Biology, Genetics and Sensory Systems. According to data from OpenAlex, Leonidas Tsiokas has authored 49 papers receiving a total of 4.7k indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Molecular Biology, 23 papers in Genetics and 15 papers in Sensory Systems. Recurrent topics in Leonidas Tsiokas's work include Genetic and Kidney Cyst Diseases (23 papers), Ion Channels and Receptors (15 papers) and Renal and related cancers (12 papers). Leonidas Tsiokas is often cited by papers focused on Genetic and Kidney Cyst Diseases (23 papers), Ion Channels and Receptors (15 papers) and Renal and related cancers (12 papers). Leonidas Tsiokas collaborates with scholars based in United States, United Kingdom and China. Leonidas Tsiokas's co-authors include Vikas P. Sukhatme, Debabrata Mukhopadhyay, Gerd Walz, Emily Kim, Thierry Arnould, Sehyun Kim, Joan S. Brugge, David A. Foster, Feng Qian and Alessandra Boletta and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Leonidas Tsiokas

48 papers receiving 4.7k citations

Hit Papers

Co-assembly of polycystin-1 and -2 produces unique cation... 1995 2026 2005 2015 2000 1995 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
Leonidas Tsiokas United States 31 3.3k 2.3k 930 787 611 49 4.7k
Guanqing Wu United States 28 3.0k 0.9× 3.1k 1.3× 1.0k 1.1× 205 0.3× 478 0.8× 45 4.3k
Michael R. Bösl Germany 28 3.4k 1.0× 498 0.2× 240 0.3× 308 0.4× 722 1.2× 40 5.0k
Andrew D. Phillips United Kingdom 9 3.0k 0.9× 2.0k 0.9× 289 0.3× 100 0.1× 305 0.5× 10 4.8k
Alessandra Boletta Italy 33 3.2k 1.0× 3.4k 1.5× 1.2k 1.3× 129 0.2× 531 0.9× 73 4.5k
Ronald van Eijk Netherlands 34 2.0k 0.6× 901 0.4× 1.3k 1.4× 106 0.1× 159 0.3× 76 4.9k
Harry Hou United States 18 3.8k 1.2× 1.4k 0.6× 552 0.6× 66 0.1× 1.6k 2.6× 18 5.0k
Eric O. Williams United States 13 1.7k 0.5× 1.3k 0.6× 380 0.4× 156 0.2× 308 0.5× 16 2.7k
Paul S. Danielian United States 28 4.8k 1.4× 2.8k 1.2× 181 0.2× 62 0.1× 657 1.1× 38 6.6k
Muriel I. Kaiser‐Kupfer United States 41 2.0k 0.6× 566 0.2× 940 1.0× 222 0.3× 620 1.0× 103 4.9k
Christian C. Dibble United States 17 3.1k 1.0× 227 0.1× 218 0.2× 166 0.2× 627 1.0× 19 4.4k

Countries citing papers authored by Leonidas Tsiokas

Since Specialization
Citations

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

Fields of papers citing papers by Leonidas Tsiokas

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Leonidas Tsiokas

This figure shows the co-authorship network connecting the top 25 collaborators of Leonidas Tsiokas. A scholar is included among the top collaborators of Leonidas Tsiokas 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 Leonidas Tsiokas. Leonidas Tsiokas 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.
Zimmerman, Kurt A., et al.. (2025). SOX9-dependent fibrosis drives renal function in nephronophthisis. EMBO Molecular Medicine. 17(6). 1238–1258. 1 indexed citations
3.
Elechalawar, Chandra Kumar, Geeta Rao, Ram Vinod Roy, et al.. (2023). Gold Nanoparticles Inhibit Macropinocytosis by Decreasing KRAS Activation. ACS Nano. 17(10). 9326–9337. 4 indexed citations
4.
Tsiokas, Leonidas, et al.. (2020). Loss of polycystins suppresses deciliation via the activation of the centrosomal integrity pathway. Life Science Alliance. 3(9). e202000750–e202000750. 12 indexed citations
5.
Eby, Bonnie, Vasyl Nesin, Megan R. Lerner, et al.. (2020). Control of PTH secretion by the TRPC1 ion channel. JCI Insight. 5(8). 9 indexed citations
6.
Tsiokas, Leonidas, et al.. (2020). Polycystins as components of large multiprotein complexes of polycystin interactors. Cellular Signalling. 72. 109640–109640. 23 indexed citations
7.
Gunnes, Gjermund, Asbjørn Holmgren, Janne E. Reseland, et al.. (2019). STIM1 R304W in mice causes subgingival hair growth and an increased fraction of trabecular bone. Cell Calcium. 85. 102110–102110. 10 indexed citations
8.
Chakraborty, Prabir K., Soumyajit Banerjee Mustafi, Xunhao Xiong, et al.. (2017). MICU1 drives glycolysis and chemoresistance in ovarian cancer. Nature Communications. 8(1). 14634–14634. 137 indexed citations
9.
Kim, Seokho, Vasyl Nesin, Uyen Tran, et al.. (2016). The polycystin complex mediates Wnt/Ca2+ signalling. Nature Cell Biology. 18(7). 752–764. 132 indexed citations
10.
Maskey, Dipak, M. Caleb Marlin, Seok‐Ho Kim, et al.. (2015). Cell cycle‐dependent ubiquitylation and destruction of NDE 1 by CDK 5‐ FBW 7 regulates ciliary length. The EMBO Journal. 34(19). 2424–2440. 64 indexed citations
11.
Nesin, Vasyl, Graham B. Wiley, Maria Kousi, et al.. (2014). Activating mutations in STIM1 and ORAI1 cause overlapping syndromes of tubular myopathy and congenital miosis. Proceedings of the National Academy of Sciences. 111(11). 4197–4202. 180 indexed citations
12.
Nesin, Vasyl & Leonidas Tsiokas. (2014). TRPC1. Handbook of experimental pharmacology. 222. 15–51. 39 indexed citations
13.
Chitalia, Vipul C., Mikhail V. Panchenko, Lirong Zeng, et al.. (2012). Polycystin-1 regulates the stability and ubiquitination of transcription factor Jade-1. Human Molecular Genetics. 21(26). 5456–5471. 15 indexed citations
14.
Kim, Sehyun & Leonidas Tsiokas. (2011). Cilia and cell cycle re-entry. Cell Cycle. 10(16). 2683–2690. 112 indexed citations
15.
Seth, Malini, Lan Mao, Victoria Graham, et al.. (2009). TRPC1 Channels Are Critical for Hypertrophic Signaling in the Heart. Circulation Research. 105(10). 1023–1030. 179 indexed citations
16.
Feng, Shuang, Andrew J. Streets, Linda J. Newby, et al.. (2008). Identification and Functional Characterization of an N-terminal Oligomerization Domain for Polycystin-2. Journal of Biological Chemistry. 283(42). 28471–28479. 46 indexed citations
17.
Felekkis, Kyriacos, Evdokia Kastanos, Ralph Witzgall, et al.. (2008). Mutant polycystin-2 induces proliferation in primary rat tubular epithelial cells in a STAT-1/p21-independent fashion accompanied instead by alterations in expression of p57KIP2and Cdk2. BMC Nephrology. 9(1). 10–10. 21 indexed citations
18.
Li, Wei-Ping, Leonidas Tsiokas, Steven C. Sansom, & Rong Ma. (2004). Epidermal Growth Factor Activates Store-operated Ca2+ Channels through an Inositol 1,4,5-Trisphosphate-independent Pathway in Human Glomerular Mesangial Cells. Journal of Biological Chemistry. 279(6). 4570–4577. 32 indexed citations
19.
Gorbsky, Gary J., et al.. (2004). PKD2 Interacts and Co-localizes with mDia1 to Mitotic Spindles of Dividing Cells. Journal of Biological Chemistry. 279(28). 29728–29739. 91 indexed citations
20.
Mukhopadhyay, Debabrata, et al.. (1995). Hypoxic induction of human vascular endothelial growth factor expression through c-Src activation. Nature. 375(6532). 577–581. 517 indexed citations breakdown →

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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