Liron David

2.0k total citations · 2 hit papers
20 papers, 1.2k citations indexed

About

Liron David is a scholar working on Molecular Biology, Immunology and Ecology, Evolution, Behavior and Systematics. According to data from OpenAlex, Liron David has authored 20 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 6 papers in Immunology and 4 papers in Ecology, Evolution, Behavior and Systematics. Recurrent topics in Liron David's work include Photosynthetic Processes and Mechanisms (8 papers), Spectroscopy and Quantum Chemical Studies (3 papers) and Inflammasome and immune disorders (3 papers). Liron David is often cited by papers focused on Photosynthetic Processes and Mechanisms (8 papers), Spectroscopy and Quantum Chemical Studies (3 papers) and Inflammasome and immune disorders (3 papers). Liron David collaborates with scholars based in United States, Israel and Canada. Liron David's co-authors include Hao Wu, Noam Adir, Xinzheng Zhang, Jianbin Ruan, Liudmila Andreeva, Chen Shen, Shaun Rawson, Pablo Pelegrı́n, Yang Li and Jiayi Wu and has published in prestigious journals such as Science, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Liron David

20 papers receiving 1.2k citations

Hit Papers

NLRP3 cages revealed by full-length mouse NLRP3 structure... 2021 2026 2022 2024 2021 2024 50 100 150

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Liron David United States 14 905 419 134 113 111 20 1.2k
Zhi‐Xin Wang China 21 1.0k 1.1× 69 0.2× 34 0.3× 68 0.6× 184 1.7× 51 1.3k
F. Lottspeich Germany 15 881 1.0× 588 1.4× 22 0.2× 557 4.9× 39 0.4× 24 1.5k
H Michel United States 14 892 1.0× 212 0.5× 101 0.8× 21 0.2× 105 0.9× 16 1.2k
John S. Reader United States 20 926 1.0× 82 0.2× 24 0.2× 42 0.4× 104 0.9× 27 1.2k
Paola Londei Italy 23 1.9k 2.1× 103 0.2× 16 0.1× 84 0.7× 49 0.4× 77 2.1k
Rinku Jain United States 23 1.3k 1.4× 121 0.3× 24 0.2× 156 1.4× 75 0.7× 40 1.7k
Takumi Ishizuka Japan 20 1.3k 1.4× 195 0.5× 28 0.2× 38 0.3× 91 0.8× 52 1.6k
Jonathan P. Schuermann United States 18 864 1.0× 78 0.2× 48 0.4× 68 0.6× 72 0.6× 25 1.2k
Andrea Scrima Germany 17 1.4k 1.6× 93 0.2× 18 0.1× 76 0.7× 154 1.4× 31 1.8k
Sebastian Klinge United States 24 2.0k 2.2× 82 0.2× 81 0.6× 71 0.6× 82 0.7× 34 2.2k

Countries citing papers authored by Liron David

Since Specialization
Citations

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

Fields of papers citing papers by Liron David

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Liron David

This figure shows the co-authorship network connecting the top 25 collaborators of Liron David. A scholar is included among the top collaborators of Liron David 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 Liron David. Liron David 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.
David, Liron, Louis Hollingsworth, Allen Volchuk, et al.. (2024). NINJ1 mediates plasma membrane rupture by cutting and releasing membrane disks. Cell. 187(9). 2224–2235.e16. 71 indexed citations breakdown →
2.
Xia, Min, Liron David, Matt Teater, et al.. (2022). BCL10 Mutations Define Distinct Dependencies Guiding Precision Therapy for DLBCL. Cancer Discovery. 12(8). OF1–OF20. 12 indexed citations
3.
David, Liron, Qiongchao Xi, Kameron Kooshesh, et al.. (2022). Piezo mechanosensory channels regulate centrosome integrity and mitotic entry. Proceedings of the National Academy of Sciences. 120(1). e2213846120–e2213846120. 7 indexed citations
4.
Andreeva, Liudmila, Liron David, Shaun Rawson, et al.. (2021). NLRP3 cages revealed by full-length mouse NLRP3 structure control pathway activation. Cell. 184(26). 6299–6312.e22. 179 indexed citations breakdown →
5.
Hollingsworth, Louis, Liron David, Yang Li, et al.. (2021). Mechanism of filament formation in UPA-promoted CARD8 and NLRP1 inflammasomes. Nature Communications. 12(1). 189–189. 57 indexed citations
6.
Wales, Thomas E., Julian Mintseris, Devin K. Schweppe, et al.. (2020). Homogeneous Oligomers of Pro-apoptotic BAX Reveal Structural Determinants of Mitochondrial Membrane Permeabilization. Molecular Cell. 79(1). 68–83.e7. 36 indexed citations
7.
Stinson, Jeffrey R., Batsukh Dorjbal, Dennis P. McDaniel, et al.. (2020). Gain-of-function mutations in CARD11 promote enhanced aggregation and idiosyncratic signalosome assembly. Cellular Immunology. 353. 104129–104129. 8 indexed citations
8.
Xia, Min, Liron David, Matthew Teater, et al.. (2020). BCL10 Gain-of-Function Mutations Aberrantly Induce Canonical and Non-Canonical NF-Kb Activation and Resistance to Ibrutinib in ABC-DLBCL. Blood. 136(Supplement 1). 2–3. 4 indexed citations
9.
David, Liron, Yang Li, Jun Ma, et al.. (2018). Assembly mechanism of the CARMA1–BCL10–MALT1–TRAF6 signalosome. Proceedings of the National Academy of Sciences. 115(7). 1499–1504. 77 indexed citations
10.
David, Liron, et al.. (2015). Linker proteins enable ultrafast excitation energy transfer in the phycobilisome antenna system of Thermosynechococcus vulcanus. Photochemical & Photobiological Sciences. 15(1). 31–44. 26 indexed citations
11.
Zhang, Liman, Shuobing Chen, Jianbin Ruan, et al.. (2015). Cryo-EM structure of the activated NAIP2-NLRC4 inflammasome reveals nucleated polymerization. Science. 350(6259). 404–409. 306 indexed citations
12.
David, Liron, et al.. (2014). Evidence of additional excitation energy transfer pathways in the phycobiliprotein antenna system of Acaryochloris marina. Photochemical & Photobiological Sciences. 14(2). 429–438. 8 indexed citations
13.
David, Liron, Mindy Prado, Ana‐Andreea Arteni, et al.. (2014). Structural studies show energy transfer within stabilized phycobilisomes independent of the mode of rod–core assembly. Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1837(3). 385–395. 43 indexed citations
14.
Yochelis, Shira, Liron David, Adam Faust, et al.. (2014). Room temperature biological quantum random walk in phycocyanin nanowires. Physical Chemistry Chemical Physics. 16(23). 11196–11201. 25 indexed citations
15.
David, Liron, et al.. (2014). Activation and deactivation of vibronic channels in intact phycocyanin rods. The Journal of Chemical Physics. 140(8). 85101–85101. 5 indexed citations
16.
Qiao, Qi, Chenghua Yang, Chao Zheng, et al.. (2013). Structural Architecture of the CARMA1/Bcl10/MALT1 Signalosome: Nucleation-Induced Filamentous Assembly. Molecular Cell. 51(6). 766–779. 138 indexed citations
17.
Yang, Chenghua, et al.. (2013). The CBM signalosome: Potential therapeutic target for aggressive lymphoma?. Cytokine & Growth Factor Reviews. 25(2). 175–183. 13 indexed citations
18.
David, Liron, et al.. (2010). High-Resolution Crystal Structures of Trimeric and Rod Phycocyanin. Journal of Molecular Biology. 405(1). 201–213. 78 indexed citations
19.
Dines, Monica, Eleonora Sendersky, Liron David, Rakefet Schwarz, & Noam Adir. (2008). Structural, Functional, and Mutational Analysis of the NblA Protein Provides Insight into Possible Modes of Interaction with the Phycobilisome. Journal of Biological Chemistry. 283(44). 30330–30340. 25 indexed citations
20.
David, Liron, et al.. (2008). Allophycocyanin Trimer Stability and Functionality Are Primarily Due to Polar Enhanced Hydrophobicity of the Phycocyanobilin Binding Pocket. Journal of Molecular Biology. 384(2). 406–421. 72 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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026