Sagi Shapira

4.7k total citations · 1 hit paper
21 papers, 2.2k citations indexed

About

Sagi Shapira is a scholar working on Immunology, Molecular Biology and Parasitology. According to data from OpenAlex, Sagi Shapira has authored 21 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Immunology, 7 papers in Molecular Biology and 7 papers in Parasitology. Recurrent topics in Sagi Shapira's work include Immune Response and Inflammation (5 papers), Toxoplasma gondii Research Studies (5 papers) and Herpesvirus Infections and Treatments (4 papers). Sagi Shapira is often cited by papers focused on Immune Response and Inflammation (5 papers), Toxoplasma gondii Research Studies (5 papers) and Herpesvirus Infections and Treatments (4 papers). Sagi Shapira collaborates with scholars based in United States, United Kingdom and Argentina. Sagi Shapira's co-authors include Piyush B. Gupta, Guozhi Jiang, Christine M. Fillmore, Charlotte Kuperwasser, Kai Tao, Eric S. Lander, Christopher A. Hunter, Jorge Caamaño, Kendra Speirs and Colleen Kane and has published in prestigious journals such as Cell, Nature Medicine and Immunity.

In The Last Decade

Sagi Shapira

21 papers receiving 2.2k citations

Hit Papers

Stochastic State Transitions Give Rise to Phenotypic Equi... 2011 2026 2016 2021 2011 250 500 750 1000
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. Stochastic State Transitions Give Rise to Phenotypic Equilibrium in Populations of Cancer Cells
    2011 1.1k citations Piyush B. Gupta, Christine M. Fillmore et al. Cell profile →

Peers

Sagi Shapira
Serena Bonin Italy
Lars Dölken Germany
Gilles Gadéa France
Michael P. Weekes United Kingdom
Marissa Vignali United States
Konstantin M. J. Sparrer Germany
Martin Meier‐Schellersheim United States
Jean‐Pierre Abastado France
Bruce T. Seet Canada
E S Vitetta United States
Serena Bonin Italy
Sagi Shapira
Citations per year, relative to Sagi Shapira Sagi Shapira (= 1×) peers Serena Bonin

Countries citing papers authored by Sagi Shapira

Since Specialization
Citations

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

Fields of papers citing papers by Sagi Shapira

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sagi Shapira

This figure shows the co-authorship network connecting the top 25 collaborators of Sagi Shapira. A scholar is included among the top collaborators of Sagi Shapira 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 Sagi Shapira. Sagi Shapira 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.
Lasso, Gorka, Barry Honig, & Sagi Shapira. (2020). A Sweep of Earth’s Virome Reveals Host-Guided Viral Protein Structural Mimicry and Points to Determinants of Human Disease. Cell Systems. 12(1). 82–91.e3. 25 indexed citations
2.
Bell, Lucy, Cem Meydan, Jacob Kim, et al.. (2020). Transcriptional response modules characterize IL-1β and IL-6 activity in COVID-19. iScience. 24(1). 101896–101896. 23 indexed citations
3.
Ramlall, Vijendra, Phyllis Thangaraj, Cem Meydan, et al.. (2020). Immune complement and coagulation dysfunction in adverse outcomes of SARS-CoV-2 infection. Nature Medicine. 26(10). 1609–1615. 207 indexed citations
4.
Lasso, Gorka, Sandra V. Mayer, E. Winkelmann, et al.. (2019). A Structure-Informed Atlas of Human-Virus Interactions. Cell. 178(6). 1526–1541.e16. 90 indexed citations
5.
Abe, Takayuki, Albert Lee, Sitharam Ramaswami, et al.. (2017). Germ-Cell-Specific Inflammasome Component NLRP14 Negatively Regulates Cytosolic Nucleic Acid Sensing to Promote Fertilization. Immunity. 46(4). 621–634. 37 indexed citations
6.
Ghamsari, Lila, et al.. (2016). A High-Throughput Strategy for Dissecting Mammalian Genetic Interactions. PLoS ONE. 11(12). e0167617–e0167617. 4 indexed citations
7.
Garzón, José Ignacio, Lei Deng, Diana Murray, et al.. (2016). A computational interactome and functional annotation for the human proteome. eLife. 5. 53 indexed citations
8.
Gupta, Piyush B., Christine M. Fillmore, Guozhi Jiang, et al.. (2011). Stochastic State Transitions Give Rise to Phenotypic Equilibrium in Populations of Cancer Cells. Cell. 147(5). 1197–1197. 48 indexed citations
9.
Gupta, Piyush B., Christine M. Fillmore, Guozhi Jiang, et al.. (2011). Stochastic State Transitions Give Rise to Phenotypic Equilibrium in Populations of Cancer Cells. Cell. 146(6). 1042–1042. 1 indexed citations
10.
Gupta, Piyush B., Christine M. Fillmore, Guozhi Jiang, et al.. (2011). Stochastic State Transitions Give Rise to Phenotypic Equilibrium in Populations of Cancer Cells. Cell. 146(4). 633–644. 1116 indexed citations breakdown →
11.
Shapira, Sagi & Nir Hacohen. (2010). Systems biology approaches to dissect mammalian innate immunity. Current Opinion in Immunology. 23(1). 71–77. 23 indexed citations
12.
Harris, Tajie H., Emma H. Wilson, Elia D. Tait Wojno, et al.. (2010). NF-κB1 contributes to T cell-mediated control of Toxoplasma gondii in the CNS. Journal of Neuroimmunology. 222(1-2). 19–28. 19 indexed citations
13.
Shapira, Sagi, Irit Gat‐Viks, Bennett O. V. Shum, et al.. (2009). A Physical and Regulatory Map of Host-Influenza Interactions Reveals Pathways in H1N1 Infection. Cell. 139(7). 1255–1267. 11 indexed citations
14.
Tato, Cristina M., Nicola J. Mason, David Artis, et al.. (2006). Opposing roles of NF-κB family members in the regulation of NK cell proliferation and production of IFN-γ. International Immunology. 18(4). 505–513. 47 indexed citations
15.
Shapira, Sagi, Omar S. Harb, Mariana Matrajt, et al.. (2005). Initiation and termination of NF-κB signaling by the intracellular protozoan parasite Toxoplasma gondii. Journal of Cell Science. 118(15). 3501–3508. 55 indexed citations
16.
Artis, David, Colleen Kane, Colby Zaph, et al.. (2005). Dendritic Cell-Intrinsic Expression of NF-κB1 Is Required to Promote Optimal Th2 Cell Differentiation. The Journal of Immunology. 174(11). 7154–7159. 47 indexed citations
17.
Kane, Colleen, Laura Cervi, Jie Sun, et al.. (2004). Helminth Antigens Modulate TLR-Initiated Dendritic Cell Activation. The Journal of Immunology. 173(12). 7454–7461. 192 indexed citations
18.
Shapira, Sagi, Omar S. Harb, Jorge Caamaño, & Christopher A. Hunter. (2004). The NF-κB signaling pathway: immune evasion and immunoregulation during toxoplasmosis. International Journal for Parasitology. 34(3). 393–400. 32 indexed citations
19.
Artis, David, Sagi Shapira, Nicola J. Mason, et al.. (2002). Differential Requirement for NF-κB Family Members in Control of Helminth Infection and Intestinal Inflammation. The Journal of Immunology. 169(8). 4481–4487. 74 indexed citations
20.
Shapira, Sagi, et al.. (2002). Suppression of NF‐κB Activation by Infection withToxoplasma gondii. The Journal of Infectious Diseases. 185(s1). S66–S72. 111 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

Breakdown of academic impact, for papers by Serena Bonin Breakdown of academic impact, for papers by Lars Dölken Breakdown of academic impact, for papers by Gilles Gadéa Breakdown of academic impact, for papers by Michael P. Weekes Breakdown of academic impact, for papers by Marissa Vignali Breakdown of academic impact, for papers by Konstantin M. J. Sparrer Breakdown of academic impact, for papers by Martin Meier‐Schellersheim Breakdown of academic impact, for papers by Jean‐Pierre Abastado Breakdown of academic impact, for papers by Bruce T. Seet Breakdown of academic impact, for papers by E S Vitetta
Rankless by CCL
2026