Matthew E. Call

3.3k total citations
41 papers, 2.6k citations indexed

About

Matthew E. Call is a scholar working on Immunology, Molecular Biology and Oncology. According to data from OpenAlex, Matthew E. Call has authored 41 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Immunology, 17 papers in Molecular Biology and 6 papers in Oncology. Recurrent topics in Matthew E. Call's work include Immune Cell Function and Interaction (21 papers), T-cell and B-cell Immunology (18 papers) and Lipid Membrane Structure and Behavior (9 papers). Matthew E. Call is often cited by papers focused on Immune Cell Function and Interaction (21 papers), T-cell and B-cell Immunology (18 papers) and Lipid Membrane Structure and Behavior (9 papers). Matthew E. Call collaborates with scholars based in Australia, United States and Switzerland. Matthew E. Call's co-authors include Kai W. Wucherpfennig, James J. Chou, Jason W. Pyrdol, Chenqi Xu, Martin Wiedmann, Melissa Call, Jianwen A. Feng, Jason R. Schnell, Étienne Gagnon and Charles D. Schwieters and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Journal of the American Chemical Society.

In The Last Decade

Matthew E. Call

38 papers receiving 2.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Matthew E. Call Australia 22 1.6k 941 592 305 140 41 2.6k
Jason W. Pyrdol United States 19 1.9k 1.2× 601 0.6× 742 1.3× 300 1.0× 153 1.1× 22 2.4k
Viia Valge-Archer United Kingdom 19 1.2k 0.8× 1.1k 1.2× 1.0k 1.7× 238 0.8× 106 0.8× 27 2.4k
Karin Reif United Kingdom 22 1.7k 1.1× 1.2k 1.2× 761 1.3× 187 0.6× 150 1.1× 29 2.7k
Julie Zikherman United States 23 1.5k 1.0× 728 0.8× 480 0.8× 163 0.5× 52 0.4× 49 2.2k
Theresa A. Kadlecek United States 24 2.3k 1.5× 1.3k 1.3× 703 1.2× 446 1.5× 98 0.7× 31 3.3k
Veronica Steri United States 17 705 0.5× 796 0.8× 827 1.4× 158 0.5× 82 0.6× 34 1.8k
Jianping Yin United States 19 1.0k 0.7× 982 1.0× 329 0.6× 242 0.8× 66 0.5× 24 2.0k
Tomáš Brdička Czechia 23 1.3k 0.8× 1.2k 1.2× 296 0.5× 239 0.8× 58 0.4× 52 2.3k
Tadashi Yokosuka Japan 24 3.0k 1.9× 1.1k 1.2× 1.4k 2.4× 384 1.3× 77 0.6× 43 4.1k
Toni Weinschenk Germany 24 2.0k 1.3× 1.6k 1.7× 1.4k 2.4× 299 1.0× 76 0.5× 50 3.2k

Countries citing papers authored by Matthew E. Call

Since Specialization
Citations

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

Fields of papers citing papers by Matthew E. Call

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Matthew E. Call. 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 Matthew E. Call. The network helps show where Matthew E. Call may publish in the future.

Co-authorship network of co-authors of Matthew E. Call

This figure shows the co-authorship network connecting the top 25 collaborators of Matthew E. Call. A scholar is included among the top collaborators of Matthew E. Call 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 Matthew E. Call. Matthew E. Call 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.
Ramsey, Jolene, J. C. K. Tovey, Daniel Cameron, et al.. (2025). Resolution of a T1-Like Bacteriophage Outbreak by Receptor Engineering. Molecular Biotechnology.
2.
Kuchel, Nathan W., Bernadine G.C. Lu, Kym N. Lowes, et al.. (2024). Mutational profiling of SARS-CoV-2 papain-like protease reveals requirements for function, structure, and drug escape. Nature Communications. 15(1). 6219–6219. 5 indexed citations
3.
Call, Matthew E., et al.. (2024). Deep mutational scanning reveals transmembrane features governing surface expression of the B cell antigen receptor. Frontiers in Immunology. 15. 1426795–1426795.
4.
Elazar, Assaf, Jonathan J. Weinstein, Raphael Trenker, et al.. (2022). De novo-designed transmembrane domains tune engineered receptor functions. eLife. 11. 34 indexed citations
5.
Trenker, Raphael, et al.. (2021). Human and viral membrane–associated E3 ubiquitin ligases MARCH1 and MIR2 recognize different features of CD86 to downregulate surface expression. Journal of Biological Chemistry. 297(1). 100900–100900. 9 indexed citations
6.
Call, Melissa, et al.. (2020). T Cell Activation Machinery: Form and Function in Natural and Engineered Immune Receptors. International Journal of Molecular Sciences. 21(19). 7424–7424. 10 indexed citations
7.
Bridgford, Jessica L., Su Min Lee, Paola Guglielmelli, et al.. (2019). Novel drivers and modifiers of MPL-dependent oncogenic transformation identified by deep mutational scanning. Blood. 135(4). 287–292. 34 indexed citations
8.
Byrne, Eamon F.X., et al.. (2018). A serine in the first transmembrane domain of the human E3 ubiquitin ligase MARCH9 is critical for down-regulation of its protein substrates. Journal of Biological Chemistry. 294(7). 2470–2485. 8 indexed citations
9.
Trenker, Raphael, Melissa Call, & Matthew E. Call. (2016). Progress and prospects for structural studies of transmembrane interactions in single-spanning receptors. Current Opinion in Structural Biology. 39. 115–123. 15 indexed citations
10.
Knoblich, Konstantin, Soohyung Park, Leonie van ‘t Hag, et al.. (2015). Transmembrane Complexes of DAP12 Crystallized in Lipid Membranes Provide Insights into Control of Oligomerization in Immunoreceptor Assembly. Cell Reports. 11(8). 1184–1192. 22 indexed citations
11.
Berry, Richard, Stephen J. Headey, Melissa Call, et al.. (2014). Structure of the Chicken CD3ϵδ/γ Heterodimer and Its Assembly with the αβT Cell Receptor. Journal of Biological Chemistry. 289(12). 8240–8251. 13 indexed citations
12.
Wucherpfennig, Kai W., Étienne Gagnon, Melissa Call, Eric S. Huseby, & Matthew E. Call. (2010). Structural Biology of the T-cell Receptor: Insights into Receptor Assembly, Ligand Recognition, and Initiation of Signaling. Cold Spring Harbor Perspectives in Biology. 2(4). a005140–a005140. 117 indexed citations
13.
Xu, Chenqi, Étienne Gagnon, Matthew E. Call, et al.. (2008). Regulation of T Cell Receptor Activation by Dynamic Membrane Binding of the CD3ɛ Cytoplasmic Tyrosine-Based Motif. Cell. 135(4). 702–713. 351 indexed citations
14.
Xu, Chenqi, Matthew E. Call, & Kai W. Wucherpfennig. (2006). A Membrane-proximal Tetracysteine Motif Contributes to Assembly of CD3δϵ and CD3γϵ Dimers with the T Cell Receptor. Journal of Biological Chemistry. 281(48). 36977–36984. 36 indexed citations
15.
Wang, Bingbing, Tara M. Love, Matthew E. Call, John G. Doench, & Carl D. Novina. (2006). Recapitulation of Short RNA-Directed Translational Gene Silencing In Vitro. Molecular Cell. 22(4). 553–560. 141 indexed citations
16.
O’Connor, Kevin C., Heiner Appel, Lisa Bregoli, et al.. (2005). Antibodies from Inflamed Central Nervous System Tissue Recognize Myelin Oligodendrocyte Glycoprotein. The Journal of Immunology. 175(3). 1974–1982. 132 indexed citations
17.
Feng, Jianwen A., et al.. (2005). Convergence on a Distinctive Assembly Mechanism by Unrelated Families of Activating Immune Receptors. Immunity. 22(4). 427–438. 65 indexed citations
18.
Call, Matthew E., Jason W. Pyrdol, & Kai W. Wucherpfennig. (2004). Stoichiometry of the T‐cell receptor–CD3 complex and key intermediates assembled in the endoplasmic reticulum. The EMBO Journal. 23(12). 2348–2357. 87 indexed citations
19.
Call, Matthew E. & Kai W. Wucherpfennig. (2004). Molecular mechanisms for the assembly of the T cell receptor–CD3 complex. Molecular Immunology. 40(18). 1295–1305. 85 indexed citations
20.
Call, Matthew E., Jason W. Pyrdol, Martin Wiedmann, & Kai W. Wucherpfennig. (2002). The Organizing Principle in the Formation of the T Cell Receptor-CD3 Complex. Cell. 111(7). 967–979. 329 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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Rankless by CCL
2026