Matthew P. DeLisa

9.7k total citations
161 papers, 7.2k citations indexed

About

Matthew P. DeLisa is a scholar working on Molecular Biology, Ecology and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, Matthew P. DeLisa has authored 161 papers receiving a total of 7.2k indexed citations (citations by other indexed papers that have themselves been cited), including 126 papers in Molecular Biology, 53 papers in Ecology and 41 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in Matthew P. DeLisa's work include Bacteriophages and microbial interactions (53 papers), Glycosylation and Glycoproteins Research (48 papers) and RNA and protein synthesis mechanisms (44 papers). Matthew P. DeLisa is often cited by papers focused on Bacteriophages and microbial interactions (53 papers), Glycosylation and Glycoproteins Research (48 papers) and RNA and protein synthesis mechanisms (44 papers). Matthew P. DeLisa collaborates with scholars based in United States, Thailand and United Kingdom. Matthew P. DeLisa's co-authors include William E. Bentley, Adam C. Fisher, George Georgiou, David Putnam, Jeffrey D. Varner, Robert Conrado, James J. Valdés, Michael C. Jewett, Tracy Palmer and Cassandra Guarino and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Matthew P. DeLisa

156 papers receiving 7.1k 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 P. DeLisa United States 48 5.2k 1.5k 1.4k 947 907 161 7.2k
Warren W. Wakarchuk Canada 53 5.2k 1.0× 651 0.4× 655 0.5× 394 0.4× 979 1.1× 156 7.7k
Antonio Villaverde Spain 54 7.6k 1.5× 1.5k 1.0× 1.9k 1.3× 1.2k 1.3× 1.2k 1.3× 348 10.5k
Roland Contreras Belgium 46 5.3k 1.0× 1.1k 0.7× 952 0.7× 705 0.7× 485 0.5× 153 7.8k
Silvia Spinelli France 48 3.7k 0.7× 1.4k 1.0× 922 0.6× 1.8k 1.9× 486 0.5× 107 6.5k
Remy Loris Belgium 47 5.3k 1.0× 1.1k 0.8× 1.7k 1.1× 1.5k 1.6× 230 0.3× 170 7.5k
Alain Charbit France 41 2.7k 0.5× 1.2k 0.8× 1.4k 1.0× 430 0.5× 191 0.2× 147 4.9k
Thilo Stehle Germany 61 5.4k 1.0× 1.1k 0.7× 2.3k 1.6× 1.1k 1.1× 328 0.4× 190 11.9k
Thierry Vernet France 48 4.4k 0.8× 566 0.4× 1.2k 0.8× 274 0.3× 268 0.3× 160 7.9k
Michel Gilbert Canada 47 3.3k 0.6× 694 0.5× 405 0.3× 443 0.5× 274 0.3× 138 6.1k
Tilman Schirmer Switzerland 55 6.9k 1.3× 1.0k 0.7× 2.9k 2.0× 162 0.2× 1.1k 1.2× 116 9.9k

Countries citing papers authored by Matthew P. DeLisa

Since Specialization
Citations

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

Fields of papers citing papers by Matthew P. DeLisa

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Matthew P. DeLisa

This figure shows the co-authorship network connecting the top 25 collaborators of Matthew P. DeLisa. A scholar is included among the top collaborators of Matthew P. DeLisa 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 P. DeLisa. Matthew P. DeLisa 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.
Mahajan, Sai Pooja, Christopher A. Alabi, Parastoo Azadi, et al.. (2025). Discovery of a single-subunit oligosaccharyltransferase that enables glycosylation of full-length IgG antibodies in bacteria. Nature Communications. 16(1). 6152–6152. 2 indexed citations
2.
Jewett, Michael C., et al.. (2024). Bacterial glycoengineering: Cell-based and cell-free routes for producing biopharmaceuticals with customized glycosylation. Current Opinion in Chemical Biology. 81. 102500–102500. 3 indexed citations
3.
DeLisa, Matthew P., et al.. (2024). Bioreversible Anionic Cloaking Enables Intracellular Protein Delivery with Ionizable Lipid Nanoparticles. ACS Central Science. 10(6). 1179–1190. 9 indexed citations
4.
Rodríguez‐López, Alexander, Ángela J. Espejo, Carolina Cardona, et al.. (2024). Novel human recombinant N-acetylgalactosamine-6-sulfate sulfatase produced in a glyco-engineered Escherichia coli strain. Heliyon. 10(12). e32555–e32555.
5.
Park, Sangwoo, Marshall J. Colville, Carolyn R. Shurer, et al.. (2023). Mucins form a nanoscale physical barrier against immune cell attack. Biophysical Journal. 122(3). 435a–435a. 1 indexed citations
6.
Jaroentomeechai, Thapakorn, Yiwen Liu, Ruchika Bhawal, et al.. (2022). A universal glycoenzyme biosynthesis pipeline that enables efficient cell-free remodeling of glycans. Nature Communications. 13(1). 6325–6325. 32 indexed citations
7.
Li, Mingji, et al.. (2021). Engineering a Supersecreting Strain of Escherichia coli by Directed Coevolution of the Multiprotein Tat Translocation Machinery. ACS Synthetic Biology. 10(11). 2947–2958. 9 indexed citations
8.
DeLisa, Matthew P., et al.. (2020). Effects of variable domain orientation on anti‐HER2 single‐chain variable fragment antibody expressed in the Escherichia coli cytoplasm. Biotechnology Progress. 37(2). e3102–e3102. 13 indexed citations
9.
Natarajan, Aravind, Thapakorn Jaroentomeechai, Asif Shajahan, et al.. (2020). Engineering orthogonal human O-linked glycoprotein biosynthesis in bacteria. Nature Chemical Biology. 16(10). 1062–1070. 36 indexed citations
10.
Merritt, Judith H., et al.. (2019). Antibody-Mediated Endocytosis of Polysialic Acid Enables Intracellular Delivery and Cytotoxicity of a Glycan-Directed Antibody–Drug Conjugate. Cancer Research. 79(8). 1810–1821. 16 indexed citations
11.
Li, Jiahe, et al.. (2019). Broad-Spectrum Proteome Editing with an Engineered Bacterial Ubiquitin Ligase Mimic. ACS Central Science. 5(5). 852–866. 34 indexed citations
12.
Kightlinger, Weston, Lin Liang, Wenhao Li, et al.. (2018). Design of glycosylation sites by rapid synthesis and analysis of glycosyltransferases. Nature Chemical Biology. 14(6). 627–635. 108 indexed citations
13.
Weyant, Kevin B., Joseph Rosenthal, Christian Heiß, et al.. (2016). Immunization with Outer Membrane Vesicles Displaying Designer Glycotopes Yields Class-Switched, Glycan-Specific Antibodies. Cell chemical biology. 23(6). 655–665. 43 indexed citations
14.
Conrado, Robert, Gabriel C. Wu, Jason T. Boock, et al.. (2011). DNA-guided assembly of biosynthetic pathways promotes improved catalytic efficiency. Nucleic Acids Research. 40(4). 1879–1889. 221 indexed citations
15.
Borrero, Ernesto E., et al.. (2010). Kinetics and Reaction Coordinates of the Reassembly of Protein Fragments Via Forward Flux Sampling. Biophysical Journal. 98(9). 1911–1920. 5 indexed citations
16.
Kim, Jae‐Young, Anne M. Doody, David J. Chen, et al.. (2008). Engineered Bacterial Outer Membrane Vesicles with Enhanced Functionality. Journal of Molecular Biology. 380(1). 51–66. 141 indexed citations
17.
Maurer, H. Carlo, et al.. (2008). Following the Path of a Twin-arginine Precursor along the TatABC Translocase of Escherichia coli. Journal of Biological Chemistry. 283(48). 33267–33275. 61 indexed citations
18.
Masip, Lluis, Jonathan L. Pan, James E. Penner‐Hahn, et al.. (2004). An Engineered Pathway for the Formation of Protein Disulfide Bonds. Science. 303(5661). 1185–1189. 65 indexed citations
19.
DeLisa, Matthew P., Philip Lee, Tracy Palmer, & George Georgiou. (2003). Phage Shock Protein PspA of Escherichia coli Relieves Saturation of Protein Export via the Tat Pathway. Journal of Bacteriology. 186(2). 366–373. 127 indexed citations
20.
DeLisa, Matthew P., et al.. (2003). Folding quality control in the export of proteins by the bacterial twin-arginine translocation pathway. Proceedings of the National Academy of Sciences. 100(10). 6115–6120. 253 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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