P. Brear

1.0k total citations
41 papers, 648 citations indexed

About

P. Brear is a scholar working on Molecular Biology, Oncology and Genetics. According to data from OpenAlex, P. Brear has authored 41 papers receiving a total of 648 indexed citations (citations by other indexed papers that have themselves been cited), including 34 papers in Molecular Biology, 8 papers in Oncology and 8 papers in Genetics. Recurrent topics in P. Brear's work include Protein Kinase Regulation and GTPase Signaling (15 papers), Enzyme Structure and Function (7 papers) and Bacterial Genetics and Biotechnology (7 papers). P. Brear is often cited by papers focused on Protein Kinase Regulation and GTPase Signaling (15 papers), Enzyme Structure and Function (7 papers) and Bacterial Genetics and Biotechnology (7 papers). P. Brear collaborates with scholars based in United Kingdom, United States and Germany. P. Brear's co-authors include Marko Hyvönen, David R. Spring, Jessica Iegre, Hannah F. Sore, Claudia De Fusco, Martin Welch, Stephen K. Dolan, Nicholas J. Westwood, Dimitri Y. Chirgadze and L. Carro and has published in prestigious journals such as Nucleic Acids Research, Journal of Biological Chemistry and Nature Communications.

In The Last Decade

P. Brear

39 papers receiving 646 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
P. Brear United Kingdom 16 483 87 85 76 73 41 648
Krisna C. Duong‐Ly United States 13 609 1.3× 62 0.7× 87 1.0× 73 1.0× 63 0.9× 21 877
Gisela Gabernet Switzerland 15 494 1.0× 30 0.3× 90 1.1× 114 1.5× 51 0.7× 33 785
Francesco Merlino Italy 21 508 1.1× 88 1.0× 82 1.0× 21 0.3× 46 0.6× 54 909
Shanhe Wan China 16 337 0.7× 172 2.0× 122 1.4× 52 0.7× 32 0.4× 44 678
Sijin Wu China 18 491 1.0× 92 1.1× 120 1.4× 33 0.4× 19 0.3× 52 779
Timothy L. Foley United States 17 591 1.2× 233 2.7× 57 0.7× 35 0.5× 41 0.6× 27 807
Wanxu Huang China 13 757 1.6× 57 0.7× 115 1.4× 34 0.4× 23 0.3× 20 926
Nahlah Makki Almansour Saudi Arabia 13 262 0.5× 31 0.4× 150 1.8× 48 0.6× 47 0.6× 27 565
Seetharama D. Satyanarayanajois United States 17 323 0.7× 81 0.9× 133 1.6× 64 0.8× 67 0.9× 29 658

Countries citing papers authored by P. Brear

Since Specialization
Citations

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

Fields of papers citing papers by P. Brear

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of P. Brear

This figure shows the co-authorship network connecting the top 25 collaborators of P. Brear. A scholar is included among the top collaborators of P. Brear 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 P. Brear. P. Brear 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.
Dolan, Stephen K., Michael Kohlstedt, Lars Gläser, et al.. (2025). The 2-methylcitrate cycle and the glyoxylate shunt in Pseudomonas aeruginosa are linked through enzymatic redundancy. Journal of Biological Chemistry. 301(4). 108355–108355. 2 indexed citations
2.
Seki, Hikaru, et al.. (2025). Pseudomonas aeruginosa PfpI is a methylglyoxalase. Journal of Biological Chemistry. 301(4). 108374–108374.
3.
Lulla, Aleksei, Matthew I. J. Raybould, Timo N. Kohler, et al.. (2024). Rapid discovery of monoclonal antibodies by microfluidics-enabled FACS of single pathogen-specific antibody-secreting cells. Nature Biotechnology. 43(6). 960–970. 10 indexed citations
4.
Sonnleitner, Elisabeth, P. Brear, Armin Resch, et al.. (2023). Catabolite repression control protein antagonist, a novel player in Pseudomonas aeruginosa carbon catabolite repression control. Frontiers in Microbiology. 14. 1195558–1195558. 5 indexed citations
5.
Reinecke, Maria, P. Brear, Larsen Vornholz, et al.. (2023). Chemical proteomics reveals the target landscape of 1,000 kinase inhibitors. Nature Chemical Biology. 20(5). 577–585. 35 indexed citations
6.
Stanway, Steven J., Yuliya Demydchuk, G.A. Bezerra, et al.. (2023). Structure-Guided Chemical Optimization of Bicyclic Peptide (Bicycle) Inhibitors of Angiotensin-Converting Enzyme 2. Journal of Medicinal Chemistry. 66(14). 9881–9893. 3 indexed citations
7.
Iegre, Jessica, Claudio D’Amore, P. Brear, et al.. (2022). Development of small cyclic peptides targeting the CK2α/β interface. Chemical Communications. 58(30). 4791–4794. 3 indexed citations
8.
Dolan, Stephen K., Michael Kohlstedt, Lars Gläser, et al.. (2022). Systems-Wide Dissection of Organic Acid Assimilation in Pseudomonas aeruginosa Reveals a Novel Path To Underground Metabolism. mBio. 13(6). e0254122–e0254122. 14 indexed citations
9.
Brear, P., Claudia De Fusco, Jessica Iegre, et al.. (2022). A fragment-based approach leading to the discovery of inhibitors of CK2α with a novel mechanism of action. RSC Medicinal Chemistry. 13(11). 1420–1426. 2 indexed citations
10.
Iegre, Jessica, et al.. (2021). Chemical probes targeting the kinase CK2: a journey outside the catalytic box. Organic & Biomolecular Chemistry. 19(20). 4380–4396. 21 indexed citations
11.
Iegre, Jessica, et al.. (2021). Downfalls of Chemical Probes Acting at the Kinase ATP-Site: CK2 as a Case Study. Molecules. 26(7). 1977–1977. 19 indexed citations
12.
Wang, Meng, et al.. (2021). Structure, Function and Regulation of a Second Pyruvate Kinase Isozyme in Pseudomonas aeruginosa. Frontiers in Microbiology. 12. 790742–790742. 7 indexed citations
13.
Brear, P., et al.. (2020). Proposed Allosteric Inhibitors Bind to the ATP Site of CK2α. Journal of Medicinal Chemistry. 63(21). 12786–12798. 16 indexed citations
14.
Kufareva, Irina, P. Brear, Renaud Prudent, et al.. (2019). Discovery of holoenzyme-disrupting chemicals as substrate-selective CK2 inhibitors. Scientific Reports. 9(1). 15893–15893. 24 indexed citations
15.
Iegre, Jessica, P. Brear, David Baker, et al.. (2019). Efficient development of stable and highly functionalised peptides targeting the CK2α/CK2β protein–protein interaction. Chemical Science. 10(19). 5056–5063. 30 indexed citations
16.
Whitehouse, Andrew, M. Daben J. Libardo, Monica Kasbekar, et al.. (2019). Targeting of Fumarate Hydratase from Mycobacterium tuberculosis Using Allosteric Inhibitors with a Dimeric-Binding Mode. Journal of Medicinal Chemistry. 62(23). 10586–10604. 7 indexed citations
17.
Brear, P., et al.. (2019). Evolutionary plasticity in the allosteric regulator-binding site of pyruvate kinase isoform PykA from Pseudomonas aeruginosa. Journal of Biological Chemistry. 294(42). 15505–15516. 14 indexed citations
18.
Iegre, Jessica, P. Brear, Claudia De Fusco, et al.. (2018). Second-generation CK2α inhibitors targeting the αD pocket. Chemical Science. 9(11). 3041–3049. 33 indexed citations
19.
Westwood, Nicholas J., et al.. (2016). A Random Forest Model for Predicting Allosteric and Functional Sites on Proteins. Molecular Informatics. 35(3-4). 125–135. 28 indexed citations
20.
Zhou, Linna, Hironori Ishizaki, Michaela Spitzer, et al.. (2012). ALDH2 Mediates 5-Nitrofuran Activity in Multiple Species. Chemistry & Biology. 19(7). 883–892. 40 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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