Patricia Reed

1.0k total citations
19 papers, 761 citations indexed

About

Patricia Reed is a scholar working on Genetics, Molecular Biology and Infectious Diseases. According to data from OpenAlex, Patricia Reed has authored 19 papers receiving a total of 761 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 12 papers in Molecular Biology and 7 papers in Infectious Diseases. Recurrent topics in Patricia Reed's work include Bacterial Genetics and Biotechnology (13 papers), Antimicrobial Resistance in Staphylococcus (7 papers) and Bacteriophages and microbial interactions (5 papers). Patricia Reed is often cited by papers focused on Bacterial Genetics and Biotechnology (13 papers), Antimicrobial Resistance in Staphylococcus (7 papers) and Bacteriophages and microbial interactions (5 papers). Patricia Reed collaborates with scholars based in Portugal, United Kingdom and United States. Patricia Reed's co-authors include Mariana G. Pinho, Helena Veiga, Sérgio R. Filipe, Pedro M. Pereira, Magda L. Atilano, James R. Yates, Ambre Jousselin, Gary J. Sharples, Nathalie T. Reichmann and Ana R. Pereira and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The EMBO Journal and PLoS ONE.

In The Last Decade

Patricia Reed

19 papers receiving 754 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Patricia Reed Portugal 14 446 297 266 150 136 19 761
Nathalie T. Reichmann Portugal 11 459 1.0× 303 1.0× 269 1.0× 142 0.9× 180 1.3× 11 816
Michael A. D’Elia Canada 11 505 1.1× 228 0.8× 263 1.0× 143 1.0× 154 1.1× 13 784
Umender Sharma India 19 526 1.2× 372 1.3× 173 0.7× 234 1.6× 178 1.3× 28 960
Sina Jordan Germany 7 429 1.0× 168 0.6× 288 1.1× 188 1.3× 102 0.8× 7 735
Wilhelm Paulander Denmark 15 387 0.9× 202 0.7× 246 0.9× 68 0.5× 255 1.9× 17 714
Sandro F. F. Pereira United States 7 428 1.0× 348 1.2× 168 0.6× 81 0.5× 81 0.6× 7 705
Ambre Jousselin Switzerland 13 417 0.9× 345 1.2× 222 0.8× 128 0.9× 124 0.9× 15 648
Ryan P. Lamers Canada 12 371 0.8× 217 0.7× 155 0.6× 80 0.5× 240 1.8× 14 674
Deborah D. Jaworski United States 8 353 0.8× 263 0.9× 150 0.6× 154 1.0× 151 1.1× 8 763
Agnieszka Bera Germany 11 491 1.1× 296 1.0× 182 0.7× 161 1.1× 89 0.7× 11 999

Countries citing papers authored by Patricia Reed

Since Specialization
Citations

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

Fields of papers citing papers by Patricia Reed

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Patricia Reed

This figure shows the co-authorship network connecting the top 25 collaborators of Patricia Reed. A scholar is included among the top collaborators of Patricia Reed 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 Patricia Reed. Patricia Reed is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

19 of 19 papers shown
1.
Saraiva, Bruno M., Helena Veiga, Simon Schäper, et al.. (2024). The role of GpsB in Staphylococcus aureus cell morphogenesis. mBio. 15(3). e0323523–e0323523. 11 indexed citations
2.
Veiga, Helena, Ambre Jousselin, Simon Schäper, et al.. (2023). Cell division protein FtsK coordinates bacterial chromosome segregation and daughter cell separation in Staphylococcus aureus. The EMBO Journal. 42(11). e112140–e112140. 18 indexed citations
3.
Reed, Patricia, et al.. (2023). A CRISPRi-based genetic resource to study essential Staphylococcus aureus genes. mBio. 15(1). e0277323–e0277323. 6 indexed citations
4.
Fernandes, Pedro B., Patricia Reed, João M. Monteiro, & Mariana G. Pinho. (2022). Revisiting the Role of VraTSR in Staphylococcus aureus Response to Cell Wall-Targeting Antibiotics. Journal of Bacteriology. 204(8). e0016222–e0016222. 14 indexed citations
5.
Barros, Dragana P.C. de, et al.. (2022). Design of Quercetin-Loaded Natural Oil-Based Nanostructured Lipid Carriers for the Treatment of Bacterial Skin Infections. Molecules. 27(24). 8818–8818. 25 indexed citations
6.
7.
Reichmann, Nathalie T., Andreia C. Tavares, Bruno M. Saraiva, et al.. (2019). SEDS–bPBP pairs direct lateral and septal peptidoglycan synthesis in Staphylococcus aureus. Nature Microbiology. 4(8). 1368–1377. 84 indexed citations
8.
Reed, Patricia, et al.. (2019). BPEI-Induced Delocalization of PBP4 Potentiates β-Lactams against MRSA. Biochemistry. 58(36). 3813–3822. 19 indexed citations
9.
Reed, Patricia, Magda L. Atilano, Renato Alves, et al.. (2015). Staphylococcus aureus Survives with a Minimal Peptidoglycan Synthesis Machine but Sacrifices Virulence and Antibiotic Resistance. PLoS Pathogens. 11(5). e1004891–e1004891. 77 indexed citations
10.
Jousselin, Ambre, Caroline Manzano, Patricia Reed, et al.. (2015). The Staphylococcus aureus Chaperone PrsA Is a New Auxiliary Factor of Oxacillin Resistance Affecting Penicillin-Binding Protein 2A. Antimicrobial Agents and Chemotherapy. 60(3). 1656–1666. 57 indexed citations
11.
Malay, Ali D., Alexander J. Trotter, Lindsay A. Wilson, et al.. (2014). Phage Orf Family Recombinases: Conservation of Activities and Involvement of the Central Channel in DNA Binding. PLoS ONE. 9(8). e102454–e102454. 5 indexed citations
12.
Atilano, Magda L., Pedro M. Pereira, Filipa Vaz, et al.. (2014). Bacterial autolysins trim cell surface peptidoglycan to prevent detection by the Drosophila innate immune system. eLife. 3. e02277–e02277. 35 indexed citations
13.
Pereira, Ana R., Patricia Reed, Helena Veiga, & Mariana G. Pinho. (2013). The Holliday junction resolvase RecU is required for chromosome segregation and DNA damage repair in Staphylococcus aureus. BMC Microbiology. 13(1). 119–119. 20 indexed citations
14.
Reed, Patricia, Helena Veiga, Ana Jorge, Mohammed Terrak, & Mariana G. Pinho. (2011). Monofunctional Transglycosylases Are Not Essential for Staphylococcus aureus Cell Wall Synthesis. Journal of Bacteriology. 193(10). 2549–2556. 46 indexed citations
15.
Reed, Patricia, Lindsay A. Wilson, Robert Yeo, et al.. (2010). The C‐terminus of the phage λ Orf recombinase is involved in DNA binding. Journal of Molecular Recognition. 24(2). 333–340. 11 indexed citations
16.
Atilano, Magda L., Pedro M. Pereira, James R. Yates, et al.. (2010). Teichoic acids are temporal and spatial regulators of peptidoglycan cross-linking in Staphylococcus aureus. Proceedings of the National Academy of Sciences. 107(44). 18991–18996. 217 indexed citations
17.
Reed, Patricia, et al.. (2005). Evolution of a phage RuvC endonuclease for resolution of both Holliday and branched DNA junctions. Molecular Microbiology. 55(5). 1332–1345. 10 indexed citations
18.
Sánchez, Humberto, Dawit Kidane, Patricia Reed, et al.. (2005). The RuvAB Branch Migration Translocase and RecU Holliday Junction Resolvase Are Required for Double-Stranded DNA Break Repair in Bacillus subtilis. Genetics. 171(3). 873–883. 63 indexed citations
19.
Maxwell, Karen L., Patricia Reed, Rongguang Zhang, et al.. (2005). Functional similarities between phage λ Orf and Escherichia coli RecFOR in initiation of genetic exchange. Proceedings of the National Academy of Sciences. 102(32). 11260–11265. 20 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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