Timothy Palzkill

8.9k total citations · 1 hit paper
180 papers, 6.8k citations indexed

About

Timothy Palzkill is a scholar working on Molecular Medicine, Molecular Biology and Genetics. According to data from OpenAlex, Timothy Palzkill has authored 180 papers receiving a total of 6.8k indexed citations (citations by other indexed papers that have themselves been cited), including 98 papers in Molecular Medicine, 71 papers in Molecular Biology and 42 papers in Genetics. Recurrent topics in Timothy Palzkill's work include Antibiotic Resistance in Bacteria (98 papers), Antibiotics Pharmacokinetics and Efficacy (26 papers) and Bacterial Genetics and Biotechnology (23 papers). Timothy Palzkill is often cited by papers focused on Antibiotic Resistance in Bacteria (98 papers), Antibiotics Pharmacokinetics and Efficacy (26 papers) and Bacterial Genetics and Biotechnology (23 papers). Timothy Palzkill collaborates with scholars based in United States, Switzerland and Canada. Timothy Palzkill's co-authors include Wanzhi Huang, Joseph F. Petrosino, B. V. Venkataram Prasad, Nicholas G. Brown, Carlos Cantu, Banumathi Sankaran, David Botstein, Dar‐Chone Chow, George M. Weinstock and Liya Hu and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Timothy Palzkill

179 papers receiving 6.7k citations

Hit Papers

Transmissible SARS-CoV-2 variants with resistance to clin... 2023 2026 2024 2025 2023 25 50 75

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Timothy Palzkill United States 49 3.1k 2.9k 1.3k 1.1k 1.0k 180 6.8k
Helen I. Zgurskaya United States 45 2.5k 0.8× 3.6k 1.2× 1.9k 1.5× 981 0.9× 833 0.8× 118 6.3k
Klaas M. Pos Germany 38 2.4k 0.8× 2.8k 1.0× 1.1k 0.9× 902 0.8× 747 0.7× 83 5.5k
Karen Joy Shaw United States 46 2.7k 0.9× 2.1k 0.7× 1.0k 0.8× 811 0.7× 2.5k 2.4× 117 6.5k
Lynn L. Silver United States 36 2.5k 0.8× 1.7k 0.6× 912 0.7× 1.0k 1.0× 654 0.6× 73 5.4k
P. Charlier Belgium 32 2.1k 0.7× 1.9k 0.7× 1.1k 0.9× 723 0.7× 757 0.7× 82 4.7k
Brian K. Coombes Canada 46 2.5k 0.8× 1.4k 0.5× 1.4k 1.1× 566 0.5× 1.3k 1.2× 121 6.8k
Taiji Nakae Japan 44 3.8k 1.2× 2.4k 0.8× 2.3k 1.9× 638 0.6× 705 0.7× 161 6.9k
M. Stephen Trent United States 48 4.3k 1.4× 3.0k 1.0× 2.2k 1.7× 485 0.4× 747 0.7× 125 9.1k
Moreno Galleni Belgium 46 2.9k 0.9× 5.0k 1.7× 441 0.4× 1.8k 1.6× 1.2k 1.2× 200 7.5k
Deborah T. Hung United States 42 6.4k 2.0× 1.3k 0.4× 957 0.8× 376 0.3× 2.2k 2.1× 118 10.6k

Countries citing papers authored by Timothy Palzkill

Since Specialization
Citations

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

Fields of papers citing papers by Timothy Palzkill

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Timothy Palzkill

This figure shows the co-authorship network connecting the top 25 collaborators of Timothy Palzkill. A scholar is included among the top collaborators of Timothy Palzkill 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 Timothy Palzkill. Timothy Palzkill 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.
Pham, Son, Banumathi Sankaran, Ketki Patil, et al.. (2025). Conformational flexibility is a critical factor in designing broad-spectrum human norovirus protease inhibitors. Journal of Virology. 99(2). e0175724–e0175724.
2.
Choby, Jacob E., Jennifer M. Colquhoun, Sarah W. Satola, et al.. (2025). Copy number flexibility facilitates heteroresistance to increasing antibiotic pressure and threatens the beta-lactam pipeline. Nature Communications. 16(1). 5721–5721. 1 indexed citations
3.
Palzkill, Timothy, et al.. (2023). Structural biology of MCR-1-mediated resistance to polymyxin antibiotics. Current Opinion in Structural Biology. 82. 102647–102647. 9 indexed citations
4.
Huang, Wanzhi, et al.. (2023). Mapping human norovirus antigens during infection reveals the breadth of the humoral immune response. npj Vaccines. 8(1). 87–87. 5 indexed citations
5.
Bradford, Patricia A., Robert A. Bonomo, Karen Bush, et al.. (2022). Consensus on β-Lactamase Nomenclature. Antimicrobial Agents and Chemotherapy. 66(4). e0033322–e0033322. 16 indexed citations
6.
Khan, Ayesha, Truc T. Tran, Rafael Ríos, et al.. (2019). Extensively Drug-Resistant Pseudomonas aeruginosa ST309 Harboring Tandem Guiana Extended Spectrum β-Lactamase Enzymes: A Newly Emerging Threat in the United States. Open Forum Infectious Diseases. 6(7). ofz273–ofz273. 40 indexed citations
7.
Zalucki, Yaramah M., Nicholas G. Brown, Timothy Palzkill, et al.. (2019). Structural, Biochemical, and In Vivo Characterization of MtrR-Mediated Resistance to Innate Antimicrobials by the Human Pathogen Neisseria gonorrhoeae. Journal of Bacteriology. 201(20). 13 indexed citations
8.
Jiang, Xiqian, Chengwei Zhang, Jianwei Chen, et al.. (2018). Quantitative Real-Time Imaging of Glutathione with Subcellular Resolution. Antioxidants and Redox Signaling. 30(16). 1900–1910. 28 indexed citations
9.
Adamski, Carolyn J. & Timothy Palzkill. (2017). Systematic substitutions at BLIP position 50 result in changes in binding specificity for class A β-lactamases. BMC Biochemistry. 18(1). 2–2. 5 indexed citations
10.
Huang, Wanzhi, et al.. (2016). Deep sequencing of phage-displayed peptide libraries reveals sequence motif that detects norovirus. Protein Engineering Design and Selection. 30(2). 129–139. 6 indexed citations
11.
Wang, Lei, Yang Yu, Fei Yan, et al.. (2015). Characterization of a Steroid Receptor Coactivator Small Molecule Stimulator that Overstimulates Cancer Cells and Leads to Cell Stress and Death. Cancer Cell. 28(2). 240–252. 68 indexed citations
12.
Adamski, Carolyn J., Ana M. Cárdenas, Nicholas G. Brown, et al.. (2014). Molecular Basis for the Catalytic Specificity of the CTX-M Extended-Spectrum β-Lactamases. Biochemistry. 54(2). 447–457. 49 indexed citations
14.
Cárdenas, Ana M., et al.. (2011). Determination of the amino acid sequence requirements for catalysis by the highly proficient orotidine monophosphate decarboxylase. Protein Science. 20(11). 1891–1906. 5 indexed citations
15.
Brown, Nicholas G., Dar‐Chone Chow, Banumathi Sankaran, et al.. (2011). Analysis of the Binding Forces Driving the Tight Interactions between β-Lactamase Inhibitory Protein-II (BLIP-II) and Class A β-Lactamases. Journal of Biological Chemistry. 286(37). 32723–32735. 18 indexed citations
16.
Brown, Nicholas G., et al.. (2010). Multiple Global Suppressors of Protein Stability Defects Facilitate the Evolution of Extended-Spectrum TEM β-Lactamases. Journal of Molecular Biology. 404(5). 832–846. 69 indexed citations
17.
Marciano, David C., Nicholas G. Brown, & Timothy Palzkill. (2009). Analysis of the plasticity of location of the Arg244 positive charge within the active site of the TEM‐1 β‐lactamase. Protein Science. 18(10). 2080–2089. 36 indexed citations
18.
Zhang, Zhen & Timothy Palzkill. (2003). Determinants of Binding Affinity and Specificity for the Interaction of TEM-1 and SME-1 β-Lactamase with β-Lactamase Inhibitory Protein. Journal of Biological Chemistry. 278(46). 45706–45712. 51 indexed citations
19.
Hoe, Nancy P., Parichher Kordari, Robert L. Cole, et al.. (2000). Human Immune Response to Streptococcal Inhibitor of Complement, a Serotype M1 Group AStreptococcusExtracellular Protein Involved in Epidemics. The Journal of Infectious Diseases. 182(5). 1425–1436. 33 indexed citations
20.
Newlon, Carol S., Irene Collins, Atul Deshpande, et al.. (1991). Analysis of a circular derivative of Saccharomyces cerevisiae chromosome III: a physical map and identification and location of ARS elements.. Genetics. 129(2). 343–357. 104 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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