Suzanne Walker

18.0k total citations · 2 hit papers
206 papers, 13.4k citations indexed

About

Suzanne Walker is a scholar working on Molecular Biology, Genetics and Organic Chemistry. According to data from OpenAlex, Suzanne Walker has authored 206 papers receiving a total of 13.4k indexed citations (citations by other indexed papers that have themselves been cited), including 161 papers in Molecular Biology, 56 papers in Genetics and 44 papers in Organic Chemistry. Recurrent topics in Suzanne Walker's work include Glycosylation and Glycoproteins Research (55 papers), Bacterial Genetics and Biotechnology (55 papers) and Carbohydrate Chemistry and Synthesis (39 papers). Suzanne Walker is often cited by papers focused on Glycosylation and Glycoproteins Research (55 papers), Bacterial Genetics and Biotechnology (55 papers) and Carbohydrate Chemistry and Synthesis (39 papers). Suzanne Walker collaborates with scholars based in United States, Ukraine and Germany. Suzanne Walker's co-authors include Daniel Kahne, John P. Santa Maria, Stephanie Brown, Jonathan G. Swoboda, Timothy C. Meredith, Yanan Hu, Bohdan Ostash, Michael B. Lazarus, Jennifer Campbell and Jiaoyang Jiang and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Suzanne Walker

196 papers receiving 13.2k citations

Hit Papers

Wall Teichoic Acids of Gram-Positive Bacteria 2013 2026 2017 2021 2013 2016 200 400 600

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Suzanne Walker United States 66 9.3k 3.8k 3.0k 1.9k 1.9k 206 13.4k
N.C.J. Strynadka Canada 69 8.5k 0.9× 1.9k 0.5× 3.3k 1.1× 1.5k 0.8× 2.3k 1.2× 219 15.5k
Yuriy A. Knirel Russia 54 7.0k 0.8× 5.2k 1.4× 2.0k 0.7× 3.1k 1.6× 871 0.5× 645 14.3k
Dominique Mengin‐Lecreulx France 59 5.2k 0.6× 1.2k 0.3× 3.0k 1.0× 1.4k 0.7× 1.1k 0.6× 167 10.1k
Eefjan Breukink Netherlands 58 6.7k 0.7× 982 0.3× 2.7k 0.9× 1.9k 1.0× 753 0.4× 160 10.9k
Gurdyal S. Besra United Kingdom 97 11.8k 1.3× 4.6k 1.2× 2.0k 0.7× 1.2k 0.6× 10.6k 5.6× 516 31.4k
Laurent Kremer France 62 4.9k 0.5× 2.4k 0.6× 889 0.3× 1.1k 0.6× 7.5k 3.9× 292 13.1k
Bernard Weisblum United States 54 7.2k 0.8× 2.6k 0.7× 2.5k 0.8× 1.3k 0.7× 1.7k 0.9× 119 11.1k
Roderich D. Süßmuth Germany 64 8.5k 0.9× 2.9k 0.8× 1.2k 0.4× 765 0.4× 648 0.3× 321 14.4k
Michael S. VanNieuwenhze United States 40 4.6k 0.5× 3.6k 1.0× 1.6k 0.5× 1.3k 0.7× 561 0.3× 102 9.8k
Michael McNeil United States 72 7.2k 0.8× 4.0k 1.1× 832 0.3× 913 0.5× 4.9k 2.6× 218 15.8k

Countries citing papers authored by Suzanne Walker

Since Specialization
Citations

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

Fields of papers citing papers by Suzanne Walker

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Suzanne Walker

This figure shows the co-authorship network connecting the top 25 collaborators of Suzanne Walker. A scholar is included among the top collaborators of Suzanne Walker 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 Suzanne Walker. Suzanne Walker 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.
Filsinger, Gabriel, et al.. (2025). A diverse single-stranded DNA–annealing protein library enables efficient genome editing across bacterial phyla. Proceedings of the National Academy of Sciences. 122(17). e2414342122–e2414342122.
2.
James, Michael J., et al.. (2025). Staphylococcus aureus uses a GGDEF protein to recruit diacylglycerol kinase to the membrane for lipid recycling. Proceedings of the National Academy of Sciences. 122(12). e2414696122–e2414696122.
3.
Hummels, Katherine R., Zhaoqi Li, Atsushi Taguchi, et al.. (2023). Coordination of bacterial cell wall and outer membrane biosynthesis. Nature. 615(7951). 300–304. 47 indexed citations
4.
Taguchi, Atsushi, et al.. (2023). A Time‐Resolved FRET Assay Identifies a Small Molecule that Inhibits the Essential Bacterial Cell Wall Polymerase FtsW. Angewandte Chemie International Edition. 62(25). e202301522–e202301522. 8 indexed citations
5.
Janetzko, John, et al.. (2021). Protein Substrates Engage the Lumen of O-GlcNAc Transferase’s Tetratricopeptide Repeat Domain in Different Ways. Biochemistry. 60(11). 847–853. 25 indexed citations
6.
Matano, Leigh M., Christopher R. Vickery, Ace George Santiago, et al.. (2020). The Length of Lipoteichoic Acid Polymers Controls Staphylococcus aureus Cell Size and Envelope Integrity. Journal of Bacteriology. 202(16). 41 indexed citations
7.
Itkonen, Harri M., Ninu Poulose, Rebecca E. Steele, et al.. (2020). Inhibition of O-GlcNAc Transferase Renders Prostate Cancer Cells Dependent on CDK9. Molecular Cancer Research. 18(10). 1512–1521. 41 indexed citations
8.
Mollo, Aurelio, Sujeet Kumar, Emily K. Butler, et al.. (2020). Detection of Transport Intermediates in the Peptidoglycan Flippase MurJ Identifies Residues Essential for Conformational Cycling. Journal of the American Chemical Society. 142(12). 5482–5486. 20 indexed citations
9.
Schaefer, Kaitlin, Tristan W. Owens, Julia E. Page, et al.. (2020). Structure and reconstitution of a hydrolase complex that may release peptidoglycan from the membrane after polymerization. Nature Microbiology. 6(1). 34–43. 26 indexed citations
10.
Do, Truc, Kaitlin Schaefer, Ace George Santiago, et al.. (2020). Staphylococcus aureus cell growth and division are regulated by an amidase that trims peptides from uncrosslinked peptidoglycan. Nature Microbiology. 5(2). 291–303. 47 indexed citations
11.
Taguchi, Atsushi, Michael A. Welsh, Lindsey S. Marmont, et al.. (2019). FtsW is a peptidoglycan polymerase that is functional only in complex with its cognate penicillin-binding protein. Nature Microbiology. 4(4). 587–594. 212 indexed citations
12.
Levine, Zebulon G., et al.. (2019). Aspartate Residues Far from the Active Site Drive O-GlcNAc Transferase Substrate Selection. Journal of the American Chemical Society. 141(33). 12974–12978. 52 indexed citations
13.
Lee, Wonsik, et al.. (2019). Multi-strain Tn-Seq reveals common daptomycin resistance determinants in Staphylococcus aureus. PLoS Pathogens. 15(11). e1007862–e1007862. 60 indexed citations
14.
Martin, Sara E., Harri M. Itkonen, Damien Duveau, et al.. (2018). Structure-Based Evolution of Low Nanomolar O-GlcNAc Transferase Inhibitors. Journal of the American Chemical Society. 140(42). 13542–13545. 122 indexed citations
15.
Lee, Wonsik, Truc Do, Ge Zhang, et al.. (2018). Antibiotic Combinations That Enable One-Step, Targeted Mutagenesis of Chromosomal Genes. ACS Infectious Diseases. 4(6). 1007–1018. 10 indexed citations
16.
Lupoli, Tania J., et al.. (2013). Lipoprotein Activators Stimulate Escherichia coli Penicillin-Binding Proteins by Different Mechanisms. Journal of the American Chemical Society. 136(1). 52–55. 70 indexed citations
17.
Brown, Stephanie, Guoqing Xia, Lyly G. Luhachack, et al.. (2012). Methicillin resistance in Staphylococcus aureus requires glycosylated wall teichoic acids. Proceedings of the National Academy of Sciences. 109(46). 18909–18914. 214 indexed citations
18.
Swoboda, Jonathan G., Timothy C. Meredith, Jennifer Campbell, et al.. (2009). Discovery of a Small Molecule that Blocks Wall Teichoic Acid Biosynthesis in Staphylococcus aureus. ACS Chemical Biology. 4(10). 875–883. 116 indexed citations
19.
Yuan, Yanqiu, Dianah Barrett, Yi Zhang, et al.. (2007). Crystal structure of a peptidoglycan glycosyltransferase suggests a model for processive glycan chain synthesis. Proceedings of the National Academy of Sciences. 104(13). 5348–5353. 118 indexed citations
20.
Gross, Benjamin, Brian Kraybill, & Suzanne Walker. (2005). Discovery of O- GlcNAc Transferase Inhibitors. Journal of the American Chemical Society. 127(42). 14588–14589. 211 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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