Mark C. Walker

1.9k total citations
19 papers, 1.4k citations indexed

About

Mark C. Walker is a scholar working on Molecular Biology, Pharmacology and Hematology. According to data from OpenAlex, Mark C. Walker has authored 19 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 9 papers in Pharmacology and 4 papers in Hematology. Recurrent topics in Mark C. Walker's work include Microbial Natural Products and Biosynthesis (9 papers), Genomics and Phylogenetic Studies (5 papers) and Biochemical and Structural Characterization (4 papers). Mark C. Walker is often cited by papers focused on Microbial Natural Products and Biosynthesis (9 papers), Genomics and Phylogenetic Studies (5 papers) and Biochemical and Structural Characterization (4 papers). Mark C. Walker collaborates with scholars based in United States, United Kingdom and Russia. Mark C. Walker's co-authors include Wilfred A. van der Donk, Michelle C. Y. Chang, Qi Zhang, Kenton J. Hetrick, Yue Hao, Manuel A. Ortega, Satish K. Nair, Richard W. Topham, Brian Lowry and Chaitan Khosla and has published in prestigious journals such as Nature, Science and Journal of the American Chemical Society.

In The Last Decade

Mark C. Walker

17 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mark C. Walker United States 16 908 588 251 161 124 19 1.4k
Bojan Bister Germany 20 884 1.0× 955 1.6× 537 2.1× 384 2.4× 38 0.3× 26 1.8k
Alessandra S. Eustáquio United States 27 1.3k 1.4× 1.1k 1.9× 521 2.1× 541 3.4× 97 0.8× 58 2.2k
Yousong Ding United States 27 1.1k 1.2× 717 1.2× 735 2.9× 311 1.9× 36 0.3× 76 2.3k
Hajo Kries Germany 21 1.2k 1.3× 505 0.9× 274 1.1× 110 0.7× 12 0.1× 40 1.5k
Kwaku Kyeremeh Ghana 18 393 0.4× 414 0.7× 184 0.7× 150 0.9× 53 0.4× 52 853
Michihiko Kobayashi Japan 24 1.2k 1.3× 205 0.3× 194 0.8× 182 1.1× 31 0.3× 72 1.7k
Tsutomu Tsuchiya Japan 22 1.2k 1.3× 694 1.2× 1.5k 5.8× 131 0.8× 276 2.2× 204 2.3k
Hao Yu China 28 893 1.0× 231 0.4× 795 3.2× 97 0.6× 86 0.7× 102 2.1k
Patrick Rabe Germany 29 1.9k 2.1× 1.5k 2.6× 281 1.1× 271 1.7× 45 0.4× 59 2.4k
Yi‐Ling Du China 21 868 1.0× 551 0.9× 389 1.5× 144 0.9× 32 0.3× 46 1.3k

Countries citing papers authored by Mark C. Walker

Since Specialization
Citations

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

Fields of papers citing papers by Mark C. Walker

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mark C. Walker

This figure shows the co-authorship network connecting the top 25 collaborators of Mark C. Walker. A scholar is included among the top collaborators of Mark C. 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 Mark C. Walker. Mark C. Walker 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.
Walker, Mark C., et al.. (2025). Genome Sequencing and Mining Expand the Natural Product Repertoire of Lysobacter. Applied Biochemistry and Microbiology. 61(3). 551–557.
2.
Stafford, James L., et al.. (2024). Assessing the Impact of the Leader Peptide in Protease Inhibition by the Microviridin Family of RiPPs. Biomedicines. 12(12). 2873–2873.
3.
Walker, Mark C., et al.. (2020). Precursor peptide-targeted mining of more than one hundred thousand genomes expands the lanthipeptide natural product family. BMC Genomics. 21(1). 387–387. 107 indexed citations
4.
Hegemann, Julian D., et al.. (2019). Assessing the Flexibility of the Prochlorosin 2.8 Scaffold for Bioengineering Applications. ACS Synthetic Biology. 8(5). 1204–1214. 32 indexed citations
5.
Yang, Xiao, et al.. (2018). A lanthipeptide library used to identify a protein–protein interaction inhibitor. Nature Chemical Biology. 14(4). 375–380. 125 indexed citations
6.
Hetrick, Kenton J., Mark C. Walker, & Wilfred A. van der Donk. (2018). Development and Application of Yeast and Phage Display of Diverse Lanthipeptides. ACS Central Science. 4(4). 458–467. 108 indexed citations
7.
Ortega, Manuel A., Yue Hao, Mark C. Walker, et al.. (2016). Structure and tRNA Specificity of MibB, a Lantibiotic Dehydratase from Actinobacteria Involved in NAI-107 Biosynthesis. Cell chemical biology. 23(3). 370–380. 61 indexed citations
8.
Walker, Mark C. & Wilfred A. van der Donk. (2015). The many roles of glutamate in metabolism. Journal of Industrial Microbiology & Biotechnology. 43(2-3). 419–430. 147 indexed citations
9.
Zhang, Qi, James R. Doroghazi, Xiling Zhao, Mark C. Walker, & Wilfred A. van der Donk. (2015). Expanded Natural Product Diversity Revealed by Analysis of Lanthipeptide-Like Gene Clusters in Actinobacteria. Applied and Environmental Microbiology. 81(13). 4339–4350. 63 indexed citations
10.
Ortega, Manuel A., Yue Hao, Qi Zhang, et al.. (2014). Structure and mechanism of the tRNA-dependent lantibiotic dehydratase NisB. Nature. 517(7535). 509–512. 249 indexed citations
11.
Walker, Mark C. & Michelle C. Y. Chang. (2014). Natural and engineered biosynthesis of fluorinated natural products. Chemical Society Reviews. 43(18). 6527–6536. 114 indexed citations
12.
Walker, Mark C., B W. Thuronyi, Louise K. Charkoudian, et al.. (2013). Expanding the Fluorine Chemistry of Living Systems Using Engineered Polyketide Synthase Pathways. Science. 341(6150). 1089–1094. 149 indexed citations
13.
Walker, Mark C., et al.. (2012). Temporal and Fluoride Control of Secondary Metabolism Regulates Cellular Organofluorine Biosynthesis. ACS Chemical Biology. 7(9). 1576–1585. 19 indexed citations
14.
Brown, Margaret E., Mark C. Walker, Toshiki G. Nakashige, Anthony T. Iavarone, & Michelle C. Y. Chang. (2011). Discovery and Characterization of Heme Enzymes from Unsequenced Bacteria: Application to Microbial Lignin Degradation. Journal of the American Chemical Society. 133(45). 18006–18009. 95 indexed citations
16.
Topham, Richard W., et al.. (1986). Studies of the ferroxidase activity of native and chemically modified xanthine oxidoreductase. Biochemical Journal. 235(1). 39–44. 12 indexed citations
17.
Topham, Richard W., et al.. (1982). Evidence for the participation of intestinal xanthine oxidase in the mucosal processing of iron. Biochemistry. 21(19). 4529–4535. 32 indexed citations
18.
Topham, Richard W., et al.. (1982). Liver xanthine dehydrogenase and iron mobilization. Biochemical and Biophysical Research Communications. 109(4). 1240–1246. 43 indexed citations
19.
Topham, Richard W., et al.. (1981). Purification and characterization of the intestinal promoter of iron(3+)-transferrin formation. Biochemistry. 20(2). 319–324. 15 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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