Seth T. Walk

6.3k total citations · 2 hit papers
87 papers, 4.5k citations indexed

About

Seth T. Walk is a scholar working on Infectious Diseases, Molecular Biology and Epidemiology. According to data from OpenAlex, Seth T. Walk has authored 87 papers receiving a total of 4.5k indexed citations (citations by other indexed papers that have themselves been cited), including 41 papers in Infectious Diseases, 29 papers in Molecular Biology and 28 papers in Epidemiology. Recurrent topics in Seth T. Walk's work include Clostridium difficile and Clostridium perfringens research (36 papers), Gut microbiota and health (25 papers) and Microscopic Colitis (24 papers). Seth T. Walk is often cited by papers focused on Clostridium difficile and Clostridium perfringens research (36 papers), Gut microbiota and health (25 papers) and Microscopic Colitis (24 papers). Seth T. Walk collaborates with scholars based in United States, Australia and France. Seth T. Walk's co-authors include Vincent B. Young, David M. Gordon, Thomas S. Whittam, James M. Tiedje, Elizabeth Wheeler Alm, Mark Young, John van der Oost, Willem M. de Vos, Pilar Manrique and Benjamin Bolduc and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Communications and Journal of Neuroscience.

In The Last Decade

Seth T. Walk

84 papers receiving 4.5k citations

Hit Papers

Healthy human gut phageome 2016 2026 2019 2022 2016 2018 100 200 300

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Seth T. Walk United States 34 1.9k 1.5k 963 960 727 87 4.5k
Raymond Ruimy France 44 2.1k 1.1× 1.6k 1.1× 950 1.0× 1.1k 1.2× 660 0.9× 128 5.2k
Gary Van Domselaar Canada 37 2.6k 1.4× 1.3k 0.9× 599 0.6× 1.1k 1.1× 772 1.1× 114 5.7k
Peter Mullany United Kingdom 37 1.7k 0.9× 1.8k 1.2× 373 0.4× 695 0.7× 863 1.2× 112 4.8k
Emmanuel F. Mongodin United States 44 4.6k 2.5× 2.4k 1.6× 536 0.6× 707 0.7× 1.1k 1.5× 123 8.3k
Derrick E. Fouts United States 41 3.0k 1.6× 536 0.4× 803 0.8× 1.8k 1.9× 1000 1.4× 98 6.7k
Kazuhiro Tateda Japan 45 2.4k 1.3× 1.7k 1.1× 1.3k 1.3× 2.2k 2.3× 368 0.5× 322 7.6k
Richard E. Isaacson United States 42 2.8k 1.5× 1.6k 1.1× 1.4k 1.4× 603 0.6× 741 1.0× 119 6.9k
Hannah M. Wexler United States 33 2.3k 1.3× 1.4k 0.9× 429 0.4× 675 0.7× 250 0.3× 116 5.3k
Hélène Marchandin France 39 1.4k 0.8× 614 0.4× 750 0.8× 730 0.8× 310 0.4× 146 3.8k

Countries citing papers authored by Seth T. Walk

Since Specialization
Citations

This map shows the geographic impact of Seth T. Walk'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 Seth T. Walk with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Seth T. Walk more than expected).

Fields of papers citing papers by Seth T. Walk

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Seth T. Walk. 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 Seth T. Walk. The network helps show where Seth T. Walk may publish in the future.

Co-authorship network of co-authors of Seth T. Walk

This figure shows the co-authorship network connecting the top 25 collaborators of Seth T. Walk. A scholar is included among the top collaborators of Seth T. Walk 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 Seth T. Walk. Seth T. Walk 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
2.
Dong, Fangcong, Andrew J. Annalora, Iain A. Murray, et al.. (2023). Contribution of Circulating Host and Microbial Tryptophan Metabolites Toward Ah Receptor Activation. PubMed. 16. 934167214–934167214. 13 indexed citations
3.
Broadaway, Susan C., Brian Tripet, Douglas J. Kominsky, et al.. (2023). Gut microbiome dysbiosis drives metabolic dysfunction in Familial dysautonomia. Nature Communications. 14(1). 218–218. 14 indexed citations
4.
Karim, Lamya, et al.. (2023). Germ‐Free C57BL /6 Mice Have Increased Bone Mass and Altered Matrix Properties but Not Decreased Bone Fracture Resistance. Journal of Bone and Mineral Research. 38(8). 1154–1174. 14 indexed citations
5.
Wiegand, Tanner, Artem Nemudryi, Anna Nemudraia, et al.. (2022). The Rise and Fall of SARS-CoV-2 Variants and Ongoing Diversification of Omicron. Viruses. 14(9). 2009–2009. 18 indexed citations
6.
Wilson, Stephanie, et al.. (2021). Temporal metabolic response yields a dynamic biosignature of inflammation. iScience. 24(8). 102817–102817. 4 indexed citations
7.
Christiansen, Bernd, et al.. (2021). The microbiome mediates epiphyseal bone loss and metabolomic changes after acute joint trauma in mice. Osteoarthritis and Cartilage. 29(6). 882–893. 18 indexed citations
8.
Rawle, Rachel A., Yoon‐Suk Kang, Qian Wang, et al.. (2021). Introducing the ArsR-Regulated Arsenic Stimulon. Frontiers in Microbiology. 12. 630562–630562. 33 indexed citations
9.
Leslie, Elaine M., et al.. (2018). Redox metabolism of ingested arsenic: Integrated activities of microbiome and host on toxicological outcomes. Current Opinion in Toxicology. 13. 90–98. 11 indexed citations
10.
Alexeev, Erica E., Jordi M. Lanis, Daniel J. Kao, et al.. (2018). Microbiota-Derived Indole Metabolites Promote Human and Murine Intestinal Homeostasis through Regulation of Interleukin-10 Receptor. American Journal Of Pathology. 188(5). 1183–1194. 391 indexed citations breakdown →
11.
Rao, Krishna, Dejan Micić, Mukil Natarajan, et al.. (2015). Clostridium difficileRibotype 027: Relationship to Age, Detectability of Toxins A or B in Stool With Rapid Testing, Severe Infection, and Mortality. Clinical Infectious Diseases. 61(2). 233–241. 109 indexed citations
12.
Aitken, Samuel L, Mohammad Jahangir Alam, Seth T. Walk, et al.. (2015). In the Endemic Setting, Clostridium difficile Ribotype 027 Is Virulent But Not Hypervirulent. Infection Control and Hospital Epidemiology. 36(11). 1318–1323. 26 indexed citations
13.
Hilmer, Jonathan K., et al.. (2014). Candidate mediators of chondrocyte mechanotransduction via targeted and untargeted metabolomic measurements. Archives of Biochemistry and Biophysics. 545. 116–123. 26 indexed citations
14.
Alam, Mohammad Jahangir, et al.. (2014). Investigation of potentially pathogenic Clostridium difficile contamination in household environs. Anaerobe. 27. 31–33. 52 indexed citations
15.
Jain, Ruchika, Seth T. Walk, David M. Aronoff, et al.. (2013). Emergence of Carbapenemase-Producing Klebsiella pneumoniae of Sequence Type 258 in Michigan, USA. Infectious Disease Reports. 5(1). e5–e5. 15 indexed citations
16.
Walk, Seth T., Dejan Micić, Ruchika Jain, et al.. (2012). Clostridium difficile Ribotype Does Not Predict Severe Infection. Clinical Infectious Diseases. 55(12). 1661–1668. 152 indexed citations
17.
Walk, Seth T., Stefan Taube, Mami Taniuchi, et al.. (2012). Disruption of the Human Gut Microbiota following Norovirus Infection. PLoS ONE. 7(10). e48224–e48224. 98 indexed citations
18.
Walk, Seth T. & Peter Feng. (2011). Population genetics of bacteria : a tribute to Thomas S. Whittam. ASM Press eBooks. 15 indexed citations
19.
Aronoff, David M., Tennille D. Thelen, Seth T. Walk, et al.. (2010). Pseudo-Outbreak ofClostridium sordelliiInfection following Probable Cross-Contamination in a Hospital Clinical Microbiology Laboratory. Infection Control and Hospital Epidemiology. 31(6). 640–642. 10 indexed citations
20.
Oaks, J. Lindsay, Thomas E. Besser, Seth T. Walk, et al.. (2010). Escherichia albertiiin Wild and Domestic Birds. Emerging infectious diseases. 16(4). 638–646. 99 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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026