James K. Lithgow

1.7k total citations · 1 hit paper
11 papers, 1.4k citations indexed

About

James K. Lithgow is a scholar working on Molecular Biology, Genetics and Infectious Diseases. According to data from OpenAlex, James K. Lithgow has authored 11 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 4 papers in Genetics and 3 papers in Infectious Diseases. Recurrent topics in James K. Lithgow's work include Bacterial Genetics and Biotechnology (4 papers), Legume Nitrogen Fixing Symbiosis (3 papers) and Bacterial biofilms and quorum sensing (3 papers). James K. Lithgow is often cited by papers focused on Bacterial Genetics and Biotechnology (4 papers), Legume Nitrogen Fixing Symbiosis (3 papers) and Bacterial biofilms and quorum sensing (3 papers). James K. Lithgow collaborates with scholars based in United Kingdom, Switzerland and Poland. James K. Lithgow's co-authors include Simon J. Foster, Lindsey N. Shaw, Malcolm J. Horsburgh, Adam C. Wilkinson, J. Allan Downie, Florence Wisniewski‐Dyé, Peter Farndon, Thierry Girard, Andrea Hardman and B. Rodelas and has published in prestigious journals such as Journal of Bacteriology, Molecular Microbiology and Microbiology.

In The Last Decade

James K. Lithgow

11 papers receiving 1.3k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

σ^BModulates Virulence Determinant Expression and Stress Resistance: Characterization of a FunctionalrsbUStrain Derived fromStaphylococcus aureus8325-4

2002 585 citations Malcolm J. Horsburgh, Lindsey N. Shaw et al. Journal of Bacteriology profile →

Peers

James K. Lithgow

MB

ID

GENET

PS

ECOLO

Joan Campbell-Tofte Denmark

M. Inês Borges‐Walmsley United Kingdom

Satoru Fukiya Japan

Paul Majcherczyk Switzerland

Alexander P. Bryant United States

Anthony D. Baughn United States

Matthew P. Fletcher United Kingdom

W. Scott Champney United States

Joeli Marrero United States

Joan Campbell-Tofte Denmark

James K. Lithgow

653 ×0.9

MB

155 ×0.3

ID

308 ×1.0

GENET

192 ×0.9

PS

134 ×0.9

ECOLO

Citations per year, relative to James K. Lithgow James K. Lithgow (= 1×) peers Joan Campbell-Tofte

Countries citing papers authored by James K. Lithgow

Since Specialization

Citations

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

Fields of papers citing papers by James K. Lithgow

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by James K. Lithgow. 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 James K. Lithgow. The network helps show where James K. Lithgow may publish in the future.

Co-authorship network of co-authors of James K. Lithgow

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

All Works

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11 of 11 papers shown

1.

Girard, Thierry, et al.. (2009). Pharmacogenetics of CYP2C19: functional and clinical implications of a new variant CYP2C19*17. British Journal of Clinical Pharmacology. 69(3). 222–230. 202 indexed citations

2.

Farndon, Peter, et al.. (2009). When Is a Genetic Test Suitable for Prime Time? Predicting the Risk of Prostate Cancer as a Case-Example. Public Health Genomics. 13(1). 55–62. 5 indexed citations

3.

Haider, Fouzia, et al.. (2008). DNA recognition by the Salmonella enterica serovar Typhimurium transcription factor SlyA.. PubMed. 11(4). 245–50. 6 indexed citations

4.

Lithgow, James K., Fouzia Haider, Ian S. Roberts, & Jeffrey Green. (2007). Alternate SlyA and H‐NS nucleoprotein complexes control hlyE expression in Escherichia coli K‐12. Molecular Microbiology. 66(3). 685–698. 67 indexed citations

5.

Shaw, Lindsey N., Jessica Davenport, James K. Lithgow, et al.. (2006). Investigations into σ ^B -Modulated Regulatory Pathways Governing Extracellular Virulence Determinant Production in Staphylococcus aureus. Journal of Bacteriology. 188(17). 6070–6080. 40 indexed citations

6.

Lithgow, James K., Emma J. Hayhurst, Gerald Cohen, Yair Aharonowitz, & Simon J. Foster. (2004). Role of a Cysteine Synthase in Staphylococcus aureus. Journal of Bacteriology. 186(6). 1579–1590. 92 indexed citations

7.

Lithgow, James K., Eileen Ingham, & Simon J. Foster. (2004). Role of the hprT–ftsH locus in Staphylococcus aureus. Microbiology. 150(2). 373–381. 42 indexed citations

8.

Horsburgh, Malcolm J., et al.. (2002). σ^BModulates Virulence Determinant Expression and Stress Resistance: Characterization of a FunctionalrsbUStrain Derived fromStaphylococcus aureus8325-4. Journal of Bacteriology. 184(19). 5457–5467. 585 indexed citations breakdown →

9.

Wilkinson, Adam C., Vittoria Danino, Florence Wisniewski‐Dyé, James K. Lithgow, & J. Allan Downie. (2002). N -Acyl-Homoserine Lactone Inhibition of Rhizobial Growth Is Mediated by Two Quorum-Sensing Genes That Regulate Plasmid Transfer. Journal of Bacteriology. 184(16). 4510–4519. 65 indexed citations

10.

Lithgow, James K., Adam C. Wilkinson, Andrea Hardman, et al.. (2000). The regulatory locus cinRI in Rhizobium leguminosarum controls a network of quorum‐sensing loci. Molecular Microbiology. 37(1). 81–97. 161 indexed citations

11.

Rodelas, B., James K. Lithgow, Florence Wisniewski‐Dyé, et al.. (1999). Analysis of Quorum-Sensing-Dependent Control of Rhizosphere-Expressed ( rhi ) Genes in Rhizobium leguminosarum bv. viciae. Journal of Bacteriology. 181(12). 3816–3823. 98 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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