Kathleen E. Kendrick

746 total citations
25 papers, 626 citations indexed

About

Kathleen E. Kendrick is a scholar working on Molecular Biology, Pharmacology and Genetics. According to data from OpenAlex, Kathleen E. Kendrick has authored 25 papers receiving a total of 626 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 12 papers in Pharmacology and 7 papers in Genetics. Recurrent topics in Kathleen E. Kendrick's work include Microbial Natural Products and Biosynthesis (12 papers), Genomics and Phylogenetic Studies (7 papers) and Bacterial Genetics and Biotechnology (7 papers). Kathleen E. Kendrick is often cited by papers focused on Microbial Natural Products and Biosynthesis (12 papers), Genomics and Phylogenetic Studies (7 papers) and Bacterial Genetics and Biotechnology (7 papers). Kathleen E. Kendrick collaborates with scholars based in United States, Australia and South Korea. Kathleen E. Kendrick's co-authors include Jerald C. Ensign, Hao Jiang, Margaret K. Hostetter, Lee Ann McCue, Mark L. Wheelis, Hao Jiang, Philip J. White, Paul Roche, James A. Triccas and Nathalie Winter and has published in prestigious journals such as Journal of Bacteriology, The Journal of Infectious Diseases and Infection and Immunity.

In The Last Decade

Kathleen E. Kendrick

25 papers receiving 603 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Kathleen E. Kendrick United States 16 375 282 159 143 107 25 626
Elke E. E. Noens Netherlands 14 519 1.4× 366 1.3× 163 1.0× 195 1.4× 98 0.9× 16 784
Carlos Hardisson Spain 16 411 1.1× 228 0.8× 159 1.0× 94 0.7× 25 0.2× 42 646
Nick Allenby United Kingdom 12 435 1.2× 224 0.8× 82 0.5× 229 1.6× 59 0.6× 24 674
Annabelle Thibessard France 14 446 1.2× 205 0.7× 90 0.6× 160 1.1× 31 0.3× 31 594
Bjørn A. Traag Netherlands 12 397 1.1× 320 1.1× 114 0.7× 147 1.0× 43 0.4× 17 600
Geneviève Girard Netherlands 14 542 1.4× 248 0.9× 242 1.5× 104 0.7× 19 0.2× 21 783
Ikuko Tomiyasu Japan 13 364 1.0× 75 0.3× 98 0.6× 28 0.2× 85 0.8× 17 544
Paul D. Facey United Kingdom 12 307 0.8× 103 0.4× 130 0.8× 69 0.5× 34 0.3× 23 508
Martha B. Arnaud United States 10 603 1.6× 263 0.9× 206 1.3× 31 0.2× 168 1.6× 10 859
Shi‐En Lu United States 20 338 0.9× 165 0.6× 661 4.2× 52 0.4× 86 0.8× 59 1.1k

Countries citing papers authored by Kathleen E. Kendrick

Since Specialization
Citations

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

Fields of papers citing papers by Kathleen E. Kendrick

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Kathleen E. Kendrick. 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 Kathleen E. Kendrick. The network helps show where Kathleen E. Kendrick may publish in the future.

Co-authorship network of co-authors of Kathleen E. Kendrick

This figure shows the co-authorship network connecting the top 25 collaborators of Kathleen E. Kendrick. A scholar is included among the top collaborators of Kathleen E. Kendrick 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 Kathleen E. Kendrick. Kathleen E. Kendrick 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.
Kendrick, Kathleen E., et al.. (2009). Analysis of Degradation Properties of Biopharmaceutical Active Ingredients as Caused by Various Process Cleaning Agents and Temperature. 15(3). 69–77. 3 indexed citations
2.
Jiang, Hao, et al.. (2002). Transformation using in vivo and in vitro methylation inStreptomyces griseus. FEMS Microbiology Letters. 209(2). 243–248. 15 indexed citations
3.
Jiang, Hao, et al.. (2001). Differential Regulation of ftsZ Transcription during Septation of Streptomyces griseus. Journal of Bacteriology. 183(17). 5092–5101. 27 indexed citations
4.
Jiang, Hao & Kathleen E. Kendrick. (2000). Cloning and characterization of the gene encoding penicillin-binding protein A ofStreptomyces griseus. FEMS Microbiology Letters. 193(1). 63–68. 4 indexed citations
5.
Jiang, Hao & Kathleen E. Kendrick. (2000). Characterization of ssfR and ssgA , Two Genes Involved in Sporulation of Streptomyces griseus. Journal of Bacteriology. 182(19). 5521–5529. 36 indexed citations
6.
Jiang, Hao & Kathleen E. Kendrick. (1998). Visualization of Penicillin-Binding Proteins during Sporulation of Streptomyces griseus. Journal of Bacteriology. 180(8). 2125–2132. 16 indexed citations
7.
Triccas, James A., et al.. (1998). Molecular and Immunological Analyses of the Mycobacterium avium Homolog of the Immunodominant Mycobacterium leprae 35-Kilodalton Protein. Infection and Immunity. 66(6). 2684–2690. 32 indexed citations
8.
McCue, Lee Ann, et al.. (1996). Identification of bldA mutants of Streptomyces griseus. Gene. 171(1). 75–78. 19 indexed citations
9.
Kendrick, Kathleen E., et al.. (1996). Bald mutants of Streptomyces griseus that prematurely undergo key events of sporulation. Journal of Bacteriology. 178(15). 4643–4650. 20 indexed citations
10.
McCue, Lee Ann, et al.. (1996). Analysis of a gene that suppresses the morphological defect of bald mutants of Streptomyces griseus. Journal of Bacteriology. 178(10). 2867–2875. 6 indexed citations
11.
Hostetter, Margaret K., et al.. (1995). Antigenic and Functional Conservation of an Integrin I-Domain in Saccharomyces cerevisiae. Biochemical and Molecular Medicine. 55(2). 122–130. 15 indexed citations
12.
Srinivasan, Kanur, et al.. (1995). Regulated expression of the histidase structural gene in Streptomyces griseus. Journal of Bacteriology. 177(3). 854–857. 5 indexed citations
13.
14.
Kendrick, Kathleen E., et al.. (1992). Histidine ammonia-lyase from Streptomyces griseus. Gene. 115(1-2). 19–25. 7 indexed citations
15.
White, Philip J., et al.. (1992). Purification of histidase from Streptomyces griseus and nucleotide sequence of the hutH structural gene. Journal of Bacteriology. 174(5). 1647–1655. 21 indexed citations
16.
McCue, Lee Ann, et al.. (1992). Molecular analysis of sporulation in Streptomyces griseus. Gene. 115(1-2). 173–179. 20 indexed citations
17.
Hostetter, Margaret K., et al.. (1990). The iC3b Receptor on Candida albicans: Subcellular Localization and Modulation of Receptor Expression by Glucose. The Journal of Infectious Diseases. 161(4). 761–768. 87 indexed citations
18.
Kendrick, Kathleen E., et al.. (1990). Transcriptional and translational features of a sporulation gene of Streptomyces griseus. Gene. 95(1). 57–63. 31 indexed citations
19.
Kendrick, Kathleen E., et al.. (1989). Cascading regulation of histidase activity in Streptomyces griseus. Journal of Bacteriology. 171(2). 1100–1105. 8 indexed citations
20.
Kendrick, Kathleen E., et al.. (1988). Cloning of DNA involved in sporulation of Streptomyces griseus. Journal of Bacteriology. 170(6). 2802–2808. 57 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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