David Zamorano‐Sánchez

1.4k total citations
24 papers, 1.0k citations indexed

About

David Zamorano‐Sánchez is a scholar working on Molecular Biology, Endocrinology and Plant Science. According to data from OpenAlex, David Zamorano‐Sánchez has authored 24 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 14 papers in Endocrinology and 6 papers in Plant Science. Recurrent topics in David Zamorano‐Sánchez's work include Bacterial biofilms and quorum sensing (15 papers), Vibrio bacteria research studies (14 papers) and Legume Nitrogen Fixing Symbiosis (5 papers). David Zamorano‐Sánchez is often cited by papers focused on Bacterial biofilms and quorum sensing (15 papers), Vibrio bacteria research studies (14 papers) and Legume Nitrogen Fixing Symbiosis (5 papers). David Zamorano‐Sánchez collaborates with scholars based in United States, Mexico and Taiwan. David Zamorano‐Sánchez's co-authors include Fitnat H. Yildiz, Gerard C. L. Wong, Andrew S. Utada, Jennifer K. Teschler, Christopher J. A. Warner, Roger G. Linington, Christopher J. Jones, Jin Hwan Park, Holger Sondermann and Jiunn C. N. Fong and has published in prestigious journals such as Nature Communications, PLoS ONE and Nature Reviews Microbiology.

In The Last Decade

David Zamorano‐Sánchez

24 papers receiving 998 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
David Zamorano‐Sánchez United States 14 679 528 205 159 148 24 1.0k
Zehra Tüzün Güvener United States 10 731 1.1× 398 0.8× 357 1.7× 150 0.9× 88 0.6× 13 1.0k
Christian Lori Switzerland 5 746 1.1× 231 0.4× 347 1.7× 170 1.1× 103 0.7× 5 1.1k
Lionel Ferrières France 13 498 0.7× 361 0.7× 363 1.8× 214 1.3× 187 1.3× 14 996
Jennifer K. Teschler United States 10 435 0.6× 482 0.9× 120 0.6× 122 0.8× 107 0.7× 13 730
Alecia N. Septer United States 16 378 0.6× 415 0.8× 215 1.0× 163 1.0× 146 1.0× 35 876
Katharina Trunk United Kingdom 11 502 0.7× 578 1.1× 255 1.2× 119 0.7× 299 2.0× 12 1.1k
Grégory Jubelin France 23 796 1.2× 443 0.8× 398 1.9× 170 1.1× 133 0.9× 40 1.5k
David Kirke United Kingdom 6 813 1.2× 362 0.7× 216 1.1× 128 0.8× 73 0.5× 6 996
Geoffrey B. Severin United States 15 392 0.6× 175 0.3× 157 0.8× 144 0.9× 75 0.5× 23 583
Aaron Hinz Canada 16 872 1.3× 229 0.4× 456 2.2× 203 1.3× 329 2.2× 31 1.2k

Countries citing papers authored by David Zamorano‐Sánchez

Since Specialization
Citations

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

Fields of papers citing papers by David Zamorano‐Sánchez

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by David Zamorano‐Sánchez. 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 David Zamorano‐Sánchez. The network helps show where David Zamorano‐Sánchez may publish in the future.

Co-authorship network of co-authors of David Zamorano‐Sánchez

This figure shows the co-authorship network connecting the top 25 collaborators of David Zamorano‐Sánchez. A scholar is included among the top collaborators of David Zamorano‐Sánchez 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 David Zamorano‐Sánchez. David Zamorano‐Sánchez 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.
Zamorano‐Sánchez, David, et al.. (2025). Insights on the regulation and function of the CRISPR/Cas transposition system located in the pathogenicity island VpaI-7 from Vibrio parahaemolyticus RIMD2210633. Infection and Immunity. 93(6). e0016925–e0016925. 1 indexed citations
2.
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Zamorano‐Sánchez, David, et al.. (2022). The GGDEF-EAL protein CdgB from Azospirillum baldaniorum Sp245, is a dual function enzyme with potential polar localization. PLoS ONE. 17(11). e0278036–e0278036. 6 indexed citations
4.
Zamorano‐Sánchez, David, et al.. (2021). CdgC, a Cyclic-di-GMP Diguanylate Cyclase of Azospirillum baldaniorum Is Involved in Internalization to Wheat Roots. Frontiers in Plant Science. 12. 748393–748393. 6 indexed citations
5.
Zamorano‐Sánchez, David, et al.. (2021). A Trigger Phosphodiesterase Modulates the Global c-di-GMP Pool, Motility, and Biofilm Formation in Vibrio parahaemolyticus. Journal of Bacteriology. 203(13). e0004621–e0004621. 32 indexed citations
6.
Correa‐Galeote, David, Mishael Sánchez-Pérez, Mario Ramı́rez, et al.. (2020). A Novel OmpR-Type Response Regulator Controls Multiple Stages of the Rhizobium etli – Phaseolus vulgaris N2-Fixing Symbiosis. Frontiers in Microbiology. 11. 615775–615775. 6 indexed citations
7.
Guzmán, Josefina, Soledad Moreno, Miguel Cocotl‐Yañez, et al.. (2020). Cyclic di-GMP-Mediated Regulation of Extracellular Mannuronan C-5 Epimerases Is Essential for Cyst Formation in Azotobacter vinelandii. Journal of Bacteriology. 202(24). 10 indexed citations
8.
Zamorano‐Sánchez, David, Fernando A. Pagliai, Jin Hwan Park, et al.. (2020). Reciprocal c-di-GMP signaling: Incomplete flagellum biogenesis triggers c-di-GMP signaling pathways that promote biofilm formation. PLoS Genetics. 16(3). e1008703–e1008703. 50 indexed citations
9.
Giglio, Krista M., David Zamorano‐Sánchez, Jin Hwan Park, et al.. (2019). A Conserved Regulatory Circuit Controls Large Adhesins in Vibrio cholerae. mBio. 10(6). 28 indexed citations
10.
Zamorano‐Sánchez, David, Wujing Xian, Calvin K. Lee, et al.. (2019). Functional Specialization in Vibrio cholerae Diguanylate Cyclases: Distinct Modes of Motility Suppression and c-di-GMP Production. mBio. 10(2). 47 indexed citations
11.
Cheng, Andrew T., et al.. (2018). NtrC Adds a New Node to the Complex Regulatory Network of Biofilm Formation and vps Expression in Vibrio cholerae. Journal of Bacteriology. 200(15). 17 indexed citations
12.
Zamorano‐Sánchez, David, et al.. (2017). The ins and outs of cyclic di-GMP signaling in Vibrio cholerae. Current Opinion in Microbiology. 36. 20–29. 101 indexed citations
13.
Chin, Ko‐Hsin, Jin He, Christopher J. Jones, et al.. (2016). Nucleotide binding by the widespread high-affinity cyclic di-GMP receptor MshEN domain. Nature Communications. 7(1). 12481–12481. 96 indexed citations
14.
15.
Teschler, Jennifer K., David Zamorano‐Sánchez, Andrew S. Utada, et al.. (2015). Living in the matrix: assembly and control of Vibrio cholerae biofilms. Nature Reviews Microbiology. 13(5). 255–268. 307 indexed citations
16.
Bilecen, Kıvanç, Jiunn C. N. Fong, Andrew T. Cheng, et al.. (2015). Polymyxin B Resistance and Biofilm Formation in Vibrio cholerae Are Controlled by the Response Regulator CarR. Infection and Immunity. 83(3). 1199–1209. 52 indexed citations
17.
Zamorano‐Sánchez, David, et al.. (2015). Identification and Characterization of VpsR and VpsT Binding Sites in Vibrio cholerae. Journal of Bacteriology. 197(7). 1221–1235. 56 indexed citations
18.
Jones, Christopher J., Andrew S. Utada, Kimberly R. Davis, et al.. (2015). C-di-GMP Regulates Motile to Sessile Transition by Modulating MshA Pili Biogenesis and Near-Surface Motility Behavior in Vibrio cholerae. PLoS Pathogens. 11(10). e1005068–e1005068. 95 indexed citations
19.
Zamorano‐Sánchez, David, et al.. (2012). FxkR Provides the Missing Link in the fixL-fixK Signal Transduction Cascade in Rhizobium etli CFN42. Molecular Plant-Microbe Interactions. 25(11). 1506–1517. 20 indexed citations
20.

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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