Gladys Alexandre

3.3k total citations
63 papers, 1.9k citations indexed

About

Gladys Alexandre is a scholar working on Molecular Biology, Plant Science and Genetics. According to data from OpenAlex, Gladys Alexandre has authored 63 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 41 papers in Molecular Biology, 29 papers in Plant Science and 16 papers in Genetics. Recurrent topics in Gladys Alexandre's work include Legume Nitrogen Fixing Symbiosis (20 papers), Bacterial Genetics and Biotechnology (16 papers) and Plant-Microbe Interactions and Immunity (12 papers). Gladys Alexandre is often cited by papers focused on Legume Nitrogen Fixing Symbiosis (20 papers), Bacterial Genetics and Biotechnology (16 papers) and Plant-Microbe Interactions and Immunity (12 papers). Gladys Alexandre collaborates with scholars based in United States, France and Mexico. Gladys Alexandre's co-authors include Igor B. Zhulin, Michael F. Hynes, Birgit E. Scharf, Amber N. Bible, Zhihong Xie, Lindsey O’Neal, Christopher K. Yost, René Bally, Tanmoy Mukherjee and René Bally and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Applied and Environmental Microbiology and Biochemistry.

In The Last Decade

Gladys Alexandre

61 papers receiving 1.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Gladys Alexandre United States 28 992 863 367 358 161 63 1.9k
Birgit E. Scharf United States 30 1.4k 1.4× 875 1.0× 496 1.4× 739 2.1× 114 0.7× 80 2.8k
Rüdiger Schmitt Germany 31 1.8k 1.8× 808 0.9× 798 2.2× 807 2.3× 180 1.1× 62 3.0k
Hoda Khouri United States 16 1.3k 1.3× 436 0.5× 279 0.8× 792 2.2× 109 0.7× 18 2.4k
R. Schmitt Germany 24 908 0.9× 480 0.6× 488 1.3× 370 1.0× 69 0.4× 46 1.7k
James E. Berleman United States 19 913 0.9× 157 0.2× 398 1.1× 402 1.1× 190 1.2× 22 1.4k
Miaomiao Shi China 21 531 0.5× 589 0.7× 321 0.9× 237 0.7× 79 0.5× 71 1.4k
Annegret Wilde Germany 38 2.7k 2.7× 676 0.8× 275 0.7× 870 2.4× 23 0.1× 90 3.3k
Amanda E. Goodman Australia 17 657 0.7× 125 0.1× 143 0.4× 330 0.9× 108 0.7× 43 1.1k
Russell D. Monds United States 16 1.3k 1.3× 254 0.3× 742 2.0× 429 1.2× 339 2.1× 16 1.9k
Burkhard A. Hense Germany 20 915 0.9× 220 0.3× 357 1.0× 247 0.7× 99 0.6× 44 1.5k

Countries citing papers authored by Gladys Alexandre

Since Specialization
Citations

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

Fields of papers citing papers by Gladys Alexandre

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Gladys Alexandre. 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 Gladys Alexandre. The network helps show where Gladys Alexandre may publish in the future.

Co-authorship network of co-authors of Gladys Alexandre

This figure shows the co-authorship network connecting the top 25 collaborators of Gladys Alexandre. A scholar is included among the top collaborators of Gladys Alexandre 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 Gladys Alexandre. Gladys Alexandre 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.
Banerjee, Ishita, John W. King, B.A. Sexton, et al.. (2025). Ethylene signals through an ethylene receptor to modulate biofilm formation and root colonization in a beneficial plant-associated bacterium. PLoS Genetics. 21(2). e1011587–e1011587.
2.
Ganusova, Elena E., et al.. (2025). Indole-3-acetic acid (IAA) protects Azospirillum brasilense from indole-induced stress. Applied and Environmental Microbiology. 91(4). e0238424–e0238424. 4 indexed citations
3.
Carrell, Alyssa A., Sara Jawdy, Wellington Muchero, et al.. (2023). Interactions with microbial consortia have variable effects in organic carbon and production of exometabolites among genotypes of Populus trichocarpa. Plant Direct. 7(11). e544–e544. 3 indexed citations
4.
O’Neal, Lindsey, et al.. (2019). A PilZ-Containing Chemotaxis Receptor Mediates Oxygen and Wheat Root Sensing in Azospirillum brasilense. Frontiers in Microbiology. 10. 312–312. 12 indexed citations
5.
Mukherjee, Tanmoy, et al.. (2019). Multiple CheY Homologs Control Swimming Reversals and Transient Pauses in Azospirillum brasilense. Biophysical Journal. 116(8). 1527–1537. 16 indexed citations
6.
Alexiades, Vasilios, et al.. (2019). Modeling aerotaxis band formation in Azospirillum brasilense. BMC Microbiology. 19(1). 101–101. 6 indexed citations
7.
Ryu, Min‐Hyung, et al.. (2017). Using Light-Activated Enzymes for Modulating Intracellular c-di-GMP Levels in Bacteria. Methods in molecular biology. 1657. 169–186. 9 indexed citations
8.
Nellas, Ricky B., et al.. (2013). Swimming motility plays a key role in the stochastic dynamics of cell clumping. Physical Biology. 10(2). 26005–26005. 6 indexed citations
9.
Alexandre, Gladys, et al.. (2012). Bovine serum albumin further enhances the effects of organic solvents on increased yield of polymerase chain reaction of GC-rich templates. BMC Research Notes. 5(1). 257–257. 74 indexed citations
10.
Siuti, Piro, et al.. (2011). The chemotaxis-like Che1 pathway has an indirect role in adhesive cell properties of Azospirillum brasilense. FEMS Microbiology Letters. 323(2). 105–112. 19 indexed citations
11.
Xie, Zhihong, Luke E. Ulrich, Igor B. Zhulin, & Gladys Alexandre. (2010). PAS domain containing chemoreceptor couples dynamic changes in metabolism with chemotaxis. Proceedings of the National Academy of Sciences. 107(5). 2235–2240. 57 indexed citations
12.
Siuti, Piro, Amber N. Bible, Gladys Alexandre, et al.. (2010). Characterization of cell surface and extracellular matrix remodeling of Azospirillum brasilense chemotaxis-like 1 signal transduction pathway mutants by atomic force microscopy. FEMS Microbiology Letters. 314(2). 131–139. 14 indexed citations
13.
Buchan, Alison, et al.. (2010). Temporal dynamics and genetic diversity of chemotactic‐competent microbial populations in the rhizosphere. Environmental Microbiology. 12(12). 3171–3184. 30 indexed citations
14.
Alexandre, Gladys, et al.. (2009). Chapter 3 Diversity in Bacterial Chemotactic Responses and Niche Adaptation. Advances in applied microbiology. 66. 53–75. 85 indexed citations
15.
Alexandre, Gladys, et al.. (2003). Aer and Tsr guide Escherichia coli in spatial gradients of oxidizable substrates. Microbiology. 149(9). 2661–2667. 43 indexed citations
16.
Alexandre, Gladys, et al.. (2003). Ecological role of energy taxis in microorganisms. FEMS Microbiology Reviews. 28(1). 113–126. 151 indexed citations
17.
Alexandre, Gladys, et al.. (2002). A major chemotaxis gene cluster inAzospirillum brasilenseand relationships between chemotaxis operons in α-proteobacteria. FEMS Microbiology Letters. 208(1). 61–67. 40 indexed citations
18.
Alexandre, Gladys. (1999). Emergence of a laccase-positive variant of Azospirillum lipoferum occurs via a two-step phenotypic switching process. FEMS Microbiology Letters. 174(2). 371–378. 2 indexed citations
19.
Alexandre, Gladys & René Bally. (1999). Emergence of a laccase-positive variant ofAzospirillum lipoferumoccurs via a two-step phenotypic switching process. FEMS Microbiology Letters. 174(2). 371–378. 26 indexed citations
20.
Alexandre, Gladys, et al.. (1996). Population dynamics of a motile and a non-motile Azospirillum lipoferum strain during rice root colonization and motility variation in the rhizosphere. FEMS Microbiology Ecology. 19(4). 271–278. 28 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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