Valérie Reeb

8.3k total citations
17 papers, 1.7k citations indexed

About

Valérie Reeb is a scholar working on Molecular Biology, Plant Science and Ecology, Evolution, Behavior and Systematics. According to data from OpenAlex, Valérie Reeb has authored 17 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 9 papers in Plant Science and 7 papers in Ecology, Evolution, Behavior and Systematics. Recurrent topics in Valérie Reeb's work include Lichen and fungal ecology (7 papers), Mycorrhizal Fungi and Plant Interactions (5 papers) and Plant Pathogens and Fungal Diseases (5 papers). Valérie Reeb is often cited by papers focused on Lichen and fungal ecology (7 papers), Mycorrhizal Fungi and Plant Interactions (5 papers) and Plant Pathogens and Fungal Diseases (5 papers). Valérie Reeb collaborates with scholars based in United States, Germany and Norway. Valérie Reeb's co-authors include François Lutzoni, Claude Roux, Mark Pagel, Stefan Zoller, Peter J. Wagner, Debashish Bhattacharya, Dawn M. Simon, Jolanta Miądlikowska, Peik Haugen and John D. Nason and has published in prestigious journals such as Nature, Nature Communications and Molecular Biology and Evolution.

In The Last Decade

Valérie Reeb

17 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Valérie Reeb United States 11 1.1k 875 700 492 183 17 1.7k
Léanne L. Dreyer South Africa 25 1.0k 0.9× 898 1.0× 561 0.8× 568 1.2× 409 2.2× 132 1.9k
Steven J. Brunsfeld United States 21 673 0.6× 850 1.0× 230 0.3× 451 0.9× 460 2.5× 35 1.8k
Francesco Dal Grande Germany 25 1.1k 1.0× 1.2k 1.4× 411 0.6× 226 0.5× 227 1.2× 74 1.6k
Stephan Nylinder Sweden 20 390 0.3× 569 0.7× 136 0.2× 411 0.8× 117 0.6× 33 1.0k
Francois Roets South Africa 24 856 0.8× 529 0.6× 746 1.1× 327 0.7× 718 3.9× 160 1.8k
Marie L. Davey Norway 23 827 0.7× 503 0.6× 475 0.7× 335 0.7× 541 3.0× 59 1.5k
Mickaël Le Gac France 19 511 0.5× 301 0.3× 368 0.5× 514 1.0× 223 1.2× 35 1.3k
Fabien Halkett France 23 1.0k 0.9× 481 0.5× 369 0.5× 392 0.8× 200 1.1× 45 1.7k
Richard C. Winkworth New Zealand 18 531 0.5× 827 0.9× 105 0.1× 486 1.0× 134 0.7× 30 1.3k
Johannes Klein Germany 6 288 0.3× 247 0.3× 142 0.2× 252 0.5× 153 0.8× 7 722

Countries citing papers authored by Valérie Reeb

Since Specialization
Citations

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

Fields of papers citing papers by Valérie Reeb

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Valérie Reeb

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

All Works

17 of 17 papers shown
1.
Reeb, Valérie, Piyali Chatterjee, Jinhua Xiang, et al.. (2025). Direct comparison of clear DX Nanopore and Illumina sequencing of SARS-CoV-2. Microbiology Spectrum. 13(9). e0042725–e0042725. 1 indexed citations
2.
Bolden, Nicholas C., L. Boyken, Andrew L. Thurman, et al.. (2023). Parallel evolution of linezolid-resistant Staphylococcus aureus in patients with cystic fibrosis. Microbiology Spectrum. 11(5). e0208423–e0208423. 2 indexed citations
3.
Moustafa, Ahmed M., Paul J. Planet, Andrea R. Thurman, et al.. (2021). 418: Linezolid-resistant Staphylococcus aureus in patients with cystic fibrosis. Journal of Cystic Fibrosis. 20. S196–S197. 1 indexed citations
4.
Porterfield, Harry S., Andrew L. Thurman, L. Boyken, et al.. (2021). MRSA strains with distinct accessory genes predominate at different ages in cystic fibrosis. Pediatric Pulmonology. 56(9). 2868–2878. 6 indexed citations
5.
Lutzoni, François, Michael Nowak, Michael E. Alfaro, et al.. (2018). Contemporaneous radiations of fungi and plants linked to symbiosis. Nature Communications. 9(1). 5451–5451. 187 indexed citations
6.
Reeb, Valérie, et al.. (2013). Cyanidiales diversity in Yellowstone National Park. Letters in Applied Microbiology. 57(5). 459–466. 22 indexed citations
7.
Schmull, Michaela, Jolanta Miądlikowska, Elfie Stocker‐Wörgötter, et al.. (2011). Phylogenetic affiliations of members of the heterogeneous lichen-forming fungi of the genus Lecidea sensu Zahlbruckner (Lecanoromycetes, Ascomycota). Mycologia. 103(5). 983–1003. 79 indexed citations
8.
Reeb, Valérie, et al.. (2010). Good to the bone: microbial community thrives within bone cavities of a bison carcass at Yellowstone National Park. Environmental Microbiology. 13(9). 2403–2415. 8 indexed citations
9.
Knudsen, Kerry, et al.. (2010). Acarospora rosulatain Europe, North America and Asia. The Lichenologist. 42(3). 291–296. 6 indexed citations
10.
Reeb, Valérie, Michael T. Peglar, Hwan Su Yoon, et al.. (2009). Interrelationships of chromalveolates within a broadly sampled tree of photosynthetic protists. Molecular Phylogenetics and Evolution. 53(1). 202–211. 20 indexed citations
11.
Reeb, Valérie, Peik Haugen, Debashish Bhattacharya, & François Lutzoni. (2007). Evolution of Pleopsidium (Lichenized Ascomycota) S943 Group I Introns and the Phylogeography of an Intron-Encoded Putative Homing Endonuclease. Journal of Molecular Evolution. 64(3). 285–298. 12 indexed citations
12.
Bhattacharya, Debashish, Valérie Reeb, Dawn M. Simon, & François Lutzoni. (2005). Phylogenetic analyses suggest reverse splicing spread of group I introns in fungal ribosomal DNA. BMC Evolutionary Biology. 5(1). 68–68. 41 indexed citations
13.
Haugen, Peik, Valérie Reeb, François Lutzoni, & Debashish Bhattacharya. (2004). The Evolution of Homing Endonuclease Genes and Group I Introns in Nuclear rDNA. Molecular Biology and Evolution. 21(1). 129–140. 60 indexed citations
14.
Reeb, Valérie, François Lutzoni, & Claude Roux. (2004). Contribution of RPB2 to multilocus phylogenetic studies of the euascomycetes (Pezizomycotina, Fungi) with special emphasis on the lichen-forming Acarosporaceae and evolution of polyspory. Molecular Phylogenetics and Evolution. 32(3). 1036–1060. 409 indexed citations
15.
Lutzoni, François, Mark Pagel, & Valérie Reeb. (2001). Major fungal lineages are derived from lichen symbiotic ancestors. Nature. 411(6840). 937–940. 380 indexed citations
16.
Bhattacharya, Debashish, François Lutzoni, Valérie Reeb, et al.. (2000). Widespread Occurrence of Spliceosomal Introns in the rDNA Genes of Ascomycetes. Molecular Biology and Evolution. 17(12). 1971–1984. 97 indexed citations
17.
Lutzoni, François, Peter J. Wagner, Valérie Reeb, & Stefan Zoller. (2000). Integrating Ambiguously Aligned Regions of DNA Sequences in Phylogenetic Analyses Without Violating Positional Homology. Systematic Biology. 49(4). 628–651. 327 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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