Varsha Mathur

970 total citations
18 papers, 489 citations indexed

About

Varsha Mathur is a scholar working on Ecology, Molecular Biology and Ecology, Evolution, Behavior and Systematics. According to data from OpenAlex, Varsha Mathur has authored 18 papers receiving a total of 489 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Ecology, 9 papers in Molecular Biology and 5 papers in Ecology, Evolution, Behavior and Systematics. Recurrent topics in Varsha Mathur's work include Microbial Community Ecology and Physiology (7 papers), Protist diversity and phylogeny (7 papers) and Genomics and Phylogenetic Studies (6 papers). Varsha Mathur is often cited by papers focused on Microbial Community Ecology and Physiology (7 papers), Protist diversity and phylogeny (7 papers) and Genomics and Phylogenetic Studies (6 papers). Varsha Mathur collaborates with scholars based in Canada, Czechia and United States. Varsha Mathur's co-authors include Patrick J. Keeling, Waldan K. Kwong, Javier del Campo, Martin Kolísko, Mark J. A. Vermeij, Nicholas A. T. Irwin, Brian S. Leander, Kevin C. Wakeman, Mark Freeman and Árni Kristmundsson and has published in prestigious journals such as Nature, Nature Communications and PLoS ONE.

In The Last Decade

Varsha Mathur

18 papers receiving 489 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Varsha Mathur Canada 12 285 272 110 84 47 18 489
Timur G. Simdyanov Russia 14 359 1.3× 379 1.4× 206 1.9× 87 1.0× 23 0.5× 26 610
Andrew G. Briscoe United Kingdom 13 273 1.0× 147 0.5× 71 0.6× 56 0.7× 21 0.4× 28 424
Martin Kostka Czechia 14 236 0.8× 310 1.1× 234 2.1× 32 0.4× 55 1.2× 26 625
Eric D. Salomaki United States 11 226 0.8× 246 0.9× 66 0.6× 119 1.4× 16 0.3× 21 420
Nicholas A. T. Irwin Canada 11 177 0.6× 244 0.9× 52 0.5× 45 0.5× 19 0.4× 19 346
Wyth L. Marshall Canada 11 294 1.0× 285 1.0× 44 0.4× 74 0.9× 88 1.9× 14 567
J. Norman Grim United States 14 276 1.0× 343 1.3× 70 0.6× 67 0.8× 27 0.6× 45 543
Michelle M. Leger Canada 10 155 0.5× 403 1.5× 62 0.6× 18 0.2× 19 0.4× 18 536
Alexis T. Howe United Kingdom 9 509 1.8× 649 2.4× 59 0.5× 92 1.1× 26 0.6× 9 833
Gita G. Paskerova Russia 11 148 0.5× 168 0.6× 176 1.6× 26 0.3× 12 0.3× 25 329

Countries citing papers authored by Varsha Mathur

Since Specialization
Citations

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

Fields of papers citing papers by Varsha Mathur

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Varsha Mathur

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

All Works

18 of 18 papers shown
1.
Mathur, Varsha, Eric D. Salomaki, Kevin C. Wakeman, et al.. (2023). Reconstruction of Plastid Proteomes of Apicomplexans and Close Relatives Reveals the Major Evolutionary Outcomes of Cryptic Plastids. Molecular Biology and Evolution. 40(1). 22 indexed citations
2.
Hehenberger, Elisabeth, Vittorio Boscaro, E. James, et al.. (2023). New Parabasalia symbionts Snyderella spp. and Daimonympha gen. nov. from South American Rugitermes termites and the parallel evolution of a cell with a rotating “head”. Journal of Eukaryotic Microbiology. 70(5). e12987–e12987. 2 indexed citations
3.
Tikhonenkov, Denis V., Kirill V. Mikhailov, Ryan M.R. Gawryluk, et al.. (2022). Microbial predators form a new supergroup of eukaryotes. Nature. 612(7941). 714–719. 43 indexed citations
4.
Holt, Corey C., Vittorio Boscaro, Niels W. L. Van Steenkiste, et al.. (2022). Microscopic marine invertebrates are reservoirs for cryptic and diverse protists and fungi. Microbiome. 10(1). 161–161. 19 indexed citations
5.
Boscaro, Vittorio, Corey C. Holt, Niels W. L. Van Steenkiste, et al.. (2022). Microbiomes of microscopic marine invertebrates do not reveal signatures of phylosymbiosis. Nature Microbiology. 7(6). 810–819. 40 indexed citations
7.
Keeling, Patrick J., Varsha Mathur, & Waldan K. Kwong. (2021). Corallicolids: The elusive coral-infecting apicomplexans. PLoS Pathogens. 17(9). e1009845–e1009845. 6 indexed citations
8.
Mathur, Varsha, Kevin C. Wakeman, & Patrick J. Keeling. (2021). Parallel functional reduction in the mitochondria of apicomplexan parasites. Current Biology. 31(13). 2920–2928.e4. 34 indexed citations
9.
Irwin, Nicholas A. T., et al.. (2021). The molecular phylogeny of Chionaster nivalis reveals a novel order of psychrophilic and globally distributed Tremellomycetes (Fungi, Basidiomycota). PLoS ONE. 16(3). e0247594–e0247594. 4 indexed citations
10.
Boscaro, Vittorio, E. James, Anna Karnkowska, et al.. (2021). Characterization of new cristamonad species from kalotermitid termites including a novel genus, Runanympha. Scientific Reports. 11(1). 7270–7270. 2 indexed citations
11.
Schön, Max Emil, Vasily V. Zlatogursky, Camille Poirier, et al.. (2021). Single cell genomics reveals plastid-lacking Picozoa are close relatives of red algae. Nature Communications. 12(1). 6651–6651. 51 indexed citations
12.
Irwin, Nicholas A. T., Alexandros A. Pittis, Varsha Mathur, et al.. (2020). The Function and Evolution of Motile DNA Replication Systems in Ciliates. Current Biology. 31(1). 66–76.e6. 11 indexed citations
13.
Mathur, Varsha, Waldan K. Kwong, Filip Husník, et al.. (2020). Phylogenomics Identifies a New Major Subgroup of Apicomplexans, Marosporida class nov., with Extreme Apicoplast Genome Reduction. Genome Biology and Evolution. 13(2). 31 indexed citations
14.
Mathur, Varsha, Martin Kolísko, Elisabeth Hehenberger, et al.. (2019). Multiple Independent Origins of Apicomplexan-Like Parasites. Current Biology. 29(17). 2936–2941.e5. 84 indexed citations
15.
Kwong, Waldan K., Javier del Campo, Varsha Mathur, Mark J. A. Vermeij, & Patrick J. Keeling. (2019). A widespread coral-infecting apicomplexan with chlorophyll biosynthesis genes. Nature. 568(7750). 103–107. 88 indexed citations
16.
Mathur, Varsha, Javier del Campo, Martin Kolísko, & Patrick J. Keeling. (2018). Global diversity and distribution of close relatives of apicomplexan parasites. Environmental Microbiology. 20(8). 2824–2833. 21 indexed citations
17.
Campo, Javier del, E. James, Yoshihisa Hirakawa, et al.. (2017). Pseudotrichonympha leei, Pseudotrichonympha lifesoni, and Pseudotrichonympha pearti, new species of parabasalian flagellates and the description of a rotating subcellular structure. Scientific Reports. 7(1). 16349–16349. 9 indexed citations
18.
Boscaro, Vittorio, E. James, Elisabeth Hehenberger, et al.. (2017). Molecular characterization and phylogeny of four new species of the genus Trichonympha (Parabasalia, Trichonymphea) from lower termite hindguts. INTERNATIONAL JOURNAL OF SYSTEMATIC AND EVOLUTIONARY MICROBIOLOGY. 67(9). 3570–3575. 10 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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