Josh T. Cuperus

4.8k total citations · 3 hit papers
38 papers, 3.3k citations indexed

About

Josh T. Cuperus is a scholar working on Molecular Biology, Plant Science and Cell Biology. According to data from OpenAlex, Josh T. Cuperus has authored 38 papers receiving a total of 3.3k indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Molecular Biology, 24 papers in Plant Science and 2 papers in Cell Biology. Recurrent topics in Josh T. Cuperus's work include Plant Molecular Biology Research (15 papers), Chromosomal and Genetic Variations (11 papers) and CRISPR and Genetic Engineering (8 papers). Josh T. Cuperus is often cited by papers focused on Plant Molecular Biology Research (15 papers), Chromosomal and Genetic Variations (11 papers) and CRISPR and Genetic Engineering (8 papers). Josh T. Cuperus collaborates with scholars based in United States, Germany and Japan. Josh T. Cuperus's co-authors include James C. Carrington, Noah Fahlgren, Taiowa A. Montgomery, Stanley Fields, Christine Queitsch, Alberto Carbonell, Elisabeth J. Chapman, Dawei Li, Edwards Allen and Jesse E. Hansen and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Nature Communications.

In The Last Decade

Josh T. Cuperus

36 papers receiving 3.3k citations

Hit Papers

Specificity of ARGONAUTE7... 2008 2026 2014 2020 2008 2011 2019 200 400 600

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Josh T. Cuperus United States 21 2.6k 2.1k 186 142 130 38 3.3k
Jeremy R. Haag United States 17 4.1k 1.6× 2.9k 1.4× 152 0.8× 200 1.4× 111 0.9× 20 4.8k
Olga Pontes United States 30 4.9k 1.9× 3.7k 1.7× 109 0.6× 149 1.0× 115 0.9× 40 5.8k
Friedrich Kragler Germany 33 2.9k 1.2× 2.4k 1.1× 111 0.6× 158 1.1× 68 0.5× 64 4.1k
Jixian Zhai China 47 5.3k 2.1× 3.6k 1.7× 290 1.6× 215 1.5× 34 0.3× 94 6.4k
Ortrun Mittelsten Scheid Austria 37 4.8k 1.9× 3.6k 1.7× 53 0.3× 58 0.4× 202 1.6× 71 5.5k
Ignacio Rubio‐Somoza Germany 22 3.3k 1.3× 2.3k 1.1× 628 3.4× 259 1.8× 47 0.4× 35 3.9k
Javier Gallego‐Bartolomé United States 26 3.3k 1.3× 2.3k 1.1× 42 0.2× 241 1.7× 55 0.4× 33 3.7k
David Turrà Spain 24 1.6k 0.6× 1.0k 0.5× 104 0.6× 36 0.3× 60 0.5× 46 2.4k
Liang Song China 18 2.4k 1.0× 2.0k 0.9× 86 0.5× 32 0.2× 75 0.6× 40 3.2k
Leslie Sieburth United States 25 3.0k 1.2× 2.6k 1.3× 138 0.7× 104 0.7× 60 0.5× 38 3.6k

Countries citing papers authored by Josh T. Cuperus

Since Specialization
Citations

This map shows the geographic impact of Josh T. Cuperus'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 Josh T. Cuperus with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Josh T. Cuperus more than expected).

Fields of papers citing papers by Josh T. Cuperus

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Josh T. Cuperus. 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 Josh T. Cuperus. The network helps show where Josh T. Cuperus may publish in the future.

Co-authorship network of co-authors of Josh T. Cuperus

This figure shows the co-authorship network connecting the top 25 collaborators of Josh T. Cuperus. A scholar is included among the top collaborators of Josh T. Cuperus 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 Josh T. Cuperus. Josh T. Cuperus 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.
Zhang, Jason Z., Josh T. Cuperus, Buwei Huang, et al.. (2025). De novo designed Hsp70 activator dissolves intracellular condensates. Cell chemical biology. 32(3). 463–473.e6. 3 indexed citations
2.
Jores, Tobias, Jackson Tonnies, Si Nian Char, et al.. (2025). Small DNA elements can act as both insulators and silencers in plants. The Plant Cell. 37(6). 2 indexed citations
3.
Bubb, Kerry L., Joseph Min, Erik J. Bergstrom, et al.. (2025). The regulatory potential of transposable elements in maize. Nature Plants. 11(6). 1181–1192. 2 indexed citations
4.
Jores, Tobias, Jackson Tonnies, Kerry L. Bubb, et al.. (2024). Arabidopsis and maize terminator strength is determined by GC content, polyadenylation motifs and cleavage probability. Nature Communications. 15(1). 5868–5868. 13 indexed citations
5.
Kwan, Elizabeth X., Gina M. Alvino, Haley M. Amemiya, et al.. (2023). Ribosomal DNA replication time coordinates completion of genome replication and anaphase in yeast. Cell Reports. 42(3). 112161–112161. 7 indexed citations
6.
Jores, Tobias, et al.. (2023). Frontiers and techniques in plant gene regulation. Current Opinion in Plant Biology. 75. 102403–102403. 8 indexed citations
7.
Lemus, Tzitziki, G. Alex Mason, Kerry L. Bubb, et al.. (2022). AGO1 and HSP90 buffer different genetic variants in Arabidopsis thaliana. Genetics. 223(2). 9 indexed citations
8.
Gala, Hardik, Amy Lanctot, Ken Jean-Baptiste, et al.. (2021). A single-cell view of the transcriptome during lateral root initiation in Arabidopsis thaliana. The Plant Cell. 33(7). 2197–2220. 95 indexed citations
9.
Jores, Tobias, Jackson Tonnies, Travis Wrightsman, et al.. (2021). Synthetic promoter designs enabled by a comprehensive analysis of plant core promoters. Nature Plants. 7(6). 842–855. 131 indexed citations
10.
Cuperus, Josh T.. (2021). Single-cell genomics in plants: current state, future directions, and hurdles to overcome. PLANT PHYSIOLOGY. 188(2). 749–755. 35 indexed citations
11.
Dorrity, Michael W., et al.. (2021). The regulatory landscape of Arabidopsis thaliana roots at single-cell resolution. Nature Communications. 12(1). 3334–3334. 116 indexed citations
12.
Jores, Tobias, Jackson Tonnies, Michael W. Dorrity, et al.. (2020). Identification of Plant Enhancers and Their Constituent Elements by STARR-seq in Tobacco Leaves. The Plant Cell. 32(7). 2120–2131. 67 indexed citations
13.
Jean-Baptiste, Ken, José L. McFaline‐Figueroa, Cristina M Alexandre, et al.. (2019). Dynamics of Gene Expression in Single Root Cells of Arabidopsis thaliana. The Plant Cell. 31(5). 993–1011. 274 indexed citations breakdown →
14.
Dorrity, Michael W., et al.. (2018). Preferences in a trait decision determined by transcription factor variants. Proceedings of the National Academy of Sciences. 115(34). E7997–E8006. 17 indexed citations
15.
Cuperus, Josh T., et al.. (2015). A tetO Toolkit To Alter Expression of Genes in Saccharomyces cerevisiae. ACS Synthetic Biology. 4(7). 842–852. 17 indexed citations
16.
Carbonell, Alberto, Atsushi Takeda, Noah Fahlgren, et al.. (2014). New Generation of Artificial MicroRNA and Synthetic Trans-Acting Small Interfering RNA Vectors for Efficient Gene Silencing in Arabidopsis. PLANT PHYSIOLOGY. 165(1). 15–29. 107 indexed citations
17.
Cuperus, Josh T., Alberto Carbonell, Noah Fahlgren, et al.. (2010). Unique functionality of 22-nt miRNAs in triggering RDR6-dependent siRNA biogenesis from target transcripts in Arabidopsis. Nature Structural & Molecular Biology. 17(8). 997–1003. 344 indexed citations
18.
Rubio‐Somoza, Ignacio, Josh T. Cuperus, Detlef Weigel, & James C. Carrington. (2009). Regulation and functional specialization of small RNA–target nodes during plant development. Current Opinion in Plant Biology. 12(5). 622–627. 91 indexed citations
19.
Bhattacharjee, Saikat, Lan‐Ying Lee, Hongbin Cao, et al.. (2008). IMPa-4, an Arabidopsis Importin α Isoform, Is Preferentially Involved in Agrobacterium -Mediated Plant Transformation. The Plant Cell. 20(10). 2661–2680. 99 indexed citations
20.
Montgomery, Taiowa A., Miya D. Howell, Josh T. Cuperus, et al.. (2008). Specificity of ARGONAUTE7-miR390 Interaction and Dual Functionality in TAS3 Trans-Acting siRNA Formation. Cell. 133(1). 128–141. 605 indexed citations breakdown →

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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