Leslie Sieburth

4.6k total citations · 1 hit paper
38 papers, 3.6k citations indexed

About

Leslie Sieburth is a scholar working on Molecular Biology, Plant Science and Biochemistry. According to data from OpenAlex, Leslie Sieburth has authored 38 papers receiving a total of 3.6k indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Molecular Biology, 27 papers in Plant Science and 2 papers in Biochemistry. Recurrent topics in Leslie Sieburth's work include Plant Molecular Biology Research (26 papers), Plant Reproductive Biology (20 papers) and Plant nutrient uptake and metabolism (8 papers). Leslie Sieburth is often cited by papers focused on Plant Molecular Biology Research (26 papers), Plant Reproductive Biology (20 papers) and Plant nutrient uptake and metabolism (8 papers). Leslie Sieburth collaborates with scholars based in United States, Canada and France. Leslie Sieburth's co-authors include Elliot M. Meyerowitz, Peter Brodersen, Patrice Dunoyer, Lali Sakvarelidze-Achard, Olivier Voinnet, Yoshiharu Y. Yamamoto, Michael K. Deyholos, Jaimie Van Norman, Gary N. Drews and Weiping Zhang and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and The EMBO Journal.

In The Last Decade

Leslie Sieburth

37 papers receiving 3.5k citations

Hit Papers

Widespread Translational Inhibition by Plant miRNAs and s... 2008 2026 2014 2020 2008 250 500 750 1000

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Leslie Sieburth United States 25 3.0k 2.6k 138 137 104 38 3.6k
Olga Pontes United States 30 4.9k 1.6× 3.7k 1.4× 109 0.8× 125 0.9× 149 1.4× 40 5.8k
Henry D. Priest United States 19 2.2k 0.7× 2.1k 0.8× 64 0.5× 77 0.6× 54 0.5× 24 3.0k
Lianfeng Gu China 30 2.3k 0.7× 2.1k 0.8× 220 1.6× 81 0.6× 77 0.7× 77 3.2k
Dong‐Hoon Jeong South Korea 25 4.0k 1.3× 2.7k 1.0× 255 1.8× 68 0.5× 118 1.1× 55 4.6k
Filipe Borges United States 19 3.2k 1.1× 2.3k 0.9× 91 0.7× 197 1.4× 102 1.0× 26 3.6k
Maria Kalyna Austria 26 2.1k 0.7× 3.2k 1.2× 137 1.0× 36 0.3× 107 1.0× 37 3.8k
Sergei A. Filichkin United States 21 1.7k 0.6× 1.8k 0.7× 57 0.4× 41 0.3× 61 0.6× 33 2.4k
Moussa Benhamed France 34 2.8k 0.9× 2.4k 0.9× 453 3.3× 56 0.4× 301 2.9× 57 3.6k
Guru Jagadeeswaran United States 23 2.6k 0.9× 1.5k 0.6× 353 2.6× 41 0.3× 79 0.8× 32 3.1k
Mee Yeon Park United States 10 3.3k 1.1× 2.3k 0.9× 130 0.9× 83 0.6× 65 0.6× 11 3.5k

Countries citing papers authored by Leslie Sieburth

Since Specialization
Citations

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

Fields of papers citing papers by Leslie Sieburth

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Leslie Sieburth

This figure shows the co-authorship network connecting the top 25 collaborators of Leslie Sieburth. A scholar is included among the top collaborators of Leslie Sieburth 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 Leslie Sieburth. Leslie Sieburth 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.
Guo, Ruipeng, Reed Sorenson, Andrew Groover, et al.. (2022). Overcoming the field-of-view to diameter trade-off in microendoscopy via computational optrode-array microscopy. Optics Express. 31(5). 7505–7505.
2.
Sorenson, Reed, Maureen Hummel, Haiyan Ke, et al.. (2020). DHH1/DDX6-like RNA helicases maintain ephemeral half-lives of stress-response mRNAs. Nature Plants. 6(6). 675–685. 55 indexed citations
3.
Sorenson, Reed, et al.. (2018). Arabidopsis mRNA decay landscape arises from specialized RNA decay substrates, decapping-mediated feedback, and redundancy. Proceedings of the National Academy of Sciences. 115(7). E1485–E1494. 83 indexed citations
4.
Roux, Milena, Magnus Wohlfahrt Rasmussen, Kristoffer Palma, et al.. (2015). The mRNA decay factor PAT 1 functions in a pathway including MAP kinase 4 and immune receptor SUMM 2. The EMBO Journal. 34(5). 593–608. 82 indexed citations
5.
Lee, Dong-Keun, et al.. (2013). Long-Distance Signaling in bypass1 Mutants: Bioassay Development Reveals the bps Signal to Be a Metabolite. Molecular Plant. 6(1). 164–173. 14 indexed citations
6.
Lee, Dong-Keun & Leslie Sieburth. (2012). Thebpssignal. Plant Signaling & Behavior. 7(6). 698–700. 4 indexed citations
7.
Norman, Jaimie Van, Caroline Murphy, & Leslie Sieburth. (2011). BYPASS1: synthesis of the mobile root-derived signal requires active root growth and arrests early leaf development. BMC Plant Biology. 11(1). 28–28. 16 indexed citations
8.
Zhang, Weiping, Caroline Murphy, & Leslie Sieburth. (2010). Conserved RNaseII domain protein functions in cytoplasmic mRNA decay and suppresses Arabidopsis decapping mutant phenotypes. Proceedings of the National Academy of Sciences. 107(36). 15981–15985. 59 indexed citations
9.
Sieburth, Leslie, et al.. (2010). BYPASS1: How a Tiny Mutant Tells a Big Story about Root‐to‐shoot Signaling. Journal of Integrative Plant Biology. 52(1). 77–85. 21 indexed citations
10.
Brodersen, Peter, Lali Sakvarelidze-Achard, Patrice Dunoyer, et al.. (2008). Widespread Translational Inhibition by Plant miRNAs and siRNAs. Science. 320(5880). 1185–1190. 1134 indexed citations breakdown →
11.
Belostotsky, Dmitry A. & Leslie Sieburth. (2008). Kill the messenger: mRNA decay and plant development. Current Opinion in Plant Biology. 12(1). 96–102. 73 indexed citations
12.
Norman, Jaimie Van, et al.. (2007). Components of the Arabidopsis mRNA Decapping Complex Are Required for Early Seedling Development. The Plant Cell. 19(5). 1549–1564. 105 indexed citations
13.
Norman, Jaimie Van & Leslie Sieburth. (2007). Dissecting the biosynthetic pathway for the bypass1 root‐derived signal. The Plant Journal. 49(4). 619–628. 55 indexed citations
14.
Sieburth, Leslie & Michael K. Deyholos. (2005). Vascular development: the long and winding road. Current Opinion in Plant Biology. 9(1). 48–54. 75 indexed citations
15.
Norman, Jaimie Van, et al.. (2004). BYPASS1 Negatively Regulates a Root-Derived Signal that Controls Plant Architecture. Current Biology. 14(19). 1739–1746. 76 indexed citations
16.
Deyholos, Michael K., et al.. (2000). The SCARFACE gene is required for cotyledon and leaf vein patterning. Development. 127(15). 3205–3213. 99 indexed citations
17.
Jack, Thomas, Leslie Sieburth, & Elliot M. Meyerowitz. (1997). Targeted misexpression of AGAMOUS in whorl 2 of Arabidopsis flowers. The Plant Journal. 11(4). 825–839. 36 indexed citations
18.
Sieburth, Leslie, Mark Running, & Elliot M. Meyerowitz. (1995). Genetic separation of third and fourth whorl functions of AGAMOUS.. The Plant Cell. 7(8). 1249–1258. 113 indexed citations
19.
Sieburth, Leslie, et al.. (1991). Chloroplast RNA Stability in Chlamydomonas: Rapid Degradation of psbB and psbC Transcripts in Two Nuclear Mutants. The Plant Cell. 3(2). 175–175. 12 indexed citations
20.
Sutton, Ann, Leslie Sieburth, & John Bennett. (1987). Light‐dependent accumulation and localization of photosystem II proteins in maize. European Journal of Biochemistry. 164(3). 571–578. 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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