Tessa M. Burch‐Smith

5.1k total citations · 1 hit paper
58 papers, 3.8k citations indexed

About

Tessa M. Burch‐Smith is a scholar working on Plant Science, Molecular Biology and Physiology. According to data from OpenAlex, Tessa M. Burch‐Smith has authored 58 papers receiving a total of 3.8k indexed citations (citations by other indexed papers that have themselves been cited), including 52 papers in Plant Science, 17 papers in Molecular Biology and 2 papers in Physiology. Recurrent topics in Tessa M. Burch‐Smith's work include Legume Nitrogen Fixing Symbiosis (20 papers), Plant Virus Research Studies (20 papers) and Plant Molecular Biology Research (20 papers). Tessa M. Burch‐Smith is often cited by papers focused on Legume Nitrogen Fixing Symbiosis (20 papers), Plant Virus Research Studies (20 papers) and Plant Molecular Biology Research (20 papers). Tessa M. Burch‐Smith collaborates with scholars based in United States, United Kingdom and France. Tessa M. Burch‐Smith's co-authors include Savithramma P. Dinesh‐Kumar, Patricia Zambryski, Michael Schiff, Yule Liu, Gregory B. Martin, Jeffrey C. Anderson, Kirk J. Czymmek, Jeffrey L. Caplan, Krzysztof Bobik and Padmavathi Mamillapalli and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Tessa M. Burch‐Smith

57 papers receiving 3.8k citations

Hit Papers

Applications and advantages of virus‐induced gene silenci... 2004 2026 2011 2018 2004 100 200 300 400 500

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Tessa M. Burch‐Smith United States 27 3.3k 1.7k 295 257 193 58 3.8k
Xiuren Zhang United States 25 4.1k 1.3× 3.0k 1.8× 267 0.9× 275 1.1× 245 1.3× 50 5.0k
Christophe Lacomme United Kingdom 24 2.8k 0.8× 1.6k 0.9× 266 0.9× 503 2.0× 243 1.3× 39 3.3k
Rosa Lozano‐Durán China 34 3.4k 1.0× 1.2k 0.7× 150 0.5× 306 1.2× 444 2.3× 95 3.7k
Peter Moffett Canada 35 4.3k 1.3× 1.4k 0.8× 334 1.1× 441 1.7× 406 2.1× 84 4.9k
Jean‐Benoit Morel France 20 3.0k 0.9× 1.6k 0.9× 152 0.5× 272 1.1× 178 0.9× 38 3.5k
Dominique Pontier France 28 3.1k 0.9× 1.9k 1.1× 106 0.4× 153 0.6× 162 0.8× 34 3.7k
Alison G. Roberts United Kingdom 29 2.9k 0.9× 1.4k 0.8× 433 1.5× 248 1.0× 118 0.6× 40 3.5k
Arthur G. Hunt United States 37 2.8k 0.8× 2.8k 1.6× 556 1.9× 395 1.5× 239 1.2× 112 4.4k
Ari Sadanandom United Kingdom 36 3.8k 1.2× 2.3k 1.4× 136 0.5× 104 0.4× 210 1.1× 76 4.8k
Guido Sessa Israel 34 3.2k 1.0× 1.2k 0.7× 129 0.4× 110 0.4× 120 0.6× 80 3.7k

Countries citing papers authored by Tessa M. Burch‐Smith

Since Specialization
Citations

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

Fields of papers citing papers by Tessa M. Burch‐Smith

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Tessa M. Burch‐Smith. 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 Tessa M. Burch‐Smith. The network helps show where Tessa M. Burch‐Smith may publish in the future.

Co-authorship network of co-authors of Tessa M. Burch‐Smith

This figure shows the co-authorship network connecting the top 25 collaborators of Tessa M. Burch‐Smith. A scholar is included among the top collaborators of Tessa M. Burch‐Smith 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 Tessa M. Burch‐Smith. Tessa M. Burch‐Smith 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.
Czymmek, Kirk J., Yoselin Benitez‐Alfonso, Tessa M. Burch‐Smith, et al.. (2025). Best practices in plant fluorescence imaging and reporting: A primer. The Plant Cell. 37(7). 1 indexed citations
2.
Adams, Nikki, Sarbottam Piya, Min Xu, et al.. (2025). Glucosinolates can act as signals to modulate intercellular trafficking via plasmodesmata. New Phytologist. 246(3). 1163–1182. 1 indexed citations
3.
Alazem, Mazen, et al.. (2025). Regulation of cell-to-cell trafficking by viral movement proteins. Journal of Experimental Botany. 77(3). 714–731. 2 indexed citations
5.
Roberts, Daniel M., et al.. (2024). Comparing Methods for Detection and Quantification of Plasmodesmal Callose in Nicotiana benthamiana Leaves During Defense Responses. Molecular Plant-Microbe Interactions. 37(5). 427–431. 4 indexed citations
6.
Alazem, Mazen, et al.. (2023). Viral synergism suppresses R gene-mediated resistance by impairing downstream defense mechanisms in soybean. PLANT PHYSIOLOGY. 192(4). 3088–3105. 9 indexed citations
7.
Kang, Byung‐Ho, Charles T. Anderson, Shin‐ichi Arimura, et al.. (2021). A glossary of plant cell structures: Current insights and future questions. The Plant Cell. 34(1). 10–52. 34 indexed citations
8.
Ganusova, Elena E., et al.. (2020). Chloroplast-to-nucleus retrograde signalling controls intercellular trafficking via plasmodesmata formation. Philosophical Transactions of the Royal Society B Biological Sciences. 375(1801). 20190408–20190408. 26 indexed citations
9.
Wang, Aiming, Tessa M. Burch‐Smith, & Yi Li. (2020). Focus on Cell Biology of Virus-Plant and Virus-Vector Interactions. Molecular Plant-Microbe Interactions. 33(1). 5–5. 1 indexed citations
10.
Piya, Sarbottam, Jinyi Liu, Tessa M. Burch‐Smith, Thomas J. Baum, & Tarek Hewezi. (2019). A role for Arabidopsis growth-regulating factors 1 and 3 in growth–stress antagonism. Journal of Experimental Botany. 71(4). 1402–1417. 41 indexed citations
12.
Ganusova, Elena E., et al.. (2018). RNA on the move: The plasmodesmata perspective. Plant Science. 275. 1–10. 36 indexed citations
13.
Hewezi, Tarek, et al.. (2017). Phytopathogen-induced changes to plant methylomes. Plant Cell Reports. 37(1). 17–23. 25 indexed citations
14.
Dunlap, John R., et al.. (2017). Spatial distribution of organelles in leaf cells and soybean root nodules revealed by focused ion beam-scanning electron microscopy. Functional Plant Biology. 45(2). 180–191. 15 indexed citations
15.
Plett, Jonathan M., Hengfu Yin, Ritesh Mewalal, et al.. (2017). Populus trichocarpa encodes small, effector-like secreted proteins that are highly induced during mutualistic symbiosis. Scientific Reports. 7(1). 382–382. 28 indexed citations
16.
Ganusova, Elena E., et al.. (2017). Altered Expression of a Chloroplast Protein Affects the Outcome of Virus and Nematode Infection. Molecular Plant-Microbe Interactions. 30(6). 478–488. 24 indexed citations
17.
Brunkard, Jacob O., Tessa M. Burch‐Smith, Anne M. Runkel, & Patricia Zambryski. (2014). Investigating Plasmodesmata Genetics with Virus-Induced Gene Silencing and an Agrobacterium-Mediated GFP Movement Assay. Methods in molecular biology. 1217. 185–198. 16 indexed citations
18.
Burch‐Smith, Tessa M., et al.. (2012). Reduced levels of class 1 reversibly glycosylated polypeptide increase intercellular transport via plasmodesmata. Plant Signaling & Behavior. 7(1). 62–67. 16 indexed citations
19.
Burch‐Smith, Tessa M. & Patricia Zambryski. (2012). Plasmodesmata Paradigm Shift: Regulation from Without Versus Within. Annual Review of Plant Biology. 63(1). 239–260. 123 indexed citations
20.
Stonebloom, Solomon, Tessa M. Burch‐Smith, In-Soon Kim, et al.. (2009). Loss of the plant DEAD-box protein ISE1 leads to defective mitochondria and increased cell-to-cell transport via plasmodesmata. Proceedings of the National Academy of Sciences. 106(40). 17229–17234. 123 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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