Thomas E. Clemente

5.4k total citations · 2 hit papers
55 papers, 3.7k citations indexed

About

Thomas E. Clemente is a scholar working on Plant Science, Molecular Biology and Biomedical Engineering. According to data from OpenAlex, Thomas E. Clemente has authored 55 papers receiving a total of 3.7k indexed citations (citations by other indexed papers that have themselves been cited), including 41 papers in Plant Science, 33 papers in Molecular Biology and 10 papers in Biomedical Engineering. Recurrent topics in Thomas E. Clemente's work include Plant tissue culture and regeneration (13 papers), CRISPR and Genetic Engineering (9 papers) and Legume Nitrogen Fixing Symbiosis (9 papers). Thomas E. Clemente is often cited by papers focused on Plant tissue culture and regeneration (13 papers), CRISPR and Genetic Engineering (9 papers) and Legume Nitrogen Fixing Symbiosis (9 papers). Thomas E. Clemente collaborates with scholars based in United States, China and Taiwan. Thomas E. Clemente's co-authors include Shirley Sato, Edgar B. Cahoon, Johnathan A. Napier, Chaofu Lu, Paul Staswick, Zhanyuan Zhang, T.J. Morris, Xiaohong Ye, Feng Qu and Aiqiu Xing and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Nature Genetics.

In The Last Decade

Thomas E. Clemente

54 papers receiving 3.6k citations

Hit Papers

Copy Number Variation of Multiple Genes at Rhg1 Mediates ... 2012 2026 2016 2021 2012 2012 100 200 300 400

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Thomas E. Clemente United States 32 2.8k 1.6k 489 325 265 55 3.7k
Jitendra P. Khurana India 43 6.0k 2.1× 4.9k 3.0× 757 1.5× 153 0.5× 65 0.2× 171 8.0k
Manish K. Pandey India 44 5.5k 1.9× 1.5k 0.9× 566 1.2× 78 0.2× 82 0.3× 219 6.1k
Muthappa Senthil‐Kumar India 38 4.9k 1.7× 2.1k 1.3× 159 0.3× 247 0.8× 72 0.3× 104 5.7k
Yan Zhou China 37 3.3k 1.2× 1.9k 1.1× 322 0.7× 170 0.5× 33 0.1× 123 4.6k
Agnelo Furtado Australia 33 2.3k 0.8× 1.3k 0.8× 577 1.2× 168 0.5× 38 0.1× 125 3.4k
Zhixi Tian China 37 4.8k 1.7× 1.8k 1.1× 1.2k 2.4× 69 0.2× 146 0.6× 91 5.6k
Ming‐Che Shih Taiwan 38 2.7k 0.9× 2.6k 1.6× 233 0.5× 274 0.8× 154 0.6× 81 4.1k
Tomonobu Kusano Japan 42 3.4k 1.2× 2.9k 1.7× 192 0.4× 146 0.4× 268 1.0× 110 4.4k
T. Lynne Reuber United States 22 5.4k 1.9× 3.4k 2.1× 237 0.5× 160 0.5× 64 0.2× 27 6.1k

Countries citing papers authored by Thomas E. Clemente

Since Specialization
Citations

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

Fields of papers citing papers by Thomas E. Clemente

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Thomas E. Clemente. 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 Thomas E. Clemente. The network helps show where Thomas E. Clemente may publish in the future.

Co-authorship network of co-authors of Thomas E. Clemente

This figure shows the co-authorship network connecting the top 25 collaborators of Thomas E. Clemente. A scholar is included among the top collaborators of Thomas E. Clemente 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 Thomas E. Clemente. Thomas E. Clemente 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.
Busta, Lucas, Ismail Dweikat, Shirley Sato, et al.. (2022). Chemical and genetic variation in feral Cannabis sativa populations across the Nebraska climate gradient. Phytochemistry. 200. 113206–113206. 13 indexed citations
2.
Trieu, Anthony, Rebecca L. Billingsley, Erik J. Sacks, et al.. (2022). Transformation and gene editing in the bioenergy grass Miscanthus. SHILAP Revista de lepidopterología. 15(1). 148–148. 7 indexed citations
3.
Smith, Thomas G., Mark A. Zaydman, Aaron DiAntonio, et al.. (2021). A phytobacterial TIR domain effector manipulates NAD + to promote virulence. New Phytologist. 233(2). 890–904. 48 indexed citations
4.
McAssey, Edward V., Priscilla S. Redd, Hanh Nguyen, et al.. (2021). Development of mPing ‐based activation tags for crop insertional mutagenesis. Plant Direct. 5(1). e00300–e00300. 8 indexed citations
5.
Li, Aixia, Shangang Jia, Abou Yobi, et al.. (2018). Editing of an Alpha-Kafirin Gene Family Increases, Digestibility and Protein Quality in Sorghum. PLANT PHYSIOLOGY. 177(4). 1425–1438. 124 indexed citations
6.
Bernacchi, Carl J., I. Köhler, Donald R. Ort, Steven Long, & Thomas E. Clemente. (2017). Agroecosystem productivity in a warmer and CO2 enriched atmosphere. EGUGA. 9391. 1 indexed citations
7.
Stacey, Minviluz G., Rebecca E. Cahoon, Hanh Nguyen, et al.. (2016). Identification of Homogentisate Dioxygenase as a Target for Vitamin E Biofortification in Oilseeds. PLANT PHYSIOLOGY. 172(3). 1506–1518. 45 indexed citations
8.
Huang, Haibo, Stephen P. Long, Thomas E. Clemente, & Vijay Singh. (2016). Technoeconomic Analysis of Biodiesel and Ethanol Production from Lipid-Producing Sugarcane and Sweet Sorghum. Industrial Biotechnology. 12(6). 357–365. 15 indexed citations
9.
Cuevas, Hugo E., Haibao Tang, Sayan Das, et al.. (2016). The Evolution of Photoperiod-Insensitive Flowering in Sorghum, A Genomic Model for Panicoid Grasses. Molecular Biology and Evolution. 33(9). 2417–2428. 35 indexed citations
10.
Kaur, Jagdeep, John P. Fellers, Alok Adholeya, et al.. (2016). Expression of apoplast-targeted plant defensin MtDef4.2 confers resistance to leaf rust pathogen Puccinia triticina but does not affect mycorrhizal symbiosis in transgenic wheat. Transgenic Research. 26(1). 37–49. 44 indexed citations
11.
Ping, Jieqing, Yunfeng Liu, Lianjun Sun, et al.. (2014). Dt2Is a Gain-of-Function MADS-Domain Factor Gene That Specifies Semideterminacy in Soybean  . The Plant Cell. 26(7). 2831–2842. 140 indexed citations
12.
Park, Hyun-Woo, Karen L. Koster, Rebecca E. Cahoon, et al.. (2014). Redirection of metabolic flux for high levels of omega‐7 monounsaturated fatty acid accumulation in camelina seeds. Plant Biotechnology Journal. 13(1). 38–50. 90 indexed citations
13.
Tang, Haibao, Hugo E. Cuevas, Sayan Das, et al.. (2013). Seed shattering in a wild sorghum is conferred by a locus unrelated to domestication. Proceedings of the National Academy of Sciences. 110(39). 15824–15829. 51 indexed citations
14.
Cook, David E., Tong Geon Lee, Xiaoli Guo, et al.. (2012). Copy Number Variation of Multiple Genes at Rhg1 Mediates Nematode Resistance in Soybean. Science. 338(6111). 1206–1209. 455 indexed citations breakdown →
15.
Clemente, Thomas E., et al.. (2012). Maize Histone H2B-mCherry: A New Fluorescent Chromatin Marker for Somatic and Meiotic Chromosome Research. DNA and Cell Biology. 31(6). 925–938. 22 indexed citations
16.
Lin, Zhongwei, Xianran Li, Laura M. Shannon, et al.. (2012). Parallel domestication of the Shattering1 genes in cereals. Nature Genetics. 44(6). 720–724. 327 indexed citations breakdown →
17.
Cook, Daniel, Agnes M. Rimando, Thomas E. Clemente, et al.. (2010). Alkylresorcinol Synthases Expressed in Sorghum bicolor Root Hairs Play an Essential Role in the Biosynthesis of the Allelopathic Benzoquinone Sorgoleone . The Plant Cell. 22(3). 867–887. 70 indexed citations
18.
Block, Anna K., Ming Guo, Guangyong Li, et al.. (2009). ThePseudomonas syringaetype III effector HopG1 targets mitochondria, alters plant development and suppresses plant innate immunity. Cellular Microbiology. 12(3). 318–330. 102 indexed citations
19.
Piller, Kenneth J., et al.. (2004). Expression and immunogenicity of an Escherichia coli K99 fimbriae subunit antigen in soybean. Planta. 222(1). 6–18. 31 indexed citations
20.
Clemente, Thomas E., Dominique Robertson, T. G. Isleib, M. K. Beute, & Arthur K. Weissinger. (1992). Evaluation of peanut (Arachis hypogaea L.) leaflets from mature zygotic embryos as recipient tissue for biolostic gene transfer. Transgenic Research. 1(6). 275–284. 17 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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