Joseph R. Ecker

130.6k total citations · 48 hit papers
272 papers, 67.3k citations indexed

About

Joseph R. Ecker is a scholar working on Plant Science, Molecular Biology and Genetics. According to data from OpenAlex, Joseph R. Ecker has authored 272 papers receiving a total of 67.3k indexed citations (citations by other indexed papers that have themselves been cited), including 185 papers in Plant Science, 168 papers in Molecular Biology and 33 papers in Genetics. Recurrent topics in Joseph R. Ecker's work include Plant Molecular Biology Research (120 papers), Epigenetics and DNA Methylation (44 papers) and Plant Stress Responses and Tolerance (43 papers). Joseph R. Ecker is often cited by papers focused on Plant Molecular Biology Research (120 papers), Epigenetics and DNA Methylation (44 papers) and Plant Stress Responses and Tolerance (43 papers). Joseph R. Ecker collaborates with scholars based in United States, Australia and United Kingdom. Joseph R. Ecker's co-authors include José M. Alonso, Joseph R. Nery, Ryan Lister, Ronan C. O’Malley, Hongwei Guo, Gregg Roman, Huaming Chen, Plinio Guzmán, Charles C. Berry and Joseph J. Kieber and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Joseph R. Ecker

270 papers receiving 66.1k citations

Hit Papers

Human DNA methylomes at base resolution ... 1990 2026 2002 2014 2009 2008 1993 2002 2002 1000 2.0k 3.0k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Joseph R. Ecker United States 135 43.3k 42.6k 7.7k 1.9k 1.6k 272 67.3k
Steven Henikoff United States 122 20.2k 0.5× 49.4k 1.2× 12.0k 1.6× 2.9k 1.5× 398 0.3× 374 64.0k
Wen‐Hsiung Li United States 91 14.2k 0.3× 27.4k 0.6× 16.2k 2.1× 1.9k 1.0× 417 0.3× 379 48.0k
Hamish McWilliam United Kingdom 15 10.7k 0.2× 25.5k 0.6× 6.1k 0.8× 907 0.5× 667 0.4× 18 46.3k
Jue Ruan China 21 11.0k 0.3× 27.6k 0.6× 12.6k 1.6× 4.4k 2.3× 339 0.2× 65 46.4k
Andreas Wilm Singapore 21 8.3k 0.2× 21.0k 0.5× 5.0k 0.7× 977 0.5× 570 0.4× 29 37.5k
Nils Homer United States 11 9.2k 0.2× 23.6k 0.6× 11.6k 1.5× 4.3k 2.2× 313 0.2× 16 41.5k
Alec Wysoker United States 8 9.1k 0.2× 24.3k 0.6× 11.6k 1.5× 4.3k 2.3× 328 0.2× 10 43.0k
Tim Fennell United States 8 10.0k 0.2× 26.6k 0.6× 14.3k 1.9× 5.3k 2.8× 348 0.2× 8 47.2k
Robert E. Handsaker United States 23 12.4k 0.3× 31.4k 0.7× 21.2k 2.8× 5.8k 3.0× 416 0.3× 28 59.7k
L. Aravind United States 123 6.5k 0.2× 39.4k 0.9× 9.0k 1.2× 2.6k 1.4× 606 0.4× 381 52.4k

Countries citing papers authored by Joseph R. Ecker

Since Specialization
Citations

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

Fields of papers citing papers by Joseph R. Ecker

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Joseph R. Ecker. 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 Joseph R. Ecker. The network helps show where Joseph R. Ecker may publish in the future.

Co-authorship network of co-authors of Joseph R. Ecker

This figure shows the co-authorship network connecting the top 25 collaborators of Joseph R. Ecker. A scholar is included among the top collaborators of Joseph R. Ecker 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 Joseph R. Ecker. Joseph R. Ecker 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.
Tian, Wei, Wubin Ding, Jiawei Shen, et al.. (2024). BAllC and BAllCools: efficient formatting and operating for single-cell DNA methylation data. Bioinformatics. 40(7). 1 indexed citations
2.
Dal-Bianco, Maximiller, João Paulo Machado, José Cleydson F. Silva, et al.. (2021). A plant-specific syntaxin-6 protein contributes to the intracytoplasmic route for the begomovirus CabLCV. PLANT PHYSIOLOGY. 187(1). 158–173. 10 indexed citations
3.
Prigge, Michael J., Kathleen Greenham, Yi Zhang, et al.. (2016). The Arabidopsis Auxin Receptor F-Box Proteins AFB4 and AFB5 Are Required for Response to the Synthetic Auxin Picloram. G3 Genes Genomes Genetics. 6(5). 1383–1390. 82 indexed citations
4.
Qiao, Hong, Zhouxin Shen, Shao‐shan Carol Huang, et al.. (2012). Processing and Subcellular Trafficking of ER-Tethered EIN2 Control Response to Ethylene Gas. Science. 338(6105). 390–393. 409 indexed citations breakdown →
5.
Schmitz, Robert J., Matthew D. Schultz, Mathew G. Lewsey, et al.. (2011). Transgenerational Epigenetic Instability Is a Source of Novel Methylation Variants. Science. 334(6054). 369–373. 479 indexed citations breakdown →
6.
Tsuchisaka, Atsunari, Guixia Yu, Hailing Jin, et al.. (2009). A Combinatorial Interplay Among the 1-Aminocyclopropane-1-Carboxylate Isoforms Regulates Ethylene Biosynthesis in Arabidopsis thaliana. Genetics. 183(3). 979–1003. 240 indexed citations
7.
Clark, Richard M., Gabriele Schweikert, Christopher Toomajian, et al.. (2007). Common Sequence Polymorphisms Shaping Genetic Diversity in Arabidopsis thaliana. Science. 317(5836). 338–342. 526 indexed citations breakdown →
8.
Kim, Sun A., Tracy Punshon, Antonio Lanzirotti, et al.. (2006). Localization of Iron in Arabidopsis Seed Requires the Vacuolar Membrane Transporter VIT1. Science. 314(5803). 1295–1298. 507 indexed citations breakdown →
9.
Olmedo, Gabriela, Hongwei Guo, Brian D. Gregory, et al.. (2006). ETHYLENE-INSENSITIVE5 encodes a 5′→3′ exoribonuclease required for regulation of the EIN3-targeting F-box proteins EBF1/2. Proceedings of the National Academy of Sciences. 103(36). 13286–13293. 139 indexed citations
10.
Chilley, Paul M., Stuart A. Casson, Petr Tarkowski, et al.. (2006). The POLARIS Peptide of Arabidopsis Regulates Auxin Transport and Root Growth via Effects on Ethylene Signaling. The Plant Cell. 18(11). 3058–3072. 112 indexed citations
11.
Lariguet, Patricia, Isabelle Schepens, Ullas V. Pedmale, et al.. (2006). PHYTOCHROME KINASE SUBSTRATE 1 is a phototropin 1 binding protein required for phototropism. Proceedings of the National Academy of Sciences. 103(26). 10134–10139. 134 indexed citations
12.
Overvoorde, Paul, Yoko Okushima, José Manuel Alonso Segura, et al.. (2005). Functional Genomic Analysis of the AUXIN/INDOLE-3-ACETIC ACID Gene Family Members in Arabidopsis thaliana  [W]. The Plant Cell. 17(12). 3282–3300. 305 indexed citations
13.
Borevitz, Justin, et al.. (2005). Quantitative trait locus mapping and DNA array hybridization identify an FLM deletion as a cause for natural flowering-time variation. Proceedings of the National Academy of Sciences. 102(7). 2460–2465. 150 indexed citations
14.
Hazen, Samuel P., Thomas F. Schultz, José L. Pruneda-Paz, et al.. (2005). LUX ARRHYTHMO encodes a Myb domain protein essential for circadian rhythms. Proceedings of the National Academy of Sciences. 102(29). 10387–10392. 349 indexed citations
15.
Borevitz, Justin, et al.. (2005). FRIGIDA-Independent Variation in Flowering Time of Natural Arabidopsis thaliana Accessions. Genetics. 170(3). 1197–1207. 127 indexed citations
17.
Alonso, José M., et al.. (2004). CBF2/DREB1C is a negative regulator of CBF1/DREB1B and CBF3/DREB1A expression and plays a central role in stress tolerance in Arabidopsis. Proceedings of the National Academy of Sciences. 101(11). 3985–3990. 440 indexed citations
18.
Catalá, Rafael, Elisa Santos, José M. Alonso, et al.. (2003). Mutations in the Ca 2 + /H + Transporter CAX1 Increase CBF/DREB1 Expression and the Cold-Acclimation Response in Arabidopsis. The Plant Cell. 15(12). 2940–2951. 143 indexed citations
19.
Alonso, José M., Anna N. Stepanova, Roberto Solano, et al.. (2003). Five components of the ethylene-response pathway identified in a screen for weak ethylene-insensitive mutants in Arabidopsis. Proceedings of the National Academy of Sciences. 100(5). 2992–2997. 311 indexed citations
20.
Hu, Jianping, Maria L. Aguirre, Charles A. Peto, et al.. (2002). A Role for Peroxisomes in Photomorphogenesis and Development of Arabidopsis. Science. 297(5580). 405–409. 125 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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