Leor Eshed Williams

3.9k total citations · 2 hit papers
24 papers, 2.9k citations indexed

About

Leor Eshed Williams is a scholar working on Plant Science, Molecular Biology and Ecology, Evolution, Behavior and Systematics. According to data from OpenAlex, Leor Eshed Williams has authored 24 papers receiving a total of 2.9k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Plant Science, 20 papers in Molecular Biology and 1 paper in Ecology, Evolution, Behavior and Systematics. Recurrent topics in Leor Eshed Williams's work include Plant Molecular Biology Research (21 papers), Plant Reproductive Biology (13 papers) and Plant tissue culture and regeneration (8 papers). Leor Eshed Williams is often cited by papers focused on Plant Molecular Biology Research (21 papers), Plant Reproductive Biology (13 papers) and Plant tissue culture and regeneration (8 papers). Leor Eshed Williams collaborates with scholars based in Israel, United States and France. Leor Eshed Williams's co-authors include Jennifer C. Fletcher, Daniel Zilberman, Assaf Zemach, Ka Thao, M. Yvonne Kim, Devin Coleman‐Derr, Ping-Hung Hsieh, Stacey L. Harmer, Cristel C. Carles and Tzung‐Fu Hsieh and has published in prestigious journals such as Science, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Leor Eshed Williams

24 papers receiving 2.9k citations

Hit Papers

The Arabidopsis Nucleosom... 2009 2026 2014 2020 2013 2009 250 500 750

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Leor Eshed Williams Israel 18 2.7k 2.0k 158 70 56 24 2.9k
Aiwu Dong China 38 3.3k 1.2× 3.0k 1.5× 188 1.2× 61 0.9× 76 1.4× 79 3.9k
Hidetoshi Saze Japan 23 2.4k 0.9× 1.6k 0.8× 205 1.3× 56 0.8× 19 0.3× 37 2.7k
Yana V. Bernatavichute United States 13 3.2k 1.2× 2.8k 1.4× 262 1.7× 27 0.4× 76 1.4× 14 4.0k
Martín A. Mecchia Argentina 16 1.7k 0.6× 1.3k 0.6× 66 0.4× 105 1.5× 37 0.7× 18 1.8k
Stéphane Pien Switzerland 13 1.6k 0.6× 1.3k 0.7× 144 0.9× 97 1.4× 19 0.3× 14 1.8k
Danhua Jiang China 24 2.0k 0.7× 1.8k 0.9× 83 0.5× 29 0.4× 31 0.6× 45 2.3k
Alice Pajoro Netherlands 15 1.1k 0.4× 946 0.5× 71 0.4× 87 1.2× 29 0.5× 16 1.3k
Michael D. Nodine Austria 20 1.3k 0.5× 1.1k 0.5× 72 0.5× 38 0.5× 64 1.1× 37 1.5k
Pablo A. Manavella Argentina 24 2.2k 0.8× 1.6k 0.8× 54 0.3× 35 0.5× 168 3.0× 52 2.5k
Alexandre Berr France 22 1.8k 0.7× 1.4k 0.7× 135 0.9× 117 1.7× 12 0.2× 38 2.0k

Countries citing papers authored by Leor Eshed Williams

Since Specialization
Citations

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

Fields of papers citing papers by Leor Eshed Williams

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Leor Eshed Williams. 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 Leor Eshed Williams. The network helps show where Leor Eshed Williams may publish in the future.

Co-authorship network of co-authors of Leor Eshed Williams

This figure shows the co-authorship network connecting the top 25 collaborators of Leor Eshed Williams. A scholar is included among the top collaborators of Leor Eshed Williams 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 Leor Eshed Williams. Leor Eshed Williams 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.
Kamai, Tamir, et al.. (2024). Characterization of gelling agents in callus inducing media: Physical properties and their effect on callus growth. Physiologia Plantarum. 176(2). e14312–e14312. 2 indexed citations
2.
Buxdorf, Kobi, et al.. (2024). Optimizing cannabis cultivation: an efficient in vitro system for flowering induction. Plant Methods. 20(1). 141–141. 2 indexed citations
3.
Kumar, Manoj, Gulzar Ahmed Rather, Hanita Zemach, et al.. (2024). A dynamic WUSCHEL/Layer 1 interplay directs shoot apical meristem formation during regeneration in tobacco. The Plant Journal. 120(2). 578–597. 1 indexed citations
4.
Berr, Alexandre, Marie Le Masson, Adi Faigenboim, et al.. (2023). Lysine 27 of histone H3 .3 is a fine modulator of developmental gene expression and stands as an epigenetic checkpoint for lignin biosynthesis in Arabidopsis. New Phytologist. 238(3). 1085–1100. 7 indexed citations
5.
McGarry, Róisín C., et al.. (2023). Altered expression of SELF-PRUNING disrupts homeostasis and facilitates signal delivery to meristems. PLANT PHYSIOLOGY. 192(2). 1517–1531. 3 indexed citations
6.
Faigenboim, Adi, et al.. (2022). Differentially Expressed Transcription Factors during Male and Female Cone Development in Pinus halepensis. Agronomy. 12(7). 1588–1588. 3 indexed citations
7.
Williams, Leor Eshed, et al.. (2019). Tradeoffs between yield components promote crop stability in sesame. Plant Science. 295. 110105–110105. 17 indexed citations
8.
Negin, Boaz, et al.. (2017). Shoot stem cell specification in roots by the WUSCHEL transcription factor. PLoS ONE. 12(4). e0176093–e0176093. 30 indexed citations
9.
Landau, Udi, et al.. (2015). The ERECTA, CLAVATA and class III HD-ZIP Pathways Display Synergistic Interactions in Regulating Floral Meristem Activities. PLoS ONE. 10(5). e0125408–e0125408. 17 indexed citations
10.
Landau, Udi, et al.. (2015). Competency for shoot regeneration from Arabidopsis root explants is regulated by DNA methylation. Plant Science. 238. 251–261. 65 indexed citations
11.
Mandel, Tali, et al.. (2014). The ERECTA receptor kinase regulates Arabidopsis shoot apical meristem size, phyllotaxy and floral meristem identity. Development. 141(4). 830–841. 61 indexed citations
12.
Zemach, Assaf, M. Yvonne Kim, Ping-Hung Hsieh, et al.. (2013). The Arabidopsis Nucleosome Remodeler DDM1 Allows DNA Methyltransferases to Access H1-Containing Heterochromatin. Cell. 153(1). 193–205. 782 indexed citations breakdown →
13.
Lee, Jung‐Eun, et al.. (2012). EMF1 and PRC2 Cooperate to Repress Key Regulators of Arabidopsis Development. PLoS Genetics. 8(3). e1002512–e1002512. 109 indexed citations
14.
Ron, Mily, et al.. (2010). Proper regulation of a sperm-specific cis-nat-siRNA is essential for double fertilization in Arabidopsis. Genes & Development. 24(10). 1010–1021. 135 indexed citations
15.
Hsieh, Tzung‐Fu, Christian Ibarra, Assaf Zemach, et al.. (2009). Genome-Wide Demethylation of Arabidopsis Endosperm. Science. 324(5933). 1451–1454. 506 indexed citations breakdown →
16.
Williams, Leor Eshed, Cristel C. Carles, Karen S. Osmont, & Jennifer C. Fletcher. (2005). A database analysis method identifies an endogenous trans-acting short-interfering RNA that targets the Arabidopsis ARF2, ARF3 , and ARF4 genes. Proceedings of the National Academy of Sciences. 102(27). 9703–9708. 242 indexed citations
17.
Williams, Leor Eshed & Jennifer C. Fletcher. (2005). Stem cell regulation in the Arabidopsis shoot apical meristem. Current Opinion in Plant Biology. 8(6). 582–586. 114 indexed citations
18.
Williams, Leor Eshed, Stephen P. Grigg, Mingtang Xie, S. Christensen, & Jennifer C. Fletcher. (2005). Regulation ofArabidopsisshoot apical meristem and lateral organ formation by microRNAmiR166gand itsAtHD-ZIPtarget genes. Development. 132(16). 3657–3668. 358 indexed citations
19.
Williams, Leor Eshed, Jing Zhao, Nadya Morozova, et al.. (2003). Chromatin reorganization accompanying cellular dedifferentiation is associated with modifications of histone H3, redistribution of HP1, and activation of E2F‐target genes. Developmental Dynamics. 228(1). 113–120. 88 indexed citations
20.
Zhao, Jing, et al.. (2001). Two Phases of Chromatin Decondensation during Dedifferentiation of Plant Cells. Journal of Biological Chemistry. 276(25). 22772–22778. 136 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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026