Elsbeth L. Walker

5.8k total citations · 1 hit paper
43 papers, 4.2k citations indexed

About

Elsbeth L. Walker is a scholar working on Plant Science, Molecular Biology and Pharmacology. According to data from OpenAlex, Elsbeth L. Walker has authored 43 papers receiving a total of 4.2k indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Plant Science, 14 papers in Molecular Biology and 4 papers in Pharmacology. Recurrent topics in Elsbeth L. Walker's work include Plant Micronutrient Interactions and Effects (20 papers), Plant Stress Responses and Tolerance (17 papers) and Plant tissue culture and regeneration (10 papers). Elsbeth L. Walker is often cited by papers focused on Plant Micronutrient Interactions and Effects (20 papers), Plant Stress Responses and Tolerance (17 papers) and Plant tissue culture and regeneration (10 papers). Elsbeth L. Walker collaborates with scholars based in United States, United Kingdom and Australia. Elsbeth L. Walker's co-authors include Gloria M. Coruzzi, Stephen L. Dellaporta, Zivile Panaviene, Louis A. Roberts, Catherine Curie, Jean‐François Briat, Sarah S. Conte, Erin L. Connolly, Raymond J. DiDonato and Jode W. Edwards and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Elsbeth L. Walker

43 papers receiving 4.0k citations

Hit Papers

Maize yellow stripe1 encodes a membrane protein directly ... 2001 2026 2009 2017 2001 200 400 600

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Elsbeth L. Walker United States 30 3.6k 1.2k 190 170 152 43 4.2k
Carolina Escobar Spain 32 2.8k 0.8× 1.3k 1.0× 47 0.2× 97 0.6× 193 1.3× 79 3.6k
Hiroshi Masuda Japan 26 2.1k 0.6× 377 0.3× 252 1.3× 306 1.8× 103 0.7× 100 2.6k
Ping Wu China 40 5.6k 1.5× 1.8k 1.5× 92 0.5× 68 0.4× 65 0.4× 67 6.3k
Grégory Vert France 33 5.8k 1.6× 2.2k 1.8× 144 0.8× 223 1.3× 229 1.5× 59 6.4k
Frédéric Gaymard France 22 2.8k 0.8× 820 0.7× 109 0.6× 203 1.2× 112 0.7× 27 3.3k
Hatem Rouached France 32 3.2k 0.9× 707 0.6× 265 1.4× 227 1.3× 99 0.7× 72 3.7k
Tobias Kretzschmar Australia 26 2.8k 0.8× 842 0.7× 99 0.5× 122 0.7× 56 0.4× 66 3.2k
Joohyun Lee United States 19 1.8k 0.5× 562 0.5× 72 0.4× 209 1.2× 269 1.8× 35 2.1k
Se Won Park South Korea 26 1.8k 0.5× 1.0k 0.8× 49 0.3× 109 0.6× 45 0.3× 56 2.5k

Countries citing papers authored by Elsbeth L. Walker

Since Specialization
Citations

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

Fields of papers citing papers by Elsbeth L. Walker

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Elsbeth L. Walker. 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 Elsbeth L. Walker. The network helps show where Elsbeth L. Walker may publish in the future.

Co-authorship network of co-authors of Elsbeth L. Walker

This figure shows the co-authorship network connecting the top 25 collaborators of Elsbeth L. Walker. A scholar is included among the top collaborators of Elsbeth L. Walker 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 Elsbeth L. Walker. Elsbeth L. Walker 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.
Chia, Ju‐Chen, Jiapei Yan, Maryam Rahmati Ishka, et al.. (2023). Loss of OPT3 function decreases phloem copper levels and impairs crosstalk between copper and iron homeostasis and shoot-to-root signaling in Arabidopsis thaliana. The Plant Cell. 35(6). 2157–2185. 26 indexed citations
2.
Walker, Elsbeth L., et al.. (2023). The Small RNA Component of Arabidopsis thaliana Phloem Sap and Its Response to Iron Deficiency. Plants. 12(15). 2782–2782. 3 indexed citations
3.
Walker, Elsbeth L., et al.. (2022). CAN OF SPINACH, a novel long non-coding RNA, affects iron deficiency responses in Arabidopsis thaliana. Frontiers in Plant Science. 13. 1005020–1005020. 5 indexed citations
4.
Escudero, Viviana, María Reguera, Julia Quintana, et al.. (2021). Medicago truncatula Yellow Stripe‐Like7 encodes a peptide transporter participating in symbiotic nitrogen fixation. Plant Cell & Environment. 44(6). 1908–1920. 12 indexed citations
5.
Walker, Elsbeth L., et al.. (2018). Analysis of Yellow Striped Mutants of Zea mays Reveals Novel Loci Contributing to Iron Deficiency Chlorosis. Frontiers in Plant Science. 9. 157–157. 24 indexed citations
6.
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8.
Conte, Sarah S. & Elsbeth L. Walker. (2012). Genetic and Biochemical Approaches for Studying the Yellow Stripe-Like Transporter Family in Plants. Current topics in membranes. 69. 295–322. 27 indexed citations
9.
Conte, Sarah S. & Elsbeth L. Walker. (2011). Transporters Contributing to Iron Trafficking in Plants. Molecular Plant. 4(3). 464–476. 164 indexed citations
10.
Walker, Elsbeth L. & Erin L. Connolly. (2008). Time to pump iron: iron-deficiency-signaling mechanisms of higher plants. Current Opinion in Plant Biology. 11(5). 530–535. 225 indexed citations
11.
Walker, Elsbeth L., et al.. (2007). Development of a Particle Bombardment-Mediated Transient Transformation System for Taxus spp. Cells in Culture. Biotechnology Progress. 0(0). 0–0. 19 indexed citations
12.
Roberts, Susan C., et al.. (2006). Expression profiling of genes involved in paclitaxel biosynthesis for targeted metabolic engineering. Metabolic Engineering. 8(5). 385–394. 83 indexed citations
13.
Panavas, Tadas, et al.. (2001). Molecular analysis of the Doppia transposable element of maize. Plant Molecular Biology. 47(3). 341–351. 14 indexed citations
14.
Curie, Catherine, et al.. (2001). Maize yellow stripe1 encodes a membrane protein directly involved in Fe(III) uptake. Nature. 409(6818). 346–349. 742 indexed citations breakdown →
15.
Panavas, Tadas, et al.. (1999). The Structure and Paramutagenicity of the R-marbled Haplotype of Zea mays. Genetics. 153(2). 979–991. 37 indexed citations
16.
Panavas, Tadas, et al.. (1999). Identification of senescence-associated genes from daylily petals. Plant Molecular Biology. 40(2). 237–248. 143 indexed citations
17.
Panavas, Tadas, Elsbeth L. Walker, & Benjamin I. P. Rubinstein. (1998). Possible involvement of abscisic acid in senescence of daylily petals. Journal of Experimental Botany. 49(329). 1987–1997. 55 indexed citations
18.
Brears, Timothy, Elsbeth L. Walker, & Gloria M. Coruzzi. (1991). A promoter sequence involved in cell‐specific expression of the pea glutamine synthetase GS3A gene in organs of transgenic tobacco and alfalfa. The Plant Journal. 1(2). 235–244. 51 indexed citations
19.
Robbins, Timothy P., Elsbeth L. Walker, Jerry L. Kermicle, Mary Alleman, & Stephen L. Dellaporta. (1991). Meiotic instability of the R-r complex arising from displaced intragenic exchange and intrachromosomal rearrangement.. Genetics. 129(1). 271–283. 65 indexed citations
20.
Walker, Elsbeth L. & Gloria M. Coruzzi. (1989). Developmentally Regulated Expression of the Gene Family for Cytosolic Glutamine Synthetase in Pisum sativum. PLANT PHYSIOLOGY. 91(2). 702–708. 48 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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