Ignacio Rubio‐Somoza

5.4k total citations · 1 hit paper
35 papers, 3.9k citations indexed

About

Ignacio Rubio‐Somoza is a scholar working on Plant Science, Molecular Biology and Biotechnology. According to data from OpenAlex, Ignacio Rubio‐Somoza has authored 35 papers receiving a total of 3.9k indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Plant Science, 22 papers in Molecular Biology and 3 papers in Biotechnology. Recurrent topics in Ignacio Rubio‐Somoza's work include Plant Molecular Biology Research (26 papers), Plant Stress Responses and Tolerance (9 papers) and Plant Reproductive Biology (9 papers). Ignacio Rubio‐Somoza is often cited by papers focused on Plant Molecular Biology Research (26 papers), Plant Stress Responses and Tolerance (9 papers) and Plant Reproductive Biology (9 papers). Ignacio Rubio‐Somoza collaborates with scholars based in Spain, Germany and United States. Ignacio Rubio‐Somoza's co-authors include Detlef Weigel, Marco Todesco, Javier Paz‐Ares, María Isabel Puga, Adrián Vallí, Isabel Mateos, José M. Franco‐Zorrilla, Antonio Leyva, Juan Antonio Garcı́a and Manuel Martínez and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Communications and Nature Genetics.

In The Last Decade

Ignacio Rubio‐Somoza

35 papers receiving 3.9k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Target mimicry provides a new mechanism for regulation of microRNA activity

2007 1.6k citations José M. Franco‐Zorrilla, Adrián Vallí et al. Nature Genetics profile →

Peers

Ignacio Rubio‐Somoza

ENDOC

GENET

Moussa Benhamed France

Cheng Lu United States

Meng Yuqi China

Yu‐Chan Zhang China

Erika Varkonyi‐Gasic New Zealand

Guru Jagadeeswaran United States

Federico Ariel Argentina

Chuyu Ye China

María Isabel Puga Spain

Josh T. Cuperus United States

Moussa Benhamed France

Ignacio Rubio‐Somoza

2.8k ×0.8

2.4k ×1.0

453 ×0.7

301 ×1.2

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99 ×1.3

GENET

Citations per year, relative to Ignacio Rubio‐Somoza Ignacio Rubio‐Somoza (= 1×) peers Moussa Benhamed

Countries citing papers authored by Ignacio Rubio‐Somoza

Since Specialization

Citations

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

Fields of papers citing papers by Ignacio Rubio‐Somoza

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ignacio Rubio‐Somoza. 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 Ignacio Rubio‐Somoza. The network helps show where Ignacio Rubio‐Somoza may publish in the future.

Co-authorship network of co-authors of Ignacio Rubio‐Somoza

This figure shows the co-authorship network connecting the top 25 collaborators of Ignacio Rubio‐Somoza. A scholar is included among the top collaborators of Ignacio Rubio‐Somoza 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 Ignacio Rubio‐Somoza. Ignacio Rubio‐Somoza is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Jiménez‐Góngora, Tamara, et al.. (2024). Conservation of molecular responses upon viral infection in the non-vascular plant Marchantia polymorpha. Nature Communications. 15(1). 8326–8326. 3 indexed citations

Rubio‐Somoza, Ignacio, et al.. (2024). After silencing suppression: miRNA targets strike back. Trends in Plant Science. 29(11). 1266–1276. 6 indexed citations

Fiorilli, Valentina, et al.. (2024). A fungal sRNA silences a host plant transcription factor to promote arbuscular mycorrhizal symbiosis. New Phytologist. 246(3). 924–935. 7 indexed citations

Vasseur, François, et al.. (2024). miR472 Deficiency Enhances Arabidopsis thaliana Defense Without Reducing Seed Production. Molecular Plant-Microbe Interactions. 37(12). 819–827. 1 indexed citations

Fiorilli, Valentina, et al.. (2023). A journey into the world of small RNAs in the arbuscular mycorrhizal symbiosis. New Phytologist. 242(4). 1534–1544. 12 indexed citations

Waelchli, Jan, Valentin Gfeller, Gabriel Deslandes‐Hérold, et al.. (2023). Bacterial tolerance to host-exuded specialized metabolites structures the maize root microbiome. Proceedings of the National Academy of Sciences. 120(44). e2310134120–e2310134120. 46 indexed citations

Rodríguez‐Negrete, Edgar A., et al.. (2021). miR825-5p targets the TIR-NBS-LRR gene MIST1 and down-regulates basal immunity against Pseudomonas syringae in Arabidopsis. Journal of Experimental Botany. 72(20). 7316–7334. 19 indexed citations

Born, Patrick von, Martí Bernardo-Faura, & Ignacio Rubio‐Somoza. (2018). An artificial miRNA system reveals that relative contribution of translational inhibition to miRNA-mediated regulation depends on environmental and developmental factors in Arabidopsis thaliana. PLoS ONE. 13(2). e0192984–e0192984. 21 indexed citations

Soto‐Suárez, Mauricio, Patricia Baldrich, Detlef Weigel, Ignacio Rubio‐Somoza, & Blanca San Segundo. (2017). The Arabidopsis miR396 mediates pathogen-associated molecular pattern-triggered immune responses against fungal pathogens. Scientific Reports. 7(1). 44898–44898. 106 indexed citations

10.

Abraham, Zamira, Raquel Iglesias‐Fernández, Manuel Martínez, et al.. (2016). A Developmental Switch of Gene Expression in the Barley Seed Mediated by HvVP1 (Viviparous-1) and HvGAMYB Interactions. PLANT PHYSIOLOGY. 170(4). 2146–2158. 26 indexed citations

11.

Martinho, Cláudia, Ana Confraria, Alexandre Elias, et al.. (2015). Dissection of miRNA Pathways Using Arabidopsis Mesophyll Protoplasts. Molecular Plant. 8(2). 261–275. 20 indexed citations

12.

Confraria, Ana, Cláudia Martinho, Alexandre Elias, Ignacio Rubio‐Somoza, & Elena Baena–González. (2013). miRNAs mediate SnRK1-dependent energy signaling in Arabidopsis. Frontiers in Plant Science. 4. 197–197. 46 indexed citations

13.

Rubio‐Somoza, Ignacio, Elise J. Tucker, Marie Javelle, et al.. (2013). A Protodermal miR394 Signal Defines a Region of Stem Cell Competence in the Arabidopsis Shoot Meristem. Developmental Cell. 24(2). 125–132. 196 indexed citations

14.

Breakfield, Natalie W., David L. Corcoran, Jalean J. Petricka, et al.. (2011). High-resolution experimental and computational profiling of tissue-specific known and novel miRNAs in Arabidopsis. Genome Research. 22(1). 163–176. 138 indexed citations

15.

Rubio‐Somoza, Ignacio & Detlef Weigel. (2011). MicroRNA networks and developmental plasticity in plants. Trends in Plant Science. 16(5). 258–264. 263 indexed citations

16.

Kawashima, Cintia Goulart, Colette Matthewman, Siqi Huang, et al.. (2011). Interplay of SLIM1 and miR395 in the regulation of sulfate assimilation in Arabidopsis. The Plant Journal. 66(5). 863–876. 157 indexed citations

17.

Sánchez‐Rodríguez, Clara, et al.. (2010). Phytohormones and the cell wall in Arabidopsis during seedling growth. Trends in Plant Science. 15(5). 291–301. 101 indexed citations

18.

Rubio‐Somoza, Ignacio, Josh T. Cuperus, Detlef Weigel, & James C. Carrington. (2009). Regulation and functional specialization of small RNA–target nodes during plant development. Current Opinion in Plant Biology. 12(5). 622–627. 91 indexed citations

19.

Franco‐Zorrilla, José M., Adrián Vallí, Marco Todesco, et al.. (2007). Target mimicry provides a new mechanism for regulation of microRNA activity. Nature Genetics. 39(8). 1033–1037. 1563 indexed citations breakdown →

20.

Dı́az, Isabel, et al.. (2005). The DOF protein, SAD, interacts with GAMYB in plant nuclei and activates transcription of endosperm‐specific genes during barley seed development. The Plant Journal. 42(5). 652–662. 121 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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