Graziano Zocchi

4.5k total citations · 2 hit papers
86 papers, 3.4k citations indexed

About

Graziano Zocchi is a scholar working on Plant Science, Molecular Biology and Soil Science. According to data from OpenAlex, Graziano Zocchi has authored 86 papers receiving a total of 3.4k indexed citations (citations by other indexed papers that have themselves been cited), including 80 papers in Plant Science, 19 papers in Molecular Biology and 4 papers in Soil Science. Recurrent topics in Graziano Zocchi's work include Plant Micronutrient Interactions and Effects (53 papers), Plant Stress Responses and Tolerance (51 papers) and Plant nutrient uptake and metabolism (20 papers). Graziano Zocchi is often cited by papers focused on Plant Micronutrient Interactions and Effects (53 papers), Plant Stress Responses and Tolerance (51 papers) and Plant nutrient uptake and metabolism (20 papers). Graziano Zocchi collaborates with scholars based in Italy, Tunisia and United States. Graziano Zocchi's co-authors include Gianpiero Vigani, Marta Dell’Orto, Patrizia De Nisi, Silvia Donnini, Daniele Daffonchio, Eleonora Rolli, Ramona Marasco, Sara Borin, C. Sorlini and Besma Ettoumi and has published in prestigious journals such as PLoS ONE, PLANT PHYSIOLOGY and New Phytologist.

In The Last Decade

Graziano Zocchi

83 papers receiving 3.3k citations

Hit Papers

Improved plant resistance to drought is promoted by the r... 2012 2026 2016 2021 2014 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
Graziano Zocchi Italy 30 3.0k 619 314 170 145 86 3.4k
Sowmyalakshmi Subramanian Canada 14 2.5k 0.8× 431 0.7× 337 1.1× 176 1.0× 113 0.8× 25 2.9k
Bruno Touraine France 28 3.7k 1.2× 1.0k 1.6× 400 1.3× 174 1.0× 74 0.5× 38 4.1k
Tōru Matoh Japan 32 3.0k 1.0× 712 1.2× 161 0.5× 141 0.8× 110 0.8× 85 3.3k
Bhoopander Giri India 20 2.6k 0.9× 649 1.0× 302 1.0× 129 0.8× 165 1.1× 45 3.2k
Rosa M. Pérez‐Clemente Spain 24 2.1k 0.7× 526 0.8× 239 0.8× 227 1.3× 77 0.5× 45 2.5k
Enéas Gomes‐Filho Brazil 32 3.4k 1.1× 745 1.2× 325 1.0× 99 0.6× 77 0.5× 130 3.9k
Carlos de Ollas Spain 15 1.7k 0.6× 520 0.8× 204 0.6× 151 0.9× 63 0.4× 23 2.1k
William Cress South Africa 17 3.8k 1.2× 1.2k 1.9× 226 0.7× 124 0.7× 168 1.2× 28 4.3k
Xiaofang Wang China 31 3.4k 1.1× 1.7k 2.8× 278 0.9× 167 1.0× 111 0.8× 81 4.2k
G. R. Kudoyarova Russia 32 3.5k 1.1× 951 1.5× 266 0.8× 137 0.8× 59 0.4× 143 3.8k

Countries citing papers authored by Graziano Zocchi

Since Specialization
Citations

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

Fields of papers citing papers by Graziano Zocchi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Graziano Zocchi. 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 Graziano Zocchi. The network helps show where Graziano Zocchi may publish in the future.

Co-authorship network of co-authors of Graziano Zocchi

This figure shows the co-authorship network connecting the top 25 collaborators of Graziano Zocchi. A scholar is included among the top collaborators of Graziano Zocchi 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 Graziano Zocchi. Graziano Zocchi 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.
Lattanzio, Vincenzo, Enrico Ercole, Marta Dell’Orto, et al.. (2021). Plasticity, exudation and microbiome-association of the root system of Pellitory-of-the-wall plants grown in environments impaired in iron availability. Plant Physiology and Biochemistry. 168. 27–42. 8 indexed citations
2.
Islam, Monirul, et al.. (2020). Temporal Responses to Direct and Induced Iron Deficiency in Parietaria judaica. Agronomy. 10(7). 1037–1037. 5 indexed citations
3.
Vigani, Gianpiero, Eleonora Rolli, Ramona Marasco, et al.. (2018). Root bacterial endophytes confer drought resistance and enhance expression and activity of a vacuolar H + ‐pumping pyrophosphatase in pepper plants. Environmental Microbiology. 21(9). 3212–3228. 52 indexed citations
4.
Vannozzi, Alessandro, Silvia Donnini, Gianpiero Vigani, et al.. (2017). Transcriptional Characterization of a Widely-Used Grapevine Rootstock Genotype under Different Iron-Limited Conditions. Frontiers in Plant Science. 7. 1994–1994. 18 indexed citations
5.
Rolli, Eleonora, Ramona Marasco, Gianpiero Vigani, et al.. (2014). Improved plant resistance to drought is promoted by the root‐associated microbiome as a water stress‐dependent trait. Environmental Microbiology. 17(2). 316–331. 411 indexed citations breakdown →
6.
Dell’Orto, Marta, Patrizia De Nisi, Gianpiero Vigani, & Graziano Zocchi. (2013). Fe deficiency differentially affects the vacuolar proton pumps in cucumber and soybean roots. Frontiers in Plant Science. 4. 326–326. 8 indexed citations
7.
Jelali, Nahida, Silvia Donnini, Marta Dell’Orto, et al.. (2013). Root antioxidant responses of two Pisum sativum cultivars to direct and induced Fe deficiency. Plant Biology. 16(3). 607–614. 24 indexed citations
8.
Vigani, Gianpiero, et al.. (2012). cDNA-AFLP analysis reveals a set of new genes differentially expressed in cucumber root apexes in response to iron deficiency. Biologia Plantarum. 56(3). 502–508. 7 indexed citations
9.
Vigani, Gianpiero, et al.. (2012). Iron deficiency affects nitrogen metabolism in cucumber (Cucumis sativusL.) plants. BMC Plant Biology. 12(1). 189–189. 87 indexed citations
10.
Dell’Orto, Marta, Gianpiero Vigani, Abderrazak Smaoui, et al.. (2011). Immunolocalization of H+-ATPase and IRT1 enzymes in N2-fixing common bean nodules subjected to iron deficiency. Journal of Plant Physiology. 169(3). 242–248. 14 indexed citations
11.
Vigani, Gianpiero, et al.. (2011). Metabolic changes of iron uptake in N2-fixing common bean nodules during iron deficiency. Plant Science. 181(2). 151–158. 25 indexed citations
12.
Jelali, Nahida, et al.. (2010). Changes of metabolic responses to direct and induced Fe deficiency of two Pisum sativum cultivars. Environmental and Experimental Botany. 68(3). 238–246. 61 indexed citations
13.
Vigani, Gianpiero & Graziano Zocchi. (2009). The fate and the role of mitochondria in Fe-deficient roots of Strategy I plants. Plant Signaling & Behavior. 4(5). 375–379. 24 indexed citations
14.
Vigani, Gianpiero, Dario Maffi, & Graziano Zocchi. (2009). Iron availability affects the function of mitochondria in cucumber roots. New Phytologist. 182(1). 127–136. 74 indexed citations
15.
16.
Zocchi, Graziano. (1985). Phosphorylation-dephosphorylation of membrane proteins controls the microsomal H+-ATPase activity of corn roots. Plant Science. 40(3). 153–159. 29 indexed citations
17.
Zocchi, Graziano & J. B. Hanson. (1983). Calcium transport and ATPase activity in a microsomal vesicle fraction from corn roots. Plant Cell & Environment. 6(3). 203–209. 5 indexed citations
18.
Zocchi, Graziano & J. B. Hanson. (1982). Calcium Influx into Corn Roots as a Result of Cold Shock. PLANT PHYSIOLOGY. 70(1). 318–319. 44 indexed citations
19.
Dell’Aquila, Alessandro, et al.. (1978). Damages at translational level in aged wheat embryos. Plant Science Letters. 12(3-4). 217–226. 2 indexed citations
20.
Zocchi, Graziano, et al.. (1976). Different forms of EF1 and viability in wheat embryos. Phytochemistry. 15(11). 1607–1610. 13 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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