Samuel Bocobza

2.3k total citations · 1 hit paper
28 papers, 1.6k citations indexed

About

Samuel Bocobza is a scholar working on Molecular Biology, Plant Science and Food Science. According to data from OpenAlex, Samuel Bocobza has authored 28 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 19 papers in Plant Science and 5 papers in Food Science. Recurrent topics in Samuel Bocobza's work include Plant tissue culture and regeneration (7 papers), Plant Reproductive Biology (7 papers) and CRISPR and Genetic Engineering (6 papers). Samuel Bocobza is often cited by papers focused on Plant tissue culture and regeneration (7 papers), Plant Reproductive Biology (7 papers) and CRISPR and Genetic Engineering (6 papers). Samuel Bocobza collaborates with scholars based in Israel, Germany and United States. Samuel Bocobza's co-authors include Asaph Aharoni, Pablo D. Cárdenas, Uwe Heinig, Ilana Rogachev, Sergey Malitsky, Michal Shapira, Yury Tikunov, Arnaud Bovy, Jules Beekwilder and Prashant D. Sonawane and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Nature Genetics.

In The Last Decade

Samuel Bocobza

26 papers receiving 1.6k citations

Hit Papers

Biosynthesis of Antinutritional Alkaloids in Solanaceous ... 2013 2026 2017 2021 2013 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
Samuel Bocobza Israel 16 1.0k 906 288 92 87 28 1.6k
Zhe Zhang China 20 705 0.7× 739 0.8× 182 0.6× 71 0.8× 55 0.6× 86 1.4k
Luisa Ugolini Italy 20 435 0.4× 810 0.9× 249 0.9× 34 0.4× 112 1.3× 43 1.3k
C. Kole India 9 432 0.4× 830 0.9× 500 1.7× 115 1.3× 54 0.6× 24 1.2k
Tahira Fatima United States 17 683 0.7× 868 1.0× 88 0.3× 34 0.4× 85 1.0× 42 1.2k
Edmundo Lozoya‐Gloria Mexico 17 564 0.5× 577 0.6× 137 0.5× 49 0.5× 46 0.5× 73 1.1k
Clive Lo Hong Kong 28 1.3k 1.2× 969 1.1× 112 0.4× 88 1.0× 44 0.5× 46 1.8k
Hexin Tan China 21 1.5k 1.4× 970 1.1× 55 0.2× 76 0.8× 75 0.9× 38 1.7k
René Höfer France 11 869 0.8× 912 1.0× 78 0.3× 22 0.2× 54 0.6× 13 1.4k
Misugi Uraji Japan 25 890 0.9× 1.4k 1.5× 71 0.2× 37 0.4× 77 0.9× 59 1.9k

Countries citing papers authored by Samuel Bocobza

Since Specialization
Citations

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

Fields of papers citing papers by Samuel Bocobza

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Samuel Bocobza

This figure shows the co-authorship network connecting the top 25 collaborators of Samuel Bocobza. A scholar is included among the top collaborators of Samuel Bocobza 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 Samuel Bocobza. Samuel Bocobza 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.
Rather, Gulzar Ahmed, et al.. (2025). Direct haploid formation in Arabidopsis using transgenic CENH3-based inducers. Plant Cell Reports. 44(8). 182–182.
2.
Kumar, Manoj, et al.. (2025). Breaking the glass ceiling of stable genetic transformation and gene editing in the popular pepper cv Cayenne. Journal of Experimental Botany. 76(10). 2688–2699. 1 indexed citations
3.
Kumar, Manoj, et al.. (2023). Morphological and Transcriptional Analyses of Regeneration Events in Pepper Plants (Capsicum annuum) Expose Patterns of Shoot Apical Meristem Formation. Journal of Plant Growth Regulation. 42(12). 7474–7487. 6 indexed citations
4.
Shavit, Reut, et al.. (2022). The transcription factor TaMYB31 regulates the benzoxazinoid biosynthetic pathway in wheat. Journal of Experimental Botany. 73(16). 5634–5649. 17 indexed citations
5.
Kumar, Manoj, et al.. (2022). Increased rates of gene-editing events using a simplified RNAi configuration designed to reduce gene silencing. Plant Cell Reports. 41(10). 1987–2003. 4 indexed citations
6.
Rather, Gulzar Ahmed, et al.. (2022). Advances in protoplast transfection promote efficient CRISPR/Cas9-mediated genome editing in tetraploid potato. Planta. 256(1). 14–14. 11 indexed citations
7.
Mopuri, Ramgopal, Alexander Rosov, Sara Yosefi, et al.. (2021). High-dose vitamin B1 therapy prevents the development of experimental fatty liver driven by overnutrition. Disease Models & Mechanisms. 14(3). 21 indexed citations
8.
Panda, Sayantan, Adam Jóźwiak, Prashant D. Sonawane, et al.. (2021). Steroidal alkaloids defence metabolism and plant growth are modulated by the joint action of gibberellin and jasmonate signalling. New Phytologist. 233(3). 1220–1237. 51 indexed citations
10.
Kazachkova, Yana, Sayantan Panda, Samuel Bocobza, et al.. (2021). The GORKY glycoalkaloid transporter is indispensable for preventing tomato bitterness. Nature Plants. 7(4). 468–480. 74 indexed citations
11.
Szymański, Jędrzej, Samuel Bocobza, Sayantan Panda, et al.. (2020). Analysis of wild tomato introgression lines elucidates the genetic basis of transcriptome and metabolome variation underlying fruit traits and pathogen response. Nature Genetics. 52(10). 1111–1121. 132 indexed citations
12.
Rosado-Souza, Laíse, Sebastian Proost, Michaël Moulin, et al.. (2019). Appropriate Thiamin Pyrophosphate Levels Are Required for Acclimation to Changes in Photoperiod. PLANT PHYSIOLOGY. 180(1). 185–197. 22 indexed citations
13.
Sonawane, Prashant D., Uwe Heinig, Sayantan Panda, et al.. (2018). Short-chain dehydrogenase/reductase governs steroidal specialized metabolites structural diversity and toxicity in the genus Solanum. Proceedings of the National Academy of Sciences. 115(23). E5419–E5428. 69 indexed citations
14.
Cárdenas, Pablo D., et al.. (2014). The bitter side of the nightshades: Genomics drives discovery in Solanaceae steroidal alkaloid metabolism. Phytochemistry. 113. 24–32. 92 indexed citations
15.
Bocobza, Samuel & Asaph Aharoni. (2014). Small molecules that interact with RNA: riboswitch‐based gene control and its involvement in metabolic regulation in plants and algae. The Plant Journal. 79(4). 693–703. 41 indexed citations
16.
Itkin, Maxim, Uwe Heinig, Oren Tzfadia, et al.. (2013). Biosynthesis of Antinutritional Alkaloids in Solanaceous Crops Is Mediated by Clustered Genes. Science. 341(6142). 175–179. 428 indexed citations breakdown →
17.
Panikashvili, David, Jianxin Shi, Samuel Bocobza, et al.. (2009). The Arabidopsis DSO/ABCG11 Transporter Affects Cutin Metabolism in Reproductive Organs and Suberin in Roots. Molecular Plant. 3(3). 563–575. 151 indexed citations
18.
Bocobza, Samuel, Idan Gabdank, Danny Barash, et al.. (2008). Computational Identification of Three-Way Junctions in Folded RNAs: A Case Study in Arabidopsis. In Silico Biology. 8(2). 105–120. 4 indexed citations
19.
Bocobza, Samuel & Asaph Aharoni. (2008). Switching the light on plant riboswitches. Trends in Plant Science. 13(10). 526–533. 41 indexed citations
20.
Bocobza, Samuel, Avital Adato, Tali Mandel, et al.. (2007). Riboswitch-dependent gene regulation and its evolution in the plant kingdom. Genes & Development. 21(22). 2874–2879. 147 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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