C. Gileadi

3.3k total citations
26 papers, 1.6k citations indexed

About

C. Gileadi is a scholar working on Molecular Biology, Insect Science and Cellular and Molecular Neuroscience. According to data from OpenAlex, C. Gileadi has authored 26 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 11 papers in Insect Science and 9 papers in Cellular and Molecular Neuroscience. Recurrent topics in C. Gileadi's work include Insect and Pesticide Research (11 papers), Neurobiology and Insect Physiology Research (9 papers) and Epigenetics and DNA Methylation (5 papers). C. Gileadi is often cited by papers focused on Insect and Pesticide Research (11 papers), Neurobiology and Insect Physiology Research (9 papers) and Epigenetics and DNA Methylation (5 papers). C. Gileadi collaborates with scholars based in United Kingdom, Israel and Japan. C. Gileadi's co-authors include Ada Rafaeli, M. Kostyukovsky, Eli Shaaya, Udo Oppermann, C. Johansson, Christopher J. Schofield, Shalom W. Applebaum, Yongliang Fan, Wyatt W. Yue and D. Doyle and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Journal of Medicinal Chemistry.

In The Last Decade

C. Gileadi

26 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
C. Gileadi United Kingdom 19 860 500 478 240 216 26 1.6k
John D. Windass United Kingdom 23 951 1.1× 305 0.6× 323 0.7× 80 0.3× 172 0.8× 36 1.4k
Frank Vanrobaeys Belgium 16 537 0.6× 222 0.4× 99 0.2× 85 0.4× 148 0.7× 18 1.0k
Masaaki Uchiyama Japan 20 444 0.5× 308 0.6× 322 0.7× 162 0.7× 116 0.5× 95 1.2k
Martin Geiser Switzerland 25 1.4k 1.7× 174 0.3× 214 0.4× 158 0.7× 528 2.4× 34 2.0k
Jingya Zhao China 23 1.3k 1.6× 82 0.2× 627 1.3× 87 0.4× 50 0.2× 74 2.0k
Severino Ronchi Italy 29 1.4k 1.6× 59 0.1× 166 0.3× 88 0.4× 100 0.5× 65 1.8k
Alexandre Nesterov United States 15 886 1.0× 234 0.5× 170 0.4× 111 0.5× 57 0.3× 16 1.3k
Paulo A. Melo Brazil 28 914 1.1× 143 0.3× 123 0.3× 217 0.9× 1.2k 5.6× 67 2.1k
Marian Kochman Poland 22 657 0.8× 194 0.4× 46 0.1× 458 1.9× 191 0.9× 71 1.3k
Shailesh Kumar India 20 898 1.0× 50 0.1× 219 0.5× 155 0.6× 107 0.5× 85 1.4k

Countries citing papers authored by C. Gileadi

Since Specialization
Citations

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

Fields of papers citing papers by C. Gileadi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of C. Gileadi

This figure shows the co-authorship network connecting the top 25 collaborators of C. Gileadi. A scholar is included among the top collaborators of C. Gileadi 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 C. Gileadi. C. Gileadi 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
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Bennett, James M., Thomas Christott, Matthew Dowling, et al.. (2023). Discovery of PFI-6, a small-molecule chemical probe for the YEATS domain of MLLT1 and MLLT3. Bioorganic & Medicinal Chemistry Letters. 98. 129546–129546. 4 indexed citations
3.
Seraphim, Thiago Vargas, Germanna Lima Righetto, Kaliandra de Almeida Gonçalves, et al.. (2019). Insights into the full-length SRPK2 structure and its hydrodynamic behavior. International Journal of Biological Macromolecules. 137. 205–214. 1 indexed citations
4.
Christott, Thomas, James M. Bennett, Carmen Coxon, et al.. (2018). Discovery of a Selective Inhibitor for the YEATS Domains of ENL/AF9. SLAS DISCOVERY. 24(2). 133–141. 40 indexed citations
5.
Walport, Louise J., Richard J. Hopkinson, M. Vollmar, et al.. (2014). Human UTY(KDM6C) Is a Male-specific Nϵ-Methyl Lysyl Demethylase. Journal of Biological Chemistry. 289(26). 18302–18313. 155 indexed citations
6.
Johansson, C., Anthony Tumber, KaHing Che, et al.. (2014). The Roles of Jumonji-Type Oxygenases in Human Disease. Epigenomics. 6(1). 89–120. 125 indexed citations
7.
Hillringhaus, Lars, Wyatt W. Yue, Nathan R. Rose, et al.. (2011). Structural and Evolutionary Basis for the Dual Substrate Selectivity of Human KDM4 Histone Demethylase Family. Journal of Biological Chemistry. 286(48). 41616–41625. 140 indexed citations
8.
Froese, D. Sean, Grazyna Kochan, J.R.C. Muniz, et al.. (2010). Structures of the Human GTPase MMAA and Vitamin B12-dependent Methylmalonyl-CoA Mutase and Insight into Their Complex Formation. Journal of Biological Chemistry. 285(49). 38204–38213. 88 indexed citations
9.
Elkins, Jonathan M., C. Gileadi, Leela Shrestha, et al.. (2010). Unusual binding interactions in PDZ domain crystal structures help explain binding mechanisms. Protein Science. 19(4). 731–741. 22 indexed citations
10.
Soundararajan, M., Francis S. Willard, Adam J. Kimple, et al.. (2008). Structural diversity in the RGS domain and its interaction with heterotrimeric G protein α-subunits. Proceedings of the National Academy of Sciences. 105(17). 6457–6462. 156 indexed citations
11.
Elkins, Jonathan M., E. Papagrigoriou, G. Berridge, et al.. (2007). Structure of PICK1 and other PDZ domains obtained with the help of self‐binding C‐terminal extensions. Protein Science. 16(4). 683–694. 56 indexed citations
12.
Kostyukovsky, M., et al.. (2002). Activation of octopaminergic receptors by essential oil constituents isolated from aromatic plants: possible mode of action against insect pests. Pest Management Science. 58(11). 1101–1106. 437 indexed citations
13.
Hirashima, Akinori, Ada Rafaeli, C. Gileadi, & Eiichi Kuwano. (1999). Three-dimensional pharmacophore hypotheses of octopamine receptor responsible for the inhibition of sex-pheromone production in Helicoverpa armigera. Journal of Molecular Graphics and Modelling. 17(1). 43–54. 23 indexed citations
14.
Hirashima, Akinori, Ada Rafaeli, C. Gileadi, & Eiichi Kuwano. (1999). Three-dimensional quantitative structure–activity studies of octopaminergic agonists responsible for the inhibition of sex-pheromone production in Hercoverpa armigera. Bioorganic & Medicinal Chemistry. 7(11). 2621–2628. 13 indexed citations
15.
Fan, Yongliang, Ada Rafaeli, C. Gileadi, Eric Kubli, & Shalom W. Applebaum. (1999). Drosophila melanogaster sex peptide stimulates juvenile hormone synthesis and depresses sex pheromone production in Helicoverpa armigera. Journal of Insect Physiology. 45(2). 127–133. 79 indexed citations
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17.
Rafaeli, Ada, C. Gileadi, & Akinori Hirashima. (1999). Identification of Novel Synthetic Octopamine Receptor Agonists Which Inhibit Moth Sex Pheromone Production. Pesticide Biochemistry and Physiology. 65(3). 194–204. 18 indexed citations
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19.
Rafaeli, Ada & C. Gileadi. (1995). Factors affecting pheromone production in the stored product moth, Plodia interpunctella: A preliminary study. Journal of Stored Products Research. 31(3). 243–247. 20 indexed citations
20.
Ben‐Arie, Nissim, C. Gileadi, & Michael Schramm. (1988). Interaction of the β‐adrenergic receptor with Gs following delipidation. European Journal of Biochemistry. 176(3). 649–654. 29 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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