Antony D. Gee

9.5k total citations · 1 hit paper
215 papers, 7.1k citations indexed

About

Antony D. Gee is a scholar working on Radiology, Nuclear Medicine and Imaging, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Antony D. Gee has authored 215 papers receiving a total of 7.1k indexed citations (citations by other indexed papers that have themselves been cited), including 80 papers in Radiology, Nuclear Medicine and Imaging, 66 papers in Molecular Biology and 45 papers in Cellular and Molecular Neuroscience. Recurrent topics in Antony D. Gee's work include Medical Imaging Techniques and Applications (59 papers), Radiopharmaceutical Chemistry and Applications (44 papers) and Neuroscience and Neuropharmacology Research (39 papers). Antony D. Gee is often cited by papers focused on Medical Imaging Techniques and Applications (59 papers), Radiopharmaceutical Chemistry and Applications (44 papers) and Neuroscience and Neuropharmacology Research (39 papers). Antony D. Gee collaborates with scholars based in United Kingdom, Denmark and Japan. Antony D. Gee's co-authors include Nicholas J. Long, Philip W. Miller, Ramón Vilar, Véronique Gouverneur, Matthew N. Hopkinson, Salvatore Bongarzone, Søren B. Hansen, Albert Gjedde, Oscar Ces and Robert V. Law and has published in prestigious journals such as Chemical Reviews, The Lancet and Chemical Society Reviews.

In The Last Decade

Antony D. Gee

213 papers receiving 7.0k citations

Hit Papers

Synthesis of 11C, 18F, 15... 2008 2026 2014 2020 2008 200 400 600

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Antony D. Gee 2.1k 1.7k 1.7k 1.2k 733 215 7.1k
Peter J. H. Scott 1.6k 0.7× 1.1k 0.6× 1.1k 0.7× 1.4k 1.1× 636 0.9× 231 5.1k
Simon M. Ametamey 2.3k 1.1× 2.0k 1.2× 1.0k 0.6× 773 0.6× 1.9k 2.5× 219 6.5k
Olof Solin 2.4k 1.1× 1.4k 0.8× 513 0.3× 699 0.6× 1.4k 1.9× 236 8.2k
Michael J. Adam 1.9k 0.9× 761 0.4× 923 0.5× 432 0.3× 428 0.6× 109 4.2k
Albert D. Windhorst 2.9k 1.4× 2.1k 1.2× 531 0.3× 547 0.4× 970 1.3× 324 9.4k
Ming‐Rong Zhang 2.0k 0.9× 2.1k 1.2× 520 0.3× 332 0.3× 1.5k 2.0× 400 7.0k
Michael Kassiou 1.9k 0.9× 3.5k 2.0× 1.7k 1.0× 221 0.2× 2.1k 2.9× 309 10.3k
Franklin I. Aigbirhio 1.6k 0.7× 1.4k 0.8× 484 0.3× 353 0.3× 1.7k 2.4× 203 8.0k
Satoshi Ueda 1.0k 0.5× 1.1k 0.7× 1.7k 1.0× 391 0.3× 324 0.4× 212 5.7k
Nagichettiar Satyamurthy 3.9k 1.8× 3.1k 1.8× 526 0.3× 452 0.4× 810 1.1× 179 11.0k

Countries citing papers authored by Antony D. Gee

Since Specialization
Citations

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

Fields of papers citing papers by Antony D. Gee

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Antony D. Gee. 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 Antony D. Gee. The network helps show where Antony D. Gee may publish in the future.

Co-authorship network of co-authors of Antony D. Gee

This figure shows the co-authorship network connecting the top 25 collaborators of Antony D. Gee. A scholar is included among the top collaborators of Antony D. Gee 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 Antony D. Gee. Antony D. Gee 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.
Feng, Minghao, Steven Kealey, P. Thuéry, et al.. (2024). Pyridine-based strategies towards nitrogen isotope exchange and multiple isotope incorporation. Nature Communications. 15(1). 6063–6063. 12 indexed citations
2.
Gee, Antony D.. (2024). Review of Zotero. Journal of Electronic Resources Librarianship. 36(4). 334–336.
3.
Bongarzone, Salvatore, et al.. (2020). Carbon-11 carboxylation of trialkoxysilane and trimethylsilane derivatives using [ 11 C]CO 2. Chemical Communications. 56(34). 4668–4671. 8 indexed citations
4.
Egerton, Alice, Joel Dunn, Nisha Singh, et al.. (2020). Evaluation of [13N]ammonia positron emission tomography as a potential method for quantifying glutamine synthetase activity in the human brain. EJNMMI Research. 10(1). 146–146. 3 indexed citations
6.
Singh, Nisha, Mattia Veronese, Jim O’Doherty, et al.. (2018). Assessing the feasibility of intranasal radiotracer administration for in brain PET imaging. Nuclear Medicine and Biology. 66. 32–39. 11 indexed citations
7.
Bongarzone, Salvatore, et al.. (2018). Development of [18F]FAMTO: A novel fluorine-18 labelled positron emission tomography (PET) radiotracer for imaging CYP11B1 and CYP11B2 enzymes in adrenal glands. Nuclear Medicine and Biology. 68-69. 14–21. 17 indexed citations
8.
Bongarzone, Salvatore, et al.. (2017). Electrochemical [11C]CO2to [11C]CO conversion for PET imaging. Chemical Communications. 53(20). 2982–2985. 12 indexed citations
9.
Coenen, Heinz H., Antony D. Gee, Michael J. Adam, et al.. (2017). Consensus nomenclature rules for radiopharmaceutical chemistry — Setting the record straight. Nuclear Medicine and Biology. 55. v–xi. 154 indexed citations
10.
Ben, Diego Dal, et al.. (2017). Design, synthesis and evaluation in an LPS rodent model of neuroinflammation of a novel 18F-labelled PET tracer targeting P2X7. EJNMMI Research. 7(1). 31–31. 48 indexed citations
11.
Wilson, Neil, Agostino Cilibrizzi, Antony D. Gee, et al.. (2016). A lipophilic copper(ii) complex as an optical probe for intracellular detection of NO. Dalton Transactions. 45(45). 18177–18182. 12 indexed citations
12.
Kikuchi, Tatsuya, T. Okamura, Maki Okada, et al.. (2016). Benzyl [11C]Hippurate as an Agent for Measuring the Activities of Organic Anion Transporter 3 in the Brain and Multidrug Resistance-Associated Protein 4 in the Heart of Mice. Journal of Medicinal Chemistry. 59(12). 5847–5856. 6 indexed citations
13.
Hosoi, Rie, et al.. (2008). Characterization of 14C-acetate uptake in cultured rat astrocytes. Brain Research. 1253. 69–73. 14 indexed citations
14.
Passchier, Jan, et al.. (2005). PRODUCTION OF THE P-GLYCOPROTEIN MARKER, [C-11]LOPERAMIDE, IN CLINICALLY USEFUL QUANTITIES. Journal of Labelled Compounds and Radiopharmaceuticals. 48. 2 indexed citations
15.
Martarello, Laurent, Maaz S. Ahmed, V J Cunningham, et al.. (2005). RADIOLABELLING AND IN VIVO EVALUATION OF [C-11]GSK215083 AS A POTENTIAL 5-HT6 PET RADIOLIGAND IN THE PORCINE BRAIN. Journal of Labelled Compounds and Radiopharmaceuticals. 48. 3 indexed citations
16.
Fujita, Masahiro, Sami S. Zoghbi, Jau‐Shyong Hong, et al.. (2004). PET imaging of brain phosphodiesterase 4 in rats using [C-11]rolipram. NeuroImage. 22.
17.
Danielsen, Erik Hvid, David A. Smith, Leif Østergaard, et al.. (1998). Positron emission tomography of living brain in minipigs and domestic pigs. Research Portal (King's College London). 25. 127–135. 16 indexed citations
18.
Svensson, Peter, Peter Johannsen, Troels S. Jensen, et al.. (1997). Cerebral representation of graded painful phasic and tonic heat in humans: A positron emission tomography study. Research Portal (King's College London). 1 indexed citations
19.
Gillings, Nic & Antony D. Gee. (1997). Aziridines in the synthesis of 11C and 18F-labelled amino acids. Journal of Labelled Compounds and Radiopharmaceuticals. 40. 764–865. 3 indexed citations
20.
Moss, TJ, Virginia H. Mansour, A Hardwick, et al.. (1992). Quantitation of Tumor Cell Removal from Bone Marrow: A Preclinical Model. Journal of Hematotherapy. 1(1). 65–73. 5 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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