Philippe Tacon

700 total citations
14 papers, 565 citations indexed

About

Philippe Tacon is a scholar working on Aquatic Science, Physiology and Genetics. According to data from OpenAlex, Philippe Tacon has authored 14 papers receiving a total of 565 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Aquatic Science, 6 papers in Physiology and 5 papers in Genetics. Recurrent topics in Philippe Tacon's work include Aquaculture Nutrition and Growth (10 papers), Reproductive biology and impacts on aquatic species (6 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers). Philippe Tacon is often cited by papers focused on Aquaculture Nutrition and Growth (10 papers), Reproductive biology and impacts on aquatic species (6 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers). Philippe Tacon collaborates with scholars based in France, China and Taiwan. Philippe Tacon's co-authors include Bernard Jalabert, Maı̈té Bueno, Brice Bouyssière, Philip Antony Jesu Prabhu, Stéphanie Fontagné-Dicharry, Sadasivam Kaushik, Simon Godin, Li Xu, Chao Ran and Ching‐Fong Chang and has published in prestigious journals such as PLoS ONE, Journal of Agricultural and Food Chemistry and Aquaculture.

In The Last Decade

Philippe Tacon

14 papers receiving 549 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Philippe Tacon France 13 317 230 173 158 93 14 565
K. Mol Belgium 17 718 2.3× 379 1.6× 113 0.7× 254 1.6× 49 0.5× 24 1.0k
Małgorzata Rzepkowska Poland 13 148 0.5× 142 0.6× 130 0.8× 87 0.6× 15 0.2× 26 436
Robert Vassallo-Agius Italy 14 599 1.9× 469 2.0× 122 0.7× 85 0.5× 45 0.5× 24 814
Marcelo Hideo Okamoto Brazil 13 267 0.8× 115 0.5× 56 0.3× 157 1.0× 15 0.2× 33 458
K. C. Majumdar India 14 254 0.8× 217 0.9× 393 2.3× 47 0.3× 30 0.3× 27 709
M. Szczepkowski Poland 17 678 2.1× 472 2.1× 158 0.9× 229 1.4× 54 0.6× 96 1.0k
Meng‐Kiat Kuah Malaysia 16 488 1.5× 206 0.9× 41 0.2× 241 1.5× 67 0.7× 23 656
Anne Sundby Norway 16 603 1.9× 245 1.1× 59 0.3× 448 2.8× 30 0.3× 20 838
Zuzana Linhartová Czechia 12 147 0.5× 258 1.1× 168 1.0× 29 0.2× 17 0.2× 30 433
Emilie Henrotte Belgium 12 296 0.9× 177 0.8× 62 0.4× 196 1.2× 12 0.1× 16 456

Countries citing papers authored by Philippe Tacon

Since Specialization
Citations

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

Fields of papers citing papers by Philippe Tacon

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Philippe Tacon

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

All Works

14 of 14 papers shown
1.
Fontagné-Dicharry, Stéphanie, Vincent Véron, Laurence Larroquet, et al.. (2020). Effect of selenium sources in plant-based diets on antioxidant status and oxidative stress-related parameters in rainbow trout juveniles under chronic stress exposure. Aquaculture. 529. 735684–735684. 31 indexed citations
2.
Ran, Chao, Lu Huang, Jun Hu, et al.. (2016). Effects of dietary live and heat-inactive baker’s yeast on growth, gut health, and disease resistance of Nile tilapia under high rearing density. Fish & Shellfish Immunology. 56. 263–271. 48 indexed citations
3.
Godin, Simon, Stéphanie Fontagné-Dicharry, Maı̈té Bueno, et al.. (2015). Influence of Dietary Selenium Species on Selenoamino Acid Levels in Rainbow Trout. Journal of Agricultural and Food Chemistry. 63(28). 6484–6492. 27 indexed citations
4.
5.
Fontagné-Dicharry, Stéphanie, Simon Godin, Haokun Liu, et al.. (2015). Influence of the forms and levels of dietary selenium on antioxidant status and oxidative stress-related parameters in rainbow trout (Oncorhynchus mykiss) fry. British Journal Of Nutrition. 113(12). 1876–1887. 79 indexed citations
6.
Bach, Svitlana V., et al.. (2015). Proteasome regulates transcription-favoring histone methylation, acetylation and ubiquitination in long-term synaptic plasticity. Neuroscience Letters. 591. 59–64. 13 indexed citations
7.
Yu, Huanhuan, Fang Han, Min Xue, et al.. (2014). Efficacy and tolerance of yeast cell wall as an immunostimulant in the diet of Japanese seabass (Lateolabrax japonicus). Aquaculture. 432. 217–224. 39 indexed citations
8.
Tacon, Philippe & Eric Auclair. (2010). Yeast in aquaculture from nutrition to well-being.. 6(4). 22–24. 2 indexed citations
9.
Forgue, Jean, Valérie Lamothe, Chantal Cauty, et al.. (2006). Tilapia (Oreochromis niloticus) vitellogenins: development of homologous and heterologous ELISAs and analysis of vitellogenin pathway through the ovarian follicle. Journal of Experimental Zoology Part A Comparative Experimental Biology. 305A(7). 576–593. 24 indexed citations
10.
Du, Jin‐Lien, Cheng‐Yen Lee, Philippe Tacon, et al.. (2001). Estradiol-17β Stimulates Gonadotropin II Expression and Release in the Protandrous Male Black Porgy Acanthopagrus schlegeli Bleeker: A Possible Role in Sex Change. General and Comparative Endocrinology. 121(2). 135–145. 20 indexed citations
11.
Lee, Yan‐Horn, Fang-Yi Lee, Wen‐Shiun Yueh, et al.. (2000). Profiles of Gonadal Development, Sex Steroids, Aromatase Activity, and Gonadotropin II in the Controlled Sex Change of Protandrous Black Porgy, Acanthopagrus schlegeli Bleeker. General and Comparative Endocrinology. 119(1). 111–120. 74 indexed citations
12.
Tacon, Philippe, Jean‐François Baroiller, P.‐Y. Le Bail, Patrick Prunet, & Bernard Jalabert. (2000). Effect of Egg Deprivation on Sex Steroids, Gonadotropin, Prolactin, and Growth Hormone Profiles during the Reproductive Cycle of the Mouthbrooding Cichlid Fish Oreochromis niloticus. General and Comparative Endocrinology. 117(1). 54–65. 61 indexed citations
13.
Chang, Ching‐Fong, En‐Lieng Lau, Wen‐Shiun Yueh, et al.. (1997). The endocrine mechanism of sex reversal in the protandrous black porgy, Acanthopagrus schlegeli: a review.. PubMed. 40(4). 197–205. 33 indexed citations
14.

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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