J. Cosson

4.4k total citations · 1 hit paper
56 papers, 3.7k citations indexed

About

J. Cosson is a scholar working on Physiology, Reproductive Medicine and Nature and Landscape Conservation. According to data from OpenAlex, J. Cosson has authored 56 papers receiving a total of 3.7k indexed citations (citations by other indexed papers that have themselves been cited), including 42 papers in Physiology, 26 papers in Reproductive Medicine and 21 papers in Nature and Landscape Conservation. Recurrent topics in J. Cosson's work include Reproductive biology and impacts on aquatic species (42 papers), Sperm and Testicular Function (26 papers) and Fish Ecology and Management Studies (21 papers). J. Cosson is often cited by papers focused on Reproductive biology and impacts on aquatic species (42 papers), Sperm and Testicular Function (26 papers) and Fish Ecology and Management Studies (21 papers). J. Cosson collaborates with scholars based in France, Czechia and United States. J. Cosson's co-authors include Sayyed Mohammad Hadi Alavi, Roland Billard, Otomar Linhart, Christian Fauvel, Marc Suquet, Catherine Dréanno, Philippe Huitorel, Marek Rodina, C. Jeulin and David Gela and has published in prestigious journals such as Nucleic Acids Research, Journal of Cell Science and European Respiratory Journal.

In The Last Decade

J. Cosson

56 papers receiving 3.4k citations

Hit Papers

Sperm motility in fishes. (II) Effects of ions and osmola... 2005 2026 2012 2019 2005 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
J. Cosson France 31 2.9k 1.9k 1.4k 1.3k 866 56 3.7k
Jacky Cosson France 29 1.9k 0.6× 1.2k 0.6× 901 0.7× 796 0.6× 671 0.8× 88 2.8k
Christian Fauvel France 30 1.9k 0.7× 850 0.5× 1.4k 1.0× 999 0.8× 700 0.8× 62 2.8k
M.P. Herráez Spain 40 2.7k 0.9× 2.5k 1.3× 1.2k 0.9× 675 0.5× 1.3k 1.6× 111 4.6k
Borys Dzyuba Czechia 25 1.4k 0.5× 935 0.5× 728 0.5× 547 0.4× 431 0.5× 94 1.8k
Vanesa Robles Spain 30 1.6k 0.5× 1.3k 0.7× 607 0.4× 337 0.3× 872 1.0× 72 2.7k
Roderick Nigel Finn Norway 35 1.5k 0.5× 185 0.1× 1.8k 1.3× 655 0.5× 560 0.6× 76 3.4k
Rolf L. Ingermann United States 22 705 0.2× 423 0.2× 367 0.3× 446 0.3× 225 0.3× 67 1.4k
Prudence Talbot United States 35 489 0.2× 1.8k 1.0× 402 0.3× 94 0.1× 394 0.5× 90 3.4k
Serafín Pérez‐Cerezales Spain 25 704 0.2× 1.2k 0.6× 232 0.2× 145 0.1× 457 0.5× 47 2.0k
G. De Metrio Italy 26 548 0.2× 87 0.0× 757 0.6× 1.2k 0.9× 272 0.3× 51 2.0k

Countries citing papers authored by J. Cosson

Since Specialization
Citations

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

Fields of papers citing papers by J. Cosson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of J. Cosson

This figure shows the co-authorship network connecting the top 25 collaborators of J. Cosson. A scholar is included among the top collaborators of J. Cosson 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 J. Cosson. J. Cosson 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.
Dzyuba, Viktoriya, J. Cosson, Borys Dzyuba, & Marek Rodina. (2015). Oxidative stress and motility in tench Tinca tinca spermatozoa. Czech Journal of Animal Science. 60(6). 250–262. 9 indexed citations
2.
Browne, Robert K., Svetlana A. Kaurova, В. К. Утешев, et al.. (2014). Sperm motility of externally fertilizing fish and amphibians. Theriogenology. 83(1). 1–13.e8. 93 indexed citations
3.
Dzyuba, Borys, J. Cosson, Sergii Boryshpolets, et al.. (2013). Motility of sturgeon spermatozoa can sustain successive activations episodes. Animal Reproduction Science. 138(3-4). 305–313. 11 indexed citations
4.
Boryshpolets, Sergii, J. Cosson, Eric Gillies, et al.. (2012). Different swimming behaviors of sterlet (Acipenser ruthenus) spermatozoa close to solid and free surfaces. Theriogenology. 79(1). 81–86. 29 indexed citations
5.
Alavi, Sayyed Mohammad Hadi, et al.. (2006). Determination of some seminal plasma indices, sperm density and sperm motility in the Persian sturgeon Acipenser persicus. Iranian journal of fisheries science. 5(2). 1–18. 3 indexed citations
6.
Alavi, Sayyed Mohammad Hadi & J. Cosson. (2005). Sperm motility in fishes. (II) Effects of ions and osmolality: A review. Cell Biology International. 30(1). 1–14. 444 indexed citations breakdown →
7.
Alavi, Sayyed Mohammad Hadi & J. Cosson. (2005). Sperm motility in fishes. I. Effects of temperature and pH: a review. Cell Biology International. 29(2). 101–110. 304 indexed citations
8.
Cosson, J., Philippe Huitorel, & C. Gagnon. (2002). How spermatozoa come to be confined to surfaces. Cell Motility and the Cytoskeleton. 54(1). 56–63. 78 indexed citations
9.
Dréanno, Catherine, J. Cosson, M. Suquet, et al.. (1999). Effects of osmolality, morphology perturbations and intracellular nucleotide content during the movement of sea bass ( Dicentrarchus labrax ) spermatozoa. Reproduction. 116(1). 113–125. 77 indexed citations
10.
Mouroux, Jérôme, et al.. (1998). Influence of external pH on ciliary beat frequency in human bronchi and bronchioles. European Respiratory Journal. 11(2). 330–333. 87 indexed citations
11.
Linhart, Otomar & J. Cosson. (1997). Cryopreservation of carp [Cyprinus carpio L.] spermatozoa: the influence of external Kplus and Naplus on post-thaw motility. Polskie Archiwum Hydrobiologii. 44. 6 indexed citations
12.
Cosson, J., et al.. (1997). Movements of fish sperm flagella studied by high speed videomicroscopy coupled to computer assisted image analysis. Polskie Archiwum Hydrobiologii. 44. 34 indexed citations
13.
Dréanno, Catherine, Marc Suquet, Loïc Quémener, et al.. (1997). Cryopreservation of turbot () spermatozoa. Theriogenology. 48(4). 589–603. 78 indexed citations
14.
Cosson, J.. (1996). A MOVING IMAGE OF FLAGELLA: NEWS AND VIEWS ON THE MECHANISMS INVOLVED IN AXONEMAL BEATING. Cell Biology International. 20(2). 83–94. 31 indexed citations
15.
Pacey, Allan, J. Cosson, & Matthew G. Bentley. (1994). Intermittent swimming in the spermatozoa of the lugworm Arenicola marina (L.) (Annelida: Polychaeta). Cell Motility and the Cytoskeleton. 29(2). 186–194. 10 indexed citations
16.
Gagnon, C., Daniel White, Philippe Huitorel, & J. Cosson. (1994). A monoclonal antibody against the dynein IC1 peptide of sea urchin spermatozoa inhibits the motility of sea urchin, dinoflagellate, and human flagellar axonemes.. Molecular Biology of the Cell. 5(9). 1051–1063. 26 indexed citations
17.
Cosson, J., et al.. (1992). Temperature effect on the ciliary beat frequency of human nasal and tracheal ciliated cells. Biology of the Cell. 76(3). 335–338. 106 indexed citations
18.
Cosson, Marie Paule, et al.. (1991). In vitro maturation of the potential for movement of carp spermatozoa. Molecular Reproduction and Development. 29(3). 259–270. 82 indexed citations
19.
Cosson, J., et al.. (1988). Promoter of a somatic histone H2B gene of the sea urchin. Nucleic Acids Research. 16(9). 4175–4175. 3 indexed citations
20.
Carré, Danièle, et al.. (1983). Calcium mediates sperm chemotaxis in siphonophores. 151. 89–93. 6 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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