Catherine Jessus

2.6k total citations
70 papers, 2.1k citations indexed

About

Catherine Jessus is a scholar working on Cell Biology, Molecular Biology and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Catherine Jessus has authored 70 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 52 papers in Cell Biology, 44 papers in Molecular Biology and 35 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Catherine Jessus's work include Microtubule and mitosis dynamics (51 papers), Reproductive Biology and Fertility (35 papers) and Genetics, Aging, and Longevity in Model Organisms (13 papers). Catherine Jessus is often cited by papers focused on Microtubule and mitosis dynamics (51 papers), Reproductive Biology and Fertility (35 papers) and Genetics, Aging, and Longevity in Model Organisms (13 papers). Catherine Jessus collaborates with scholars based in France, United States and Morocco. Catherine Jessus's co-authors include René Ozon, Olivier Haccard, Catherine Thibier, David Beach, Anthi Karaı̈skou, Konstantin Galaktionov, Aude Dupré, Hélène Rime, Xavier Cayla and Dorothée Huchon and has published in prestigious journals such as Journal of Biological Chemistry, Nature Communications and Genes & Development.

In The Last Decade

Catherine Jessus

67 papers receiving 2.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Catherine Jessus France 28 1.5k 1.0k 813 283 224 70 2.1k
Andrea L. Lewellyn United States 26 1.6k 1.1× 1.1k 1.0× 798 1.0× 260 0.9× 227 1.0× 34 2.2k
Olivier Haccard France 19 971 0.7× 791 0.8× 677 0.8× 121 0.4× 189 0.8× 35 1.4k
J C Cavadore France 21 2.5k 1.7× 1.4k 1.4× 473 0.6× 828 2.9× 147 0.7× 38 3.1k
Gérard Peaucellier France 21 869 0.6× 495 0.5× 414 0.5× 147 0.5× 198 0.9× 40 1.4k
Noriyuki Sagata Japan 31 2.9k 1.9× 1.7k 1.7× 1.5k 1.8× 540 1.9× 465 2.1× 60 4.0k
Manfred J. Lohka United States 21 3.5k 2.3× 2.1k 2.1× 981 1.2× 518 1.8× 425 1.9× 30 4.4k
Didier Fesquet France 27 2.5k 1.7× 1.6k 1.6× 448 0.6× 958 3.4× 158 0.7× 36 3.0k
Ellen K. Shibuya Canada 15 890 0.6× 586 0.6× 320 0.4× 202 0.7× 103 0.5× 18 1.2k
Michèle Weber France 12 1.0k 0.7× 461 0.4× 600 0.7× 172 0.6× 172 0.8× 16 1.4k
Marie‐Emilie Terret France 23 1.6k 1.1× 1.2k 1.2× 871 1.1× 233 0.8× 168 0.8× 42 2.2k

Countries citing papers authored by Catherine Jessus

Since Specialization
Citations

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

Fields of papers citing papers by Catherine Jessus

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Catherine Jessus

This figure shows the co-authorship network connecting the top 25 collaborators of Catherine Jessus. A scholar is included among the top collaborators of Catherine Jessus 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 Catherine Jessus. Catherine Jessus 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.
Peshkin, Leonid, Enrico Maria Daldello, Elizabeth Van Itallie, et al.. (2025). Decoding protein phosphorylation during oocyte meiotic divisions using phosphoproteomics. eLife. 13.
2.
Daldello, Enrico Maria, et al.. (2021). The M-phase regulatory phosphatase PP2A-B55δ opposes protein kinase A on Arpp19 to initiate meiotic division. Nature Communications. 12(1). 5 indexed citations
3.
Dupré, Aude, et al.. (2020). The G2-to-M transition from a phosphatase perspective: a new vision of the meiotic division. Cell Division. 15(1). 9–9. 24 indexed citations
4.
Dupré, Aude, et al.. (2020). Translational Control of Xenopus Oocyte Meiosis: Toward the Genomic Era. Cells. 9(6). 1502–1502. 20 indexed citations
5.
Haccard, Olivier, et al.. (2017). The greatwall kinase is dominant over PKA in controlling the antagonistic function of ARPP19 in Xenopus oocytes. Cell Cycle. 16(15). 1440–1452. 7 indexed citations
6.
Haccard, Olivier, Aude Dupré, Philippe Lière, et al.. (2012). Naturally occurring steroids in Xenopus oocyte during meiotic maturation. Unexpected presence and role of steroid sulfates. Molecular and Cellular Endocrinology. 362(1-2). 110–119. 20 indexed citations
7.
Zhao, Yong, Olivier Haccard, Ruoning Wang, et al.. (2008). Roles of Greatwall Kinase in the Regulation of Cdc25 Phosphatase. Molecular Biology of the Cell. 19(4). 1317–1327. 60 indexed citations
8.
Dehennaut, Vanessa, Marie‐Christine Slomianny, Adeline Page, et al.. (2008). Identification of Structural and Functional O-Linked N-Acetylglucosamine-bearing Proteins in Xenopus laevis Oocyte. Molecular & Cellular Proteomics. 7(11). 2229–2245. 71 indexed citations
9.
Dupré, Aude, et al.. (2006). Deciphering the H-Ras pathway in Xenopus oocyte. Oncogene. 25(37). 5155–5162. 8 indexed citations
10.
Smedt, Véronique De, Robert Poulhe, Xavier Cayla, et al.. (2002). Thr-161 Phosphorylation of Monomeric Cdc2. Journal of Biological Chemistry. 277(32). 28592–28600. 49 indexed citations
11.
Frank-Vaillant, Marie, Olivier Haccard, René Ozon, & Catherine Jessus. (2001). Interplay between Cdc2 Kinase and the c-Mos/MAPK Pathway between Metaphase I and Metaphase II in Xenopus Oocytes. Developmental Biology. 231(1). 279–288. 20 indexed citations
12.
Karaı̈skou, Anthi, et al.. (1998). MPF amplification in Xenopus oocyte extracts depends on a two-step activation of Cdc25 phosphatase. HAL (Le Centre pour la Communication Scientifique Directe). 1 indexed citations
13.
Taïeb, Frédéric, Catherine Thibier, & Catherine Jessus. (1997). On cyclins, oocytes, and eggs. Molecular Reproduction and Development. 48(3). 397–411. 76 indexed citations
14.
Taïeb, Frédéric, Isabelle Chartrain, Stéphan Chevalier, Olivier Haccard, & Catherine Jessus. (1997). Cyclin D2 ArrestsXenopusEarly Embryonic Cell Cycles. Experimental Cell Research. 237(2). 338–346. 10 indexed citations
15.
Rime, Hélène, Catherine Jessus, & René Ozon. (1995). Tyrosine Phosphorylation of p34cdc2 Is Regulated by Protein Phosphatase 2A in Growing Immature Xenopus Oocytes. Experimental Cell Research. 219(1). 29–38. 24 indexed citations
16.
Rime, Hélène, Jing Yang, Catherine Jessus, & René Ozon. (1991). MPF is activated in growing immature Xenopus oocytes in the absence of detectable tyrosine dephosphorylation of p34cdc2. Experimental Cell Research. 196(2). 241–245. 18 indexed citations
17.
Jessus, Catherine, Bernard Ducommun, & David Beach. (1990). Direct activation of cdc2 with phosphatase: identification of p13sucl‐sensitive and insensitive steps. FEBS Letters. 266(1-2). 4–8. 34 indexed citations
18.
Haccard, Olivier, Catherine Jessus, Xavier Cayla, et al.. (1990). In vivo activation of a microtubule‐associated protein kinase during meiotic maturation of the Xenopus oocyte. European Journal of Biochemistry. 192(3). 633–642. 63 indexed citations
19.
Rime, Hélène, et al.. (1990). Characterization of MPF activation by okadaic acid in Xenopus oocyte. Cell Differentiation and Development. 29(1). 47–58. 57 indexed citations
20.
Huchon, Dorothée, Catherine Jessus, Catherine Thibier, & René Ozon. (1988). Presence of microtubules in isolated cortices of prophase I and metaphase II oocytes in Xenopus laevis. Cell and Tissue Research. 254(2). 415–20. 23 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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