Olivier Destrée

7.3k total citations · 2 hit papers
80 papers, 6.1k citations indexed

About

Olivier Destrée is a scholar working on Molecular Biology, Genetics and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Olivier Destrée has authored 80 papers receiving a total of 6.1k indexed citations (citations by other indexed papers that have themselves been cited), including 64 papers in Molecular Biology, 16 papers in Genetics and 11 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Olivier Destrée's work include Cancer-related gene regulation (22 papers), Wnt/β-catenin signaling in development and cancer (21 papers) and Developmental Biology and Gene Regulation (15 papers). Olivier Destrée is often cited by papers focused on Cancer-related gene regulation (22 papers), Wnt/β-catenin signaling in development and cancer (21 papers) and Developmental Biology and Gene Regulation (15 papers). Olivier Destrée collaborates with scholars based in Netherlands, United States and France. Olivier Destrée's co-authors include Hans Clevers, Miranda Molenaar, Jeroen P. Roose, Marc van de Wetering, Mariëtte A. Oosterwegel, Vladimír Kořínek, Josi Peterson-Maduro, Susan F. Godsave, Giulietta Roël and Harry Begthel and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Olivier Destrée

80 papers receiving 5.9k citations

Hit Papers

XTcf-3 Transcription Factor Mediates β-Catenin-Induced Ax... 1996 2026 2006 2016 1996 1998 500 1000 1.5k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Olivier Destrée Netherlands 34 5.2k 1.0k 623 556 423 80 6.1k
Masanori Taira Japan 42 5.0k 1.0× 957 0.9× 393 0.6× 728 1.3× 135 0.3× 133 6.0k
Miguel Ramalho‐Santos United States 35 6.2k 1.2× 1.1k 1.0× 454 0.7× 459 0.8× 404 1.0× 57 7.4k
Nancy A. Jenkins United States 27 3.7k 0.7× 1.0k 1.0× 533 0.9× 427 0.8× 208 0.5× 44 5.0k
Licia Selleri United States 42 3.3k 0.6× 1.1k 1.1× 426 0.7× 284 0.5× 254 0.6× 110 5.0k
Brigitte Royer‐Pokora Germany 37 3.8k 0.7× 1.3k 1.3× 598 1.0× 378 0.7× 262 0.6× 118 5.5k
Mathias Treier Germany 34 4.3k 0.8× 2.1k 2.0× 609 1.0× 481 0.9× 720 1.7× 47 6.0k
Grady F. Saunders United States 39 5.5k 1.1× 2.0k 1.9× 380 0.6× 348 0.6× 228 0.5× 114 6.8k
Catherine E. Ovitt United States 31 3.0k 0.6× 1.1k 1.1× 480 0.8× 412 0.7× 529 1.3× 57 4.7k
Lawrence Lum United States 37 5.3k 1.0× 993 1.0× 1.2k 2.0× 652 1.2× 186 0.4× 64 6.5k
Anne K. Voss Australia 45 4.1k 0.8× 981 0.9× 475 0.8× 433 0.8× 646 1.5× 113 5.6k

Countries citing papers authored by Olivier Destrée

Since Specialization
Citations

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

Fields of papers citing papers by Olivier Destrée

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Olivier Destrée

This figure shows the co-authorship network connecting the top 25 collaborators of Olivier Destrée. A scholar is included among the top collaborators of Olivier Destrée 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 Olivier Destrée. Olivier Destrée 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.
Gent, Yoony Y. J., et al.. (2009). Lef1 plays a role in patterning the mesoderm and ectoderm in Xenopus tropicalis. The International Journal of Developmental Biology. 53(1). 81–89. 6 indexed citations
2.
Coudreuse, Damien, Giulietta Roël, Marco C. Betist, Olivier Destrée, & Hendrik C. Korswagen. (2006). Wnt Gradient Formation Requires Retromer Function in Wnt-Producing Cells. Science. 312(5775). 921–924. 202 indexed citations
3.
Boer, Teun P. de, Bart Kok, Giulietta Roël, et al.. (2006). Cloning, embryonic expression, and functional characterization of two novel connexins from Xenopus laevis. Biochemical and Biophysical Research Communications. 349(2). 855–862. 5 indexed citations
4.
Kuiper, George G. J. M., Willem Klootwijk, Ghislaine Morvan-Dubois, et al.. (2006). Characterization of Recombinant Xenopus laevis Type I Iodothyronine Deiodinase: Substitution of a Proline Residue in the Catalytic Center by Serine (Pro132Ser) Restores Sensitivity to 6-Propyl-2-Thiouracil. Endocrinology. 147(7). 3519–3529. 39 indexed citations
5.
Standley, Henrietta J., Olivier Destrée, Matthew Kofron, Chris Wylie, & Janet Heasman. (2005). Maternal XTcf1 and XTcf4 have distinct roles in regulating Wnt target genes. Developmental Biology. 289(2). 318–328. 42 indexed citations
6.
Heyden, Marcel A. G. van der, et al.. (2001). Connexin43 expression during Xenopus development. Mechanisms of Development. 108(1-2). 217–220. 10 indexed citations
7.
Destrée, Olivier, et al.. (2001). Expression of Tcf/Lef and sFrp and localization of β-catenin in the developing mouse lung. Mechanisms of Development. 109(2). 437–440. 63 indexed citations
8.
Heyden, Marcel A. G. van der, Jacqueline M. Veltmaat, Jeanine Hendriks, Olivier Destrée, & Libert H.K. Defize. (2000). Dynamic connexin43 expression and gap junctional communication during endoderm differentiation of F9 embryonal carcinoma cells. European Journal of Cell Biology. 79(4). 272–282. 8 indexed citations
9.
Molenaar, Miranda, et al.. (2000). Differential expression of the Groucho-related genes 4 and 5 during early development of Xenopus laevis. Mechanisms of Development. 91(1-2). 311–315. 43 indexed citations
10.
Jonkers, Jos, Renée van Amerongen, Martin van der Valk, et al.. (1999). In vivo analysis of Frat1 deficiency suggests compensatory activity of Frat3. Mechanisms of Development. 88(2). 183–194. 32 indexed citations
11.
Molenaar, Miranda, et al.. (1998). Differential expression of the HMG box transcription factors XTcf-3 and XLef-1 during early Xenopus development. Mechanisms of Development. 75(1-2). 151–154. 67 indexed citations
12.
Roose, Jeroen P., Miranda Molenaar, Petra Moerer, et al.. (1998). The Xenopus Wnt effector XTcf-3 interacts with Groucho-related transcriptional repressors. Nature. 395(6702). 608–612. 572 indexed citations breakdown →
13.
Veenstra, Gert Jan C., et al.. (1998). Non-cell autonomous induction of apoptosis and loss of posterior structures by activation domain-specific interactions of Oct-1 in the Xenopus embryo. Cell Death and Differentiation. 5(9). 774–784. 20 indexed citations
14.
Biewenga, Jeike, Olivier Destrée, & Loes H. Schrama. (1997). Plasmid-mediated gene transfer in neurons using the biolistics technique. Journal of Neuroscience Methods. 71(1). 67–75. 36 indexed citations
15.
Joore, Jos, Johanna E. Speksnijder, W. Kruijer, et al.. (1996). Regulation of the zebrafish goosecoid promoter by mesoderm inducing factors and Xwnt1. Mechanisms of Development. 55(1). 3–18. 25 indexed citations
16.
Beumer, Tim L., et al.. (1995). Whole-mount immunohistochemistry on Xenopus embryos using far-red fluorescent dyes. Trends in Genetics. 11(1). 9–9. 17 indexed citations
17.
Gispen, Willem Hendrik, Joost Verhaagen, Loes H. Schrama, et al.. (1993). The rat B-50(GAP43) promoter directs neural-preferred expression of a reporter gene in xenopus laevis embryos. Utrecht University Repository (Utrecht University). 7 indexed citations
18.
Hulshof, S.C.J., P.M.M. Kastrop, M.M. Bevers, Olivier Destrée, & Th.A.M. Kruip. (1989). The effect of inhibitors on bovine oocyte maturation. Cell Differentiation and Development. 27. 38–38. 1 indexed citations
19.
Dongen, Walter Van, et al.. (1981). The organization of the histone genes in the genome of Xenopus laevis. Nucleic Acids Research. 9(10). 2297–2311. 38 indexed citations
20.
Kasinsky, Harold E., et al.. (1979). Newly synthesized histones in chromatin of early embryos of Xenopus laevis. Cell Differentiation. 8(2). 93–104. 20 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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