Vincent Pasque

3.1k total citations
44 papers, 1.6k citations indexed

About

Vincent Pasque is a scholar working on Molecular Biology, Genetics and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Vincent Pasque has authored 44 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 42 papers in Molecular Biology, 10 papers in Genetics and 5 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Vincent Pasque's work include Pluripotent Stem Cells Research (27 papers), CRISPR and Genetic Engineering (24 papers) and Epigenetics and DNA Methylation (10 papers). Vincent Pasque is often cited by papers focused on Pluripotent Stem Cells Research (27 papers), CRISPR and Genetic Engineering (24 papers) and Epigenetics and DNA Methylation (10 papers). Vincent Pasque collaborates with scholars based in Belgium, United Kingdom and United States. Vincent Pasque's co-authors include J. B. Gurdon, Jérôme Jullien, Kei Miyamoto, Richard P. Halley‐Stott, Astrid Gillich, Nigel Garrett, Kathrin Plath, M. Azim Surani, Patrick Motté and Joseph Martial and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Vincent Pasque

43 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Vincent Pasque Belgium 23 1.4k 335 211 151 112 44 1.6k
Monika Bialecka Netherlands 17 989 0.7× 348 1.0× 254 1.2× 68 0.5× 125 1.1× 26 1.3k
Jay L. Vivian United States 20 947 0.7× 247 0.7× 107 0.5× 119 0.8× 111 1.0× 45 1.3k
Steffen Biechele Canada 13 1.3k 0.9× 311 0.9× 145 0.7× 193 1.3× 125 1.1× 18 1.7k
Electra Coucouvanis United States 10 1.1k 0.7× 208 0.6× 190 0.9× 137 0.9× 150 1.3× 10 1.3k
Nobuaki Kikyo United States 24 1.5k 1.1× 309 0.9× 276 1.3× 54 0.4× 152 1.4× 46 1.8k
Louise Hyslop United Kingdom 11 1.0k 0.7× 132 0.4× 334 1.6× 185 1.2× 145 1.3× 17 1.4k
Elen Gócza Hungary 16 1.1k 0.8× 411 1.2× 207 1.0× 45 0.3× 244 2.2× 50 1.5k
Misuzu Yamashita Japan 21 616 0.4× 254 0.8× 412 2.0× 98 0.6× 97 0.9× 26 1.2k
Nicoletta Corbi Italy 19 1.2k 0.9× 326 1.0× 75 0.4× 77 0.5× 69 0.6× 40 1.5k
Aitana Perea-Gómez France 15 1.4k 1.0× 249 0.7× 258 1.2× 114 0.8× 181 1.6× 27 1.5k

Countries citing papers authored by Vincent Pasque

Since Specialization
Citations

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

Fields of papers citing papers by Vincent Pasque

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Vincent Pasque

This figure shows the co-authorship network connecting the top 25 collaborators of Vincent Pasque. A scholar is included among the top collaborators of Vincent Pasque 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 Vincent Pasque. Vincent Pasque 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.
Migeotte, Isabelle, et al.. (2025). Extra-embryonic mesoderm during development and in in vitro models. Development. 152(5). 2 indexed citations
2.
Casas-Delucchi, Corella S., Paulina Prorok, Sunil Kumar Pradhan, et al.. (2024). Histone variant macroH2A1 regulates synchronous firing of replication origins in the inactive X chromosome. Nucleic Acids Research. 52(19). 11659–11688.
3.
Georgolopoulos, Grigorios, Rob Lavigne, Ophélie Renoult, et al.. (2024). Unraveling hallmark suitability for staging pre- and post-implantation stem cell models. Cell Reports. 43(5). 114232–114232. 7 indexed citations
4.
Shahbazi, Marta N. & Vincent Pasque. (2024). Early human development and stem cell-based human embryo models. Cell stem cell. 31(10). 1398–1418. 22 indexed citations
5.
Chai, Yoke Chin, San Kit To, Samantha Zaunz, et al.. (2023). Spatially Self‐Organized Three‐Dimensional Neural Concentroid as a Novel Reductionist Humanized Model to Study Neurovascular Development. Advanced Science. 11(5). e2304421–e2304421. 8 indexed citations
6.
Hermans, Florian, Benoit Cox, Elodie Modave, et al.. (2021). Interleukin-6 is an activator of pituitary stem cells upon local damage, a competence quenched in the aging gland. Proceedings of the National Academy of Sciences. 118(25). 34 indexed citations
7.
Talón, Irene, Adrian Janiszewski, Juan Song, et al.. (2021). Enhanced chromatin accessibility contributes to X chromosome dosage compensation in mammals. Genome biology. 22(1). 302–302. 18 indexed citations
8.
Pósfai, Eszter, John P. Schell, Adrian Janiszewski, et al.. (2021). Evaluating totipotency using criteria of increasing stringency. Nature Cell Biology. 23(1). 49–60. 132 indexed citations
9.
Luo, Xinlong, Rita Khoueiry, Adrian Janiszewski, et al.. (2020). Regulatory Dynamics of Tet1 and Oct4 Resolve Stages of Global DNA Demethylation and Transcriptomic Changes in Reprogramming. Cell Reports. 30(7). 2150–2169.e9. 11 indexed citations
10.
Quarta, Alessandra, Debbie Le Blon, Francesc Miró‐Mur, et al.. (2019). Murine iPSC-derived microglia and macrophage cell culture models recapitulate distinct phenotypical and functional properties of classical and alternative neuro-immune polarisation. Brain Behavior and Immunity. 82. 406–421. 21 indexed citations
11.
Song, Juan, Adrian Janiszewski, Natalie De Geest, et al.. (2019). X-Chromosome Dosage Modulates Multiple Molecular and Cellular Properties of Mouse Pluripotent Stem Cells Independently of Global DNA Methylation Levels. Stem Cell Reports. 12(2). 333–350. 21 indexed citations
12.
Pasque, Vincent, Rahul Karnik, Constantinos Chronis, et al.. (2018). X Chromosome Dosage Influences DNA Methylation Dynamics during Reprogramming to Mouse iPSCs. Stem Cell Reports. 10(5). 1537–1550. 32 indexed citations
13.
Jullien, Jérôme, Munender Vodnala, Vincent Pasque, et al.. (2017). Gene Resistance to Transcriptional Reprogramming following Nuclear Transfer Is Directly Mediated by Multiple Chromatin-Repressive Pathways. Molecular Cell. 65(5). 873–884.e8. 38 indexed citations
14.
Pasque, Vincent, et al.. (2012). RUNX3, EGR1 and SOX9B Form a Regulatory Cascade Required to Modulate BMP-Signaling during Cranial Cartilage Development in Zebrafish. PLoS ONE. 7(11). e50140–e50140. 39 indexed citations
15.
Teperek, Marta, Vincent Pasque, George E. Gentsch, & Anne C. Ferguson‐Smith. (2011). Epigenetic reprogramming: is deamination key to active DNA demethylation?. Reproduction. 142(5). 621–632. 43 indexed citations
16.
Miyamoto, Kei, Vincent Pasque, Jérôme Jullien, & J. B. Gurdon. (2011). Nuclear actin polymerization is required for transcriptional reprogramming of Oct4 by oocytes. Genes & Development. 25(9). 946–958. 138 indexed citations
17.
Pasque, Vincent, Richard P. Halley‐Stott, Astrid Gillich, Nigel Garrett, & J. B. Gurdon. (2011). Epigenetic stability of repressed states involving the histone variant macroH2A revealed by nuclear transfer to Xenopus oocytes. Nucleus. 2(6). 533–539. 24 indexed citations
18.
Jullien, Jérôme, Vincent Pasque, Richard P. Halley‐Stott, Kei Miyamoto, & J. B. Gurdon. (2011). Mechanisms of nuclear reprogramming by eggs and oocytes: a deterministic process?. Nature Reviews Molecular Cell Biology. 12(7). 453–459. 84 indexed citations
19.
Pasque, Vincent, Jérôme Jullien, Kei Miyamoto, Richard P. Halley‐Stott, & J. B. Gurdon. (2011). Epigenetic factors influencing resistance to nuclear reprogramming. Trends in Genetics. 27(12). 516–525. 76 indexed citations
20.
Pendeville, Hélène, Marie Winandy, Olivier Nivelles, et al.. (2008). Zebrafish Sox7 and Sox18 function together to control arterial–venous identity. Developmental Biology. 317(2). 405–416. 100 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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