Erwan Watrin

2.3k total citations
28 papers, 1.0k citations indexed

About

Erwan Watrin is a scholar working on Molecular Biology, Cell Biology and Plant Science. According to data from OpenAlex, Erwan Watrin has authored 28 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 9 papers in Cell Biology and 4 papers in Plant Science. Recurrent topics in Erwan Watrin's work include Genomics and Chromatin Dynamics (19 papers), RNA Research and Splicing (13 papers) and Microtubule and mitosis dynamics (9 papers). Erwan Watrin is often cited by papers focused on Genomics and Chromatin Dynamics (19 papers), RNA Research and Splicing (13 papers) and Microtubule and mitosis dynamics (9 papers). Erwan Watrin collaborates with scholars based in France, Austria and Netherlands. Erwan Watrin's co-authors include Jan‐Michael Peters, Vincent Legagneux, Péter Lénárt, Karl Mechtler, Julia Schmitz, Kim Nasmyth, Kōichi Tanaka, Frank Eisenhaber, Alexander Schleiffer and Frank J. Kaiser and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Clinical Investigation and The EMBO Journal.

In The Last Decade

Erwan Watrin

28 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Erwan Watrin France 16 922 208 203 159 88 28 1.0k
John A. Schmiesing United States 11 987 1.1× 164 0.8× 215 1.1× 107 0.7× 106 1.2× 11 1.1k
Silvia Remeseiro Spain 14 973 1.1× 119 0.6× 187 0.9× 138 0.9× 78 0.9× 26 1.1k
Olivier Ganier France 11 879 1.0× 198 1.0× 93 0.5× 165 1.0× 127 1.4× 15 991
Heather C. Gregson United States 9 1.4k 1.6× 257 1.2× 457 2.3× 215 1.4× 65 0.7× 9 1.6k
Anne Helmrich Germany 8 859 0.9× 88 0.4× 87 0.4× 302 1.9× 101 1.1× 9 936
Philip A. Knobel Spain 13 517 0.6× 131 0.6× 160 0.8× 137 0.9× 188 2.1× 15 737
Miguel G. Blanco Spain 13 1.3k 1.4× 333 1.6× 180 0.9× 164 1.0× 163 1.9× 28 1.4k
E. Ozeri-Galai Israel 8 430 0.5× 145 0.7× 57 0.3× 172 1.1× 81 0.9× 10 556
Suzanne A. Hartford United States 12 686 0.7× 111 0.5× 84 0.4× 206 1.3× 117 1.3× 16 833
Tyrone Ryba United States 16 1.8k 1.9× 85 0.4× 283 1.4× 317 2.0× 41 0.5× 21 1.9k

Countries citing papers authored by Erwan Watrin

Since Specialization
Citations

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

Fields of papers citing papers by Erwan Watrin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Erwan Watrin

This figure shows the co-authorship network connecting the top 25 collaborators of Erwan Watrin. A scholar is included among the top collaborators of Erwan Watrin 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 Erwan Watrin. Erwan Watrin 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.
Gagné, Jean‐Philippe, Malgorzata Ewa Rogalska, Amit K. Behera, et al.. (2024). Proteomic study identifies Aurora-A–mediated regulation of alternative splicing through multiple splicing factors. Journal of Biological Chemistry. 301(1). 108000–108000. 3 indexed citations
2.
Diebold, Marie-Laure, T.B. Shaik, A. Durand, et al.. (2024). The cohesin ATPase cycle is mediated by specific conformational dynamics and interface plasticity of SMC1A and SMC3 ATPase domains. Cell Reports. 43(9). 114656–114656. 1 indexed citations
3.
Éot-Houllier, Grégory, Laura Magnaghi-Jaulin, Fátima Smagulova, et al.. (2023). The histone methyltransferase NSD3 contributes to sister chromatid cohesion and to cohesin loading at mitotic exit. Journal of Cell Science. 136(11). 3 indexed citations
4.
Leschik, Julia, et al.. (2021). Targeting the histone demethylase LSD1 prevents cardiomyopathy in a mouse model of laminopathy. Journal of Clinical Investigation. 131(1). 34 indexed citations
5.
Courthéoux, Thibault, et al.. (2020). Alteration of SC35 localization by transfection reagents. Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1867(4). 118650–118650. 2 indexed citations
6.
Dubourg, Christèle, Sylvie Odent, Valérie Dupé, et al.. (2020). Synonymous variants in holoprosencephaly alter codon usage and impact the Sonic Hedgehog protein. Brain. 143(7). 2027–2038. 11 indexed citations
7.
Akloul, Linda, Wilfrid Carré, Chloé Quēlin, et al.. (2019). Targeted panel sequencing establishes the implication of planar cell polarity pathway and involves new candidate genes in neural tube defect disorders. Human Genetics. 138(4). 363–374. 17 indexed citations
8.
Pozojevic, Jelena, Ilaria Parenti, Luitgard Graul‐Neumann, et al.. (2017). Novel mosaic variants in two patients with Cornelia de Lange syndrome. European Journal of Medical Genetics. 61(11). 680–684. 7 indexed citations
9.
Zuin, Jessica, Valentina Casà, Jelena Pozojevic, et al.. (2017). Regulation of the cohesin-loading factor NIPBL: Role of the lncRNA NIPBL-AS1 and identification of a distal enhancer element. PLoS Genetics. 13(12). e1007137–e1007137. 11 indexed citations
10.
Watrin, Erwan, Frank J. Kaiser, & Kerstin S. Wendt. (2016). Gene regulation and chromatin organization: relevance of cohesin mutations to human disease. Current Opinion in Genetics & Development. 37. 59–66. 44 indexed citations
11.
Watrin, Erwan, et al.. (2014). Sororin pre‐ mRNA splicing is required for proper sister chromatid cohesion in human cells. EMBO Reports. 15(9). 948–955. 30 indexed citations
12.
Braunholz, Diana, Ilaria Parenti, Jelena Pozojevic, et al.. (2014). Hidden Mutations in Cornelia de Lange Syndrome Limitations of Sanger Sequencing in Molecular Diagnostics. Human Mutation. 36(1). 26–29. 19 indexed citations
13.
Watrin, Erwan & Jan‐Michael Peters. (2009). The cohesin complex is required for the DNA damage‐induced G2/M checkpoint in mammalian cells. The EMBO Journal. 28(17). 2625–2635. 110 indexed citations
14.
Schmitz, Julia, Erwan Watrin, Péter Lénárt, Karl Mechtler, & Jan‐Michael Peters. (2007). Sororin Is Required for Stable Binding of Cohesin to Chromatin and for Sister Chromatid Cohesion in Interphase. Current Biology. 17(7). 630–636. 191 indexed citations
15.
Watrin, Erwan, Alexander Schleiffer, Kōichi Tanaka, et al.. (2006). Human Scc4 Is Required for Cohesin Binding to Chromatin, Sister-Chromatid Cohesion, and Mitotic Progression. Current Biology. 16(9). 863–874. 198 indexed citations
16.
Watrin, Erwan & Jan‐Michael Peters. (2006). Cohesin and DNA damage repair. Experimental Cell Research. 312(14). 2687–2693. 92 indexed citations
17.
Watrin, Erwan & Vincent Legagneux. (2005). Contribution of hCAP-D2, a Non-SMC Subunit of Condensin I, to Chromosome and Chromosomal Protein Dynamics during Mitosis. Molecular and Cellular Biology. 25(2). 740–750. 37 indexed citations
18.
Legagneux, Vincent, Fabien Cubizolles, & Erwan Watrin. (2004). Multiple roles of Condensins: a complex story. Biology of the Cell. 96(3). 201–213. 27 indexed citations
19.
Watrin, Erwan & Vincent Legagneux. (2003). Introduction to chromosome dynamics in mitosis. Biology of the Cell. 95(8). 507–513. 7 indexed citations
20.
Beenders, Brent, Erwan Watrin, Vincent Legagneux, Igor I. Kireev, & Michel Bellini. (2003). Distribution of XCAP-E and XCAP-D2 in the Xenopus oocyte nucleus. Chromosome Research. 11(6). 549–564. 13 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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