Valérie Borde

3.5k total citations
44 papers, 2.4k citations indexed

About

Valérie Borde is a scholar working on Molecular Biology, Cell Biology and Plant Science. According to data from OpenAlex, Valérie Borde has authored 44 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 42 papers in Molecular Biology, 9 papers in Cell Biology and 6 papers in Plant Science. Recurrent topics in Valérie Borde's work include DNA Repair Mechanisms (38 papers), Genomics and Chromatin Dynamics (16 papers) and CRISPR and Genetic Engineering (11 papers). Valérie Borde is often cited by papers focused on DNA Repair Mechanisms (38 papers), Genomics and Chromatin Dynamics (16 papers) and CRISPR and Genetic Engineering (11 papers). Valérie Borde collaborates with scholars based in France, United Kingdom and United States. Valérie Borde's co-authors include Michael Lichten, Alain Nicolas, Alastair S. H. Goldman, Waka Lin, Nicolas Robine, Cyril Buhler, Bernard de Massy, Vincent Géli, Arnaud De Muyt and Franz Klein and has published in prestigious journals such as Nature, Science and Proceedings of the National Academy of Sciences.

In The Last Decade

Valérie Borde

42 papers receiving 2.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Valérie Borde France 25 2.3k 544 362 259 189 44 2.4k
Beth Rockmill United States 21 1.9k 0.8× 491 0.9× 479 1.3× 196 0.8× 126 0.7× 26 2.0k
Hideo Tsubouchi Japan 18 1.5k 0.7× 227 0.4× 310 0.9× 128 0.5× 211 1.1× 37 1.6k
Fekret Osman United Kingdom 21 2.0k 0.9× 274 0.5× 448 1.2× 215 0.8× 311 1.6× 38 2.0k
Igor Chesnokov United States 19 1.3k 0.5× 249 0.5× 227 0.6× 226 0.9× 66 0.3× 32 1.4k
Hildo H. Offenberg Netherlands 20 2.0k 0.9× 605 1.1× 409 1.1× 394 1.5× 148 0.8× 24 2.2k
Patricia W. Greenwell United States 18 1.6k 0.7× 397 0.7× 224 0.6× 306 1.2× 195 1.0× 21 1.8k
Martin E. Budd United States 23 2.1k 0.9× 282 0.5× 207 0.6× 241 0.9× 284 1.5× 33 2.2k
J. Kent Moore United States 9 2.3k 1.0× 454 0.8× 204 0.6× 180 0.7× 297 1.6× 9 2.4k
Monica Boselli United States 9 830 0.4× 267 0.5× 461 1.3× 211 0.8× 132 0.7× 10 1.1k
Eugenio Sánchez‐Morán United Kingdom 24 2.1k 0.9× 1.4k 2.6× 229 0.6× 259 1.0× 237 1.3× 42 2.5k

Countries citing papers authored by Valérie Borde

Since Specialization
Citations

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

Fields of papers citing papers by Valérie Borde

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Valérie Borde

This figure shows the co-authorship network connecting the top 25 collaborators of Valérie Borde. A scholar is included among the top collaborators of Valérie Borde 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 Valérie Borde. Valérie Borde 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.
Cohen, Sarah, Aude Guénolé, Ikrame Lazar, et al.. (2022). A POLD3/BLM dependent pathway handles DSBs in transcribed chromatin upon excessive RNA:DNA hybrid accumulation. Nature Communications. 13(1). 2012–2012. 23 indexed citations
2.
Reginato, Giordano, Céline Adam, Lepakshi Ranjha, et al.. (2021). The Pif1 helicase is actively inhibited during meiotic recombination which restrains gene conversion tract length. Nucleic Acids Research. 49(8). 4522–4533. 16 indexed citations
3.
Sanchez, Aurore, Céline Adam, Lepakshi Ranjha, et al.. (2021). Molecular basis of the dual role of the Mlh1-Mlh3 endonuclease in MMR and in meiotic crossover formation. Proceedings of the National Academy of Sciences. 118(23). 21 indexed citations
4.
Sanchez, Aurore, Céline Adam, Yann Duroc, et al.. (2020). Exo1 recruits Cdc5 polo kinase to MutLγ to ensure efficient meiotic crossover formation. Proceedings of the National Academy of Sciences. 117(48). 30577–30588. 26 indexed citations
5.
Mohiuddin, Mohiuddin, Masataka Tsuda, Hiroyuki Sasanuma, et al.. (2020). Genetic evidence for the involvement of mismatch repair proteins, PMS2 and MLH3, in a late step of homologous recombination. Journal of Biological Chemistry. 295(51). 17460–17475. 17 indexed citations
6.
Borde, Valérie, et al.. (2019). Crossing and zipping: molecular duties of the ZMM proteins in meiosis. Chromosoma. 128(3). 181–198. 95 indexed citations
7.
Duroc, Yann, Rajeev Kumar, Lepakshi Ranjha, et al.. (2017). Concerted action of the MutLβ heterodimer and Mer3 helicase regulates the global extent of meiotic gene conversion. eLife. 6. 49 indexed citations
8.
Borde, Valérie, et al.. (2015). The CAF-1 and Hir Histone Chaperones Associate with Sites of Meiotic Double-Strand Breaks in Budding Yeast. PLoS ONE. 10(5). e0125965–e0125965. 11 indexed citations
9.
Borde, Valérie, et al.. (2012). The spatial regulation of meiotic recombination hotspots: Are all DSB hotspots crossover hotspots?. Experimental Cell Research. 318(12). 1347–1352. 47 indexed citations
11.
Martini, Emmanuelle, Valérie Borde, Matthieu Legendre, et al.. (2011). Genome-Wide Analysis of Heteroduplex DNA in Mismatch Repair–Deficient Yeast Cells Reveals Novel Properties of Meiotic Recombination Pathways. PLoS Genetics. 7(9). e1002305–e1002305. 97 indexed citations
12.
Borde, Valérie, et al.. (2011). Interplay between modifications of chromatin and meiotic recombination hotspots. Biology of the Cell. 104(2). 51–69. 28 indexed citations
13.
Schlecht, Ulrich, Ionas Erb, Philippe Demougin, et al.. (2008). Genome-wide Expression Profiling, In Vivo DNA Binding Analysis, and Probabilistic Motif Prediction Reveal Novel Abf1 Target Genes during Fermentation, Respiration, and Sporulation in Yeast. Molecular Biology of the Cell. 19(5). 2193–2207. 26 indexed citations
14.
Buhler, Cyril, Valérie Borde, & Michael Lichten. (2008). Correction: Mapping Meiotic Single-Strand DNA Reveals a New Landscape of DNA Double-Strand Breaks in Saccharomyces cerevisiae. PLoS Biology. 6(4). e104–e104.
15.
Johnson, Rebecca A., Valérie Borde, Matthew J. Neale, et al.. (2007). Excess Single-Stranded DNA Inhibits Meiotic Double-Strand Break Repair. PLoS Genetics. 3(11). e223–e223. 23 indexed citations
16.
Robine, Nicolas, Norio Uematsu, Franck Amiot, et al.. (2006). Genome-Wide Redistribution of Meiotic Double-Strand Breaks in Saccharomyces cerevisiae. Molecular and Cellular Biology. 27(5). 1868–1880. 80 indexed citations
17.
Penkner, Alexandra, et al.. (2005). The control of Spo11's interaction with meiotic recombination hotspots. Genes & Development. 19(2). 255–269. 78 indexed citations
18.
Johnson, Rebecca, Valérie Borde, Matthew J. Neale, et al.. (2005). Excess single-stranded DNA inhibits meiotic double-strand break repair. PLoS Genetics. preprint(2007). e223–e223. 1 indexed citations
19.
Borde, Valérie, Waka Lin, Eugene Novikov, et al.. (2004). Association of Mre11p with Double-Strand Break Sites during Yeast Meiosis. Molecular Cell. 13(3). 389–401. 115 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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