Christophe Lachaud

1.3k total citations
22 papers, 893 citations indexed

About

Christophe Lachaud is a scholar working on Molecular Biology, Cell Biology and Genetics. According to data from OpenAlex, Christophe Lachaud has authored 22 papers receiving a total of 893 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 5 papers in Cell Biology and 4 papers in Genetics. Recurrent topics in Christophe Lachaud's work include DNA Repair Mechanisms (10 papers), CRISPR and Genetic Engineering (7 papers) and Microtubule and mitosis dynamics (4 papers). Christophe Lachaud is often cited by papers focused on DNA Repair Mechanisms (10 papers), CRISPR and Genetic Engineering (7 papers) and Microtubule and mitosis dynamics (4 papers). Christophe Lachaud collaborates with scholars based in United Kingdom, France and Spain. Christophe Lachaud's co-authors include John Rouse, Rachel Toth, Thomas Macartney, Paul L. Appleton, Iván Muñoz, Dennis Castor, Christian Brière, Valérie Cotelle, Francesco Marchesi and Christian Mazars and has published in prestigious journals such as Science, Nucleic Acids Research and Genes & Development.

In The Last Decade

Christophe Lachaud

20 papers receiving 889 citations

Peers

Christophe Lachaud
Christophe Lachaud
Citations per year, relative to Christophe Lachaud Christophe Lachaud (= 1×) peers Philip A. Knobel

Countries citing papers authored by Christophe Lachaud

Since Specialization
Citations

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

Fields of papers citing papers by Christophe Lachaud

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Christophe Lachaud

This figure shows the co-authorship network connecting the top 25 collaborators of Christophe Lachaud. A scholar is included among the top collaborators of Christophe Lachaud 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 Christophe Lachaud. Christophe Lachaud 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.
Braud, Laura, Manuel Bernabé, Antonio M. A. Miranda, et al.. (2025). TERT expression attenuates metabolic disorders in obese mice by promoting adipose stem and progenitor cell expansion and differentiation. Molecular Metabolism. 102. 102262–102262.
2.
Pozo‐Guisado, Eulalia, Alberto Álvarez, Sérgio Lilla, et al.. (2024). STIM1 translocation to the nucleus protects cells from DNA damage. Nucleic Acids Research. 52(5). 2389–2415.
3.
Larcher, Lise, Nadia Vasquez, Mélanie Da Costa, et al.. (2023). A clickable melphalan for monitoring DNA interstrand crosslink accumulation and detecting ICL repair defects in Fanconi anemia patient cells. Nucleic Acids Research. 51(15). 7988–8004. 3 indexed citations
4.
Guervilly, Jean-Hugues, et al.. (2023). Beyond current treatment of Fanconi Anemia: What do advances in cell and gene-based approaches offer?. Blood Reviews. 60. 101094–101094. 5 indexed citations
5.
Martínez‐López, Alicia, Christophe Lachaud, Miguel Blanquer, et al.. (2023). ZAKα / P38 kinase signaling pathway regulates hematopoiesis by activating the NLRP1 inflammasome. EMBO Molecular Medicine. 15(10). e18142–e18142. 8 indexed citations
6.
Pérez‐Oliva, Ana B., Dmitri Churikov, Joshua Peter, et al.. (2021). UFMylation of MRE11 is essential for telomere length maintenance and hematopoietic stem cell survival. Science Advances. 7(39). eabc7371–eabc7371. 37 indexed citations
7.
Lachaud, Christophe, Pablo Mesa-del-Castillo, María Luz Cayuela, et al.. (2020). Zebrafish Models to Study Inflammasome-Mediated Regulation of Hematopoiesis. Trends in Immunology. 41(12). 1116–1127. 12 indexed citations
8.
Tyrkalska, Sylwia D., Ana B. Pérez‐Oliva, Francisca Alcaraz‐Pérez, et al.. (2019). Inflammasome Regulates Hematopoiesis through Cleavage of the Master Erythroid Transcription Factor GATA1. Immunity. 51(1). 50–63.e5. 63 indexed citations
9.
Feeney, Laura, Iván Muñoz, Christophe Lachaud, et al.. (2017). RPA-Mediated Recruitment of the E3 Ligase RFWD3 Is Vital for Interstrand Crosslink Repair and Human Health. Molecular Cell. 66(5). 610–621.e4. 60 indexed citations
10.
Lachaud, Christophe, Meghan M. Slean, Francesco Marchesi, et al.. (2016). Karyomegalic interstitial nephritis and DNA damage-induced polyploidy in Fan1 nuclease-defective knock-in mice. Genes & Development. 30(6). 639–644. 31 indexed citations
11.
Lachaud, Christophe & John Rouse. (2016). A route to new cancer therapies: the FA pathway is essential in BRCA1- or BRCA2-deficient cells. Nature Structural & Molecular Biology. 23(8). 701–703. 2 indexed citations
12.
Rojas‐Fernández, Alejandro, Lina Herhaus, Thomas Macartney, et al.. (2015). Rapid generation of endogenously driven transcriptional reporters in cells through CRISPR/Cas9. Scientific Reports. 5(1). 9811–9811. 29 indexed citations
13.
Muñoz, Iván, Piotr Szyniarowski, Rachel Toth, John Rouse, & Christophe Lachaud. (2014). Improved Genome Editing in Human Cell Lines Using the CRISPR Method. PLoS ONE. 9(10). e109752–e109752. 40 indexed citations
14.
Lachaud, Christophe, Dennis Castor, Iván Muñoz, et al.. (2014). Distinct functional roles for the SLX4 ubiquitin-binding UBZ domains mutated in Fanconi anemia. Journal of Cell Science. 127(Pt 13). 2811–7. 41 indexed citations
15.
Pérez‐Oliva, Ana B., Christophe Lachaud, Piotr Szyniarowski, et al.. (2014). USP 45 deubiquitylase controls ERCC 1– XPF endonuclease‐mediated DNA damage responses. The EMBO Journal. 34(3). 326–343. 41 indexed citations
16.
Castor, Dennis, Nidhi Nair, Anne‐Cécile Déclais, et al.. (2013). Cooperative Control of Holliday Junction Resolution and DNA Repair by the SLX1 and MUS81-EME1 Nucleases. Molecular Cell. 52(2). 221–233. 117 indexed citations
17.
Lachaud, Christophe, Patrice Thuleau, Sabine Grat, et al.. (2012). 14-3-3-Regulated Ca2+-dependent protein kinase CPK3 is required for sphingolipid-induced cell death in Arabidopsis. Cell Death and Differentiation. 20(2). 209–217. 67 indexed citations
18.
Lachaud, Christophe, et al.. (2012). DVC1 (C1orf124) recruits the p97 protein segregase to sites of DNA damage. Nature Structural & Molecular Biology. 19(11). 1093–1100. 117 indexed citations
19.
Lachaud, Christophe, Valérie Cotelle, Christian Brière, et al.. (2011). Nitric oxide production is not required for dihydrosphingosine-induced cell death in tobacco BY-2 cells. Plant Signaling & Behavior. 6(5). 736–739. 12 indexed citations
20.
Lachaud, Christophe, Valérie Cotelle, Patrice Thuleau, et al.. (2009). Nuclear calcium controls the apoptotic-like cell death induced by d-erythro-sphinganine in tobacco cells. Cell Calcium. 47(1). 92–100. 67 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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