Emmanuelle Martini

2.5k total citations
25 papers, 1.8k citations indexed

About

Emmanuelle Martini is a scholar working on Molecular Biology, Oncology and Pathology and Forensic Medicine. According to data from OpenAlex, Emmanuelle Martini has authored 25 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 5 papers in Oncology and 2 papers in Pathology and Forensic Medicine. Recurrent topics in Emmanuelle Martini's work include DNA Repair Mechanisms (20 papers), Genomics and Chromatin Dynamics (9 papers) and CRISPR and Genetic Engineering (8 papers). Emmanuelle Martini is often cited by papers focused on DNA Repair Mechanisms (20 papers), Genomics and Chromatin Dynamics (9 papers) and CRISPR and Genetic Engineering (8 papers). Emmanuelle Martini collaborates with scholars based in France, United States and Germany. Emmanuelle Martini's co-authors include Geneviève Almouzni, Scott Keeney, Neil Hunter, Robert L. Diaz, Christine Scamps, Marc Lipinski, Dominique Ray-Gallet, Jean‐Pierre Quivy, Paul D. Kaufman and Pierre-Henri L. Gaillard and has published in prestigious journals such as Nature, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Emmanuelle Martini

25 papers receiving 1.8k citations

Peers

Emmanuelle Martini
M. Mitchell Smith United States
Nicola Reynolds United Kingdom
Nicolas Lacoste France
Malik Lutzmann France
Olivier Ganier France
Nabieh Ayoub Israel
Lisa Kadyk United States
Simona Giunta Italy
Olga V. Iarovaia Russia
Prabha Sarangi United States
M. Mitchell Smith United States
Emmanuelle Martini
Citations per year, relative to Emmanuelle Martini Emmanuelle Martini (= 1×) peers M. Mitchell Smith

Countries citing papers authored by Emmanuelle Martini

Since Specialization
Citations

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

Fields of papers citing papers by Emmanuelle Martini

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Emmanuelle Martini

This figure shows the co-authorship network connecting the top 25 collaborators of Emmanuelle Martini. A scholar is included among the top collaborators of Emmanuelle Martini 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 Emmanuelle Martini. Emmanuelle Martini 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.
Guerquin, Marie-Justine, Antoine D. Rolland, Sébastien Messiaen, et al.. (2025). Genome-wide transcriptional silencing and mRNA stabilization allow the coordinated expression of the meiotic program in mice. Nucleic Acids Research. 53(5). 1 indexed citations
2.
Matos‐Rodrigues, Gabriel, Vilma Barroca, Elodie Dardillac, et al.. (2023). In vivo reduction of RAD51 ‐mediated homologous recombination triggers aging but impairs oncogenesis. The EMBO Journal. 42(20). e110844–e110844. 7 indexed citations
3.
Mabondzo, Aloı̈se, Rania Harati, Anne-Cécile Guyot, et al.. (2023). Dodecyl creatine ester improves cognitive function and identifies key protein drivers including KIF1A and PLCB1 in a mouse model of creatine transporter deficiency. Frontiers in Molecular Neuroscience. 16. 1118707–1118707. 6 indexed citations
4.
Moison, Delphine, Sébastien Messiaen, Emmanuelle Martini, et al.. (2022). Foetal exposure to the bisphenols BADGE and BPAF impairs meiosis through DNA oxidation in mouse ovaries. Environmental Pollution. 317. 120791–120791. 15 indexed citations
5.
Barroca, Vilma, Sébastien Messiaen, Delphine Moison, et al.. (2021). Mouse model of radiation-induced premature ovarian insufficiency reveals compromised oocyte quality: implications for fertility preservation. Reproductive BioMedicine Online. 43(5). 799–809. 13 indexed citations
6.
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
7.
Dupaigne, P., Cécile Ducrot, Clotilde Duquenne, et al.. (2021). The meiosis-specific MEIOB–SPATA22 complex cooperates with RPA to form a compacted mixed MEIOB/SPATA22/RPA/ssDNA complex. DNA repair. 102. 103097–103097. 15 indexed citations
8.
Matos‐Rodrigues, Gabriel, Josée Guirouilh‐Barbat, Emmanuelle Martini, & Bernard S. López. (2021). Homologous recombination, cancer and the ‘RAD51 paradox’. NAR Cancer. 3(2). zcab016–zcab016. 29 indexed citations
9.
Barroca, Vilma, Nathalie Lailler, Gabriel Livéra, et al.. (2020). shani mutation in mouse affects splicing of Spata22 and leads to impaired meiotic recombination. Chromosoma. 129(2). 161–179. 6 indexed citations
10.
Zhang, Jingjing, Manickam Gurusaran, Yasuhiro Fujiwara, et al.. (2020). The BRCA2-MEILB2-BRME1 complex governs meiotic recombination and impairs the mitotic BRCA2-RAD51 function in cancer cells. Nature Communications. 11(1). 2055–2055. 41 indexed citations
11.
Caburet, Sandrine, Anne‐Laure Todeschini, Emmanuelle Martini, et al.. (2019). A truncating MEIOB mutation responsible for familial primary ovarian insufficiency abolishes its interaction with its partner SPATA22 and their recruitment to DNA double-strand breaks. EBioMedicine. 42. 524–531. 51 indexed citations
12.
Abby, Emilie, Sophie Tourpin, Katrin Daniel, et al.. (2016). Implementation of meiosis prophase I programme requires a conserved retinoid-independent stabilizer of meiotic transcripts. Nature Communications. 7(1). 10324–10324. 92 indexed citations
13.
Abby, Emilie, et al.. (2015). RPA homologs and ssDNA processing during meiotic recombination. Chromosoma. 125(2). 265–276. 56 indexed citations
14.
Souquet, Benoît, Emilie Abby, Roxane Hervé, et al.. (2013). MEIOB Targets Single-Strand DNA and Is Necessary for Meiotic Recombination. PLoS Genetics. 9(9). e1003784–e1003784. 91 indexed citations
15.
Costelloe, Thomas, Nozomi Tomimatsu, Bipasha Mukherjee, et al.. (2012). The yeast Fun30 and human SMARCAD1 chromatin remodellers promote DNA end resection. Nature. 489(7417). 581–584. 212 indexed citations
16.
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
17.
Martini, Emmanuelle, Robert L. Diaz, Neil Hunter, & Scott Keeney. (2006). Crossover Homeostasis in Yeast Meiosis. Cell. 126(2). 285–295. 260 indexed citations
18.
Ray-Gallet, Dominique, Jean‐Pierre Quivy, Christine Scamps, et al.. (2002). HIRA Is Critical for a Nucleosome Assembly Pathway Independent of DNA Synthesis. Molecular Cell. 9(5). 1091–1100. 329 indexed citations
19.
Martini, Emmanuelle & Scott Keeney. (2002). Sex and the Single (Double-Strand) Break. Molecular Cell. 9(4). 700–702. 15 indexed citations
20.
Gaillard, Pierre-Henri L., Emmanuelle Martini, Paul D. Kaufman, et al.. (1996). Chromatin Assembly Coupled to DNA Repair: A New Role for Chromatin Assembly Factor I. Cell. 86(6). 887–896. 283 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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