Mathilde Lefebvre

1.8k total citations
18 papers, 400 citations indexed

About

Mathilde Lefebvre is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Mathilde Lefebvre has authored 18 papers receiving a total of 400 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 4 papers in Genetics and 3 papers in Surgery. Recurrent topics in Mathilde Lefebvre's work include Mitochondrial Function and Pathology (2 papers), Prenatal Screening and Diagnostics (2 papers) and Chromatin Remodeling and Cancer (2 papers). Mathilde Lefebvre is often cited by papers focused on Mitochondrial Function and Pathology (2 papers), Prenatal Screening and Diagnostics (2 papers) and Chromatin Remodeling and Cancer (2 papers). Mathilde Lefebvre collaborates with scholars based in France, Italy and Belgium. Mathilde Lefebvre's co-authors include Judith St‐Onge, Philippe Lachaume, Yannis Duffourd, Patrick Callier, Patrick Vernet, Laurence Faivre, Frédéric Morel, Julien Thévenon, Géraldine Farge and Amandine Moretton and has published in prestigious journals such as PLoS ONE, FEBS Letters and Science Advances.

In The Last Decade

Mathilde Lefebvre

18 papers receiving 396 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mathilde Lefebvre France 8 207 136 67 43 36 18 400
Renius Owen United States 12 130 0.6× 139 1.0× 37 0.6× 26 0.6× 26 0.7× 23 329
Makiko Yamada Japan 13 236 1.1× 52 0.4× 26 0.4× 53 1.2× 46 1.3× 26 401
Hideo Sasai Japan 13 220 1.1× 75 0.6× 179 2.7× 32 0.7× 51 1.4× 51 432
Mitsuo Toyoshima Japan 9 78 0.4× 43 0.3× 43 0.6× 62 1.4× 23 0.6× 24 253
Stephanie Lu United States 10 293 1.4× 130 1.0× 24 0.4× 21 0.5× 12 0.3× 15 497
Elizabeth G. Ames United States 11 129 0.6× 39 0.3× 26 0.4× 13 0.3× 33 0.9× 23 291
Gianni Russo Italy 15 340 1.6× 193 1.4× 40 0.6× 15 0.3× 43 1.2× 29 559
Semra Gürsoy Türkiye 9 85 0.4× 93 0.7× 17 0.3× 10 0.2× 23 0.6× 39 260
Ioana Streață Romania 10 97 0.5× 64 0.5× 11 0.2× 15 0.3× 45 1.3× 54 296
Yunhai Dai China 10 125 0.6× 22 0.2× 23 0.3× 58 1.3× 18 0.5× 27 385

Countries citing papers authored by Mathilde Lefebvre

Since Specialization
Citations

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

Fields of papers citing papers by Mathilde Lefebvre

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mathilde Lefebvre

This figure shows the co-authorship network connecting the top 25 collaborators of Mathilde Lefebvre. A scholar is included among the top collaborators of Mathilde Lefebvre 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 Mathilde Lefebvre. Mathilde Lefebvre is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

18 of 18 papers shown
1.
Lefebvre, Mathilde, Caterina Zanus, Irene Bruno, et al.. (2024). In-Depth Phenotyping of PIGW-Related Disease and Its Role in 17q12 Genomic Disorder. Biomolecules. 14(12). 1626–1626. 1 indexed citations
2.
Liu, Tengyuan, Azadeh Saffarian, Jun Komatsu, et al.. (2023). The temporal balance between self-renewal and differentiation of human neural stem cells requires the amyloid precursor protein. Science Advances. 9(24). eadd5002–eadd5002. 7 indexed citations
3.
Lefebvre, Mathilde, A. Gélot, Solveig Heide, et al.. (2023). First reports of fetal SMARCC1 related hydrocephalus. European Journal of Medical Genetics. 66(8). 104797–104797. 1 indexed citations
4.
Lambert, Véronique, Antoine Enfissi, Mathilde Lefebvre, et al.. (2022). Tonate Virus and Fetal Abnormalities, French Guiana, 2019. Emerging infectious diseases. 28(2). 445–448. 7 indexed citations
5.
Gilbert, Alice, Armelle Rancillac, Audrey Chagnot, et al.. (2022). In mice and humans, brain microvascular contractility matures postnatally. Brain Structure and Function. 228(2). 475–492. 7 indexed citations
6.
Schnuriger, Aurélie, et al.. (2021). Description of a late miscarriage case at 16 Weeks of Gestation associated with a SARS-CoV-2 infection. Journal of Gynecology Obstetrics and Human Reproduction. 50(3). 102064–102064. 6 indexed citations
7.
Bernard‐Valnet, Raphaël, Xavier Moisset, Nicolas Maubeuge, et al.. (2021). CCR5 Blockade in Inflammatory PML and PML-IRIS Associated With Chronic Inflammatory Diseases' Treatments. Neurology Neuroimmunology & Neuroinflammation. 9(1). 9 indexed citations
8.
Slavotinek, Anne, Mathilde Lefebvre, Anne‐Claire Bréhin, et al.. (2021). Prenatal presentation of multiple anomalies associated with haploinsufficiency for ARID1A. European Journal of Medical Genetics. 65(2). 104407–104407. 8 indexed citations
9.
Lefebvre, Mathilde, Marie Cassart, Lucie Guilbaud, et al.. (2019). Prenatal ultrasonography of autosomal dominant polycystic kidney disease mimicking recessive type: case series. Pediatric Radiology. 49(7). 906–912. 5 indexed citations
10.
Lefebvre, Mathilde, Christine Francannet, Hélène Laurichesse, et al.. (2018). Extending the ALDH18A1 clinical spectrum to severe autosomal recessive fetal cutis laxa with corpus callosum agenesis. American Journal of Medical Genetics Part A. 176(11). 2509–2512. 6 indexed citations
11.
Tonni, Gabriele, Gianpaolo Grisolia, Federico Prefumo, et al.. (2018). TRAP Sequence in Monochorionic/Monoamniotic (MC/MA) Discordant Twins: Two Cases Treated with Fetoscopic Laser Surgery. Fetal and Pediatric Pathology. 37(6). 433–447. 7 indexed citations
12.
Moretton, Amandine, Frédéric Morel, Bertil Macao, et al.. (2017). Selective mitochondrial DNA degradation following double-strand breaks. PLoS ONE. 12(4). e0176795–e0176795. 103 indexed citations
13.
Moretton, Amandine, Mathilde Lefebvre, Serge Alziari, et al.. (2016). DNA maintenance following bleomycin-induced strand breaks does not require poly(ADP-ribosyl)ation activation in Drosophila S2 cells. DNA repair. 48. 8–16. 1 indexed citations
14.
Lefebvre, Mathilde, Yannis Duffourd, Charlotte Pöe, et al.. (2016). Autosomal recessive variations of TBX6, from congenital scoliosis to spondylocostal dysostosis. Clinical Genetics. 91(6). 908–912. 26 indexed citations
15.
Thévenon, Julien, Yannis Duffourd, Alice Masurel‐Paulet, et al.. (2016). Diagnostic odyssey in severe neurodevelopmental disorders: toward clinical whole‐exome sequencing as a first‐line diagnostic test. Clinical Genetics. 89(6). 700–707. 138 indexed citations
16.
Batard, Éric, Mathilde Lefebvre, Guillaume Ghislain Aubin, Nathalie Caroff, & Stéphane Corvec. (2015). High prevalence of cross-resistance to fluoroquinolone and cotrimoxazole in tetracycline-resistant Escherichia coli human clinical isolates. Journal of Chemotherapy. 28(6). 510–512. 7 indexed citations
17.
Lefebvre, Mathilde, Sylvain Caillat, Frédéric Morel, et al.. (2014). A comprehensive approach to determining BER capacities and their change with aging in Drosophila melanogaster mitochondria by oligonucleotide microarray. FEBS Letters. 588(9). 1673–1679. 8 indexed citations
18.
Lefebvre, Mathilde, Cédric Jacqueline, Gilles Amador, et al.. (2010). Efficacy of daptomycin combined with rifampicin for the treatment of experimental meticillin-resistant Staphylococcus aureus (MRSA) acute osteomyelitis. International Journal of Antimicrobial Agents. 36(6). 542–544. 53 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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