Caroline Lefèvre

2.2k total citations
12 papers, 1.3k citations indexed

About

Caroline Lefèvre is a scholar working on Molecular Biology, Cell Biology and Epidemiology. According to data from OpenAlex, Caroline Lefèvre has authored 12 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 5 papers in Cell Biology and 2 papers in Epidemiology. Recurrent topics in Caroline Lefèvre's work include Skin and Cellular Biology Research (5 papers), Protein Kinase Regulation and GTPase Signaling (3 papers) and Wnt/β-catenin signaling in development and cancer (3 papers). Caroline Lefèvre is often cited by papers focused on Skin and Cellular Biology Research (5 papers), Protein Kinase Regulation and GTPase Signaling (3 papers) and Wnt/β-catenin signaling in development and cancer (3 papers). Caroline Lefèvre collaborates with scholars based in France, Algeria and Morocco. Caroline Lefèvre's co-authors include Judith Fischer, Mark Lathrop, B. Bouadjar, Florence Jobard, Pascal Laforêt, Anne Nègre‐Salvayre, Jean‐Marie Mussini, Robert Salvayre, Jean-François Prud’homme and Éva Morava and has published in prestigious journals such as Nature Genetics, Scientific Reports and The American Journal of Human Genetics.

In The Last Decade

Caroline Lefèvre

10 papers receiving 1.3k citations

Peers

Caroline Lefèvre
Maria Matzaris Australia
John E. Pawlowski United States
Terumi Kambe Japan
Abigail S. Krall United States
Hugo B. Sanchez United States
Myron E. Hinsdale United States
Shanmugam Panneer Selvam United States
Andrey Frolov United States
George Talbott United States
Jyoti Athanikar United States
Maria Matzaris Australia
Caroline Lefèvre
Citations per year, relative to Caroline Lefèvre Caroline Lefèvre (= 1×) peers Maria Matzaris

Countries citing papers authored by Caroline Lefèvre

Since Specialization
Citations

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

Fields of papers citing papers by Caroline Lefèvre

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Caroline Lefèvre

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

All Works

12 of 12 papers shown
1.
Lefèvre, Caroline, et al.. (2025). Key domains involved in the interaction and assembly of the HCMV terminase complex. Scientific Reports. 15(1). 44943–44943.
2.
Flores, T, et al.. (2025). Deciphering letermovir's mode of action and resistance mutation effects. Antiviral Research. 244. 106289–106289.
3.
Colson, Cindy, Évelyne Aubry, Maryse Cartigny, et al.. (2016). SF1 and spleen development: new heterozygous mutation, literature review and consequences for NR5A1‐mutated patient's management. Clinical Genetics. 92(1). 99–103. 16 indexed citations
4.
Lesueur, Fabienne, Caroline Lefèvre, Cristina Has, et al.. (2007). Confirmation of Psoriasis Susceptibility Loci on Chromosome 6p21 and 20p13 in French Families. Journal of Investigative Dermatology. 127(6). 1403–1409. 20 indexed citations
5.
Lefèvre, Caroline, B. Bouadjar, Gianluca Tadini, et al.. (2006). Mutations in a new cytochrome P450 gene in lamellar ichthyosis type 3. Human Molecular Genetics. 15(5). 767–776. 148 indexed citations
6.
Lesueur, Fabienne, B. Bouadjar, Caroline Lefèvre, et al.. (2006). Novel Mutations in ALOX12B in Patients with Autosomal Recessive Congenital Ichthyosis and Evidence for Genetic Heterogeneity on Chromosome 17p13. Journal of Investigative Dermatology. 127(4). 829–834. 33 indexed citations
7.
Fischer, Judith, Caroline Lefèvre, Éva Morava, et al.. (2006). The gene encoding adipose triglyceride lipase (PNPLA2) is mutated in neutral lipid storage disease with myopathy. Nature Genetics. 39(1). 28–30. 357 indexed citations
8.
Lefèvre, Caroline, B. Bouadjar, Ayşen Karaduman, et al.. (2004). Mutations in ichthyin a new gene on chromosome 5q33 in a new form of autosomal recessive congenital ichthyosis. Human Molecular Genetics. 13(20). 2473–2482. 126 indexed citations
9.
10.
Lefèvre, Caroline. (2003). Mutations in the transporter ABCA12 are associated with lamellar ichthyosis type 2. Human Molecular Genetics. 12(18). 2369–2378. 202 indexed citations
11.
Lefèvre, Caroline, Florence Jobard, F. Caux, et al.. (2001). Mutations in CGI-58, the Gene Encoding a New Protein of the Esterase/Lipase/Thioesterase Subfamily, in Chanarin-Dorfman Syndrome. The American Journal of Human Genetics. 69(5). 1002–1012. 346 indexed citations
12.
Blanchet‐Bardon, C, B. Bouadjar, J.‐F. Stalder, et al.. (2001). Novel Point Mutations, Deletions, and Polymorphisms in the Cathepsin C Gene in Nine Families from Europe and North Africa with Papillon–Lefèvre Syndrome. Journal of Investigative Dermatology. 117(6). 1657–1661. 30 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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