S. Lefebvre

1.2k total citations
16 papers, 882 citations indexed

About

S. Lefebvre is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, S. Lefebvre has authored 16 papers receiving a total of 882 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 9 papers in Genetics and 3 papers in Surgery. Recurrent topics in S. Lefebvre's work include Neurogenetic and Muscular Disorders Research (9 papers), RNA modifications and cancer (7 papers) and Nicotinic Acetylcholine Receptors Study (5 papers). S. Lefebvre is often cited by papers focused on Neurogenetic and Muscular Disorders Research (9 papers), RNA modifications and cancer (7 papers) and Nicotinic Acetylcholine Receptors Study (5 papers). S. Lefebvre collaborates with scholars based in France, United States and Netherlands. S. Lefebvre's co-authors include P Burlet, Arnold Münnich, Olivier Clermont, Judith Melki, Lydie Bürglen, Solange Bertrandy, Céline Huber, Pierre‐Jean Corringer, Louis Viollet and Ingrid Zwaenepoel and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Journal of Clinical Investigation.

In The Last Decade

S. Lefebvre

16 papers receiving 859 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
S. Lefebvre France	12	720	531	198	85	57	16	882
Bénédicte Desforges France	17	665 0.9×	108 0.2×	53 0.3×	77 0.9×	19 0.3×	33	948
Michael J. Francis United Kingdom	12	246 0.3×	136 0.3×	35 0.2×	49 0.6×	27 0.5×	14	495
Mária Nagy United States	18	515 0.7×	76 0.1×	37 0.2×	64 0.8×	62 1.1×	30	754
Mihaela‐Rita Mihailescu United States	18	781 1.1×	55 0.1×	9 0.0×	25 0.3×	215 3.8×	34	927
Zhushan Zhang United States	11	255 0.4×	19 0.0×	59 0.3×	67 0.8×	178 3.1×	16	708
Yasuo Shikamoto Japan	9	264 0.4×	37 0.1×	15 0.1×	64 0.8×	151 2.6×	17	593
Samuel J. Seguin Italy	6	838 1.2×	73 0.1×	11 0.1×	150 1.8×	14 0.2×	6	1.1k
Fenfen Wu United States	16	993 1.4×	16 0.0×	66 0.3×	298 3.5×	46 0.8×	32	1.2k
Márta Szaszák Germany	14	428 0.6×	11 0.0×	53 0.3×	136 1.6×	24 0.4×	20	685
Moniek Riemersma Netherlands	10	489 0.7×	21 0.0×	18 0.1×	67 0.8×	90 1.6×	11	613

Countries citing papers authored by S. Lefebvre

Since Specialization

Citations

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

Fields of papers citing papers by S. Lefebvre

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of S. Lefebvre

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

All Works

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16 of 16 papers shown

Lefebvre, S., et al.. (2024). Bidirectional ATP-driven transport of cobalamin by the mycobacterial ABC transporter BacA. Nature Communications. 15(1). 2626–2626. 7 indexed citations

Lefebvre, S., et al.. (2023). Illumination of a progressive allosteric mechanism mediating the glycine receptor activation. Nature Communications. 14(1). 795–795. 9 indexed citations

Lefebvre, S., et al.. (2021). Mutational analysis to explore long-range allosteric couplings involved in a pentameric channel receptor pre-activation and activation. eLife. 10. 9 indexed citations

Lefebvre, S. & Catherine Sarret. (2020). Pathogenesis and therapeutic targets in spinal muscular atrophy (SMA). Archives de Pédiatrie. 27(7). 7S3–7S8. 14 indexed citations

Ruan, Yi, Kevin S. Kao, S. Lefebvre, et al.. (2018). Structural titration of receptor ion channel GLIC gating by HS-AFM. Proceedings of the National Academy of Sciences. 115(41). 10333–10338. 36 indexed citations

Hassaı̈ne, Ghérici, Emmanuelle Neumann, Anders A. Jensen, et al.. (2018). Conformational transitions of the serotonin 5-HT3 receptor. Nature. 563(7730). 275–279. 113 indexed citations

Menny, Anaïs, S. Lefebvre, Philipp A. M. Schmidpeter, et al.. (2017). Identification of a pre-active conformation of a pentameric channel receptor. eLife. 6. 31 indexed citations

Maystadt, Isabelle, Mohammed Zarhrate, B. Estournet, et al.. (2006). A gene for an autosomal recessive lower motor neuron disease with childhood onset maps to 1p36. Neurology. 67(1). 120–124. 8 indexed citations

Lefebvre, S.. (2002). A novel association of the SMN protein with two major non-ribosomal nucleolar proteins and its implication in spinal muscular atrophy. Human Molecular Genetics. 11(9). 1017–1027. 43 indexed citations

10.

Bertrandy, Solange, P Burlet, Olivier Clermont, et al.. (1999). The RNA-Binding Properties of SMN: Deletion Analysis of the Zebrafish Orthologue Defines Domains Conserved in Evolution. Human Molecular Genetics. 8(5). 775–782. 77 indexed citations

11.

Lefebvre, S.. (1998). The role of the SMN gene in proximal spinal muscular atrophy. Human Molecular Genetics. 7(10). 1531–1536. 120 indexed citations

12.

Burlet, P, Céline Huber, Solange Bertrandy, et al.. (1998). The distribution of SMN protein complex in human fetal tissues and its alteration in spinal muscular atrophy. Human Molecular Genetics. 7(12). 1927–1933. 122 indexed citations

13.

Bürglen, Lydie, Thierry Seroz, Pierre Miniou, et al.. (1997). The gene encoding p44, a subunit of the transcription factor TFIIH, is involved in large-scale deletions associated with Werdnig-Hoffmann disease.. PubMed. 60(1). 72–9. 91 indexed citations

14.

Bürglen, Lydie, Jeanne Amiel, Louis Viollet, et al.. (1996). Survival motor neuron gene deletion in the arthrogryposis multiplex congenita-spinal muscular atrophy association.. Journal of Clinical Investigation. 98(5). 1130–1132. 56 indexed citations

15.

Burlet, P, Lydie Bürglen, Olivier Clermont, et al.. (1996). Large scale deletions of the 5q13 region are specific to Werdnig-Hoffmann disease.. Journal of Medical Genetics. 33(4). 281–283. 79 indexed citations

16.

Bureau, Jean‐François, Xavier Montagutelli, S. Lefebvre, et al.. (1992). The interaction of two groups of murine genes determines the persistence of Theiler's virus in the central nervous system. Journal of Virology. 66(8). 4698–4704. 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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