Sophie Lebon

2.9k total citations · 1 hit paper
40 papers, 2.0k citations indexed

About

Sophie Lebon is a scholar working on Molecular Biology, Clinical Biochemistry and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Sophie Lebon has authored 40 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 16 papers in Clinical Biochemistry and 7 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Sophie Lebon's work include Mitochondrial Function and Pathology (18 papers), Metabolism and Genetic Disorders (16 papers) and ATP Synthase and ATPases Research (9 papers). Sophie Lebon is often cited by papers focused on Mitochondrial Function and Pathology (18 papers), Metabolism and Genetic Disorders (16 papers) and ATP Synthase and ATPases Research (9 papers). Sophie Lebon collaborates with scholars based in France, United Kingdom and Italy. Sophie Lebon's co-authors include Pierre Gressèns, Pierre Rustin, Tifenn Le Charpentier, Vibol Chhor, Vincent Degos, Bobbi Fleiss, Henrik Hagberg, Agnès Rötig, Étienne Jacotot and Julien Josserand and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Investigation and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Sophie Lebon

40 papers receiving 2.0k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Characterization of phenotype markers and neuronotoxic potential of polarised primary microglia in vitro

2013 510 citations Vibol Chhor, Tifenn Le Charpentier et al. Brain Behavior and Immunity profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Sophie Lebon France	24	1.0k	499	489	252	223	40	2.0k
Giuseppe Scalabrino Italy	27	1.0k 1.0×	164 0.3×	268 0.5×	53 0.2×	134 0.6×	74	1.8k
Marcelle Bergeron United States	19	811 0.8×	76 0.2×	226 0.5×	95 0.4×	241 1.1×	26	1.9k
Catherine I. Rousset France	20	472 0.5×	70 0.1×	213 0.4×	153 0.6×	727 3.3×	26	1.5k
Atsushi Nishiyori Japan	18	348 0.3×	153 0.3×	351 0.7×	317 1.3×	65 0.3×	48	1.3k
Seung Kyoon Woo United States	28	1.1k 1.1×	74 0.1×	190 0.4×	133 0.5×	449 2.0×	41	2.5k
Robert Surtees United Kingdom	23	848 0.8×	757 1.5×	133 0.3×	72 0.3×	249 1.1×	45	2.2k
Leonardo Cavone Italy	22	580 0.6×	85 0.2×	189 0.4×	186 0.7×	41 0.2×	31	1.3k
Ajaib S. Paintlia United States	21	510 0.5×	48 0.1×	262 0.5×	327 1.3×	122 0.5×	29	1.3k
Chi‐un Choe Germany	20	470 0.5×	113 0.2×	755 1.5×	406 1.6×	47 0.2×	58	2.0k
Marco Pedrazzi Italy	20	578 0.6×	556 1.1×	284 0.6×	409 1.6×	24 0.1×	51	1.5k

Countries citing papers authored by Sophie Lebon

Since Specialization

Citations

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

Fields of papers citing papers by Sophie Lebon

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sophie Lebon

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

All Works

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20 of 20 papers shown

Boccazzi, Marta, Giulia Macchiarulo, Sophie Lebon, et al.. (2023). G protein-coupled receptor 17 is regulated by WNT pathway during oligodendrocyte precursor cell differentiation. Neurobiology of Disease. 187. 106315–106315. 9 indexed citations

Ghouzzi, Vincent El, F. Bianchi, Ivan Molineris, et al.. (2016). ZIKA virus elicits P53 activation and genotoxic stress in human neural progenitors similar to mutations involved in severe forms of genetic microcephaly and p53. Cell Death and Disease. 7(10). e2440–e2440. 101 indexed citations

Dupuis, Nina, Andréy Mazarati, Béatrice Desnous, et al.. (2016). Pro-epileptogenic effects of viral-like inflammation in both mature and immature brains. Journal of Neuroinflammation. 13(1). 307–307. 19 indexed citations

Moretti, Raffaella, Vibol Chhor, Silvana De Lucia, et al.. (2016). Contribution of mast cells to injury mechanisms in a mouse model of pediatric traumatic brain injury. Journal of Neuroscience Research. 94(12). 1546–1560. 25 indexed citations

Fleiss, Bobbi, Vibol Chhor, Sophie Lebon, et al.. (2015). The Anti-Inflammatory Effects of the Small Molecule Pifithrin-µ on BV2 Microglia. Developmental Neuroscience. 37(4-5). 363–375. 12 indexed citations

Chhor, Vibol, Tifenn Le Charpentier, Sophie Lebon, et al.. (2013). Characterization of phenotype markers and neuronotoxic potential of polarised primary microglia in vitro. Brain Behavior and Immunity. 32. 70–85. 510 indexed citations breakdown →

Bayot, Aurélien, Sacha Reichman, Sophie Lebon, et al.. (2013). Cis-silencing of PIP5K1B evidenced in Friedreich's ataxia patient cells results in cytoskeleton anomalies. Human Molecular Genetics. 22(14). 2894–2904. 23 indexed citations

Baulny, Hélène Ogier de, Renata Kozyraki, Sandrine Passemard, et al.. (2012). How can cobalamin injections be spaced in long-term therapy for inborn errors of vitamin B12 absorption?. Molecular Genetics and Metabolism. 107(1-2). 66–71. 15 indexed citations

Perrin, Laurence, Odile Fenneteau, Brice Ilharreborde, et al.. (2012). A new lysosomal storage disorder resembling Morquio syndrome in sibs. European Journal of Medical Genetics. 55(3). 157–162. 1 indexed citations

10.

Dupuis, Nina, Sophie Lebon, Manoj Kumar, et al.. (2012). A NovelRAB33BMutation in Smith-McCort Dysplasia. Human Mutation. 34(2). 283–286. 27 indexed citations

11.

Carlsson, Ylva, Leslie Schwendimann, Regina Vontell, et al.. (2011). Genetic inhibition of caspase‐2 reduces hypoxic‐ischemic and excitotoxic neonatal brain injury. Annals of Neurology. 70(5). 781–789. 49 indexed citations

12.

Passemard, Sandrine, Vincent El Ghouzzi, Catherine Verney, et al.. (2011). VIP blockade leads to microcephaly in mice via disruption of Mcph1-Chk1 signaling. Journal of Clinical Investigation. 121(8). 3072–3087. 22 indexed citations

13.

Bénit, Paule, Sophie Lebon, & Pierre Rustin. (2008). Respiratory-chain diseases related to complex III deficiency. Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1793(1). 181–185. 74 indexed citations

14.

Lebon, Sophie, Diana Rodriguez, Delphine Bridoux, et al.. (2007). A novel mutation in the human complex I NDUFS7 subunit associated with Leigh syndrome. Molecular Genetics and Metabolism. 90(4). 379–382. 38 indexed citations

15.

Rötig, Agnès, Sophie Lebon, Elena Zinovieva, et al.. (2004). Molecular diagnostics of mitochondrial disorders. Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1659(2-3). 129–135. 28 indexed citations

16.

Gigarel, Nadine, Pierre F. Ray, Philippe Burlet, et al.. (2004). Single cell quantification of the 8993T>G NARP mitochondrial DNA mutation by fluorescent PCR. Molecular Genetics and Metabolism. 84(3). 289–292. 23 indexed citations

17.

Bénit, Paule, Julie Steffann, Sophie Lebon, et al.. (2003). Genotyping microsatellite DNA markers at putative disease loci in inbred/multiplex families with respiratory chain complex I deficiency allows rapid identification of a novel nonsense mutation (IVS1nt −1) in the NDUFS4 gene in Leigh syndrome. Human Genetics. 112(5-6). 563–566. 53 indexed citations

18.

Guéry, Benoît, Gabriel Choukroun, Laure‐Hélène Noël, et al.. (2003). The Spectrum of Systemic Involvement in Adults Presenting with Renal Lesion and Mitochondrial tRNA(Leu) Gene Mutation. Journal of the American Society of Nephrology. 14(8). 2099–2108. 86 indexed citations

19.

Lebon, Sophie, et al.. (2003). Recurrent de novo mitochondrial DNA mutations in respiratory chain deficiency. Journal of Medical Genetics. 40(12). 896–899. 107 indexed citations

20.

Brivet, M., Guy Touati, Pierre Rustin, et al.. (2003). A deletion in the human QP-C gene causes a complex III deficiency resulting in hypoglycaemia and lactic acidosis. Human Genetics. 113(2). 118–122. 98 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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