Sophie Lebon

2.9k citations

40 papers · 2.0k indexed · 1 hit paper · h-index 24

Molecular Biology top 10%
Clinical Biochemistry top 0.5%
Neurology top 2%
Immunology top 10%
Pediatrics, Perinatology and Child Health top 5%

Co-authors: Pierre Gressèns Pierre Rustin Tifenn Le Charpentier Vibol Chhor Vincent Degos Bobbi Fleiss Henrik Hagberg Agnès Rötig
Topics: Mitochondrial Function and Pathology (18 papers)Metabolism and Genetic Disorders (16 papers)ATP Synthase and ATPases Research (9 papers)
Cited by: Clinical Biochemistry Neurology Developmental Neuroscience
Journals: Proceedings of the National Academy of Sciences Journal of Clinical Investigation The Journal of Clinical Endocrinology & Metabolism
Partner nations: France United Kingdom Italy

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

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

#	Work	Indexed citations
1	G protein-coupled receptor 17 is regulated by WNT pathway during oligodendrocyte precursor cell differentiation 2023 ·Neurobiology of Disease ·Marta Boccazzi,Giulia Macchiarulo,Sophie Lebon,(unknown),Tifenn Le Charpentier,Valérie Faivre,Jennifer Hua,Davide Marangon,Davide Lecca,Marta Fumagalli,Shyamala Mani,Maria P. Abbracchio,Pierre Gressèns,Anne‐Laure Schang,Juliette Van Steenwinckel	9
2	ZIKA virus elicits P53 activation and genotoxic stress in human neural progenitors similar to mutations involved in severe forms of genetic microcephaly and p53 2016 ·Cell Death and Disease ·Vincent El Ghouzzi,F. Bianchi,Ivan Molineris,Bryan C. Mounce,Gaia Berto,Malgorzata Rak,Sophie Lebon,Laëtitia Aubry,Chiara Tocco,Marta Gai,(unknown),Francesco Sgrò,Gianmarco Pallavicini,Etienne Simon‐Lorière,Sandrine Passemard,Marco Vignuzzi,Pierre Gressèns,Ferdinando Di Cunto	101
3	Pro-epileptogenic effects of viral-like inflammation in both mature and immature brains 2016 ·Journal of Neuroinflammation ·Nina Dupuis,Andréy Mazarati,Béatrice Desnous,Vibol Chhor,Bobbi Fleiss,Tifenn Le Charpentier,Sophie Lebon,Zsolt Csaba,Pierre Gressèns,Pascal Dournaud,Stéphane Auvin	19
4	The Anti-Inflammatory Effects of the Small Molecule Pifithrin-µ on BV2 Microglia 2015 ·Developmental Neuroscience ·Bobbi Fleiss,Vibol Chhor,(unknown),Sophie Lebon,Henrik Hagberg,Pierre Gressèns,Claire Thornton	12
5	Characterization of phenotype markers and neuronotoxic potential of polarised primary microglia in vitrobreakdown → 2013 ·Brain Behavior and Immunity ·Vibol Chhor,Tifenn Le Charpentier,Sophie Lebon,(unknown),(unknown),Julien Josserand,Vincent Degos,Étienne Jacotot,Henrik Hagberg,Karin Sävman,Carina Mallard,Pierre Gressèns,Bobbi Fleiss	510
6	Cis-silencing of PIP5K1B evidenced in Friedreich's ataxia patient cells results in cytoskeleton anomalies 2013 ·Human Molecular Genetics ·Aurélien Bayot,Sacha Reichman,Sophie Lebon,Zsolt Csaba,Laëtitia Aubry,Ghislaine Sterkers,Isabelle Husson,Malgorzata Rak,Pierre Rustin	23
7	How can cobalamin injections be spaced in long-term therapy for inborn errors of vitamin B12 absorption? 2012 ·Molecular Genetics and Metabolism ·(unknown),Hélène Ogier de Baulny,Renata Kozyraki,Sandrine Passemard,Odile Fenneteau,Sophie Lebon,Odile Rigal,Bettina Mesplès,Karima Yacouben,Stéphane Giraudier,Jean‐François Benoist,Manuel Schiff	15
8	A NovelRAB33BMutation in Smith-McCort Dysplasia 2012 ·Human Mutation ·Nina Dupuis,Sophie Lebon,Manoj Kumar,Séverine Drunat,Luitgard Graul‐Neumann,Pierre Gressèns,Vincent El Ghouzzi	27
9	Genetic inhibition of caspase‐2 reduces hypoxic‐ischemic and excitotoxic neonatal brain injury 2011 ·Annals of Neurology ·Ylva Carlsson,Leslie Schwendimann,Regina Vontell,Catherine I. Rousset,Xiaoyang Wang,Sophie Lebon,Christiane Charriaut‐Marlangue,Veena G. Supramaniam,Henrik Hagberg,Pierre Gressèns,Étienne Jacotot	49
10	VIP blockade leads to microcephaly in mice via disruption of Mcph1-Chk1 signaling 2011 ·Journal of Clinical Investigation ·Sandrine Passemard,Vincent El Ghouzzi,(unknown),Catherine Verney,Guilan Vodjdani,Adrien Lacaud,Sophie Lebon,Marc Laburthe,Patrick Robberecht,Jeannette Nardelli,Shyamala Mani,Alain Verloès,Pierre Gressèns,Vincent Lelièvre	22
11	Respiratory-chain diseases related to complex III deficiency 2008 ·Biochimica et Biophysica Acta (BBA) - Molecular Cell Research ·Paule Bénit,Sophie Lebon,Pierre Rustin	74
12	A novel mutation in the human complex I NDUFS7 subunit associated with Leigh syndrome 2007 ·Molecular Genetics and Metabolism ·Sophie Lebon,Diana Rodriguez,Delphine Bridoux,Amal Zerrad-Saadi,Agnès Rötig,Arnold Münnich,Alain Legrand,Abdelhamid Slama	38
13	Fatal manifestation of a de novo ND5 mutation: Insights into the pathogenetic mechanisms of mtDNA ND5 gene defects 2007 ·Mitochondrion ·Sergey Zhadanov,(unknown),(unknown),Vladislava Gusar,(unknown),Sophie Lebon,(unknown),Theodore G. Schurr	22
14	A novel recurrent mitochondrial DNA mutation in ND3 gene is associated with isolated complex I deficiency causing Leigh syndrome and dystonia 2006 ·American Journal of Medical Genetics Part A ·Emmanuelle Sarzi,Michael D. Brown,Sophie Lebon,Dominique Chrétien,Arnold Münnich,Agnès Rötig,Vincent Procaccio	86
15	Molecular diagnostics of mitochondrial disorders 2004 ·Biochimica et Biophysica Acta (BBA) - Bioenergetics ·Agnès Rötig,Sophie Lebon,Elena Zinovieva,(unknown),Emmanuelle Sarzi,Jean‐Paul Bonnefont,Arnold Münnich	28
16	Genotypes and Clinical Phenotypes in Children with Cytochrome-cOxidase Deficiency 2003 ·Neuropediatrics ·Niklas Darín,(unknown),Sophie Lebon,Pierre Rustin,E Holme,Anders Oldfors,M. Tulinius	27
17	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 2003 ·Human Genetics ·Paule Bénit,Julie Steffann,Sophie Lebon,Dominique Chrétien,Noman Kadhom,Pascale de Lonlay,Alice Goldenberg,Yves Dumez,Marc Dommergues,Pierre Rustin,Arnold Münnich,Agnès Rötig	53
18	The Spectrum of Systemic Involvement in Adults Presenting with Renal Lesion and Mitochondrial tRNA(Leu) Gene Mutation 2003 ·Journal of the American Society of Nephrology ·Benoît Guéry,Gabriel Choukroun,Laure‐Hélène Noël,P. Clavel,Agnès Rötig,Sophie Lebon,Pierre Rustin,Christine Bellané‐Chantelot,B. Mougenot,Jean‐Pierre Grünfeld,Dominique Chauveau	86
19	Recurrent de novo mitochondrial DNA mutations in respiratory chain deficiency 2003 ·Journal of Medical Genetics ·Sophie Lebon,(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown)	107
20	A deletion in the human QP-C gene causes a complex III deficiency resulting in hypoglycaemia and lactic acidosis 2003 ·Human Genetics ·(unknown),M. Brivet,Guy Touati,Pierre Rustin,Sophie Lebon,(unknown),Jean Marie Saudubray,Audrey Boutron,Alain Legrand,Abdelhamid Slama	98

About Sophie Lebon

Sophie Lebon is a scholar working on Clinical Biochemistry, Developmental Neuroscience and Neurology, having authored 40 papers that have together received 2.0k indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (18 papers), Metabolism and Genetic Disorders (16 papers) and ATP Synthase and ATPases Research (9 papers). The work is most often cited by research in Clinical Biochemistry (499 citations), Neurology (489 citations) and Developmental Neuroscience (209 citations). Sophie Lebon has collaborated with scholars based in France, United Kingdom and Italy. Frequent 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. Their work appears in journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Investigation and The Journal of Clinical Endocrinology & Metabolism.

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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