Anne-Sophie Lèbre

2.2k total citations
38 papers, 1.1k citations indexed

About

Anne-Sophie Lèbre is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Anne-Sophie Lèbre has authored 38 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Molecular Biology, 14 papers in Clinical Biochemistry and 10 papers in Genetics. Recurrent topics in Anne-Sophie Lèbre's work include Mitochondrial Function and Pathology (21 papers), Metabolism and Genetic Disorders (14 papers) and ATP Synthase and ATPases Research (7 papers). Anne-Sophie Lèbre is often cited by papers focused on Mitochondrial Function and Pathology (21 papers), Metabolism and Genetic Disorders (14 papers) and ATP Synthase and ATPases Research (7 papers). Anne-Sophie Lèbre collaborates with scholars based in France, United Kingdom and United States. Anne-Sophie Lèbre's co-authors include Agnès Rötig, Arnold Münnich, Marlène Rio, Vincent Morinière, Nathalie Boddaert, Corinne Antignac, Bertrand Knebelmann, Laurence Heidet, Vincent Guigonis and Rémi Salomon and has published in prestigious journals such as Brain, Neurology and Free Radical Biology and Medicine.

In The Last Decade

Anne-Sophie Lèbre

38 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Anne-Sophie Lèbre France 18 769 316 218 132 103 38 1.1k
Christine Barnérias France 20 704 0.9× 236 0.7× 283 1.3× 137 1.0× 145 1.4× 73 1.4k
Amal Alhashem Saudi Arabia 19 616 0.8× 163 0.5× 447 2.1× 90 0.7× 126 1.2× 76 1.1k
Caterina Garone Italy 21 1.3k 1.7× 641 2.0× 182 0.8× 131 1.0× 71 0.7× 45 1.7k
Reeval Segel Israel 18 649 0.8× 174 0.6× 249 1.1× 69 0.5× 87 0.8× 40 1.1k
Ivo Kremensky Bulgaria 18 753 1.0× 127 0.4× 295 1.4× 395 3.0× 104 1.0× 75 1.4k
Hui Xiong China 17 652 0.8× 130 0.4× 97 0.4× 126 1.0× 121 1.2× 116 1.0k
Gunter Scharer United States 17 616 0.8× 583 1.8× 232 1.1× 67 0.5× 33 0.3× 29 1.1k
Rıza Köksal Özgül Türkiye 17 457 0.6× 183 0.6× 194 0.9× 124 0.9× 37 0.4× 69 873
Alberto Blázquez Spain 18 750 1.0× 323 1.0× 141 0.6× 84 0.6× 37 0.4× 50 1.1k
Denise Cassandrini Italy 23 735 1.0× 228 0.7× 176 0.8× 222 1.7× 126 1.2× 62 1.3k

Countries citing papers authored by Anne-Sophie Lèbre

Since Specialization
Citations

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

Fields of papers citing papers by Anne-Sophie Lèbre

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anne-Sophie Lèbre

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

All Works

20 of 20 papers shown
1.
2.
Oudart, Jean‐Baptiste, et al.. (2022). Mutational Characteristics of Primary Mucosal Melanoma: A Systematic Review. Molecular Diagnosis & Therapy. 26(2). 189–202. 10 indexed citations
3.
Lèbre, Anne-Sophie, et al.. (2021). Prolidase Deficiency Causing Recalcitrant Leg Ulcerations in Siblings. Advances in Skin & Wound Care. 34(11). 1–4. 3 indexed citations
4.
Boulagnon‐Rombi, Camille, Christophe Schneider, Chloé Leandri, et al.. (2018). LRP1 expression in colon cancer predicts clinical outcome. Oncotarget. 9(10). 8849–8869. 28 indexed citations
5.
Benfodda, M., Anne-Sophie Lèbre, Udaya Raj Paudel, et al.. (2017). Clinical and genetic characteristics of xeroderma pigmentosum in Nepal. Journal of the European Academy of Dermatology and Venereology. 32(5). 832–839. 4 indexed citations
6.
Kuster, Alice, Jean‐Baptiste Arnoux, Magalie Barth, et al.. (2017). Diagnostic approach to neurotransmitter monoamine disorders: experience from clinical, biochemical, and genetic profiles. Journal of Inherited Metabolic Disease. 41(1). 129–139. 11 indexed citations
7.
Slama, Abdelhamid, et al.. (2016). Resveratrol attenuates oxidative stress in mitochondrial Complex I deficiency: Involvement of SIRT3. Free Radical Biology and Medicine. 96. 190–198. 46 indexed citations
8.
Leman, Géraldine, Naïg Guéguen, Valérie Desquiret‐Dumas, et al.. (2015). Assembly defects induce oxidative stress in inherited mitochondrial complex I deficiency. The International Journal of Biochemistry & Cell Biology. 65. 91–103. 35 indexed citations
9.
Grévent, D., Anne-Sophie Lèbre, Marlène Rio, et al.. (2014). Aspect en IRM cérébrale des maladies mitochondriales. Algorithme décisionnel des maladies mitochondriales les plus fréquentes. Revue Neurologique. 170(5). 381–389. 2 indexed citations
10.
Rigaud, Charlotte, Anne-Sophie Lèbre, Renaud Touraine, et al.. (2013). Natural history of Barth syndrome: a national cohort study of 22 patients. Orphanet Journal of Rare Diseases. 8(1). 70–70. 97 indexed citations
11.
Rouzier, Cécile, Annabelle Chaussenot, Valérie Serre, et al.. (2013). Quantitative multiplex PCR of short fluorescent fragments for the detection of large intragenic POLG rearrangements in a large French cohort. European Journal of Human Genetics. 22(4). 542–550. 28 indexed citations
12.
Galmiche, Louise, Valérie Serre, Marine Beinat, et al.. (2011). Exome sequencing identifies MRPL3 mutation in mitochondrial cardiomyopathy. Human Mutation. 32(11). 1225–1231. 110 indexed citations
13.
Galmiche, Louise, Valérie Serre, Marine Beinat, et al.. (2011). Toward genotype phenotype correlations in GFM1 mutations. Mitochondrion. 12(2). 242–247. 14 indexed citations
14.
Sabbagh, Sandra, Anne-Sophie Lèbre, Nadia Bahi‐Buisson, et al.. (2010). Epileptic phenotypes in children with respiratory chain disorders. Epilepsia. 51(7). 1225–1235. 77 indexed citations
15.
Takahashi‐Fujigasaki, Junko, Tilo Breidert, Hiroto Fujigasaki, et al.. (2010). Amyloid precursor-like protein 2 cleavage contributes to neuronal intranuclear inclusions and cytotoxicity in spinocerebellar ataxia-7 (SCA7). Neurobiology of Disease. 41(1). 33–42. 5 indexed citations
16.
Leshinsky‐Silver, Esther, Anne-Sophie Lèbre, Limor Minai, et al.. (2009). NDUFS4 mutations cause Leigh syndrome with predominant brainstem involvement. Molecular Genetics and Metabolism. 97(3). 185–189. 46 indexed citations
17.
Lèbre, Anne-Sophie, Vincent Morinière, Olivier Dunand, et al.. (2009). Maternal uniparental heterodisomy of chromosome 17 in a patient with nephropathic cystinosis. European Journal of Human Genetics. 17(8). 1019–1023. 20 indexed citations
18.
Baujat, Geneviève, Anne-Sophie Lèbre, Valérie Cormier‐Daire, & M. Le Merrer. (2008). Ostéogenèse imparfaite, annonce du diagnostic (classification clinique et génétique). Archives de Pédiatrie. 15(5). 789–791. 8 indexed citations
19.
Lèbre, Anne-Sophie & Alexis Brice. (2001). Maladies par expansion de polyglutamine : données moléculaires et physiopathologiques. médecine/sciences. 17(11). 1149–1157. 2 indexed citations
20.
Lèbre, Anne-Sophie, Alexandra Dürr, G Ponsot, et al.. (1999). DYT1 mutation in French families with idiopathic torsion dystonia. Brain. 122(1). 41–45. 40 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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