Laurence Lion‐François

1.3k total citations
32 papers, 535 citations indexed

About

Laurence Lion‐François is a scholar working on Neurology, Genetics and Nutrition and Dietetics. According to data from OpenAlex, Laurence Lion‐François has authored 32 papers receiving a total of 535 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Neurology, 8 papers in Genetics and 7 papers in Nutrition and Dietetics. Recurrent topics in Laurence Lion‐François's work include Trace Elements in Health (7 papers), Neurofibromatosis and Schwannoma Cases (7 papers) and Heavy Metal Exposure and Toxicity (6 papers). Laurence Lion‐François is often cited by papers focused on Trace Elements in Health (7 papers), Neurofibromatosis and Schwannoma Cases (7 papers) and Heavy Metal Exposure and Toxicity (6 papers). Laurence Lion‐François collaborates with scholars based in France, United States and India. Laurence Lion‐François's co-authors include V. des Portes, Laurent Guibaud, Isabelle Kemlin, Daniel Gérard, Gaëtan Lesca, Diana Rodriguez, David Cheillan, Gajja S. Salomons, Alain Lachaux and Christine Vianey‐Saban and has published in prestigious journals such as Neurology, The Journal of Physiology and Behavioral Neuroscience.

In The Last Decade

Laurence Lion‐François

29 papers receiving 522 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Laurence Lion‐François France 13 160 157 96 87 86 32 535
Zhengjin Cao United States 8 598 3.7× 15 0.1× 55 0.6× 141 1.6× 74 0.9× 8 755
Iris Noyman Israel 9 207 1.3× 23 0.1× 55 0.6× 23 0.3× 32 0.4× 26 455
D. R. Johns United States 18 781 4.9× 176 1.1× 48 0.5× 382 4.4× 30 0.3× 20 1.0k
Su‐Kyeong Hwang South Korea 16 285 1.8× 43 0.3× 44 0.5× 16 0.2× 106 1.2× 47 720
Stanley D. Johnsen United States 13 510 3.2× 87 0.6× 34 0.4× 350 4.0× 32 0.4× 29 895
Namiko Nomura Japan 17 291 1.8× 117 0.7× 122 1.3× 10 0.1× 17 0.2× 30 652
Majid Fardaei Iran 14 742 4.6× 82 0.5× 21 0.2× 22 0.3× 36 0.4× 58 1.0k
Robert E. Greenberg United States 15 97 0.6× 58 0.4× 24 0.3× 42 0.5× 36 0.4× 39 540
M. Pineda Spain 13 285 1.8× 59 0.4× 48 0.5× 127 1.5× 38 0.4× 26 533
Gabriel Sturm United States 11 222 1.4× 17 0.1× 55 0.6× 31 0.4× 29 0.3× 16 470

Countries citing papers authored by Laurence Lion‐François

Since Specialization
Citations

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

Fields of papers citing papers by Laurence Lion‐François

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Laurence Lion‐François. 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 Laurence Lion‐François. The network helps show where Laurence Lion‐François may publish in the future.

Co-authorship network of co-authors of Laurence Lion‐François

This figure shows the co-authorship network connecting the top 25 collaborators of Laurence Lion‐François. A scholar is included among the top collaborators of Laurence Lion‐François 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 Laurence Lion‐François. Laurence Lion‐François 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.
Curie, Aurore, Laurence Lion‐François, Vassili Valayannopoulos, et al.. (2024). Clinical Characteristics, Developmental Trajectory, and Caregiver Burden of Patients With Creatine Transporter Deficiency ( SLC6A8 ). Neurology. 102(8). e209243–e209243. 3 indexed citations
2.
Taïeb, Guillaume, Emmanuel Roze, Laurence Lion‐François, et al.. (2023). Clinical and Electrophysiological Characterization of Essential Tremor in 18 Children and Adolescents. Tremor and Other Hyperkinetic Movements. 13. 46–46. 1 indexed citations
3.
Lesca, Gaëtan, Dorothée Ville, Anne‐Lise Poulat, et al.. (2022). CNTNAP1-encephalopathy: Six novel patients surviving the neonatal period. European Journal of Paediatric Neurology. 37. 98–104. 5 indexed citations
4.
Guillaud, Olivier, France Woimant, Jérôme Dumortier, et al.. (2022). Maintenance therapy simplification using a single daily dose: A preliminary real-life feasibility study in patients with Wilson disease. Clinics and Research in Hepatology and Gastroenterology. 46(9). 101978–101978. 7 indexed citations
5.
Sandahl, Thomas Damgaard, Cécile Pagan, Laurence Lion‐François, et al.. (2021). ATP7B variant spectrum in a French pediatric Wilson disease cohort. European Journal of Medical Genetics. 64(10). 104305–104305. 11 indexed citations
6.
Lion‐François, Laurence, Olivier Guillaud, Dalila Habès, et al.. (2021). Pediatric Wilson's Disease. Journal of Pediatric Gastroenterology and Nutrition. 73(4). e80–e86. 21 indexed citations
7.
Sarret, Catherine, Laurence Lion‐François, Olivier Revol, et al.. (2020). Normal intellectual skills in patients with Rhombencephalosynapsis. European Journal of Paediatric Neurology. 29. 92–100. 4 indexed citations
8.
Lamboux, Aline, Olivier Guillaud, Chloé Laurencin, et al.. (2020). The blood copper isotopic composition is a prognostic indicator of the hepatic injury in Wilson disease. Metallomics. 12(11). 1781–1790. 21 indexed citations
9.
Pons, Linda, Gaëtan Lesca, Damien Sanlaville, et al.. (2018). Neonatal tremor episodes and hyperekplexia‐like presentation at onset in a child with SCN8A developmental and epileptic encephalopathy. Epileptic Disorders. 20(4). 289–294. 9 indexed citations
10.
Michael, George A., et al.. (2017). Is aggressive behavior in Neurofibromatosis Type 1 due to dysregulated inhibitory control, difficulties in interpreting emotional cues, or both?. European Journal of Paediatric Neurology. 21. e171–e171.
11.
Laurencin, Chloé, Anne Brunet, Jérôme Dumortier, et al.. (2016). Liver Transplantation in Wilson's Disease with Neurological Impairment: Evaluation in 4 Patients. European Neurology. 77(1-2). 5–15. 18 indexed citations
12.
Spitz, Marie‐Aude, Sylvain Roche, Bénédicte Héron, et al.. (2016). Chronic Diarrhea in l-Amino Acid Decarboxylase (AADC) Deficiency: A Prominent Clinical Finding Among a Series of Ten French Patients. JIMD Reports. 31. 85–93. 13 indexed citations
13.
Favre, Émilie, et al.. (2016). Cognitive Abilities of Children With Neurological and Liver Forms of Wilson Disease. Journal of Pediatric Gastroenterology and Nutrition. 64(3). 436–439. 8 indexed citations
14.
Mercimek‐Mahmutoglu, Saadet, Joseph Ndika, Warsha A. Kanhai, et al.. (2014). Thirteen New Patients with Guanidinoacetate Methyltransferase Deficiency and Functional Characterization of Nineteen Novel Missense Variants in theGAMTGene. Human Mutation. 35(4). 462–469. 38 indexed citations
15.
Poulat, Anne‐Lise, Gaëtan Lesca, Damien Sanlaville, et al.. (2013). A proposed diagnostic approach for infantile spasms based on a spectrum of variable aetiology. European Journal of Paediatric Neurology. 18(2). 176–182. 20 indexed citations
16.
Simkin, Dina, Isabelle Léna, P. Landrieu, et al.. (2011). Mechanisms underlying a life‐threatening skeletal muscle Na+ channel disorder. The Journal of Physiology. 589(13). 3115–3124. 12 indexed citations
17.
Szathmári, Alexandru, Philippe Thiesse, C. Mottolèse, et al.. (2010). Correlation between pre‐ or postoperative MRI findings and cerebellar sequelae in patients with medulloblastomas. Pediatric Blood & Cancer. 55(7). 1310–1316. 13 indexed citations
18.
Michael, George A., et al.. (2009). Reactivity to visual signals and the cerebellar vermis: Evidence from a rare case with rhombencephalosynapsis.. Behavioral Neuroscience. 123(1). 86–96. 12 indexed citations
19.
Colombani, Marina, Mondher Chouchane, G. Pitelet, et al.. (2006). A new case of megalencephaly and perisylvian polymicrogyria with post-axial polydactyly and hydrocephalus: MPPH syndrome. European Journal of Medical Genetics. 49(6). 466–471. 15 indexed citations
20.
Lion‐François, Laurence, David Cheillan, G. Pitelet, et al.. (2006). High frequency of creatine deficiency syndromes in patients with unexplained mental retardation. Neurology. 67(9). 1713–1714. 74 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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