Florence Renaldo

1.1k total citations
19 papers, 339 citations indexed

About

Florence Renaldo is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Florence Renaldo has authored 19 papers receiving a total of 339 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 3 papers in Cellular and Molecular Neuroscience and 3 papers in Neurology. Recurrent topics in Florence Renaldo's work include RNA regulation and disease (8 papers), RNA Research and Splicing (6 papers) and RNA and protein synthesis mechanisms (3 papers). Florence Renaldo is often cited by papers focused on RNA regulation and disease (8 papers), RNA Research and Splicing (6 papers) and RNA and protein synthesis mechanisms (3 papers). Florence Renaldo collaborates with scholars based in France, United States and Italy. Florence Renaldo's co-authors include Odile Boespflug‐Tanguy, Imen Dorboz, Monique Elmaleh, Diana Rodriguez, Gillian Rice, Yanick J. Crow, Davide Tonduti, Joseph G. Gleeson, John H. Livingston and Vincent Laugel and has published in prestigious journals such as Neurology, Annals of Neurology and Epilepsia.

In The Last Decade

Florence Renaldo

18 papers receiving 335 citations

Peers

Florence Renaldo
J.A.P. Hiel Netherlands
Tatsuo Itakura United States
Veronica Diesl United States
Lanjun Xu China
Monica Nagendran United States
Kenian Liu United States
Kip D. Zimmerman United States
Florence Renaldo
Citations per year, relative to Florence Renaldo Florence Renaldo (= 1×) peers Isabelle Rouvet

Countries citing papers authored by Florence Renaldo

Since Specialization
Citations

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

Fields of papers citing papers by Florence Renaldo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Florence Renaldo

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

All Works

19 of 19 papers shown
1.
Bélot, Alexandre, Odile Boespflug‐Tanguy, Guilaine Boursier, et al.. (2025). French protocol for diagnosis and management of type 1 interferonopathies. La Revue de Médecine Interne. 46(6). 320–340.
2.
Zaki, Maha S., Mahmoud Y. Issa, Boris Keren, et al.. (2024). Biallelic variants in ERLIN1: a series of 13 individuals with spastic paraparesis. Human Genetics. 143(11). 1353–1362. 1 indexed citations
3.
Ntorkou, Alexandra, Florence Renaldo, Diane Doummar, et al.. (2021). Enlargement of the Optic Chiasm: A Novel Imaging Finding in Glutaric Aciduria Type 1. American Journal of Neuroradiology. 42(9). 1722–1726. 2 indexed citations
4.
Renaldo, Florence, Sylvain Renolleau, Étienne Javouhey, et al.. (2021). Mortality and Neurologic Sequelae in Influenza-Associated Encephalopathy: Retrospective Multicenter PICU Cohort in France. Pediatric Critical Care Medicine. 22(11). e582–e587. 10 indexed citations
5.
Renaldo, Florence, François Chalard, Stéphanie Valence, Lydie Bürglen, & Diana Rodriguez. (2021). Area Postrema Syndrome as the Initial Presentation of Alexander Disease. Neurology. 97(11). 548–549. 3 indexed citations
6.
Ellul, Pierre, Florence Renaldo, Odile Boespflug‐Tanguy, et al.. (2020). Catatonia in a patient with Aicardi-Goutières syndrome efficiently treated with immunoadsorption. Schizophrenia Research. 222. 484–486. 4 indexed citations
7.
Maillart, Élisabeth, Florence Renaldo, Caroline Papeix, et al.. (2020). Dramatic efficacy of ofatumumab in refractory pediatric-onset AQP4-IgG neuromyelitis optica spectrum disorder. Neurology Neuroimmunology & Neuroinflammation. 7(3). 10 indexed citations
8.
Dewulf, Joseph P., Elsa Wiame, Imen Dorboz, et al.. (2019). SLC13A3 variants cause acute reversible leukoencephalopathy and α‐ketoglutarate accumulation. Annals of Neurology. 85(3). 385–395. 19 indexed citations
9.
Kraoua, Ichraf, C. Drissi, Hanène Benrhouma, et al.. (2019). Novel POLR1C mutation in RNA polymerase III‐related leukodystrophy with severe myoclonus and dystonia. Molecular Genetics & Genomic Medicine. 7(9). e914–e914. 8 indexed citations
10.
Dorboz, Imen, Hélène Dumay‐Odelot, Yosra Bouyacoub, et al.. (2018). Mutation in POLR3K causes hypomyelinating leukodystrophy and abnormal ribosomal RNA regulation. Neurology Genetics. 4(6). e289–e289. 55 indexed citations
11.
Tonduti, Davide, Simona Orcesi, Emma M. Jenkinson, et al.. (2016). Clinical, radiological and possible pathological overlap of cystic leukoencephalopathy without megalencephaly and Aicardi-Goutières syndrome. European Journal of Paediatric Neurology. 20(4). 604–610. 24 indexed citations
12.
Tonduti, Davide, Chiara Aiello, Florence Renaldo, et al.. (2015). TUBB4A-related hypomyelinating leukodystrophy: New insights from a series of 12 patients. European Journal of Paediatric Neurology. 20(2). 323–330. 24 indexed citations
13.
Masliah‐Planchon, Julien, Céline Dupont, Aurélien Trimouille, et al.. (2015). Insertion of an extra copy of Xq22.2 into 1p36 results in functional duplication of the PLP1 gene in a girl with classical Pelizaeus-Merzbacher disease. BMC Medical Genetics. 16(1). 7 indexed citations
14.
Tonduti, Davide, Imen Dorboz, Florence Renaldo, et al.. (2015). Cystic leukoencephalopathy with cortical dysplasia related to LAMB1 mutations. Neurology. 84(21). 2195–2197. 15 indexed citations
15.
Zaki, Maha S., Mohamed Abdel‐Hamid, Ghada M. H. Abdel‐Salam, et al.. (2014). Mutations in ADAR1, IFIH1, and RNASEH2B Presenting As Spastic Paraplegia. Neuropediatrics. 45(6). 386–391. 57 indexed citations
16.
Lévy, Jonathan, Aline Receveur, Guillaume Jedraszak, et al.. (2014). Involvement of interstitial telomeric sequences in two new cases of mosaicism for autosomal structural rearrangements. American Journal of Medical Genetics Part A. 167(2). 428–433. 6 indexed citations
17.
Terracciano, Antonio, Florence Renaldo, Ginevra Zanni, et al.. (2011). The use of muscle biopsy in the diagnosis of undefined ataxia with cerebellar atrophy in children. European Journal of Paediatric Neurology. 16(3). 248–256. 25 indexed citations
18.
Mignot, Cyril, I. Desguerre, Lydie Bürglen, et al.. (2008). Tumor-like enlargement of the optic chiasm in an infant with Alexander disease. Brain and Development. 31(3). 244–247. 10 indexed citations
19.
Madhavan, Deepak, Alexis Arzimanoglou, Florence Renaldo, et al.. (2007). Surgical Outcome in Tuberous Sclerosis Complex: A Multicenter Survey. Epilepsia. 48(8). 1625–1628. 59 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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