Catherine Sarret

1.8k total citations
43 papers, 599 citations indexed

About

Catherine Sarret is a scholar working on Molecular Biology, Neurology and Epidemiology. According to data from OpenAlex, Catherine Sarret has authored 43 papers receiving a total of 599 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 7 papers in Neurology and 7 papers in Epidemiology. Recurrent topics in Catherine Sarret's work include RNA Research and Splicing (5 papers), Thyroid Disorders and Treatments (4 papers) and RNA regulation and disease (4 papers). Catherine Sarret is often cited by papers focused on RNA Research and Splicing (5 papers), Thyroid Disorders and Treatments (4 papers) and RNA regulation and disease (4 papers). Catherine Sarret collaborates with scholars based in France, Italy and United States. Catherine Sarret's co-authors include Odile Boespflug‐Tanguy, Vincent des Portes, Catherine Vaurs‐Barrière, Renaud Touraine, Jean‐Jacques Lemaire, Anna Sontheimer, Bruno Pereira, Davide Tonduti, Diana Rodriguez and Giuseppe De Michele and has published in prestigious journals such as Annals of Neurology, Neuroscience and The American Journal of Human Genetics.

In The Last Decade

Catherine Sarret

42 papers receiving 591 citations

Peers

Catherine Sarret
Annick Sévely France
A. Hori Germany
Maria Grazia Egitto Italy
Pasquale F. Finelli United States
Sabrina Avignone Italy
Ichiro Kuki Japan
Rainer Guthoff Germany
Sueng‐Han Han South Korea
Robert McWilliam United Kingdom
Charu Deshpande United Kingdom
Annick Sévely France
Catherine Sarret
Citations per year, relative to Catherine Sarret Catherine Sarret (= 1×) peers Annick Sévely

Countries citing papers authored by Catherine Sarret

Since Specialization
Citations

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

Fields of papers citing papers by Catherine Sarret

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Catherine Sarret

This figure shows the co-authorship network connecting the top 25 collaborators of Catherine Sarret. A scholar is included among the top collaborators of Catherine Sarret 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 Catherine Sarret. Catherine Sarret 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.
Bouvier, Damien, Aymeric Cantais, Philippe Fournier, et al.. (2024). Serum S100B Level in the Management of Pediatric Minor Head Trauma. JAMA Network Open. 7(3). e242366–e242366. 4 indexed citations
2.
Oris, Charlotte, Bruno Pereira, Philippe Gonzalo, et al.. (2024). Serum GFAP and UCH-L1 for the identification of clinically important traumatic brain injury in children in France: a diagnostic accuracy substudy. The Lancet Child & Adolescent Health. 9(1). 47–56. 3 indexed citations
3.
Masnada, Silvia, Catherine Sarret, Clara E. Antonello, et al.. (2021). Movement disorders in MCT8 deficiency/Allan-Herndon-Dudley Syndrome. Molecular Genetics and Metabolism. 135(1). 109–113. 20 indexed citations
4.
5.
Lefebvre, S. & Catherine Sarret. (2020). Pathogenesis and therapeutic targets in spinal muscular atrophy (SMA). Archives de Pédiatrie. 27(7). 7S3–7S8. 14 indexed citations
6.
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
7.
8.
Sarret, Catherine. (2019). Leukodystrophies and genetic leukoencephalopathies in children. Revue Neurologique. 176(1-2). 10–19. 7 indexed citations
9.
Rochette, Emmanuelle, Bruno Pereira, Corinne Borderon, et al.. (2019). Impaired Muscular Fat Metabolism in Juvenile Idiopathic Arthritis in Inactive Disease. Frontiers in Physiology. 10. 528–528. 7 indexed citations
10.
Sarret, Catherine, Zahra Ashkavand, Imen Dorboz, et al.. (2019). Deleterious mutations in ALDH1L2 suggest a novel cause for neuro-ichthyotic syndrome. npj Genomic Medicine. 4(1). 17–17. 15 indexed citations
11.
Sarret, Catherine, Jean‐Jacques Lemaire, Anna Sontheimer, et al.. (2018). Brain Diffusion Imaging and Tractography to Distinguish Clinical Severity of Human <b><i>PLP1</i></b>-Related Disorders. Developmental Neuroscience. 40(4). 301–311. 5 indexed citations
12.
Dorboz, Imen, et al.. (2017). Mutation in the AGK gene in two siblings with unusual Sengers syndrome. Metabolic Brain Disease. 32(6). 2149–2154. 12 indexed citations
13.
Merlin, Étienne, et al.. (2016). Initiation à la pédagogie narrative en pédiatrie : le focus-groupe pédagogique. Archives de Pédiatrie. 23(8). 792–797. 1 indexed citations
14.
Lemaire, Jean‐Jacques, Laurent Sakka, Yves Boirie‌, et al.. (2013). Maps of the adult human hypothalamus. Surgical Neurology International. 4(4). 156–156. 31 indexed citations
15.
Coste, Karen, et al.. (2012). Le syndrome macrocéphalie – malformation capillaire. Intérêt du diagnostic en période néonatale. Archives de Pédiatrie. 19(9). 917–920. 2 indexed citations
16.
Sarret, Catherine, et al.. (2012). Atteintes neurologiques à Bartonella henselae : à propos de 2 cas pédiatriques. Archives de Pédiatrie. 19(8). 823–826. 6 indexed citations
17.
Sarret, Catherine, Catherine Vaurs‐Barrière, Imen Dorboz, et al.. (2011). Sjögren–Larsson syndrome: Novel mutations in the ALDH3A2 gene in a French cohort. Journal of the Neurological Sciences. 312(1-2). 123–126. 8 indexed citations
18.
Mochel, Fanny, Catherine Sarret, Éléonore Eymard-Pierre, et al.. (2010). Elevated CSF N-acetylaspartylglutamate suggests specific molecular diagnostic abnormalities in patients with white matter diseases. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1802(11). 1112–1117. 15 indexed citations
19.
Vaurs‐Barrière, Catherine, Catherine Sarret, G Giraud, et al.. (2009). Pelizaeus–Merzbacher–Like disease presentation of MCT8 mutated male subjects. Annals of Neurology. 65(1). 114–118. 84 indexed citations
20.
Sarret, Catherine, et al.. (2005). Érythème noueux et adénopathies chez un adolescent : Mode de révélation rare de la maladie des griffes du chat. Archives de Pédiatrie. 12(3). 295–297. 6 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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