Caroline Sevin

2.9k total citations
54 papers, 1.4k citations indexed

About

Caroline Sevin is a scholar working on Physiology, Molecular Biology and Clinical Biochemistry. According to data from OpenAlex, Caroline Sevin has authored 54 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Physiology, 24 papers in Molecular Biology and 12 papers in Clinical Biochemistry. Recurrent topics in Caroline Sevin's work include Lysosomal Storage Disorders Research (27 papers), Metabolism and Genetic Disorders (11 papers) and RNA regulation and disease (9 papers). Caroline Sevin is often cited by papers focused on Lysosomal Storage Disorders Research (27 papers), Metabolism and Genetic Disorders (11 papers) and RNA regulation and disease (9 papers). Caroline Sevin collaborates with scholars based in France, United States and Germany. Caroline Sevin's co-authors include Nathalie Cartier, Patrick Aubourg, Guy Touati, Pascale de Lonlay, Claire Nihoul‐Feketé, Francesca Menni, Valérie Barbier, Jean-Marie Saudubray, Patrick Aubourg and Françoise Piguet and has published in prestigious journals such as Molecular and Cellular Biology, Neurology and PEDIATRICS.

In The Last Decade

Caroline Sevin

52 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Caroline Sevin France 20 551 444 358 268 202 54 1.4k
Kanya Suphapeetiporn Thailand 23 804 1.5× 144 0.3× 119 0.3× 714 2.7× 150 0.7× 131 2.0k
Luisella Alberti Italy 26 997 1.8× 192 0.4× 625 1.7× 275 1.0× 343 1.7× 41 2.1k
György Fekete Hungary 18 530 1.0× 196 0.4× 67 0.2× 322 1.2× 105 0.5× 94 1.3k
David Coman Australia 20 583 1.1× 302 0.7× 73 0.2× 227 0.8× 131 0.6× 79 1.2k
Tawfeg Ben‐Omran Qatar 25 608 1.1× 133 0.3× 132 0.4× 348 1.3× 69 0.3× 62 1.4k
Agnieszka Jurecka Poland 21 405 0.7× 649 1.5× 81 0.2× 143 0.5× 446 2.2× 63 1.2k
Rachel Laframboise Canada 25 974 1.8× 227 0.5× 116 0.3× 544 2.0× 84 0.4× 57 1.7k
Filippo Pinto e Vairo Brazil 20 569 1.0× 602 1.4× 59 0.2× 226 0.8× 211 1.0× 111 1.4k
Stephanie Austin United States 25 375 0.7× 776 1.7× 80 0.2× 622 2.3× 179 0.9× 72 2.0k
Anne‐Marie Madec France 23 516 0.9× 167 0.4× 694 1.9× 551 2.1× 154 0.8× 49 1.7k

Countries citing papers authored by Caroline Sevin

Since Specialization
Citations

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

Fields of papers citing papers by Caroline Sevin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Caroline Sevin

This figure shows the co-authorship network connecting the top 25 collaborators of Caroline Sevin. A scholar is included among the top collaborators of Caroline Sevin 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 Caroline Sevin. Caroline Sevin 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.
Sevin, Caroline & Fanny Mochel. (2024). Hematopoietic stem cell transplantation in leukodystrophies. Handbook of clinical neurology. 204. 355–366. 2 indexed citations
2.
Sevin, Caroline, et al.. (2023). Childhood cerebral adrenoleukodystrophy (CCALD) in France: epidemiology, natural history, and burden of disease - A population-based study. Orphanet Journal of Rare Diseases. 18(1). 238–238. 2 indexed citations
3.
Brassier, Anaïs, Pierre Broué, Claude Cancés, et al.. (2023). Effects of miglustat therapy on neurological disorder and survival in early-infantile Niemann-Pick disease type C: a national French retrospective study. Orphanet Journal of Rare Diseases. 18(1). 204–204. 7 indexed citations
4.
Boespflug‐Tanguy, Odile, Caroline Sevin, & Françoise Piguet. (2023). Gene therapy for neurodegenerative disorders in children: dreams and realities. Archives de Pédiatrie. 30(8). 8S32–8S40. 1 indexed citations
5.
Eichler, Florian, et al.. (2022). Understanding caregiver descriptions of initial signs and symptoms to improve diagnosis of metachromatic leukodystrophy. Orphanet Journal of Rare Diseases. 17(1). 370–370. 8 indexed citations
6.
Orchard, Paul J., Christine Duncan, Florian Eichler, et al.. (2021). Elivaldogene Autotemcel (eli-cel, Lenti-D) Gene Therapy for the Treatment of Cerebral Adrenoleukodystrophy: Updated Results from the Phase 2/3 ALD-102 Study and First Report on Safety Outcomes from the Phase 3 ALD-104 Study. Transplantation and Cellular Therapy. 27(3). S114–S114. 2 indexed citations
7.
Chiesa, Robert, Jaap Jan Boelens, Christine Duncan, et al.. (2021). Variables affecting outcomes after allogeneic hematopoietic stem cell transplant for cerebral adrenoleukodystrophy. Blood Advances. 6(5). 1512–1524. 19 indexed citations
8.
9.
Audouard, Emilie, et al.. (2021). Complete Correction of Brain and Spinal Cord Pathology in Metachromatic Leukodystrophy Mice. Frontiers in Molecular Neuroscience. 14. 677895–677895. 12 indexed citations
10.
Bost, Chloé, Hélène Maurey, Céline Bellesme, et al.. (2020). Mild Encephalitis/Encephalopathy with reversible splenial lesion syndrome: An unusual presentation of anti-GFAP astrocytopathy. European Journal of Paediatric Neurology. 26. 89–91. 20 indexed citations
11.
Piguet, Françoise, Emilie Audouard, Kévin Beccaria, et al.. (2020). The Challenge of Gene Therapy for Neurological Diseases: Strategies and Tools to Achieve Efficient Delivery to the Central Nervous System. Human Gene Therapy. 32(7-8). 349–374. 30 indexed citations
12.
Demir, Zeynep, Caroline Sevin, Dalila Habès, et al.. (2020). Adenosine kinase deficiency: Three new cases and diagnostic value of hypermethioninemia. Molecular Genetics and Metabolism. 132(1). 38–43. 8 indexed citations
13.
Wijburg, Frits A., Chester B. Whitley, Joseph Muenzer, et al.. (2018). Intrathecal heparan-N-sulfatase in patients with Sanfilippo syndrome type A: A phase IIb randomized trial. Molecular Genetics and Metabolism. 126(2). 121–130. 37 indexed citations
14.
15.
Piguet, Françoise, Dolan Sondhi, Monique Piraud, et al.. (2012). Correction of Brain Oligodendrocytes by AAVrh.10 Intracerebral Gene Therapy in Metachromatic Leukodystrophy Mice. Human Gene Therapy. 23(8). 903–914. 66 indexed citations
16.
Colle, Marie‐Anne, Françoise Piguet, Sylvie Raoul, et al.. (2009). Efficient intracerebral delivery of AAV5 vector encoding human ARSA in non-human primate. Human Molecular Genetics. 19(1). 147–158. 58 indexed citations
17.
Sevin, Caroline, et al.. (2009). Gene therapy in metachromatic leukodystrophy. International Journal of Clinical Pharmacology and Therapeutics. 47 Suppl 1. S128–31. 3 indexed citations
18.
Sevin, Caroline, Patrick Aubourg, & Nathalie Cartier. (2007). Enzyme, cell and gene‐based therapies for metachromatic leukodystrophy. Journal of Inherited Metabolic Disease. 30(2). 175–183. 57 indexed citations
19.
Thuillier, Laure, Caroline Sevin, France Demaugre, et al.. (2000). Genotype/phenotype correlation in carnitine palmitoyl transferase II deficiency: lessons from a compound heterozygous patient. Neuromuscular Disorders. 10(3). 200–205. 25 indexed citations
20.
Mikaeloff, Yann, Florence Pinton, Caroline Sevin, Jean‐Louis Dhondt, & G Ponsot. (1999). Encéphalopathie progressive convulsivante : penser aux anomalies du métabolisme des bioptérines. Archives de Pédiatrie. 6(7). 759–761. 1 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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