Vincent Laugel

6.3k total citations
88 papers, 2.3k citations indexed

About

Vincent Laugel is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Vincent Laugel has authored 88 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 51 papers in Molecular Biology, 30 papers in Genetics and 11 papers in Cellular and Molecular Neuroscience. Recurrent topics in Vincent Laugel's work include DNA Repair Mechanisms (22 papers), Genetics and Neurodevelopmental Disorders (18 papers) and Muscle Physiology and Disorders (11 papers). Vincent Laugel is often cited by papers focused on DNA Repair Mechanisms (22 papers), Genetics and Neurodevelopmental Disorders (18 papers) and Muscle Physiology and Disorders (11 papers). Vincent Laugel collaborates with scholars based in France, United Kingdom and United States. Vincent Laugel's co-authors include Jocelyn Laporte, Jean‐Louis Mandel, Alain Sarasin, Michel Fischbach, Tiziana Nardò, Miria Stefanini, Nadia Messaddeq, Hala Fahs, Jean‐François Pellissier and Hélène Dollfus and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Investigation and Molecular Cell.

In The Last Decade

Vincent Laugel

81 papers receiving 2.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Vincent Laugel France 26 1.7k 475 355 339 184 88 2.3k
Abdelaziz Sefiani Morocco 21 964 0.6× 526 1.1× 119 0.3× 104 0.3× 150 0.8× 123 1.8k
Tuula Lönnqvist Finland 29 1.4k 0.8× 286 0.6× 150 0.4× 347 1.0× 93 0.5× 80 2.4k
Yasuhiro Takeshima Japan 31 2.7k 1.6× 496 1.0× 138 0.4× 183 0.5× 451 2.5× 194 3.5k
Avinash Abhyankar United States 20 959 0.6× 650 1.4× 89 0.3× 134 0.4× 124 0.7× 30 1.9k
Hammadi Ayadi Tunisia 29 1.3k 0.8× 673 1.4× 129 0.4× 116 0.3× 83 0.5× 137 2.6k
C. Ronald Scott United States 26 966 0.6× 545 1.1× 517 1.5× 82 0.2× 53 0.3× 75 2.5k
Paola Carrera Italy 27 936 0.6× 383 0.8× 80 0.2× 267 0.8× 63 0.3× 128 2.3k
Luisa Bonafé Switzerland 36 1.8k 1.1× 1.4k 2.9× 378 1.1× 178 0.5× 53 0.3× 97 3.5k
Craig B. Woda United States 17 1.4k 0.9× 329 0.7× 111 0.3× 107 0.3× 132 0.7× 21 2.4k
Sarah Collins United States 21 635 0.4× 189 0.4× 143 0.4× 110 0.3× 52 0.3× 58 1.4k

Countries citing papers authored by Vincent Laugel

Since Specialization
Citations

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

Fields of papers citing papers by Vincent Laugel

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Vincent Laugel

This figure shows the co-authorship network connecting the top 25 collaborators of Vincent Laugel. A scholar is included among the top collaborators of Vincent Laugel 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 Vincent Laugel. Vincent Laugel 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.
Grimaldi‐Bensouda, Lamiae, Céline Tard, Pascale Saugier-Véber, et al.. (2025). REGISTRE SMA FRANCE: A nationwide observational registry of patients with spinal muscular atrophy in France. Journal of Neuromuscular Diseases. 12(6). 793–803.
2.
3.
McMillan, Hugh J., Giovanni Baranello, Michelle A. Farrar, et al.. (2024). Safety and Efficacy of IV Onasemnogene Abeparvovec for Pediatric Patients With Spinal Muscular Atrophy. Neurology. 104(2). e210268–e210268. 5 indexed citations
4.
Laugel, Vincent, Jean‐Baptiste Davion, Nathalie Danièle, et al.. (2024). 410P GNT0004, Genethon's AAV8 vector-delivered microdystrophin gene therapy of Duchenne muscular dystrophy, first data of the phase I/II part of the GNT-016-MDYF all-in-one clinical trial in ambulant boys. Neuromuscular Disorders. 43. 104441.281–104441.281. 6 indexed citations
5.
Mantyh, William G., Christina A. Pacak, Paul D. Robbins, et al.. (2024). Cognitive Decline and Other Late-Stage Neurologic Complications in Cockayne Syndrome. Neurology Clinical Practice. 14(4). e200309–e200309. 2 indexed citations
6.
Ehlinger, Virginie, Maëlle Biotteau, Ulrike Walther‐Louvier, et al.. (2023). Confirmatory validation of the french version of the Duchenne Muscular Dystrophy module of the pediatric quality of life inventory (PedsQLTM3.0DMDfv). BMC Pediatrics. 23(1). 563–563. 1 indexed citations
7.
8.
Kraoua, Ichraf, Nadège Calmels, Cathy Obringer, et al.. (2022). Heterogeneous clinical features in Cockayne syndrome patients and siblings carrying the same CSA mutations. Orphanet Journal of Rare Diseases. 17(1). 121–121. 7 indexed citations
9.
Baer, Sarah, Cathy Obringer, Sophie Julia, et al.. (2020). Early‐onset nucleotide excision repair disorders with neurological impairment: Clues for early diagnosis and prognostic counseling. Clinical Genetics. 98(3). 251–260. 11 indexed citations
10.
Boyer, Anthony, R. Bellance, Martin Krahn, et al.. (2019). Identification of novel pathogenic copy number variations in Charcot-Marie-Tooth disease. Journal of Human Genetics. 65(3). 313–323. 7 indexed citations
11.
Spitz, Marie‐Aude, M. Durand, Cathy Obringer, et al.. (2019). Renal disease in Cockayne syndrome. European Journal of Medical Genetics. 63(1). 103612–103612. 6 indexed citations
12.
May, Nicolas Le, et al.. (2018). Xeroderma Pigmentosum Groups C and A in Algerian Patients with Deregulation of both Transcription and DNA Repair. HAL (Le Centre pour la Communication Scientifique Directe). 6(4). 3 indexed citations
13.
Epanchintsev, Alexey, Tao Ye, Luca Proietti‐De‐Santis, et al.. (2017). Cockayne’s Syndrome A and B Proteins Regulate Transcription Arrest after Genotoxic Stress by Promoting ATF3 Degradation. Molecular Cell. 68(6). 1054–1066.e6. 69 indexed citations
14.
Laugel, Vincent. (2013). Cockayne syndrome: The expanding clinical and mutational spectrum. Mechanisms of Ageing and Development. 134(5-6). 161–170. 157 indexed citations
15.
Amor-Guéret, Mounira, Anthony Laugé, Rosine Onclercq-Delic, et al.. (2008). Three New BLM Gene Mutations Associated with Bloom Syndrome. Genetic Testing. 12(2). 257–261. 11 indexed citations
16.
Laugel, Vincent, Mireille Cossée, Jacqueline Matis, et al.. (2007). Diagnostic approach to neonatal hypotonia: retrospective study on 144 neonates. European Journal of Pediatrics. 167(5). 517–523. 36 indexed citations
17.
Martin, Anne de Saint, Vincent Laugel, & Édouard Hirsch. (2006). Épilepsies de l’enfant : choix des antiépileptiques et surveillance. MTP. Médecine thérapeutique pédiatrie. 9(5). 313–324.
18.
Laugel, Vincent, Benoı̂t Escande, Natacha Entz‐Werlé, et al.. (2004). Pancréatites aiguës sévères à l’asparaginase chez l’enfant : étude rétrospective multicentrique. Archives de Pédiatrie. 12(1). 34–41. 12 indexed citations
19.
Laugel, Vincent, et al.. (2001). Tétralogie de Fallot chez un couple de jumeaux monozygotes. Archives de Pédiatrie. 8(4). 385–388. 3 indexed citations
20.
Laugel, Vincent, et al.. (2001). Pemphigoïde gravidique et lésions bulleuses chez le nouveau-né. Archives de Pédiatrie. 8(10). 1071–1074. 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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