Edgard Verdura

1.1k total citations
17 papers, 389 citations indexed

About

Edgard Verdura is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Edgard Verdura has authored 17 papers receiving a total of 389 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 5 papers in Genetics and 3 papers in Cell Biology. Recurrent topics in Edgard Verdura's work include RNA Research and Splicing (6 papers), RNA regulation and disease (3 papers) and Muscle Physiology and Disorders (3 papers). Edgard Verdura is often cited by papers focused on RNA Research and Splicing (6 papers), RNA regulation and disease (3 papers) and Muscle Physiology and Disorders (3 papers). Edgard Verdura collaborates with scholars based in Spain, France and Argentina. Edgard Verdura's co-authors include Jonàs Juan‐Mateu, P. Gallano, Lidia González‐Quereda, A. Nascimento, Montserrat Baiget, Maria José Rodríguez, Manel Baena, C. Ortez, Françoise Bergametti and Elisabeth Tournier‐Lasserve and has published in prestigious journals such as Journal of Clinical Investigation, PLoS ONE and Brain.

In The Last Decade

Edgard Verdura

16 papers receiving 387 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Edgard Verdura Spain 8 255 122 85 67 57 17 389
Manu Jokela Finland 12 236 0.9× 114 0.9× 46 0.5× 51 0.8× 83 1.5× 35 356
Maurice Overzier Netherlands 8 216 0.8× 92 0.8× 38 0.4× 27 0.4× 64 1.1× 15 317
Matthew Wicklund United States 12 223 0.9× 111 0.9× 23 0.3× 74 1.1× 127 2.2× 34 412
Meyke Schouten Netherlands 10 221 0.9× 60 0.5× 49 0.6× 82 1.2× 124 2.2× 19 420
Daniel Kjellgren Sweden 9 168 0.7× 70 0.6× 68 0.8× 37 0.6× 40 0.7× 11 455
David S. Lynch United Kingdom 13 346 1.4× 97 0.8× 210 2.5× 25 0.4× 145 2.5× 30 578
Dong-Hui Chen United States 9 370 1.5× 127 1.0× 39 0.5× 26 0.4× 277 4.9× 10 579
Tomokatsu Yoshida Japan 12 342 1.3× 140 1.1× 57 0.7× 12 0.2× 51 0.9× 54 546
Çiğdem Köroğlu United States 11 151 0.6× 115 0.9× 58 0.7× 11 0.2× 91 1.6× 20 361
Jean Christophe Antoine France 7 118 0.5× 179 1.5× 67 0.8× 19 0.3× 106 1.9× 10 384

Countries citing papers authored by Edgard Verdura

Since Specialization
Citations

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

Fields of papers citing papers by Edgard Verdura

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Edgard Verdura

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

All Works

17 of 17 papers shown
1.
Launay, Nathalie, Edgard Verdura, Gorka Fernández‐Eulate, et al.. (2024). Altered tubulin detyrosination due to SVBP malfunction induces cytokinesis failure and senescence, underlying a complex hereditary spastic paraplegia. Aging Cell. 24(1). e14355–e14355.
2.
Larasati, Yonika Arum, Gonzalo P. Solis, Alexey Koval, et al.. (2024). Clinical and Molecular Profiling in GNAO1 Permits Phenotype–Genotype Correlation. Movement Disorders. 39(9). 1578–1591. 6 indexed citations
3.
Launay, Nathalie, Montserrat Ruíz, Laura Planas‐Serra, et al.. (2023). RINT1 deficiency disrupts lipid metabolism and underlies a complex hereditary spastic paraplegia. Journal of Clinical Investigation. 133(14). 7 indexed citations
4.
Verdura, Edgard, Bruno Senger, Miquel Raspall‐Chaure, et al.. (2022). Loss of seryl-tRNA synthetase (SARS1) causes complex spastic paraplegia and cellular senescence. Journal of Medical Genetics. 59(12). 1227–1233. 7 indexed citations
5.
Dubail, Johanne, Sergio Aguilera, Chiara Paganini, et al.. (2022). Biallelic variants in SLC35B2 cause a novel chondrodysplasia with hypomyelinating leukodystrophy. Brain. 145(10). 3711–3722. 6 indexed citations
6.
Verdura, Edgard, et al.. (2021). Heterogeneity in Fragile X Syndrome Highlights the Need for Precision Medicine-Based Treatments. Frontiers in Psychiatry. 12. 722378–722378. 11 indexed citations
7.
Aloui, Chaker, Dominique Hervé, Gaëlle Marenne, et al.. (2021). End‐Truncated LAMB1 Causes a Hippocampal Memory Defect and a Leukoencephalopathy. Annals of Neurology. 90(6). 962–975. 10 indexed citations
8.
Rodríguez‐Palmero, Agustí, Agatha Schlüter, Edgard Verdura, et al.. (2020). A novel hypomorphic splice variant in EIF2B5 gene is associated with mild ovarioleukodystrophy. Annals of Clinical and Translational Neurology. 7(9). 1574–1579. 4 indexed citations
9.
Verdura, Edgard, Agatha Schlüter, Montserrat Ruíz, et al.. (2019). Complete loss of KCNA1 activity causes neonatal epileptic encephalopathy and dyskinesia. Journal of Medical Genetics. 57(2). 132–137. 31 indexed citations
10.
Verdura, Edgard, Agatha Schlüter, Gorka Fernández‐Eulate, et al.. (2019). A deep intronic splice variant advises reexamination of presumably dominant SPG7 Cases. Annals of Clinical and Translational Neurology. 7(1). 105–111. 14 indexed citations
11.
Casasnovas, Carlos, Edgard Verdura, Valentina Vélez-Santamaría, et al.. (2019). A novel mutation in the GFAP gene expands the phenotype of Alexander disease. Journal of Medical Genetics. 56(12). 846–849. 5 indexed citations
12.
Verdura, Edgard, Dominique Hervé, Eva Scharrer, et al.. (2015). HeterozygousHTRA1mutations are associated with autosomal dominant cerebral small vessel disease. Brain. 138(8). 2347–2358. 123 indexed citations
13.
Juan‐Mateu, Jonàs, Lidia González‐Quereda, Maria José Rodríguez, et al.. (2015). DMD Mutations in 576 Dystrophinopathy Families: A Step Forward in Genotype-Phenotype Correlations. PLoS ONE. 10(8). e0135189–e0135189. 109 indexed citations
14.
Gazal, Steven, Edgard Verdura, Françoise Bergametti, et al.. (2015). Can whole-exome sequencing data be used for linkage analysis?. European Journal of Human Genetics. 24(4). 581–586. 8 indexed citations
15.
Juan‐Mateu, Jonàs, Lidia González‐Quereda, Maria José Rodríguez, et al.. (2013). Interplay between DMD Point Mutations and Splicing Signals in Dystrophinopathy Phenotypes. PLoS ONE. 8(3). e59916–e59916. 39 indexed citations
16.
González‐Quereda, Lidia, Jonàs Juan‐Mateu, Edgard Verdura, et al.. (2011). LMNA mutation in progeroid syndrome in association with strokes. European Journal of Medical Genetics. 54(6). e576–e579. 4 indexed citations
17.
Juan‐Mateu, Jonàs, Carmen Paradas, Montse Olivé, et al.. (2011). Isolated cardiomyopathy caused by a DMD nonsense mutation in somatic mosaicism: genetic normalization in skeletal muscle. Clinical Genetics. 82(6). 574–578. 5 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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