Jorge A. Bevilacqua

1.6k total citations
54 papers, 928 citations indexed

About

Jorge A. Bevilacqua is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Cell Biology. According to data from OpenAlex, Jorge A. Bevilacqua has authored 54 papers receiving a total of 928 indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Molecular Biology, 16 papers in Cellular and Molecular Neuroscience and 15 papers in Cell Biology. Recurrent topics in Jorge A. Bevilacqua's work include Muscle Physiology and Disorders (19 papers), Genetic Neurodegenerative Diseases (13 papers) and Cellular transport and secretion (13 papers). Jorge A. Bevilacqua is often cited by papers focused on Muscle Physiology and Disorders (19 papers), Genetic Neurodegenerative Diseases (13 papers) and Cellular transport and secretion (13 papers). Jorge A. Bevilacqua collaborates with scholars based in Chile, France and United States. Jorge A. Bevilacqua's co-authors include Pablo Caviedes, Ana M. Cárdenas, Marc Bitoun, Pascale Guicheney, Norma B. Romero, Arlek M. González‐Jamett, Michel Fardeau, Bernard Prudhon, B. Eymard and Soledad Monges and has published in prestigious journals such as Journal of Neuroscience, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Jorge A. Bevilacqua

53 papers receiving 919 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jorge A. Bevilacqua Chile 18 657 303 279 225 147 54 928
Pervin Dinçer Türkiye 14 825 1.3× 313 1.0× 258 0.9× 176 0.8× 73 0.5× 45 947
Anne-Sophie Nicot France 11 559 0.9× 331 1.1× 164 0.6× 136 0.6× 134 0.9× 14 879
Eloisa De Sá Moreira Brazil 9 905 1.4× 195 0.6× 267 1.0× 244 1.1× 188 1.3× 13 1.1k
Andrea O’Neill United States 17 629 1.0× 285 0.9× 289 1.0× 139 0.6× 142 1.0× 27 969
Johann Böhm France 22 1.2k 1.8× 327 1.1× 311 1.1× 431 1.9× 116 0.8× 80 1.5k
Ikuya Nonaka Japan 17 977 1.5× 150 0.5× 228 0.8× 146 0.6× 195 1.3× 31 1.2k
S. Britton United Kingdom 6 914 1.4× 189 0.6× 227 0.8× 240 1.1× 242 1.6× 9 1.0k
R. Bashir United Kingdom 13 930 1.4× 173 0.6× 478 1.7× 137 0.6× 169 1.1× 25 1.2k
Susana Quijano‐Roy France 18 1.0k 1.6× 151 0.5× 233 0.8× 379 1.7× 95 0.6× 32 1.2k
Beate Schlotter‐Weigel Germany 15 779 1.2× 240 0.8× 338 1.2× 112 0.5× 348 2.4× 24 1.3k

Countries citing papers authored by Jorge A. Bevilacqua

Since Specialization
Citations

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

Fields of papers citing papers by Jorge A. Bevilacqua

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jorge A. Bevilacqua. 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 Jorge A. Bevilacqua. The network helps show where Jorge A. Bevilacqua may publish in the future.

Co-authorship network of co-authors of Jorge A. Bevilacqua

This figure shows the co-authorship network connecting the top 25 collaborators of Jorge A. Bevilacqua. A scholar is included among the top collaborators of Jorge A. Bevilacqua 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 Jorge A. Bevilacqua. Jorge A. Bevilacqua 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.
Bevilacqua, Jorge A., Hacer Durmuş, Josiah Chai, et al.. (2024). Detection of gene variants associated with recessive limb–girdle muscular weakness and Pompe disease in a global cohort of patients through the application of next-generation sequencing analysis. Frontiers in Genetics. 15. 1477291–1477291. 1 indexed citations
2.
Palmero, María José Guerra, Jorge A. Bevilacqua, Ana M. Cárdenas, et al.. (2023). A centronuclear myopathy‐causing mutation in dynamin‐2 disrupts neuronal morphology and excitatory synaptic transmission in a murine model of the disease. Neuropathology and Applied Neurobiology. 49(4). e12918–e12918. 3 indexed citations
3.
Bevilacqua, Jorge A., et al.. (2022). Novel autosomal dominant TPM3 mutation causes a combined congenital fibre type disproportion-cap disease histological pattern. Neuromuscular Disorders. 32(8). 687–691. 3 indexed citations
4.
Bevilacqua, Jorge A., et al.. (2021). Acute myopathy with skin manifestations, not always idiopathic and autoimmune. Neuromuscular Disorders. 31(11). 1218–1219.
5.
Bevilacqua, Jorge A., Alberto Dubrovsky, Marcondes C. França, et al.. (2020). The Latin American experience with a next generation sequencing genetic panel for recessive limb-girdle muscular weakness and Pompe disease. Orphanet Journal of Rare Diseases. 15(1). 11–11. 21 indexed citations
6.
Garibaldi, Matteo, John Rendu, Julie Brocard, et al.. (2019). ‘Dusty core disease’ (DuCD): expanding morphological spectrum of RYR1 recessive myopathies. Acta Neuropathologica Communications. 7(1). 3–3. 33 indexed citations
7.
Basualto-Alarcón, Carla, et al.. (2017). AB0176 Mitochondrial dysfunction in idiopathic inflammatory myopathy derived myoblasts. Annals of the Rheumatic Diseases. 76. 1108–1108. 4 indexed citations
8.
González‐Jamett, Arlek M., María José Guerra Palmero, Mai Thao Bui, et al.. (2017). Dynamin-2 mutations linked to Centronuclear Myopathy impair actin-dependent trafficking in muscle cells. Scientific Reports. 7(1). 28 indexed citations
9.
Cárdenas, Ana M., Arlek M. González‐Jamett, A. Luis, Jorge A. Bevilacqua, & Pablo Caviedes. (2016). Dysferlin function in skeletal muscle: Possible pathological mechanisms and therapeutical targets in dysferlinopathies. Experimental Neurology. 283(Pt A). 246–254. 51 indexed citations
10.
Luis, A., Jorge A. Bevilacqua, Ana M. Cárdenas, et al.. (2016). The absence of dysferlin induces the expression of functional connexin-based hemichannels in human myotubes. BMC Cell Biology. 17(S1). 15–15. 19 indexed citations
11.
Castiglioni, Claudia, et al.. (2015). Utilidad de la resonancia magnética en el diagnóstico de las enfermedades musculares hereditarias. Revista de Fomento Social. 21(4). 144–150. 2 indexed citations
12.
González‐Jamett, Arlek M., et al.. (2013). Dynamin-2 Function and Dysfunction Along the Secretory Pathway. Frontiers in Endocrinology. 4. 126–126. 51 indexed citations
13.
Bevilacqua, Jorge A., Nicole Monnier, Marc Bitoun, et al.. (2010). Recessive RYR1 mutations cause unusual congenital myopathy with prominent nuclear internalization and large areas of myofibrillar disorganization. Neuropathology and Applied Neurobiology. 37(3). 271–284. 75 indexed citations
14.
Bevilacqua, Jorge A., et al.. (2009). Dysferlinopathy in Chile: Evidence of Two Novel Mutations in the First Reported Cases. Genetic Testing and Molecular Biomarkers. 13(1). 105–108. 4 indexed citations
15.
Bitoun, Marc, Anne‐Cécile Durieux, Bernard Prudhon, et al.. (2009). Dynamin 2 mutations associated with human diseases impair clathrin-mediated receptor endocytosis. Human Mutation. 30(10). 1419–1427. 67 indexed citations
16.
Bitoun, Marc, Jorge A. Bevilacqua, B. Eymard, et al.. (2009). A NEW CENTRONUCLEAR MYOPATHY PHENOTYPE DUE TO A NOVEL DYNAMIN 2 MUTATION. Neurology. 72(1). 93–95. 28 indexed citations
17.
Bitoun, Marc, Jorge A. Bevilacqua, Bernard Prudhon, et al.. (2007). Dynamin 2 mutations cause sporadic centronuclear myopathy with neonatal onset. Annals of Neurology. 62(6). 666–670. 104 indexed citations
18.
Bevilacqua, Jorge A., Marc Bitoun, Svetlana Maugenre, et al.. (2006). G.P.8 11 Towards the identification of new morphological subtypes of congenital myopathy. Neuromuscular Disorders. 16(9-10). 709–710. 1 indexed citations
19.
Bevilacqua, Jorge A., et al.. (2002). Neuropatía por disulfiram: Comunicación de tres casos clínicos. Revista médica de Chile. 130(9). 1037–42. 5 indexed citations
20.

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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