Soledad Monges

2.9k total citations
28 papers, 509 citations indexed

About

Soledad Monges is a scholar working on Molecular Biology, Genetics and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Soledad Monges has authored 28 papers receiving a total of 509 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 7 papers in Genetics and 6 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Soledad Monges's work include Muscle Physiology and Disorders (10 papers), Neurogenetic and Muscular Disorders Research (7 papers) and Nuclear Structure and Function (6 papers). Soledad Monges is often cited by papers focused on Muscle Physiology and Disorders (10 papers), Neurogenetic and Muscular Disorders Research (7 papers) and Nuclear Structure and Function (6 papers). Soledad Monges collaborates with scholars based in Argentina, France and Chile. Soledad Monges's co-authors include Fabiana Lubieniecki, Jorge A. Bevilacqua, Pascale Guicheney, Michel Fardeau, Marc Bitoun, Ana Lía Taratuto, Norma B. Romero, Emmanuelle Uro‐Coste, Svetlana Maugenre and Claude Cancès and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Annals of Neurology.

In The Last Decade

Soledad Monges

28 papers receiving 501 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Soledad Monges Argentina 12 360 135 110 109 107 28 509
C. Scotton Italy 14 443 1.2× 89 0.7× 84 0.8× 65 0.6× 60 0.6× 20 541
Francesco Laschena Italy 12 419 1.2× 192 1.4× 172 1.6× 104 1.0× 20 0.2× 18 534
Claudia Castiglioni Chile 15 320 0.9× 99 0.7× 111 1.0× 125 1.1× 54 0.5× 47 566
Nicoletta Checcarelli Italy 14 531 1.5× 88 0.7× 71 0.6× 38 0.3× 48 0.4× 23 731
Tiziana Mongini Italy 14 399 1.1× 117 0.9× 141 1.3× 48 0.4× 103 1.0× 46 595
Matthew Wicklund United States 12 223 0.6× 74 0.5× 127 1.2× 83 0.8× 31 0.3× 34 412
M.L. Mostacciuolo Italy 12 289 0.8× 119 0.9× 113 1.0× 88 0.8× 29 0.3× 18 466
Robyn Labrum United Kingdom 14 488 1.4× 145 1.1× 400 3.6× 44 0.4× 41 0.4× 21 772
Marie‐Louise Sveen Denmark 11 546 1.5× 173 1.3× 256 2.3× 144 1.3× 90 0.8× 14 716
Dan Cox United Kingdom 11 221 0.6× 36 0.3× 71 0.6× 25 0.2× 98 0.9× 18 389

Countries citing papers authored by Soledad Monges

Since Specialization
Citations

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

Fields of papers citing papers by Soledad Monges

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Soledad Monges

This figure shows the co-authorship network connecting the top 25 collaborators of Soledad Monges. A scholar is included among the top collaborators of Soledad Monges 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 Soledad Monges. Soledad Monges 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.
Foncuberta, María Eugenia, et al.. (2024). A novel deep intronic variant in the DMD gene causes Duchenne muscular dystrophy by pseudoexon activation encoding a nonsense codon. Gene. 930. 148862–148862. 1 indexed citations
2.
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
3.
Moreno, Cristiane Araújo Martins, Eduardo de Paula Estephan, Soledad Monges, et al.. (2019). Congenital fiber type disproportion caused by TPM3 mutation: A report of two atypical cases. Neuromuscular Disorders. 30(1). 54–58. 6 indexed citations
4.
Monges, Soledad, Edoardo Malfatti, Fabiana Lubieniecki, et al.. (2018). Sarcomeric disorganization and nemaline bodies in muscle biopsies of patients with EXOSC3‐related type 1 pontocerebellar hypoplasia. Muscle & Nerve. 59(1). 137–141. 6 indexed citations
5.
Monges, Soledad & Alberto L. Rosa. (2017). Management of neuromuscular diseases and spinal muscular atrophy in Latin America. Gene Therapy. 24(9). 578–580. 6 indexed citations
6.
Monges, Soledad, et al.. (2017). Energy expenditure, body composition, and prevalence of metabolic disorders in patients with Duchenne muscular dystrophy. Diabetes & Metabolic Syndrome Clinical Research & Reviews. 12(2). 81–85. 46 indexed citations
7.
Dabaj, Ivana, Rabah Ben Yaou, C. Bönnemann, et al.. (2017). Corticosteroid treatment in early-onset lamin A/C related muscular dystrophies. Neuromuscular Disorders. 27. S138–S138. 1 indexed citations
8.
Yaou, Rabah Ben, Ivana Dabaj, Gina Norato, et al.. (2017). First results from the international LMNA-related congenital and childhood onset muscular dystrophy retrospective natural history study. Neuromuscular Disorders. 27. S137–S138. 1 indexed citations
9.
Monges, Soledad, Laura Alías, Sara Bernal, et al.. (2016). Genotype–phenotype correlation of SMN locus genes in spinal muscular atrophy children from Argentina. European Journal of Paediatric Neurology. 20(6). 910–917. 18 indexed citations
10.
Malfatti, Edoardo, Soledad Monges, Vilma‐Lotta Lehtokari, et al.. (2015). Bilateral foot-drop as predominant symptom in nebulin (NEB) gene related “core-rod” congenital myopathy. European Journal of Medical Genetics. 58(10). 556–561. 11 indexed citations
11.
12.
Dubrovsky, Alberto, E. Fulgenzi, Hernán Amartino, et al.. (2014). Consenso argentino para el diagnóstico, seguimiento y tratamiento de la enfermedad de Pompe. Neurología Argentina. 6(2). 96–113. 2 indexed citations
13.
Ruggieri, Víctor, Soledad Monges, Roberto Caraballo, et al.. (2013). Encefalitis aguda mediada por anticuerpos contra el receptor ionotrópico de glutamato activado por N-metil-D-aspartato (NMDAR): análisis de once casos pediátricos en Argentina (Premio Benito Yelín). SHILAP Revista de lepidopterología. 73. 1–9. 8 indexed citations
14.
Caraballo, Roberto, et al.. (2013). Rasmussen syndrome: An Argentinean experience in 32 patients. Seizure. 22(5). 360–367. 16 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.
Cho, Tae‐Joon, Kazu Matsumoto, Virginia Fano, et al.. (2012). TRPV4‐pathy manifesting both skeletal dysplasia and peripheral neuropathy: A report of three patients. American Journal of Medical Genetics Part A. 158A(4). 795–802. 45 indexed citations
17.
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
18.
Lubieniecki, Fabiana, Soledad Monges, Alberto Dubrovsky, et al.. (2007). G.P.5.01 Inflammatory or ‘congenital myopathy’ type findings in muscle biopsies of patients with LMNA mutations. Neuromuscular Disorders. 17(9-10). 797–797. 2 indexed citations
19.
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
20.
Monges, Soledad, et al.. (2003). Epilepsia mioclónica refleja del lactante: un nuevo síndrome epiléptico reflejo o una variante de la epilepsia mioclónica benigna del lactante. Revista de Neurología. 36(5). 429–429. 12 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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