Monica Traverso

1.8k total citations
32 papers, 488 citations indexed

About

Monica Traverso is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Monica Traverso has authored 32 papers receiving a total of 488 indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 8 papers in Genetics and 6 papers in Cellular and Molecular Neuroscience. Recurrent topics in Monica Traverso's work include Muscle Physiology and Disorders (10 papers), Cardiomyopathy and Myosin Studies (5 papers) and Genomics and Rare Diseases (4 papers). Monica Traverso is often cited by papers focused on Muscle Physiology and Disorders (10 papers), Cardiomyopathy and Myosin Studies (5 papers) and Genomics and Rare Diseases (4 papers). Monica Traverso collaborates with scholars based in Italy, United States and Canada. Monica Traverso's co-authors include Federico Zara, Carlo Minetti, Marina Pedemonte, Claudio Bruno, Stefania Assereto, Pasquale Striano, Elisabetta Gazzerro, Roberta Biancheri, Silvia Stringara and Michael P. Lisanti and has published in prestigious journals such as Annals of Neurology, Biochemical and Biophysical Research Communications and International Journal of Molecular Sciences.

In The Last Decade

Monica Traverso

30 papers receiving 479 citations

Peers

Monica Traverso
Roula Ghaoui Australia
Marcello Scala Italy
David S. Lynch United Kingdom
Eric Noé France
Soledad Monges Argentina
Tara Newcomb United States
Marc D’Hooghe Belgium
Saeko Ishida Japan
Takuya Hiraide Japan
Hanna Mierzewska Poland
Roula Ghaoui Australia
Monica Traverso
Citations per year, relative to Monica Traverso Monica Traverso (= 1×) peers Roula Ghaoui

Countries citing papers authored by Monica Traverso

Since Specialization
Citations

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

Fields of papers citing papers by Monica Traverso

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Monica Traverso

This figure shows the co-authorship network connecting the top 25 collaborators of Monica Traverso. A scholar is included among the top collaborators of Monica Traverso 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 Monica Traverso. Monica Traverso 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.
Haanpää, Maria K., John R. Pollard, Monica Traverso, et al.. (2024). Expanding the phenotype of UPF3B‐related disorder: Case reports and literature review. American Journal of Medical Genetics Part A. 194(6). e63534–e63534. 3 indexed citations
2.
Traverso, Monica, Michele Iacomino, Marco Di Duca, et al.. (2024). DAG1 haploinsufficiency is associated with sporadic and familial isolated or pauci-symptomatic hyperCKemia. European Journal of Human Genetics. 32(3). 342–349. 1 indexed citations
3.
Fossa, Paola, Chiara Fiorillo, Chiara Gemelli, et al.. (2024). Case report: A single novel calpain 3 gene variant associated with mild myopathy. Frontiers in Genetics. 15. 1437859–1437859.
4.
Panicucci, Chiara, Monica Traverso, Noemi Brolatti, et al.. (2023). Early Muscle MRI Findings in a Pediatric Case of Emery-Dreifuss Muscular Dystrophy Type 1. Neuropediatrics. 54(6). 426–429.
5.
Iacomino, Michele, Monica Traverso, Mariasavina Severino, et al.. (2023). Refining the electroclinical spectrum of NPRL3‐related epilepsy: A novel multiplex family and literature review. Epilepsia Open. 8(4). 1314–1330. 6 indexed citations
6.
Scala, Marcello, Patrizia De Marco, Monica Traverso, et al.. (2023). Case report: Revascularization failure in NF1-related moyamoya syndrome after selumetinib: A possible pathophysiological correlation?. Frontiers in Pediatrics. 11. 1051026–1051026. 4 indexed citations
7.
Baldassari, Sımona, Chiara Cervetto, Floriana Fruscione, et al.. (2022). Vesicular Glutamate Release from Feeder-FreehiPSC-Derived Neurons. International Journal of Molecular Sciences. 23(18). 10545–10545. 8 indexed citations
8.
Conteduca, Giuseppina, Chiara Baldo, Monica Traverso, et al.. (2022). Generation of induced pluripotent stem cell lines from a patient with Sotos syndrome carrying 5q35 microdeletion. Stem Cell Research. 66. 103007–103007. 1 indexed citations
9.
Miano, Maurizio, Alice Grossi, Elena Palmisani, et al.. (2022). Underlying Inborn Errors of Immunity in Patients With Evans Syndrome and Multilineage Cytopenias: A Single-Centre Analysis. Frontiers in Immunology. 13. 869033–869033. 14 indexed citations
10.
Fiorillo, Chiara, Paolo Broda, Monica Traverso, et al.. (2021). The Role of Muscle Biopsy in Diagnostic Process of Infant Hypotonia: From Clinical Classification to the Genetic Outcome. Frontiers in Neurology. 12. 735488–735488. 2 indexed citations
11.
Traverso, Monica, Stefania Assereto, Michele Iacomino, et al.. (2018). Clinical and molecular consequences of exon 78 deletion in DMD gene. Journal of Human Genetics. 63(6). 761–764. 7 indexed citations
12.
Bernardo, Pia, Francesca Madia, Lia Santulli, et al.. (2016). 17q21.31 microdeletion syndrome: Description of a case further contributing to the delineation of Koolen-de Vries syndrome. Brain and Development. 38(7). 663–668. 7 indexed citations
13.
Dilena, Robertino, Pasquale Striano, Monica Traverso, et al.. (2015). Dramatic effect of levetiracetam in early-onset epileptic encephalopathy due to STXBP1 mutation. Brain and Development. 38(1). 128–131. 37 indexed citations
14.
Trivisano, Marina, Pasquale Striano, Lucio Giordano, et al.. (2015). CHD2 mutations are a rare cause of generalized epilepsy with myoclonic–atonic seizures. Epilepsy & Behavior. 51. 53–56. 27 indexed citations
15.
Papa, Riccardo, Francesca Madia, Federica Trucco, et al.. (2015). Genetic and Early Clinical Manifestations of Females Heterozygous for Duchenne/Becker Muscular Dystrophy. Pediatric Neurology. 55. 58–63. 32 indexed citations
16.
Traverso, Monica, Stefania Assereto, Elisabetta Gazzerro, et al.. (2013). Novel FAM126A mutations in hypomyelination and congenital cataract disease. Biochemical and Biophysical Research Communications. 439(3). 369–372. 13 indexed citations
17.
Traverso, Monica, Özge Özalp Yüreğir, Aviva Mimouni-Bloch, et al.. (2012). Hypomyelination and congenital cataract: Identification of novel mutations in two unrelated families. European Journal of Paediatric Neurology. 17(1). 108–111. 4 indexed citations
18.
Assereto, Stefania, Silvia Stringara, Federica Sotgia, et al.. (2005). Pharmacological rescue of the dystrophin-glycoprotein complex in Duchenne and Becker skeletal muscle explants by proteasome inhibitor treatment. American Journal of Physiology-Cell Physiology. 290(2). C577–C582. 56 indexed citations
19.
Traverso, Monica, Mauro Malnati, Carlo Minetti, et al.. (2005). Multiplex real-time PCR for detection of deletions and duplications in dystrophin gene. Biochemical and Biophysical Research Communications. 339(1). 145–150. 31 indexed citations
20.
Bruno, Claudio, Filippo M. Santorelli, Stefania Assereto, et al.. (2003). Progressive exercise intolerance associated with a new muscle‐restricted nonsense mutation (G142X) in the mitochondrial cytochrome b gene. Muscle & Nerve. 28(4). 508–511. 40 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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