Marina Pedemonte

3.5k total citations
57 papers, 1.3k citations indexed

About

Marina Pedemonte is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Marina Pedemonte has authored 57 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 39 papers in Molecular Biology, 16 papers in Genetics and 9 papers in Surgery. Recurrent topics in Marina Pedemonte's work include Muscle Physiology and Disorders (18 papers), Neurogenetic and Muscular Disorders Research (16 papers) and RNA modifications and cancer (11 papers). Marina Pedemonte is often cited by papers focused on Muscle Physiology and Disorders (18 papers), Neurogenetic and Muscular Disorders Research (16 papers) and RNA modifications and cancer (11 papers). Marina Pedemonte collaborates with scholars based in Italy, United States and United Kingdom. Marina Pedemonte's co-authors include Carlo Minetti, Claudio Bruno, Federico Zara, Ugo Carraro, Enrico Bertini, Marco Sandri, Roberta Biancheri, Michael P. Lisanti, Filippo M. Santorelli and Adele D’Amico and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Genetics and American Journal of Clinical Nutrition.

In The Last Decade

Marina Pedemonte

51 papers receiving 1.3k citations

Peers

Marina Pedemonte

GENET

CCM

SURGE

Raffaella Adami Italy

Luca Bello Italy

Christophe Hourdé France

A. Reha United States

Peter Reilich Germany

Chiara Fiorillo Italy

Diana M. Escolar United States

Susana Quijano‐Roy France

Antonella Pini Italy

Theodoros Kyriakides Cyprus

Raffaella Adami Italy

Marina Pedemonte

996 ×1.0

233 ×1.0

GENET

161 ×0.8

142 ×0.8

CCM

132 ×0.8

SURGE

Citations per year, relative to Marina Pedemonte Marina Pedemonte (= 1×) peers Raffaella Adami

Countries citing papers authored by Marina Pedemonte

Since Specialization

Citations

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

Fields of papers citing papers by Marina Pedemonte

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marina Pedemonte

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

All Works

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20 of 20 papers shown

Panicucci, Chiara, Francesca Bovis, Noemi Brolatti, et al.. (2025). Hand X-ray metrics for assessing bone health and fracture risk in Duchenne muscular dystrophy: a cross-sectional study. European Journal of Pediatrics. 184(12). 767–767.

Panicucci, Chiara, Noemi Brolatti, Marina Pedemonte, et al.. (2024). Bone Health Determinants in Ambulant Prepubertal Boys With Duchenne Muscular Dystrophy Treated With Deflazacort: Findings From a 3‐Year Study. Muscle & Nerve. 71(2). 191–199. 2 indexed citations

Panicucci, Chiara, Martina Bartolucci, Noemi Brolatti, et al.. (2024). Proteomics profiling and machine learning in nusinersen-treated patients with spinal muscular atrophy. Cellular and Molecular Life Sciences. 81(1). 393–393. 3 indexed citations

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.

Brolatti, Noemi, Federica Trucco, Paola Tacchetti, et al.. (2023). Structured Light Plethysmography for Non-Invasive Assessment of Respiratory Pattern in Spinal Muscular Atrophy Type 1. Journal of Clinical Medicine. 12(24). 7553–7553.

Panicucci, Chiara, Maria Beatrice Damasio, Noemi Brolatti, et al.. (2023). Long-term clinical and MRI follow-up in two POMT2-related limb girdle muscular dystrophy (LGMDR14) patients. Brain and Development. 45(5). 306–313.

Foppiani, Andrea, Ramona De Amicis, Alessandro Leone, et al.. (2021). Predictive fat mass equations for spinal muscular atrophy type I children: Development and internal validation. Clinical Nutrition. 40(4). 1578–1587. 3 indexed citations

Sansone, Valeria, Giorgia Coratti, Maria Carmela Pera, et al.. (2020). Sometimes they come back: New and old spinal muscular atrophy adults in the era of nusinersen. European Journal of Neurology. 28(2). 602–608. 8 indexed citations

Bertoli, Simona, Ramona De Amicis, Giorgio Bedogni, et al.. (2020). Predictive energy equations for spinal muscular atrophy type I children. American Journal of Clinical Nutrition. 111(5). 983–996. 10 indexed citations

10.

Coratti, Giorgia, Maria Carmela Pera, Simona Lucibello, et al.. (2020). Age and baseline values predict 12 and 24-month functional changes in type 2 SMA. Neuromuscular Disorders. 30(9). 756–764. 26 indexed citations

11.

Scala, Marcello, Giorgia Brigati, Chiara Fiorillo, et al.. (2019). Novel homozygous TSFM pathogenic variant associated with encephalocardiomyopathy with sensorineural hearing loss and peculiar neuroradiologic findings. Neurogenetics. 20(3). 165–172. 7 indexed citations

12.

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

13.

Trucco, Federica, Marina Pedemonte, Chiara Fiorillo, et al.. (2016). Respiratory pattern in a FSHD pediatric population. Respiratory Medicine. 119. 78–80. 7 indexed citations

14.

Biancheri, Roberta, Denise Cassandrini, Rosanna Trovato, et al.. (2013). EXOSC3 mutations in isolated cerebellar hypoplasia and spinal anterior horn involvement. Journal of Neurology. 260(7). 1866–1870. 19 indexed citations

15.

Ottonello, G., Chiara Mastella, Andrea Wolfler, et al.. (2011). Spinal Muscular Atrophy Type 1. American Journal of Physical Medicine & Rehabilitation. 90(11). 895–900. 11 indexed citations

16.

Zara, Federico, Roberta Biancheri, Claudio Bruno, et al.. (2006). Deficiency of hyccin, a newly identified membrane protein, causes hypomyelination and congenital cataract. Nature Genetics. 38(10). 1111–1113. 74 indexed citations

17.

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

18.

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

19.

Minetti, Carlo, Marco Gattorno, Silvia Repetto, et al.. (2005). Chemokine receptor CCR7 is expressed in muscle fibers in juvenile dermatomyositis. Biochemical and Biophysical Research Communications. 333(2). 540–543. 8 indexed citations

20.

Cordone, G, M. Bado, Giuseppe Morreale, Marina Pedemonte, & Carlo Minetti. (1996). Severe dystrophinopathy in a patient with congenital hypotonia. Child s Nervous System. 12(8). 466–9. 2 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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