Anna Modoni

1.9k total citations
58 papers, 1.1k citations indexed

About

Anna Modoni is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Anna Modoni has authored 58 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 34 papers in Molecular Biology, 28 papers in Cellular and Molecular Neuroscience and 17 papers in Neurology. Recurrent topics in Anna Modoni's work include Genetic Neurodegenerative Diseases (26 papers), Mitochondrial Function and Pathology (12 papers) and Ion channel regulation and function (10 papers). Anna Modoni is often cited by papers focused on Genetic Neurodegenerative Diseases (26 papers), Mitochondrial Function and Pathology (12 papers) and Ion channel regulation and function (10 papers). Anna Modoni collaborates with scholars based in Italy, United States and Japan. Anna Modoni's co-authors include Gabriella Silvestri, Pietro Tonali, Camillo Marra, Enzo Ricci, Marcella Masciullo, Maria Grazia Pomponi, Massimo Santoro, Adele D’Amico, Massimiliano Mirabella and Giorgio Tasca and has published in prestigious journals such as SHILAP Revista de lepidopterología, Blood and Neurology.

In The Last Decade

Anna Modoni

55 papers receiving 1.1k citations

Peers

Anna Modoni
Anna Modoni
Citations per year, relative to Anna Modoni Anna Modoni (= 1×) peers Enrico Bugiardini

Countries citing papers authored by Anna Modoni

Since Specialization
Citations

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

Fields of papers citing papers by Anna Modoni

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anna Modoni

This figure shows the co-authorship network connecting the top 25 collaborators of Anna Modoni. A scholar is included among the top collaborators of Anna Modoni 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 Anna Modoni. Anna Modoni 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.
Galli, Eugenio, Roberta Di Blasi, Alice Di Rocco, et al.. (2025). Routine prophylaxis with levetiracetam offers no benefit in CD19 CAR-T for LBCL: a multicenter propensity-matched study. Blood Advances. 9(21). 5501–5509.
2.
Modoni, Anna, Catello Vollono, Eugenio Galli, et al.. (2025). Predictors of Neurotoxicity in a Large Cohort of Italian Patients Undergoing Anti‐CD19 Chimeric Antigen Receptor (CAR) T‐Cell Therapy. Brain and Behavior. 15(9). e70891–e70891.
3.
Galli, Eugenio, Anna Modoni, Luca Battistini, et al.. (2023). Blood-Brain Barrier and Neuronal Damage during Icans in Patients Treated with Anti-CD19 CAR-T Cells. Blood. 142(Supplement 1). 2128–2128. 2 indexed citations
4.
Luigetti, Marco, Valeria Guglielmino, Marina Romozzi, et al.. (2022). Nerve Conduction Studies of Dorsal Sural Nerve: Normative Data and Its Potential Application in ATTRv Pre-Symptomatic Subjects. Brain Sciences. 12(8). 1037–1037. 4 indexed citations
5.
Nicoletti, Tommaso, Salvatore Rossi, Maria Gabriella Vita, et al.. (2022). Elevated serum Neurofilament Light chain (NfL) as a potential biomarker of neurological involvement in Myotonic Dystrophy type 1 (DM1). Journal of Neurology. 269(9). 5085–5092. 6 indexed citations
6.
Santoro, Massimo, Alessia Perna, Piergiorgio La Rosa, et al.. (2020). Compound heterozygosity for an expanded (GAA) and a (GAAGGA) repeat at FXN locus: from a diagnostic pitfall to potential clues to the pathogenesis of Friedreich ataxia. Neurogenetics. 21(4). 279–287. 3 indexed citations
7.
Bruno, Carmine, Francesco D’Argento, Alfredo Pontecorvi, et al.. (2019). A Late Onset of Wernicke-Korsakoff Encephalopathy After Biliopancreatic Diversion: a Case Report. Obesity Surgery. 29(7). 2309–2311. 1 indexed citations
8.
Silvestri, Gabriella, Elide Mantuano, Anna Modoni, et al.. (2017). A channelopathy mutation in the voltage-sensor discloses contributions of a conserved phenylalanine to gating properties of Kv1.1 channels and ataxia. Scientific Reports. 7(1). 174–174. 14 indexed citations
9.
Vanacore, Nicola, Emanuele Rastelli, Giovanni Antonini, et al.. (2016). An Age-Standardized Prevalence Estimate and a Sex and Age Distribution of Myotonic Dystrophy Types 1 and 2 in the Rome Province, Italy. Neuroepidemiology. 46(3). 191–197. 32 indexed citations
10.
Bianchi, Maria Laura Ester, Emanuele Leoncini, Marcella Masciullo, et al.. (2016). Increased risk of tumor in DM1 is not related to exposure to common lifestyle risk factors. Journal of Neurology. 263(3). 492–498. 23 indexed citations
11.
Monaco, Mauro Lo, Adele D’Amico, Marco Luigetti, Jean‐François Desaphy, & Anna Modoni. (2014). Effect of mexiletine on transitory depression of compound motor action potential in recessive myotonia congenita. Clinical Neurophysiology. 126(2). 399–403. 21 indexed citations
12.
Santoro, Massimo, Marcella Masciullo, Roberta Pietrobono, et al.. (2012). Molecular, clinical, and muscle studies in myotonic dystrophy type 1 (DM1) associated with novel variant CCG expansions. Journal of Neurology. 260(5). 1245–1257. 31 indexed citations
13.
Lecchi, Marzia, Valeria Sansone, Elisa Redaelli, et al.. (2012). Myotonia congenita: Novel mutations in CLCN1 gene and functional characterizations in Italian patients. Journal of the Neurological Sciences. 318(1-2). 65–71. 21 indexed citations
14.
Vadacca, Marta, et al.. (2011). Neuropsychiatric Lupus Erythematosus. Reumatismo. 58(3). 177–86. 7 indexed citations
15.
Modoni, Anna, Maria Laura Ester Bianchi, Nicola Vitulano, et al.. (2011). Lack of Any Cardiac Involvement in a Patient with Andersen-Tawil Syndrome Associated with the c.574A→G Mutation in <i>KCNJ2</i>. Cardiology. 120(4). 200–203. 3 indexed citations
16.
Modoni, Anna, Adele D’Amico, Bruno Dallapiccola, et al.. (2011). Low-Rate Repetitive Nerve Stimulation Protocol in an Italian Cohort of Patients Affected by Recessive Myotonia Congenita. Journal of Clinical Neurophysiology. 28(1). 39–44. 16 indexed citations
17.
Modoni, Anna, Marcella Masciullo, Pietro Spinelli, et al.. (2009). Successful Treatment of Acute Autoimmune Limbic Encephalitis With Negative VGKC and NMDAR Antibodies. Cognitive and Behavioral Neurology. 22(1). 63–66. 26 indexed citations
18.
Modoni, Anna, Gabriella Silvestri, Maria Gabriella Vita, et al.. (2008). Cognitive impairment in myotonic dystrophy type 1 (DM1). Journal of Neurology. 255(11). 1737–1742. 66 indexed citations
19.
Gidaro, Teresa, Anna Modoni, Mario Sabatelli, et al.. (2007). An Italian family with inclusion‐body myopathy and frontotemporal dementia due to mutation in the VCP gene. Muscle & Nerve. 37(1). 111–114. 36 indexed citations
20.
Odoardi, Francesca, Michele Rana, Aldobrando Broccolini, et al.. (2003). Pathogenic role of mtDNA duplications in mitochondrial diseases associated with mtDNA deletions. American Journal of Medical Genetics Part A. 118A(3). 247–254. 15 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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