Stefania Magri

2.1k total citations
33 papers, 477 citations indexed

About

Stefania Magri is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Stefania Magri has authored 33 papers receiving a total of 477 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 22 papers in Cellular and Molecular Neuroscience and 6 papers in Neurology. Recurrent topics in Stefania Magri's work include Hereditary Neurological Disorders (15 papers), Genetic Neurodegenerative Diseases (14 papers) and Mitochondrial Function and Pathology (10 papers). Stefania Magri is often cited by papers focused on Hereditary Neurological Disorders (15 papers), Genetic Neurodegenerative Diseases (14 papers) and Mitochondrial Function and Pathology (10 papers). Stefania Magri collaborates with scholars based in Italy, United Kingdom and United States. Stefania Magri's co-authors include Franco Taroni, Daniela Di Bella, Davide Pareyson, Cinzia Gellera, Paola Saveri, Giuseppe Piscosquito, Caterina Mariotti, Lorenzo Nanetti, Alexis Brice and Daniel R. Scoles and has published in prestigious journals such as PLoS ONE, Epilepsia and Movement Disorders.

In The Last Decade

Stefania Magri

29 papers receiving 471 citations

Peers

Stefania Magri
Marie‐Josée Dicaire Canada
S. A. Klyushnikov Russia
Fiorella Speziani United States
Stéphanie Efthymiou United Kingdom
Marie Coutelier France
Afagh Alavi Iran
Alleene V. Strickland United States
Lemuel Racacho Canada
Naïma Bouslam Morocco
Dolores Martínez‐Rubio Spain
Marie‐Josée Dicaire Canada
Stefania Magri
Citations per year, relative to Stefania Magri Stefania Magri (= 1×) peers Marie‐Josée Dicaire

Countries citing papers authored by Stefania Magri

Since Specialization
Citations

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

Fields of papers citing papers by Stefania Magri

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Stefania Magri

This figure shows the co-authorship network connecting the top 25 collaborators of Stefania Magri. A scholar is included among the top collaborators of Stefania Magri 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 Stefania Magri. Stefania Magri 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.
Tedesco, B., Veronica Ferrari, Marta Chierichetti, et al.. (2025). One gene, many phenotypes: the role of KIF5A in neurodegenerative and neurodevelopmental diseases. Cell Communication and Signaling. 23(1). 287–287.
2.
Ciaccio, Claudia, Chiara Pantaleoni, Marina Grisoli, et al.. (2024). Phenotypic Spectrum and Natural History of Gillespie Syndrome. An Updated Literature Review with 2 New Cases. The Cerebellum. 23(6). 2655–2670.
3.
Castellotti, Barbara, Laura Canafoglia, Elena Freri, et al.. (2023). Progressive myoclonus epilepsies due to SEMA6B mutations. New variants and appraisal of published phenotypes. Epilepsia Open. 8(2). 645–650. 6 indexed citations
4.
Nanetti, Lorenzo, Stefania Magri, Mario Fichera, et al.. (2023). Complex Ataxia‐Dementia Phenotype in Patients with Digenic TBP/STUB1 Spinocerebellar Ataxia. Movement Disorders. 38(4). 665–675. 10 indexed citations
5.
Saveri, Paola, Stefania Magri, Emanuela Maderna, et al.. (2022). DNAJB2‐related Charcot‐Marie‐Tooth disease type 2: Pathomechanism insights and phenotypic spectrum widening. European Journal of Neurology. 29(7). 2056–2065. 11 indexed citations
6.
Bossolasco, Patrizia, Stefania Magri, Claudia Colombrita, et al.. (2022). Generation of an iPSC line from a patient with spastic paraplegia type 10 carrying a novel mutation in KIF5A gene. Stem Cell Research. 66. 103008–103008. 2 indexed citations
7.
Abati, Elena, Stefania Magri, Megi Meneri, et al.. (2021). Charcot–Marie–Tooth disease type 2F associated with biallelic HSPB1 mutations. Annals of Clinical and Translational Neurology. 8(5). 1158–1164. 6 indexed citations
8.
Magri, Stefania, Lorenzo Nanetti, Cinzia Gellera, et al.. (2021). Digenic inheritance of STUB1 variants and TBP polyglutamine expansions explains the incomplete penetrance of SCA17 and SCA48. Genetics in Medicine. 24(1). 29–40. 32 indexed citations
9.
Freri, Elena, Barbara Castellotti, Laura Canafoglia, et al.. (2021). Severe epilepsy in CNTNAP2-related Pitt-Hopkins-like syndrome successfully treated with stiripentol. Seizure. 88. 143–145. 7 indexed citations
10.
Gatti, Marta, Stefania Magri, Daniela Di Bella, et al.. (2021). Spastic paraplegia type 46: novel and recurrent GBA2 gene variants in a compound heterozygous Italian patient with spastic ataxia phenotype. Neurological Sciences. 42(11). 4741–4745. 4 indexed citations
11.
Almomani, Rowida, Margherita Marchi, Patrick Lindsey, et al.. (2020). Evaluation of molecular inversion probe versus TruSeq® custom methods for targeted next-generation sequencing. PLoS ONE. 15(9). e0238467–e0238467. 13 indexed citations
12.
Pensato, Viviana, Stefania Magri, Eleonora Dalla Bella, et al.. (2020). Sorting Rare ALS Genetic Variants by Targeted Re-Sequencing Panel in Italian Patients: OPTN, VCP, and SQSTM1 Variants Account for 3% of Rare Genetic Forms. Journal of Clinical Medicine. 9(2). 412–412. 23 indexed citations
13.
Saveri, Paola, Maria De Luca, Chiara Pisciotta, et al.. (2020). Charcot-Marie-Tooth Type 2B: A New Phenotype Associated with a Novel RAB7A Mutation and Inhibited EGFR Degradation. Cells. 9(4). 1028–1028. 24 indexed citations
14.
Magri, Stefania, Elena Salvatore, Elena Rizzo, et al.. (2020). Frequency and distribution of polyQ disease intermediate-length repeat alleles in healthy Italian population. Neurological Sciences. 41(6). 1475–1482. 6 indexed citations
15.
Nanetti, Lorenzo, Elisa Sarto, Anna Castaldo, et al.. (2018). ANO10 mutational screening in recessive ataxia: genetic findings and refinement of the clinical phenotype. Journal of Neurology. 266(2). 378–385. 12 indexed citations
16.
Ragona, Francesca, Barbara Castellotti, Stefania Magri, et al.. (2017). Alternating Hemiplegia and Epilepsia Partialis Continua: A new phenotype for a novel compound TBC1D24 mutation. Seizure. 47. 71–73. 15 indexed citations
17.
Cortese, Andrea, Matilde Laurá, Carlo Casali, et al.. (2017). Altered TDP‐43‐dependent splicing in HSPB8‐related distal hereditary motor neuropathy and myofibrillar myopathy. European Journal of Neurology. 25(1). 154–163. 25 indexed citations
18.
Corrado, Lucia, Stefania Magri, Alessandra Bagarotti, et al.. (2016). A novel synonymous mutation in the MPZ gene causing an aberrant splicing pattern and Charcot-Marie-Tooth disease type 1b. Neuromuscular Disorders. 26(8). 516–520. 19 indexed citations
19.
Piscosquito, Giuseppe, Stefania Magri, Paola Saveri, et al.. (2016). A novel NDRG1 mutation in a non‐Romani patient with CMT4D/HMSN‐Lom. Journal of the Peripheral Nervous System. 22(1). 47–50. 8 indexed citations
20.
Piscosquito, Giuseppe, Paola Saveri, Stefania Magri, et al.. (2015). Mutational mechanisms in MFN2‐related neuropathy: compound heterozygosity for recessive and semidominant mutations. Journal of the Peripheral Nervous System. 20(4). 380–386. 23 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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