Stefano Gambardella

2.5k total citations
74 papers, 1.7k citations indexed

About

Stefano Gambardella is a scholar working on Molecular Biology, Neurology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Stefano Gambardella has authored 74 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Molecular Biology, 17 papers in Neurology and 14 papers in Cellular and Molecular Neuroscience. Recurrent topics in Stefano Gambardella's work include Parkinson's Disease Mechanisms and Treatments (10 papers), Genetic Neurodegenerative Diseases (9 papers) and Autophagy in Disease and Therapy (9 papers). Stefano Gambardella is often cited by papers focused on Parkinson's Disease Mechanisms and Treatments (10 papers), Genetic Neurodegenerative Diseases (9 papers) and Autophagy in Disease and Therapy (9 papers). Stefano Gambardella collaborates with scholars based in Italy, Albania and United States. Stefano Gambardella's co-authors include Francesco Fornai, Francesca Biagioni, Fiona Limanaqi, Giuseppe Novelli, Rosangela Ferese, Carla L. Busceti, Alessandro Frati, Larisa Ryskalin, Emiliano Giardina and Fabrizio Rinaldi and has published in prestigious journals such as Journal of Biological Chemistry, American Journal of Respiratory and Critical Care Medicine and Brain Research.

In The Last Decade

Stefano Gambardella

72 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Stefano Gambardella Italy	24	759	291	256	236	217	74	1.7k
Murat Digicaylioglu United States	19	768 1.0×	316 1.1×	195 0.8×	155 0.7×	228 1.1×	28	1.9k
Dong Seok Kim South Korea	30	672 0.9×	426 1.5×	471 1.8×	229 1.0×	243 1.1×	90	2.4k
Chuanzhu Yan China	24	1.4k 1.8×	311 1.1×	328 1.3×	301 1.3×	366 1.7×	172	2.4k
Ingrid Lang Austria	28	557 0.7×	247 0.8×	355 1.4×	237 1.0×	239 1.1×	60	2.3k
Gerald Pfeffer Canada	22	1.2k 1.6×	307 1.1×	271 1.1×	191 0.8×	105 0.5×	75	1.9k
Alpa Trivedi United States	21	1.1k 1.4×	310 1.1×	176 0.7×	138 0.6×	113 0.5×	45	2.3k
George E. Farmer United States	17	957 1.3×	127 0.4×	299 1.2×	125 0.5×	133 0.6×	41	2.2k
Luca Peruzzotti‐Jametti United Kingdom	26	890 1.2×	377 1.3×	158 0.6×	286 1.2×	152 0.7×	46	2.0k
Meenakshi B. Bhattacharjee United States	19	662 0.9×	135 0.5×	241 0.9×	251 1.1×	202 0.9×	59	1.4k

Countries citing papers authored by Stefano Gambardella

Since Specialization

Citations

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

Fields of papers citing papers by Stefano Gambardella

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Stefano Gambardella

This figure shows the co-authorship network connecting the top 25 collaborators of Stefano Gambardella. A scholar is included among the top collaborators of Stefano Gambardella 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 Stefano Gambardella. Stefano Gambardella 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

Paparella, Giulia, et al.. (2025). Isolated Generalized Chorea in a Patient with Small-Expanded Allele Spinocerebellar Ataxia 17. The Cerebellum. 24(4). 110–110.

Dolcetti, Ettore, Fabio Buttari, Antonio Bruno, et al.. (2024). An IL-5 Single-Nucleotide Polymorphism Influences Neuroinflammation and Prospective Disease Activity in Multiple Sclerosis. International Journal of Molecular Sciences. 25(16). 9108–9108. 1 indexed citations

Ferese, Rosangela, Simona Scala, Antonio Suppa, et al.. (2023). Cohort analysis of novel SPAST variants in SPG4 patients and implementation of in vitro and in vivo studies to identify the pathogenic mechanism caused by splicing mutations. Frontiers in Neurology. 14. 1296924–1296924. 3 indexed citations

Bruno, Antonio, Ettore Dolcetti, Alessandro Moscatelli, et al.. (2022). Interleukin 6 SNP rs1818879 Regulates Radiological and Inflammatory Activity in Multiple Sclerosis. Genes. 13(5). 897–897. 6 indexed citations

Dolcetti, Ettore, Antonio Bruno, Luana Gilio, et al.. (2022). The BDNF Val66Met Polymorphism (rs6265) Modulates Inflammation and Neurodegeneration in the Early Phases of Multiple Sclerosis. Genes. 13(2). 332–332. 10 indexed citations

Iannielli, Angelo, Mirko Luoni, Serena Giannelli, et al.. (2022). Modeling native and seeded Synuclein aggregation and related cellular dysfunctions in dopaminergic neurons derived by a new set of isogenic iPSC lines with SNCA multiplications. Cell Death and Disease. 13(10). 881–881. 10 indexed citations

Fusco, Carmela, Dario Ronchi, Stefano Gambardella, et al.. (2021). Improving clinical interpretation of five KRIT1 and PDCD10 intronic variants. Clinical Genetics. 99(6). 829–835.

Strafella, Claudia, Valerio Caputo, Andrea Termine, et al.. (2020). Analysis of ACE2 Genetic Variability among Populations Highlights a Possible Link with COVID-19-Related Neurological Complications. Genes. 11(7). 741–741. 60 indexed citations

Bassi, Mario Stampanoni, Fabio Buttari, Ilaria Simonelli, et al.. (2020). A Single Nucleotide ADA Genetic Variant Is Associated to Central Inflammation and Clinical Presentation in MS: Implications for Cladribine Treatment. Genes. 11(10). 1152–1152. 6 indexed citations

10.

Ferese, Rosangela, Paola Lenzi, Federica Fulceri, et al.. (2020). Quantitative Ultrastructural Morphometry and Gene Expression of mTOR-Related Mitochondriogenesis within Glioblastoma Cells. International Journal of Molecular Sciences. 21(13). 4570–4570. 19 indexed citations

11.

Ferese, Rosangela, Stefania Zampatti, Emiliano Giardina, et al.. (2020). A novel POLR3A genotype leads to leukodystrophy type-7 in two siblings with unusually late age of onset. BMC Neurology. 20(1). 258–258. 7 indexed citations

12.

Mancini, Valentina, Viviana Frantellizzi, Stefania Zampatti, et al.. (2019). Migrainous Infarction in a Patient With Sporadic Hemiplegic Migraine and Cystic Fibrosis: A 99mTc‐HMPAO Brain SPECT Study. Headache The Journal of Head and Face Pain. 59(2). 253–258. 8 indexed citations

13.

Gambardella, Stefano, et al.. (2019). Unusual Segregation of <b><i>APP</i></b> Mutations in Monogenic Alzheimer Disease. Neurodegenerative Diseases. 19(2). 96–100. 3 indexed citations

14.

Limanaqi, Fiona, Stefano Gambardella, Francesca Biagioni, Carla L. Busceti, & Francesco Fornai. (2018). Epigenetic Effects Induced by Methamphetamine and Methamphetamine‐Dependent Oxidative Stress. Oxidative Medicine and Cellular Longevity. 2018(1). 4982453–4982453. 64 indexed citations

15.

Ferrucci, Michela, Francesca Biagioni, Paola Lenzi, et al.. (2017). Rapamycin promotes differentiation increasing βIII-tubulin, NeuN, and NeuroD while suppressing nestin expression in glioblastoma cells. Oncotarget. 8(18). 29574–29599. 26 indexed citations

16.

Palumbo, Orazio, Pietro Palumbo, Rosangela Ferese, et al.. (2017). Developmental Coordination Disorder in a Patient with Mental Disability and a Mild Phenotype Carrying Terminal 6q26-qter Deletion. Frontiers in Genetics. 8. 206–206. 5 indexed citations

17.

Cascella, Raffaella, Claudia Strafella, L. Manzo, et al.. (2017). Assessing individual risk for AMD with genetic counseling, family history, and genetic testing. Eye. 32(2). 446–450. 20 indexed citations

18.

Gambardella, Stefano, Francesca Biagioni, Rosangela Ferese, et al.. (2016). Vacuolar Protein Sorting Genes in Parkinson's Disease: A Re-appraisal of Mutations Detection Rate and Neurobiology of Disease. Frontiers in Neuroscience. 10. 532–532. 16 indexed citations

19.

Mineo, Davide, Vincenzo Ambrogi, Maria Elena Cufari, et al.. (2010). Variations of Inflammatory Mediators and α1-Antitrypsin Levels after Lung Volume Reduction Surgery for Emphysema. American Journal of Respiratory and Critical Care Medicine. 181(8). 806–814. 27 indexed citations

20.

Conte, Chiara, Stefano Gambardella, Fabrizio Rinaldi, et al.. (2008). Screening of EDA1 Gene in X-Linked Anhidrotic Ectodermal Dysplasia Using DHPLC: Identification of 14 Novel Mutations in Italian Patients. Genetic Testing. 12(3). 437–442. 11 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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