Giovanni Duro

2.6k total citations
105 papers, 1.9k citations indexed

About

Giovanni Duro is a scholar working on Physiology, Molecular Biology and Epidemiology. According to data from OpenAlex, Giovanni Duro has authored 105 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 53 papers in Physiology, 30 papers in Molecular Biology and 25 papers in Epidemiology. Recurrent topics in Giovanni Duro's work include Lysosomal Storage Disorders Research (44 papers), Cellular transport and secretion (16 papers) and Carbohydrate Chemistry and Synthesis (15 papers). Giovanni Duro is often cited by papers focused on Lysosomal Storage Disorders Research (44 papers), Cellular transport and secretion (16 papers) and Carbohydrate Chemistry and Synthesis (15 papers). Giovanni Duro collaborates with scholars based in Italy, Spain and United States. Giovanni Duro's co-authors include Calogero Caruso, Giuseppina Candore, V. Izzo, Carmela Zizzo, Paolo Colomba, Francesco Iemolo, Sonya Vasto, Paolo Colombo, Maria Assunta Costa and Domenico Nuzzo and has published in prestigious journals such as Nucleic Acids Research, SHILAP Revista de lepidopterología and The Journal of Immunology.

In The Last Decade

Giovanni Duro

99 papers receiving 1.9k citations

Peers

Giovanni Duro

PHYSI

EPIDE

Zhongjian Zhang United States

Yoshiya Aze Japan

Kyungho Chang Japan

Thomas Jansen Germany

Takanobu Taniguchi Japan

Dominique Thomas Germany

Clara Paolucci Italy

N. M. Muñoz United States

Harm Maarsingh Netherlands

Zhongjian Zhang United States

Giovanni Duro

1.2k ×1.4

PHYSI

1.2k ×2.5

342 ×1.0

EPIDE

112 ×0.4

754 ×3.9

Citations per year, relative to Giovanni Duro Giovanni Duro (= 1×) peers Zhongjian Zhang

Countries citing papers authored by Giovanni Duro

Since Specialization

Citations

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

Fields of papers citing papers by Giovanni Duro

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Giovanni Duro

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Marano, Massimo, Immacolata Tartaglione, Marco Spada, et al.. (2025). Identification of Novel Mutations in Patients Affected by Gaucher Disease. International Journal of Molecular Sciences. 26(8). 3918–3918.

Biddeci, Giuseppa, et al.. (2025). Fabry Disease Beyond Storage: The Role of Inflammation in Disease Progression. International Journal of Molecular Sciences. 26(15). 7054–7054. 1 indexed citations

Battaglia, Yuri, Simone Russo, Giuliana Sartori, et al.. (2025). Expanded screening for Fabry disease in patients with chronic kidney disease not on dialysis: a multicenter Italian experience. Renal Failure. 47(1). 2454295–2454295. 1 indexed citations

Moschetti, Marta, et al.. (2024). Mutation Spectrum of GAA Gene in Pompe Disease: Current Knowledge and Results of an Italian Study. International Journal of Molecular Sciences. 25(17). 9139–9139. 1 indexed citations

Colomba, Paolo, Giovanni Caocci, Gaetano Giuffrida, et al.. (2024). Gaucher Disease or Acid Sphingomyelinase Deficiency? The Importance of Differential Diagnosis. Journal of Clinical Medicine. 13(5). 1487–1487. 2 indexed citations

Faro, Denise Cristiana, et al.. (2023). Sex Differences in Anderson–Fabry Cardiomyopathy: Clinical, Genetic, and Imaging Analysis in Women. Genes. 14(9). 1804–1804. 10 indexed citations

Rubino, Marta, Emanuele Monda, Martina Caiazza, et al.. (2022). Diagnosis of Fabry Disease in a Patient with a Surgically Repaired Congenital Heart Defect: When Clinical History and Genetics Make the Difference. SHILAP Revista de lepidopterología. 12(1). 102–108. 1 indexed citations

Caruso, Calogero, Mattia Emanuela Ligotti, Giulia Accardi, et al.. (2022). How Important Are Genes to Achieve Longevity?. International Journal of Molecular Sciences. 23(10). 5635–5635. 23 indexed citations

Ligotti, Mattia Emanuela, Anna Aiello, Giulia Accardi, et al.. (2022). Distribution of KIR Genes and Their HLA Ligands in Different Viral Infectious Diseases: Frequency Study in Sicilian Population. International Journal of Molecular Sciences. 23(24). 15466–15466. 7 indexed citations

10.

Gragnaniello, Vincenza, Alessandro P. Burlina, Giulia Polo, et al.. (2021). Newborn Screening for Fabry Disease in Northeastern Italy: Results of Five Years of Experience. Biomolecules. 11(7). 951–951. 33 indexed citations

11.

Russo, Camilla, Sirio Cocozza, Eleonora Riccio, et al.. (2020). Prevalence of GLA gene mutations and polymorphisms in patients with multiple sclerosis: A cross-sectional study. Journal of the Neurological Sciences. 412. 116782–116782. 2 indexed citations

12.

Cammarata, Giuseppe, et al.. (2019). Circulating miRNAs in Successful and Unsuccessful Aging. A Mini-review. Current Pharmaceutical Design. 25(39). 4150–4153. 10 indexed citations

13.

Burlina, Alberto, Giulia Polo, Laura Rubert, et al.. (2019). Implementation of Second-Tier Tests in Newborn Screening for Lysosomal Disorders in North Eastern Italy. International Journal of Neonatal Screening. 5(2). 24–24. 53 indexed citations

14.

Polo, Giulia, Alessandro P. Burlina, Enzo Ranieri, et al.. (2019). Plasma and dried blood spot lysosphingolipids for the diagnosis of different sphingolipidoses: a comparative study. Clinical Chemistry and Laboratory Medicine (CCLM). 57(12). 1863–1874. 67 indexed citations

15.

Tuttolomondo, Antonino, Giovanni Duro, Rosaria Pecoraro, et al.. (2014). A family with various symptomatology suggestive of Anderson–Fabry disease and a genetic polymorphism of alpha galactosidase A gene. Clinical Biochemistry. 48(1-2). 55–62. 16 indexed citations

16.

Cigna, Diego, Claudia D’Anna, Carmela Zizzo, et al.. (2013). Alteration of proteomic profiles in PBMC isolated from patients with Fabry disease: preliminary findings. Molecular BioSystems. 9(6). 1162–1168. 33 indexed citations

17.

Duro, Giovanni, et al.. (1998). Enhanced hybridization labeling signals in Southern blotted DNAs fractionated with voltage gradient gel electrophoresis. Electrophoresis. 19(5). 643–645. 6 indexed citations

18.

Duro, Giovanni, et al.. (1996). Rapid DNA Elution Procedure from Agarose Gels. Analytical Biochemistry. 235(1). 106–107. 10 indexed citations

19.

Barbieri, Raffaella, Giovanni Duro, Maria Assunta Costa, & V. Izzo. (1994). Simple and Inexpensive Dot-Blot Apparatus. Analytical Biochemistry. 216(2). 461–462. 6 indexed citations

20.

Farina, Mário, et al.. (1987). Intragenomic recombination between homologous regions of genes II and IV promotes formation of bacteriophage f1 miniphages. Nucleic Acids Research. 15(17). 7190–7190. 1 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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