Carmela Zizzo

872 total citations
34 papers, 490 citations indexed

About

Carmela Zizzo is a scholar working on Physiology, Organic Chemistry and Molecular Biology. According to data from OpenAlex, Carmela Zizzo has authored 34 papers receiving a total of 490 indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Physiology, 12 papers in Organic Chemistry and 10 papers in Molecular Biology. Recurrent topics in Carmela Zizzo's work include Lysosomal Storage Disorders Research (30 papers), Carbohydrate Chemistry and Synthesis (12 papers) and Cellular transport and secretion (10 papers). Carmela Zizzo is often cited by papers focused on Lysosomal Storage Disorders Research (30 papers), Carbohydrate Chemistry and Synthesis (12 papers) and Cellular transport and secretion (10 papers). Carmela Zizzo collaborates with scholars based in Italy, United States and Canada. Carmela Zizzo's co-authors include Giovanni Duro, Paolo Colomba, Giuseppe Albeggiani, Giuseppe Cammarata, Francesco Iemolo, Alessandro P. Burlina, Riccardo Alessandro, Andrea Dardis, Simone Scalia and Giulia Polo and has published in prestigious journals such as SHILAP Revista de lepidopterología, International Journal of Molecular Sciences and Gene.

In The Last Decade

Carmela Zizzo

29 papers receiving 483 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Carmela Zizzo Italy 14 384 140 137 122 118 34 490
Tom Wagemans Netherlands 12 383 1.0× 191 1.4× 147 1.1× 105 0.9× 73 0.6× 14 510
Margaret Timmons United States 8 603 1.6× 267 1.9× 191 1.4× 196 1.6× 180 1.5× 10 761
Marie T. Vanier France 8 496 1.3× 94 0.7× 183 1.3× 193 1.6× 75 0.6× 9 611
Julie Simon United States 8 234 0.6× 118 0.8× 82 0.6× 66 0.5× 76 0.6× 8 429
Roberta Taurisano Italy 14 257 0.7× 72 0.5× 174 1.3× 58 0.5× 107 0.9× 28 501
Hadhami Ben Turkia Tunisia 13 417 1.1× 151 1.1× 171 1.2× 151 1.2× 53 0.4× 46 524
Ana Marcão Portugal 12 402 1.0× 169 1.2× 188 1.4× 128 1.0× 160 1.4× 22 616
Andrea M. Atherton United States 8 191 0.5× 73 0.5× 116 0.8× 44 0.4× 75 0.6× 18 341
Linda van der Tol Netherlands 7 493 1.3× 234 1.7× 78 0.6× 161 1.3× 156 1.3× 10 529
Alexander Broomfield United Kingdom 14 358 0.9× 124 0.9× 205 1.5× 81 0.7× 137 1.2× 54 613

Countries citing papers authored by Carmela Zizzo

Since Specialization
Citations

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

Fields of papers citing papers by Carmela Zizzo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Carmela Zizzo

This figure shows the co-authorship network connecting the top 25 collaborators of Carmela Zizzo. A scholar is included among the top collaborators of Carmela Zizzo 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 Carmela Zizzo. Carmela Zizzo 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.
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.
2.
Moschetti, Marta, et al.. (2025). Highlights of Precision Medicine, Genetics, Epigenetics and Artificial Intelligence in Pompe Disease. International Journal of Molecular Sciences. 26(2). 757–757. 1 indexed citations
3.
Zizzo, Carmela, et al.. (2025). The Identification of a Novel Pathogenic Variant of the GLA Gene Associated with a Classic Phenotype of Anderson–Fabry Disease: A Clinical and Molecular Study. International Journal of Molecular Sciences. 26(2). 470–470. 1 indexed citations
4.
Ottaviani, Donatella, Raffaella Di Giacopo, Mauro Catalan, et al.. (2025). Distinctive cognitive phenotypes in Parkinson’s disease patients with GBA mutations and without dementia: a multicentre cross-sectional retrospective study. Clinical Parkinsonism & Related Disorders. 13. 100365–100365.
5.
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
6.
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
7.
Fiori, Laura M., Veronica Maria Tagi, C Montanari, et al.. (2024). Desensitization of olipudase alfa-induced anaphylaxis in a child with chronic neurovisceral acid sphingomyelinase deficiency. Molecular Genetics and Metabolism Reports. 40. 101120–101120. 1 indexed citations
8.
Duro, Giovanni, et al.. (2024). Diagnosis of Fabry Disease Using Alpha-Galactosidase A Activity or LysoGb3 in Blood Fails to Identify Up to Two Thirds of Female Patients. International Journal of Molecular Sciences. 25(10). 5158–5158. 6 indexed citations
9.
Marotto, Daniela, et al.. (2023). Late-Onset Pompe Disease with Normal Creatine Kinase Levels: The Importance of Rheumatological Suspicion. International Journal of Molecular Sciences. 24(21). 15924–15924. 1 indexed citations
10.
Esposito, Pasquale, Monica Repetto, Alberto Somaschini, et al.. (2023). Diagnosing Fabry nephropathy: the challenge of multiple kidney disease. BMC Nephrology. 24(1). 344–344. 7 indexed citations
11.
Accardi, Giulia, Giuseppe Cammarata, Anna Aiello, et al.. (2022). miR-126-3p and miR-21-5p as Hallmarks of Bio-Positive Ageing; Correlation Analysis and Machine Learning Prediction in Young to Ultra-Centenarian Sicilian Population. Cells. 11(9). 1505–1505. 23 indexed citations
12.
Burlina, Alberto, Giulia Polo, Leonardo Salviati, et al.. (2017). Newborn screening for lysosomal storage disorders by tandem mass spectrometry in North East Italy. Journal of Inherited Metabolic Disease. 41(2). 209–219. 123 indexed citations
13.
Cammarata, Giuseppe, Pasquale Fatuzzo, Margherita Stefania Rodolico, et al.. (2015). High Variability of Fabry Disease Manifestations in an Extended Italian Family. BioMed Research International. 2015. 1–5. 25 indexed citations
14.
Colomba, Paolo, Giuseppe Cammarata, Carmela Zizzo, et al.. (2015). Anderson-Fabry: una malattia rara?. SHILAP Revista de lepidopterología. 27(2). 73–77.
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.
Iemolo, Francesco, Giuseppe Albeggiani, Carmela Zizzo, et al.. (2014). De novo mutation in a male patient with Fabry disease: a case report. BMC Research Notes. 7(1). 11–11. 15 indexed citations
17.
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
18.
Firinu, Davide, Paolo Colomba, Paolo Emilio Manconi, et al.. (2013). Identification of a novel and recurrent mutation in the SERPING1 gene in patients with hereditary angioedema. Clinical Immunology. 147(2). 129–132. 7 indexed citations
19.
Colomba, Paolo, Antonia Nucera, Carmela Zizzo, et al.. (2012). Identification of a novel mutation in the alpha-galactosidase A gene in patients with Fabry disease. Clinical Biochemistry. 45(10-11). 839–841. 9 indexed citations
20.
Nuzzo, Domenico, et al.. (2011). Genetic screening of Fabry patients with EcoTILLING and HRM technology. BMC Research Notes. 4(1). 323–323. 22 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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