Chiara Cazzorla

1.1k total citations
45 papers, 760 citations indexed

About

Chiara Cazzorla is a scholar working on Physiology, Clinical Biochemistry and Molecular Biology. According to data from OpenAlex, Chiara Cazzorla has authored 45 papers receiving a total of 760 indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Physiology, 24 papers in Clinical Biochemistry and 14 papers in Molecular Biology. Recurrent topics in Chiara Cazzorla's work include Metabolism and Genetic Disorders (24 papers), Lysosomal Storage Disorders Research (20 papers) and Diet and metabolism studies (10 papers). Chiara Cazzorla is often cited by papers focused on Metabolism and Genetic Disorders (24 papers), Lysosomal Storage Disorders Research (20 papers) and Diet and metabolism studies (10 papers). Chiara Cazzorla collaborates with scholars based in Italy, Switzerland and Germany. Chiara Cazzorla's co-authors include Alberto Burlina, Alessandro P. Burlina, Giulia Polo, Leonardo Salviati, Laura Rubert, Giovanni Duro, Vincenza Gragnaniello, Andrea Dardis, Giacomo Biasucci and Carmela Zizzo and has published in prestigious journals such as Gene, Nutrients and BMC Public Health.

In The Last Decade

Chiara Cazzorla

44 papers receiving 748 citations

Peers

Chiara Cazzorla
Daniel Gruskin United States
A Baldellou Spain
Teodor Podskarbi Germany
Shauna Kearney United Kingdom
Margreet van Rijn Netherlands
Serap Sivri Türkiye
İlyas Okur Türkiye
Elaina Jurecki United States
H Gröbe Germany
Sabrina Paci Italy
Daniel Gruskin United States
Chiara Cazzorla
Citations per year, relative to Chiara Cazzorla Chiara Cazzorla (= 1×) peers Daniel Gruskin

Countries citing papers authored by Chiara Cazzorla

Since Specialization
Citations

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

Fields of papers citing papers by Chiara Cazzorla

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Chiara Cazzorla

This figure shows the co-authorship network connecting the top 25 collaborators of Chiara Cazzorla. A scholar is included among the top collaborators of Chiara Cazzorla 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 Chiara Cazzorla. Chiara Cazzorla 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.
Gragnaniello, Vincenza, et al.. (2025). Natural history of inflammation and impaired autophagy in children with Gaucher disease identified by newborn screening. Molecular Genetics and Metabolism Reports. 42. 101187–101187. 1 indexed citations
2.
Gragnaniello, Vincenza, et al.. (2025). The Hidden Burden: Gastrointestinal Involvement in Lysosomal Storage Disorders. Metabolites. 15(6). 361–361.
3.
Gragnaniello, Vincenza, Chiara Cazzorla, Elena Porcù, et al.. (2024). Newborn Screening for Acid Sphingomyelinase Deficiency: Prevalence and Genotypic Findings in Italy. International Journal of Neonatal Screening. 10(4). 79–79. 1 indexed citations
4.
Burlina, Alberto, Alessandro P. Burlina, Renzo Mignani, et al.. (2024). Non‐Hodgkin lymphoma in a kidney transplanted patient with methylmalonic acidemia: Metabolic susceptibility and the role of immunosuppression. JIMD Reports. 65(2). 56–62. 1 indexed citations
5.
Cazzorla, Chiara, et al.. (2024). Parents’ Perspectives of Children with PKU: Assessing Parental Stress and Psychological Adjustment. 6(3). 779–785. 1 indexed citations
6.
Scala, Iris, Lucia Brodosi, Filippo Manti, et al.. (2024). Pegvaliase therapy for phenylketonuria: Real-world case series and clinical insights. Molecular Genetics and Metabolism. 142(1). 108151–108151. 3 indexed citations
7.
Gragnaniello, Vincenza, Chiara Cazzorla, Elena Porcù, et al.. (2023). Abnormal activation of MAPKs pathways and inhibition of autophagy in a group of patients with Zellweger spectrum disorders and X-linked adrenoleukodystrophy. Orphanet Journal of Rare Diseases. 18(1). 358–358. 1 indexed citations
8.
Polloni, Laura, et al.. (2023). On-line psycho-educational antenatal classes during COVID-19 pandemic in Italy: women’s opinion and satisfaction. Current Psychology. 43(13). 11447–11457. 2 indexed citations
9.
Gragnaniello, Vincenza, et al.. (2023). Newborn Screening for Fabry Disease: Current Status of Knowledge. International Journal of Neonatal Screening. 9(2). 31–31. 18 indexed citations
10.
Muri, Raphaela, Michel Hochuli, Péter Reismann, et al.. (2023). Health-related quality of life in a european sample of adults with early-treated classical PKU. Orphanet Journal of Rare Diseases. 18(1). 300–300. 6 indexed citations
11.
Gragnaniello, Vincenza, Alessandro P. Burlina, Stijn L.M. in ‘t Groen, et al.. (2022). Newborn screening for Pompe disease in Italy: Long-term results and future challenges. Molecular Genetics and Metabolism Reports. 33. 100929–100929. 22 indexed citations
12.
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
13.
Burlina, Alberto, Giulia Polo, Vincenza Gragnaniello, et al.. (2021). Detection of 3-O-methyldopa in dried blood spots for neonatal diagnosis of aromatic L-amino-acid decarboxylase deficiency: The northeastern Italian experience. Molecular Genetics and Metabolism. 133(1). 56–62. 17 indexed citations
14.
Landolt, Markus A., Matthias R. Baumgartner, Stefan Kölker, et al.. (2020). Health‐related quality of life in paediatric patients with intoxication‐type inborn errors of metabolism: Analysis of an international data set. Journal of Inherited Metabolic Disease. 44(1). 215–225. 22 indexed citations
15.
Gragnaniello, Vincenza, Laura Rubert, Francesca Manzoni, et al.. (2020). Report of Five Years of Experience in Neonatal Screening for Mucopolysaccharidosis Type I and Review of the Literature. International Journal of Neonatal Screening. 6(4). 85–85. 12 indexed citations
16.
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
17.
Burlina, Alessandro P., et al.. (2019). Large Neutral Amino Acid Therapy Increases Tyrosine Levels in Adult Patients with Phenylketonuria: A Long-Term Study. Nutrients. 11(10). 2541–2541. 16 indexed citations
18.
19.
Rizzo, Monica, Alessandro P. Burlina, Jörn Oliver Sass, et al.. (2013). Metabolic stroke in a late-onset form of isolated sulfite oxidase deficiency. Molecular Genetics and Metabolism. 108(4). 263–266. 26 indexed citations
20.
Cazzorla, Chiara, Monica Rizzo, Peter Burgard, et al.. (2012). Application of the WHOQOL-100 for the assessment of quality of life of adult patients with inherited metabolic diseases. Molecular Genetics and Metabolism. 106(1). 25–30. 19 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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