Sara Boenzi

1.5k total citations
43 papers, 1.0k citations indexed

About

Sara Boenzi is a scholar working on Molecular Biology, Clinical Biochemistry and Rheumatology. According to data from OpenAlex, Sara Boenzi has authored 43 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 24 papers in Clinical Biochemistry and 15 papers in Rheumatology. Recurrent topics in Sara Boenzi's work include Metabolism and Genetic Disorders (24 papers), Folate and B Vitamins Research (12 papers) and Lysosomal Storage Disorders Research (8 papers). Sara Boenzi is often cited by papers focused on Metabolism and Genetic Disorders (24 papers), Folate and B Vitamins Research (12 papers) and Lysosomal Storage Disorders Research (8 papers). Sara Boenzi collaborates with scholars based in Italy, United States and Australia. Sara Boenzi's co-authors include Carlo Dionisi‐Vici, Federica Deodato, Filippo M. Santorelli, Cristiano Rizzo, Diego Martinelli, Daria Diodato, Roberta Taurisano, Enrico Bertini, Rosalba Carrozzo and Bianca Maria Goffredo and has published in prestigious journals such as Analytical Chemistry, Neurology and PEDIATRICS.

In The Last Decade

Sara Boenzi

43 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sara Boenzi Italy 20 539 524 263 247 136 43 1.0k
Hilary Vallance Canada 18 519 1.0× 469 0.9× 221 0.8× 145 0.6× 153 1.1× 65 1.0k
María Antònia Vilaseca Spain 20 639 1.2× 652 1.2× 269 1.0× 251 1.0× 139 1.0× 45 1.1k
Uta Lichter‐Konecki United States 20 608 1.1× 717 1.4× 223 0.8× 113 0.5× 203 1.5× 35 1.1k
Uta Lichter‐Konecki United States 23 774 1.4× 969 1.8× 260 1.0× 388 1.6× 121 0.9× 47 1.3k
Wulf Röschinger Germany 21 925 1.7× 955 1.8× 301 1.1× 250 1.0× 375 2.8× 48 1.6k
Steven L Hillman United States 12 633 1.2× 723 1.4× 209 0.8× 161 0.7× 322 2.4× 14 1.1k
Joy Yaplito‐Lee Australia 17 653 1.2× 575 1.1× 193 0.7× 163 0.7× 164 1.2× 29 1.1k
E. Holme Sweden 22 1.1k 2.0× 926 1.8× 303 1.2× 115 0.5× 121 0.9× 45 1.7k
Anupam Chakrapani United Kingdom 19 646 1.2× 1.2k 2.3× 449 1.7× 316 1.3× 389 2.9× 47 1.6k
Mübeccel Demirkol Türkiye 20 632 1.2× 685 1.3× 294 1.1× 202 0.8× 155 1.1× 43 1.2k

Countries citing papers authored by Sara Boenzi

Since Specialization
Citations

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

Fields of papers citing papers by Sara Boenzi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sara Boenzi

This figure shows the co-authorship network connecting the top 25 collaborators of Sara Boenzi. A scholar is included among the top collaborators of Sara Boenzi 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 Sara Boenzi. Sara Boenzi 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.
Deodato, Federica, et al.. (2025). Case Report: Two years of compassionate use with Olipudase-alfa in a child with neurovisceral acid sphingomyelinase deficiency. Frontiers in Pediatrics. 12. 1518344–1518344. 2 indexed citations
2.
Cocciadiferro, Dario, Tommaso Mazza, Davide Vecchio, et al.. (2024). Exploiting in silico structural analysis to introduce emerging genotype–phenotype correlations in DHCR24-related sterol biosynthesis disorder: a case study. Frontiers in Genetics. 14. 1307934–1307934. 5 indexed citations
3.
Deodato, Federica, Turgay Coşkun, İncilay Lay, et al.. (2021). A new UHPLC-MS/MS method for the screening of urinary oligosaccharides expands the detection of storage disorders. Orphanet Journal of Rare Diseases. 16(1). 24–24. 9 indexed citations
4.
Maines, Evelina, Sara Boenzi, Antonella Mosca, et al.. (2020). Plasma methylcitric acid and its correlations with other disease biomarkers: The impact in the follow up of patients with propionic and methylmalonic acidemia. Journal of Inherited Metabolic Disease. 43(6). 1173–1185. 20 indexed citations
5.
Boenzi, Sara, Rosalba Carrozzo, Daria Diodato, et al.. (2018). The urinary organic acids profile in single large-scale mitochondrial DNA deletion disorders. Clinica Chimica Acta. 481. 156–160. 8 indexed citations
6.
Deodato, Federica, et al.. (2018). The impact of biomarkers analysis in the diagnosis of Niemann-Pick C disease and acid sphingomyelinase deficiency. Clinica Chimica Acta. 486. 387–394. 37 indexed citations
7.
8.
Caterino, Marianna, Anna Pastore, Gianna Di Giovamberardino, et al.. (2015). The proteome of cblC defect: in vivo elucidation of altered cellular pathways in humans. Journal of Inherited Metabolic Disease. 38(5). 969–979. 36 indexed citations
9.
Maiorana, Arianna, Monica Malamisura, Francesco Emma, et al.. (2014). Early effect of NTBC on renal tubular dysfunction in hereditary tyrosinemia type 1. Molecular Genetics and Metabolism. 113(3). 188–193. 20 indexed citations
10.
Muraca, Maurizio, et al.. (2014). Determination of plasma pipecolic acid by an easy and rapid liquid chromatography–tandem mass spectrometry method. Clinica Chimica Acta. 440. 108–112. 8 indexed citations
11.
Boenzi, Sara, Federica Deodato, Roberta Taurisano, et al.. (2014). A new simple and rapid LC–ESI-MS/MS method for quantification of plasma oxysterols as dimethylaminobutyrate esters. Its successful use for the diagnosis of Niemann–Pick type C disease. Clinica Chimica Acta. 437. 93–100. 57 indexed citations
12.
Masotti, Andrea, Sara Boenzi, Anna Pastore, et al.. (2013). Gender-related effects on urine l-cystine metastability. Amino Acids. 46(2). 415–427. 3 indexed citations
13.
Pastore, Anna, Gianna Di Giovamberardino, Sara Petrillo, et al.. (2012). Pediatric reference intervals for muscle coenzyme Q10. Biomarkers. 17(8). 764–766. 3 indexed citations
14.
Boenzi, Sara, Cristiano Rizzo, Vincenzo Di Ciommo, et al.. (2011). Simultaneous determination of creatine and guanidinoacetate in plasma by liquid chromatography–tandem mass spectrometry (LC–MS/MS). Journal of Pharmaceutical and Biomedical Analysis. 56(4). 792–798. 14 indexed citations
15.
Martinelli, Diego, Andrea Dotta, Laura Massella, et al.. (2010). Cobalamin C defect presenting as severe neonatal hyperammonemia. European Journal of Pediatrics. 170(7). 887–890. 10 indexed citations
16.
Sirleto, Pietro, Cecilia Surace, Helena G. Dos Santos, et al.. (2009). Lyonization Effects of the t(X;16) Translocation on the Phenotypic Expression in a Rare Female With Menkes Disease. Pediatric Research. 65(3). 347–351. 18 indexed citations
17.
Duranti, Guglielmo, Sara Boenzi, Cristiano Rizzo, et al.. (2008). Urine acylcarnitine analysis by ESI–MS/MS: A new tool for the diagnosis of peroxisomal biogenesis disorders. Clinica Chimica Acta. 398(1-2). 86–89. 20 indexed citations
18.
Rosa, Gabriella Di, Federica Deodato, Ference J. Loupatty, et al.. (2006). Hypertrophic cardiomyopathy, cataract, developmental delay, lactic acidosis: A novel subtype of 3‐methylglutaconic aciduria. Journal of Inherited Metabolic Disease. 29(4). 546–550. 24 indexed citations
19.
Deodato, Federica, Sara Boenzi, Cristiano Rizzo, et al.. (2004). Inborn errors of metabolism: an update on epidemiology and on neonatal‐onset hyperammonemia. Acta Paediatrica. 93(s445). 18–21. 27 indexed citations
20.
Rizzo, Cristiano, Sara Boenzi, Ronald J. A. Wanders, et al.. (2003). Characteristic Acylcarnitine Profiles in Inherited Defects of Peroxisome Biogenesis: A Novel Tool for Screening Diagnosis Using Tandem Mass Spectrometry. Pediatric Research. 53(6). 1013–1018. 43 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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