Lucia Santoro

1.2k total citations
35 papers, 775 citations indexed

About

Lucia Santoro is a scholar working on Physiology, Molecular Biology and Epidemiology. According to data from OpenAlex, Lucia Santoro has authored 35 papers receiving a total of 775 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Physiology, 11 papers in Molecular Biology and 11 papers in Epidemiology. Recurrent topics in Lucia Santoro's work include Lysosomal Storage Disorders Research (16 papers), Trypanosoma species research and implications (9 papers) and Carbohydrate Chemistry and Synthesis (8 papers). Lucia Santoro is often cited by papers focused on Lysosomal Storage Disorders Research (16 papers), Trypanosoma species research and implications (9 papers) and Carbohydrate Chemistry and Synthesis (8 papers). Lucia Santoro collaborates with scholars based in Italy, United States and Lebanon. Lucia Santoro's co-authors include Orazio Gabrielli, Lucia Zampini, Giovanni V. Coppa, Lucia Padella, Tiziana Galeazzi, Enrico Bertino, Nicola Volpi, Chiara Peila, Francesca Giuliani and C Fabris and has published in prestigious journals such as PEDIATRICS, Analytical Biochemistry and Food Chemistry.

In The Last Decade

Lucia Santoro

34 papers receiving 753 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Lucia Santoro Italy 14 419 329 223 175 152 35 775
G V Coppa Italy 13 260 0.6× 258 0.8× 103 0.5× 72 0.4× 69 0.5× 24 641
Joanna S. Hawkes Australia 18 553 1.3× 226 0.7× 96 0.4× 121 0.7× 65 0.4× 32 839
Karen C. Goehring United States 8 924 2.2× 416 1.3× 182 0.8× 335 1.9× 30 0.2× 8 1.1k
Jürgen Jelinek Italy 15 729 1.7× 291 0.9× 228 1.0× 149 0.9× 36 0.2× 23 1.1k
Dennis S. Acton Netherlands 14 275 0.7× 163 0.5× 218 1.0× 45 0.3× 75 0.5× 16 879
Sanxia Wang United States 12 349 0.8× 114 0.3× 202 0.9× 202 1.2× 24 0.2× 20 885
Philippe Alliët Belgium 13 308 0.7× 131 0.4× 213 1.0× 61 0.3× 51 0.3× 25 688
Kerstin Goth United States 9 328 0.8× 162 0.5× 124 0.6× 191 1.1× 15 0.1× 14 541
Ruud Schoemaker Netherlands 9 225 0.5× 88 0.3× 121 0.5× 53 0.3× 31 0.2× 13 412
Antoine Soliman United States 10 386 0.9× 129 0.4× 224 1.0× 341 1.9× 23 0.2× 13 1.1k

Countries citing papers authored by Lucia Santoro

Since Specialization
Citations

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

Fields of papers citing papers by Lucia Santoro

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lucia Santoro

This figure shows the co-authorship network connecting the top 25 collaborators of Lucia Santoro. A scholar is included among the top collaborators of Lucia Santoro 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 Lucia Santoro. Lucia Santoro 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.
Pedrini, Elena, Morena Tremosini, Dario Cocciadiferro, et al.. (2025). Further Evidence of Early-Onset Osteoporosis and Bone Fractures as a New FGFR2-Related Phenotype. International Journal of Molecular Sciences. 26(9). 4204–4204.
2.
Santoro, Lucia, Lucia Padella, Lucia Zampini, et al.. (2022). 18‐year follow‐up of enzyme‐replacement therapy in two siblings with attenuated mucopolysaccharidosis I. American Journal of Medical Genetics Part A. 191(2). 564–569. 4 indexed citations
3.
Sestito, Simona, Angelica Rampazzo, Francesca D’Avanzo, et al.. (2022). Cardiac involvement in MPS patients: incidence and response to therapy in an Italian multicentre study. Orphanet Journal of Rare Diseases. 17(1). 251–251. 12 indexed citations
4.
Zanetti, Alessandra, Francesca D’Avanzo, Laura Rigon, et al.. (2019). Molecular diagnosis of patients affected by mucopolysaccharidosis: a multicenter study. European Journal of Pediatrics. 178(5). 739–753. 19 indexed citations
5.
Monachesi, Chiara, Lucia Zampini, Lucia Padella, et al.. (2018). False positive screen test for mucopolysaccharidoses in healthy female newborns. Clinica Chimica Acta. 486. 221–223. 3 indexed citations
6.
Zampini, Lucia, Lucia Padella, Lucia Santoro, et al.. (2016). Importance of the combined urinary procedure for the diagnosis of Mucopolysaccharidoses. Clinica Chimica Acta. 464. 165–169. 3 indexed citations
7.
Coppa, G V, Orazio Gabrielli, Lucia Zampini, et al.. (2015). Mental retardation in mucopolysaccharidoses correlates with high molecular weight urinary heparan sulphate derived glucosamine. Metabolic Brain Disease. 30(6). 1343–1348. 6 indexed citations
8.
Coppa, Giovanni V., Bruna Facinelli, Gloria Magi, et al.. (2015). Human milk glycosaminoglycans inhibit in vitro the adhesion of Escherichia coli and Salmonella fyris to human intestinal cells. Pediatric Research. 79(4). 603–607. 29 indexed citations
9.
Nino, Fabiano, et al.. (2015). Genetics of Vesicoureteral Reflux. Current Genomics. 17(1). 70–79. 26 indexed citations
10.
Santoro, Lucia, et al.. (2014). Cognitive‐motor profile, clinical characteristics and diagnosis of CHARGE syndrome: An Italian experience. American Journal of Medical Genetics Part A. 164(12). 3042–3051. 3 indexed citations
11.
Volpi, Nicola, Lucia Zampini, Francesca Maccari, et al.. (2013). Plasmatic kinetics of dermatan sulfate during enzyme replacement therapy with iduronate-2-sulfatase in a mucopolysaccharidosis II Patient. Glycoconjugate Journal. 30(7). 727–732. 1 indexed citations
12.
Volpi, Nicola, Francesca Maccari, Fabio Galeotti, et al.. (2013). Plasmatic dermatan sulfate and chondroitin sulfate determination in mucopolysaccharidoses. Journal of Pharmaceutical and Biomedical Analysis. 85. 40–45. 11 indexed citations
13.
Coppa, Giovanni V., Orazio Gabrielli, Enrico Bertino, et al.. (2013). Human milk glycosaminoglycans: the state of the art and future perspectives. ˜The œItalian Journal of Pediatrics/Italian journal of pediatrics. 39(1). 2–2. 26 indexed citations
14.
Coppa, Giovanni V., Fabio Galeotti, Lucia Zampini, et al.. (2012). Mild mental retardation and low levels of urinary heparan sulfate in a patient with the attenuated phenotype of mucopolysaccharidosis type IIIA. Clinical Biochemistry. 46(7-8). 688–690. 5 indexed citations
15.
Galeotti, Fabio, Giovanni V. Coppa, Lucia Zampini, et al.. (2012). On-line high-performance liquid chromatography–fluorescence detection–electrospray ionization–mass spectrometry profiling of human milk oligosaccharides derivatized with 2-aminoacridone. Analytical Biochemistry. 430(1). 97–104. 35 indexed citations
16.
Tiano, Luca, Lucia Padella, Lucia Santoro, et al.. (2011). Prolonged coenzyme Q10 treatment in Down syndrome patients, effect on DNA oxidation. Neurobiology of Aging. 33(3). 626.e1–626.e8. 34 indexed citations
17.
Coppa, Giovanni V., Lucia Zampini, Francesca Maccari, et al.. (2011). Plasmatic and Urinary Glycosaminoglycans Characterization in Mucopolysaccharidosis II Patient Treated with Enzyme-Replacement Therapy with Idursulfase. JIMD Reports. 4. 79–90. 3 indexed citations
18.
Ficcadenti, Anna, et al.. (2009). Mental retardation, facial anomalies, brachydactyly, cerebral angiomas, femoral nucleus necrosis: A new entity or Hall–Riggs syndrome?. American Journal of Medical Genetics Part A. 149A(5). 1001–1005. 1 indexed citations
19.
Opitz, John M., James F. Smith, & Lucia Santoro. (2008). The FG Syndromes (Online Mendelian Inheritance in Man 305450): Perspective in 2008. Advances in Pediatrics. 55(1). 123–170. 7 indexed citations
20.
Tiano, Luca, Gian Paolo Littarru, Federica Principi, et al.. (2005). Assessment of DNA damage in Down Syndrome patients by means of a new, optimised single cell gel electrophoresis technique. BioFactors. 25(1-4). 187–195. 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by G V Coppa Breakdown of academic impact, for papers by Joanna S. Hawkes Breakdown of academic impact, for papers by Karen C. Goehring Breakdown of academic impact, for papers by Jürgen Jelinek Breakdown of academic impact, for papers by Dennis S. Acton Breakdown of academic impact, for papers by Sanxia Wang Breakdown of academic impact, for papers by Philippe Alliët Breakdown of academic impact, for papers by Kerstin Goth Breakdown of academic impact, for papers by Ruud Schoemaker Breakdown of academic impact, for papers by Antoine Soliman
Rankless by CCL
2026