Roberta Taurisano

757 total citations
28 papers, 501 citations indexed

About

Roberta Taurisano is a scholar working on Physiology, Molecular Biology and Clinical Biochemistry. According to data from OpenAlex, Roberta Taurisano has authored 28 papers receiving a total of 501 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Physiology, 9 papers in Molecular Biology and 8 papers in Clinical Biochemistry. Recurrent topics in Roberta Taurisano's work include Lysosomal Storage Disorders Research (12 papers), Metabolism and Genetic Disorders (8 papers) and Glycogen Storage Diseases and Myoclonus (4 papers). Roberta Taurisano is often cited by papers focused on Lysosomal Storage Disorders Research (12 papers), Metabolism and Genetic Disorders (8 papers) and Glycogen Storage Diseases and Myoclonus (4 papers). Roberta Taurisano collaborates with scholars based in Italy, United Kingdom and Australia. Roberta Taurisano's co-authors include Carlo Dionisi‐Vici, Federica Deodato, Sara Boenzi, Cristiano Rizzo, Rosalba Carrozzo, Bianca Maria Goffredo, Arianna Maiorana, Maria Alice Donati, Diego Martinelli and Daniela Melis and has published in prestigious journals such as Neurology, Journal of Lipid Research and The Journal of Pediatrics.

In The Last Decade

Roberta Taurisano

27 papers receiving 496 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Roberta Taurisano Italy 14 257 174 107 72 70 28 501
Hana Vlášková Czechia 13 272 1.1× 179 1.0× 119 1.1× 96 1.3× 28 0.4× 27 483
Alexander Broomfield United Kingdom 14 358 1.4× 205 1.2× 137 1.3× 124 1.7× 28 0.4× 54 613
Fatih Süheyl Ezgü Türkiye 15 262 1.0× 296 1.7× 139 1.3× 75 1.0× 51 0.7× 100 724
Toju Tanaka Japan 10 274 1.1× 101 0.6× 106 1.0× 121 1.7× 28 0.4× 16 417
Miriam Rigoldi Italy 16 286 1.1× 119 0.7× 228 2.1× 114 1.6× 27 0.4× 29 544
Christine Broissand France 7 175 0.7× 138 0.8× 66 0.6× 82 1.1× 37 0.5× 10 416
Chuan‐Hong Kao Taiwan 7 204 0.8× 158 0.9× 102 1.0× 103 1.4× 17 0.2× 10 411
A Baldellou Spain 10 194 0.8× 160 0.9× 80 0.7× 77 1.1× 22 0.3× 23 392
Dimitar Gavrilov United States 15 345 1.3× 403 2.3× 152 1.4× 102 1.4× 74 1.1× 35 901
Elisabeth Jameson United Kingdom 11 185 0.7× 120 0.7× 93 0.9× 88 1.2× 14 0.2× 22 402

Countries citing papers authored by Roberta Taurisano

Since Specialization
Citations

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

Fields of papers citing papers by Roberta Taurisano

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Roberta Taurisano

This figure shows the co-authorship network connecting the top 25 collaborators of Roberta Taurisano. A scholar is included among the top collaborators of Roberta Taurisano 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 Roberta Taurisano. Roberta Taurisano 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.
Martinelli, Diego, Sara Cairoli, Daniela Longo, et al.. (2025). Positive Clinical, Neuropsychological, and Metabolic Impact of Liver Transplantation in Patients With Argininosuccinate Lyase Deficiency. Journal of Inherited Metabolic Disease. 48(1). e12843–e12843. 3 indexed citations
2.
Servais, Aude, Miriam Zacchia, Rukshana Shroff, et al.. (2024). Clinical Practice Recommendations on Kidney Management in Methylmalonic Acidemia: an Expert Consensus Statement From ERKNet and MetabERN. Kidney International Reports. 9(12). 3362–3374. 1 indexed citations
3.
Porta, Francesco, Arianna Maiorana, Vincenza Gragnaniello, et al.. (2024). Triheptanoin in patients with long-chain fatty acid oxidation disorders: clinical experience in Italy. ˜The œItalian Journal of Pediatrics/Italian journal of pediatrics. 50(1). 204–204. 4 indexed citations
4.
Toscano, António, Olimpia Musumeci, Michele Sacchini, et al.. (2023). Safety outcomes and patients’ preferences for home-based intravenous enzyme replacement therapy (ERT) in pompe disease and mucopolysaccharidosis type I (MPS I) disorder: COVID-19 and beyond. Orphanet Journal of Rare Diseases. 18(1). 338–338. 2 indexed citations
5.
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
6.
Piga, Simone, Carlo Dionisi‐Vici, Pasquale Parisi, et al.. (2020). Hypoglycemia in a Pediatric Emergency Department. Pediatric Emergency Care. 38(1). e404–e409. 4 indexed citations
7.
Baban, Anwar, Rachele Adorisio, Bernadette Corica, et al.. (2019). Delayed appearance of 3‐methylglutaconic aciduria in neonates with early onset metabolic cardiomyopathies: A potential pitfall for the diagnosis. American Journal of Medical Genetics Part A. 182(1). 64–70. 5 indexed citations
8.
Caciotti, Anna, Matthew Mort, D.N. Cooper, et al.. (2018). Mis-splicing of the GALNS gene resulting from deep intronic mutations as a cause of Morquio a disease. BMC Medical Genetics. 19(1). 183–183. 15 indexed citations
9.
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
10.
Ponzi, Emanuela, Arianna Maiorana, Francesca Romana Lepri, et al.. (2018). Persistent Hypoglycemia in Children: Targeted Gene Panel Improves the Diagnosis of Hypoglycemia Due to Inborn Errors of Metabolism. The Journal of Pediatrics. 202. 272–278.e4. 13 indexed citations
11.
Martinelli, Domenico, Arianna Maiorana, Alessia Liguori, et al.. (2018). P017 Impact of liver transplant on plasma and cerebrospinal fluid amino acids in patients with argininosuccinic aciduria. Digestive and Liver Disease. 50(4). e365–e365. 1 indexed citations
12.
Parini, Rossella, Paola De Lorenzo, Andrea Dardis, et al.. (2018). Long term clinical history of an Italian cohort of infantile onset Pompe disease treated with enzyme replacement therapy. Orphanet Journal of Rare Diseases. 13(1). 32–32. 57 indexed citations
13.
14.
Deodato, Federica, Elena Procopio, Angelica Rampazzo, et al.. (2017). The treatment of juvenile/adult GM1-gangliosidosis with Miglustat may reverse disease progression. Metabolic Brain Disease. 32(5). 1529–1536. 30 indexed citations
15.
Boenzi, Sara, Federica Deodato, Roberta Taurisano, et al.. (2016). Evaluation of plasma cholestane-3β,5α,6β-triol and 7-ketocholesterol in inherited disorders related to cholesterol metabolism. Journal of Lipid Research. 57(3). 361–367. 61 indexed citations
16.
Taurisano, Roberta, Arianna Maiorana, Fabrizio De Benedetti, et al.. (2014). Wolman disease associated with hemophagocytic lymphohistiocytosis: attempts for an explanation. European Journal of Pediatrics. 173(10). 1391–1394. 36 indexed citations
17.
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
18.
Mozzillo, Enza, Daniela Melis, Mariateresa Falco, et al.. (2013). Thiamine responsive megaloblastic anemia: a novelSLC19A2compound heterozygous mutation in two siblings. Pediatric Diabetes. 14(5). 384–387. 19 indexed citations
19.
Melis, Daniela, Rita Genesio, Ennio Del Giudice, et al.. (2011). Selective cognitive impairment and tall stature due to chromosome 19 supernumerary ring. Clinical Dysmorphology. 21(1). 27–32. 4 indexed citations
20.
Orrico, Alfredo, Lucia Galli, Laurence Faivre, et al.. (2010). Aarskog–Scott syndrome: Clinical update and report of nine novel mutations of the FGD1 gene. American Journal of Medical Genetics Part A. 152A(2). 313–318. 39 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 Hana Vlášková Breakdown of academic impact, for papers by Alexander Broomfield Breakdown of academic impact, for papers by Fatih Süheyl Ezgü Breakdown of academic impact, for papers by Toju Tanaka Breakdown of academic impact, for papers by Miriam Rigoldi Breakdown of academic impact, for papers by Christine Broissand Breakdown of academic impact, for papers by Chuan‐Hong Kao Breakdown of academic impact, for papers by A Baldellou Breakdown of academic impact, for papers by Dimitar Gavrilov Breakdown of academic impact, for papers by Elisabeth Jameson
Rankless by CCL
2026