S. De Virgiliis

3.0k total citations
88 papers, 2.1k citations indexed

About

S. De Virgiliis is a scholar working on Epidemiology, Genetics and Hematology. According to data from OpenAlex, S. De Virgiliis has authored 88 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Epidemiology, 20 papers in Genetics and 19 papers in Hematology. Recurrent topics in S. De Virgiliis's work include Hemoglobinopathies and Related Disorders (18 papers), Celiac Disease Research and Management (16 papers) and Iron Metabolism and Disorders (15 papers). S. De Virgiliis is often cited by papers focused on Hemoglobinopathies and Related Disorders (18 papers), Celiac Disease Research and Management (16 papers) and Iron Metabolism and Disorders (15 papers). S. De Virgiliis collaborates with scholars based in Italy, United States and United Kingdom. S. De Virgiliis's co-authors include Antonio Cao, Mauro Congia, Maria Grazia Clemente, Francesco Cucca, Fulvia Frau, Franco Frau, Rosanna Lampis, R Lampis, F Argiolu and Giovanna Cornacchia and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Gastroenterology and Hepatology.

In The Last Decade

S. De Virgiliis

86 papers receiving 2.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
S. De Virgiliis Italy 27 646 600 568 547 365 88 2.1k
Nobuo Hiwatashi Japan 33 1.1k 1.7× 1.6k 2.7× 1.0k 1.8× 394 0.7× 730 2.0× 126 3.4k
N. D. Gallagher Australia 22 374 0.6× 134 0.2× 613 1.1× 129 0.2× 260 0.7× 78 1.5k
Eduardo Luiz Rachid Cançado Brazil 23 1.1k 1.7× 140 0.2× 451 0.8× 155 0.3× 84 0.2× 77 2.0k
Helen Stevens United Kingdom 14 224 0.3× 1.9k 3.1× 1.0k 1.8× 329 0.6× 810 2.2× 15 2.9k
Shinobu Ida Japan 19 135 0.2× 224 0.4× 454 0.8× 185 0.3× 94 0.3× 83 1.1k
Orazio Palmieri Italy 24 376 0.6× 779 1.3× 475 0.8× 212 0.4× 472 1.3× 78 1.7k
GianFranco Bottazzo United Kingdom 12 506 0.8× 1.6k 2.6× 1.3k 2.2× 114 0.2× 829 2.3× 16 3.1k
S A McMillan United Kingdom 24 562 0.9× 163 0.3× 444 0.8× 558 1.0× 320 0.9× 59 1.5k
Thomas Greuter Switzerland 28 714 1.1× 747 1.2× 972 1.7× 190 0.3× 302 0.8× 109 2.1k
Aaron Lerner Israel 25 653 1.0× 501 0.8× 543 1.0× 825 1.5× 215 0.6× 49 1.7k

Countries citing papers authored by S. De Virgiliis

Since Specialization
Citations

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

Fields of papers citing papers by S. De Virgiliis

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by S. De Virgiliis. 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 S. De Virgiliis. The network helps show where S. De Virgiliis may publish in the future.

Co-authorship network of co-authors of S. De Virgiliis

This figure shows the co-authorship network connecting the top 25 collaborators of S. De Virgiliis. A scholar is included among the top collaborators of S. De Virgiliis 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 S. De Virgiliis. S. De Virgiliis 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.
Loudianos, Georgios, et al.. (2012). Wilson's disease in two consecutive generations: The detection of three mutated alleles in the ATP7B gene in two Sardinian families. Digestive and Liver Disease. 45(4). 342–345. 9 indexed citations
2.
Lovicu, Mario, Antonietta Zappu, Raffaele Iorio, et al.. (2009). RNA Analysis of Consensus Sequence Splicing Mutations: Implications for the Diagnosis of Wilson Disease. Genetic Testing and Molecular Biomarkers. 13(2). 185–191. 10 indexed citations
3.
Lovicu, Mario, Antonietta Zappu, Lucia Zancan, et al.. (2007). Twenty-Four Novel Mutations in Wilson Disease Patients of Predominantly Italian Origin. Genetic Testing. 11(3). 328–332. 26 indexed citations
4.
Usai–Satta, Paolo, Francesco Cucca, S. De Virgiliis, et al.. (2007). Genetic testing improves the diagnosis of adult type hypolactasia in the Mediterranean population of Sardinia. European Journal of Clinical Nutrition. 61(10). 1220–1225. 24 indexed citations
5.
Bonamico, Margherita, P. Mariani, Pinella Failla, et al.. (2001). Prevalence and Clinical Picture of Celiac Disease in Italian Down Syndrome Patients: A Multicenter Study. Journal of Pediatric Gastroenterology and Nutrition. 33(2). 139–143. 108 indexed citations
6.
Bonamico, Margherita, P. Mariani, Pinella Failla, et al.. (2001). Prevalence and Clinical Picture of Celiac Disease in Italian Down Syndrome Patients: A Multicenter Study. Journal of Pediatric Gastroenterology and Nutrition. 33(2). 139–143. 7 indexed citations
7.
Clemente, Maria Grazia & S. De Virgiliis. (2000). Autoantigen characterization in liver/kidney microsome positive hepatitis. Digestive and Liver Disease. 32(1). 39–45. 3 indexed citations
8.
Clemente, Maria Grazia, et al.. (2000). Guinea pig transglutaminase ELISA: pitfalls in the celiac disease diagnosis. UNICA IRIS Institutional Research Information System (University of Cagliari). 1 indexed citations
9.
Clemente, Maria Grazia, Franco Frau, G Brusco, et al.. (1999). IMMUNE REACTION AGAINST CYTOSKELETON IN COELIAC DISEASE. Journal of Pediatric Gastroenterology and Nutrition. 28(5). 551–551. 1 indexed citations
10.
Clemente, Maria Grazia, Petra Obermayer–Straub, Antonella Meloni, et al.. (1997). Cytochrome P450 1A2 Is a Hepatic Autoantigen in Autoimmune Polyglandular Syndrome Type 11. The Journal of Clinical Endocrinology & Metabolism. 82(5). 1353–1361. 78 indexed citations
11.
Clemente, Maria Grazia, et al.. (1996). Cytochrome P450 2A6: a new autoantigen in autoimmune liver disease. UNICA IRIS Institutional Research Information System (University of Cagliari). 28(6). 354–354. 1 indexed citations
12.
Congia, Mauro, Maria Grazia Clemente, C. Dessì, et al.. (1996). Hla Class Ii Genes in Chronic Hepatitis C Virus–Infection and Associated Immunological Disorders. Hepatology. 24(6). 1338–1341. 73 indexed citations
13.
Greco, L., M Mayer, Giuseppe Mazzarella, et al.. (1996). In siblings of celiac children, rectal gluten challenge reveals gluten sensitization not restricted to celiac HLA. Gastroenterology. 111(2). 318–324. 40 indexed citations
14.
Rosatelli, Maria Cristina, et al.. (1993). A novel cystic fibrosis mutation: deletion of seventeen nucleotides at the exon 10-intron 10 boundary of the CFTR gene, in a Sardinian patient. Human Molecular Genetics. 2(1). 83–84. 1 indexed citations
15.
Virgiliis, S. De, et al.. (1982). Therapy of HBsAg-negative chronic active hepatitis in transfusion-dependent thalassemia major.. PubMed. 18(7). 355–60. 1 indexed citations
16.
Sanna, G., et al.. (1981). Glucose-6-Phosphate Dehydrogenase Red Blood Cell Phenotype in GdMediterranean Heterozygous Females and Hemizygous Males at Birth. Pediatric Research. 15(11). 1443–1446. 9 indexed citations
17.
Cao, Aili, Carlo Cianchetti, E Signorini, et al.. (1977). Agenesis of the corpus callosum, infantile spasms, spastic quadriplegia, microcephaly and severe mental retardation in three siblings. Clinical Genetics. 12(5). 290–296. 16 indexed citations
18.
Cao, Antonio, et al.. (1972). Characterization of serum alkaline phosphatase in infancy and childhood. European Journal of Pediatrics. 113(4). 289–296. 3 indexed citations
19.
Cao, Antonio, S. De Virgiliis, C Lippi, & Giovanni V. Coppa. (1971). Serum and Muscle Creatine Kinase Isoenzymes andSerum Aspartate Aminotransferase Isoenzymes inProgressive Muscular Dystrophy. Enzyme. 12(1). 49–62. 22 indexed citations
20.
Cao, Antonio, et al.. (1971). Characterization of platelet alkaline phosphatase in normal subjects and in trisomy 21 Down's syndrome patients. Clinica Chimica Acta. 35(1). 165–172. 4 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 Nobuo Hiwatashi Breakdown of academic impact, for papers by N. D. Gallagher Breakdown of academic impact, for papers by Eduardo Luiz Rachid Cançado Breakdown of academic impact, for papers by Helen Stevens Breakdown of academic impact, for papers by Shinobu Ida Breakdown of academic impact, for papers by Orazio Palmieri Breakdown of academic impact, for papers by GianFranco Bottazzo Breakdown of academic impact, for papers by S A McMillan Breakdown of academic impact, for papers by Thomas Greuter Breakdown of academic impact, for papers by Aaron Lerner
Rankless by CCL
2026