Disma Renda

987 total citations
29 papers, 630 citations indexed

About

Disma Renda is a scholar working on Genetics, Hematology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Disma Renda has authored 29 papers receiving a total of 630 indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Genetics, 19 papers in Hematology and 8 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Disma Renda's work include Hemoglobinopathies and Related Disorders (25 papers), Iron Metabolism and Disorders (17 papers) and Prenatal Screening and Diagnostics (8 papers). Disma Renda is often cited by papers focused on Hemoglobinopathies and Related Disorders (25 papers), Iron Metabolism and Disorders (17 papers) and Prenatal Screening and Diagnostics (8 papers). Disma Renda collaborates with scholars based in Italy, Greece and United Kingdom. Disma Renda's co-authors include Aurelio Maggio, Antonino Giambona, Cristina Passarello, Paolo Rigano, Maria Domenica Cappellini, Antonella Mandas, Caterina Borgna‐Pignatti, Paolo Cianciulli, Maria Grazia Bisconte and Antonio Piga and has published in prestigious journals such as SHILAP Revista de lepidopterología, Blood and Gut.

In The Last Decade

Disma Renda

26 papers receiving 610 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Disma Renda Italy 15 513 431 150 74 57 29 630
Paloma Ropero Spain 11 313 0.6× 262 0.6× 61 0.4× 26 0.4× 80 1.4× 85 443
M Laulicht United Kingdom 9 298 0.6× 356 0.8× 52 0.3× 112 1.5× 56 1.0× 12 539
Victor Hoffbrand United Kingdom 11 176 0.3× 203 0.5× 37 0.2× 20 0.3× 73 1.3× 18 393
Harry Bos Netherlands 7 125 0.2× 197 0.5× 67 0.4× 17 0.2× 134 2.4× 9 647
B.R. Bacon United States 7 127 0.2× 161 0.4× 8 0.1× 114 1.5× 34 0.6× 15 360
S. Schrier United States 10 167 0.3× 169 0.4× 51 0.3× 46 0.6× 174 3.1× 25 431
José Manuel Vagace Spain 10 92 0.2× 102 0.2× 68 0.5× 30 0.4× 34 0.6× 19 328
Airie Kim United States 8 165 0.3× 227 0.5× 14 0.1× 20 0.3× 38 0.7× 13 345
Egemen Tütüncüoğlu United States 8 158 0.3× 131 0.3× 9 0.1× 16 0.2× 103 1.8× 18 324
Noémi Roy United Kingdom 12 131 0.3× 147 0.3× 15 0.1× 32 0.4× 119 2.1× 26 419

Countries citing papers authored by Disma Renda

Since Specialization
Citations

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

Fields of papers citing papers by Disma Renda

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Disma Renda

This figure shows the co-authorship network connecting the top 25 collaborators of Disma Renda. A scholar is included among the top collaborators of Disma Renda 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 Disma Renda. Disma Renda 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.
Calvaruso, Giuseppina, Disma Renda, Simona Raso, et al.. (2022). The First Case of Haemophagocytic Lymphohistiocytosis Triggered by the Booster Dose of Anti-SARS-CoV-2 Vaccine in a Patient with β-Thalassemia. SHILAP Revista de lepidopterología. 12(2). 46–50.
2.
Vitrano, Angela, Salvatore Scondotto, Gabriella Dardanoni, et al.. (2018). β-Thalassemia heterozygote state detrimentally affects health expectation. European Journal of Internal Medicine. 54. 76–80. 8 indexed citations
3.
Cassarà, Filippo, Disma Renda, Giuseppina Calvaruso, et al.. (2017). Phenotypic evaluations of HBB:c.93-23T>C, a nucleotide substitution in the IVS I nt 108 of β-globin gene. Journal of Clinical Pathology. 71(4). 298–302.
4.
Giambona, Antonino, Gianfranco Damiani, Filippo Cassarà, et al.. (2015). Incidence of haemoglobinopathies in Sicily: the impact of screening and prenatal diagnosis. International Journal of Clinical Practice. 69(10). 1129–1138. 14 indexed citations
5.
Vitrano, Angela, Rosario Di Maggio, Samir K. Ballas, et al.. (2014). Deferiprone versus Deferoxamine in Sickle Cell Disease: Results from a 5-year long-term Italian multi-center randomized clinical trial. Blood Cells Molecules and Diseases. 53(4). 265–271. 16 indexed citations
6.
Giambona, Antonino, Filippo Cassarà, G Fiorentino, et al.. (2011). The genetic heterogeneity of β-globin gene defects in Sicily reflects the historic population migrations of the island. Blood Cells Molecules and Diseases. 46(4). 282–287. 22 indexed citations
7.
Giambona, Antonino, George Makrydimas, Francesco Picciotto, et al.. (2011). Feasibility of DNA diagnosis of haemoglobinopathies on coelocentesis. British Journal of Haematology. 153(2). 268–272. 14 indexed citations
8.
Renda, Maria Concetta, Antonino Giambona, Emanuela Fecarotta, et al.. (2010). Embryo‐fetal erythroid megaloblasts in the human coelomic cavity. Journal of Cellular Physiology. 225(2). 385–389. 7 indexed citations
9.
Rigano, Paolo, Roberta Calzolari, Santina Acuto, et al.. (2010). Desensitization to hydroxycarbamide following long‐term treatment of thalassaemia intermedia as observed in vivo and in primary erythroid cultures from treated patients. British Journal of Haematology. 151(5). 509–515. 37 indexed citations
10.
Giambona, Antonino, Cristina Passarello, Disma Renda, & Aurelio Maggio. (2009). The significance of the hemoglobin A2 value in screening for hemoglobinopathies. Clinical Biochemistry. 42(18). 1786–1796. 70 indexed citations
11.
Giambona, Antonino, et al.. (2008). Significance of borderline hemoglobin A2 values in an Italian population with a high prevalence of  -thalassemia. Haematologica. 93(9). 1380–1384. 62 indexed citations
12.
Passarello, Cristina, Antonino Giambona, Luciano Prossomariti, et al.. (2008). Hb Southern Italy: coexistence of two missence mutations (the Hb Sun Prairie α2 130 Ala → Pro and Hb Caserta α2 26 Ala → Thr) in a single HBA2 gene. British Journal of Haematology. 143(1). 138–142. 3 indexed citations
13.
Filosa, Aldo, Luca Valgimigli, Gian Franco Pedulli, et al.. (2005). Quantitative evaluation of oxidative stress status on peripheral blood in β‐thalassaemic patients by means of electron paramagnetic resonance spectroscopy. British Journal of Haematology. 131(1). 135–140. 10 indexed citations
14.
Borgna‐Pignatti, Caterina, Gianluca Vergine, T. Lombardo, et al.. (2003). Hepatocellular carcinoma in the thalassaemia syndromes. British Journal of Haematology. 124(1). 114–117. 127 indexed citations
15.
Mancuso, Luigi, et al.. (2003). Cardiac complications in thalassemia: noninvasive detection methods and new directions in the clinical management. Expert Review of Cardiovascular Therapy. 1(3). 439–452. 7 indexed citations
16.
Rigano, Paolo, Griffin P. Rodgers, Disma Renda, et al.. (2001). CLINICAL AND HEMATOLOGICAL RESPONSES TO HYDROXYUREA IN SICILIAN PATIENTS WITH Hb S/β-THALASSEMIA. Hemoglobin. 25(1). 9–17. 19 indexed citations
17.
Tesoriere, Luisa, Daniele D’Arpa, Daniela Butera, et al.. (2001). Oral supplements of vitamin E improve measures of oxidative stress in plasma and reduce oxidative damage to LDL and erythrocytes in β-thalassemia intermedia patients. Free Radical Research. 34(5). 529–540. 68 indexed citations
18.
Lerut, Jan, E Lavenne-Pardonge, Olga Ciccarelli, et al.. (1999). HEPATIC SICKLING. Transplantation. 67(1). 65–68. 21 indexed citations
19.
Rigano, Paolo, L. Manfrè, Disma Renda, et al.. (1997). Clinical and Hematological Response to Hydroxyurea in a Patient with Hb Leporbp-Thalassemia. Hemoglobin. 21(3). 219–226. 24 indexed citations
20.
Marco, V. Di, Oreste Lo Iacono, Stefania La Grutta, et al.. (1993). Alpha interferon treatment of chronic hepatitis C in beta-thalassaemia.. Gut. 34(2 Suppl). S142–S143. 16 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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