Roberta Russo

7.9k total citations
136 papers, 2.6k citations indexed

About

Roberta Russo is a scholar working on Physiology, Genetics and Hematology. According to data from OpenAlex, Roberta Russo has authored 136 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 60 papers in Physiology, 42 papers in Genetics and 30 papers in Hematology. Recurrent topics in Roberta Russo's work include Erythrocyte Function and Pathophysiology (58 papers), Hemoglobinopathies and Related Disorders (41 papers) and Blood properties and coagulation (23 papers). Roberta Russo is often cited by papers focused on Erythrocyte Function and Pathophysiology (58 papers), Hemoglobinopathies and Related Disorders (41 papers) and Blood properties and coagulation (23 papers). Roberta Russo collaborates with scholars based in Italy, United States and France. Roberta Russo's co-authors include Achille Iolascon, Immacolata Andolfo, Antonella Gambale, Mario Capasso, Maria Rosaria Esposito, Barbara Eleni Rosato, Francesco Manna, Roberta Marra, Claudio Tiribelli and J. Delaunay and has published in prestigious journals such as SHILAP Revista de lepidopterología, Blood and Analytical Chemistry.

In The Last Decade

Roberta Russo

124 papers receiving 2.6k 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 Russo Italy 30 1.1k 698 578 571 546 136 2.6k
Irene Schmid Germany 32 312 0.3× 243 0.3× 281 0.5× 697 1.2× 778 1.4× 134 3.0k
G. Fiorelli Italy 27 567 0.5× 1.4k 2.0× 642 1.1× 1.2k 2.0× 555 1.0× 103 3.4k
Guy Touchard France 38 244 0.2× 776 1.1× 368 0.6× 870 1.5× 2.1k 3.9× 163 4.8k
Marc C. Levesque United States 39 418 0.4× 448 0.6× 602 1.0× 263 0.5× 885 1.6× 124 4.6k
Tibor J. Greenwalt United States 26 1.0k 0.9× 274 0.4× 269 0.5× 849 1.5× 507 0.9× 122 2.6k
Maurizio Sampietro Italy 31 291 0.3× 1.2k 1.8× 190 0.3× 1.4k 2.4× 663 1.2× 83 3.1k
Bruce H. Davis United States 36 563 0.5× 554 0.8× 234 0.4× 747 1.3× 812 1.5× 96 3.2k
Shingo Kato Japan 35 322 0.3× 117 0.2× 432 0.7× 461 0.8× 691 1.3× 188 4.1k
Byron P. Croker United States 41 433 0.4× 184 0.3× 427 0.7× 144 0.3× 1.3k 2.4× 100 5.3k
Francesco Perfumo Italy 32 285 0.3× 238 0.3× 357 0.6× 209 0.4× 684 1.3× 145 3.6k

Countries citing papers authored by Roberta Russo

Since Specialization
Citations

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

Fields of papers citing papers by Roberta Russo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Roberta Russo

This figure shows the co-authorship network connecting the top 25 collaborators of Roberta Russo. A scholar is included among the top collaborators of Roberta Russo 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 Russo. Roberta Russo 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.
Spagnoli, Carlotta, A Cavalli, Stefano Giuseppe Caraffi, et al.. (2025). Myoclonic reflex and non‐reflex seizures in a female child with Coffin–Lowry syndrome: Clinical vignette. Epileptic Disorders. 27(2). 299–303. 1 indexed citations
2.
Siciliano, Angela, Angelo D’Alessandro, Alessandro Mattè, et al.. (2025). Mitapivat metabolically reprograms human β-thalassemic erythroblasts, increasing their responsiveness to oxidation. Blood Advances. 9(11). 2818–2830. 1 indexed citations
3.
Ferrigno, Rosario, Immacolata Andolfo, Roberta Russo, et al.. (2024). Genotype–Phenotype Correlation of GNAS Gene: Review and Disease Management of a Hotspot Mutation. International Journal of Molecular Sciences. 25(20). 10913–10913.
4.
5.
Rosato, Barbara Eleni, Roberta Marra, Vito Alessandro Lasorsa, et al.. (2024). RAS signaling pathway is essential in regulating PIEZO1 ‐mediated hepatic iron overload in dehydrated hereditary stomatocytosis. American Journal of Hematology. 100(1). 52–65. 4 indexed citations
6.
Santoro, Antonella, Silvia De Santis, Ferdinando Palmieri, et al.. (2024). P2 Receptor Antagonists Rescue Defective Heme Content in an In Vitro SLC25A38-Associated Congenital Sideroblastic Anemia Cell Model. International Journal of Molecular Sciences. 25(24). 13314–13314.
7.
Mattè, Alessandro, Federica Gevi, Enrica Federti, et al.. (2023). Mitapivat reprograms the RBC metabolome and improves anemia in a mouse model of hereditary spherocytosis. JCI Insight. 8(20). 6 indexed citations
8.
Andolfo, Immacolata, Vittoria Monaco, Barbara Eleni Rosato, et al.. (2023). Proteome alterations in erythrocytes with PIEZO1 gain-of-function mutations. Blood Advances. 7(12). 2681–2693. 8 indexed citations
9.
Rosato, Barbara Eleni, Roberta Marra, Maddalena Raia, et al.. (2023). Unraveling the Role of PIEZO1 in Stressed Erythropoiesis: Implications for Dyserythropoiesis and Potential Therapeutic Targets in Dehydrated Hereditary Stomatocytosis. Blood. 142(Supplement 1). 2446–2446.
10.
Caterino, Marianna, Michele Costanzo, Roberta Fedele, et al.. (2021). The Serum Metabolome of Moderate and Severe COVID-19 Patients Reflects Possible Liver Alterations Involving Carbon and Nitrogen Metabolism. International Journal of Molecular Sciences. 22(17). 9548–9548. 57 indexed citations
11.
Andolfo, Immacolata, Barbara Eleni Rosato, Roberta Marra, et al.. (2021). Complex Modes of Inheritance in Hereditary Red Blood Cell Disorders: A Case Series Study of 155 Patients. Genes. 12(7). 958–958. 25 indexed citations
12.
Iolascon, Achille, Immacolata Andolfo, & Roberta Russo. (2020). Congenital dyserythropoietic anemias. Blood. 136(11). 1274–1283. 62 indexed citations
13.
Gambale, Antonella, Roberta Russo, Immacolata Andolfo, et al.. (2019). Germline mutations and new copy number variants among 40 pediatric cancer patients suspected for genetic predisposition. Clinical Genetics. 96(4). 359–365. 14 indexed citations
14.
Andolfo, Immacolata, Barbara Eleni Rosato, Roberta Marra, et al.. (2019). The BMP‐SMAD pathway mediates the impaired hepatic iron metabolism associated with the ERFE‐A260S variant. American Journal of Hematology. 94(11). 1227–1235. 19 indexed citations
15.
Andolfo, Immacolata, Roberta Russo, Barbara Eleni Rosato, et al.. (2018). Genotype‐phenotype correlation and risk stratification in a cohort of 123 hereditary stomatocytosis patients. American Journal of Hematology. 93(12). 1509–1517. 40 indexed citations
16.
Russo, Roberta, Immacolata Andolfo, Francesco Manna, et al.. (2018). Multi‐gene panel testing improves diagnosis and management of patients with hereditary anemias. American Journal of Hematology. 93(5). 672–682. 105 indexed citations
17.
Andolfo, Immacolata, Roberta Russo, Antonella Gambale, & Achille Iolascon. (2017). Hereditary stomatocytosis: An underdiagnosed condition. American Journal of Hematology. 93(1). 107–121. 49 indexed citations
18.
Pierro, Elena Di, Roberta Russo, Zeynep Karakaş, et al.. (2014). Congenital erythropoietic porphyria linked to GATA 1‐ R 216 W mutation: challenges for diagnosis. European Journal Of Haematology. 94(6). 491–497. 30 indexed citations
19.
Russo, Roberta, Maria Rosaria Esposito, Antonella Gambale, et al.. (2013). Hypomorphic mutations of SEC23B gene account for mild phenotypes of congenital dyserythropoietic anemia type II. Blood Cells Molecules and Diseases. 51(1). 17–21. 29 indexed citations
20.
Russo, Roberta, Antonella Gambale, Maria Rosaria Esposito, et al.. (2011). Two founder mutations in the SEC23B gene account for the relatively high frequency of CDA II in the Italian population. American Journal of Hematology. 86(9). 727–732. 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.

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