Laura Frogheri

1.0k total citations
13 papers, 82 citations indexed

About

Laura Frogheri is a scholar working on Genetics, Hematology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Laura Frogheri has authored 13 papers receiving a total of 82 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 9 papers in Hematology and 3 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Laura Frogheri's work include Hemoglobinopathies and Related Disorders (11 papers), Iron Metabolism and Disorders (8 papers) and Erythrocyte Function and Pathophysiology (3 papers). Laura Frogheri is often cited by papers focused on Hemoglobinopathies and Related Disorders (11 papers), Iron Metabolism and Disorders (8 papers) and Erythrocyte Function and Pathophysiology (3 papers). Laura Frogheri collaborates with scholars based in Italy, United States and Vietnam. Laura Frogheri's co-authors include Maurizio Longinotti, Sylvain Doré, Susanna Pardini, Bruno Masala, Laura Manca, John G. Gilman, Giuseppe Corona, Re G, Massimo Madonia and Antonio Cao and has published in prestigious journals such as Cancers, Journal of Translational Medicine and American Journal of Hematology.

In The Last Decade

Laura Frogheri

12 papers receiving 80 citations

Peers

Laura Frogheri

GENET

HEMAT

PPCH

ONCOL

A. M. Vannucchi Italy

Liesl Mathias United Kingdom

Annelore Cortoos United States

Caterina Consarino Italy

Emilio Usala Italy

Sophie Dimicoli‐Salazar France

Julia Herzig Germany

Cláudia Moreira Portugal

Thomas Creasey United Kingdom

Viktor Rossiev Russia

A. M. Vannucchi Italy

Laura Frogheri

33 ×0.5

GENET

61 ×1.0

HEMAT

4 ×0.3

PPCH

12 ×0.9

ONCOL

21 ×1.9

Citations per year, relative to Laura Frogheri Laura Frogheri (= 1×) peers A. M. Vannucchi

Countries citing papers authored by Laura Frogheri

Since Specialization

Citations

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

Fields of papers citing papers by Laura Frogheri

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Laura Frogheri

This figure shows the co-authorship network connecting the top 25 collaborators of Laura Frogheri. A scholar is included among the top collaborators of Laura Frogheri 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 Laura Frogheri. Laura Frogheri is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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13 of 13 papers shown

Sini, Maria Cristina, Laura Frogheri, Angelo Zinellu, et al.. (2024). Combination of mutations in genes controlling DNA repair and high mutational load plays a prognostic role in pancreatic ductal adenocarcinoma (PDAC): a retrospective real-life study in Sardinian population. Journal of Translational Medicine. 22(1). 108–108. 1 indexed citations

Santeufemia, Davide Adriano, Giuseppe Palmieri, Gianmaria Miolo, et al.. (2023). Current Trends in Mucosal Melanomas: An Overview. Cancers. 15(5). 1356–1356. 14 indexed citations

Casu, Giuseppina, Laura Frogheri, Ivana Persico, et al.. (2017). Molecular Characterization of β-Thalassemia Mutations in Central Vietnam. Hemoglobin. 41(2). 96–99. 4 indexed citations

Frogheri, Laura, et al.. (2008). Haematological phenotypes in a family with triplicated α-globin gene, β∘39 and δ+27 thalassaemia mutations. Clinical & Laboratory Haematology. 14(4). 289–292.

Frogheri, Laura, et al.. (2002). The homozygous state of Hb J Sardegna. The Hematology Journal. 3(4). 176–178. 3 indexed citations

Frogheri, Laura, et al.. (1997). Maximal γ‐globin expression in the compound heterozygous state for –175 ^Gγ HPFH and β°39 nonsense thalassaemia: a case study. European Journal Of Haematology. 58(5). 320–325. 3 indexed citations

Frogheri, Laura, et al.. (1996). Frequency of delta+ 27-thalassaemia in Sardinians.. PubMed. 18(4). 241–4. 13 indexed citations

Frogheri, Laura, et al.. (1996). Frequency of δ⁺27-thalassaemia in Sardinians. Clinical & Laboratory Haematology. 18(4). 241–244. 10 indexed citations

Frogheri, Laura, Laura Manca, Sylvain Doré, et al.. (1995). Fetal hemoglobin expression in compound heterozygotes for −117 (G→A) ^Aγ HPFH and β⁰39 nonsense thalassemia. American Journal of Hematology. 49(4). 267–270. 7 indexed citations

10.

Longinotti, Maurizio, Laura Frogheri, Sylvain Doré, et al.. (1994). A 12‐year preventive program for β‐thalassemia in Northern Sardinia. Clinical Genetics. 46(3). 238–243. 8 indexed citations

11.

Gilman, John G., et al.. (1994). Mild β⁺(−87)‐thalassemia CACCC box mutation is associated with elevated fetal hemoglobin expression in cis. American Journal of Hematology. 45(3). 265–267. 10 indexed citations

12.

Frogheri, Laura, et al.. (1994). A novel mediterranean “δβ‐thalassemia” determinant containing the δ⁺27 and β°39 point mutations in cis. American Journal of Hematology. 45(1). 81–84. 8 indexed citations

13.

Doré, Sylvain, et al.. (1992). [Differential diagnosis of thalassemia syndromes].. PubMed. 7(1). 34–41. 1 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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