Matteo Francese

452 total citations
15 papers, 337 citations indexed

About

Matteo Francese is a scholar working on Genetics, Hematology and Surgery. According to data from OpenAlex, Matteo Francese has authored 15 papers receiving a total of 337 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 5 papers in Hematology and 4 papers in Surgery. Recurrent topics in Matteo Francese's work include Hemoglobinopathies and Related Disorders (7 papers), Blood properties and coagulation (4 papers) and Erythrocyte Function and Pathophysiology (4 papers). Matteo Francese is often cited by papers focused on Hemoglobinopathies and Related Disorders (7 papers), Blood properties and coagulation (4 papers) and Erythrocyte Function and Pathophysiology (4 papers). Matteo Francese collaborates with scholars based in Italy and United States. Matteo Francese's co-authors include Silverio Perrotta, Brúno Nobili, Achille Iolascon, Emanuele Miraglia del Giudice, Luigi Esposito, Francesca Rossi, Giulia Bellini, Chiara Tortora, Antonietta Coppola and Marco Torella and has published in prestigious journals such as The Journal of Pediatrics, British Journal of Haematology and Haematologica.

In The Last Decade

Matteo Francese

15 papers receiving 329 citations

Peers

Matteo Francese

PHYSI

GENET

HEMAT

PPCH

PRM

Christopher Denton United States

Florin Tripon Romania

Agnes J. Bishop Canada

Balázs Stenczer Hungary

H Bertz Germany

M. Pilar Sardà Spain

Anwar Al‐Awadhi Kuwait

Junichi Kitagawa Japan

M A Hussain United Kingdom

Hiromitsu Takakura Japan

Christopher Denton United States

Matteo Francese

40 ×0.3

PHYSI

96 ×0.8

GENET

96 ×0.9

HEMAT

73 ×0.7

PPCH

32 ×0.4

PRM

Citations per year, relative to Matteo Francese Matteo Francese (= 1×) peers Christopher Denton

Countries citing papers authored by Matteo Francese

Since Specialization

Citations

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

Fields of papers citing papers by Matteo Francese

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Matteo Francese

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

All Works

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15 of 15 papers shown

Rossi, Francesca, Silverio Perrotta, Giulia Bellini, et al.. (2014). Iron overload causes osteoporosis in thalassemia major patients through interaction with transient receptor potential vanilloid type 1 (TRPV1) channels. Haematologica. 99(12). 1876–1884. 70 indexed citations

D’Angelo, V., Matteo Francese, Elvira Pota, et al.. (2013). Influence of methylenetetrahydrofolate reductase gene polymorphisms on the outcome of pediatric patients with non-Hodgkin lymphoma treated with high-dose methotrexate. Leukemia & lymphoma. 54(12). 2639–2644. 13 indexed citations

D’Angelo, V., Stefania Crisci, Paolo Indolfi, et al.. (2011). Methotrexate toxicity and efficacy during the consolidation phase in paediatric acute lymphoblastic leukaemia and MTHFR polymorphisms as pharmacogenetic determinants. Cancer Chemotherapy and Pharmacology. 68(5). 1339–1346. 37 indexed citations

Vitale, Elsa, Andrea Ungar, Roberto Maggi, et al.. (2010). Discrepancy between clinical practice and standardized indications for an implantable loop recorder in patients with unexplained syncope. EP Europace. 12(10). 1475–1479. 20 indexed citations

Rossi, Francesca, Matteo Francese, Rosa Iodice, et al.. (2005). [Inherited disorders of bilirubin metabolism].. PubMed. 57(2). 53–63. 11 indexed citations

Francese, Matteo, et al.. (2005). Impact of excess weight and estrogen receptor gene polymorphisms on clinical course of homozygous β thalassemia. Hematology. 10(5). 407–411. 3 indexed citations

Francese, Matteo, et al.. (2003). Role of polymorphic sequences 5′ to the^Gγ gene and 5′ to the β gene on the homozygous β thalassemic phenotype. Hemoglobin. 27(3). 167–175. 7 indexed citations

Francese, Matteo, et al.. (2002). Effect of VDR polymorphisms on growth and bone mineral density in homozygous beta thalassaemia. British Journal of Haematology. 117(2). 436–440. 38 indexed citations

Francese, Matteo, et al.. (2001). HEMATOLOGICAL AND MOLECULAR ANALYSIS OF β-THALASSEMIA AND Hb LEPORE IN CAMPANIA, ITALY. Hemoglobin. 25(1). 29–34. 7 indexed citations

10.

Nobili, Brúno, et al.. (2001). Clinical and molecular evaluation of non‐dominant hereditary spherocytosis. British Journal of Haematology. 112(1). 42–47. 41 indexed citations

11.

Giudice, Emanuele Miraglia del, et al.. (1998). High frequency of de novo mutations in ankyrin gene (ANK1) in children with hereditary spherocytosis. The Journal of Pediatrics. 132(1). 117–120. 31 indexed citations

12.

Giudice, Emanuele Miraglia del, Cinzia Lombardi, Matteo Francese, et al.. (1998). Frequent de novo monoallelic expression of β‐spectrin gene (SPTB) in children with hereditary spherocytosis and isolated spectrin deficiency. British Journal of Haematology. 101(2). 251–254. 29 indexed citations

13.

Perrone, Laura, et al.. (1998). Leptin level and structure in Italian obese children. Nutrition Research. 18(9). 1493–1498. 2 indexed citations

14.

Alfinito, Fiorella, Amelia Cimmino, Maria Vittoria Cubellis, et al.. (1997). Molecular characterization of G6PD deficiency in Southern Italy: heterogeneity, correlation genotype–phenotype and description of a new variant (G6PD Neapolis). British Journal of Haematology. 98(1). 41–46. 16 indexed citations

15.

Giudice, Emanuele Miraglia del, et al.. (1997). Apparently normal ankyrin content in unsplenectomized hereditary spherocytosis patients with the inactivation of one ankyrin (ANK1) allele.. PubMed. 82(3). 332–3. 12 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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