Luisa Ronzoni

1.1k total citations
43 papers, 455 citations indexed

About

Luisa Ronzoni is a scholar working on Epidemiology, Genetics and Molecular Biology. According to data from OpenAlex, Luisa Ronzoni has authored 43 papers receiving a total of 455 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Epidemiology, 14 papers in Genetics and 11 papers in Molecular Biology. Recurrent topics in Luisa Ronzoni's work include Liver Disease Diagnosis and Treatment (13 papers), Erythrocyte Function and Pathophysiology (10 papers) and Genomic variations and chromosomal abnormalities (7 papers). Luisa Ronzoni is often cited by papers focused on Liver Disease Diagnosis and Treatment (13 papers), Erythrocyte Function and Pathophysiology (10 papers) and Genomic variations and chromosomal abnormalities (7 papers). Luisa Ronzoni collaborates with scholars based in Italy, United States and Sweden. Luisa Ronzoni's co-authors include Maria Domenica Cappellini, F. Turrini, Luca Valenti, Donatella Milani, Susanna Esposito, Achille Iolascon, Lucia De Franceschi, Amina Khadjavi, Franca Mannu and Arianna Tucci and has published in prestigious journals such as Nucleic Acids Research, SHILAP Revista de lepidopterología and Blood.

In The Last Decade

Luisa Ronzoni

41 papers receiving 442 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Luisa Ronzoni Italy 13 188 131 116 86 78 43 455
Virginie Helias France 7 104 0.6× 144 1.1× 97 0.8× 32 0.4× 47 0.6× 8 340
Flávia Roche Moreira Latini Brazil 11 101 0.5× 98 0.7× 56 0.5× 48 0.6× 79 1.0× 34 342
Pavlos Fanis Cyprus 12 283 1.5× 81 0.6× 274 2.4× 31 0.4× 146 1.9× 36 618
R Kastally France 12 126 0.7× 234 1.8× 83 0.7× 71 0.8× 82 1.1× 29 513
Shigeko Nishimura Japan 9 323 1.7× 84 0.6× 133 1.1× 23 0.3× 37 0.5× 31 543
Gianfranco Savoldi Italy 15 177 0.9× 55 0.4× 40 0.3× 48 0.6× 206 2.6× 36 670
Cristina Clissa Italy 15 341 1.8× 42 0.3× 124 1.1× 83 1.0× 54 0.7× 31 723
Christina Lisk United States 9 150 0.8× 46 0.4× 51 0.4× 28 0.3× 50 0.6× 18 335
Mushfequr R. Haq United Kingdom 9 130 0.7× 29 0.2× 47 0.4× 45 0.5× 67 0.9× 10 413
Mônica Barbosa de Melo Brazil 16 362 1.9× 31 0.2× 108 0.9× 25 0.3× 131 1.7× 67 791

Countries citing papers authored by Luisa Ronzoni

Since Specialization
Citations

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

Fields of papers citing papers by Luisa Ronzoni

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Luisa Ronzoni

This figure shows the co-authorship network connecting the top 25 collaborators of Luisa Ronzoni. A scholar is included among the top collaborators of Luisa Ronzoni 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 Luisa Ronzoni. Luisa Ronzoni 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.
Shi, Hongxue, Xiaobo Wang, Brennan D. Gerlach, et al.. (2025). Impaired TIM4-mediated efferocytosis by liver macrophages contributes to fibrosis in metabolic dysfunction–associated steatohepatitis. Science Translational Medicine. 17(815). eadv2106–eadv2106. 2 indexed citations
2.
Moore, Mary P., Xiaobo Wang, John P. Kennelly, et al.. (2024). Low MBOAT7 expression, a genetic risk for MASH, promotes a profibrotic pathway involving hepatocyte TAZ upregulation. Hepatology. 81(2). 576–590. 7 indexed citations
3.
Pelusi, Serena, Luisa Ronzoni, Chiara Rosso, et al.. (2024). Prevalence and Determinants of Liver Disease in Relatives of Italian Patients With Advanced MASLD. Clinical Gastroenterology and Hepatology. 22(11). 2231–2239.e4. 7 indexed citations
4.
Pietro, Giada Di, Luisa Ronzoni, Claudia Tagliabue, et al.. (2023). SARS-CoV-2 infection in children: A 24 months experience with focus on risk factors in a pediatric tertiary care hospital in Milan, Italy. Frontiers in Pediatrics. 11. 1082083–1082083. 4 indexed citations
5.
Ronzoni, Luisa, Francesco Malvestiti, Cristiana Bianco, et al.. (2023). Liver Involvement in Patients with Rare MBOAT7 Variants and Intellectual Disability: A Case Report and Literature Review. Genes. 14(8). 1633–1633. 2 indexed citations
6.
Shalaby, Sarah, Luisa Ronzoni, Virginia Hernández–Gea, & Luca Valenti. (2023). The genetics of portal hypertension: Recent developments and the road ahead. Liver International. 43(12). 2592–2603. 6 indexed citations
7.
Bianco, Cristiana, Serena Pelusi, Federica Tavaglione, et al.. (2023). Predictors of controlled attenuation parameter in metabolic dysfunction. United European Gastroenterology Journal. 12(3). 364–373. 5 indexed citations
8.
Valenti, Luca, Armando Tripodi, Vincenzo La Mura, et al.. (2022). Clinical and genetic determinants of the fatty liver–coagulation balance interplay in individuals with metabolic dysfunction. JHEP Reports. 4(12). 100598–100598. 17 indexed citations
9.
Ronzoni, Luisa, et al.. (2020). Ultrasound 2-D and 3-D diagnosis of Rubinstein–Taybi syndrome in a 21-week-old fetus. Journal of Ultrasound. 25(2). 301–304. 4 indexed citations
10.
Ronzoni, Luisa, Antonio Novelli, Giulia Brisighelli, et al.. (2016). 2q33.1q34 Deletion in a Girl with Brain Anomalies and Anorectal Malformation. Cytogenetic and Genome Research. 150(1). 23–28. 2 indexed citations
11.
Tucci, Arianna, Lidia Pezzani, Giulietta Scuvera, et al.. (2016). Is cutis verticis Gyrata‐Intellectual Disability syndrome an underdiagnosed condition? A case report and review of 62 cases. American Journal of Medical Genetics Part A. 173(3). 638–646. 15 indexed citations
12.
Ronzoni, Luisa, Angela Peron, Vera Bianchi, et al.. (2015). Molecular cytogenetic characterization of a 2q35‐q37 duplication and a 4q35.1‐q35.2 deletion in two cousins: A genotype–phenotype analysis. American Journal of Medical Genetics Part A. 167(7). 1551–1559. 4 indexed citations
13.
Ferru, Emanuela, Antonella Pantaleo, Franco Carta, et al.. (2013). Thalassemic erythrocytes release microparticles loaded with hemichromes by redox activation of p72Syk kinase. Haematologica. 99(3). 570–578. 55 indexed citations
14.
Franceschi, Lucia De, Mariarita Bertoldi, Luigia De Falco, et al.. (2011). Oxidative stress modulates heme synthesis and induces peroxiredoxin-2 as a novel cytoprotective response in  -thalassemic erythropoiesis. Haematologica. 96(11). 1595–1604. 60 indexed citations
15.
Punzo, Francesca, Aida M. Bertoli‐Avella, Saverio Scianguetta, et al.. (2011). Congenital Dyserythropoietic Anemia Type II: molecular analysis and expression of the SEC23B Gene. Orphanet Journal of Rare Diseases. 6(1). 89–89. 15 indexed citations
16.
Finaurini, Sara, Luisa Ronzoni, Alessandra Cattaneo, et al.. (2010). Selective toxicity of dihydroartemisinin on human CD34+ erythroid cell differentiation. Toxicology. 276(2). 128–134. 26 indexed citations
17.
Borriello, Adriana, Ilaria Caldarelli, Debora Bencivenga, et al.. (2010). p57 Kip2 is a downstream effector of BCR–ABL kinase inhibitors in chronic myelogenous leukemia cells. Carcinogenesis. 32(1). 10–18. 21 indexed citations
18.
Finaurini, Sara, et al.. (2009). Effect of dihydroartemisinis (DHA) on human erythroid cell differentiation : implications for malaria treatment in pregnancy. Clinical Biochemistry. 42(18). 1860–1861. 1 indexed citations
19.
Franceschi, Lucia De, Luisa Ronzoni, Maria Domenica Cappellini, et al.. (2007). K-CL co-transport plays an important role in normal and   thalassemic erythropoiesis. Haematologica. 92(10). 1319–1326. 15 indexed citations
20.
Tringali, Cristina, Luigi Anastasia, Nadia Papini, et al.. (2006). Modification of sialidase levels and sialoglycoconjugate pattern during erythroid and erytroleukemic cell differentiation. Glycoconjugate Journal. 24(1). 67–79. 17 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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