Claudia Cesaretti

913 total citations
34 papers, 504 citations indexed

About

Claudia Cesaretti is a scholar working on Genetics, Neurology and Genetics. According to data from OpenAlex, Claudia Cesaretti has authored 34 papers receiving a total of 504 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 9 papers in Neurology and 9 papers in Genetics. Recurrent topics in Claudia Cesaretti's work include Hemoglobinopathies and Related Disorders (9 papers), Neurofibromatosis and Schwannoma Cases (9 papers) and Iron Metabolism and Disorders (6 papers). Claudia Cesaretti is often cited by papers focused on Hemoglobinopathies and Related Disorders (9 papers), Neurofibromatosis and Schwannoma Cases (9 papers) and Iron Metabolism and Disorders (6 papers). Claudia Cesaretti collaborates with scholars based in Italy, United States and Lebanon. Claudia Cesaretti's co-authors include Maria Domenica Cappellini, Khaled M. Musallam, Alì Taher, Mehran Karimi, Shahina Daar, Khawla Belhoul, Amal El‐Beshlawy, Cecilia Parazzini, Andrea Righini and Mario Anichini and has published in prestigious journals such as SHILAP Revista de lepidopterología, Blood and Journal of Thrombosis and Haemostasis.

In The Last Decade

Claudia Cesaretti

27 papers receiving 487 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Claudia Cesaretti Italy 12 235 197 92 81 68 34 504
Amy Hughes United States 11 147 0.6× 208 1.1× 20 0.2× 55 0.7× 30 0.4× 27 506
Marta S. Gallego Argentina 15 98 0.4× 317 1.6× 95 1.0× 61 0.8× 34 0.5× 43 644
Lulin Choubtum Thailand 11 161 0.7× 124 0.6× 61 0.7× 15 0.2× 30 0.4× 22 454
Eva Simmons-OʼBrien United States 6 48 0.2× 112 0.6× 22 0.2× 54 0.7× 86 1.3× 7 429
Guopan Yu China 14 199 0.8× 428 2.2× 80 0.9× 37 0.5× 26 0.4× 69 763
Raine Tatara Japan 10 132 0.6× 95 0.5× 22 0.2× 22 0.3× 19 0.3× 23 286
Laura Dell’Arti Italy 11 79 0.3× 45 0.2× 23 0.3× 52 0.6× 32 0.5× 21 391
Giulia Ceglie Italy 11 115 0.5× 63 0.3× 15 0.2× 34 0.4× 72 1.1× 22 261
Paula Polk United States 8 112 0.5× 77 0.4× 30 0.3× 14 0.2× 15 0.2× 11 334
Dale Wright Australia 8 31 0.1× 56 0.3× 88 1.0× 41 0.5× 29 0.4× 23 420

Countries citing papers authored by Claudia Cesaretti

Since Specialization
Citations

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

Fields of papers citing papers by Claudia Cesaretti

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Claudia Cesaretti

This figure shows the co-authorship network connecting the top 25 collaborators of Claudia Cesaretti. A scholar is included among the top collaborators of Claudia Cesaretti 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 Claudia Cesaretti. Claudia Cesaretti 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.
Bettinaglio, Paola, Eleonora Mangano, Claudia Cesaretti, et al.. (2024). Genetic/epigenetic effects in NF1 microdeletion syndrome: beyond the haploinsufficiency, looking at the contribution of not deleted genes. Human Genetics. 143(6). 775–795.
2.
Milani, Donatella, Federica Alberti, Claudia Cesaretti, et al.. (2023). CATSHL syndrome, a new family and phenotypic expansion. Clinical Genetics. 105(3). 313–316. 1 indexed citations
3.
Bettinaglio, Paola, Eleonora Mangano, Roberta Bordoni, et al.. (2023). New insights into the molecular basis of spinal neurofibromatosis type 1. European Journal of Human Genetics. 31(8). 931–938. 1 indexed citations
4.
Rimoldi, M., Berardo Rinaldi, Roberta Villa, et al.. (2022). Congenital diaphragmatic hernia in Coffin Siris syndrome: Further evidence from two cases. American Journal of Medical Genetics Part A. 191(2). 605–611.
5.
Paterra, Rosina, Paola Bettinaglio, Eleonora Mangano, et al.. (2022). A Translational Approach to Spinal Neurofibromatosis: Clinical and Molecular Insights from a Wide Italian Cohort. Cancers. 15(1). 59–59. 3 indexed citations
6.
Esposito, Andrea, Gianmarco Della Pepa, Giulia Cagnoli, et al.. (2021). Neurofibromatosis Type 1 with Neck and Thoraco-Abdominal Involvement: A Case Series Showing Different Localization and MRI Features. SHILAP Revista de lepidopterología. Volume 14. 41–51.
7.
Bianchessi, Donatella, Veronica Saletti, Rosina Paterra, et al.. (2020). Simultaneous Detection of NF1, SPRED1, LZTR1, and NF2 Gene Mutations by Targeted NGS in an Italian Cohort of Suspected NF1 Patients. Genes. 11(6). 671–671. 8 indexed citations
8.
Curcio, Cristina, et al.. (2020). Unexpected Genotype in a Non-Transfusion Dependent Thalassemia Family. Journal of Medical Cases. 11(4). 90–93.
9.
Tucci, Arianna, Veronica Saletti, Francesca Menni, et al.. (2017). The absence that makes the difference: choroidal abnormalities in Legius syndrome. Journal of Human Genetics. 62(11). 1001–1004. 5 indexed citations
10.
Righini, Andrea, Claudia Cesaretti, Giorgio Conte, et al.. (2015). Expanding the spectrum of human ganglionic eminence region anomalies on fetal magnetic resonance imaging. Neuroradiology. 58(3). 293–300. 11 indexed citations
11.
Conte, Giorgio, et al.. (2015). Diagnostic Value of Prenatal MR Imaging in the Detection of Brain Malformations in Fetuses before the 26th Week of Gestational Age. American Journal of Neuroradiology. 37(5). 946–951. 20 indexed citations
12.
Martino, Francesca, Mariya Malova, Claudia Cesaretti, et al.. (2015). Prenatal MR imaging features of isolated cerebellar haemorrhagic lesions. European Radiology. 26(8). 2685–2696. 15 indexed citations
13.
Cesaretti, Claudia, M. Nanni, T. Ghi, et al.. (2015). Variability of Forebrain Commissures in Callosal Agenesis: A Prenatal MR Imaging Study. American Journal of Neuroradiology. 37(3). 521–527. 7 indexed citations
14.
Cesaretti, Claudia, Luigina Spaccini, Mariangela Rustico, et al.. (2014). Prenatal magnetic resonance imaging detection of temporal lobes and hippocampal anomalies in hypochondroplasia. Prenatal Diagnosis. 34(10). 1015–1017. 8 indexed citations
15.
Cesaretti, Claudia, Giulia Melloni, Roberto Fogliani, et al.. (2013). Neurofibromatosis type 1 and pregnancy: Maternal complications and attitudes about prenatal diagnosis. American Journal of Medical Genetics Part A. 161(2). 386–388. 16 indexed citations
16.
Musallam, Khaled M., Alì Taher, Lorena Duca, et al.. (2011). Levels of growth differentiation factor-15 are high and correlate with clinical severity in transfusion-independent patients with β thalassemia intermedia. Blood Cells Molecules and Diseases. 47(4). 232–234. 53 indexed citations
17.
Cesaretti, Claudia, Barbara Gentilin, Vera Bianchi, et al.. (2011). Occurrence of complete arhinia in two siblings with a clinical picture of Treacher Collins syndrome negative for TCOF1, POLR1D and POLR1C mutations. Clinical Dysmorphology. 20(4). 229–231. 8 indexed citations
18.
Colombo, Elisa Adele, Elena Cassinerio, Claudia Cesaretti, et al.. (2010). Pregnant women affected by thalassemia major: A controlled study of traits and personality. SHILAP Revista de lepidopterología. 2 indexed citations
19.
Taher, Alì, Khaled M. Musallam, Mehran Karimi, et al.. (2010). Splenectomy and thrombosis: the case of thalassemia intermedia. Journal of Thrombosis and Haemostasis. 8(10). 2152–2158. 118 indexed citations
20.
Roghi, Alberto, Maria Domenica Cappellini, John C. Wood, et al.. (2009). Absence of cardiac siderosis despite hepatic iron overload in Italian patients with thalassemia intermedia: an MRI T2* study. Annals of Hematology. 89(6). 585–589. 60 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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