Giulio Calcagni

1.6k total citations
52 papers, 584 citations indexed

About

Giulio Calcagni is a scholar working on Epidemiology, Molecular Biology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Giulio Calcagni has authored 52 papers receiving a total of 584 indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Epidemiology, 25 papers in Molecular Biology and 24 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Giulio Calcagni's work include Congenital Heart Disease Studies (25 papers), Congenital heart defects research (17 papers) and Coronary Artery Anomalies (14 papers). Giulio Calcagni is often cited by papers focused on Congenital Heart Disease Studies (25 papers), Congenital heart defects research (17 papers) and Coronary Artery Anomalies (14 papers). Giulio Calcagni collaborates with scholars based in Italy, France and United Kingdom. Giulio Calcagni's co-authors include M. Cristina Digilio, Bruno Marino, Paolo Versacci, Anwar Baban, Bruno Dallapiccola, Françis Brunelle, Daniel Sidi, Marco Tartaglia, Fabrizio Drago and Marta Unolt and has published in prestigious journals such as PLoS ONE, European Heart Journal and Journal of Thoracic and Cardiovascular Surgery.

In The Last Decade

Giulio Calcagni

48 papers receiving 573 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Giulio Calcagni Italy 13 319 304 165 152 149 52 584
G. Buheitel Germany 10 229 0.7× 218 0.7× 123 0.7× 121 0.8× 90 0.6× 39 467
Jae Sook South Korea 10 89 0.3× 76 0.3× 232 1.4× 221 1.5× 106 0.7× 50 445
Mitsuru Seki Japan 13 78 0.2× 168 0.6× 253 1.5× 206 1.4× 216 1.4× 38 474
Erin Pinto United States 12 48 0.2× 174 0.6× 115 0.7× 341 2.2× 58 0.4× 22 475
Hubert Jockin United States 11 80 0.3× 102 0.3× 217 1.3× 115 0.8× 55 0.4× 15 431
M R Dische United States 10 53 0.2× 183 0.6× 167 1.0× 133 0.9× 166 1.1× 14 433
Songling Fu China 15 138 0.4× 49 0.2× 296 1.8× 474 3.1× 158 1.1× 34 668
Louise Ekholm Sweden 10 112 0.4× 486 1.6× 75 0.5× 30 0.2× 33 0.2× 11 587
Martina Finetti Italy 10 392 1.2× 129 0.4× 41 0.2× 159 1.0× 274 1.8× 30 740
Jonathan Anderson United Kingdom 8 65 0.2× 60 0.2× 37 0.2× 108 0.7× 82 0.6× 15 362

Countries citing papers authored by Giulio Calcagni

Since Specialization
Citations

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

Fields of papers citing papers by Giulio Calcagni

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Giulio Calcagni

This figure shows the co-authorship network connecting the top 25 collaborators of Giulio Calcagni. A scholar is included among the top collaborators of Giulio Calcagni 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 Giulio Calcagni. Giulio Calcagni 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.
Calcagni, Giulio, Federica Ferrigno, Maria Lisa Dentici, et al.. (2024). Congenital Heart Defects in Patients with Molecularly Confirmed Sotos Syndrome. Diagnostics. 14(6). 594–594. 1 indexed citations
2.
Leonardi, Benedetta, Federica Gentili, Massimiliano Bianco, et al.. (2024). Cardiopulmonary Exercise Testing after Surgical Repair of Tetralogy of Fallot—Does Modality Matter?. Journal of Clinical Medicine. 13(5). 1192–1192. 2 indexed citations
3.
Monda, Emanuele, Michele Lioncino, Gabrielle Norrish, et al.. (2023). Natural History of Hypertrophic Cardiomyopathy in Noonan Syndrome With Multiple Lentigines. Circulation Genomic and Precision Medicine. 16(4). 350–358. 9 indexed citations
4.
Lioncino, Michele, Giulio Calcagni, Giovanni Antonelli, et al.. (2023). Double-Outlet Left Ventricle: Case Series and Systematic Review of the Literature. Diagnostics. 13(20). 3175–3175.
5.
Gentili, Federica, Giulio Calcagni, Nicoletta Cantarutti, et al.. (2023). Cardiopulmonary Exercise Testing in Children and Young Adolescents after a Multisystem Inflammatory Syndrome: Physical Deconditioning or Residual Pathology?. Journal of Clinical Medicine. 12(6). 2375–2375. 4 indexed citations
6.
Calcagni, Giulio, Camilla Calvieri, Anwar Baban, et al.. (2022). Syndromic and Non-Syndromic Patients with Repaired Tetralogy of Fallot: Does It Affect the Long-Term Outcome?. Journal of Clinical Medicine. 11(3). 850–850. 5 indexed citations
7.
Calcagni, Giulio, Silvia Anaclerio, Flaminia Pugnaloni, et al.. (2022). Crossed pulmonary arteries: An underestimated cardiovascular variant with a strong association with genetic syndromes—A report of 74 cases with systematic review of the literature. American Journal of Medical Genetics Part A. 188(8). 2351–2359. 3 indexed citations
8.
Putotto, Carolina, Flaminia Pugnaloni, Marta Unolt, et al.. (2022). 22q11.2 Deletion Syndrome: Impact of Genetics in the Treatment of Conotruncal Heart Defects. Children. 9(6). 772–772. 12 indexed citations
9.
Onesimo, Roberta, Paolo Versacci, Angelica Bibiana Delogu, et al.. (2021). Smith–Magenis syndrome: Report of morphological and new functional cardiac findings with review of the literature. American Journal of Medical Genetics Part A. 185(7). 2003–2011. 5 indexed citations
10.
Gallo, Giovanna, Vittoria Mastromarino, Giulio Calcagni, et al.. (2021). Insights from Cardiopulmonary Exercise Testing in Pediatric Patients with Hypertrophic Cardiomyopathy. Biomolecules. 11(3). 376–376. 5 indexed citations
11.
Capitello, Teresa Grimaldi, Francesca Bevilacqua, Roberta Vallone, et al.. (2021). Validity and reliability of the Italian version of the cardiac quality of life questionnaire for pediatric patients with heart disease (PedsQLTM). BMC Cardiovascular Disorders. 21(1). 398–398. 8 indexed citations
12.
Lioncino, Michele, Emanuele Monda, Federica Verrillo, et al.. (2021). Hypertrophic Cardiomyopathy in RASopathies. Heart Failure Clinics. 18(1). 19–29. 35 indexed citations
13.
Dentici, Maria Lisa, Sara Loddo, Luigi Laino, et al.. (2021). Congenital heart defects in the recurrent 2q13 deletion syndrome. European Journal of Medical Genetics. 65(1). 104381–104381. 12 indexed citations
14.
Baban, Anwar, Nicoletta Cantarutti, Rachele Adorisio, et al.. (2018). Long-term survival and phenotypic spectrum in heterotaxy syndrome: A 25-year follow-up experience. International Journal of Cardiology. 268. 100–105. 25 indexed citations
15.
Unolt, Marta, Paolo Versacci, Silvia Anaclerio, et al.. (2018). Congenital heart diseases and cardiovascular abnormalities in 22q11.2 deletion syndrome: From well‐established knowledge to new frontiers. American Journal of Medical Genetics Part A. 176(10). 2087–2098. 43 indexed citations
16.
Putotto, Carolina, Giulio Calcagni, Marta Unolt, et al.. (2018). Impact of genetic studies on comprehension and treatment of congenital heart disease. Progress in Pediatric Cardiology. 51. 31–36.
17.
Ferese, Rosangela, Monica Bonetti, Federica Consoli, et al.. (2018). Heterozygous missense mutations inNFATC1are associated with atrioventricular septal defect. Human Mutation. 39(10). 1428–1441. 14 indexed citations
18.
Calcagni, Giulio, Françis Brunelle, Pascal Vouhé, et al.. (2008). CT demonstration of “chicken trachea” resulting from complete cartilaginous rings of the trachea in ring-sling complex. Pediatric Radiology. 38(7). 798–800. 4 indexed citations
19.
Calcagni, Giulio, Francesco Gesualdo, Daniel Tamisier, et al.. (2008). Arterial aneurysms and tuberous sclerosis: a classic but little known association. Pediatric Radiology. 38(7). 795–797. 14 indexed citations
20.
Ou, Phalla, Giulio Calcagni, Davide Marini, et al.. (2007). Unusual systemic venous return with absence of superior caval veins. Journal of Thoracic and Cardiovascular Surgery. 133(5). 1368–1369. 5 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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