Antonio Correra

838 total citations
20 papers, 639 citations indexed

About

Antonio Correra is a scholar working on Immunology, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Antonio Correra has authored 20 papers receiving a total of 639 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Immunology, 5 papers in Molecular Biology and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Antonio Correra's work include Metabolism and Genetic Disorders (3 papers), Vascular Malformations and Hemangiomas (3 papers) and Child and Adolescent Health (3 papers). Antonio Correra is often cited by papers focused on Metabolism and Genetic Disorders (3 papers), Vascular Malformations and Hemangiomas (3 papers) and Child and Adolescent Health (3 papers). Antonio Correra collaborates with scholars based in Italy, United States and United Kingdom. Antonio Correra's co-authors include Duilio Brugnoni, Alessandra Bettinardi, Eugenia Quirós-Roldán, Luigi D. Notarangelo, Stefania La Grutta, Umberto Dianzani, Sara Bonissoni, Daniela DiFranco, Carla Alliaudi and Donatella Buonfiglio and has published in prestigious journals such as Blood, PLoS ONE and PEDIATRICS.

In The Last Decade

Antonio Correra

17 papers receiving 616 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Antonio Correra Italy 12 310 259 122 83 76 20 639
Stefania Gaspari Italy 15 180 0.6× 218 0.8× 96 0.8× 241 2.9× 50 0.7× 46 659
J. Jansen Netherlands 10 137 0.4× 124 0.5× 76 0.6× 26 0.3× 72 0.9× 18 845
Hirayasu Kai Japan 14 452 1.5× 100 0.4× 158 1.3× 63 0.8× 56 0.7× 41 810
Irina Costea Canada 17 151 0.5× 336 1.3× 137 1.1× 159 1.9× 120 1.6× 23 1.1k
Judit Laki Hungary 13 216 0.7× 96 0.4× 57 0.5× 69 0.8× 40 0.5× 18 566
Hisashi Tsutsumi Japan 10 181 0.6× 102 0.4× 135 1.1× 100 1.2× 80 1.1× 28 488
Monica Arenas United Kingdom 11 96 0.3× 216 0.8× 62 0.5× 116 1.4× 138 1.8× 19 874
Yoshinobu Fuke Japan 13 164 0.5× 102 0.4× 45 0.4× 54 0.7× 75 1.0× 39 498
Toshio Yanagihara Japan 17 124 0.4× 351 1.4× 29 0.2× 31 0.4× 42 0.6× 36 1.1k
Iman I. Salama Egypt 12 148 0.5× 345 1.3× 80 0.7× 42 0.5× 205 2.7× 38 721

Countries citing papers authored by Antonio Correra

Since Specialization
Citations

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

Fields of papers citing papers by Antonio Correra

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Antonio Correra

This figure shows the co-authorship network connecting the top 25 collaborators of Antonio Correra. A scholar is included among the top collaborators of Antonio Correra 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 Antonio Correra. Antonio Correra 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.
Nunziato, Marcella, Maria Valeria Esposito, Antonio Correra, et al.. (2023). One-step NGS molecular analysis of the CFTR gene on newborn dried blood spots gives a higher diagnostic sensitivity in affected and carrier subjects: A pilot study. Clinica Chimica Acta. 552. 117625–117625.
2.
Correra, Antonio, et al.. (2021). Multifocal lymphangioendotheliomatosis with thrombocytopenia. Minerva Pediatrics. 74(4). 482–484.
3.
4.
Veropalumbo, C., Angelo Campanozzi, Fabiola De Gregorio, et al.. (2014). Shwachman-Diamond syndrome with autoimmune-like liver disease and enteropathy mimicking celiac disease. Clinics and Research in Hepatology and Gastroenterology. 39(1). e1–e4. 7 indexed citations
5.
Agostiniani, Rino, Antonio Correra, Ernesto d’Aloja, et al.. (2014). Pediatric claims in Italy during a 8-years survey. ˜The œItalian Journal of Pediatrics/Italian journal of pediatrics. 40(S1). 4 indexed citations
6.
Fanos, Vassilios, Paolo Tagliabue, Luigi Greco, et al.. (2011). Neonatal malpractice claims in Italy: how big is the problem and which are the causes?. The Journal of Maternal-Fetal & Neonatal Medicine. 25(5). 493–497. 11 indexed citations
7.
Rapacciuolo, Antonio, et al.. (2010). Infantile facial haemangioma and subclinical left ventricular dysfunction: the importance of z score in the diagnostic and therapeutic process. Journal of Cardiovascular Medicine. 11(9). 692–694. 2 indexed citations
8.
Daniele, Aurora, Giuseppe Cardillo, Maria Teresa Carbone, et al.. (2008). Five human phenylalanine hydroxylase proteins identified in mild hyperphenylalaninemia patients are disease-causing variants. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1782(6). 378–384. 12 indexed citations
9.
Guarino, Alfredo, Filippo Ansaldi, Alberto G. Ugazio, et al.. (2008). [Italian Pediatrician's consensus statement on anti-Rotavirus vaccines].. PubMed. 60(1). 3–16. 3 indexed citations
10.
Daniele, Aurora, Giuseppe Cardillo, Maria Teresa Carbone, et al.. (2006). Molecular Epidemiology of Phenylalanine Hydroxylase Deficiency in Southern Italy: a 96% Detection Rate with Ten Novel Mutations. Annals of Human Genetics. 71(2). 185–193. 35 indexed citations
11.
Fecarotta, Simona, Giancarlo Parenti, Pietro Vajro, et al.. (2006). HHH syndrome (hyperornithinaemia, hyperammonaemia, homocitrullinuria), with fulminant hepatitis‐like presentation. Journal of Inherited Metabolic Disease. 29(1). 186–189. 28 indexed citations
12.
13.
Albano, F., Dario Ummarino, Antonio Correra, et al.. (2003). Short duration of breastfeeding and early introduction of cow's milk as a result of mothers’low level of education. Acta Paediatrica. 92(s441). 12–17. 21 indexed citations
14.
Dianzani, Umberto, Manuela Bragardo, Daniela DiFranco, et al.. (1997). Deficiency of the Fas Apoptosis Pathway Without Fas Gene Mutations in Pediatric Patients With Autoimmunity/Lymphoproliferation. Blood. 89(8). 2871–2879. 137 indexed citations
15.
Bettinardi, Alessandra, Duilio Brugnoni, Eugenia Quirós-Roldán, et al.. (1997). Missense mutations in the Fas gene resulting in autoimmune lymphoproliferative syndrome: a molecular and immunological analysis.. PubMed. 89(3). 902–9. 151 indexed citations
16.
Bettinardi, Alessandra, Duilio Brugnoni, Eugenia Quirós-Roldán, et al.. (1997). Missense Mutations in the Fas Gene Resulting in Autoimmune Lymphoproliferative Syndrome: A Molecular and Immunological Analysis. Blood. 89(3). 902–909. 145 indexed citations
17.
Pelliccia, Andrea, et al.. (1989). The incidence of infectious complications during the childhood ALL induction phase with BFM/ALL/NHL/86 protocol.. PubMed. 4 Suppl 3. 103–103. 1 indexed citations
18.
Trautman, Paul D., et al.. (1988). Prediction of Intellectual Deficits in Children with Acute Lymphoblastic Leukemia. Journal of Developmental & Behavioral Pediatrics. 9(3). 122???128–122???128. 14 indexed citations
19.
Correra, Antonio, et al.. (1984). Radiotherapy of a pseudotumor in a hemophiliac with Factor VIII inhibitor. Journal of Pediatric Hematology/Oncology. 6(3). 325–326. 22 indexed citations
20.
Comelli, A, et al.. (1976). Peptichemio in children with neoplastic disease.. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 9(9). 76–83. 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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