G. Ottonello

1.2k total citations
21 papers, 538 citations indexed

About

G. Ottonello is a scholar working on Pulmonary and Respiratory Medicine, Endocrine and Autonomic Systems and Surgery. According to data from OpenAlex, G. Ottonello has authored 21 papers receiving a total of 538 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Pulmonary and Respiratory Medicine, 11 papers in Endocrine and Autonomic Systems and 9 papers in Surgery. Recurrent topics in G. Ottonello's work include Neonatal Respiratory Health Research (12 papers), Neuroscience of respiration and sleep (11 papers) and Respiratory Support and Mechanisms (6 papers). G. Ottonello is often cited by papers focused on Neonatal Respiratory Health Research (12 papers), Neuroscience of respiration and sleep (11 papers) and Respiratory Support and Mechanisms (6 papers). G. Ottonello collaborates with scholars based in Italy, France and United States. G. Ottonello's co-authors include Isabella Ceccherini, Renato Cutrera, Andrea Wolfler, Ida Salvo, Chiara Mastella, Cesare Gregoretti, Sara Parodi, Andrea Moscatelli, Maria Beatrice Chiarini Testa and Lucilla Ravà and has published in prestigious journals such as American Journal of Respiratory and Critical Care Medicine, PEDIATRICS and Surgical Endoscopy.

In The Last Decade

G. Ottonello

21 papers receiving 522 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
G. Ottonello Italy 14 360 209 150 77 71 21 538
Janet Stocks United Kingdom 11 203 0.6× 63 0.3× 95 0.6× 72 0.9× 207 2.9× 11 521
Bruno Langevin France 9 718 2.0× 332 1.6× 93 0.6× 24 0.3× 10 0.1× 12 971
Elia Gómez-Merino Spain 9 312 0.9× 84 0.4× 33 0.2× 102 1.3× 7 0.1× 18 493
Nicole Sheers Australia 10 359 1.0× 89 0.4× 27 0.2× 149 1.9× 13 0.2× 27 539
Gabriela Ferreyra Italy 8 452 1.3× 39 0.2× 91 0.6× 38 0.5× 9 0.1× 14 638
Jesús Sancho Spain 17 678 1.9× 57 0.3× 43 0.3× 395 5.1× 14 0.2× 35 1.1k
Brian Weaver United States 4 139 0.4× 25 0.1× 138 0.9× 214 2.8× 17 0.2× 4 370
Karl Leroux France 16 490 1.4× 217 1.0× 35 0.2× 32 0.4× 5 0.1× 31 603
William Prentice United States 8 189 0.5× 22 0.1× 32 0.2× 32 0.4× 24 0.3× 9 304
Cathy Worwa United States 12 335 0.9× 145 0.7× 78 0.5× 45 0.6× 216 3.0× 13 633

Countries citing papers authored by G. Ottonello

Since Specialization
Citations

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

Fields of papers citing papers by G. Ottonello

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of G. Ottonello

This figure shows the co-authorship network connecting the top 25 collaborators of G. Ottonello. A scholar is included among the top collaborators of G. Ottonello 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 G. Ottonello. G. Ottonello 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.
Trang, Ha, Martin Samuels, Isabella Ceccherini, et al.. (2020). Guidelines for diagnosis and management of congenital central hypoventilation syndrome. Orphanet Journal of Rare Diseases. 15(1). 252–252. 68 indexed citations
2.
Blanot, Stéphane, et al.. (2016). Évaluation rétrospective de l’épreuve d’apnée chez l’enfant en mort encéphalique. Réanimation. 1 indexed citations
3.
Trang, Ha, Jean‐François Brunet, Hermann Rohrer, et al.. (2014). Proceedings of the fourth international conference on central hypoventilation. Orphanet Journal of Rare Diseases. 9(1). 194–194. 11 indexed citations
4.
Gregoretti, Cesare, G. Ottonello, Maria Beatrice Chiarini Testa, et al.. (2013). Survival of Patients With Spinal Muscular Atrophy Type 1. PEDIATRICS. 131(5). e1509–e1514. 80 indexed citations
5.
Ottonello, G., Chiara Mastella, Andrea Wolfler, et al.. (2011). Spinal Muscular Atrophy Type 1. American Journal of Physical Medicine & Rehabilitation. 90(11). 895–900. 11 indexed citations
6.
Agosto, Caterina, et al.. (2011). Congenital central hypoventilation syndrome and hypoglycaemia. Acta Paediatrica. 101(2). e92–6. 17 indexed citations
7.
Racca, Fabrizio, Maurizio Bonati, Lorenzo Del Sorbo, et al.. (2011). Invasive and non-invasive long-term mechanical ventilation in Italian children.. PubMed. 77(9). 892–901. 33 indexed citations
8.
Wolfler, Andrea, G. Ottonello, Giorgio Conti, et al.. (2010). Daily practice of mechanical ventilation in Italian pediatric intensive care units: A prospective survey*. Pediatric Critical Care Medicine. 12(2). 141–146. 41 indexed citations
9.
Ottonello, G., Chiara Mastella, Elisabetta Lampugnani, et al.. (2010). Parental role in the Intensive Care Unit for children affected by Werdnig Hoffmann disease.. PubMed. 62(2). 147–51. 1 indexed citations
10.
Racca, Fabrizio, Marco Sequi, Renato Cutrera, et al.. (2010). Long‐term home ventilation of children in Italy: A national survey. Pediatric Pulmonology. 46(6). 566–572. 60 indexed citations
11.
Parodi, Sara, Catello Vollono, Martina Balestri, et al.. (2010). Congenital central hypoventilation syndrome: genotype–phenotype correlation in parents of affected children carrying a PHOX2B expansion mutation. Clinical Genetics. 78(3). 289–293. 17 indexed citations
13.
Parodi, Sara, Alessio Pini Prato, Francesco Caroli, et al.. (2008). A novel missense mutation in the PHOX2Bgene is associated with late onset central hypoventilation syndrome. Pediatric Pulmonology. 43(10). 1036–1039. 13 indexed citations
14.
Ottonello, G., et al.. (2007). Home mechanical ventilation in children: Retrospective survey of a pediatric population. Pediatrics International. 49(6). 801–805. 51 indexed citations
15.
Parodi, Sara, Tiziana Bachetti, Francesca Lantieri, et al.. (2007). Parental origin and somatic mosaicism of PHOX2B mutations in Congenital Central Hypoventilation Syndrome. Human Mutation. 29(1). 206–206. 48 indexed citations
16.
Bachetti, Tiziana, Angela Robbiano, Sara Parodi, et al.. (2006). Brainstem Anomalies in Two Patients Affected by Congenital Central Hypoventilation Syndrome. American Journal of Respiratory and Critical Care Medicine. 174(6). 706–709. 20 indexed citations
17.
Ottonello, G., et al.. (2006). Noninvasive ventilation in a child affected by achondroplasia respiratory difficulty syndrome. Pediatric Anesthesia. 17(1). 75–79. 10 indexed citations
18.
Villa, G., et al.. (2006). Sudden Death in an Infant Revealing Atypical Kawasaki Disease. Pediatric Emergency Care. 22(1). 35–37. 13 indexed citations
19.
Mattioli, Girolamo, Klaas N.M.A. Bax, F. Becmeur, et al.. (2005). European multicenter survey on the laparoscopic treatment of gastroesophageal reflux in patients aged less than 12 months with supraesophageal symptoms. Surgical Endoscopy. 19(10). 1309–1314. 8 indexed citations
20.
Matera, Ivana, Tiziana Bachetti, R. Cinti, et al.. (2002). Mutational analysis of the RNX gene in congenital central hypoventilation syndrome. American Journal of Medical Genetics. 113(2). 178–182. 13 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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