Carla Olivieri

1.8k total citations
50 papers, 1.0k citations indexed

About

Carla Olivieri is a scholar working on Genetics, Pulmonary and Respiratory Medicine and Surgery. According to data from OpenAlex, Carla Olivieri has authored 50 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Genetics, 31 papers in Pulmonary and Respiratory Medicine and 13 papers in Surgery. Recurrent topics in Carla Olivieri's work include Vascular Anomalies and Treatments (31 papers), Tracheal and airway disorders (24 papers) and Sharing Economy and Platforms (9 papers). Carla Olivieri is often cited by papers focused on Vascular Anomalies and Treatments (31 papers), Tracheal and airway disorders (24 papers) and Sharing Economy and Platforms (9 papers). Carla Olivieri collaborates with scholars based in Italy, France and Spain. Carla Olivieri's co-authors include Cesare Danesino, Fabio Pagella, Elisabetta Buscarini, Alberto Zambelli, Elina Matti, Gaëtan Lesca, Maurizio Grosso, H Plauchu, L Reduzzi and Giacomo Pongiglione and has published in prestigious journals such as SHILAP Revista de lepidopterología, Blood and PLoS ONE.

In The Last Decade

Carla Olivieri

46 papers receiving 1.0k citations

Peers

Carla Olivieri
Christopher Dittus United States
Alberto Sinico Italy
Abeed A. Pall United Kingdom
G. Pinotti Italy
Gill Gaskin United Kingdom
Sang Hun Jung South Korea
Alex P.W.M. Maat Netherlands
Marco A. Alba Spain
Ian C. Duncan South Africa
E. Christiaan Hagen Netherlands
Christopher Dittus United States
Carla Olivieri
Citations per year, relative to Carla Olivieri Carla Olivieri (= 1×) peers Christopher Dittus

Countries citing papers authored by Carla Olivieri

Since Specialization
Citations

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

Fields of papers citing papers by Carla Olivieri

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Carla Olivieri

This figure shows the co-authorship network connecting the top 25 collaborators of Carla Olivieri. A scholar is included among the top collaborators of Carla Olivieri 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 Carla Olivieri. Carla Olivieri 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.
Danesino, Cesare, Federico Biglioli, Laura Moneghini, et al.. (2024). Pleomorphic Parotid Adenoma in a Child Affected with Cri du Chat Syndrome: Clinical, Cytogenetic, and Molecular Analysis. International Journal of Molecular Sciences. 25(19). 10664–10664.
2.
Matti, Elina, et al.. (2023). Silicone septal splint for recurrent epistaxis in HHT patients: experience of a national referral centre. Acta Otorhinolaryngologica Italica. 43(2 (Suppl. 1)). S28–S33. 1 indexed citations
3.
Matti, Elina, Annalisa De Silvestri, Gian Luigi Marseglia, et al.. (2021). Nasal Endoscopy in the Clinical Diagnosis of Hereditary Hemorrhagic Telangiectasia. The Journal of Pediatrics. 238. 74–79.e2. 4 indexed citations
4.
Ruiz, Lı́dia, Cesare Danesino, Pınar Bayrak‐Toydemir, et al.. (2019). Characterization of a mutation in the zona pellucida module of Endoglin that causes Hereditary Hemorrhagic Telangiectasia. Gene. 696. 33–39. 5 indexed citations
5.
Ruiz, Lı́dia, Carmen Langa, Gabriele Babini, et al.. (2018). Functional analysis of a novel ENG variant in a patient with hereditary hemorrhagic telangiectasia (HHT) identifies a new Sp1 binding-site. Gene. 647. 85–92. 5 indexed citations
6.
Invernizzi, Rosangela, Federica Quaglia, Catherine Klersy, et al.. (2015). Efficacy and safety of thalidomide for the treatment of severe recurrent epistaxis in hereditary haemorrhagic telangiectasia: results of a non-randomised, single-centre, phase 2 study. The Lancet Haematology. 2(11). e465–e473. 73 indexed citations
7.
Massa, Margherita, Rita Campanelli, Fabio Pagella, et al.. (2014). Increase of circulating endothelial cells in patients with Hereditary Hemorrhagic Telangiectasia. International Journal of Hematology. 101(1). 23–31. 2 indexed citations
8.
Radi, Orietta, Elisabetta Buscarini, Antonella Minelli, et al.. (2013). Hereditary Hemorrhagic Telangiectasia: Breakpoint Characterization of a Novel Large Deletion in ACVRL1 Suggests the Causing Mechanism. Molecular Syndromology. 4(3). 119–124. 1 indexed citations
9.
Pagella, Fabio, Elina Matti, Francesco Chu, et al.. (2012). Argon plasma coagulation is an effective treatment for hereditary hemorrhagic telangiectasia patients with severe nosebleeds. Acta Oto-Laryngologica. 133(2). 174–180. 13 indexed citations
10.
Lesca, Gaëtan, Emmanuelle Génin, Carla Olivieri, et al.. (2008). Hereditary hemorrhagic telangiectasia: evidence for regional founder effects of ACVRL1 mutations in French and Italian patients. European Journal of Human Genetics. 16(6). 742–749. 30 indexed citations
11.
Olivieri, Carla, et al.. (2007). Epidemiology and clinical aspects of Werner's syndrome in North Sardinia: description of a cluster.. PubMed. 17(3). 213–6. 29 indexed citations
12.
Lesca, Gaëtan, Carla Olivieri, Nelly Burnichon, et al.. (2007). Genotype-phenotype correlations in hereditary hemorrhagic telangiectasia: Data from the French-Italian HHT network. Genetics in Medicine. 9(1). 14–22. 157 indexed citations
13.
Olivieri, Carla, Fabio Pagella, L Semino, et al.. (2007). Analysis of ENG and ACVRL1 genes in 137 HHT Italian families identifies 76 different mutations (24 novel). Comparison with other European studies. Journal of Human Genetics. 52(10). 820–829. 55 indexed citations
14.
Olivieri, Carla, Fabio Pagella, L Semino, et al.. (2006). Echocardiographic screening discloses increased values of pulmonary artery systolic pressure in 9 of 68 unselected patients affected with hereditary hemorrhagic telangiectasia. Genetics in Medicine. 8(3). 183–190. 39 indexed citations
15.
Buscarini, Elisabetta, Cesare Danesino, Carla Olivieri, G. Lupinacci, & Alberto Zambelli. (2005). Liver involvement in hereditary haemorrhagic telangiectasia or Rendu-Osler-Weber disease. Digestive and Liver Disease. 37(9). 635–645. 39 indexed citations
16.
Olivieri, Carla, Cesare Danesino, Susi Scappaticci, & Mauro Bozzola. (2004). Can GH induce chromosome breaks or microsatellite instability in GH-deficient children?. Journal of Endocrinological Investigation. 27(4). 308–310. 1 indexed citations
17.
Buscarini, Elisabetta, Cesare Danesino, Carla Olivieri, et al.. (2004). Doppler Ultrasonographic Grading of Hepatic Vascular Malformations in Hereditary Hemorrhagic Telangiectasia - Results of Extensive Screening. Ultraschall in der Medizin - European Journal of Ultrasound. 25(5). 348–355. 73 indexed citations
18.
Buscarini, Elisabetta, Cesare Danesino, H Plauchu, et al.. (2004). High prevalence of hepatic focal nodular hyperplasia in subjects with hereditary hemorrhagic telangiectasia. Ultrasound in Medicine & Biology. 30(9). 1089–1097. 74 indexed citations
19.
Olivieri, Carla, et al.. (2002). Identification of 13 new mutations in the ACVRL1 gene in a group of 52 unselected Italian patients affected by hereditary haemorrhagic telangiectasia. Journal of Medical Genetics. 39(7). e39–e39. 47 indexed citations
20.
Dellavecchia, Claudia, Andrea Guala, Carla Olivieri, et al.. (1999). Early Onset of Gastric Carcinoma and Constitutional Deletion of 18p. Cancer Genetics and Cytogenetics. 113(1). 96–99. 12 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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