Antonella Fabretto

1.0k total citations
20 papers, 194 citations indexed

About

Antonella Fabretto is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Antonella Fabretto has authored 20 papers receiving a total of 194 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 9 papers in Molecular Biology and 3 papers in Surgery. Recurrent topics in Antonella Fabretto's work include Genomic variations and chromosomal abnormalities (6 papers), Genomics and Rare Diseases (5 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Antonella Fabretto is often cited by papers focused on Genomic variations and chromosomal abnormalities (6 papers), Genomics and Rare Diseases (5 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Antonella Fabretto collaborates with scholars based in Italy, Netherlands and Germany. Antonella Fabretto's co-authors include Paolo Gasparini, Vanna Pecile, Emmanouil Athanasakis, Danilo Licastro, Flavio Faletra, Diego Vozzi, Aldo Skabar, Pio D’Adamo, Anna Morgan and Sandro Banfi and has published in prestigious journals such as PLoS ONE, Radiology and Gene.

In The Last Decade

Antonella Fabretto

20 papers receiving 190 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Antonella Fabretto Italy 7 99 84 38 25 17 20 194
Érika L. Freitas Brazil 10 112 1.1× 122 1.5× 31 0.8× 18 0.7× 21 1.2× 16 260
Joon Suk Lee South Korea 10 123 1.2× 67 0.8× 80 2.1× 49 2.0× 17 1.0× 14 284
Alisdair McNeill United Kingdom 6 152 1.5× 93 1.1× 10 0.3× 19 0.8× 13 0.8× 13 218
Michaela Thoenes Germany 7 132 1.3× 88 1.0× 24 0.6× 34 1.4× 22 1.3× 9 226
R. Farcas Germany 6 210 2.1× 54 0.6× 35 0.9× 9 0.4× 24 1.4× 8 282
Joy Samanich United States 10 141 1.4× 88 1.0× 86 2.3× 9 0.4× 30 1.8× 17 289
Teresa Palladino Italy 9 123 1.2× 141 1.7× 52 1.4× 6 0.2× 13 0.8× 15 246
Amjad Khan Pakistan 12 170 1.7× 124 1.5× 11 0.3× 18 0.7× 10 0.6× 40 291
Souad Gherbi France 8 103 1.0× 50 0.6× 80 2.1× 8 0.3× 15 0.9× 11 199
Jost Schönberger Germany 7 351 3.5× 39 0.5× 54 1.4× 15 0.6× 21 1.2× 8 515

Countries citing papers authored by Antonella Fabretto

Since Specialization
Citations

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

Fields of papers citing papers by Antonella Fabretto

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Antonella Fabretto

This figure shows the co-authorship network connecting the top 25 collaborators of Antonella Fabretto. A scholar is included among the top collaborators of Antonella Fabretto 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 Antonella Fabretto. Antonella Fabretto 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.
Lucafò, Marianna, et al.. (2024). Preanalytical Stability of 13 Antibiotics in Biological Samples: A Crucial Factor for Therapeutic Drug Monitoring. Antibiotics. 13(7). 675–675. 3 indexed citations
2.
Tamaro, Gianluca, Antonella Fabretto, F. Buonomo, et al.. (2023). Prevalence and characteristics of thelarche variant. Frontiers in Endocrinology. 14. 1303989–1303989. 6 indexed citations
3.
Lucafò, Marianna, Matteo Bramuzzo, Marco Rabusin, et al.. (2022). A Validated HPLC–Diode Array Detection Method for Therapeutic Drug Monitoring of Thiopurines in Pediatric Patients: From Bench to Bedside. Metabolites. 12(12). 1173–1173. 2 indexed citations
4.
Menichelli, Alina, et al.. (2018). A new MAPT deletion in a case of speech apraxia leading to corticobasal syndrome. Neurocase. 24(3). 140–144. 6 indexed citations
5.
Russo, Silvia, Chiara Luoni, Francesca Cogliati, et al.. (2015). Somatic Mosaicism as Modulator of the Global and Intellectual Phenotype in Epimutated Angelman Syndrome Patients. Journal of Intellectual Disability - Diagnosis and Treatment. 3(3). 126–137. 1 indexed citations
6.
Pecile, Vanna, et al.. (2015). CTNND2 deletion and intellectual disability. Gene. 565(1). 146–149. 20 indexed citations
7.
Naviglio, Samuele, Serena Arrigo, Stefano Martelossi, et al.. (2014). Severe inflammatory bowel disease associated with congenital alteration of transforming growth factor beta signaling. Journal of Crohn s and Colitis. 8(8). 770–774. 21 indexed citations
8.
Athanasakis, Emmanouil, Danilo Licastro, Flavio Faletra, et al.. (2013). Next generation sequencing in nonsyndromic intellectual disability: From a negative molecular karyotype to a possible causative mutation detection. American Journal of Medical Genetics Part A. 164(1). 170–176. 31 indexed citations
9.
Vozzi, Diego, Danilo Licastro, Stefano Martelossi, et al.. (2013). Alagille Syndrome: A New Missense Mutation Detected by Whole-Exome Sequencing in a Case Previously Found to Be Negative by DHPLC and MLPA. Molecular Syndromology. 4(4). 207–210. 4 indexed citations
10.
Licastro, Danilo, Margherita Mutarelli, Ivana Peluso, et al.. (2012). Molecular Diagnosis of Usher Syndrome: Application of Two Different Next Generation Sequencing-Based Procedures. PLoS ONE. 7(8). e43799–e43799. 24 indexed citations
11.
Athanasakis, Emmanouil, et al.. (2012). Two Novel <b><i>COH1</i></b> Mutations in an Italian Patient with Cohen Syndrome. Molecular Syndromology. 3(1). 30–33. 2 indexed citations
12.
Fabretto, Antonella, et al.. (2012). De novo 6.9 Mb interstitial deletion on chromosome 4q31.1‐q32.1 in a girl with severe speech delay and dysmorphic features. American Journal of Medical Genetics Part A. 158A(4). 882–887. 4 indexed citations
13.
Rocca, Maria Santa, Antonella Fabretto, Flavio Faletra, et al.. (2011). Contribution of SNP arrays in diagnosis of deletion 2p11.2–p12. Gene. 492(1). 315–318. 5 indexed citations
14.
Travan, Laura, et al.. (2011). Opitz trigonocephaly syndrome presenting with sudden unexplained death in the operating room: a case report. Journal of Medical Case Reports. 5(1). 222–222. 3 indexed citations
15.
Vozzi, Diego, Anu Aaspõllu, Emmanouil Athanasakis, et al.. (2011). Molecular epidemiology of Usher syndrome in Italy.. PubMed. 17. 1662–8. 28 indexed citations
16.
Fabretto, Antonella, et al.. (2010). A Case of Lymphedema-Distichiasis Syndrome Carrying a New de novo Frameshift FOXC2 Mutation. Ophthalmic Genetics. 31(2). 98–100. 6 indexed citations
17.
Faletra, Flavio, et al.. (2010). A new case of duplication of the MDS region identified by high-density SNP arrays and a review of the literature. Journal of Applied Genetics. 52(1). 77–80. 3 indexed citations
18.
Fabretto, Antonella, et al.. (2010). Two cases of Noonan syndrome with severe respiratory and gastroenteral involvement and the SOS1 mutation F623I. European Journal of Medical Genetics. 53(5). 322–324. 6 indexed citations
19.
Parentin, Fulvio, Antonella Fabretto, Federico Marchetti, et al.. (2009). Ophthalmic Features in a Dysmorphic Boy with Chromosome 4q Deletion and Duplication. Ophthalmic Genetics. 30(2). 103–105. 2 indexed citations
20.
Guerci, Veronica Ileana, Antonella Fabretto, Flavio Faletra, et al.. (2009). Detection of Epidermal Thickening inGJB2Carriers with Epidermal US. Radiology. 251(1). 280–286. 17 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Érika L. Freitas Breakdown of academic impact, for papers by Joon Suk Lee Breakdown of academic impact, for papers by Alisdair McNeill Breakdown of academic impact, for papers by Michaela Thoenes Breakdown of academic impact, for papers by R. Farcas Breakdown of academic impact, for papers by Joy Samanich Breakdown of academic impact, for papers by Teresa Palladino Breakdown of academic impact, for papers by Amjad Khan Breakdown of academic impact, for papers by Souad Gherbi Breakdown of academic impact, for papers by Jost Schönberger
Rankless by CCL
2026