Alice Bruson

842 total citations
21 papers, 225 citations indexed

About

Alice Bruson is a scholar working on Molecular Biology, Oncology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Alice Bruson has authored 21 papers receiving a total of 225 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 4 papers in Oncology and 3 papers in Cellular and Molecular Neuroscience. Recurrent topics in Alice Bruson's work include Retinal Development and Disorders (3 papers), Vascular Tumors and Angiosarcomas (2 papers) and Skin and Cellular Biology Research (2 papers). Alice Bruson is often cited by papers focused on Retinal Development and Disorders (3 papers), Vascular Tumors and Angiosarcomas (2 papers) and Skin and Cellular Biology Research (2 papers). Alice Bruson collaborates with scholars based in Italy, Türkiye and United States. Alice Bruson's co-authors include Monica Forzan, Maurizio Clementi, Matteo Bertelli, Paolo Enrico Maltese, Sandro Michelini, Paolo Santonastaso, Elena Tenconi, Angela Favaro, Daniela Degortes and Renzo Manara and has published in prestigious journals such as Fertility and Sterility, Journal of Vascular Surgery and Molecular Phylogenetics and Evolution.

In The Last Decade

Alice Bruson

21 papers receiving 221 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Alice Bruson Italy 9 69 47 33 32 29 21 225
Liang Huo China 8 74 1.1× 12 0.3× 19 0.6× 21 0.7× 16 0.6× 22 346
Shinji Ono Japan 11 153 2.2× 23 0.5× 13 0.4× 34 1.1× 38 1.3× 26 383
Immaculada Ponsa Spain 9 156 2.3× 56 1.2× 21 0.6× 39 1.2× 26 0.9× 16 380
Michael Davenport United States 9 44 0.6× 20 0.4× 12 0.4× 64 2.0× 15 0.5× 21 284
Adnan Maqsood Choudhry Pakistan 7 151 2.2× 28 0.6× 100 3.0× 23 0.7× 12 0.4× 9 350
Maxine Chen United States 7 52 0.8× 23 0.5× 40 1.2× 7 0.2× 7 0.2× 12 261
Dóra Török Hungary 12 178 2.6× 15 0.3× 16 0.5× 8 0.3× 7 0.2× 47 373
Barry J. Lewis United Kingdom 6 65 0.9× 28 0.6× 6 0.2× 11 0.3× 7 0.2× 8 377
Run Xiao United States 12 127 1.8× 50 1.1× 4 0.1× 30 0.9× 20 0.7× 17 413
Sarah L. Jensen United States 9 32 0.5× 46 1.0× 7 0.2× 12 0.4× 88 3.0× 14 290

Countries citing papers authored by Alice Bruson

Since Specialization
Citations

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

Fields of papers citing papers by Alice Bruson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alice Bruson

This figure shows the co-authorship network connecting the top 25 collaborators of Alice Bruson. A scholar is included among the top collaborators of Alice Bruson 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 Alice Bruson. Alice Bruson 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.
Paolacci, Stefano, Alessandra Zulian, Alice Bruson, et al.. (2019). Vascular anomalies: molecular bases, genetic testing and therapeutic approaches. International Angiology. 38(2). 157–170. 11 indexed citations
2.
Maltese, Paolo Enrico, Sandro Michelini, Silvia Maitz, et al.. (2019). Increasing evidence of hereditary lymphedema caused by CELSR1 loss‐of‐function variants. American Journal of Medical Genetics Part A. 179(9). 1718–1724. 30 indexed citations
3.
Maltese, Paolo Enrico, Elena Manara, Stefano Paolacci, et al.. (2019). Putative role of Brugada syndrome genes in familial atrial fibrillation.. PubMed. 23(17). 7582–7598. 3 indexed citations
4.
Maltese, Paolo Enrico, et al.. (2018). Genetic testing for Ebstein anomaly. The EuroBiotech Journal. 2(s1). 55–57. 1 indexed citations
5.
Bruson, Alice, et al.. (2017). Genetic testing for non syndromic retinitis pigmentosa. The EuroBiotech Journal. 1(s1). 92–95. 3 indexed citations
6.
Bruson, Alice, et al.. (2017). Genetic testing for Usher syndrome. The EuroBiotech Journal. 1(s1). 108–110. 2 indexed citations
7.
Bruson, Alice, et al.. (2017). Genetic testing for Bietti crystalline dystrophy. The EuroBiotech Journal. 1(s1). 20–22. 2 indexed citations
8.
Mattassi, Raúl, Elena Manara, Piergiuseppe Colombo, et al.. (2017). Variant discovery in patients with Mendelian vascular anomalies by next-generation sequencing and their use in patient clinical management. Journal of Vascular Surgery. 67(3). 922–932.e11. 16 indexed citations
9.
Iarossi, Giancarlo, Matteo Bertelli, Paolo Enrico Maltese, et al.. (2017). Genotype-Phenotype Characterization of Novel Variants in Six Italian Patients with Familial Exudative Vitreoretinopathy. Journal of Ophthalmology. 2017. 1–10. 8 indexed citations
10.
Bruson, Alice, et al.. (2017). Genetic testing for color vision deficiency. The EuroBiotech Journal. 1(s1). 32–34. 1 indexed citations
11.
Michelini, Sandro, Andrea Vettori, Paolo Enrico Maltese, et al.. (2016). Genetic Screening in a Large Cohort of Italian Patients Affected by Primary Lymphedema Using a Next Generation Sequencing (NGS) Approach.. PubMed. 49(2). 57–72. 20 indexed citations
12.
Michelini, Sandro, et al.. (2016). A Rare Case of Emberger Syndrome Caused By a De Novo Mutation in the GATA2 Gene.. PubMed. 49(1). 15–20. 4 indexed citations
13.
Favaro, Angela, Renzo Manara, Michela Pievani, et al.. (2014). Neural signatures of the interaction between the 5-HTTLPR genotype and stressful life events in healthy women. Psychiatry Research Neuroimaging. 223(2). 157–163. 13 indexed citations
14.
Virzì, Grazia Maria, Alice Bruson, Valentina Corradi, et al.. (2014). High‐Resolution Melt as a Screening Method in Autosomal Dominant Polycystic Kidney Disease (ADPKD). Journal of Clinical Laboratory Analysis. 28(4). 328–334. 2 indexed citations
15.
Pujolar, José Martín, Laura Astolfi, Elisa Boscari, et al.. (2012). Tana1, a new putatively active Tc1-like transposable element in the genome of sturgeons. Molecular Phylogenetics and Evolution. 66(1). 223–232. 13 indexed citations
16.
Bruson, Alice, Fabio Sambataro, Giorgia Querin, et al.. (2012). CAG repeat length in androgen receptor gene is not associated with amyotrophic lateral sclerosis. European Journal of Neurology. 19(10). 1373–1375. 7 indexed citations
17.
Toldo, Irene, Alice Bruson, Alberto Casarin, et al.. (2011). Polymorphisms of the SCN1A gene in children and adolescents with primary headache and idiopathic or cryptogenic epilepsy: is there a linkage?. The Journal of Headache and Pain. 12(4). 435–441. 4 indexed citations
18.
Rigon, Chiara, Alessandra Andrisani, Monica Forzan, et al.. (2009). Association study of AMH and AMHRII polymorphisms with unexplained infertility. Fertility and Sterility. 94(4). 1244–1248. 26 indexed citations
19.
Forzan, Monica, Leonardo Salviati, Vanessa Pertegato, et al.. (2009). Is CFTR 621+3 A>G a cystic fibrosis causing mutation?. Journal of Human Genetics. 55(1). 23–26. 13 indexed citations
20.
Arpesella, Giorgio, Alberto Giannoni, Corrado Rizzi, et al.. (1995). Functional and Structural Characteristic of Sheep LD Conditioned to Fatigue Resistance by a Half-Day Cardiac-Like Electrostimulation Protocol: Implications for Dynamic Cardiomyoplasty. 103–107. 4 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 Liang Huo Breakdown of academic impact, for papers by Shinji Ono Breakdown of academic impact, for papers by Immaculada Ponsa Breakdown of academic impact, for papers by Michael Davenport Breakdown of academic impact, for papers by Adnan Maqsood Choudhry Breakdown of academic impact, for papers by Maxine Chen Breakdown of academic impact, for papers by Dóra Török Breakdown of academic impact, for papers by Barry J. Lewis Breakdown of academic impact, for papers by Run Xiao Breakdown of academic impact, for papers by Sarah L. Jensen
Rankless by CCL
2026