Alessandro Bruselles

3.1k total citations
49 papers, 1.0k citations indexed

About

Alessandro Bruselles is a scholar working on Molecular Biology, Genetics and Virology. According to data from OpenAlex, Alessandro Bruselles has authored 49 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Molecular Biology, 19 papers in Genetics and 9 papers in Virology. Recurrent topics in Alessandro Bruselles's work include HIV Research and Treatment (9 papers), HIV/AIDS drug development and treatment (6 papers) and Genetics and Neurodevelopmental Disorders (6 papers). Alessandro Bruselles is often cited by papers focused on HIV Research and Treatment (9 papers), HIV/AIDS drug development and treatment (6 papers) and Genetics and Neurodevelopmental Disorders (6 papers). Alessandro Bruselles collaborates with scholars based in Italy, United States and Belarus. Alessandro Bruselles's co-authors include Maria Rosaria Capobianchi, Giuseppe Ippolito, Giovanni Chillemi, Mattia Prosperi, Marco Tartaglia, Gabriella Rozera, Isabella Abbate, Donatella Vincenti, Alessandro Desideri and Mariacarmela Solmone and has published in prestigious journals such as Nucleic Acids Research, Journal of Biological Chemistry and PLoS ONE.

In The Last Decade

Alessandro Bruselles

48 papers receiving 991 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Alessandro Bruselles Italy 20 508 195 188 184 173 49 1.0k
Scott W. Eastman United States 17 402 0.8× 294 1.5× 619 3.3× 187 1.0× 119 0.7× 20 1.2k
Szecheng J. Lo Taiwan 22 581 1.1× 416 2.1× 67 0.4× 170 0.9× 57 0.3× 84 1.3k
Marina Vaysburd United Kingdom 21 462 0.9× 178 0.9× 123 0.7× 121 0.7× 96 0.6× 29 1.2k
Kathleen Börner Germany 19 1.2k 2.4× 155 0.8× 329 1.8× 410 2.2× 100 0.6× 31 1.8k
Nicholas M. Stamatos United States 19 658 1.3× 114 0.6× 141 0.8× 96 0.5× 98 0.6× 23 1.1k
Steven J. Madore United States 22 1.3k 2.5× 111 0.6× 343 1.8× 176 1.0× 156 0.9× 28 1.7k
Eugen Buehler United States 16 715 1.4× 300 1.5× 97 0.5× 130 0.7× 89 0.5× 25 1.1k
Gabriele Fuchs United States 19 1.2k 2.4× 120 0.6× 71 0.4× 108 0.6× 54 0.3× 27 1.8k
Mikhail K. Levin United States 18 952 1.9× 143 0.7× 54 0.3× 195 1.1× 30 0.2× 30 1.3k
Joseph M. Luna United States 14 1.1k 2.1× 378 1.9× 157 0.8× 96 0.5× 183 1.1× 24 1.9k

Countries citing papers authored by Alessandro Bruselles

Since Specialization
Citations

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

Fields of papers citing papers by Alessandro Bruselles

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alessandro Bruselles

This figure shows the co-authorship network connecting the top 25 collaborators of Alessandro Bruselles. A scholar is included among the top collaborators of Alessandro Bruselles 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 Alessandro Bruselles. Alessandro Bruselles 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.
Bruselles, Alessandro, Paola D′Ambrosio, Andrea Ciolfi, et al.. (2025). The p.Ile202Thr Substitution in TUBB2B Can Be Associated with Syndromic Presentation of Congenital Fibrosis of the Extraocular Muscles. Genes. 16(10). 1182–1182. 1 indexed citations
2.
Stellacci, Emilia, Marcello Niceta, Alessandro Bruselles, et al.. (2024). Whole Genome Sequencing Solves an Atypical Form of Bardet–Biedl Syndrome: Identification of Novel Pathogenic Variants of BBS9. International Journal of Molecular Sciences. 25(15). 8313–8313.
3.
Galosi, Serena, Cecilia Mancini, Paolo Calligari, et al.. (2024). Biallelic Variants of MRPS36 Cause a New Form of Leigh Syndrome. Movement Disorders. 39(7). 1225–1231. 2 indexed citations
4.
Francescangeli, Federica, et al.. (2022). Analysis of Dormancy-Associated Transcriptional Networks Reveals a Shared Quiescence Signature in Lung and Colorectal Cancer. International Journal of Molecular Sciences. 23(17). 9869–9869. 15 indexed citations
5.
Ziccardi, Lucia, Marcello Niceta, Emilia Stellacci, et al.. (2022). Biallelic Inactivating TUB Variants Cause Retinal Ciliopathy Impairing Biogenesis and the Structure of the Primary Cilium. International Journal of Molecular Sciences. 23(23). 14656–14656. 2 indexed citations
6.
Leoni, Chiara, Francesca Clementina Radio, Giovanni Chillemi, et al.. (2021). Broadening the phenotypic spectrum of Beta3GalT6 ‐associated phenotypes. American Journal of Medical Genetics Part A. 185(10). 3153–3160. 4 indexed citations
7.
Flex, Elisabetta, Giovanna Carpentieri, Alessandro Bruselles, et al.. (2021). A Rare Case of Brachyolmia with Amelogenesis Imperfecta Caused by a New Pathogenic Splicing Variant in LTBP3. Genes. 12(9). 1406–1406. 3 indexed citations
8.
Stellacci, Emilia, Gian Marco Moneta, Alessandro Bruselles, et al.. (2019). The activating p.Ser466Arg change in STAT1 causes a peculiar phenotype with features of interferonopathies. Clinical Genetics. 96(6). 585–589. 10 indexed citations
9.
Sferra, Antonella, Fabiana Fattori, Teresa Rizza, et al.. (2018). Defective kinesin binding of TUBB2A causes progressive spastic ataxia syndrome resembling sacsinopathy. Human Molecular Genetics. 27(11). 1892–1904. 28 indexed citations
10.
Servidei, Tiziana, Daniela Meco, Valentina Muto, et al.. (2017). Novel SEC61GEGFR Fusion Gene in Pediatric Ependymomas Discovered by Clonal Expansion of Stem Cells in Absence of Exogenous Mitogens. Cancer Research. 77(21). 5860–5872. 20 indexed citations
11.
Verdina, Alessandra, Giuliana Di Rocco, Veronica Gatti, et al.. (2017). HIPK2-T566 autophosphorylation diversely contributes to UV- and doxorubicin-induced HIPK2 activation. Oncotarget. 8(10). 16744–16754. 5 indexed citations
12.
Dorboz, Imen, Chiara Aiello, Cas Simons, et al.. (2017). Biallelic mutations in the homeodomain of NKX6-2 underlie a severe hypomyelinating leukodystrophy. Brain. 140(10). 2550–2556. 15 indexed citations
13.
Stellacci, Emilia, Roberta Onesimo, Alessandro Bruselles, et al.. (2016). Congenital immunodeficiency in an individual with Wiedemann–Steiner syndrome due to a novel missense mutation in KMT2A. American Journal of Medical Genetics Part A. 170(9). 2389–2393. 23 indexed citations
14.
Giorgio, Elisa, Alessandro Brussino, Elisa Biamino, et al.. (2016). Exome sequencing in children of women with skewed X-inactivation identifies atypical cases and complex phenotypes. European Journal of Paediatric Neurology. 21(3). 475–484. 11 indexed citations
15.
Svicher, Valentina, Valeria Cento, Gabriella Rozera, et al.. (2013). The Genotypic False Positive Rate Determined by V3 Population Sequencing Can Predict the Burden of HIV-1 CXCR4-using Species Detected by Pyrosequencing. PLoS ONE. 8(1). e53603–e53603. 10 indexed citations
16.
Rozera, Gabriella, Isabella Abbate, Massimo Ciccozzi, et al.. (2012). Ultra‐deep sequencing reveals hidden HIV‐1 minority lineages and shifts of viral population between the main cellular reservoirs of the infection after therapy interruption. Journal of Medical Virology. 84(6). 839–844. 11 indexed citations
17.
Prosperi, Mattia, Alessandro Bruselles, Isabella Abbate, et al.. (2011). Combinatorial analysis and algorithms for quasispecies reconstruction using next-generation sequencing. BMC Bioinformatics. 12(1). 5–5. 60 indexed citations
18.
Abbate, Isabella, Gabriella Rozera, Chiara Tommasi, et al.. (2010). Analysis of co‐receptor usage of circulating viral and proviral HIV genome quasispecies by ultra‐deep pyrosequencing in patients who are candidates for CCR5 antagonist treatment. Clinical Microbiology and Infection. 17(5). 725–731. 30 indexed citations
19.
Bruselles, Alessandro, Gabriella Rozera, Barbara Bartolini, et al.. (2009). Use of Massive Parallel Pyrosequencing for Near Full-Length Characterization of a Unique HIV Type 1 BF Recombinant Associated with a Fatal Primary Infection. AIDS Research and Human Retroviruses. 25(9). 937–942. 24 indexed citations
20.
Rozera, Gabriella, Isabella Abbate, Alessandro Bruselles, et al.. (2009). Massively parallel pyrosequencing highlights minority variants in the HIV-1 env quasispecies deriving from lymphomonocyte sub-populations. Retrovirology. 6(1). 15–15. 86 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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