Roberto Bertorelli

2.8k total citations · 1 hit paper
20 papers, 977 citations indexed

About

Roberto Bertorelli is a scholar working on Molecular Biology, Epidemiology and Genetics. According to data from OpenAlex, Roberto Bertorelli has authored 20 papers receiving a total of 977 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 6 papers in Epidemiology and 4 papers in Genetics. Recurrent topics in Roberto Bertorelli's work include RNA modifications and cancer (4 papers), Genomics and Phylogenetic Studies (3 papers) and Mycobacterium research and diagnosis (3 papers). Roberto Bertorelli is often cited by papers focused on RNA modifications and cancer (4 papers), Genomics and Phylogenetic Studies (3 papers) and Mycobacterium research and diagnosis (3 papers). Roberto Bertorelli collaborates with scholars based in Italy, United States and Belgium. Roberto Bertorelli's co-authors include Veronica De Sanctis, Olivier Jousson, Nicola Segata, Stylianos E. Antonarakis, Serena Ziglio, Annachiara Rosa, Massimo Pizzato, Sean Matthew McCauley, Ajit Chande and Jeremy Luban and has published in prestigious journals such as Nature, PLoS ONE and Cancer.

In The Last Decade

Roberto Bertorelli

20 papers receiving 961 citations

Hit Papers

HIV-1 Nef promotes infection by excluding SERINC5 from vi... 2015 2026 2018 2022 2015 100 200 300

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Roberto Bertorelli Italy 13 371 351 303 262 192 20 977
Veronica De Sanctis Italy 14 470 1.3× 355 1.0× 286 0.9× 262 1.0× 196 1.0× 30 1.0k
Tanja M. Kaptein Netherlands 13 552 1.5× 278 0.8× 334 1.1× 99 0.4× 719 3.7× 21 1.3k
Suganya Selvarajah United States 12 529 1.4× 399 1.1× 248 0.8× 300 1.1× 203 1.1× 20 1.3k
Giuliana Magri Spain 15 341 0.9× 234 0.7× 208 0.7× 165 0.6× 836 4.4× 26 1.4k
John Hural United States 18 544 1.5× 414 1.2× 360 1.2× 619 2.4× 804 4.2× 35 1.6k
Debra Chester Kalter United States 22 216 0.6× 522 1.5× 645 2.1× 1.1k 4.1× 657 3.4× 34 1.8k
Shiki Takamura Japan 26 353 1.0× 412 1.2× 322 1.1× 157 0.6× 1.5k 7.7× 53 2.1k
Peter J. Heidt Netherlands 20 610 1.6× 257 0.7× 467 1.5× 121 0.5× 537 2.8× 35 1.6k
Janet Ruby Australia 16 217 0.6× 387 1.1× 185 0.6× 234 0.9× 648 3.4× 25 1.1k
Thera Mulvania United States 7 145 0.4× 132 0.4× 113 0.4× 142 0.5× 661 3.4× 10 965

Countries citing papers authored by Roberto Bertorelli

Since Specialization
Citations

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

Fields of papers citing papers by Roberto Bertorelli

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Roberto Bertorelli

This figure shows the co-authorship network connecting the top 25 collaborators of Roberto Bertorelli. A scholar is included among the top collaborators of Roberto Bertorelli 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 Roberto Bertorelli. Roberto Bertorelli 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.
Barozzi, Chiara, Margherita Serra, Veronica De Sanctis, et al.. (2023). Alterations of ribosomal RNA pseudouridylation in human breast cancer. NAR Cancer. 5(2). zcad026–zcad026. 16 indexed citations
2.
Venturi, Giulia, Veronica De Sanctis, Roberto Bertorelli, et al.. (2022). Human dyskerin binds to cytoplasmic H/ACA-box-containing transcripts affecting nuclear hormone receptor dependence. Genome biology. 23(1). 177–177. 10 indexed citations
3.
Buratto, Mattia, Silvia Fuselli, Andrea Benazzo, et al.. (2022). Suppressing gain-of-function proteins via CRISPR/Cas9 system in SCA1 cells. Scientific Reports. 12(1). 20285–20285. 5 indexed citations
4.
Romagnoli, Dario, Giulia Boccalini, Martina Bonechi, et al.. (2018). ddSeeker: a tool for processing Bio-Rad ddSEQ single cell RNA-seq data. BMC Genomics. 19(1). 960–960. 16 indexed citations
5.
Tortoli, Enrico, Tarcisio Fedrizzi, Conor J. Meehan, et al.. (2017). The new phylogeny of the genus Mycobacterium : The old and the news. Infection Genetics and Evolution. 56. 19–25. 109 indexed citations
6.
Tett, Adrian, Edoardo Pasolli, Duy Tin Truong, et al.. (2017). Unexplored diversity and strain-level structure of the skin microbiome associated with psoriasis. npj Biofilms and Microbiomes. 3(1). 14–14. 131 indexed citations
7.
Fedrizzi, Tarcisio, Conor J. Meehan, Antonella Grottola, et al.. (2017). Genomic characterization of Nontuberculous Mycobacteria. Scientific Reports. 7(1). 45258–45258. 149 indexed citations
8.
Catarsi, Paolo, Vittorio Rosti, Giacomo Morreale, et al.. (2015). JAK2 Exon 14 Skipping in Patients with Primary Myelofibrosis: A Minor Splice Variant Modulated by the JAK2-V617F Allele Burden. PLoS ONE. 10(1). e0116636–e0116636. 6 indexed citations
9.
Stanghellini, Ilaria, Erik Dassi, Roberto Bertorelli, et al.. (2015). Exome sequencing in a patient with Catel–Manzke-like syndrome excludes the involvement of the known genes and reveals a possible candidate. European Journal of Medical Genetics. 58(11). 597–602. 2 indexed citations
10.
Rosa, Annachiara, Ajit Chande, Serena Ziglio, et al.. (2015). HIV-1 Nef promotes infection by excluding SERINC5 from virion incorporation. Nature. 526(7572). 212–217. 325 indexed citations breakdown →
11.
Andreotti, Virginia, Alessandra Bisio, Brigitte Bressac–de Paillerets, et al.. (2015). The CDKN2A/p16INK4a 5′UTR sequence and translational regulation: impact of novel variants predisposing to melanoma. Pigment Cell & Melanoma Research. 29(2). 210–221. 8 indexed citations
12.
Tortoli, Enrico, Tarcisio Fedrizzi, Monica Pecorari, et al.. (2014). The new phylogenesis of the genus Mycobacterium. International Journal of Mycobacteriology. 4. 77–77. 2 indexed citations
13.
Dassi, Erik, Annalisa Ballarini, Giuseppina Covello, et al.. (2014). Enhanced microbial diversity in the saliva microbiome induced by short-term probiotic intake revealed by 16S rRNA sequencing on the IonTorrent PGM platform. Journal of Biotechnology. 190. 30–39. 32 indexed citations
14.
Potrich, Cristina, Valentina Vaghi, Lorenzo Lunelli, et al.. (2014). OncomiR detection in circulating body fluids: a PDMS microdevice perspective. Lab on a Chip. 14(20). 4067–4075. 21 indexed citations
15.
Iughetti, Lorenzo, Heba Elsedfy, Roberto Bertorelli, et al.. (2010). Unexpected Phenotype in a Boy with Trisomy of the SHOX Gene. Journal of Pediatric Endocrinology and Metabolism. 23(1-2). 159–69. 17 indexed citations
16.
Stanghellini, Ilaria, et al.. (2006). Quantitation of fetal DNA in maternal serum during the first trimester of pregnancy by the use of a DAZ repetitive probe. Molecular Human Reproduction. 12(9). 587–591. 32 indexed citations
17.
Bonioli, E, Carmen La Rosa, Roberto Bertorelli, et al.. (2005). Heterozygous mutations of growth hormone receptor gene in children with idiopathic short stature. Growth Hormone & IGF Research. 15(6). 405–410. 36 indexed citations
18.
Coviello, Domenico, B. Brambati, Lucia Tului, et al.. (2004). First‐trimester prenatal screening for the common 35delG GJB2 mutation causing prelingual deafness. Prenatal Diagnosis. 24(8). 631–634. 6 indexed citations
19.
Iughetti, Lorenzo, Roberto Bertorelli, Domenico Coviello, et al.. (2003). Genotype/Phenotype Correlations of Males Affected by Simpson-Golabi-Behmel Syndrome with GPC3 Gene Mutations: Patient Report and Review of the Literature. Journal of Pediatric Endocrinology and Metabolism. 16(2). 225–32. 36 indexed citations
20.
Ballestrero, Alberto, Domenico Coviello, Anna Garuti, et al.. (2001). Reverse-transcriptase polymerase chain reaction of the maspin gene in the detection of bone marrow breast carcinoma cell contamination. Cancer. 92(8). 2030–2035. 18 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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