Stefano Berri

1.1k total citations
19 papers, 658 citations indexed

About

Stefano Berri is a scholar working on Genetics, Cancer Research and Molecular Biology. According to data from OpenAlex, Stefano Berri has authored 19 papers receiving a total of 658 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 7 papers in Cancer Research and 6 papers in Molecular Biology. Recurrent topics in Stefano Berri's work include Genomic variations and chromosomal abnormalities (8 papers), Cancer Genomics and Diagnostics (6 papers) and Genomics and Phylogenetic Studies (4 papers). Stefano Berri is often cited by papers focused on Genomic variations and chromosomal abnormalities (8 papers), Cancer Genomics and Diagnostics (6 papers) and Genomics and Phylogenetic Studies (4 papers). Stefano Berri collaborates with scholars based in United Kingdom, Italy and Saudi Arabia. Stefano Berri's co-authors include Jordan H. Boyle, Netta Cohen, Henry M. Wood, Pamela Rabbitts, Arief Gusnanto, Ian A. Hope, Manlio Tassieri, Yudi Pawitan, Mario Enrico Pè and Piero Morandini and has published in prestigious journals such as Bioinformatics, PLoS ONE and The Journal of Pathology.

In The Last Decade

Stefano Berri

19 papers receiving 643 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Stefano Berri United Kingdom 13 272 160 148 146 143 19 658
Derek M. Pavelec United States 13 814 3.0× 39 0.2× 200 1.4× 356 2.4× 149 1.0× 23 1.1k
Karin Aumayr Austria 5 528 1.9× 100 0.6× 24 0.2× 84 0.6× 346 2.4× 6 890
Huiling Xue China 13 1.1k 3.9× 75 0.5× 80 0.5× 76 0.5× 633 4.4× 25 1.4k
Julien Pontabry France 11 599 2.2× 86 0.5× 192 1.3× 61 0.4× 39 0.3× 17 798
Johannes Landskron Norway 14 238 0.9× 121 0.8× 78 0.5× 30 0.2× 20 0.1× 20 827
Jan Padeken Switzerland 14 1.1k 4.1× 157 1.0× 427 2.9× 129 0.9× 59 0.4× 21 1.3k
Ian A. Swinburne United States 15 705 2.6× 88 0.6× 77 0.5× 24 0.2× 44 0.3× 18 978
Inna Inashkina Latvia 15 433 1.6× 97 0.6× 38 0.3× 14 0.1× 74 0.5× 35 697
Anthony P. Fejes Canada 11 969 3.6× 229 1.4× 75 0.5× 23 0.2× 161 1.1× 15 1.2k
Christopher Barry Canada 16 390 1.4× 152 0.9× 44 0.3× 10 0.1× 40 0.3× 18 756

Countries citing papers authored by Stefano Berri

Since Specialization
Citations

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

Fields of papers citing papers by Stefano Berri

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Stefano Berri

This figure shows the co-authorship network connecting the top 25 collaborators of Stefano Berri. A scholar is included among the top collaborators of Stefano Berri 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 Stefano Berri. Stefano Berri is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

19 of 19 papers shown
1.
Berri, Stefano, John F. Peden, Claire Fielding, et al.. (2025). A dedicated caller for DUX4 rearrangements from whole-genome sequencing data. BMC Medical Genomics. 18(1). 24–24. 1 indexed citations
2.
Ivakhno, Sergii, Camilla Colombo, Stephen Tanner, et al.. (2016). tHapMix: simulating tumour samples through haplotype mixtures. Bioinformatics. 33(2). 280–282. 7 indexed citations
3.
Fateen, Waleed, Henry M. Wood, Stefano Berri, et al.. (2016). OC-033 Nine-Gene Signature Implicated in the Early Development of Hepatitis C Virus (HCV) Related Hepatocellular Carcinoma (HCC). A20.1–A20. 1 indexed citations
4.
Wood, Henry M., Caroline Conway, Catherine Daly, et al.. (2015). The clonal relationships between pre‐cancer and cancer revealed by ultra‐deep sequencing. The Journal of Pathology. 237(3). 296–306. 24 indexed citations
5.
Wood, Henry M., Caroline Conway, Stefano Berri, et al.. (2014). Next-generation sequencing analysis for detecting human papillomavirus in oral verrucous carcinoma. Oral Surgery Oral Medicine Oral Pathology and Oral Radiology. 118(1). 117–125.e1. 14 indexed citations
6.
Gusnanto, Arief, et al.. (2014). Estimating optimal window size for analysis of low-coverage next-generation sequence data. Bioinformatics. 30(13). 1823–1829. 18 indexed citations
7.
8.
Hayes, Josie, Helene Thygesen, Stefano Berri, et al.. (2013). Diagnosis of copy number variation by Illumina next generation sequencing is comparable in performance to oligonucleotide array comparative genomic hybridisation. Genomics. 102(3). 174–181. 43 indexed citations
9.
Stead, Lucy F., Philip Egan, Aoife Devery, et al.. (2013). An Integrated Inspection of the Somatic Mutations in a Lung Squamous Cell Carcinoma Using Next-Generation Sequencing. PLoS ONE. 8(11). e78823–e78823. 5 indexed citations
10.
Boyle, Jordan H., Stefano Berri, & Netta Cohen. (2012). Gait Modulation in C. elegans: An Integrated Neuromechanical Model. Frontiers in Computational Neuroscience. 6. 10–10. 92 indexed citations
11.
Conway, Caroline, Rebecca Chalkley, A.S. High, et al.. (2012). Next-Generation Sequencing for Simultaneous Determination of Human Papillomavirus Load, Subtype, and Associated Genomic Copy Number Changes in Tumors. Journal of Molecular Diagnostics. 14(2). 104–111. 35 indexed citations
12.
Stead, Lucy F., Stefano Berri, Henry M. Wood, et al.. (2012). The Transcriptional Consequences of Somatic Amplifications, Deletions, and Rearrangements in a Human Lung Squamous Cell Carcinoma. Neoplasia. 14(11). 1075–IN16. 15 indexed citations
13.
Belvedere, Ornella, Stefano Berri, Rebecca Chalkley, et al.. (2011). A computational index derived from whole-genome copy number analysis is a novel tool for prognosis in early stage lung squamous cell carcinoma. Genomics. 99(1). 18–24. 12 indexed citations
14.
Boyle, Jordan H., Stefano Berri, Manlio Tassieri, Ian A. Hope, & Netta Cohen. (2011). Gait Modulation in C. Elegans: It's Not a Choice, It's a Reflex!. Frontiers in Behavioral Neuroscience. 5. 10–10. 15 indexed citations
15.
Gusnanto, Arief, Henry M. Wood, Yudi Pawitan, Pamela Rabbitts, & Stefano Berri. (2011). Correcting for cancer genome size and tumour cell content enables better estimation of copy number alterations from next-generation sequence data. Bioinformatics. 28(1). 40–47. 117 indexed citations
16.
Cohen, Kelly, Joanne Morgan, Henry M. Wood, et al.. (2011). Molecular karyotyping using massively parallel sequencing – a next generation approach to prenatal diagnosis?. Archives of Disease in Childhood Fetal & Neonatal. 96(Suppl 1). Fa54.3–Fa54. 1 indexed citations
17.
Berri, Stefano, Pamela Abbruscato, Odile Faivre‐Rampant, et al.. (2009). Characterization of WRKYco-regulatory networks in rice and Arabidopsis. BMC Plant Biology. 9(1). 120–120. 139 indexed citations
18.
Berri, Stefano, Jordan H. Boyle, Manlio Tassieri, Ian A. Hope, & Netta Cohen. (2009). Forward locomotion of the nematodeC. elegansis achieved through modulation of a single gait. PubMed. 3(3). 186–193. 96 indexed citations
19.
Berri, Stefano, Jordan H. Boyle, Manlio Tassieri, Ian A. Hope, & Netta Cohen. (2009). C. elegans locomotion: a unified multidisciplinary perspective. BMC Neuroscience. 10(S1). 2 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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