Beatrice Bodega

6.6k total citations · 1 hit paper
32 papers, 2.3k citations indexed

About

Beatrice Bodega is a scholar working on Molecular Biology, Plant Science and Genetics. According to data from OpenAlex, Beatrice Bodega has authored 32 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Molecular Biology, 10 papers in Plant Science and 9 papers in Genetics. Recurrent topics in Beatrice Bodega's work include Genomics and Chromatin Dynamics (14 papers), Chromosomal and Genetic Variations (9 papers) and Epigenetics and DNA Methylation (8 papers). Beatrice Bodega is often cited by papers focused on Genomics and Chromatin Dynamics (14 papers), Chromosomal and Genetic Variations (9 papers) and Epigenetics and DNA Methylation (8 papers). Beatrice Bodega collaborates with scholars based in Italy, Germany and Saudi Arabia. Beatrice Bodega's co-authors include Luca Azzolin, Mattia Forcato, Antonio Rosato, Erika Quaranta, Silvio Bicciato, Stefano Piccolo, Francesca Zanconato, Giusy Battilana, Michelangelo Cordenonsi and Enrico Ginelli and has published in prestigious journals such as Cell, Nucleic Acids Research and Journal of Clinical Investigation.

In The Last Decade

Beatrice Bodega

31 papers receiving 2.3k citations

Hit Papers

Genome-wide association between YAP/TAZ/TEAD and AP-1 at ... 2015 2026 2018 2022 2015 250 500 750

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Beatrice Bodega Italy 17 1.6k 694 499 351 184 32 2.3k
Manuel Sánchez‐Martín Spain 25 1.5k 0.9× 412 0.6× 214 0.4× 304 0.9× 363 2.0× 64 2.3k
Toshiyuki Habu Japan 18 1.5k 0.9× 504 0.7× 181 0.4× 341 1.0× 192 1.0× 38 2.1k
Sabine Loewer United States 10 1.8k 1.1× 401 0.6× 193 0.4× 290 0.8× 44 0.2× 11 2.3k
Kristina Vintersten Germany 19 1.8k 1.1× 204 0.3× 137 0.3× 444 1.3× 104 0.6× 84 2.3k
Anne Harrington United States 13 1.1k 0.7× 236 0.3× 112 0.2× 289 0.8× 180 1.0× 20 1.5k
Gary Brown United States 12 2.1k 1.3× 193 0.3× 226 0.5× 274 0.8× 269 1.5× 14 3.0k
Makoto Matsuyama Japan 22 1.2k 0.7× 489 0.7× 101 0.2× 481 1.4× 66 0.4× 58 1.8k
Wen‐Hui Lien United States 19 1.7k 1.1× 834 1.2× 187 0.4× 212 0.6× 39 0.2× 24 2.5k
Claire M. Schreiner United States 17 1.7k 1.0× 333 0.5× 172 0.3× 403 1.1× 86 0.5× 30 2.4k
Markus Stümm Germany 24 2.5k 1.5× 437 0.6× 761 1.5× 898 2.6× 170 0.9× 78 3.5k

Countries citing papers authored by Beatrice Bodega

Since Specialization
Citations

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

Fields of papers citing papers by Beatrice Bodega

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Beatrice Bodega

This figure shows the co-authorship network connecting the top 25 collaborators of Beatrice Bodega. A scholar is included among the top collaborators of Beatrice Bodega 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 Beatrice Bodega. Beatrice Bodega 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.
Mauri, Gianluca, Giorgio Patelli, Andrea Sartore‐Bianchi, et al.. (2024). Early-onset cancers: Biological bases and clinical implications. Cell Reports Medicine. 5(9). 101737–101737. 18 indexed citations
2.
Bettinaglio, Paola, Eleonora Mangano, Claudia Cesaretti, et al.. (2024). Genetic/epigenetic effects in NF1 microdeletion syndrome: beyond the haploinsufficiency, looking at the contribution of not deleted genes. Human Genetics. 143(6). 775–795.
3.
Fontana, Camilla, Sara Mancinelli, Nicola Pesenti, et al.. (2021). Early maternal care restores LINE-1 methylation and enhances neurodevelopment in preterm infants. BMC Medicine. 19(1). 14 indexed citations
4.
Cafora, Marco, Cinzia Bragato, Daniele Capitanio, et al.. (2021). Targeting HDAC8 to ameliorate skeletal muscle differentiation in Duchenne muscular dystrophy. Pharmacological Research. 170. 105750–105750. 27 indexed citations
5.
Bianchi, Andrea, Chiara Mozzetta, Sara Valsoni, et al.. (2020). Dysfunctional polycomb transcriptional repression contributes to lamin A/C–dependent muscular dystrophy. Journal of Clinical Investigation. 130(5). 2408–2421. 39 indexed citations
6.
Manganaro, Lara, et al.. (2020). 3D Multicolor DNA FISH Tool to Study Nuclear Architecture in Human Primary Cells. Journal of Visualized Experiments. 2 indexed citations
7.
Fontana, Laura, Silvia Maitz, Silvia Tabano, et al.. (2020). Profound alterations of the chromatin architecture at chromosome 11p15.5 in cells from Beckwith-Wiedemann and Silver-Russell syndromes patients. Scientific Reports. 10(1). 8275–8275. 12 indexed citations
8.
Sinha, Shruti, Francesco Gregoretti, Laura Antonelli, et al.. (2019). 4q-D4Z4 chromatin architecture regulates the transcription of muscle atrophic genes in facioscapulohumeral muscular dystrophy. Genome Research. 29(6). 883–895. 11 indexed citations
9.
Deflorian, Gianluca, Grazia Fazio, Erica Bresciani, et al.. (2019). NIPBL: a new player in myeloid cell differentiation. Haematologica. 104(7). 1332–1341. 19 indexed citations
10.
Bodega, Beatrice, Valeria Ranzani, Alessandro Cherubini, et al.. (2017). A cytosolic Ezh1 isoform modulates a PRC2–Ezh1 epigenetic adaptive response in postmitotic cells. Nature Structural & Molecular Biology. 24(5). 444–452. 31 indexed citations
11.
Ranzani, Valeria, Grazisa Rossetti, Ilaria Panzeri, et al.. (2015). The long intergenic noncoding RNA landscape of human lymphocytes highlights the regulation of T cell differentiation by linc-MAF-4. Nature Immunology. 16(3). 318–325. 268 indexed citations
12.
Zanconato, Francesca, Mattia Forcato, Giusy Battilana, et al.. (2015). Genome-wide association between YAP/TAZ/TEAD and AP-1 at enhancers drives oncogenic growth. Nature Cell Biology. 17(9). 1218–1227. 840 indexed citations breakdown →
13.
Bodega, Beatrice & Valerio Orlando. (2014). Repetitive elements dynamics in cell identity programming, maintenance and disease. Current Opinion in Cell Biology. 31. 67–73. 31 indexed citations
14.
Giussani, Marta, Maria Francesca Cardone, Beatrice Bodega, Enrico Ginelli, & Raffaella Meneveri. (2012). Evolutionary history of linked D4Z4 and Beta satellite clusters at the FSHD locus (4q35). Genomics. 100(5). 289–296. 4 indexed citations
15.
Cabianca, Daphne S., Valentina Casà, Beatrice Bodega, et al.. (2012). A Long ncRNA Links Copy Number Variation to a Polycomb/Trithorax Epigenetic Switch in FSHD Muscular Dystrophy. Cell. 149(4). 819–831. 301 indexed citations
16.
Cheli, Stefania, Stéphanie François, Beatrice Bodega, et al.. (2011). Expression Profiling of FSHD-1 and FSHD-2 Cells during Myogenic Differentiation Evidences Common and Distinctive Gene Dysregulation Patterns. PLoS ONE. 6(6). e20966–e20966. 41 indexed citations
17.
Bodega, Beatrice, Maria Francesca Cardone, Stefan Müller, et al.. (2007). Evolutionary genomic remodelling of the human 4q subtelomere (4q35.2). BMC Evolutionary Biology. 7(1). 39–39. 9 indexed citations
18.
Bodega, Beatrice, Maria Francesca Cardone, Mariano Rocchi, et al.. (2006). The boundary of macaque rDNA is constituted by low-copy sequences conserved during evolution. Genomics. 88(5). 564–571. 5 indexed citations
19.
Bodega, Beatrice, Silvia Bione, Leda Dalprà, et al.. (2005). Influence of intermediate and uninterrupted FMR1 CGG expansions in premature ovarian failure manifestation. Human Reproduction. 21(4). 952–957. 143 indexed citations
20.
Bodega, Beatrice. (2004). Mutations in the coding region of the FOXL2 gene are not a major cause of idiopathic premature ovarian failure. Molecular Human Reproduction. 10(8). 555–557. 29 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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