Simona Cavalieri

1.1k total citations
25 papers, 740 citations indexed

About

Simona Cavalieri is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Simona Cavalieri has authored 25 papers receiving a total of 740 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 9 papers in Genetics and 4 papers in Cellular and Molecular Neuroscience. Recurrent topics in Simona Cavalieri's work include DNA Repair Mechanisms (10 papers), CRISPR and Genetic Engineering (5 papers) and Mitochondrial Function and Pathology (4 papers). Simona Cavalieri is often cited by papers focused on DNA Repair Mechanisms (10 papers), CRISPR and Genetic Engineering (5 papers) and Mitochondrial Function and Pathology (4 papers). Simona Cavalieri collaborates with scholars based in Italy, United States and Russia. Simona Cavalieri's co-authors include Alfredo Brusco, Luigi Naldini, Massimo Geuna, Laurie Ailles, Richard A. Gatti, Chiara Bonini, Claudio Bordignon, Zulma Magnani, Rainer Loew and Hermann Bujard and has published in prestigious journals such as SHILAP Revista de lepidopterología, Blood and Scientific Reports.

In The Last Decade

Simona Cavalieri

24 papers receiving 717 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Simona Cavalieri Italy	17	498	329	160	103	95	25	740
Sabine Endele Germany	14	701 1.4×	309 0.9×	84 0.5×	74 0.7×	74 0.8×	22	908
Aaron Mammoser United States	11	462 0.9×	225 0.7×	92 0.6×	41 0.4×	56 0.6×	25	765
Jiong Yan United States	15	650 1.3×	487 1.5×	73 0.5×	117 1.1×	92 1.0×	27	1.0k
K. Binley United Kingdom	11	415 0.8×	230 0.7×	79 0.5×	89 0.9×	81 0.9×	14	691
Tatsuaki Kurosaki United States	13	1.1k 2.1×	211 0.6×	76 0.5×	92 0.9×	63 0.7×	24	1.3k
Diego Ottaviani United Kingdom	15	570 1.1×	115 0.3×	179 1.1×	97 0.9×	134 1.4×	35	935
Alexander Saveliev United Kingdom	13	611 1.2×	165 0.5×	75 0.5×	153 1.5×	177 1.9×	17	827
Reinhard Grausenburger Austria	14	702 1.4×	92 0.3×	181 1.1×	106 1.0×	126 1.3×	25	1.1k
T. Nagase Japan	9	533 1.1×	185 0.6×	119 0.7×	54 0.5×	54 0.6×	11	774
Jennifer Coleman United States	7	668 1.3×	267 0.8×	57 0.4×	87 0.8×	50 0.5×	7	905

Countries citing papers authored by Simona Cavalieri

Since Specialization

Citations

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

Fields of papers citing papers by Simona Cavalieri

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Simona Cavalieri

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

All Works

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20 of 20 papers shown

Cavalieri, Simona, et al.. (2021). Moving between the boundaries of physical and digital contexts: a case study about a shared project by a group of children. SHILAP Revista de lepidopterología.

Pozzi, Elisa, Elisa Giorgio, Cecilia Mancini, et al.. (2020). In vitro dexamethasone treatment does not induce alternative ATM transcripts in cells from Ataxia–Telangiectasia patients. Scientific Reports. 10(1). 20182–20182. 2 indexed citations

Cagnoli, Claudia, Alessandro Brussino, Cecilia Mancini, et al.. (2018). Spinocerebellar Ataxia Tethering PCR. Journal of Molecular Diagnostics. 20(3). 289–297. 15 indexed citations

Sirchia, Fabio, Eleonora Di Gregorio, Gabriella Restagno, et al.. (2017). A case of Feingold type 2 syndrome associated with keratoconus refines keratoconus type 7 locus on chromosome 13q. European Journal of Medical Genetics. 60(4). 224–227. 8 indexed citations

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

Squadrone, Stefania, Paola Brizio, Cecilia Mancini, et al.. (2015). Blood metal levels and related antioxidant enzyme activities in patients with ataxia telangiectasia. Neurobiology of Disease. 81. 162–167. 11 indexed citations

Biamino, Elisa, Eleonora Di Gregorio, Elga Fabia Belligni, et al.. (2015). A novel 3q29 deletion associated with autism, intellectual disability, psychiatric disorders, and obesity. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 171(2). 290–299. 25 indexed citations

Gregorio, Eleonora Di, Giovanni Botta, Alessandro Calcia, et al.. (2015). Array-Comparative Genomic Hybridization Analysis in Fetuses with Major Congenital Malformations Reveals that 24% of Cases Have Pathogenic Deletions/Duplications. Cytogenetic and Genome Research. 147(1). 10–16. 2 indexed citations

Giorgio, Elisa, Giovanna Vaula, Cecilia Mancini, et al.. (2015). Two families with novel missense mutations in COL4A1: When diagnosis can be missed. Journal of the Neurological Sciences. 352(1-2). 99–104. 16 indexed citations

10.

Mancini, Cecilia, Yiran Guo, Yulan Chen, et al.. (2014). Adult-onset autosomal recessive ataxia associated with neuronal ceroid lipofuscinosis type 5 gene (CLN5) mutations. Journal of Neurology. 262(1). 173–178. 30 indexed citations

11.

Nanetti, Lorenzo, Simona Cavalieri, Viviana Pensato, et al.. (2013). SETX mutations are a frequent genetic cause of juvenile and adult onset cerebellar ataxia with neuropathy and elevated serum alpha-fetoprotein. Orphanet Journal of Rare Diseases. 8(1). 123–123. 24 indexed citations

12.

Cavalieri, Simona, Elisa Pozzi, Richard A. Gatti, & Alfredo Brusco. (2012). Deep-intronic ATM mutation detected by genomic resequencing and corrected in vitro by antisense morpholino oligonucleotide (AMO). European Journal of Human Genetics. 21(7). 774–778. 30 indexed citations

13.

Cirillo, Emilia, Rosa Romano, Alfonso Romano, et al.. (2012). De novo 13q12.3–q14.11 deletion involving BRCA2 gene in a patient with developmental delay, elevated IgM levels, transient ataxia, and cerebellar hypoplasia, mimicking an A‐T like phenotype. American Journal of Medical Genetics Part A. 158A(10). 2571–2576. 19 indexed citations

14.

Nakamura, Kotoka, Liutao Du, Francesca Fike, et al.. (2011). Functional characterization and targeted correction of ATM mutations identified in Japanese patients with ataxia-telangiectasia. Human Mutation. 33(1). 198–208. 37 indexed citations

15.

Porcedda, Paola, Valentina Turinetto, Alfredo Brusco, et al.. (2008). A rapid flow cytometry test based on histone H2AX phosphorylation for the sensitive and specific diagnosis of ataxia telangiectasia. Cytometry Part A. 73A(6). 508–516. 53 indexed citations

16.

Degan, Paolo, Marco d’Ischia, Federico V. Pallardó, et al.. (2007). Glutathione levels in blood from ataxia telangiectasia patients suggest in vivo adaptive mechanisms to oxidative stress. Clinical Biochemistry. 40(9-10). 666–670. 16 indexed citations

17.

Cavalieri, Simona, Ada Funaro, Patrizia Pappi, et al.. (2007). Large Genomic Mutations within the ATM Gene Detected by MLPA, Including a Duplication of 41 kb from Exon 4 to 20. Annals of Human Genetics. 72(1). 10–18. 24 indexed citations

18.

Cavalieri, Simona, Ada Funaro, Paola Porcedda, et al.. (2006). ATM mutations in Italian families with ataxia telangiectasia include two distinct large genomic deletions. Human Mutation. 27(10). 1061–1061. 30 indexed citations

19.

Vigna, Elisa, Simona Cavalieri, Laurie Ailles, et al.. (2002). Robust and Efficient Regulation of Transgene Expression in Vivo by Improved Tetracycline-Dependent Lentiviral Vectors. Molecular Therapy. 5(3). 252–261. 119 indexed citations

20.

Ceda, Gian Paolo, Licia Denti, Graziano Ceresini, et al.. (1989). Calcitonin inhibition of growth hormone-releasing hormone-induced GH secretion in normal men. European Journal of Endocrinology. 120(4). 416–422. 5 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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