Simona Cavalieri

1.1k citations

25 papers · 740 indexed · h-index 17

Impact in

Genetics top 10%
- Virus-based gene therapy research
Molecular Biology
- DNA Repair Mechanisms
- CRISPR and Genetic Engineering
- RNA Interference and Gene Delivery
- Mitochondrial Function and Pathology

Papers in ⓘ

Molecular Biology 19
- DNA Repair Mechanisms 10
- CRISPR and Genetic Engineering 5
- Mitochondrial Function and Pathology 4
Genetics 9
- Genomic variations and chromosomal abnormalities 4
- Virus-based gene therapy research 3
- Genetics and Neurodevelopmental Disorders 3

Co-authors: Luigi Naldini (3 shared papers)Alfredo Brusco (20 shared papers)Massimo Geuna (2 shared papers)Laurie Ailles (2 shared papers)Richard A. Gatti (5 shared papers)Claudio Bordignon (1 shared paper)Zulma Magnani (1 shared paper)Chiara Bonini (1 shared paper)
Journals: Molecular Therapy (2 papers)Journal of Neurology (2 papers)Human Mutation (2 papers)Cytometry Part A (1 paper)Scientific Reports (1 paper)
Partner nations: Italy United States Russia

In The Last Decade

Simona Cavalieri

24 papers receiving 717 citations

Peers

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-authors

The 25 scholars most cited alongside Simona Cavalieri, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Simona Cavalieri Line = papers co-authored together Simona Cavalieri links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 25 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Human T lymphocytes transduced by lentiviral vectors in the absence of TCR activation maintain an intact immune competence Blood ·Simona Cavalieri, Sabrina Cazzaniga, Massimo Geuna, Zulma Magnani, Claudio Bordignon, Luigi Naldini, Chiara Bonini	2003	126
2	Robust and Efficient Regulation of Transgene Expression in Vivo by Improved Tetracycline-Dependent Lentiviral Vectors Molecular Therapy ·Elisa Vigna, Simona Cavalieri, Laurie Ailles, Massimo Geuna, Rainer Loew, Hermann Bujard, Luigi Naldini	2002	119
3	Molecular Evidence of Lentiviral Vector-Mediated Gene Transfer into Human Self-Renewing, Multi-potent, Long-Term NOD/SCID Repopulating Hematopoietic Cells Molecular Therapy ·Laurie Ailles, Manfred Schmidt, Francesca R. Santoni de Sio, Hanno Glimm, Simona Cavalieri, Stefania Bruno, Wanda Piacibello, Christof von Kalle, Luigi Naldini	2002	74
4	A rapid flow cytometry test based on histone H2AX phosphorylation for the sensitive and specific diagnosis of ataxia telangiectasia Cytometry Part A ·Paola Porcedda, Valentina Turinetto, Alfredo Brusco, Simona Cavalieri, Erica Lantelme, Luca Orlando, Umberto Ricardi, Antonio Amoroso, Darío Gregori, Claudia Giachino	2008	53
5	Functional characterization and targeted correction of ATM mutations identified in Japanese patients with ataxia-telangiectasia Human Mutation ·Kotoka Nakamura, Liutao Du, Rashmi Tunuguntla, Francesca Fike, Simona Cavalieri, Tomohiro Morio, Shuki Mizutani, Alfredo Brusco, Richard A. Gatti	2011	37
6	Deep-intronic ATM mutation detected by genomic resequencing and corrected in vitro by antisense morpholino oligonucleotide (AMO) European Journal of Human Genetics ·Simona Cavalieri, Elisa Pozzi, Richard A. Gatti, Alfredo Brusco	2012	30
7	Adult-onset autosomal recessive ataxia associated with neuronal ceroid lipofuscinosis type 5 gene (CLN5) mutations Journal of Neurology ·Cecilia Mancini, Stefano Nassani, Yiran Guo, Yulan Chen, Elisa Giorgio, Alessandro Brussino, Eleonora Di Gregorio, Simona Cavalieri, Nicola Lo Buono, Ada Funaro, Nicola Renato Pizio, Bruce Nmezi, Aija Kyttälä, Filippo M. Santorelli, Quasar Salem Padiath, Håkon Håkonarson, Hao Zhang, Alfredo Brusco	2014	30
8	ATM mutations in Italian families with ataxia telangiectasia include two distinct large genomic deletions Human Mutation ·Simona Cavalieri, Ada Funaro, Paola Porcedda, Valentina Turinetto, Nicola Migone, Richard A. Gatti, Alfredo Brusco	2006	30
9	A novel 3q29 deletion associated with autism, intellectual disability, psychiatric disorders, and obesity American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Elisa Biamino, Eleonora Di Gregorio, Elga Fabia Belligni, Roberto Keller, Evelise Riberi, Marina Gandione, Alessandro Calcia, Cecilia Mancini, Elisa Giorgio, Simona Cavalieri, Patrizia Pappi, Flavia Talarico, Antonio Maria Fea, Silvia De Rubeis, Margherita Silengo, Giovanni Battista Ferrero, Alfredo Brusco	2015	25
10	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 ·Lorenzo Nanetti, Simona Cavalieri, Viviana Pensato, Alessandra Erbetta, Davide Pareyson, Marta Panzeri, Giovanna Zorzi, Carlo Antozzi, Isabella Moroni, Cinzia Gellera, Alfredo Brusco, Caterina Mariotti	2013	24
11	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 ·Simona Cavalieri, Ada Funaro, Patrizia Pappi, Nicola Migone, Richard A. Gatti, Alfredo Brusco	2007	24
12	Long-term treatment with thiamine as possible medical therapy for Friedreich ataxia Journal of Neurology ·Antonio Costantini, Tiziana Laureti, Maria Immacolata Pala, Marco Colangeli, Simona Cavalieri, Elisa Pozzi, Alfredo Brusco, S. Salvarani, Carlo Serrati, Roberto Fancellu	2016	24
13	Whole exome sequencing is necessary to clarify ID/DD cases with de novo copy number variants of uncertain significance: Two proof‐of‐concept examples American Journal of Medical Genetics Part A ·Elisa Giorgio, Andrea Ciolfi, Elisa Biamino, Viviana Caputo, Eleonora Di Gregorio, Elga Fabia Belligni, Alessandro Calcia, Elena Gaidolfi, Alessandro Bruselles, Cecilia Mancini, Simona Cavalieri, Cristina Molinatto, Margherita Silengo, Giovanni Battista Ferrero, Marco Tartaglia, Alfredo Brusco	2016	22
14	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 ·Emilia Cirillo, Rosa Romano, Alfonso Romano, Giuliana Giardino, Anne Durandy, Lucio Nitsch, Rita Genesio, Eleonora Di Gregorio, Simona Cavalieri, Giovanna Abate, Luigi Del Vecchio, Alfredo Brusco, Claudio Pignata	2012	19
15	Megalencephalic leukoencephalopathy with subcortical cysts type 1 (MLC1) due to a homozygous deep intronic splicing mutation (c.895-226T>G) abrogated in vitro using an antisense morpholino oligonucleotide Neurogenetics ·Cecilia Mancini, Giovanna Vaula, L Scalzitti, Simona Cavalieri, Enrico Bertini, Chiara Aiello, C Lucchini, Richard A. Gatti, Alessandro Brussino, Alfredo Brusco	2012	17
16	Glutathione levels in blood from ataxia telangiectasia patients suggest in vivo adaptive mechanisms to oxidative stress Clinical Biochemistry ·Paolo Degan, Marco d’Ischia, Federico V. Pallardó, Adriana Zatterale, Alfredo Brusco, Rita Calzone, Simona Cavalieri, Kaan Kavaklı, Ana Lloret, Paola Manini, Maria Antonietta Pisanti, Emilia Vuttariello, Giovanni Pagano	2007	16
17	Two families with novel missense mutations in COL4A1: When diagnosis can be missed Journal of the Neurological Sciences ·Elisa Giorgio, Giovanna Vaula, Giovanni Bosco, S Giacone, Cecilia Mancini, Alessandro Calcia, Simona Cavalieri, Eleonora Di Gregorio, Roberta Rigault De Longrais, S. Leombruni, Lorenzo Pinessi, Paolo Cerrato, Alfredo Brusco, Alessandro Brussino	2015	16
18	Spinocerebellar Ataxia Tethering PCR Journal of Molecular Diagnostics ·Claudia Cagnoli, Alessandro Brussino, Cecilia Mancini, Marina Ferrone, Laura Orsi, Paola Salmin, Patrizia Pappi, Elisa Giorgio, Elisa Pozzi, Simona Cavalieri, Eleonora Di Gregorio, Marta Ferrero, Alessandro Filla, Giuseppe De Michele, Cinzia Gellera, Caterina Mariotti, Suran Nethisinghe, Paola Giunti, Giovanni Stévanin, Alfredo Brusco	2018	15
19	Blood metal levels and related antioxidant enzyme activities in patients with ataxia telangiectasia Neurobiology of Disease ·Stefania Squadrone, Paola Brizio, Cecilia Mancini, Elisa Pozzi, Simona Cavalieri, Maria Cesarina Abete, Alfredo Brusco	2015	11
20	Exome sequencing in children of women with skewed X-inactivation identifies atypical cases and complex phenotypes European Journal of Paediatric Neurology ·Elisa Giorgio, Alessandro Brussino, Elisa Biamino, Elga Fabia Belligni, Alessandro Bruselles, Andrea Ciolfi, Viviana Caputo, Simone Pizzi, Alessandro Calcia, Eleonora Di Gregorio, Simona Cavalieri, Cecilia Mancini, Elisa Pozzi, Marta Ferrero, Evelise Riberi, I Borelli, Antonio Amoroso, Giovanni Battista Ferrero, Marco Tartaglia, Alfredo Brusco	2016	11

About Simona Cavalieri

Simona Cavalieri is a scholar working on Molecular Biology, Genetics, Cellular and Molecular Neuroscience, Neurology and Oncology, having authored 25 papers that have together received 740 indexed citations. Recurring topics across this work include DNA Repair Mechanisms (10 papers), CRISPR and Genetic Engineering (5 papers), Genetic Neurodegenerative Diseases (4 papers), Mitochondrial Function and Pathology (4 papers), Genomic variations and chromosomal abnormalities (4 papers), Virus-based gene therapy research (3 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Carcinogens and Genotoxicity Assessment (3 papers). The work is most often cited by research in Genetics (329 citations), Molecular Biology (498 citations), Oncology (160 citations), Cellular and Molecular Neuroscience (103 citations) and Cancer Research (77 citations). Simona Cavalieri has collaborated with scholars based in Italy, United States and Russia. Frequent co-authors include Luigi Naldini, Alfredo Brusco, Massimo Geuna, Laurie Ailles, Richard A. Gatti, Claudio Bordignon, Zulma Magnani, Chiara Bonini, Hermann Bujard and Rainer Loew. Their work appears in journals such as Molecular Therapy, Journal of Neurology, Human Mutation, Cytometry Part A and Scientific Reports.

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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