Roberta Petillo
Impact in
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- Cardiomyopathy and Myosin Studies
- Cardiac electrophysiology and arrhythmias
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- Neurogenetic and Muscular Disorders Research
Papers in
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- Muscle Physiology and Disorders 5
- Ion channel regulation and function 2
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- Cardiac electrophysiology and arrhythmias 4
- Cardiomyopathy and Myosin Studies 4
- Cardiac pacing and defibrillation studies 2
- Co-authors
- Luisa Politano (10 shared papers)Paola D′Ambrosio (9 shared papers)Alberto Palladino (6 shared papers)Andrea Antonio Papa (5 shared papers)Marianna Scutifero (7 shared papers)Gerardo Nigro (3 shared papers)Manuela Ergoli (4 shared papers)Luigia Passamano (5 shared papers)
In The Last Decade
Roberta Petillo
15 papers receiving 161 citations
Peers
Comparison fields: 5 of 36
- Cardiology and Cardiovascular Medicine 64
- Genetics 27
- Molecular Biology 125
- Sensory Systems 8
- Cellular and Molecular Neuroscience 22
Countries citing papers authored by Roberta Petillo
This map shows the geographic impact of Roberta Petillo'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 Roberta Petillo with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Roberta Petillo more than expected).
Fields of papers citing papers by Roberta Petillo
This network shows the impact of papers produced by Roberta Petillo. 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 Roberta Petillo. The network helps show where Roberta Petillo may publish in the future.
Co-authors
The 25 scholars most cited alongside Roberta Petillo, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | Clinical features of patients with dystrophinopathy sharing the 45-55 exon deletion of DMD gene. | 2015 | 37 |
| 2 | 2017 | 31 | |
| 3 | Novel mutations in LMNA A/C gene and associated phenotypes. | 2015 | 18 |
| 4 | 2022 | 16 | |
| 5 | 2018 | 14 | |
| 6 | 2022 | 11 | |
| 7 | 2018 | 10 | |
| 8 | Management of cardiac involvement in muscular dystrophies: paediatric versus adult forms. | 2016 | 8 |
| 9 | 2020 | 5 | |
| 10 | 2017 | 4 | |
| 11 | Cardiac diseases as a predictor warning of hereditary muscle diseases. The case of laminopathies. | 2019 | 3 |
| 12 | 2023 | 2 | |
| 13 | 2022 | 2 | |
| 14 | 2016 | 1 | |
| 15 | Is the epicardial left ventricular lead implantation an alternative approach to percutaneous attempt in patients with Steinert disease? A case report. | 2017 | 1 |
About Roberta Petillo
Roberta Petillo is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine, Cellular and Molecular Neuroscience, Genetics and Genetics, having authored 15 papers that have together received 163 indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (5 papers), Cardiac electrophysiology and arrhythmias (4 papers), Genetic Neurodegenerative Diseases (4 papers), Cardiomyopathy and Myosin Studies (4 papers), Genomic variations and chromosomal abnormalities (3 papers), Genetics and Neurodevelopmental Disorders (2 papers), Ion channel regulation and function (2 papers) and Cardiac pacing and defibrillation studies (2 papers). The work is most often cited by research in Cardiology and Cardiovascular Medicine (64 citations), Genetics (27 citations), Molecular Biology (125 citations), Sensory Systems (8 citations) and Cellular and Molecular Neuroscience (22 citations). Roberta Petillo has collaborated with scholars based in Italy, Poland and France. Frequent co-authors include Luisa Politano, Paola D′Ambrosio, Alberto Palladino, Andrea Antonio Papa, Marianna Scutifero, Gerardo Nigro, Manuela Ergoli, Luigia Passamano, Annalaura Torella and Antonella Taglia. Their work appears in journals such as Frontiers in Neurology, European Journal of Medical Genetics, Genes, Human Mutation and Intractable & Rare Diseases Research.
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.