Manuela Ergoli
Impact in
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- Neurogenetic and Muscular Disorders Research
- Virus-based gene therapy research
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- Cardiomyopathy and Myosin Studies
Papers in
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- Muscle Physiology and Disorders 7
- Nuclear Structure and Function 4
- Ubiquitin and proteasome pathways 2
- RNA Research and Splicing 2
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- Cardiomyopathy and Myosin Studies 3
- Cardiovascular Effects of Exercise 2
- Co-authors
- Luisa Politano (12 shared papers)Esther Picillo (9 shared papers)Emanuela Viggiano (3 shared papers)Paola D′Ambrosio (5 shared papers)Gerardo Nigro (3 shared papers)Roberta Petillo (4 shared papers)Annalaura Torella (3 shared papers)Antonella Taglia (2 shared papers)
In The Last Decade
Manuela Ergoli
12 papers receiving 212 citations
Peers
Comparison fields: 5 of 38
- Genetics 27
- Cardiology and Cardiovascular Medicine 54
- Molecular Biology 176
- Aging 3
- Cellular and Molecular Neuroscience 28
Countries citing papers authored by Manuela Ergoli
This map shows the geographic impact of Manuela Ergoli'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 Manuela Ergoli with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Manuela Ergoli more than expected).
Fields of papers citing papers by Manuela Ergoli
This network shows the impact of papers produced by Manuela Ergoli. 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 Manuela Ergoli. The network helps show where Manuela Ergoli may publish in the future.
Co-authors
The 25 scholars most cited alongside Manuela Ergoli, 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 | 2016 | 52 | |
| 2 | Clinical features of patients with dystrophinopathy sharing the 45-55 exon deletion of DMD gene. | 2015 | 37 |
| 3 | 2018 | 28 | |
| 4 | 2017 | 21 | |
| 5 | 2019 | 18 | |
| 6 | Novel mutations in LMNA A/C gene and associated phenotypes. | 2015 | 18 |
| 7 | 2016 | 12 | |
| 8 | Are there real benefits to implanting cardiac devices in patients with end-stage dilated dystrophinopathic cardiomyopathy? Review of literature and personal results. | 2019 | 10 |
| 9 | 2019 | 7 | |
| 10 | 2020 | 5 | |
| 11 | Cardiac diseases as a predictor warning of hereditary muscle diseases. The case of laminopathies. | 2019 | 3 |
| 12 | Study of anti-Müllerian hormone levels in patients with Myotonic Dystrophy Type 1. Preliminary results. | 2017 | 3 |
About Manuela Ergoli
Manuela Ergoli is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine, Cellular and Molecular Neuroscience, Physiology and Clinical Biochemistry, having authored 12 papers that have together received 214 indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (7 papers), Nuclear Structure and Function (4 papers), Genetic Neurodegenerative Diseases (3 papers), Cardiomyopathy and Myosin Studies (3 papers), Cardiovascular Effects of Exercise (2 papers), Ubiquitin and proteasome pathways (2 papers), RNA Research and Splicing (2 papers) and Adipose Tissue and Metabolism (2 papers). The work is most often cited by research in Genetics (27 citations), Cardiology and Cardiovascular Medicine (54 citations), Molecular Biology (176 citations), Aging (3 citations) and Cellular and Molecular Neuroscience (28 citations). Manuela Ergoli has collaborated with scholars based in Italy, Poland and France. Frequent co-authors include Luisa Politano, Esther Picillo, Emanuela Viggiano, Paola D′Ambrosio, Gerardo Nigro, Roberta Petillo, Annalaura Torella, Antonella Taglia, Alberto Palladino and Sergio Minucci. Their work appears in journals such as Neuromuscular Disorders, Human Genetics, Frontiers in Neurology, The Journal of Gene Medicine and Journal of Cellular and Molecular Medicine.
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.