Maria Sframeli
Impact in
- Genetics top 5%
- Neurogenetic and Muscular Disorders Research
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- Cell Adhesion Molecules Research
Papers in
- Genetics 15
- Neurogenetic and Muscular Disorders Research 15
- Genetics and Neurodevelopmental Disorders 2
- Genetic Syndromes and Imprinting 2
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- RNA modifications and cancer 6
- Muscle Physiology and Disorders 5
- Co-authors
- Sonia Messina (19 shared papers)Eugenio Mercuri (6 shared papers)Adele D’Amico (6 shared papers)Valeria Sansone (7 shared papers)Giuseppe Vita (10 shared papers)Giorgia Coratti (5 shared papers)Claudio Bruno (5 shared papers)Gian Luca Vita (12 shared papers)
- Journals
- Neuromuscular Disorders (8 papers)Neurological Sciences (5 papers)Pharmaceuticals (1 paper)Clinical Epigenetics (1 paper)PLoS ONE (1 paper)
- Partner nations
- ItalyUnited KingdomUnited States
In The Last Decade
Maria Sframeli
28 papers receiving 459 citations
Peers
Comparison fields: 5 of 63
- Genetics 284
- Immunology and Allergy 20
- Molecular Biology 227
- Surgery 111
- Neurology 29
Countries citing papers authored by Maria Sframeli
This map shows the geographic impact of Maria Sframeli'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 Maria Sframeli with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Maria Sframeli more than expected).
Fields of papers citing papers by Maria Sframeli
This network shows the impact of papers produced by Maria Sframeli. 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 Maria Sframeli. The network helps show where Maria Sframeli may publish in the future.
Co-authors
The 25 scholars most cited alongside Maria Sframeli, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 29 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2020 | 108 | |
| 2 | 2018 | 69 | |
| 3 | 2017 | 67 | |
| 4 | 2020 | 43 | |
| 5 | 2016 | 22 | |
| 6 | 2020 | 21 | |
| 7 | 2021 | 17 | |
| 8 | 2020 | 14 | |
| 9 | 2021 | 11 | |
| 10 | Activation of NF-kB pathway in Duchennemuscular dystrophy: relation to age | 2011 | 11 |
| 11 | 2020 | 10 | |
| 12 | 2020 | 9 | |
| 13 | 2020 | 9 | |
| 14 | 2020 | 8 | |
| 15 | 2021 | 8 | |
| 16 | 2018 | 8 | |
| 17 | Intrathecal Administration of Nusinersen in Patients with SMA1: Too Little is Known | 2019 | 6 |
| 18 | 2018 | 5 | |
| 19 | 2020 | 5 | |
| 20 | 2020 | 5 |
About Maria Sframeli
Maria Sframeli is a scholar working on Genetics, Molecular Biology, Surgery, Genetics and Neurology, having authored 29 papers that have together received 467 indexed citations. Recurring topics across this work include Neurogenetic and Muscular Disorders Research (15 papers), RNA modifications and cancer (6 papers), Muscle Physiology and Disorders (5 papers), Amyotrophic Lateral Sclerosis Research (4 papers), Congenital Anomalies and Fetal Surgery (4 papers), Cardiomyopathy and Myosin Studies (3 papers), Genetics and Neurodevelopmental Disorders (2 papers) and Genetic Syndromes and Imprinting (2 papers). The work is most often cited by research in Genetics (284 citations), Immunology and Allergy (20 citations), Molecular Biology (227 citations), Surgery (111 citations) and Neurology (29 citations). Maria Sframeli has collaborated with scholars based in Italy, United Kingdom and United States. Frequent co-authors include Sonia Messina, Eugenio Mercuri, Adele D’Amico, Valeria Sansone, Giuseppe Vita, Giorgia Coratti, Claudio Bruno, Gian Luca Vita, Emilio Albamonte and Marika Pane. Their work appears in journals such as Neuromuscular Disorders, Neurological Sciences, Pharmaceuticals, Clinical Epigenetics and PLoS ONE.
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.