Massimo Plumari
Impact in
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- Genetic Neurodegenerative Diseases
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- Neurological disorders and treatments
- Neurological diseases and metabolism
Papers in
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- Mitochondrial Function and Pathology 4
- RNA modifications and cancer 2
- Connexins and lens biology 1
- Ion channel regulation and function 1
- Protein purification and stability 1
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- Genetic Neurodegenerative Diseases 3
- Hereditary Neurological Disorders 1
- Co-authors
- Franco Taroni (4 shared papers)Daniela Di Bella (3 shared papers)Roberto Fancellu (2 shared papers)Caterina Mariotti (2 shared papers)Cinzia Gellera (3 shared papers)Lorena Duca (1 shared paper)Alessandra Solari (1 shared paper)Maria Domenica Cappellini (1 shared paper)
- Journals
- Human Mutation (1 paper)Clinical Genetics (1 paper)Neurogenetics (1 paper)Neuropediatrics (1 paper)Movement Disorders (1 paper)
- Partner nations
- ItalyUnited KingdomUnited States
In The Last Decade
Massimo Plumari
9 papers receiving 123 citations
Peers
Comparison fields: 5 of 34
- Cellular and Molecular Neuroscience 76
- Neurology 27
- Molecular Biology 107
- Neurology 10
- Aging 2
Countries citing papers authored by Massimo Plumari
This map shows the geographic impact of Massimo Plumari'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 Massimo Plumari with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Massimo Plumari more than expected).
Fields of papers citing papers by Massimo Plumari
This network shows the impact of papers produced by Massimo Plumari. 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 Massimo Plumari. The network helps show where Massimo Plumari may publish in the future.
Co-authors
The 25 scholars most cited alongside Massimo Plumari, 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 | 2012 | 47 | |
| 2 | 2011 | 33 | |
| 3 | 2018 | 27 | |
| 4 | 2020 | 6 | |
| 5 | 2021 | 5 | |
| 6 | 2022 | 4 | |
| 7 | 2024 | 2 | |
| 8 | 2024 | 1 | |
| 9 | 2010 | 1 | |
| 10 | 2024 | 1 |
About Massimo Plumari
Massimo Plumari is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience, Genetics, Genetics and Neurology, having authored 10 papers that have together received 127 indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (4 papers), Genetic Neurodegenerative Diseases (3 papers), RNA modifications and cancer (2 papers), Connexins and lens biology (1 paper), Metabolism and Genetic Disorders (1 paper), Ion channel regulation and function (1 paper), Hereditary Neurological Disorders (1 paper) and Protein purification and stability (1 paper). The work is most often cited by research in Cellular and Molecular Neuroscience (76 citations), Neurology (27 citations), Molecular Biology (107 citations), Neurology (10 citations) and Aging (2 citations). Massimo Plumari has collaborated with scholars based in Italy, United Kingdom and United States. Frequent co-authors include Franco Taroni, Daniela Di Bella, Roberto Fancellu, Caterina Mariotti, Cinzia Gellera, Lorena Duca, Alessandra Solari, Maria Domenica Cappellini, Giuseppe Lauria and Lorenzo Nanetti. Their work appears in journals such as Human Mutation, Clinical Genetics, Neurogenetics, Neuropediatrics and Movement Disorders.
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.