Massimo Zeviani
Impact in
- Clinical Biochemistry top 0.01%
- Metabolism and Genetic Disorders
- Molecular Biology top 0.02%
- Mitochondrial Function and Pathology
- ATP Synthase and ATPases Research
- RNA modifications and cancer
- RNA and protein synthesis mechanisms
- RNA Research and Splicing
Papers in
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- Metabolism and Genetic Disorders 218
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- Mitochondrial Function and Pathology 373
- ATP Synthase and ATPases Research 159
- RNA modifications and cancer 51
- RNA and protein synthesis mechanisms 25
- Photosynthetic Processes and Mechanisms 22
- Ubiquitin and proteasome pathways 16
- Co-authors
- Valeria Tiranti (67 shared papers)Salvatore DiMauro (26 shared papers)Carlo Fiore Viscomi (57 shared papers)Erika Fernández‐Vizarra (42 shared papers)Antonella Spinazzola (22 shared papers)Eric A. Schon (23 shared papers)Graziella Uziel (36 shared papers)Stefano DiDonato (22 shared papers)
- Journals
- Neurology (26 papers)The American Journal of Human Genetics (25 papers)Human Molecular Genetics (19 papers)Annals of Neurology (19 papers)Neuromuscular Disorders (17 papers)
- Partner nations
- ItalyUnited KingdomUnited States
In The Last Decade
Massimo Zeviani
470 papers receiving 42.0k citations
Massimo Zeviani's Hit Papers
Peers
Comparison fields: 5 of 181
- Clinical Biochemistry 15.1k
- Molecular Biology 34.6k
- Genetics 3.8k
- Aging 536
- Cellular and Molecular Neuroscience 4.1k
Countries citing papers authored by Massimo Zeviani
This map shows the geographic impact of Massimo Zeviani'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 Zeviani with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Massimo Zeviani more than expected).
Fields of papers citing papers by Massimo Zeviani
This network shows the impact of papers produced by Massimo Zeviani. 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 Zeviani. The network helps show where Massimo Zeviani may publish in the future.
Co-authors
The 25 scholars most cited alongside Massimo Zeviani, 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 475 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Identification and characterization of a spinal muscular atrophy-determining gene Hit paper breakdown → | 1995 | 3348 |
| 2 | Mitochondrial diseases Hit paper breakdown → | 2016 | 1181 |
| 3 | Mitochondrial DNA Deletions in Progressive External Ophthalmoplegia and Kearns-Sayre Syndrome Hit paper breakdown → | 1989 | 866 |
| 4 | Human mitochondrial DNA deletions associated with mutations in the gene encoding Twinkle, a phage T7 gene 4-like protein localized in mitochondria Hit paper breakdown → | 2001 | 737 |
| 5 | 1998 | 688 | |
| 6 | Deletions of mitochondrial DNA in Kearns‐Sayre syndrome Hit paper breakdown → | 1988 | 661 |
| 7 | 2005 | 643 | |
| 8 | Mitochondrial myopathies Hit paper breakdown → | 1985 | 603 |
| 9 | An autosomal dominant disorder with multiple deletions of mitochondrial DNA starting at the D-loop region Hit paper breakdown → | 1989 | 557 |
| 10 | 2000 | 525 | |
| 11 | A Direct Repeat Is a Hotspot for Large-Scale Deletion of Human Mitochondrial DNA Hit paper breakdown → | 1989 | 506 |
| 12 | 2003 | 457 | |
| 13 | 1998 | 454 | |
| 14 | 1998 | 454 | |
| 15 | Haplotype and phylogenetic analyses suggest that one European-specific mtDNA background plays a role in the expression of Leber hereditary optic neuropathy by increasing the penetrance of the primary mutations 11778 and 14484. | 1997 | 390 |
| 16 | 2015 | 388 | |
| 17 | 2004 | 381 | |
| 18 | 2006 | 367 | |
| 19 | 2010 | 362 | |
| 20 | 2009 | 356 |
About Massimo Zeviani
Massimo Zeviani is a scholar working on Clinical Biochemistry, Molecular Biology, Cellular and Molecular Neuroscience, Biochemistry and Physiology, having authored 475 papers that have together received 43.6k indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (373 papers), Metabolism and Genetic Disorders (218 papers), ATP Synthase and ATPases Research (159 papers), RNA modifications and cancer (51 papers), Genetic Neurodegenerative Diseases (33 papers), RNA and protein synthesis mechanisms (25 papers), Photosynthetic Processes and Mechanisms (22 papers) and Ubiquitin and proteasome pathways (16 papers). The work is most often cited by research in Clinical Biochemistry (15.1k citations), Molecular Biology (34.6k citations), Genetics (3.8k citations), Aging (536 citations) and Cellular and Molecular Neuroscience (4.1k citations). Massimo Zeviani has collaborated with scholars based in Italy, United Kingdom and United States. Frequent co-authors include Valeria Tiranti, Salvatore DiMauro, Carlo Fiore Viscomi, Erika Fernández‐Vizarra, Antonella Spinazzola, Eric A. Schon, Graziella Uziel, Stefano DiDonato, Eleonora Lamantea and Daniele Ghezzi. Their work appears in journals such as Neurology, The American Journal of Human Genetics, Human Molecular Genetics, Annals of Neurology and Neuromuscular 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.