Massimo Mogni
Impact in
Papers in
- Genetics 8
- Hemoglobinopathies and Related Disorders 5
- Mesenchymal stem cell research 3
- Genomic variations and chromosomal abnormalities 3
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- DNA Repair Mechanisms 2
- Epigenetics and DNA Methylation 2
- Co-authors
- Nadia Sessarego (2 shared papers)Francesco Frassoni (2 shared papers)Ranieri Cancedda (4 shared papers)Annalisa Kunkl (2 shared papers)Domenico Coviello (7 shared papers)Mario Lituania (2 shared papers)Federica Benvenuto (1 shared paper)Marina Podestà (1 shared paper)
- Journals
- Genes (2 papers)Frontiers in Pediatrics (1 paper)Clinical Chemistry and Laboratory Medicine (CCLM) (1 paper)Haematologica (1 paper)Journal of Child Neurology (1 paper)
- Partner nations
- ItalyNetherlandsJapan
In The Last Decade
Massimo Mogni
13 papers receiving 422 citations
Peers
Comparison fields: 5 of 51
- Genetics 178
- Urology 32
- Surgery 157
- Cancer Research 49
- Biomaterials 45
Countries citing papers authored by Massimo Mogni
This map shows the geographic impact of Massimo Mogni'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 Mogni with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Massimo Mogni more than expected).
Fields of papers citing papers by Massimo Mogni
This network shows the impact of papers produced by Massimo Mogni. 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 Mogni. The network helps show where Massimo Mogni may publish in the future.
Co-authors
The 25 scholars most cited alongside Massimo Mogni, 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 | 2008 | 140 | |
| 2 | 2017 | 109 | |
| 3 | 2007 | 46 | |
| 4 | 2013 | 42 | |
| 5 | 2017 | 39 | |
| 6 | 2011 | 30 | |
| 7 | 2016 | 14 | |
| 8 | 2015 | 5 | |
| 9 | 2012 | 4 | |
| 10 | 2006 | 3 | |
| 11 | 2020 | 1 | |
| 12 | 2022 | 1 | |
| 13 | 2021 | 1 | |
| 14 | 2021 | 0 | |
| 15 | 2024 | 0 |
About Massimo Mogni
Massimo Mogni is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Genetics and Surgery, having authored 15 papers that have together received 435 indexed citations. Recurring topics across this work include Hemoglobinopathies and Related Disorders (5 papers), Mesenchymal stem cell research (3 papers), Genomic variations and chromosomal abnormalities (3 papers), DNA Repair Mechanisms (2 papers), Epigenetics and DNA Methylation (2 papers), Chromosomal and Genetic Variations (2 papers), Neonatal Health and Biochemistry (2 papers) and Tissue Engineering and Regenerative Medicine (2 papers). The work is most often cited by research in Genetics (178 citations), Urology (32 citations), Surgery (157 citations), Cancer Research (49 citations) and Biomaterials (45 citations). Massimo Mogni has collaborated with scholars based in Italy, Netherlands and Japan. Frequent co-authors include Nadia Sessarego, Francesco Frassoni, Ranieri Cancedda, Annalisa Kunkl, Domenico Coviello, Mario Lituania, Federica Benvenuto, Marina Podestà, F. Dagna Bricarelli and Alessandro Parodi. Their work appears in journals such as Genes, Frontiers in Pediatrics, Clinical Chemistry and Laboratory Medicine (CCLM), Haematologica and Journal of Child Neurology.
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.