Mario Sirito
Impact in
- Hematology top 1%
- Iron Metabolism and Disorders
- Erythropoietin and Anemia Treatment
- Genetics top 2%
- Hemoglobinopathies and Related Disorders
Papers in
-
- Mitochondrial Function and Pathology 7
- DNA Repair Mechanisms 5
- Muscle Physiology and Disorders 4
- Ubiquitin and proteasome pathways 3
- Genomics and Chromatin Dynamics 3
-
- Genetic Neurodegenerative Diseases 13
- Co-authors
- Michèle Sawadogo (6 shared papers)Qun Lin (3 shared papers)Tapati Maity (1 shared paper)Gaël Nicolas (1 shared paper)Axel Kahn (1 shared paper)Myriam Bennoun (1 shared paper)Carole Beaumont (1 shared paper)Sophie Vaulont (1 shared paper)
- Journals
- Neuromuscular Disorders (3 papers)American Journal Of Pathology (3 papers)Proceedings of the National Academy of Sciences (3 papers)Gene (2 papers)Human Molecular Genetics (2 papers)
- Partner nations
- United StatesFinlandItaly
In The Last Decade
Mario Sirito
25 papers receiving 2.0k citations
Mario Sirito's Hit Papers
Peers
Comparison fields: 5 of 92
- Hematology 641
- Genetics 429
- Nutrition and Dietetics 434
- Cellular and Molecular Neuroscience 348
- Molecular Biology 979
Countries citing papers authored by Mario Sirito
This map shows the geographic impact of Mario Sirito'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 Mario Sirito with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Mario Sirito more than expected).
Fields of papers citing papers by Mario Sirito
This network shows the impact of papers produced by Mario Sirito. 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 Mario Sirito. The network helps show where Mario Sirito may publish in the future.
Co-authors
The 25 scholars most cited alongside Mario Sirito, 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 25 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Severe iron deficiency anemia in transgenic mice expressing liver hepcidin Hit paper breakdown → | 2002 | 701 |
| 2 | 1994 | 303 | |
| 3 | 1998 | 139 | |
| 4 | Members of the USF family of helix-loop-helix proteins bind DNA as homo- as well as heterodimers. | 1992 | 137 |
| 5 | 1992 | 123 | |
| 6 | 1992 | 92 | |
| 7 | 2009 | 70 | |
| 8 | 2010 | 61 | |
| 9 | 2010 | 59 | |
| 10 | 2010 | 48 | |
| 11 | 2004 | 37 | |
| 12 | 2020 | 35 | |
| 13 | 2022 | 29 | |
| 14 | 2005 | 29 | |
| 15 | 2013 | 29 | |
| 16 | 2009 | 25 | |
| 17 | 2012 | 23 | |
| 18 | 2003 | 21 | |
| 19 | 2021 | 17 | |
| 20 | 1994 | 16 |
About Mario Sirito
Mario Sirito is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience, Genetics, Cardiology and Cardiovascular Medicine and Oncology, having authored 25 papers that have together received 2.0k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (13 papers), Mitochondrial Function and Pathology (7 papers), DNA Repair Mechanisms (5 papers), Muscle Physiology and Disorders (4 papers), Ubiquitin and proteasome pathways (3 papers), Genomics and Chromatin Dynamics (3 papers), Cardiomyopathy and Myosin Studies (3 papers) and Trace Elements in Health (2 papers). The work is most often cited by research in Hematology (641 citations), Genetics (429 citations), Nutrition and Dietetics (434 citations), Cellular and Molecular Neuroscience (348 citations) and Molecular Biology (979 citations). Mario Sirito has collaborated with scholars based in United States, Finland and Italy. Frequent co-authors include Michèle Sawadogo, Qun Lin, Tapati Maity, Gaël Nicolas, Axel Kahn, Myriam Bennoun, Carole Beaumont, Sophie Vaulont, Bernard Grandchamp and Arlette Porteu. Their work appears in journals such as Neuromuscular Disorders, American Journal Of Pathology, Proceedings of the National Academy of Sciences, Gene and Human Molecular Genetics.
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.