Marco Ritelli
Impact in
- Genetics top 2%
- Connective tissue disorders research
- Dermatological and Skeletal Disorders
- Rheumatology top 5%
- Dupuytren's Contracture and Treatments
Papers in
- Genetics 65
- Connective tissue disorders research 62
- Dermatological and Skeletal Disorders 26
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- Ubiquitin and proteasome pathways 6
- Wnt/β-catenin signaling in development and cancer 5
- Protein Tyrosine Phosphatases 4
- Co-authors
- Marina Colombi (71 shared papers)Nicola Chiarelli (37 shared papers)Nicoletta Zoppi (27 shared papers)Marina Venturini (32 shared papers)Chiara Dordoni (19 shared papers)Valeria Cinquina (21 shared papers)Piergiacomo Calzavara‐Pinton (12 shared papers)Marco Castori (14 shared papers)
- Journals
- Genes (6 papers)Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease (4 papers)Orphanet Journal of Rare Diseases (4 papers)European Journal of Human Genetics (3 papers)Clinical Genetics (3 papers)
- Partner nations
- ItalyUnited StatesSwitzerland
In The Last Decade
Marco Ritelli
78 papers receiving 1.6k citations
Peers
Comparison fields: 5 of 100
- Genetics 1.1k
- Rheumatology 208
- Medical Terminology 2
- Immunology and Allergy 40
- Nephrology 44
Countries citing papers authored by Marco Ritelli
This map shows the geographic impact of Marco Ritelli'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 Marco Ritelli with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Marco Ritelli more than expected).
Fields of papers citing papers by Marco Ritelli
This network shows the impact of papers produced by Marco Ritelli. 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 Marco Ritelli. The network helps show where Marco Ritelli may publish in the future.
Co-authors
The 25 scholars most cited alongside Marco Ritelli, 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 80 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2015 | 99 | |
| 2 | 2013 | 99 | |
| 3 | 2012 | 76 | |
| 4 | 2014 | 70 | |
| 5 | 2019 | 53 | |
| 6 | 2013 | 52 | |
| 7 | 2016 | 44 | |
| 8 | 2015 | 41 | |
| 9 | 2018 | 38 | |
| 10 | 2014 | 38 | |
| 11 | 2013 | 37 | |
| 12 | 2018 | 36 | |
| 13 | 2016 | 34 | |
| 14 | 2015 | 32 | |
| 15 | 2017 | 31 | |
| 16 | 2020 | 31 | |
| 17 | 2014 | 30 | |
| 18 | 2017 | 30 | |
| 19 | 2016 | 30 | |
| 20 | 2014 | 30 |
About Marco Ritelli
Marco Ritelli is a scholar working on Genetics, Molecular Biology, Oncology, Rheumatology and Cell Biology, having authored 80 papers that have together received 1.7k indexed citations. Recurring topics across this work include Connective tissue disorders research (62 papers), Dermatological and Skeletal Disorders (26 papers), Ubiquitin and proteasome pathways (6 papers), Bone health and treatments (6 papers), Wnt/β-catenin signaling in development and cancer (5 papers), Dupuytren's Contracture and Treatments (5 papers), Protein Tyrosine Phosphatases (4 papers) and NF-κB Signaling Pathways (4 papers). The work is most often cited by research in Genetics (1.1k citations), Rheumatology (208 citations), Medical Terminology (2 citations), Immunology and Allergy (40 citations) and Nephrology (44 citations). Marco Ritelli has collaborated with scholars based in Italy, United States and Switzerland. Frequent co-authors include Marina Colombi, Nicola Chiarelli, Nicoletta Zoppi, Marina Venturini, Chiara Dordoni, Valeria Cinquina, Piergiacomo Calzavara‐Pinton, Marco Castori, Paola Grammatico and Silvia Morlino. Their work appears in journals such as Genes, Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, Orphanet Journal of Rare Diseases, European Journal of Human Genetics and Clinical 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.