Daniela Melis
Impact in
- Rheumatology top 1%
- Glycogen Storage Diseases and Myoclonus
- Genetics top 5%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Connective tissue disorders research
- Genetic Syndromes and Imprinting
Papers in
- Rheumatology 45
- Glycogen Storage Diseases and Myoclonus 35
- Genetics 36
- Genomic variations and chromosomal abnormalities 12
- Genetics and Neurodevelopmental Disorders 7
- Connective tissue disorders research 6
- Co-authors
- Generoso Andria (32 shared papers)Giancarlo Parenti (26 shared papers)Roberto Della Casa (17 shared papers)Rosario Pivonello (16 shared papers)Rossella Parini (11 shared papers)Annamaria Colao (8 shared papers)Gaetano Lombardi (4 shared papers)Antongiulio Faggiano (3 shared papers)
- Journals
- The Journal of Pediatrics (5 papers)Orphanet Journal of Rare Diseases (5 papers)Journal of Inherited Metabolic Disease (5 papers)European Journal of Pediatrics (4 papers)Human Mutation (3 papers)
- Partner nations
- ItalyUnited StatesUnited Kingdom
In The Last Decade
Daniela Melis
106 papers receiving 1.8k citations
Peers
Comparison fields: 5 of 106
- Rheumatology 633
- Genetics 599
- Pharmacy 66
- Nephrology 83
- Neurology 158
Countries citing papers authored by Daniela Melis
This map shows the geographic impact of Daniela Melis'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 Daniela Melis with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Daniela Melis more than expected).
Fields of papers citing papers by Daniela Melis
This network shows the impact of papers produced by Daniela Melis. 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 Daniela Melis. The network helps show where Daniela Melis may publish in the future.
Co-authors
The 25 scholars most cited alongside Daniela Melis, 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 109 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2007 | 96 | |
| 2 | 2012 | 78 | |
| 3 | 2003 | 74 | |
| 4 | 2005 | 65 | |
| 5 | 2020 | 45 | |
| 6 | 1999 | 44 | |
| 7 | 2013 | 40 | |
| 8 | 2011 | 40 | |
| 9 | 2010 | 39 | |
| 10 | 2017 | 37 | |
| 11 | 2012 | 34 | |
| 12 | 2014 | 33 | |
| 13 | 2005 | 32 | |
| 14 | 2006 | 32 | |
| 15 | 2007 | 32 | |
| 16 | 2004 | 31 | |
| 17 | 2005 | 30 | |
| 18 | 2012 | 30 | |
| 19 | 2003 | 30 | |
| 20 | 2018 | 29 |
About Daniela Melis
Daniela Melis is a scholar working on Rheumatology, Genetics, Molecular Biology, Neurology and Physiology, having authored 109 papers that have together received 1.8k indexed citations. Recurring topics across this work include Glycogen Storage Diseases and Myoclonus (35 papers), Genomic variations and chromosomal abnormalities (12 papers), Carbohydrate Chemistry and Synthesis (10 papers), Neurofibromatosis and Schwannoma Cases (9 papers), Protein Tyrosine Phosphatases (7 papers), Lysosomal Storage Disorders Research (7 papers), Genetics and Neurodevelopmental Disorders (7 papers) and Connective tissue disorders research (6 papers). The work is most often cited by research in Rheumatology (633 citations), Genetics (599 citations), Pharmacy (66 citations), Nephrology (83 citations) and Neurology (158 citations). Daniela Melis has collaborated with scholars based in Italy, United States and United Kingdom. Frequent co-authors include Generoso Andria, Giancarlo Parenti, Roberto Della Casa, Rosario Pivonello, Rossella Parini, Annamaria Colao, Gaetano Lombardi, Antongiulio Faggiano, Mariagiovanna Filippella and Rita Genesio. Their work appears in journals such as The Journal of Pediatrics, Orphanet Journal of Rare Diseases, Journal of Inherited Metabolic Disease, European Journal of Pediatrics and Human Mutation.
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.