Miriam Iannicelli
- Co-authors
- Bruno DallapiccolaFrancesco BrancatiIrene BottilloEmanuele BellacchioGiandomenico PalkaSigmar StrickerAlfredo RossiMarc Lopez
- Topics
- Genetic Syndromes and Imprinting (1 paper)Wnt/β-catenin signaling in development and cancer (1 paper)Skin and Cellular Biology Research (1 paper)
In The Last Decade
Miriam Iannicelli
3 papers receiving 145 citations
Peers
Comparison fields: 5 of 45
- Molecular Biology 70
- Genetics 42
- Immunology 29
- Pathology and Forensic Medicine 26
- Rheumatology 25
Countries citing papers authored by Miriam Iannicelli
This map shows the geographic impact of Miriam Iannicelli'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 Miriam Iannicelli with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Miriam Iannicelli more than expected).
Fields of papers citing papers by Miriam Iannicelli
This network shows the impact of papers produced by Miriam Iannicelli. 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 Miriam Iannicelli. The network helps show where Miriam Iannicelli may publish in the future.
Co-authorship network of co-authors of Miriam Iannicelli
This figure shows the co-authorship network connecting the top 25 collaborators of Miriam Iannicelli. A scholar is included among the top collaborators of Miriam Iannicelli based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Miriam Iannicelli. Miriam Iannicelli is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 91 | |
| 2 | A novel homozygous splice site mutation in the HPGD gene causes mild primary hypertrophic osteoarthropathy. | 29 |
| 3 | 25 |
About Miriam Iannicelli
Miriam Iannicelli is a scholar working on Immunology and Allergy, Rheumatology and Cell Biology, having authored 3 papers that have together received 145 indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (1 paper), Wnt/β-catenin signaling in development and cancer (1 paper) and Skin and Cellular Biology Research (1 paper). The work is most often cited by research in Rheumatology (25 citations), Genetics (42 citations) and Pathology and Forensic Medicine (26 citations). Miriam Iannicelli has collaborated with scholars based in Italy, France and Algeria. Frequent co-authors include Bruno Dallapiccola, Francesco Brancati, Irene Bottillo, Emanuele Bellacchio, Giandomenico Palka, Sigmar Stricker, Alfredo Rossi, Marc Lopez, Giovanna Zambruno and Uwe Kornak. Their work appears in journals such as The American Journal of Human Genetics, American Journal of Medical Genetics Part A and PubMed.
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.