Rosamaria Silipigni
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- Genomic variations and chromosomal abnormalities 12
- Genomics and Rare Diseases 5
- Genetic Syndromes and Imprinting 4
- Glioma Diagnosis and Treatment 3
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- MicroRNA in disease regulation 3
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- Genomic variations and chromosomal abnormalities 12
- Genomics and Rare Diseases 5
- Genetic Syndromes and Imprinting 4
- Glioma Diagnosis and Treatment 3
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- Congenital heart defects research 4
- Pluripotent Stem Cells Research 4
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- Prenatal Screening and Diagnostics 5
- Co-authors
- Silvana GuerneriMonica MiozzoLaura FontanaSilvia TabanoGiovanni MarfiaChiara PesentiAndrea TerrasiSilvano Bòsari
- Cited by
- GeneticsCancer ResearchNephrology
- Journals
- Stem Cell Research (6 papers)Journal of Intellectual Disability Research (2 papers)Prenatal Diagnosis (2 papers)
- Partner nations
- ItalyGermanyUnited States
In The Last Decade
Rosamaria Silipigni
32 papers receiving 262 citations
Peers
Comparison fields: 5 of 63
- Genetics 50
- Cancer Research 54
- Genetics 79
- Nephrology 15
- Molecular Biology 144
Countries citing papers authored by Rosamaria Silipigni
This map shows the geographic impact of Rosamaria Silipigni'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 Rosamaria Silipigni with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Rosamaria Silipigni more than expected).
Fields of papers citing papers by Rosamaria Silipigni
This network shows the impact of papers produced by Rosamaria Silipigni. 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 Rosamaria Silipigni. The network helps show where Rosamaria Silipigni may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Rosamaria Silipigni, 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 | 2024 | 0 | |
| 2 | 2024 | 2 | |
| 3 | 2023 | 1 | |
| 4 | 2022 | 0 | |
| 5 | 2022 | 27 | |
| 6 | 2022 | 1 | |
| 7 | 2021 | 1 | |
| 8 | 2021 | 5 | |
| 9 | 2020 | 12 | |
| 10 | 2019 | 18 | |
| 11 | 2019 | 4 | |
| 12 | 2018 | 13 | |
| 13 | 2017 | 3 | |
| 14 | 2017 | 2 | |
| 15 | 2016 | 19 | |
| 16 | 2015 | 8 | |
| 17 | 2015 | 2 | |
| 18 | 2015 | 4 | |
| 19 | 2015 | 23 | |
| 20 | 2015 | 2 |
About Rosamaria Silipigni
Rosamaria Silipigni is a scholar working on Genetics, Genetics, Developmental Biology, Molecular Biology and Cancer Research, having authored 35 papers that have together received 264 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (12 papers), Genomics and Rare Diseases (5 papers), Prenatal Screening and Diagnostics (5 papers), Genetic Syndromes and Imprinting (4 papers), Congenital heart defects research (4 papers), Pluripotent Stem Cells Research (4 papers), Glioma Diagnosis and Treatment (3 papers) and MicroRNA in disease regulation (3 papers). The work is most often cited by research in Genetics (50 citations), Cancer Research (54 citations), Genetics (79 citations), Nephrology (15 citations) and Molecular Biology (144 citations). Rosamaria Silipigni has collaborated with scholars based in Italy, Germany and United States. Frequent co-authors include Silvana Guerneri, Monica Miozzo, Laura Fontana, Silvia Tabano, Giovanni Marfia, Chiara Pesenti, Andrea Terrasi, Silvano Bòsari, Leda Paganini and Rolando Campanella. Their work appears in journals such as Stem Cell Research, Journal of Intellectual Disability Research, Prenatal Diagnosis, Journal of Visualized Experiments and Cytogenetic and Genome Research.
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.