Silvia Russo
Impact in
- Genetics top 0.5%
- Genetic Syndromes and Imprinting
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 88
- Genetic Syndromes and Imprinting 39
- Genomic variations and chromosomal abnormalities 32
- Genetics and Neurodevelopmental Disorders 29
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- Epigenetics and DNA Methylation 33
- Genomics and Chromatin Dynamics 23
- RNA Research and Splicing 16
- RNA modifications and cancer 14
- Co-authors
- Lidia Larizza (63 shared papers)Angelo Selicorni (33 shared papers)Cristina Gervasini (22 shared papers)Andrea Riccio (14 shared papers)Donatella Milani (14 shared papers)Giovanni Battista Ferrero (11 shared papers)Alessandro Mussa (9 shared papers)Maria Luisa Focarelli (1 shared paper)
- Journals
- Clinical Genetics (9 papers)International Journal of Molecular Sciences (5 papers)Clinical Epigenetics (4 papers)European Journal of Human Genetics (4 papers)The Journal of Clinical Endocrinology & Metabolism (4 papers)
- Partner nations
- ItalyUnited StatesUnited Kingdom
In The Last Decade
Silvia Russo
132 papers receiving 3.2k citations
Peers
Comparison fields: 5 of 115
- Genetics 1.9k
- Pediatrics, Perinatology and Child Health 900
- Molecular Biology 1.9k
- Developmental Biology 54
- Pathology and Forensic Medicine 298
Countries citing papers authored by Silvia Russo
This map shows the geographic impact of Silvia Russo'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 Silvia Russo with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Silvia Russo more than expected).
Fields of papers citing papers by Silvia Russo
This network shows the impact of papers produced by Silvia Russo. 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 Silvia Russo. The network helps show where Silvia Russo may publish in the future.
Co-authors
The 25 scholars most cited alongside Silvia Russo, 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 136 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2006 | 335 | |
| 2 | 2008 | 151 | |
| 3 | 2013 | 142 | |
| 4 | 2011 | 98 | |
| 5 | 2016 | 98 | |
| 6 | 2013 | 84 | |
| 7 | 2006 | 76 | |
| 8 | 2007 | 72 | |
| 9 | 2009 | 71 | |
| 10 | 2007 | 71 | |
| 11 | 2016 | 70 | |
| 12 | 2010 | 63 | |
| 13 | 1992 | 61 | |
| 14 | 2009 | 58 | |
| 15 | 2009 | 55 | |
| 16 | 2015 | 54 | |
| 17 | 2019 | 54 | |
| 18 | 2015 | 52 | |
| 19 | 2015 | 51 | |
| 20 | 2010 | 48 |
About Silvia Russo
Silvia Russo is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Cognitive Neuroscience and Plant Science, having authored 136 papers that have together received 3.3k indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (39 papers), Prenatal Screening and Diagnostics (33 papers), Epigenetics and DNA Methylation (33 papers), Genomic variations and chromosomal abnormalities (32 papers), Genetics and Neurodevelopmental Disorders (29 papers), Genomics and Chromatin Dynamics (23 papers), RNA Research and Splicing (16 papers) and RNA modifications and cancer (14 papers). The work is most often cited by research in Genetics (1.9k citations), Pediatrics, Perinatology and Child Health (900 citations), Molecular Biology (1.9k citations), Developmental Biology (54 citations) and Pathology and Forensic Medicine (298 citations). Silvia Russo has collaborated with scholars based in Italy, United States and United Kingdom. Frequent co-authors include Lidia Larizza, Angelo Selicorni, Cristina Gervasini, Andrea Riccio, Donatella Milani, Giovanni Battista Ferrero, Alessandro Mussa, Maria Luisa Focarelli, Paolo Vezzoni and Francesca Cogliati. Their work appears in journals such as Clinical Genetics, International Journal of Molecular Sciences, Clinical Epigenetics, European Journal of Human Genetics and The Journal of Clinical Endocrinology & Metabolism.
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.