Elisa Savin
Impact in
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- Prenatal Screening and Diagnostics
- Fetal and Pediatric Neurological Disorders
Papers in
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- Hedgehog Signaling Pathway Studies 2
- Congenital heart defects research 1
- DNA and Nucleic Acid Chemistry 1
- Genetics 4
- Genomic variations and chromosomal abnormalities 3
- Genomics and Rare Diseases 1
- Co-authors
- Cristiana Marchese (1 shared paper)Mario Marchi (1 shared paper)A. O. Carbonara (1 shared paper)G Pagliano (1 shared paper)E. Viora (2 shared papers)Francesca Carozzi (1 shared paper)M Campogrande (1 shared paper)Eleonora Di Gregorio (3 shared papers)
In The Last Decade
Elisa Savin
6 papers receiving 54 citations
Peers
Comparison fields: 5 of 22
- Pediatrics, Perinatology and Child Health 30
- Developmental Biology 2
- Surgery 29
- Urology 4
- Pathology and Forensic Medicine 10
Countries citing papers authored by Elisa Savin
This map shows the geographic impact of Elisa Savin'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 Elisa Savin with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Elisa Savin more than expected).
Fields of papers citing papers by Elisa Savin
This network shows the impact of papers produced by Elisa Savin. 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 Elisa Savin. The network helps show where Elisa Savin may publish in the future.
Co-authors
The 25 scholars most cited alongside Elisa Savin, 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 | 1985 | 36 | |
| 2 | 2017 | 8 | |
| 3 | 1987 | 6 | |
| 4 | 1989 | 4 | |
| 5 | 2015 | 2 | |
| 6 | 2014 | 1 |
About Elisa Savin
Elisa Savin is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Surgery and Developmental Biology, having authored 6 papers that have together received 57 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (3 papers), Prenatal Screening and Diagnostics (2 papers), Hedgehog Signaling Pathway Studies (2 papers), Congenital heart defects research (1 paper), interferon and immune responses (1 paper), Congenital limb and hand anomalies (1 paper), DNA and Nucleic Acid Chemistry (1 paper) and Genomics and Rare Diseases (1 paper). The work is most often cited by research in Pediatrics, Perinatology and Child Health (30 citations), Developmental Biology (2 citations), Surgery (29 citations), Urology (4 citations) and Pathology and Forensic Medicine (10 citations). Elisa Savin has collaborated with scholars based in Italy, Singapore and Sudan. Frequent co-authors include Cristiana Marchese, Mario Marchi, A. O. Carbonara, G Pagliano, E. Viora, Francesca Carozzi, M Campogrande, Eleonora Di Gregorio, Cecilia Mancini and Fabio Sirchia. Their work appears in journals such as European Journal of Medical Genetics, Journal of Medical Genetics, Prenatal Diagnosis, Cytogenetic and Genome Research and Cancer Genetics and Cytogenetics.
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.