Stefania Gimelli
Impact in
- Genetics top 2%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Developmental Biology top 10%
Papers in
- Genetics 44
- Genomic variations and chromosomal abnormalities 22
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 8
- Genetics and Neurodevelopmental Disorders 8
- Genomics and Rare Diseases 5
- Genetic Mapping and Diversity in Plants and Animals 3
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- Congenital heart defects research 12
- Sexual Differentiation and Disorders 4
- Co-authors
- Giorgio Gimelli (26 shared papers)Orsetta Zuffardi (16 shared papers)Frédérique Béna (16 shared papers)Roberto Giorda (9 shared papers)Maria Teresa Divizia (10 shared papers)Stylianos E. Antonarakis (8 shared papers)Margherita Lerone (10 shared papers)Silvana Beri (7 shared papers)
- Journals
- European Journal of Medical Genetics (8 papers)PLoS ONE (5 papers)European Journal of Human Genetics (3 papers)Orphanet Journal of Rare Diseases (3 papers)Human Mutation (3 papers)
- Partner nations
- SwitzerlandItalyUnited States
In The Last Decade
Stefania Gimelli
64 papers receiving 1.6k citations
Peers
Comparison fields: 5 of 95
- Genetics 886
- Developmental Biology 33
- Pediatrics, Perinatology and Child Health 200
- Molecular Biology 712
- Developmental Neuroscience 33
Countries citing papers authored by Stefania Gimelli
This map shows the geographic impact of Stefania Gimelli'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 Stefania Gimelli with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Stefania Gimelli more than expected).
Fields of papers citing papers by Stefania Gimelli
This network shows the impact of papers produced by Stefania Gimelli. 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 Stefania Gimelli. The network helps show where Stefania Gimelli may publish in the future.
Co-authors
The 25 scholars most cited alongside Stefania Gimelli, 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 64 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2013 | 139 | |
| 2 | 2007 | 135 | |
| 3 | 2009 | 110 | |
| 4 | 2007 | 108 | |
| 5 | 2007 | 98 | |
| 6 | 2008 | 96 | |
| 7 | 2010 | 69 | |
| 8 | 2006 | 63 | |
| 9 | 2012 | 54 | |
| 10 | 2010 | 46 | |
| 11 | 2010 | 45 | |
| 12 | 2011 | 42 | |
| 13 | 2010 | 40 | |
| 14 | 2013 | 33 | |
| 15 | 2005 | 29 | |
| 16 | 2015 | 28 | |
| 17 | 2012 | 28 | |
| 18 | 2014 | 26 | |
| 19 | 2008 | 26 | |
| 20 | 2014 | 26 |
About Stefania Gimelli
Stefania Gimelli is a scholar working on Genetics, Molecular Biology, Plant Science, Surgery and Pediatrics, Perinatology and Child Health, having authored 64 papers that have together received 1.7k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (22 papers), Congenital heart defects research (12 papers), Chromosomal and Genetic Variations (11 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (8 papers), Genetics and Neurodevelopmental Disorders (8 papers), Genomics and Rare Diseases (5 papers), Sexual Differentiation and Disorders (4 papers) and Genetic Mapping and Diversity in Plants and Animals (3 papers). The work is most often cited by research in Genetics (886 citations), Developmental Biology (33 citations), Pediatrics, Perinatology and Child Health (200 citations), Molecular Biology (712 citations) and Developmental Neuroscience (33 citations). Stefania Gimelli has collaborated with scholars based in Switzerland, Italy and United States. Frequent co-authors include Giorgio Gimelli, Orsetta Zuffardi, Frédérique Béna, Roberto Giorda, Maria Teresa Divizia, Stylianos E. Antonarakis, Margherita Lerone, Silvana Beri, Elisa Tassano and Renata Bocciardi. Their work appears in journals such as European Journal of Medical Genetics, PLoS ONE, European Journal of Human Genetics, Orphanet Journal of Rare Diseases 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.