Stefania Gimelli
Impact in
- Genetics top 1%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetic Associations and Epidemiology
- Developmental Biology top 2%
Papers in
- Genetics 61
- Genomic variations and chromosomal abnormalities 46
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 7
- Genetics and Neurodevelopmental Disorders 5
- Genomics and Rare Diseases 3
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- Congenital limb and hand anomalies 5
- Co-authors
- Giorgio Gimelli (26 shared papers)Orsetta Zuffardi (17 shared papers)Frederique Sloan Bena (27 shared papers)Roberto Giorda (9 shared papers)Maria Teresa Divizia (10 shared papers)Stylianos E. Antonarakis (9 shared papers)Margherita Lerone (10 shared papers)Silvana Beri (7 shared papers)
- Journals
- European Journal of Medical Genetics (9 papers)PLoS ONE (5 papers)Journal of Medical Genetics (4 papers)Human Mutation (4 papers)European Journal of Human Genetics (3 papers)
- Partner nations
- SwitzerlandItalyUnited States
In The Last Decade
Stefania Gimelli
78 papers receiving 3.4k citations
Stefania Gimelli's Hit Papers
Peers
Comparison fields: 5 of 98
- Genetics 2.3k
- Developmental Biology 84
- Pediatrics, Perinatology and Child Health 295
- Developmental Neuroscience 59
- Psychiatry and Mental health 172
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 79 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Recurrent Rearrangements of Chromosome 1q21.1 and Variable Pediatric Phenotypes Hit paper breakdown → | 2008 | 629 |
| 2 | 2011 | 371 | |
| 3 | 2007 | 256 | |
| 4 | 2011 | 176 | |
| 5 | 2007 | 150 | |
| 6 | 2013 | 145 | |
| 7 | 2009 | 116 | |
| 8 | 2007 | 111 | |
| 9 | 2007 | 107 | |
| 10 | 2007 | 106 | |
| 11 | 2008 | 101 | |
| 12 | 2013 | 95 | |
| 13 | 2009 | 77 | |
| 14 | 2014 | 73 | |
| 15 | 2010 | 69 | |
| 16 | 2015 | 65 | |
| 17 | 2006 | 63 | |
| 18 | 2012 | 57 | |
| 19 | 2010 | 53 | |
| 20 | 2011 | 49 |
About Stefania Gimelli
Stefania Gimelli is a scholar working on Genetics, Developmental Biology, Pediatrics, Perinatology and Child Health, Molecular Biology and Reproductive Medicine, having authored 79 papers that have together received 3.8k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (46 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (7 papers), Pluripotent Stem Cells Research (5 papers), Congenital limb and hand anomalies (5 papers), Genetics and Neurodevelopmental Disorders (5 papers), Down syndrome and intellectual disability research (3 papers), Genomics and Rare Diseases (3 papers) and Congenital gastrointestinal and neural anomalies (3 papers). The work is most often cited by research in Genetics (2.3k citations), Developmental Biology (84 citations), Pediatrics, Perinatology and Child Health (295 citations), Developmental Neuroscience (59 citations) and Psychiatry and Mental health (172 citations). Stefania Gimelli has collaborated with scholars based in Switzerland, Italy and United States. Frequent co-authors include Giorgio Gimelli, Orsetta Zuffardi, Frederique Sloan Bena, 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, Journal of Medical Genetics, Human Mutation and European Journal of Human Genetics.
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.