Giorgio Gimelli
- Genetics top 0.5%
- Genomic variations and chromosomal abnormalities 50
- Genetics and Neurodevelopmental Disorders 20
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 14
- Plant Science top 2%
- Chromosomal and Genetic Variations 19
- Molecular Biology top 5%
- Congenital heart defects research 14
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- Prenatal Screening and Diagnostics 11
- Developmental Biology top 10%
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- Coronary Interventions and Diagnostics 8
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- Immunodeficiency and Autoimmune Disorders 8
- Co-authors
- Orsetta ZuffardiCristina CuocoStefania GimelliRoberto GiordaSabrina GiglioElisa TassanoPeter E. WarburtonChris Tyler‐Smith
- Journals
- Human Genetics (15 papers)European Journal of Medical Genetics (9 papers)Molecular Cytogenetics (8 papers)
- Partner nations
- ItalyUnited StatesSwitzerland
In The Last Decade
Giorgio Gimelli
126 papers receiving 3.3k citations
Peers
Comparison fields: 5 of 106
- Genetics 1.9k
- Plant Science 949
- Molecular Biology 1.7k
- Pediatrics, Perinatology and Child Health 495
- Developmental Biology 36
Countries citing papers authored by Giorgio Gimelli
This map shows the geographic impact of Giorgio 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 Giorgio Gimelli with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Giorgio Gimelli more than expected).
Fields of papers citing papers by Giorgio Gimelli
This network shows the impact of papers produced by Giorgio 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 Giorgio Gimelli. The network helps show where Giorgio Gimelli may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Giorgio 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
| # | Work | ||
|---|---|---|---|
| 1 | 2022 | 0 | |
| 2 | 2020 | 9 | |
| 3 | 2018 | 10 | |
| 4 | 2018 | 6 | |
| 5 | 2015 | 26 | |
| 6 | 2015 | 1 | |
| 7 | 2015 | 4 | |
| 8 | 2015 | 13 | |
| 9 | 2013 | 9 | |
| 10 | 2013 | 14 | |
| 11 | 2012 | 2 | |
| 12 | 2009 | 4 | |
| 13 | 2008 | 75 | |
| 14 | 2006 | 24 | |
| 15 | 2005 | 14 | |
| 16 | 2001 | 288 | |
| 17 | Endovascular treatment of a noninfected anastomotic juxtarenal aortic aneurysm. | 2000 | 13 |
| 18 | 1999 | 98 | |
| 19 | 1996 | 14 | |
| 20 | 1994 | 3 |
About Giorgio Gimelli
Giorgio Gimelli is a scholar working on Genetics, Developmental Biology, Molecular Biology, Immunology and Allergy and Cardiology and Cardiovascular Medicine, having authored 128 papers that have together received 3.4k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (50 papers), Genetics and Neurodevelopmental Disorders (20 papers), Chromosomal and Genetic Variations (19 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (14 papers), Congenital heart defects research (14 papers), Prenatal Screening and Diagnostics (11 papers), Coronary Interventions and Diagnostics (8 papers) and Immunodeficiency and Autoimmune Disorders (8 papers). The work is most often cited by research in Genetics (1.9k citations), Plant Science (949 citations), Molecular Biology (1.7k citations), Pediatrics, Perinatology and Child Health (495 citations) and Developmental Biology (36 citations). Giorgio Gimelli has collaborated with scholars based in Italy, United States and Switzerland. Frequent co-authors include Orsetta Zuffardi, Cristina Cuoco, Stefania Gimelli, Roberto Giorda, Sabrina Giglio, Elisa Tassano, Peter E. Warburton, Chris Tyler‐Smith, William C. Earnshaw and Margherita Lerone. Their work appears in journals such as Human Genetics, European Journal of Medical Genetics, Molecular Cytogenetics, Cytogenetic and Genome Research 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.