Sabrina Giglio
- Genetics top 1%
- Genomic variations and chromosomal abnormalities 25
- Genetics and Neurodevelopmental Disorders 18
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 9
- Genomics and Rare Diseases 8
- Connective tissue disorders research 6
- Nephrology top 5%
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- Prenatal Screening and Diagnostics 8
- Molecular Biology top 5%
- RNA modifications and cancer 7
- Genetics top 10%
- Genomic variations and chromosomal abnormalities 25
- Genetics and Neurodevelopmental Disorders 18
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 9
- Genomics and Rare Diseases 8
- Connective tissue disorders research 6
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- Chromosomal and Genetic Variations 11
- Co-authors
- Orsetta ZuffardiGiorgio GimelliRoberto GiordaVladimiro CalvariElena RossiLucille VoullaireRenzo GuerriniKarl W. Broman
- Journals
- European Journal of Human Genetics (5 papers)Clinical Genetics (5 papers)European Journal of Medical Genetics (4 papers)
- Partner nations
- ItalyUnited StatesGermany
In The Last Decade
Sabrina Giglio
112 papers receiving 2.5k citations
Peers
Comparison fields: 5 of 104
- Genetics 1.3k
- Nephrology 195
- Pediatrics, Perinatology and Child Health 422
- Molecular Biology 1.5k
- Genetics 149
Countries citing papers authored by Sabrina Giglio
This map shows the geographic impact of Sabrina Giglio'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 Sabrina Giglio with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sabrina Giglio more than expected).
Fields of papers citing papers by Sabrina Giglio
This network shows the impact of papers produced by Sabrina Giglio. 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 Sabrina Giglio. The network helps show where Sabrina Giglio may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Sabrina Giglio, 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 | 2025 | 2 | |
| 2 | 2023 | 3 | |
| 3 | 2022 | 4 | |
| 4 | 2022 | 2 | |
| 5 | 2022 | 29 | |
| 6 | 2021 | 3 | |
| 7 | 2021 | 6 | |
| 8 | 2021 | 3 | |
| 9 | 2021 | 2 | |
| 10 | 2021 | 34 | |
| 11 | 2020 | 5 | |
| 12 | 2020 | 3 | |
| 13 | 2020 | 28 | |
| 14 | 2019 | 21 | |
| 15 | 2019 | 14 | |
| 16 | 2018 | 12 | |
| 17 | 2017 | 0 | |
| 18 | Anti-miR21 oligonucleotide enhances chemosensitivity of T98G cell line to doxorubicin by inducing apoptosis. | 2015 | 36 |
| 19 | Heterogeneous Genetic Alterations Predict Resistance To Immunosuppressive Treatments In Sporadic Steroid-resistant Nephrotic Syndrome. | 2014 | 3 |
| 20 | 2000 | 53 |
About Sabrina Giglio
Sabrina Giglio is a scholar working on Genetics, Nephrology and Developmental Biology, having authored 116 papers that have together received 2.6k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (25 papers), Genetics and Neurodevelopmental Disorders (18 papers), Chromosomal and Genetic Variations (11 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (9 papers), Genomics and Rare Diseases (8 papers), Prenatal Screening and Diagnostics (8 papers), RNA modifications and cancer (7 papers) and Connective tissue disorders research (6 papers). The work is most often cited by research in Genetics (1.3k citations), Nephrology (195 citations) and Pediatrics, Perinatology and Child Health (422 citations). Sabrina Giglio has collaborated with scholars based in Italy, United States and Germany. Frequent co-authors include Orsetta Zuffardi, Giorgio Gimelli, Roberto Giorda, Vladimiro Calvari, Elena Rossi, Lucille Voullaire, Renzo Guerrini, Karl W. Broman, Daniela Larizza and Hirofumi Ohashi. Their work appears in journals such as European Journal of Human Genetics, Clinical Genetics, European Journal of Medical Genetics, Nephrology Dialysis Transplantation and The American 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.