Giulia Arrigo
Impact in
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 5
- Genomic variations and chromosomal abnormalities 5
- Mesenchymal stem cell research 3
- Myeloproliferative Neoplasms: Diagnosis and Treatment 2
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- Acute Myeloid Leukemia Research 3
- Co-authors
- Orsetta Zuffardi (14 shared papers)Andrea Ballabio (2 shared papers)Cinzia Felicita Sala (3 shared papers)Daniela Toniolo (3 shared papers)Philippe Jonveaux (2 shared papers)Silvia Bione (1 shared paper)Christophe Philippe (1 shared paper)Sandro Banfi (1 shared paper)
- Journals
- Genomics (6 papers)Journal of Medical Genetics (2 papers)European Journal of Medical Genetics (1 paper)PLoS Genetics (1 paper)Cytogenetic and Genome Research (1 paper)
- Partner nations
- ItalyUnited StatesGermany
In The Last Decade
Giulia Arrigo
24 papers receiving 1.1k citations
Peers
Comparison fields: 5 of 72
- Genetics 644
- Pediatrics, Perinatology and Child Health 185
- Reproductive Medicine 69
- Molecular Biology 528
- Genetics 48
Countries citing papers authored by Giulia Arrigo
This map shows the geographic impact of Giulia Arrigo'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 Giulia Arrigo with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Giulia Arrigo more than expected).
Fields of papers citing papers by Giulia Arrigo
This network shows the impact of papers produced by Giulia Arrigo. 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 Giulia Arrigo. The network helps show where Giulia Arrigo may publish in the future.
Co-authors
The 25 scholars most cited alongside Giulia Arrigo, 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 25 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2007 | 255 | |
| 2 | 1998 | 221 | |
| 3 | 2011 | 173 | |
| 4 | 1997 | 112 | |
| 5 | 1996 | 110 | |
| 6 | 2007 | 105 | |
| 7 | 2000 | 42 | |
| 8 | 1998 | 33 | |
| 9 | 2015 | 27 | |
| 10 | 2012 | 24 | |
| 11 | 1997 | 23 | |
| 12 | 2023 | 20 | |
| 13 | 2011 | 19 | |
| 14 | 1999 | 12 | |
| 15 | 2014 | 11 | |
| 16 | 1998 | 7 | |
| 17 | 1999 | 6 | |
| 18 | 2022 | 5 | |
| 19 | 1998 | 4 | |
| 20 | 2021 | 3 |
About Giulia Arrigo
Giulia Arrigo is a scholar working on Genetics, Genetics, Hematology, Molecular Biology and Cancer Research, having authored 25 papers that have together received 1.2k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (5 papers), Chromosomal and Genetic Variations (4 papers), Cancer-related molecular mechanisms research (3 papers), Peptidase Inhibition and Analysis (3 papers), Acute Myeloid Leukemia Research (3 papers), Mesenchymal stem cell research (3 papers), Prenatal Screening and Diagnostics (2 papers) and Myeloproliferative Neoplasms: Diagnosis and Treatment (2 papers). The work is most often cited by research in Genetics (644 citations), Pediatrics, Perinatology and Child Health (185 citations), Reproductive Medicine (69 citations), Molecular Biology (528 citations) and Genetics (48 citations). Giulia Arrigo has collaborated with scholars based in Italy, United States and Germany. Frequent co-authors include Orsetta Zuffardi, Andrea Ballabio, Cinzia Felicita Sala, Daniela Toniolo, Philippe Jonveaux, Silvia Bione, Christophe Philippe, Sandro Banfi, Maurizio Zuccotti and M. Chiara Manzini. Their work appears in journals such as Genomics, Journal of Medical Genetics, European Journal of Medical Genetics, PLoS Genetics and Cytogenetic and Genome Research.
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.