Simone Pizzi
Impact in
- Genetics top 5%
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Molecular Biology top 10%
- Epigenetics and DNA Methylation
- Ion channel regulation and function
Papers in
- Genetics 37
- Genomics and Rare Diseases 22
- Genetics and Neurodevelopmental Disorders 12
- Genetic and Kidney Cyst Diseases 4
- Glioma Diagnosis and Treatment 3
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- Epigenetics and DNA Methylation 7
- Protein Tyrosine Phosphatases 4
- dental development and anomalies 3
- Co-authors
- Marco Tartaglia (34 shared papers)Sabina Barresi (13 shared papers)Alessandro Bruselles (10 shared papers)Andrea Ciolfi (13 shared papers)Bruno Dallapiccola (6 shared papers)Marcello Niceta (8 shared papers)Maria Lisa Dentici (4 shared papers)Emilia Stellacci (4 shared papers)
- Journals
- The American Journal of Human Genetics (10 papers)Genes (6 papers)Clinical Genetics (5 papers)European Journal of Human Genetics (4 papers)Nature Communications (3 papers)
- Partner nations
- ItalyUnited StatesNetherlands
In The Last Decade
Simone Pizzi
68 papers receiving 1.5k citations
Peers
Comparison fields: 5 of 85
- Genetics 701
- Molecular Biology 539
- Clinical Biochemistry 38
- Developmental Biology 16
- Cellular and Molecular Neuroscience 89
Countries citing papers authored by Simone Pizzi
This map shows the geographic impact of Simone Pizzi'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 Simone Pizzi with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Simone Pizzi more than expected).
Fields of papers citing papers by Simone Pizzi
This network shows the impact of papers produced by Simone Pizzi. 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 Simone Pizzi. The network helps show where Simone Pizzi may publish in the future.
Co-authors
The 25 scholars most cited alongside Simone Pizzi, 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 69 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2020 | 231 | |
| 2 | 2019 | 140 | |
| 3 | 2021 | 118 | |
| 4 | 2018 | 82 | |
| 5 | 2020 | 69 | |
| 6 | 2016 | 65 | |
| 7 | 2021 | 54 | |
| 8 | 2018 | 53 | |
| 9 | 2019 | 51 | |
| 10 | 2020 | 45 | |
| 11 | 2020 | 44 | |
| 12 | 2016 | 32 | |
| 13 | 2021 | 28 | |
| 14 | 2024 | 26 | |
| 15 | 2021 | 25 | |
| 16 | 2017 | 24 | |
| 17 | 2019 | 24 | |
| 18 | 2017 | 22 | |
| 19 | 2018 | 20 | |
| 20 | 2021 | 19 |
About Simone Pizzi
Simone Pizzi is a scholar working on Genetics, Molecular Biology, Cell Biology, Neurology and Immunology, having authored 69 papers that have together received 1.6k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (22 papers), Genetics and Neurodevelopmental Disorders (12 papers), Epigenetics and DNA Methylation (7 papers), Immunodeficiency and Autoimmune Disorders (5 papers), Protein Tyrosine Phosphatases (4 papers), Genetic and Kidney Cyst Diseases (4 papers), dental development and anomalies (3 papers) and Glioma Diagnosis and Treatment (3 papers). The work is most often cited by research in Genetics (701 citations), Molecular Biology (539 citations), Clinical Biochemistry (38 citations), Developmental Biology (16 citations) and Cellular and Molecular Neuroscience (89 citations). Simone Pizzi has collaborated with scholars based in Italy, United States and Netherlands. Frequent co-authors include Marco Tartaglia, Sabina Barresi, Alessandro Bruselles, Andrea Ciolfi, Bruno Dallapiccola, Marcello Niceta, Maria Lisa Dentici, Emilia Stellacci, Francesca Pantaleoni and Francesca Clementina Radio. Their work appears in journals such as The American Journal of Human Genetics, Genes, Clinical Genetics, European Journal of Human Genetics and Nature Communications.
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.