Tommaso Pippucci
- Genetics top 5%
- Genomics and Rare Diseases 22
- Genetics and Neurodevelopmental Disorders 15
- Genomic variations and chromosomal abnormalities 12
- Cancer Research top 10%
- Cancer Genomics and Diagnostics 7
- Clinical Biochemistry top 5%
- Metabolism and Genetic Disorders 6
- Molecular Biology top 10%
- Ion channel regulation and function 6
- Genomics and Phylogenetic Studies 5
- Psychiatry and Mental health top 10%
- Epilepsy research and treatment 7
- Co-authors
- Alberto MagiMarco SeriLorenzo TattiniMatteo BenelliBetti GiustiFrancesca BisulliFlavia PalomboG. Cara Romeo
- Partner nations
- ItalyUnited StatesGermany
In The Last Decade
Tommaso Pippucci
69 papers receiving 1.5k citations
Peers
Comparison fields: 5 of 103
- Genetics 663
- Cancer Research 215
- Clinical Biochemistry 82
- Molecular Biology 708
- Psychiatry and Mental health 154
Countries citing papers authored by Tommaso Pippucci
This map shows the geographic impact of Tommaso Pippucci'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 Tommaso Pippucci with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Tommaso Pippucci more than expected).
Fields of papers citing papers by Tommaso Pippucci
This network shows the impact of papers produced by Tommaso Pippucci. 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 Tommaso Pippucci. The network helps show where Tommaso Pippucci may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Tommaso Pippucci, 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 | 2024 | 2 | |
| 2 | 2024 | 17 | |
| 3 | 2024 | 0 | |
| 4 | 2024 | 1 | |
| 5 | 2024 | 5 | |
| 6 | 2022 | 11 | |
| 7 | 2020 | 0 | |
| 8 | 2020 | 27 | |
| 9 | 2020 | 6 | |
| 10 | 2019 | 30 | |
| 11 | 2019 | 6 | |
| 12 | 2018 | 37 | |
| 13 | 2018 | 25 | |
| 14 | 2017 | 7 | |
| 15 | 2017 | 11 | |
| 16 | 2016 | 70 | |
| 17 | 2014 | 4 | |
| 18 | 2013 | 32 | |
| 19 | 2011 | 13 | |
| 20 | 2008 | 12 |
About Tommaso Pippucci
Tommaso Pippucci is a scholar working on Genetics, Clinical Biochemistry and Hematology, having authored 71 papers that have together received 1.5k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (22 papers), Genetics and Neurodevelopmental Disorders (15 papers), Genomic variations and chromosomal abnormalities (12 papers), Cancer Genomics and Diagnostics (7 papers), Epilepsy research and treatment (7 papers), Metabolism and Genetic Disorders (6 papers), Ion channel regulation and function (6 papers) and Genomics and Phylogenetic Studies (5 papers). The work is most often cited by research in Genetics (663 citations), Cancer Research (215 citations) and Clinical Biochemistry (82 citations). Tommaso Pippucci has collaborated with scholars based in Italy, United States and Germany. Frequent co-authors include Alberto Magi, Marco Seri, Lorenzo Tattini, Matteo Benelli, Betti Giusti, Francesca Bisulli, Flavia Palombo, G. Cara Romeo, Romina D’Aurizio and Laura Licchetta. Their work appears in journals such as Nucleic Acids Research, Blood and Bioinformatics.
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.