Francesca Mattioli
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- Genetics and Neurodevelopmental Disorders 5
- Genomics and Rare Diseases 4
- Genomic variations and chromosomal abnormalities 2
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- Congenital limb and hand anomalies 1
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- RNA modifications and cancer 4
- RNA Research and Splicing 2
- RNA and protein synthesis mechanisms 2
- Glycosylation and Glycoproteins Research 1
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- Genetics and Neurodevelopmental Disorders 5
- Genomics and Rare Diseases 4
- Genomic variations and chromosomal abnormalities 2
- Co-authors
- Jean‐Louis MandelAmélie PitonAlexandre ReymondSheila UngerBénédicte GérardAndrea Superti‐FurgaÉlise SchaeferMuhammad Ansar
- Partner nations
- SwitzerlandFrancePakistan
In The Last Decade
Francesca Mattioli
11 papers receiving 137 citations
Peers
Comparison fields: 5 of 44
- Genetics 74
- Developmental Biology 3
- Molecular Biology 90
- Genetics 9
- Developmental Neuroscience 3
Countries citing papers authored by Francesca Mattioli
This map shows the geographic impact of Francesca Mattioli'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 Francesca Mattioli with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Francesca Mattioli more than expected).
Fields of papers citing papers by Francesca Mattioli
This network shows the impact of papers produced by Francesca Mattioli. 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 Francesca Mattioli. The network helps show where Francesca Mattioli may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Francesca Mattioli, 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 | 2023 | 12 | |
| 2 | 2023 | 6 | |
| 3 | 2021 | 4 | |
| 4 | 2021 | 12 | |
| 5 | 2021 | 7 | |
| 6 | 2019 | 5 | |
| 7 | 2018 | 6 | |
| 8 | 2018 | 11 | |
| 9 | 2018 | 13 | |
| 10 | 2016 | 20 | |
| 11 | 2016 | 42 |
About Francesca Mattioli
Francesca Mattioli is a scholar working on Developmental Biology, Genetics and Genetics, having authored 11 papers that have together received 138 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (5 papers), RNA modifications and cancer (4 papers), Genomics and Rare Diseases (4 papers), Genomic variations and chromosomal abnormalities (2 papers), RNA Research and Splicing (2 papers), RNA and protein synthesis mechanisms (2 papers), Glycosylation and Glycoproteins Research (1 paper) and Congenital limb and hand anomalies (1 paper). The work is most often cited by research in Genetics (74 citations), Developmental Biology (3 citations) and Molecular Biology (90 citations). Francesca Mattioli has collaborated with scholars based in Switzerland, France and Pakistan. Frequent co-authors include Jean‐Louis Mandel, Amélie Piton, Alexandre Reymond, Sheila Unger, Bénédicte Gérard, Andrea Superti‐Furga, Élise Schaefer, Muhammad Ansar, Paul R. Mark and Gaëlle Vieville.
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.