Francesca Novara
- Genetics top 1%
- Molecular Biology top 10%
- Genetics top 5%
- Surgery top 10%
- Oncology top 10%
- Co-authors
- Orsetta ZuffardiRita MaccarioAngela CometaMaria Antonietta AvanziniAntonia MorettaMaria Ester BernardoFranco LocatelliRaffaella Villa
- Topics
- Genomic variations and chromosomal abnormalities (16 papers)Genetics and Neurodevelopmental Disorders (14 papers)Mesenchymal stem cell research (8 papers)
- Journals
- Nature CommunicationsBloodNeurology
- Partner nations
- ItalyUnited StatesUnited Kingdom
In The Last Decade
Francesca Novara
55 papers receiving 2.2k citations
Hit Papers
Peers
Comparison fields: 5 of 100
- Genetics 895
- Molecular Biology 881
- Genetics 579
- Surgery 505
- Oncology 289
Countries citing papers authored by Francesca Novara
This map shows the geographic impact of Francesca Novara'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 Novara with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Francesca Novara more than expected).
Fields of papers citing papers by Francesca Novara
This network shows the impact of papers produced by Francesca Novara. 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 Novara. The network helps show where Francesca Novara may publish in the future.
Co-authorship network of co-authors of Francesca Novara
This figure shows the co-authorship network connecting the top 25 collaborators of Francesca Novara. A scholar is included among the top collaborators of Francesca Novara based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Francesca Novara. Francesca Novara is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 11 | |
| 2 | 7 | |
| 3 | 3 | |
| 4 | 18 | |
| 5 | 19 | |
| 6 | 31 | |
| 7 | 11 | |
| 8 | 24 | |
| 9 | 11 | |
| 10 | 5 | |
| 11 | 2 | |
| 12 | 11 | |
| 13 | 18 | |
| 14 | Refining the phenotype associated with MEF2C haploinsufficiency | 4 |
| 15 | 171 | |
| 16 | 65 | |
| 17 | 99 | |
| 18 | 12 | |
| 19 | 50 | |
| 20 | 34 |
About Francesca Novara
Francesca Novara is a scholar working on Genetics, Genetics and Developmental Neuroscience, having authored 56 papers that have together received 2.3k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (16 papers), Genetics and Neurodevelopmental Disorders (14 papers) and Mesenchymal stem cell research (8 papers). The work is most often cited by research in Genetics (895 citations), Urology (143 citations) and Genetics (579 citations). Francesca Novara has collaborated with scholars based in Italy, United States and United Kingdom. Frequent co-authors include Orsetta Zuffardi, Rita Maccario, Angela Cometa, Maria Antonietta Avanzini, Antonia Moretta, Maria Ester Bernardo, Franco Locatelli, Raffaella Villa, Nadia Zaffaroni and Maria Grazia Daidone. Their work appears in journals such as Nature Communications, Blood and Neurology.
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.