Francesca Faravelli
Impact in
- Immunology top 2%
- T-cell and B-cell Immunology
- Immune Cell Function and Interaction
- Immunotherapy and Immune Responses
- Genetics top 2%
- Genomic variations and chromosomal abnormalities
- Diabetes and associated disorders
- Genetics and Neurodevelopmental Disorders
- Genetic Syndromes and Imprinting
Papers in
- Genetics 38
- Genomic variations and chromosomal abnormalities 18
- Genetics and Neurodevelopmental Disorders 11
- Genomics and Rare Diseases 5
- Connective tissue disorders research 4
- Co-authors
- F. Dagna BricarelliL PerroniJane PeakeMassimo MazzellaSean ProllGeoffrey C ByrneJean‐Laurent CasanovaOlivier Goulet
- Journals
- European Journal of Human Genetics (3 papers)The American Journal of Human Genetics (3 papers)European Journal of Medical Genetics (2 papers)Prenatal Diagnosis (2 papers)Human Mutation (2 papers)
- Partner nations
- ItalyUnited KingdomUnited States
In The Last Decade
Francesca Faravelli
60 papers receiving 2.8k citations
Hit Papers
Peers
Comparison fields: 5 of 105
- Immunology 1.2k
- Genetics 1.2k
- Developmental Biology 82
- Pediatrics, Perinatology and Child Health 294
- Molecular Biology 869
Countries citing papers authored by Francesca Faravelli
This map shows the geographic impact of Francesca Faravelli'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 Faravelli with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Francesca Faravelli more than expected).
Fields of papers citing papers by Francesca Faravelli
This network shows the impact of papers produced by Francesca Faravelli. 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 Faravelli. The network helps show where Francesca Faravelli may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Francesca Faravelli, 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 | 2025 | 0 | |
| 2 | 2024 | 3 | |
| 3 | 2023 | 3 | |
| 4 | 2023 | 9 | |
| 5 | 2022 | 1 | |
| 6 | 2018 | 104 | |
| 7 | 2016 | 30 | |
| 8 | 2013 | 12 | |
| 9 | 2012 | 21 | |
| 10 | 2010 | 16 | |
| 11 | 2010 | 19 | |
| 12 | 2009 | 15 | |
| 13 | 2008 | 4 | |
| 14 | 2007 | 42 | |
| 15 | 2006 | 34 | |
| 16 | 2006 | 9 | |
| 17 | 2005 | 8 | |
| 18 | 2003 | 156 | |
| 19 | 2002 | 3 | |
| 20 | X-linked neonatal diabetes mellitus, enteropathy and endocrinopathy syndrome is the human equivalent of mouse scurfy Hit paper breakdown → | 2001 | 1422 |
About Francesca Faravelli
Francesca Faravelli is a scholar working on Developmental Biology, Genetics, Immunology and Allergy, Pediatrics, Perinatology and Child Health and Molecular Biology, having authored 61 papers that have together received 2.9k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (18 papers), Genetics and Neurodevelopmental Disorders (11 papers), Congenital heart defects research (9 papers), Autism Spectrum Disorder Research (6 papers), Prenatal Screening and Diagnostics (6 papers), Genomics and Rare Diseases (5 papers), Hedgehog Signaling Pathway Studies (5 papers) and Connective tissue disorders research (4 papers). The work is most often cited by research in Immunology (1.2k citations), Genetics (1.2k citations), Developmental Biology (82 citations), Pediatrics, Perinatology and Child Health (294 citations) and Molecular Biology (869 citations). Francesca Faravelli has collaborated with scholars based in Italy, United Kingdom and United States. Frequent co-authors include F. Dagna Bricarelli, L Perroni, Jane Peake, Massimo Mazzella, Sean Proll, Geoffrey C Byrne, Jean‐Laurent Casanova, Olivier Goulet, Robert S. Wildin and Mark W. Appleby. Their work appears in journals such as European Journal of Human Genetics, The American Journal of Human Genetics, European Journal of Medical Genetics, Prenatal Diagnosis and Human Mutation.
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.