Francesca Faravelli
Impact in
- Immunology top 2%
- T-cell and B-cell Immunology
- Immune Cell Function and Interaction
- Immunotherapy and Immune Responses
- Genetics top 1%
- Genomic variations and chromosomal abnormalities
- Diabetes and associated disorders
- Genetics and Neurodevelopmental Disorders
- Genetic Syndromes and Imprinting
Papers in
- Genetics 33
- Genomic variations and chromosomal abnormalities 16
- Genetics and Neurodevelopmental Disorders 7
- Connective tissue disorders research 4
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- Congenital heart defects research 9
- Hedgehog Signaling Pathway Studies 5
- Co-authors
- F. Dagna Bricarelli (8 shared papers)L Perroni (5 shared papers)Olivier Goulet (1 shared paper)Massimo Mazzella (1 shared paper)Geoffrey C Byrne (1 shared paper)Fred Ramsdell (1 shared paper)Robert S. Wildin (1 shared paper)Sean Proll (1 shared paper)
- 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
61 papers receiving 2.8k citations
Francesca Faravelli's Hit Papers
Peers
Comparison fields: 5 of 102
- Immunology 1.1k
- Genetics 1.1k
- Developmental Biology 80
- Pediatrics, Perinatology and Child Health 207
- Molecular Biology 779
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-authors
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
Showing the 20 most-cited of 63 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | X-linked neonatal diabetes mellitus, enteropathy and endocrinopathy syndrome is the human equivalent of mouse scurfy Hit paper breakdown → | 2001 | 1431 |
| 2 | 2005 | 224 | |
| 3 | 2003 | 156 | |
| 4 | 2018 | 105 | |
| 5 | 2011 | 58 | |
| 6 | 2015 | 51 | |
| 7 | 2006 | 51 | |
| 8 | 2005 | 45 | |
| 9 | 2007 | 41 | |
| 10 | 2016 | 39 | |
| 11 | 2006 | 38 | |
| 12 | 2005 | 37 | |
| 13 | 2006 | 34 | |
| 14 | 2007 | 34 | |
| 15 | 2012 | 32 | |
| 16 | 2016 | 30 | |
| 17 | 2014 | 29 | |
| 18 | 2013 | 26 | |
| 19 | 2006 | 26 | |
| 20 | 1999 | 25 |
About Francesca Faravelli
Francesca Faravelli is a scholar working on Genetics, Molecular Biology, Surgery, Pediatrics, Perinatology and Child Health and Cognitive Neuroscience, having authored 63 papers that have together received 2.9k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (16 papers), Congenital heart defects research (9 papers), Genetics and Neurodevelopmental Disorders (7 papers), Autism Spectrum Disorder Research (6 papers), Hedgehog Signaling Pathway Studies (5 papers), Prenatal Screening and Diagnostics (4 papers), Connective tissue disorders research (4 papers) and Genetic factors in colorectal cancer (4 papers). The work is most often cited by research in Immunology (1.1k citations), Genetics (1.1k citations), Developmental Biology (80 citations), Pediatrics, Perinatology and Child Health (207 citations) and Molecular Biology (779 citations). Francesca Faravelli has collaborated with scholars based in Italy, United Kingdom and United States. Frequent co-authors include F. Dagna Bricarelli, L Perroni, Olivier Goulet, Massimo Mazzella, Geoffrey C Byrne, Fred Ramsdell, Robert S. Wildin, Sean Proll, Mary E. Brunkow 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.