D. Franceschini
Impact in
- Developmental Biology top 10%
- Genetics top 10%
- Connective tissue disorders research
- Genetic Syndromes and Imprinting
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
Papers in
- Genetics 10
- Connective tissue disorders research 4
- Dermatological and Skeletal Disorders 3
- Genomic variations and chromosomal abnormalities 2
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- Protein Tyrosine Phosphatases 3
- Co-authors
- Andrea Guala (19 shared papers)P Franceschini (18 shared papers)Giuseppe Di Cara (13 shared papers)Piergiorgio Franceschini (4 shared papers)Andrea Saporito (2 shared papers)Luciano Anselmi (2 shared papers)José Aguirre (1 shared paper)Alain Borgeat (1 shared paper)
- Journals
- American Journal of Medical Genetics (15 papers)European Journal of Pediatrics (1 paper)Prenatal Diagnosis (1 paper)British Journal of Anaesthesia (1 paper)American Journal of Medical Genetics Part A (2 papers)
- Partner nations
- ItalySwitzerland
In The Last Decade
D. Franceschini
23 papers receiving 396 citations
Peers
Comparison fields: 5 of 57
- Developmental Biology 18
- Genetics 193
- Pharmacy 19
- Critical Care and Intensive Care Medicine 17
- Pediatrics, Perinatology and Child Health 56
Countries citing papers authored by D. Franceschini
This map shows the geographic impact of D. Franceschini'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 D. Franceschini with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites D. Franceschini more than expected).
Fields of papers citing papers by D. Franceschini
This network shows the impact of papers produced by D. Franceschini. 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 D. Franceschini. The network helps show where D. Franceschini may publish in the future.
Co-authors
The 25 scholars most cited alongside D. Franceschini, 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 25 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2017 | 47 | |
| 2 | 2000 | 45 | |
| 3 | 1993 | 42 | |
| 4 | 1993 | 41 | |
| 5 | 2000 | 38 | |
| 6 | 1999 | 32 | |
| 7 | 1995 | 28 | |
| 8 | 1995 | 27 | |
| 9 | 2013 | 17 | |
| 10 | 1992 | 13 | |
| 11 | 1996 | 11 | |
| 12 | 2003 | 10 | |
| 13 | 2021 | 10 | |
| 14 | 2001 | 10 | |
| 15 | The Williams syndrome: an Italian collaborative study. | 1996 | 7 |
| 16 | 1997 | 5 | |
| 17 | 1998 | 5 | |
| 18 | 1993 | 4 | |
| 19 | 1999 | 4 | |
| 20 | 2000 | 3 |
About D. Franceschini
D. Franceschini is a scholar working on Genetics, Molecular Biology, Developmental Biology, Surgery and Rheumatology, having authored 25 papers that have together received 407 indexed citations. Recurring topics across this work include Congenital limb and hand anomalies (6 papers), Connective tissue disorders research (4 papers), Dermatological and Skeletal Disorders (3 papers), Protein Tyrosine Phosphatases (3 papers), Oropharyngeal Anatomy and Pathologies (2 papers), Genomic variations and chromosomal abnormalities (2 papers), Chromosomal and Genetic Variations (2 papers) and Synthesis and Reactions of Organic Compounds (2 papers). The work is most often cited by research in Developmental Biology (18 citations), Genetics (193 citations), Pharmacy (19 citations), Critical Care and Intensive Care Medicine (17 citations) and Pediatrics, Perinatology and Child Health (56 citations). D. Franceschini has collaborated with scholars based in Italy and Switzerland. Frequent co-authors include Andrea Guala, P Franceschini, Giuseppe Di Cara, Piergiorgio Franceschini, Andrea Saporito, Luciano Anselmi, José Aguirre, Alain Borgeat, Samuele Ceruti and Lorenzo Genitori. Their work appears in journals such as American Journal of Medical Genetics, European Journal of Pediatrics, Prenatal Diagnosis, British Journal of Anaesthesia and American Journal of Medical Genetics Part A.
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.