Elisabetta Lenzini
- Co-authors
- C BaccichettiSveva BolliniMichela PozzobonU. WolfW. SchemppGerd SchererRomano TenconiMartina Piccoli
- Topics
- Genomic variations and chromosomal abnormalities (12 papers)Prenatal Screening and Diagnostics (8 papers)Chromosomal and Genetic Variations (4 papers)
- Partner nations
- ItalyUnited KingdomSwitzerland
In The Last Decade
Elisabetta Lenzini
25 papers receiving 398 citations
Peers
Comparison fields: 5 of 52
- Molecular Biology 212
- Genetics 205
- Surgery 112
- Genetics 105
- Pediatrics, Perinatology and Child Health 71
Countries citing papers authored by Elisabetta Lenzini
This map shows the geographic impact of Elisabetta Lenzini'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 Elisabetta Lenzini with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Elisabetta Lenzini more than expected).
Fields of papers citing papers by Elisabetta Lenzini
This network shows the impact of papers produced by Elisabetta Lenzini. 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 Elisabetta Lenzini. The network helps show where Elisabetta Lenzini may publish in the future.
Co-authorship network of co-authors of Elisabetta Lenzini
This figure shows the co-authorship network connecting the top 25 collaborators of Elisabetta Lenzini. A scholar is included among the top collaborators of Elisabetta Lenzini 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 Elisabetta Lenzini. Elisabetta Lenzini is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 2 | |
| 2 | 8 | |
| 3 | 21 | |
| 4 | 3 | |
| 5 | 3 | |
| 6 | 30 | |
| 7 | 114 | |
| 8 | 9 | |
| 9 | 19 | |
| 10 | Hypomelanosis of Ito: involvement of chromosome aberrations in this syndrome. | 11 |
| 11 | 7 | |
| 12 | 64 | |
| 13 | 29 | |
| 14 | Partial duplication of 17 long arm. | 7 |
| 15 | 10 | |
| 16 | 1 | |
| 17 | Dermatoglyphic pattern of the 9p syndrome. | 1 |
| 18 | 8 | |
| 19 | [The syndrome of trisomy 9p and presentation of 2 new cases]. | 1 |
| 20 | 13 |
About Elisabetta Lenzini
Elisabetta Lenzini is a scholar working on Genetics, Developmental Biology and Pediatrics, Perinatology and Child Health, having authored 25 papers that have together received 415 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (12 papers), Prenatal Screening and Diagnostics (8 papers) and Chromosomal and Genetic Variations (4 papers). The work is most often cited by research in Genetics (105 citations), Genetics (205 citations) and Pediatrics, Perinatology and Child Health (71 citations). Elisabetta Lenzini has collaborated with scholars based in Italy, United Kingdom and Switzerland. Frequent co-authors include C Baccichetti, Sveva Bollini, Michela Pozzobon, U. Wolf, W. Schempp, Gerd Scherer, Romano Tenconi, Martina Piccoli, Paolo De Coppi and Igor Vendramin. Their work appears in journals such as Gene, Journal of Molecular and Cellular Cardiology 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.