Federica Natacci
Impact in
- Neurology top 5%
- Neurofibromatosis and Schwannoma Cases
- Vascular Malformations Diagnosis and Treatment
- Neuroblastoma Research and Treatments
-
- Prenatal Screening and Diagnostics
Papers in
- Co-authors
- Faustina Lalatta (14 shared papers)Lidia Larizza (13 shared papers)Paola Riva (10 shared papers)Maria Francesca Bedeschi (14 shared papers)Cristina Curcio (3 shared papers)Angelo Selicorni (5 shared papers)Giulia Melloni (6 shared papers)The‐Hung Bui (1 shared paper)
- Journals
- Prenatal Diagnosis (4 papers)Human Genetics (3 papers)Journal of Child Neurology (2 papers)Cancers (2 papers)European Journal of Human Genetics (2 papers)
- Partner nations
- ItalyUnited StatesUnited Kingdom
In The Last Decade
Federica Natacci
49 papers receiving 679 citations
Peers
Comparison fields: 5 of 56
- Neurology 251
- Pediatrics, Perinatology and Child Health 160
- Genetics 229
- Developmental Neuroscience 24
- Rheumatology 58
Countries citing papers authored by Federica Natacci
This map shows the geographic impact of Federica Natacci'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 Federica Natacci with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Federica Natacci more than expected).
Fields of papers citing papers by Federica Natacci
This network shows the impact of papers produced by Federica Natacci. 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 Federica Natacci. The network helps show where Federica Natacci may publish in the future.
Co-authors
The 25 scholars most cited alongside Federica Natacci, 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 54 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2011 | 96 | |
| 2 | 2000 | 71 | |
| 3 | 2004 | 65 | |
| 4 | 2013 | 36 | |
| 5 | 2004 | 33 | |
| 6 | 2003 | 28 | |
| 7 | 2016 | 27 | |
| 8 | 2015 | 26 | |
| 9 | 2002 | 23 | |
| 10 | 2009 | 23 | |
| 11 | 2011 | 22 | |
| 12 | 2012 | 21 | |
| 13 | 2015 | 19 | |
| 14 | 2000 | 17 | |
| 15 | 2019 | 17 | |
| 16 | 2013 | 16 | |
| 17 | 2000 | 15 | |
| 18 | 2008 | 15 | |
| 19 | 2008 | 14 | |
| 20 | 2008 | 14 |
About Federica Natacci
Federica Natacci is a scholar working on Neurology, Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health and Pulmonary and Respiratory Medicine, having authored 54 papers that have together received 731 indexed citations. Recurring topics across this work include Neurofibromatosis and Schwannoma Cases (18 papers), Genomic variations and chromosomal abnormalities (10 papers), Sarcoma Diagnosis and Treatment (7 papers), Prenatal Screening and Diagnostics (6 papers), Genetics and Neurodevelopmental Disorders (6 papers), Neuroblastoma Research and Treatments (4 papers), Chromatin Remodeling and Cancer (4 papers) and Congenital heart defects research (3 papers). The work is most often cited by research in Neurology (251 citations), Pediatrics, Perinatology and Child Health (160 citations), Genetics (229 citations), Developmental Neuroscience (24 citations) and Rheumatology (58 citations). Federica Natacci has collaborated with scholars based in Italy, United States and United Kingdom. Frequent co-authors include Faustina Lalatta, Lidia Larizza, Paola Riva, Maria Francesca Bedeschi, Cristina Curcio, Angelo Selicorni, Giulia Melloni, The‐Hung Bui, Umberto Nicolini and Chiara Mapelli. Their work appears in journals such as Prenatal Diagnosis, Human Genetics, Journal of Child Neurology, Cancers and European Journal of Human Genetics.
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.