Federica Natacci
Impact in
- Neurology top 5%
- Neurofibromatosis and Schwannoma Cases
- Vascular Malformations Diagnosis and Treatment
-
- Prenatal Screening and Diagnostics
Papers in
- Genetics 25
- Genomic variations and chromosomal abnormalities 15
- Genetics and Neurodevelopmental Disorders 7
- Genetic Syndromes and Imprinting 4
-
- Chromatin Remodeling and Cancer 4
- Co-authors
- Faustina Lalatta (14 shared papers)Lidia Larizza (13 shared papers)Paola Riva (10 shared papers)Cristina Curcio (3 shared papers)Maria Francesca Bedeschi (14 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)European Journal of Human Genetics (2 papers)Cancers (2 papers)The American Journal of Human Genetics (2 papers)
- Partner nations
- ItalyUnited StatesUnited Kingdom
In The Last Decade
Federica Natacci
48 papers receiving 667 citations
Peers
Comparison fields: 5 of 60
- Neurology 250
- Pediatrics, Perinatology and Child Health 184
- Genetics 258
- Developmental Neuroscience 24
- Rheumatology 70
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 53 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2011 | 95 | |
| 2 | 2000 | 71 | |
| 3 | 2004 | 64 | |
| 4 | 2013 | 36 | |
| 5 | 2004 | 33 | |
| 6 | 2003 | 28 | |
| 7 | 2016 | 27 | |
| 8 | 2015 | 25 | |
| 9 | 2009 | 23 | |
| 10 | 2002 | 23 | |
| 11 | 2011 | 22 | |
| 12 | 2012 | 21 | |
| 13 | 2015 | 19 | |
| 14 | 2019 | 17 | |
| 15 | 2013 | 16 | |
| 16 | 2000 | 16 | |
| 17 | 2008 | 15 | |
| 18 | 2000 | 15 | |
| 19 | 2008 | 14 | |
| 20 | 2019 | 14 |
About Federica Natacci
Federica Natacci is a scholar working on Genetics, Molecular Biology, Neurology, Pediatrics, Perinatology and Child Health and Pulmonary and Respiratory Medicine, having authored 53 papers that have together received 720 indexed citations. Recurring topics across this work include Neurofibromatosis and Schwannoma Cases (18 papers), Genomic variations and chromosomal abnormalities (15 papers), Prenatal Screening and Diagnostics (8 papers), Sarcoma Diagnosis and Treatment (7 papers), Genetics and Neurodevelopmental Disorders (7 papers), Genetic Syndromes and Imprinting (4 papers), Chromatin Remodeling and Cancer (4 papers) and Neuroblastoma Research and Treatments (4 papers). The work is most often cited by research in Neurology (250 citations), Pediatrics, Perinatology and Child Health (184 citations), Genetics (258 citations), Developmental Neuroscience (24 citations) and Rheumatology (70 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, Cristina Curcio, Maria Francesca Bedeschi, Angelo Selicorni, Giulia Melloni, The‐Hung Bui, Umberto Nicolini and Chiara Mapelli. Their work appears in journals such as Prenatal Diagnosis, Human Genetics, European Journal of Human Genetics, Cancers and The American 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.