Federica Natacci

1.4k total citations
53 papers, 720 citations indexed

About

Federica Natacci is a scholar working on Genetics, Molecular Biology and Neurology. According to data from OpenAlex, Federica Natacci has authored 53 papers receiving a total of 720 indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Genetics, 19 papers in Molecular Biology and 19 papers in Neurology. Recurrent topics in Federica Natacci's work include Neurofibromatosis and Schwannoma Cases (18 papers), Genomic variations and chromosomal abnormalities (15 papers) and Prenatal Screening and Diagnostics (8 papers). Federica Natacci is often cited by papers focused on Neurofibromatosis and Schwannoma Cases (18 papers), Genomic variations and chromosomal abnormalities (15 papers) and Prenatal Screening and Diagnostics (8 papers). Federica Natacci collaborates with scholars based in Italy, United States and United Kingdom. Federica Natacci's co-authors include Faustina Lalatta, Lidia Larizza, Paola Riva, Maria Francesca Bedeschi, Cristina Curcio, Angelo Selicorni, Giulia Melloni, Umberto Nicolini, The‐Hung Bui and Diego Vezzola and has published in prestigious journals such as SHILAP Revista de lepidopterología, The Journal of Clinical Endocrinology & Metabolism and Ophthalmology.

In The Last Decade

Federica Natacci

48 papers receiving 667 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Federica Natacci Italy	16	258	250	214	184	101	53	720
Diane Beysen Belgium	12	357 1.4×	326 1.3×	397 1.9×	60 0.3×	95 0.9×	20	951
Charles W. McCluggage United States	13	190 0.7×	193 0.8×	175 0.8×	57 0.3×	105 1.0×	15	689
Leah W. Burke United States	13	247 1.0×	105 0.4×	182 0.9×	74 0.4×	51 0.5×	22	552
Chin‐To Fong United States	11	197 0.8×	138 0.6×	282 1.3×	65 0.4×	54 0.5×	22	738
Diana Carli Italy	14	272 1.1×	97 0.4×	279 1.3×	152 0.8×	90 0.9×	51	599
Yaşar Bayri Türkiye	13	57 0.2×	179 0.7×	75 0.4×	74 0.4×	67 0.7×	48	496
Maria Michela Rinaldi Italy	13	305 1.2×	61 0.2×	408 1.9×	139 0.8×	18 0.2×	17	631
Cameron F. Parsa United States	14	128 0.5×	279 1.1×	127 0.6×	54 0.3×	201 2.0×	32	821
Dimitris P. Agamanolis United States	16	62 0.2×	128 0.5×	237 1.1×	74 0.4×	86 0.9×	27	844
Fady M. Mikhail United States	19	551 2.1×	124 0.5×	700 3.3×	338 1.8×	70 0.7×	61	1.5k

Countries citing papers authored by Federica Natacci

Since Specialization

Citations

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

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Federica Natacci

This figure shows the co-authorship network connecting the top 25 collaborators of Federica Natacci. A scholar is included among the top collaborators of Federica Natacci 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 Federica Natacci. Federica Natacci is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Lettieri, Antonella, Chiara Parodi, Elisa Adele Colombo, et al.. (2024). Characterization of a novel HDAC2 pathogenetic variant: a missing puzzle piece for chromatinopathies. Human Genetics. 143(6). 747–759. 1 indexed citations

Bettinaglio, Paola, Eleonora Mangano, Claudia Cesaretti, et al.. (2024). Genetic/epigenetic effects in NF1 microdeletion syndrome: beyond the haploinsufficiency, looking at the contribution of not deleted genes. Human Genetics. 143(6). 775–795.

Milani, Donatella, Alessia Dolci, Ilaria Muller, et al.. (2023). Thyroid findings in pediatric and adult patients with PTEN hamartoma tumor syndrome: A retrospective analysis, and literature review. Endocrine. 81(1). 98–106. 5 indexed citations

Kuhn, Elisabetta, Federica Natacci, Massimo Corbo, et al.. (2023). The Contribution of Oxidative Stress to NF1-Altered Tumors. Antioxidants. 12(8). 1557–1557. 3 indexed citations

Paterra, Rosina, Paola Bettinaglio, Eleonora Mangano, et al.. (2022). A Translational Approach to Spinal Neurofibromatosis: Clinical and Molecular Insights from a Wide Italian Cohort. Cancers. 15(1). 59–59. 3 indexed citations

Bianchessi, Donatella, Veronica Saletti, Rosina Paterra, et al.. (2020). Simultaneous Detection of NF1, SPRED1, LZTR1, and NF2 Gene Mutations by Targeted NGS in an Italian Cohort of Suspected NF1 Patients. Genes. 11(6). 671–671. 8 indexed citations

Filopanti, Marcello, Uberta Verga, Fabio Massimo Ulivieri, et al.. (2018). Trabecular Bone Score (TBS) and Bone Metabolism in Patients Affected with Type 1 Neurofibromatosis (NF1). Calcified Tissue International. 104(2). 207–213. 13 indexed citations

Tucci, Arianna, Veronica Saletti, Francesca Menni, et al.. (2017). The absence that makes the difference: choroidal abnormalities in Legius syndrome. Journal of Human Genetics. 62(11). 1001–1004. 5 indexed citations

Natacci, Federica, Enrico Alfei, Stefano D’Arrigo, et al.. (2015). Chromosome 17q21.31 duplication syndrome: Description of a new familiar case and further delineation of the clinical spectrum. European Journal of Paediatric Neurology. 20(1). 183–187. 19 indexed citations

10.

Menni, Francesca, Maria Francesca Bedeschi, Federica Natacci, et al.. (2013). Healthcare transition in patients with rare genetic disorders with and without developmental disability: Neurofibromatosis 1 and williams–beuren syndrome. American Journal of Medical Genetics Part A. 161(7). 1666–1674. 36 indexed citations

11.

Finelli, Palma, Silvia Maria Sirchia, Maura Masciadri, et al.. (2012). Juxtaposition of heterochromatic and euchromatic regions by chromosomal translocation mediates a heterochromatic long-range position effect associated with a severe neurological phenotype. Molecular Cytogenetics. 5(1). 16–16. 21 indexed citations

12.

Viola, Francesco, Edoardo Villani, Federica Natacci, et al.. (2011). Choroidal Abnormalities Detected by Near-Infrared Reflectance Imaging as a New Diagnostic Criterion for Neurofibromatosis 1. Ophthalmology. 119(2). 369–375. 95 indexed citations

13.

Bedeschi, Maria Francesca, Vera Bianchi, Federica Natacci, et al.. (2011). Clinical follow‐up of young adults affected by Williams syndrome: Experience of 45 Italian patients. American Journal of Medical Genetics Part A. 155(2). 353–359. 22 indexed citations

14.

Gentilin, Barbara, Silvana Guerneri, Vera Bianchi, et al.. (2008). Discordant Prenatal Phenotype and Karyotype of Monozygotic Twins Characterized by the Unequal Distribution of Two Cell Lines Investigated by Different Methods: A Review. Twin Research and Human Genetics. 11(3). 352–356. 13 indexed citations

15.

Natacci, Federica, Maria Francesca Bedeschi, Andrea Righini, et al.. (2007). Norman–Roberts syndrome: characterization of the phenotype in early fetal life. Prenatal Diagnosis. 27(6). 568–572. 5 indexed citations

16.

Ruggeri, Anna, Francesca Dulcetti, Monica Miozzo, et al.. (2004). Prenatal search for UPD 14 and UPD 15 in 83 cases of familial and de novo heterologous Robertsonian translocations. Prenatal Diagnosis. 24(12). 997–1000. 33 indexed citations

17.

Colapietro, Patrizia, Cristina Gervasini, Federica Natacci, et al.. (2003). NF1 exon�7 skipping and sequence alterations in exonic splice enhancers (ESEs) in a neurofibromatosis�1 patient. Human Genetics. 113(6). 551–554. 28 indexed citations

18.

Riva, Paola, Marco Venturin, Paolo Guarnieri, et al.. (2002). Genotype-phenotype correlation in patients with NF1 microdeletion syndrome: identification of candidate genes for mental retardation. The American Journal of Human Genetics. 71(4). 308–308.

19.

Giardino, Daniela, Palma Finelli, Silvia Russo, et al.. (2002). Small familial supernumerary ring chromosome 2: FISH characterization and genotype‐phenotype correlation. American Journal of Medical Genetics. 111(3). 319–323. 23 indexed citations

20.

Finelli, Palma, Pietro Cavalli, Daniela Giardino, et al.. (2001). FISH characterization of a supernumerary r(1)(::cen?q22::q22?sq21::) chromosome associated with multiple anomalies and bilateral cataracts. American Journal of Medical Genetics. 104(2). 157–164. 13 indexed citations

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.

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