Silvia Russo

7.5k total citations
136 papers, 3.3k citations indexed

About

Silvia Russo is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Silvia Russo has authored 136 papers receiving a total of 3.3k indexed citations (citations by other indexed papers that have themselves been cited), including 88 papers in Genetics, 80 papers in Molecular Biology and 37 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Silvia Russo's work include Genetic Syndromes and Imprinting (39 papers), Epigenetics and DNA Methylation (33 papers) and Prenatal Screening and Diagnostics (33 papers). Silvia Russo is often cited by papers focused on Genetic Syndromes and Imprinting (39 papers), Epigenetics and DNA Methylation (33 papers) and Prenatal Screening and Diagnostics (33 papers). Silvia Russo collaborates with scholars based in Italy, United States and United Kingdom. Silvia Russo's co-authors include Lidia Larizza, Angelo Selicorni, Cristina Gervasini, Andrea Riccio, Donatella Milani, Giovanni Battista Ferrero, Alessandro Mussa, Paolo Vezzoni, Antonio Musio and Francesca Cogliati and has published in prestigious journals such as Nature Genetics, PLoS ONE and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Silvia Russo

132 papers receiving 3.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Silvia Russo Italy 30 1.9k 1.9k 900 298 271 136 3.3k
Sanaa Choufani Canada 30 1.3k 0.7× 2.5k 1.3× 1.1k 1.2× 106 0.4× 106 0.4× 71 3.5k
Leda Dalprà Italy 32 1.2k 0.6× 1.5k 0.8× 490 0.5× 93 0.3× 206 0.8× 119 3.3k
Ana Cristina Victorino Krepischi Brazil 27 1.4k 0.7× 1.4k 0.7× 295 0.3× 183 0.6× 115 0.4× 146 2.7k
Howard R. Slater Australia 32 1.8k 0.9× 1.3k 0.7× 795 0.9× 53 0.2× 452 1.7× 99 3.0k
Sylvie Langlois Canada 32 1.6k 0.8× 1.1k 0.6× 1.5k 1.6× 73 0.2× 63 0.2× 107 2.8k
Sabrina Giglio Italy 29 1.3k 0.7× 1.5k 0.8× 422 0.5× 150 0.5× 43 0.2× 116 2.6k
Laura Bernardini Italy 27 1.0k 0.5× 797 0.4× 317 0.4× 70 0.2× 103 0.4× 126 2.1k
Daniela del Gaudio United States 18 1.0k 0.5× 854 0.4× 388 0.4× 55 0.2× 121 0.4× 47 1.8k
Ann Nordgren Sweden 29 997 0.5× 1.1k 0.6× 391 0.4× 165 0.6× 151 0.6× 134 2.6k
Mieke M. van Haelst Netherlands 28 1.4k 0.7× 1.2k 0.6× 303 0.3× 163 0.5× 55 0.2× 105 2.7k

Countries citing papers authored by Silvia Russo

Since Specialization
Citations

This map shows the geographic impact of Silvia Russo'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 Silvia Russo with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Silvia Russo more than expected).

Fields of papers citing papers by Silvia Russo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Silvia Russo. 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 Silvia Russo. The network helps show where Silvia Russo may publish in the future.

Co-authorship network of co-authors of Silvia Russo

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

All Works

20 of 20 papers shown
1.
Pezzani, Lidia, Rosamaria Silipigni, Silvia Russo, et al.. (2024). A long way to syndromic short stature. ˜The œItalian Journal of Pediatrics/Italian journal of pediatrics. 50(1). 192–192.
2.
Cogliati, Francesca, Letizia Straniero, Valeria Rimoldi, et al.. (2024). Low‐grade parental gonosomal mosaicism in CHD2 siblings with Smith–Magenis‐like syndrome. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 195(6). e32976–e32976. 2 indexed citations
3.
Patti, Giuseppa, Maria Grazia Calevo, Silvia Russo, et al.. (2022). Pubertal timing in children with Silver Russell syndrome compared to those born small for gestational age. Frontiers in Endocrinology. 13. 975511–975511. 4 indexed citations
4.
Tannorella, Pierpaola, Sara Guzzetti, Luciano Calzari, et al.. (2021). Maternal Uniparental Disomy of Chromosome 20 (UPD(20)mat) as Differential Diagnosis of Silver Russell Syndrome: Identification of Three New Cases. Genes. 12(4). 588–588. 8 indexed citations
5.
Masciadri, Maura, et al.. (2019). A novel RAD21 mutation in a boy with mild Cornelia de Lange presentation: Further delineation of the phenotype. European Journal of Medical Genetics. 63(1). 103620–103620. 5 indexed citations
6.
Crippa, M., Maria Teresa Bonati, Luciano Calzari, et al.. (2019). Molecular Etiology Disclosed by Array CGH in Patients With Silver–Russell Syndrome or Similar Phenotypes. Frontiers in Genetics. 10. 955–955. 10 indexed citations
7.
Sparago, Angela, Ankit Verma, Maria Grazia Patricelli, et al.. (2019). The phenotypic variations of multi-locus imprinting disturbances associated with maternal-effect variants of NLRP5 range from overt imprinting disorder to apparently healthy phenotype. Clinical Epigenetics. 11(1). 190–190. 24 indexed citations
8.
Masciadri, Maura, Anna Ficcadenti, Donatella Milani, et al.. (2018). Recurrence and Familial Inheritance of Intronic NIPBL Pathogenic Variant Associated With Mild CdLS. Frontiers in Neurology. 9. 967–967. 5 indexed citations
9.
Roversi, Gaia, M. Crippa, Daniela Perotti, et al.. (2015). Constitutional de novo deletion of the FBXW7 gene in a patient with focal segmental glomerulosclerosis and multiple primitive tumors. Scientific Reports. 5(1). 15454–15454. 7 indexed citations
10.
Mussa, Alessandro, Stefania Di Candia, Silvia Russo, et al.. (2015). Recommendations of the Scientific Committee of the Italian Beckwith–Wiedemann Syndrome Association on the diagnosis, management and follow-up of the syndrome. European Journal of Medical Genetics. 59(1). 52–64. 54 indexed citations
11.
Castronovo, Chiara, M. Crippa, Silvia Russo, et al.. (2014). Complex de novo chromosomal rearrangement at 15q11–q13 involving an intrachromosomal triplication in a patient with a severe neuropsychological phenotype: Clinical report and review of the literature. American Journal of Medical Genetics Part A. 167(1). 221–230. 12 indexed citations
12.
Russo, Silvia, et al.. (2013). Think About It. Journal of Child Neurology. 29(9). NP74–NP77. 11 indexed citations
13.
Gervasini, Cristina, Silvia Russo, Anna Cereda, et al.. (2013). Cornelia de Lange individuals with new and recurrent SMC1A mutations enhance delineation of mutation repertoire and phenotypic spectrum. American Journal of Medical Genetics Part A. 161(11). 2909–2919. 24 indexed citations
14.
Limongelli, Giuseppe, Silvia Russo, M. Cristina Digilio, et al.. (2010). Hypertrophic cardiomyopathy in a girl with Cornelia de Lange syndrome due to mutation in SMC1A. American Journal of Medical Genetics Part A. 152A(8). 2127–2129. 19 indexed citations
15.
Castronovo, Paola, Andrée Delahaye‐Duriez, Cristina Gervasini, et al.. (2010). Somatic mosaicism in Cornelia de Lange syndrome: a further contributor to the wide clinical expressivity?. Clinical Genetics. 78(6). 560–564. 24 indexed citations
16.
Mari, Francesca, Rossella Caselli, Silvia Russo, et al.. (2005). Germline mosaicism in Rett syndrome identified by prenatal diagnosis. Clinical Genetics. 67(3). 258–260. 21 indexed citations
17.
Russo, Silvia, et al.. (2003). A fluorescent method for detecting low-grade 11patUPD mosaicism in Beckwith–Wiedemann syndrome. Molecular and Cellular Probes. 17(6). 295–299. 8 indexed citations
18.
Resta, Nicoletta, Alessandro Stella, Francesco Susca, et al.. (2001). Nine novel APC mutations in Italian FAP patients. Human Mutation. 17(5). 434–435. 11 indexed citations
19.
Finelli, Palma, Daniela Giardino, Silvia Russo, et al.. (2001). Refined FISH characterization of a de novo 1p22-p36.2 paracentric inversion and associated 1p21-22 deletion in a patient with signs of 1p36 microdeletion syndrome. American Journal of Medical Genetics. 99(4). 308–313. 7 indexed citations
20.
Russo, Silvia, et al.. (2000). Mapping to distal Xq28 of nonspecific X-linked mental retardation MRX72: Linkage analysis and clinical findings in a three-generation Sardinian family. American Journal of Medical Genetics. 94(5). 376–382. 8 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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