Silvia Guarducci

834 total citations
18 papers, 243 citations indexed

About

Silvia Guarducci is a scholar working on Genetics, Molecular Biology and Infectious Diseases. According to data from OpenAlex, Silvia Guarducci has authored 18 papers receiving a total of 243 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 9 papers in Molecular Biology and 3 papers in Infectious Diseases. Recurrent topics in Silvia Guarducci's work include Genomic variations and chromosomal abnormalities (4 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Genomics and Rare Diseases (2 papers). Silvia Guarducci is often cited by papers focused on Genomic variations and chromosomal abnormalities (4 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Genomics and Rare Diseases (2 papers). Silvia Guarducci collaborates with scholars based in Italy, Switzerland and China. Silvia Guarducci's co-authors include Maria Luisa Giovannucci Uzielli, Elisabetta Lapi, U. Ricci, Antonella Cecconi, Guglielmo Bonaccorsi, Chiara Lorini, E. D. Pellegrino, Francesca Santomauro, Paolo Bonanni and Benedetta Scarselli and has published in prestigious journals such as Journal of Medical Genetics, Electrophoresis and Forensic Science International.

In The Last Decade

Silvia Guarducci

17 papers receiving 239 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 Guarducci Italy 9 167 82 54 47 44 18 243
Ryan L. Jensen United States 5 244 1.5× 195 2.4× 40 0.7× 15 0.3× 82 1.9× 5 372
Ziad Al Bkhetan Australia 4 38 0.2× 80 1.0× 18 0.3× 4 0.1× 19 0.4× 7 242
David Owen United Kingdom 9 112 0.7× 87 1.1× 18 0.3× 2 0.0× 16 0.4× 19 272
Wayne Huggins United States 9 42 0.3× 294 3.6× 9 0.2× 5 0.1× 32 0.7× 21 427
Geneva DeGregorio United States 6 86 0.5× 37 0.5× 83 1.5× 3 0.1× 68 1.5× 9 219
Sarah Gray United States 9 97 0.6× 331 4.0× 18 0.3× 2 0.0× 20 0.5× 13 434
Jennifer Daily United States 8 166 1.0× 133 1.6× 29 0.5× 4 0.1× 23 0.5× 11 296
Cíntia Tusset Brazil 9 88 0.5× 89 1.1× 2 0.0× 5 0.1× 58 1.3× 20 282
Sherry Vinson United States 7 81 0.5× 67 0.8× 31 0.6× 112 2.5× 7 229
Shan Tang United Kingdom 8 77 0.5× 47 0.6× 25 0.5× 1 0.0× 46 1.0× 16 225

Countries citing papers authored by Silvia Guarducci

Since Specialization
Citations

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

Fields of papers citing papers by Silvia Guarducci

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Silvia Guarducci

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

All Works

18 of 18 papers shown
1.
Salvetti, Sara, Simone Vanni, Luca Masotti, et al.. (2022). A rapid and cost-effective diagnostic algorithm for the detection of SARS-CoV-2 infection in the emergency area by combining highly sensitive antigenic test and RT-PCR. Diagnostic Microbiology and Infectious Disease. 103(4). 115727–115727. 1 indexed citations
2.
Rubegni, Anna, Claudia Nesti, Melissa Barghigiani, et al.. (2021). Learning from massive testing of mitochondrial disorders: UPD explaining unorthodox transmission. Journal of Medical Genetics. 58(8). 543–546. 5 indexed citations
3.
Fichera, Marco, Susan Marelli, Anna Cavallini, et al.. (2020). Assigning single clinical features to their disease-locus in large deletions: the example of chromosome 1q23-25 deletion syndrome. UNICA IRIS Institutional Research Information System (University of Cagliari). 1 indexed citations
4.
Giunti, Laura, Anna Maria Buccoliero, M Lucchesi, et al.. (2016). Molecular characterization of paediatric glioneuronal tumours with neuropil-like islands: a genome-wide copy number analysis.. PubMed. 6(12). 2910–2918.
5.
Guarducci, Silvia, Chiara Lorini, Anderson Soares da Silva, et al.. (2015). Budget impact analysis of universal rotavirus vaccination in the Local Health Unit 11 Empoli, Tuscany, Italy. PubMed. 56(2). E66–71. 2 indexed citations
6.
Stagi, Stefano, Elisabetta Lapi, Salvatore Seminara, et al.. (2014). Long-term auxological and endocrinological evaluation of patients with 9p trisomy: a focus on the growth hormone-insulin-like growth factor-I axis. BMC Endocrine Disorders. 14(1). 3–3. 13 indexed citations
7.
Marini, Carla, Antonella Cecconi, Elisa Contini, et al.. (2013). Clinical and genetic study of a family with a paternally inherited 15q11–q13 duplication. American Journal of Medical Genetics Part A. 161(6). 1459–1464. 18 indexed citations
8.
Bonaccorsi, Guglielmo, Chiara Lorini, Francesca Santomauro, et al.. (2013). Predictive factors associated with the acceptance of pandemic and seasonal influenza vaccination in health care workers and students in Tuscany, Central Italy. Human Vaccines & Immunotherapeutics. 9(12). 2603–2612. 54 indexed citations
9.
Bonaccorsi, Guglielmo, et al.. (2013). Diabetes screening in primary care: the PRE.DI.CO. study.. PubMed. 24(6). 527–34. 3 indexed citations
10.
Ricci, U., Elisabetta Lapi, Silvia Guarducci, et al.. (2004). Twin zygosity studies with the formula from DNA-View's Kinship Module after molecular analyses by polymorphic markers. International Congress Series. 1261. 452–453. 1 indexed citations
11.
Ricci, U., et al.. (2002). Analysis of 13 tetrameric short tandem repeat loci in a population of Tuscany (Central Italy) performed by means of an automated infrared sequencer. Forensic Science International. 125(1). 83–85. 8 indexed citations
12.
13.
Baumer, Alessandra, Maria Luisa Giovannucci Uzielli, Silvia Guarducci, et al.. (2002). Meiotic origin of two ring chromosomes 18 in a girl with developmental delay. American Journal of Medical Genetics. 113(1). 101–104. 12 indexed citations
14.
Giunti, Laura, Silvia Guarducci, Elisabetta Lapi, et al.. (2001). Spectrum and distribution of MECP2 mutations in 64 Italian Rett syndrome girls: tentative genotype/phenotype correlation. Brain and Development. 23. S242–S245. 18 indexed citations
15.
Ricci, U., Ilaria Sani, Silvia Guarducci, et al.. (2000). Infrared fluorescent automated detection of thirteen short tandem repeat polymorphisms and one gender-determining system of the CODIS core system. Electrophoresis. 21(17). 3564–3570. 20 indexed citations
16.
Uzielli, Maria Luisa Giovannucci, Silvia Guarducci, Elisabetta Lapi, et al.. (1999). Premature ovarian failure (POF) and fragile X premutation females: From POF to fragile X carrier identification, from fragile X carrier diagnosis to POF association data. American Journal of Medical Genetics. 84(3). 300–303. 65 indexed citations
17.
Uzielli, Maria Luisa Giovannucci, Silvia Guarducci, Elisabetta Lapi, et al.. (1999). Premature ovarian failure (POF) and fragile X premutation females: From POF to fragile X carrier identification, from fragile X carrier diagnosis to POF association data. American Journal of Medical Genetics. 84(3). 300–303. 4 indexed citations
18.
Guarducci, Silvia, et al.. (1991). Four cases of trisomy 9p syndrome with particular chromosome rearrangements.. PubMed. 34(2). 115–9. 12 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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