Silvana Briuglia

1.4k total citations
52 papers, 812 citations indexed

About

Silvana Briuglia is a scholar working on Genetics, Molecular Biology and Immunology. According to data from OpenAlex, Silvana Briuglia has authored 52 papers receiving a total of 812 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Genetics, 20 papers in Molecular Biology and 8 papers in Immunology. Recurrent topics in Silvana Briuglia's work include Genomic variations and chromosomal abnormalities (9 papers), Genetics and Neurodevelopmental Disorders (7 papers) and Genetic Syndromes and Imprinting (6 papers). Silvana Briuglia is often cited by papers focused on Genomic variations and chromosomal abnormalities (9 papers), Genetics and Neurodevelopmental Disorders (7 papers) and Genetic Syndromes and Imprinting (6 papers). Silvana Briuglia collaborates with scholars based in Italy, United Kingdom and United States. Silvana Briuglia's co-authors include Carmelo Salpietro, Luciana Rigoli, Maria Merlino, Chiara Di Bella, Bruno Dallapiccola, Sebastiano Gangemi, Domenico Trombetta, Antonella Saija, Salvatore Leonardi and Paola Lucia Minciullo and has published in prestigious journals such as The American Journal of Human Genetics, Frontiers in Immunology and Journal of the American Academy of Dermatology.

In The Last Decade

Silvana Briuglia

49 papers receiving 789 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Silvana Briuglia Italy 16 315 215 121 113 89 52 812
Katarzyna Jarząbek Poland 16 326 1.0× 234 1.1× 49 0.4× 34 0.3× 65 0.7× 37 813
Rebecca E. Slager United States 11 241 0.8× 230 1.1× 110 0.9× 28 0.2× 18 0.2× 16 701
Jianzhong Zhang China 20 420 1.3× 49 0.2× 80 0.7× 65 0.6× 14 0.2× 75 1.1k
Haibo Xue China 16 177 0.6× 64 0.3× 250 2.1× 42 0.4× 74 0.8× 38 785
Núria Torán Spain 24 608 1.9× 339 1.6× 37 0.3× 179 1.6× 26 0.3× 71 1.5k
Uta Tacke Germany 13 329 1.0× 124 0.6× 53 0.4× 217 1.9× 162 1.8× 27 1.3k
Juan Antonio Aguilar‐Pimentel Germany 13 177 0.6× 41 0.2× 135 1.1× 21 0.2× 90 1.0× 22 730
Tamara R. Jones United States 19 743 2.4× 169 0.8× 190 1.6× 228 2.0× 18 0.2× 32 1.7k
Andrea Casasco Italy 17 348 1.1× 58 0.3× 43 0.4× 37 0.3× 53 0.6× 76 1.0k
M.J. Benito Spain 14 149 0.5× 38 0.2× 280 2.3× 20 0.2× 41 0.5× 22 864

Countries citing papers authored by Silvana Briuglia

Since Specialization
Citations

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

Fields of papers citing papers by Silvana Briuglia

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Silvana Briuglia

This figure shows the co-authorship network connecting the top 25 collaborators of Silvana Briuglia. A scholar is included among the top collaborators of Silvana Briuglia 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 Silvana Briuglia. Silvana Briuglia 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.
2.
Mondello, Cristina, Mariacarmela Santarpía, Natasha Irrera, et al.. (2025). Genetic Insight into Expression-Defined Melanoma Subtypes and Network Mechanisms: An in Silico Study. Genes. 16(12). 1428–1428.
3.
Capra, Anna Paola, et al.. (2023). Coexistence of Genetic Diseases Is a New Clinical Challenge: Three Unrelated Cases of Dual Diagnosis. Genes. 14(2). 484–484. 6 indexed citations
4.
Capra, Anna Paola, Domenico Corica, Giorgia Pepe, et al.. (2023). A novel case of 16q22.3 duplication syndrome in a child with overgrowth: case report and literature review. BMC Medical Genomics. 16(1). 315–315.
5.
Sticht, Heinrich, François Lecoquierre, Alice Goldenberg, et al.. (2022). Heterozygous and homozygous variants in STX1A cause a neurodevelopmental disorder with or without epilepsy. European Journal of Human Genetics. 31(3). 345–352. 4 indexed citations
6.
Capra, Anna Paola, Alessio Ardizzone, Silvana Briuglia, et al.. (2022). A Systematic Review and Meta-Analysis of the Association between the FV H1299R Variant and the Risk of Recurrent Pregnancy Loss. Biology. 11(11). 1608–1608. 6 indexed citations
7.
Ardizzone, Alessio, Anna Paola Capra, Michela Campolo, et al.. (2022). Neurofibromatosis: New Clinical Challenges in the Era of COVID-19. Biomedicines. 10(5). 940–940. 5 indexed citations
8.
Ardizzone, Alessio, Anna Paola Capra, Stefania Mondello, et al.. (2022). H1299R Variant in Factor V and Recurrent Pregnancy Loss: A Systematic Review and Meta-Analysis Protocol. Genes. 13(6). 1019–1019. 8 indexed citations
9.
Capra, Anna Paola, Silvana Briuglia, Chiara Baldo, et al.. (2021). 8p23.2-pter Microdeletions: Seven New Cases Narrowing the Candidate Region and Review of the Literature. Genes. 12(5). 652–652. 12 indexed citations
10.
Briuglia, Silvana, et al.. (2021). Molecular Pathways within Autism Spectrum Disorder Endophenotypes. Journal of Molecular Neuroscience. 71(7). 1357–1367. 4 indexed citations
11.
Calabrò, Marco, et al.. (2021). Suicide Related Phenotypes in a Bipolar Sample: Genetic Underpinnings. Genes. 12(10). 1482–1482. 8 indexed citations
12.
Bruno, Rocco, Francesco Galletti, Chiara Di Bella, et al.. (2015). Prevalence of Deafness‐Associated Connexin‐26 (GJB2) and Connexin‐30 (GJB6) Pathogenic Alleles in a Large Patient Cohort from Eastern Sicily. Annals of Human Genetics. 79(5). 341–349. 12 indexed citations
13.
Chirico, Valeria, Valeria Ferraù, Italia Loddo, et al.. (2014). LMNA gene mutation as a model of cardiometabolic dysfunction: From genetic analysis to treatment response. Diabetes & Metabolism. 40(3). 224–228. 7 indexed citations
14.
Salpietro, Vincenzo, Agata Polizzi, Francesca Granata, et al.. (2012). Upper Respiratory Tract Infection and Torticollis in Children. Clinical Neuroradiology. 22(4). 351–353. 8 indexed citations
15.
Salpietro, Carmelo, Silvana Briuglia, Maria Concetta Cutrupi, et al.. (2009). Apparent third patient with cutaneous mastocytosis, microcephaly, conductive hearing loss, and microtia. American Journal of Medical Genetics Part A. 149A(10). 2270–2273. 2 indexed citations
16.
Trombetta, Domenico, Sebastiano Gangemi, Antonella Saija, et al.. (2006). Increased protein carbonyl groups in the serum of patients affected by thalassemia major. Annals of Hematology. 85(8). 520–522. 22 indexed citations
17.
Vaccaro, Mario, et al.. (2005). Cutis laxa in Kabuki make-up syndrome. Journal of the American Academy of Dermatology. 53(5). S247–S251. 5 indexed citations
18.
Valente, Enza Maria, Francesco Brancati, Enrico Bertini, et al.. (2003). Description, Nomenclature, and Mapping of a Novel Cerebello-Renal Syndrome with the Molar Tooth Malformation. The American Journal of Human Genetics. 73(3). 663–670. 54 indexed citations
19.
Salpietro, Carmelo, Silvana Briuglia, Maria Merlino, Chiara Di Bella, & Luciana Rigoli. (2003). A mitochondrial DNA mutation (A3243G mtDNA) in a family with cyclic vomiting. European Journal of Pediatrics. 162(10). 727–728. 21 indexed citations
20.
Gangemi, Sebastiano, Antonella Saija, Antonio Tomaino, et al.. (2003). Protein carbonyl group content in patients affected by familiar chronic nail candidiasis. Mediators of Inflammation. 12(4). 247–249. 2 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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