Manuela Priolo

2.1k total citations
48 papers, 882 citations indexed

About

Manuela Priolo is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Manuela Priolo has authored 48 papers receiving a total of 882 indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Molecular Biology, 26 papers in Genetics and 8 papers in Surgery. Recurrent topics in Manuela Priolo's work include Congenital heart defects research (7 papers), Genomics and Rare Diseases (6 papers) and Genetic Syndromes and Imprinting (6 papers). Manuela Priolo is often cited by papers focused on Congenital heart defects research (7 papers), Genomics and Rare Diseases (6 papers) and Genetic Syndromes and Imprinting (6 papers). Manuela Priolo collaborates with scholars based in Italy, France and United States. Manuela Priolo's co-authors include Margherita Lerone, Margherita Silengo, Roberto Ravazzolo, Carmelo Laganà, Isabella Ceccherini, Corrado Mammì, Marco Seri, Andrea Riccio, Angela Sparago and Flavia Cerrato and has published in prestigious journals such as Blood, Gene and International Journal of Environmental Research and Public Health.

In The Last Decade

Manuela Priolo

46 papers receiving 826 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Manuela Priolo Italy 18 542 404 126 90 76 48 882
Irfan Saadi United States 18 623 1.1× 347 0.9× 57 0.5× 85 0.9× 75 1.0× 36 1.1k
Jacqueline Siegel‐Bartelt Canada 8 820 1.5× 477 1.2× 89 0.7× 36 0.4× 63 0.8× 10 1.1k
Yao‐Shan Fan United States 18 346 0.6× 432 1.1× 202 1.6× 29 0.3× 131 1.7× 39 913
Sylvie Manouvrier‐Hanu France 18 504 0.9× 395 1.0× 117 0.9× 37 0.4× 99 1.3× 57 846
M Shohat Israel 15 329 0.6× 387 1.0× 88 0.7× 20 0.2× 134 1.8× 29 911
Aleksander Jamsheer Poland 16 433 0.8× 397 1.0× 57 0.5× 31 0.3× 112 1.5× 77 731
Yves Lacassie United States 18 475 0.9× 425 1.1× 174 1.4× 9 0.1× 92 1.2× 70 952
Martine Blayau France 18 649 1.2× 404 1.0× 118 0.9× 12 0.1× 102 1.3× 44 1.1k
J. Siegel‐Bartelt Canada 13 666 1.2× 524 1.3× 97 0.8× 24 0.3× 105 1.4× 20 903
R. Sid Wilroy United States 21 635 1.2× 778 1.9× 166 1.3× 20 0.2× 275 3.6× 53 1.3k

Countries citing papers authored by Manuela Priolo

Since Specialization
Citations

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

Fields of papers citing papers by Manuela Priolo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Manuela Priolo

This figure shows the co-authorship network connecting the top 25 collaborators of Manuela Priolo. A scholar is included among the top collaborators of Manuela Priolo 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 Manuela Priolo. Manuela Priolo 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.
Bruselles, Alessandro, Paola D′Ambrosio, Andrea Ciolfi, et al.. (2025). The p.Ile202Thr Substitution in TUBB2B Can Be Associated with Syndromic Presentation of Congenital Fibrosis of the Extraocular Muscles. Genes. 16(10). 1182–1182. 1 indexed citations
2.
Chetta, Massimiliano, Anna Basile, Marina Tarsitano, et al.. (2024). The Target Therapy Hyperbole: “KRAS (p.G12C)”—The Simplification of a Complex Biological Problem. Cancers. 16(13). 2389–2389. 1 indexed citations
3.
Alesi, Viola, Silvia Genovese, Silvia Di Tommaso, et al.. (2024). Structural rearrangements as a recurrent pathogenic mechanism for SETBP1 haploinsufficiency. Human Genomics. 18(1). 29–29. 1 indexed citations
4.
Alfieri, Paolo, Marina Macchiaiolo, Marcella Zollino, et al.. (2023). Behavioral profiling in children and adolescents with Malan syndrome. PubMed. 2. 1106228–1106228. 2 indexed citations
5.
Priolo, Manuela, Francesca Clementina Radio, Andrea Ciolfi, et al.. (2023). Natural history of MRAS‐related Noonan syndrome: Evidence of mild adult‐onset left ventricular hypertrophy and neuropsychiatric features. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 193(2). 160–166.
6.
Priolo, Manuela, Francesca Clementina Radio, Andrea Ciolfi, et al.. (2023). Clinical profiling of MRD48 and functional characterization of two novel pathogenic RAC1 variants. European Journal of Human Genetics. 31(7). 805–814. 4 indexed citations
7.
Priolo, Manuela & Marco Tartaglia. (2023). The Right to Ask, the Need to Answer—When Patients Meet Research: How to Cope with Time. International Journal of Environmental Research and Public Health. 20(5). 4573–4573. 2 indexed citations
8.
Priolo, Manuela, Andrea Ciolfi, Luca Pannone, et al.. (2022). SHP2 's gain‐of‐function in Werner syndrome causes childhood disease onset likely resulting from negative genetic interaction. Clinical Genetics. 102(1). 12–21. 2 indexed citations
9.
Callea, Michele, Roberto Teggi, İzzet Yavuz, et al.. (2013). Ear nose throat manifestations in hypoidrotic ectodermal dysplasia. International Journal of Pediatric Otorhinolaryngology. 77(11). 1801–1804. 24 indexed citations
10.
Priolo, Manuela, et al.. (2012). A peculiar mutation in the DNA-binding/dimerization domain of NFIX causes Sotos-like overgrowth syndrome: A new case. Gene. 511(1). 103–105. 25 indexed citations
11.
Basinko, Audrey, et al.. (2011). Clinical and molecular cytogenetic studies in ring chromosome 5: Report of a child with congenital abnormalities. European Journal of Medical Genetics. 55(2). 112–116. 24 indexed citations
12.
Priolo, Manuela. (2009). Ectodermal dysplasias: An overview and update of clinical and molecular‐functional mechanisms. American Journal of Medical Genetics Part A. 149A(9). 2003–2013. 23 indexed citations
13.
Rossi, Pia, Antonio Terracciano, Manuela Priolo, et al.. (2009). The metabotropic glutamate receptor 1, GRM1: evaluation as a candidate gene for inherited forms of cerebellar ataxia. Journal of Neurology. 257(4). 598–602. 17 indexed citations
14.
Uliana, Vera, N. Giordano, Rossella Caselli, et al.. (2008). Expanding the phenotype of 22q11 deletion syndrome: the MURCS association. Clinical Dysmorphology. 17(1). 13–17. 15 indexed citations
15.
Priolo, Manuela, Angela Sparago, Corrado Mammì, et al.. (2008). MS-MLPA is a specific and sensitive technique for detecting all chromosome 11p15.5 imprinting defects of BWS and SRS in a single-tube experiment. European Journal of Human Genetics. 16(5). 565–571. 57 indexed citations
16.
Priolo, Manuela, et al.. (2006). Malpuech syndrome: Broadening the clinical spectrum and molecular analysis by array-CGH. European Journal of Medical Genetics. 50(2). 139–143. 4 indexed citations
17.
Pescucci, Chiara, Rossella Caselli, Salvatore Grosso, et al.. (2006). 2q24–q31 Deletion: Report of a case and review of the literature. European Journal of Medical Genetics. 50(1). 21–32. 61 indexed citations
18.
Silengo, Margherita, Margherita Lerone, Marco Seri, Manuela Priolo, & Laura Jarre. (2000). New clinical findings in oculo-ecNew clinical findings in oculo-ectodermal syndrome.. Clinical Dysmorphology. 39–41. 3 indexed citations
19.
Priolo, Manuela, et al.. (2000). Question mark ears, temporo-mandibular joint malformation and hypotonia: auriculo-condylar syndrome or a distinct entity?. Clinical Dysmorphology. 9(4). 277–280. 20 indexed citations
20.
Lerone, Margherita, Manuela Priolo, Arturo Naselli, et al.. (1997). Ectodermal abnormalities in Kabuki syndrome. American Journal of Medical Genetics. 73(3). 263–266. 28 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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