Raffaella Stallone

523 total citations
16 papers, 312 citations indexed

About

Raffaella Stallone is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Raffaella Stallone has authored 16 papers receiving a total of 312 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 9 papers in Molecular Biology and 5 papers in Plant Science. Recurrent topics in Raffaella Stallone's work include Genomic variations and chromosomal abnormalities (9 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Chromosomal and Genetic Variations (4 papers). Raffaella Stallone is often cited by papers focused on Genomic variations and chromosomal abnormalities (9 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Chromosomal and Genetic Variations (4 papers). Raffaella Stallone collaborates with scholars based in Italy, Germany and United Kingdom. Raffaella Stallone's co-authors include Massimo Carella, Orazio Palumbo, Leopoldo Zelante, Teresa Palladino, Pietro Palumbo, Raffaela Barbano, Antonio Laborante, Patrizia De Bonis, Luigi Bisceglia and Maurizio Delvecchio and has published in prestigious journals such as Nucleic Acids Research, Frontiers in Immunology and Gene.

In The Last Decade

Raffaella Stallone

16 papers receiving 276 citations

Peers

Raffaella Stallone

GENET

RNMI

PHEOH

OPHTH

Filomena Tiziana Papa Italy

Sophie Julia France

Marc Pauper Netherlands

Kelly E. Jackson United States

Marie‐Claire Vincent France

G.J. te Meerman Netherlands

Ada Rosenmann Israel

Hannah Verdin Belgium

Aman George India

Luís Nunes Portugal

Filomena Tiziana Papa Italy

Raffaella Stallone

257 ×1.7

GENET

182 ×1.7

15 ×0.2

RNMI

33 ×0.8

PHEOH

51 ×1.4

OPHTH

Citations per year, relative to Raffaella Stallone Raffaella Stallone (= 1×) peers Filomena Tiziana Papa

Countries citing papers authored by Raffaella Stallone

Since Specialization

Citations

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

Fields of papers citing papers by Raffaella Stallone

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Raffaella Stallone

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

All Works

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16 of 16 papers shown

Summa, Simona De, Antonella Daniele, Orazio Palumbo, et al.. (2023). miRNA deregulation and relationship with metabolic parameters after Mediterranean dietary intervention in BRCA-mutated women. Frontiers in Oncology. 13. 1147190–1147190. 3 indexed citations

Etna, Marilena P., Martina Severa, Valerio Licursi, et al.. (2021). Genome-Wide Gene Expression Analysis of Mtb-Infected DC Highlights the Rapamycin-Driven Modulation of Regulatory Cytokines via the mTOR/GSK-3β Axis. Frontiers in Immunology. 12. 649475–649475. 7 indexed citations

Palumbo, Pietro, Stefano Castellana, Orazio Palumbo, et al.. (2017). Putative TMPRSS3/GJB2 digenic inheritance of hearing loss detected by targeted resequencing. Molecular and Cellular Probes. 33. 24–27. 8 indexed citations

Palumbo, Orazio, Maria Accadia, Pietro Palumbo, et al.. (2017). Refinement of the critical 7p22.1 deletion region: Haploinsufficiency of ACTB is the cause of the 7p22.1 microdeletion-related developmental disorders. European Journal of Medical Genetics. 61(5). 248–252. 8 indexed citations

Palumbo, Pietro, Maria Accadia, Teresa Palladino, et al.. (2017). Clinical and molecular characterization of an emerging chromosome 22q13.31 microdeletion syndrome. American Journal of Medical Genetics Part A. 176(2). 391–398. 16 indexed citations

Mazza, Tommaso, Gianluigi Mazzoccoli, Caterina Fusilli, et al.. (2016). Multifaceted enrichment analysis of RNA–RNA crosstalk reveals cooperating micro-societies in human colorectal cancer. Nucleic Acids Research. 44(9). 4025–4036. 13 indexed citations

Palumbo, Pietro, Orazio Palumbo, Raffaella Stallone, et al.. (2016). Clinical and molecular characterization of a de novo 19p13.3 microdeletion. Molecular Cytogenetics. 9(1). 40–40. 4 indexed citations

Palumbo, Orazio, Pietro Palumbo, Raffaella Stallone, et al.. (2016). <b><i>PARK2</i></b> Microduplication: Clinical and Molecular Characterization of a Further Case and Review of the Literature. Molecular Syndromology. 7(5). 282–286. 6 indexed citations

Palumbo, Orazio, Pietro Palumbo, Maurizio Delvecchio, et al.. (2014). Microdeletion of 12q24.31: Report of a girl with intellectual disability, stereotypies, seizures and facial dysmorphisms. American Journal of Medical Genetics Part A. 167(2). 438–444. 37 indexed citations

10.

Palumbo, Orazio, Pietro Palumbo, Raffaella Stallone, et al.. (2012). 8q12.1q12.3 de novo microdeletion involving the CHD7 gene in a patient without the major features of CHARGE syndrome: Case report and critical review of the literature. Gene. 513(1). 209–213. 20 indexed citations

11.

Palumbo, Orazio, Pietro Palumbo, Teresa Palladino, et al.. (2012). An emerging phenotype of interstitial 15q25.2 microdeletions: Clinical report and review. American Journal of Medical Genetics Part A. 158A(12). 3182–3189. 14 indexed citations

12.

Delvecchio, Maurizio, Ornella Ludovico, Emanuele Bellacchio, et al.. (2012). MODY type 2 P59S GCK mutant: founder effect in South of Italy. Clinical Genetics. 83(1). 83–87. 3 indexed citations

13.

Mattina, Teresa, et al.. (2012). Interstitial 16p13.3 microduplication: Case report and critical review of genotype–phenotype correlation. European Journal of Medical Genetics. 55(12). 747–752. 28 indexed citations

14.

Palumbo, Orazio, Pietro Palumbo, Teresa Palladino, et al.. (2012). A novel deletion in 2q24.1q24.2 in a girl with mental retardation and generalized hypotonia: a case report. Molecular Cytogenetics. 5(1). 1–1. 28 indexed citations

15.

Palumbo, Orazio, Leonardo D’Agruma, Pietro Palumbo, et al.. (2012). 3p14.1 de novo microdeletion involving the FOXP1 gene in an adult patient with autism, severe speech delay and deficit of motor coordination. Gene. 516(1). 107–113. 33 indexed citations

16.

Bonis, Patrizia De, Antonio Laborante, Raffaella Stallone, et al.. (2011). Mutational screening of VSX1, SPARC, SOD1, LOX, and TIMP3 in keratoconus.. PubMed. 17. 2482–94. 84 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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