Davide Vecchio

872 total citations
33 papers, 333 citations indexed

About

Davide Vecchio is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Davide Vecchio has authored 33 papers receiving a total of 333 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Genetics, 10 papers in Molecular Biology and 8 papers in Surgery. Recurrent topics in Davide Vecchio's work include Genomics and Rare Diseases (5 papers), Genomic variations and chromosomal abnormalities (5 papers) and Genetic Syndromes and Imprinting (4 papers). Davide Vecchio is often cited by papers focused on Genomics and Rare Diseases (5 papers), Genomic variations and chromosomal abnormalities (5 papers) and Genetic Syndromes and Imprinting (4 papers). Davide Vecchio collaborates with scholars based in Italy, Australia and South Korea. Davide Vecchio's co-authors include Giovanni Corsello, Mario Giuffrè, Ettore Piro, Caterina Mammina, Aurora Aléo, Celestino Bonura, Marina Macchiaiolo, Laura Saporito, Giorgio Graziano and Daniela Maria Geraci and has published in prestigious journals such as The FASEB Journal, The American Journal of Human Genetics and Frontiers in Microbiology.

In The Last Decade

Davide Vecchio

30 papers receiving 328 citations

Peers

Davide Vecchio

GENET

EPIDE

PPCH

SPS

Melahat Melek Oğuz Türkiye

Rose Geransar Canada

Ahmad Abulaban Saudi Arabia

Elizabeth Prout Parks United States

Amy MacDougall United Kingdom

Annette Uwineza Rwanda

Caoimhe McKenna United Kingdom

Jane M. DeLuca United States

Ann-Cathrin Svensson Sweden

Melahat Melek Oğuz Türkiye

Davide Vecchio

33 ×0.3

24 ×0.3

GENET

80 ×1.4

EPIDE

46 ×1.1

PPCH

64 ×1.6

SPS

Citations per year, relative to Davide Vecchio Davide Vecchio (= 1×) peers Melahat Melek Oğuz

Countries citing papers authored by Davide Vecchio

Since Specialization

Citations

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

Fields of papers citing papers by Davide Vecchio

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Davide Vecchio

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

All Works

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20 of 20 papers shown

Macchiaiolo, Marina, Michaela Veronika Gonfiantini, Antonella Cacchione, et al.. (2025). Reduction of tumor burden via precise photothermal release of sirolimus by carbon nanodots in 3D plexiform neurofibroma-in-a-dish models. Surfaces and Interfaces. 59. 105978–105978. 3 indexed citations

Travaglini, Lorena, Marina Macchiaiolo, Giacomo Garone, et al.. (2024). Spectrum of ERCC6-Related Cockayne Syndrome (Type B): From Mild to Severe Forms. Genes. 15(4). 508–508.

Cocciadiferro, Dario, Tommaso Mazza, Davide Vecchio, et al.. (2024). Exploiting in silico structural analysis to introduce emerging genotype–phenotype correlations in DHCR24-related sterol biosynthesis disorder: a case study. Frontiers in Genetics. 14. 1307934–1307934. 5 indexed citations

Valente, Paola, Davide Vecchio, Michaela Veronika Gonfiantini, et al.. (2023). Long-term follow-up in a pediatric patient with Ligneous Conjunctivitis due to PLG gene mutation in topical plasminogen treatment after successful use of ocular prosthesis for aesthetic rehabilitation: a case report. The Italian Journal of Pediatrics/Italian journal of pediatrics. 49(1). 101–101.

Macchiaiolo, Marina, Davide Vecchio, Michaela Veronika Gonfiantini, et al.. (2022). Expanding phenotype of FAM111B‐related disease focusing on liver involvement: Literature review, report of a case with end‐stage liver disease and proposal for a new acronym. American Journal of Medical Genetics Part A. 188(10). 2920–2931. 5 indexed citations

Buonuomo, Paola Sabrina, Giovanna Leone, Michaela Veronika Gonfiantini, et al.. (2021). Evolocumab in the management of children <10 years of age affected by homozygous familial hypercholesterolemia. Atherosclerosis. 324. 148–150. 2 indexed citations

Bozzola, Elena, Giulia Spina, Massimiliano Valeriani, et al.. (2021). Management of pediatric post-infectious neurological syndromes. The Italian Journal of Pediatrics/Italian journal of pediatrics. 47(1). 6 indexed citations

Rossi, Michela, Paola Sabrina Buonuomo, Giulia Battafarano, et al.. (2021). Dysregulated miRNAs in bone cells of patients with Gorham‐Stout disease. The FASEB Journal. 35(3). e21424–e21424. 12 indexed citations

Vecchio, Davide, Marina Macchiaiolo, Michaela Veronika Gonfiantini, & Andrea Bartuli. (2021). Ancient Romans and Down Syndrome. Pediatric Research. 90(6). 1266–1267.

10.

Rossi, Michela, Paola Sabrina Buonuomo, Giulia Battafarano, et al.. (2021). Stimulation of Treg Cells to Inhibit Osteoclastogenesis in Gorham-Stout Disease. Frontiers in Cell and Developmental Biology. 9. 706596–706596. 9 indexed citations

11.

Vecchio, Davide, et al.. (2020). Deciphering the Invdupdel(8p) Genotype–Phenotype Correlation: Our Opinion. Brain Sciences. 10(7). 451–451. 5 indexed citations

12.

Dong, Xiaomin, Natalie B. Tan, Katherine B. Howell, et al.. (2020). Bi-allelic LoF NRROS Variants Impairing Active TGF-β1 Delivery Cause a Severe Infantile-Onset Neurodegenerative Condition with Intracranial Calcification. The American Journal of Human Genetics. 106(4). 559–569. 18 indexed citations

13.

Bozzola, Elena, Giulia Spina, Davide Vecchio, et al.. (2019). Media use during adolescence: the recommendations of the Italian Pediatric Society. The Italian Journal of Pediatrics/Italian journal of pediatrics. 45(1). 149–149. 40 indexed citations

14.

Giuffrè, Mario, Daniela Maria Geraci, Celestino Bonura, et al.. (2016). The Increasing Challenge of Multidrug-Resistant Gram-Negative Bacilli. Medicine. 95(10). e3016–e3016. 50 indexed citations

15.

Geraci, Daniela Maria, Mario Giuffrè, Celestino Bonura, et al.. (2016). A Snapshot on MRSA Epidemiology in a Neonatal Intensive Care Unit Network, Palermo, Italy. Frontiers in Microbiology. 7. 815–815. 5 indexed citations

16.

Biasio, Luigi Roberto, Giovanni Corsello, Claudio Costantino, et al.. (2016). Communication about vaccination: A shared responsibility. Human Vaccines & Immunotherapeutics. 12(11). 2984–2987. 33 indexed citations

17.

Vecchio, Davide & Mario Giuffrè. (2016). The Coat-Hanger Angle Sign. The Journal of Pediatrics. 177. 325–325.e1. 4 indexed citations

18.

Piccione, Maria, et al.. (2015). 4p16.1-p15.31 duplication and 4p terminal deletion in a 3-years old Chinese girl: Array-CGH, genotype-phenotype and neurological characterization. European Journal of Paediatric Neurology. 19(4). 477–483. 6 indexed citations

19.

Corsello, Giovanni & Davide Vecchio. (2014). Green nail syndrome. Pediatrics International. 56(5). 801–801. 2 indexed citations

20.

Piccione, Maria, Davide Vecchio, Simona Cavani, et al.. (2011). The first case of myoclonic epilepsy in a child with a de novo 22q11.2 microduplication. American Journal of Medical Genetics Part A. 155(12). 3054–3059. 15 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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