Davide Vecchio

956 citations
50 papers · 632 · h-index 14

Impact in

    • Antibiotic Resistance in Bacteria
    • Genetics and Neurodevelopmental Disorders
    • Genomic variations and chromosomal abnormalities
    • Genomics and Rare Diseases

Papers in

    • Genomic variations and chromosomal abnormalities 7
    • Genomics and Rare Diseases 6
    • Genetics and Neurodevelopmental Disorders 6
    • Genetic Syndromes and Imprinting 3
    • Vascular Malformations and Hemangiomas 4
    • Lipoproteins and Cardiovascular Health 3

Davide Vecchio

43 papers receiving 624 citations

Peers

Davide Vecchio
Comparison fields: 5 of 95
  • Molecular Medicine 35
  • Genetics 161
  • Applied Microbiology and Biotechnology 10
  • Health 30
  • Molecular Biology 186
Replace Michael Crowley with:
Michael Crowley United States
Gianfranco Di Gennaro Italy
Richard Chawana South Africa
Christina Landwehr Germany
Elizabeth Lindsay United States
Paul J. Bonthuis United States
Jeffrey Cohen United States
Irena Drašković France
Elizabeth Kim United States
Robert Buttery Australia
Davide Vecchio relative to Michael Crowley United States Michael Crowley's profile →
Citations per field
00.5×2×3.2×
Michael Crowley · 1×
Citations per year

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-authors

The 25 scholars most cited alongside Davide Vecchio, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Davide Vecchio Line = papers co-authored together Davide Vecchio links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 50 papers — load more, or switch the sort, to bring in the rest.

#Work
1 2020138
2 201653
3 202249
4 201947
5 201636
6 201830
7 202122
8 202021
9 201819
10 202218
11 201118
12 202117
13 201516
14
A case of femoral-facial syndrome in a patient with autism spectrum disorders.
201115
15 202114
16 201614
17 202110
18 202010
19 20206
20 20216

About Davide Vecchio

Davide Vecchio is a scholar working on Genetics, Surgery, Pediatrics, Perinatology and Child Health, Molecular Biology and Molecular Medicine, having authored 50 papers that have together received 632 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (7 papers), Genomics and Rare Diseases (6 papers), Genetics and Neurodevelopmental Disorders (6 papers), Vascular Malformations and Hemangiomas (4 papers), Lipoproteins and Cardiovascular Health (3 papers), Prenatal Screening and Diagnostics (3 papers), Genetic Syndromes and Imprinting (3 papers) and Neonatal and Maternal Infections (2 papers). The work is most often cited by research in Molecular Medicine (35 citations), Genetics (161 citations), Applied Microbiology and Biotechnology (10 citations), Health (30 citations) and Molecular Biology (186 citations). Davide Vecchio has collaborated with scholars based in Italy, Spain and United States. Frequent co-authors include Giovanni Corsello, Mario Giuffrè, Celestino Bonura, Giorgio Graziano, Daniela Maria Geraci, Ettore Piro, Vincenzo Antona, Caterina Mammina, Marina Macchiaiolo and Laura Saporito. Their work appears in journals such as Orphanet Journal of Rare Diseases, Frontiers in Genetics, The Journal of Pediatrics, Atherosclerosis and Frontiers in Microbiology.

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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