V. Ventruto
Impact in
- Developmental Biology top 5%
- Congenital limb and hand anomalies
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Connective tissue disorders research
Papers in
- Genetics 19
- Hemoglobinopathies and Related Disorders 8
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 5
- Genomic variations and chromosomal abnormalities 5
- Genetic Syndromes and Imprinting 3
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- Retinal Development and Disorders 3
- Ubiquitin and proteasome pathways 2
- Co-authors
- Michael T. Trese (1 shared paper)Xiaodong Jiao (1 shared paper)J. Fielding Hejtmancik (1 shared paper)Barkur S. Shastry (1 shared paper)Corrado Baglioni (3 shared papers)M Stabile (13 shared papers)Michele D’Urso (7 shared papers)Maria Giuseppina Miano (6 shared papers)
- Journals
- Journal of Medical Genetics (9 papers)Clinical Genetics (3 papers)Acta Haematologica (2 papers)Annals of Hematology (2 papers)Ophthalmic Genetics (2 papers)
- Partner nations
- ItalyUnited StatesSpain
In The Last Decade
V. Ventruto
46 papers receiving 777 citations
Peers
Comparison fields: 5 of 68
- Developmental Biology 50
- Genetics 281
- Genetics 73
- Molecular Biology 447
- Ophthalmology 41
Countries citing papers authored by V. Ventruto
This map shows the geographic impact of V. Ventruto'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 V. Ventruto with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites V. Ventruto more than expected).
Fields of papers citing papers by V. Ventruto
This network shows the impact of papers produced by V. Ventruto. 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 V. Ventruto. The network helps show where V. Ventruto may publish in the future.
Co-authors
The 25 scholars most cited alongside V. Ventruto, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 49 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2004 | 161 | |
| 2 | 1998 | 53 | |
| 3 | 2002 | 42 | |
| 4 | 2001 | 36 | |
| 5 | 1998 | 30 | |
| 6 | 1999 | 30 | |
| 7 | 1965 | 29 | |
| 8 | 1989 | 26 | |
| 9 | 1989 | 24 | |
| 10 | 2007 | 24 | |
| 11 | 2005 | 24 | |
| 12 | 1968 | 23 | |
| 13 | 1984 | 22 | |
| 14 | 1977 | 22 | |
| 15 | 1988 | 21 | |
| 16 | 1984 | 20 | |
| 17 | 1983 | 19 | |
| 18 | 1985 | 19 | |
| 19 | 1982 | 16 | |
| 20 | 1985 | 16 |
About V. Ventruto
V. Ventruto is a scholar working on Genetics, Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health and Surgery, having authored 49 papers that have together received 822 indexed citations. Recurring topics across this work include Hemoglobinopathies and Related Disorders (8 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers), Genomic variations and chromosomal abnormalities (5 papers), Prenatal Screening and Diagnostics (3 papers), Congenital limb and hand anomalies (3 papers), Genetic Syndromes and Imprinting (3 papers), Retinal Development and Disorders (3 papers) and Ubiquitin and proteasome pathways (2 papers). The work is most often cited by research in Developmental Biology (50 citations), Genetics (281 citations), Genetics (73 citations), Molecular Biology (447 citations) and Ophthalmology (41 citations). V. Ventruto has collaborated with scholars based in Italy, United States and Spain. Frequent co-authors include Michael T. Trese, Xiaodong Jiao, J. Fielding Hejtmancik, Barkur S. Shastry, Corrado Baglioni, M Stabile, Michele D’Urso, Maria Giuseppina Miano, Maria Luigia Cavaliere and Gioacchino Scarano. Their work appears in journals such as Journal of Medical Genetics, Clinical Genetics, Acta Haematologica, Annals of Hematology and Ophthalmic Genetics.
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.