Vanna Pecile
Impact in
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genetic Syndromes and Imprinting
- Genomics and Rare Diseases
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 35
- Genomic variations and chromosomal abnormalities 22
- Genetics and Neurodevelopmental Disorders 14
- Genomics and Rare Diseases 8
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 7
- Genetic Syndromes and Imprinting 4
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- Epigenetics and DNA Methylation 5
- Co-authors
- Marcella Zollino (4 shared papers)Giuseppe Marangi (3 shared papers)Giovanni Neri (2 shared papers)Flavio Faletra (13 shared papers)Paolo Gasparini (10 shared papers)Laura Mazzanti (1 shared paper)Marina Murdolo (2 shared papers)Cinzia Galasso (1 shared paper)
- Journals
- European Journal of Medical Genetics (3 papers)Gene (3 papers)Journal of Medical Genetics (3 papers)Clinical Genetics (3 papers)European Journal of Human Genetics (2 papers)
- Partner nations
- ItalyUnited StatesSpain
In The Last Decade
Vanna Pecile
53 papers receiving 787 citations
Peers
Comparison fields: 5 of 72
- Genetics 499
- Pediatrics, Perinatology and Child Health 175
- Molecular Biology 443
- Sensory Systems 25
- Cancer Research 50
Countries citing papers authored by Vanna Pecile
This map shows the geographic impact of Vanna Pecile'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 Vanna Pecile with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Vanna Pecile more than expected).
Fields of papers citing papers by Vanna Pecile
This network shows the impact of papers produced by Vanna Pecile. 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 Vanna Pecile. The network helps show where Vanna Pecile may publish in the future.
Co-authors
The 25 scholars most cited alongside Vanna Pecile, 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 54 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2008 | 112 | |
| 2 | Molecular basis of Diamond-Blackfan anemia: new findings from the Italian registry and a review of the literature. | 2004 | 71 |
| 3 | 2012 | 54 | |
| 4 | 2009 | 39 | |
| 5 | 1997 | 39 | |
| 6 | 1990 | 38 | |
| 7 | 2014 | 36 | |
| 8 | 2013 | 31 | |
| 9 | 2003 | 31 | |
| 10 | 2016 | 28 | |
| 11 | 2018 | 25 | |
| 12 | 2018 | 24 | |
| 13 | 2015 | 20 | |
| 14 | 2014 | 20 | |
| 15 | 2018 | 19 | |
| 16 | 2019 | 18 | |
| 17 | 2011 | 17 | |
| 18 | 2011 | 15 | |
| 19 | 2017 | 14 | |
| 20 | 1985 | 12 |
About Vanna Pecile
Vanna Pecile is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Plant Science and Genetics, having authored 54 papers that have together received 825 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (22 papers), Genetics and Neurodevelopmental Disorders (14 papers), Prenatal Screening and Diagnostics (12 papers), Chromosomal and Genetic Variations (8 papers), Genomics and Rare Diseases (8 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (7 papers), Epigenetics and DNA Methylation (5 papers) and Genetic Syndromes and Imprinting (4 papers). The work is most often cited by research in Genetics (499 citations), Pediatrics, Perinatology and Child Health (175 citations), Molecular Biology (443 citations), Sensory Systems (25 citations) and Cancer Research (50 citations). Vanna Pecile has collaborated with scholars based in Italy, United States and Spain. Frequent co-authors include Marcella Zollino, Giuseppe Marangi, Giovanni Neri, Flavio Faletra, Paolo Gasparini, Laura Mazzanti, Marina Murdolo, Cinzia Galasso, G Filippi and Daniela Orteschi. Their work appears in journals such as European Journal of Medical Genetics, Gene, Journal of Medical Genetics, Clinical Genetics and European Journal of Human 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.