Daniela Orteschi
Impact in
- Genetics top 5%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Genetic Syndromes and Imprinting
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 35
- Genomic variations and chromosomal abnormalities 21
- Genetics and Neurodevelopmental Disorders 12
- Genomics and Rare Diseases 10
- Genetic Syndromes and Imprinting 2
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- Prenatal Screening and Diagnostics 3
- Co-authors
- Marcella Zollino (33 shared papers)Giovanni Neri (15 shared papers)Giuseppe Marangi (19 shared papers)Domenica Battaglia (7 shared papers)Serena Lattante (7 shared papers)Vincenzo Leuzzi (4 shared papers)Fiorella Gurrieri (5 shared papers)Marina Murdolo (5 shared papers)
- Journals
- European Journal of Human Genetics (6 papers)Genes (4 papers)Journal of Medical Genetics (3 papers)PLoS ONE (3 papers)Epilepsia (2 papers)
- Partner nations
- ItalyUnited StatesSwitzerland
In The Last Decade
Daniela Orteschi
47 papers receiving 1.3k citations
Peers
Comparison fields: 5 of 61
- Genetics 825
- Pediatrics, Perinatology and Child Health 92
- Ophthalmology 65
- Psychiatry and Mental health 100
- Cognitive Neuroscience 109
Countries citing papers authored by Daniela Orteschi
This map shows the geographic impact of Daniela Orteschi'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 Daniela Orteschi with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Daniela Orteschi more than expected).
Fields of papers citing papers by Daniela Orteschi
This network shows the impact of papers produced by Daniela Orteschi. 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 Daniela Orteschi. The network helps show where Daniela Orteschi may publish in the future.
Co-authors
The 25 scholars most cited alongside Daniela Orteschi, 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 48 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2012 | 191 | |
| 2 | 2012 | 128 | |
| 3 | 2009 | 87 | |
| 4 | 2019 | 70 | |
| 5 | 2009 | 60 | |
| 6 | 2012 | 60 | |
| 7 | 2011 | 59 | |
| 8 | 2013 | 53 | |
| 9 | 2015 | 52 | |
| 10 | 2009 | 50 | |
| 11 | 2008 | 46 | |
| 12 | 2009 | 45 | |
| 13 | 2012 | 43 | |
| 14 | 2013 | 36 | |
| 15 | 2015 | 34 | |
| 16 | 2009 | 32 | |
| 17 | 2009 | 32 | |
| 18 | 2010 | 30 | |
| 19 | 2014 | 28 | |
| 20 | 2012 | 27 |
About Daniela Orteschi
Daniela Orteschi is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Psychiatry and Mental health, Ophthalmology and Developmental Biology, having authored 48 papers that have together received 1.4k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (21 papers), Genetics and Neurodevelopmental Disorders (12 papers), Genomics and Rare Diseases (10 papers), Epilepsy research and treatment (3 papers), Prenatal Screening and Diagnostics (3 papers), Ocular Oncology and Treatments (2 papers), Genetic Syndromes and Imprinting (2 papers) and Pluripotent Stem Cells Research (1 paper). The work is most often cited by research in Genetics (825 citations), Pediatrics, Perinatology and Child Health (92 citations), Ophthalmology (65 citations), Psychiatry and Mental health (100 citations) and Cognitive Neuroscience (109 citations). Daniela Orteschi has collaborated with scholars based in Italy, United States and Switzerland. Frequent co-authors include Marcella Zollino, Giovanni Neri, Giuseppe Marangi, Domenica Battaglia, Serena Lattante, Vincenzo Leuzzi, Fiorella Gurrieri, Marina Murdolo, Eugenio Maria Mercuri and Vanna Pecile. Their work appears in journals such as European Journal of Human Genetics, Genes, Journal of Medical Genetics, PLoS ONE and Epilepsia.
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.