Daniela Orteschi
Impact in
- Genetics top 5%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Genetic Syndromes and Imprinting
- Cognitive Neuroscience top 10%
- Autism Spectrum Disorder Research
Papers in
- Genetics 24
- Genomic variations and chromosomal abnormalities 19
- Genetics and Neurodevelopmental Disorders 12
- Genomics and Rare Diseases 8
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- Chromatin Remodeling and Cancer 3
- Genomics and Chromatin Dynamics 3
- Glycosylation and Glycoproteins Research 2
- Co-authors
- Marcella Zollino (31 shared papers)Giuseppe Marangi (19 shared papers)Giovanni Neri (14 shared papers)Domenica Battaglia (7 shared papers)Serena Lattante (7 shared papers)Fiorella Gurrieri (5 shared papers)Vincenzo Leuzzi (4 shared papers)Marina Murdolo (4 shared papers)
- Journals
- European Journal of Human Genetics (5 papers)Genes (3 papers)PLoS ONE (3 papers)Epilepsia (2 papers)Journal of Medical Genetics (2 papers)
- Partner nations
- ItalyUnited StatesNetherlands
In The Last Decade
Daniela Orteschi
36 papers receiving 913 citations
Peers
Comparison fields: 5 of 66
- Genetics 584
- Cognitive Neuroscience 142
- Ophthalmology 55
- Pediatrics, Perinatology and Child Health 105
- Molecular Biology 405
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 37 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2012 | 187 | |
| 2 | 2012 | 114 | |
| 3 | 2019 | 65 | |
| 4 | 2009 | 59 | |
| 5 | 2012 | 56 | |
| 6 | 2013 | 53 | |
| 7 | 2009 | 46 | |
| 8 | 2008 | 42 | |
| 9 | 2012 | 40 | |
| 10 | 2013 | 32 | |
| 11 | 2015 | 31 | |
| 12 | 2010 | 27 | |
| 13 | 2009 | 27 | |
| 14 | 2014 | 24 | |
| 15 | 2012 | 23 | |
| 16 | 2008 | 23 | |
| 17 | 2013 | 21 | |
| 18 | 2017 | 20 | |
| 19 | 2017 | 20 | |
| 20 | 2015 | 12 |
About Daniela Orteschi
Daniela Orteschi is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Plant Science and Cancer Research, having authored 37 papers that have together received 1.0k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (19 papers), Genetics and Neurodevelopmental Disorders (12 papers), Genomics and Rare Diseases (8 papers), Prenatal Screening and Diagnostics (5 papers), Chromatin Remodeling and Cancer (3 papers), Genomics and Chromatin Dynamics (3 papers), Glycosylation and Glycoproteins Research (2 papers) and Cancer Genomics and Diagnostics (2 papers). The work is most often cited by research in Genetics (584 citations), Cognitive Neuroscience (142 citations), Ophthalmology (55 citations), Pediatrics, Perinatology and Child Health (105 citations) and Molecular Biology (405 citations). Daniela Orteschi has collaborated with scholars based in Italy, United States and Netherlands. Frequent co-authors include Marcella Zollino, Giuseppe Marangi, Giovanni Neri, Domenica Battaglia, Serena Lattante, Fiorella Gurrieri, Vincenzo Leuzzi, Marina Murdolo, Eugenio Mercuri and Vanna Pecile. Their work appears in journals such as European Journal of Human Genetics, Genes, PLoS ONE, Epilepsia and Journal of Medical 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.