Sara Loddo
Impact in
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
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- Prenatal Screening and Diagnostics
- Fetal and Pediatric Neurological Disorders
Papers in
- Genetics 28
- Genomic variations and chromosomal abnormalities 20
- Genetics and Neurodevelopmental Disorders 8
- Genomics and Rare Diseases 8
- Congenital Ear and Nasal Anomalies 3
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- Congenital heart defects research 6
- Chromatin Remodeling and Cancer 3
- Co-authors
- Antonio Novelli (34 shared papers)Laura Bernardini (9 shared papers)Agatino Battaglia (3 shared papers)Viola Alesi (19 shared papers)Anna Capalbo (2 shared papers)Viola Doccini (2 shared papers)Tiziana Filippi (2 shared papers)Bruno Dallapiccola (17 shared papers)
- Journals
- International Journal of Molecular Sciences (3 papers)Neurogenetics (2 papers)European Journal of Medical Genetics (2 papers)Cytogenetic and Genome Research (2 papers)Orphanet Journal of Rare Diseases (2 papers)
- Partner nations
- ItalyUnited StatesFrance
In The Last Decade
Sara Loddo
39 papers receiving 613 citations
Peers
Comparison fields: 5 of 55
- Genetics 369
- Pediatrics, Perinatology and Child Health 97
- Molecular Biology 239
- Genetics 33
- Cognitive Neuroscience 60
Countries citing papers authored by Sara Loddo
This map shows the geographic impact of Sara Loddo'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 Sara Loddo with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sara Loddo more than expected).
Fields of papers citing papers by Sara Loddo
This network shows the impact of papers produced by Sara Loddo. 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 Sara Loddo. The network helps show where Sara Loddo may publish in the future.
Co-authors
The 25 scholars most cited alongside Sara Loddo, 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 39 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2013 | 147 | |
| 2 | 2014 | 59 | |
| 3 | 2019 | 47 | |
| 4 | 2009 | 45 | |
| 5 | 2018 | 44 | |
| 6 | 2011 | 34 | |
| 7 | 2015 | 30 | |
| 8 | 2013 | 27 | |
| 9 | 2020 | 23 | |
| 10 | 2019 | 23 | |
| 11 | 2010 | 19 | |
| 12 | 2013 | 15 | |
| 13 | 2021 | 12 | |
| 14 | 2019 | 11 | |
| 15 | 2012 | 11 | |
| 16 | 2020 | 9 | |
| 17 | 2018 | 9 | |
| 18 | 2018 | 9 | |
| 19 | 2017 | 9 | |
| 20 | 2020 | 7 |
About Sara Loddo
Sara Loddo is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Plant Science and Genetics, having authored 39 papers that have together received 649 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (20 papers), Genetics and Neurodevelopmental Disorders (8 papers), Genomics and Rare Diseases (8 papers), Congenital heart defects research (6 papers), Chromosomal and Genetic Variations (6 papers), Congenital Ear and Nasal Anomalies (3 papers), Fetal and Pediatric Neurological Disorders (3 papers) and Chromatin Remodeling and Cancer (3 papers). The work is most often cited by research in Genetics (369 citations), Pediatrics, Perinatology and Child Health (97 citations), Molecular Biology (239 citations), Genetics (33 citations) and Cognitive Neuroscience (60 citations). Sara Loddo has collaborated with scholars based in Italy, United States and France. Frequent co-authors include Antonio Novelli, Laura Bernardini, Agatino Battaglia, Viola Alesi, Anna Capalbo, Viola Doccini, Tiziana Filippi, Bruno Dallapiccola, John C. Carey and Marco Tartaglia. Their work appears in journals such as International Journal of Molecular Sciences, Neurogenetics, European Journal of Medical Genetics, Cytogenetic and Genome Research and Orphanet Journal of Rare Diseases.
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.