Fabiola Ceroni
Impact in
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- Reading and Literacy Development
- Language Development and Disorders
- Genetics top 10%
- Ocular Disorders and Treatments
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genetic Associations and Epidemiology
- Genomics and Rare Diseases
Papers in
- Genetics 10
- Ocular Disorders and Treatments 8
- Genomics and Rare Diseases 1
- Genomic variations and chromosomal abnormalities 1
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- Reading and Literacy Development 3
- Language Development and Disorders 1
- Co-authors
- Nicola Ragge (7 shared papers)Julie Plaisancié (3 shared papers)Patrick Calvas (3 shared papers)Nicolas Chassaing (3 shared papers)Celia Zazo Seco (1 shared paper)Elena Maestrini (6 shared papers)Dianne F. Newbury (4 shared papers)Nuala H. Simpson (3 shared papers)
- Journals
- European Journal of Human Genetics (6 papers)The American Journal of Human Genetics (2 papers)Human Genetics (2 papers)Scientific Reports (2 papers)Proceedings of the National Academy of Sciences (1 paper)
- Partner nations
- United KingdomUnited StatesItaly
In The Last Decade
Fabiola Ceroni
20 papers receiving 553 citations
Fabiola Ceroni's Hit Papers
Peers
Comparison fields: 5 of 39
- Developmental and Educational Psychology 112
- Genetics 167
- Cognitive Neuroscience 43
- Cell Biology 13
- Molecular Biology 40
Countries citing papers authored by Fabiola Ceroni
This map shows the geographic impact of Fabiola Ceroni'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 Fabiola Ceroni with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Fabiola Ceroni more than expected).
Fields of papers citing papers by Fabiola Ceroni
This network shows the impact of papers produced by Fabiola Ceroni. 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 Fabiola Ceroni. The network helps show where Fabiola Ceroni may publish in the future.
Co-authors
The 25 scholars most cited alongside Fabiola Ceroni, 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 22 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Discovery of 42 genome-wide significant loci associated with dyslexia Hit paper breakdown → | 2022 | 83 |
| 2 | Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people Hit paper breakdown → | 2022 | 80 |
| 3 | 2019 | 73 | |
| 4 | 2018 | 48 | |
| 5 | 2014 | 42 | |
| 6 | 2015 | 41 | |
| 7 | 2019 | 34 | |
| 8 | 2014 | 32 | |
| 9 | 2014 | 20 | |
| 10 | 2020 | 18 | |
| 11 | 2024 | 14 | |
| 12 | 2024 | 14 | |
| 13 | 2017 | 11 | |
| 14 | 2016 | 10 | |
| 15 | 2022 | 9 | |
| 16 | 2022 | 9 | |
| 17 | 2022 | 9 | |
| 18 | 2021 | 4 | |
| 19 | 2023 | 3 | |
| 20 | 2024 | 1 |
About Fabiola Ceroni
Fabiola Ceroni is a scholar working on Genetics, Developmental and Educational Psychology, Cognitive Neuroscience, Nuclear Energy and Engineering and Waste Management and Disposal, having authored 22 papers that have together received 555 indexed citations. Recurring topics across this work include Ocular Disorders and Treatments (8 papers), Autism Spectrum Disorder Research (4 papers), Reading and Literacy Development (3 papers), Neurobiology of Language and Bilingualism (1 paper), Genomics and Rare Diseases (1 paper), Genomic variations and chromosomal abnormalities (1 paper) and Language Development and Disorders (1 paper). The work is most often cited by research in Developmental and Educational Psychology (112 citations), Genetics (167 citations), Cognitive Neuroscience (43 citations), Cell Biology (13 citations) and Molecular Biology (40 citations). Fabiola Ceroni has collaborated with scholars based in United Kingdom, United States and Italy. Frequent co-authors include Nicola Ragge, Julie Plaisancié, Patrick Calvas, Nicolas Chassaing, Celia Zazo Seco, Elena Maestrini, Dianne F. Newbury, Nuala H. Simpson, Elena Bacchelli and Dalila Pinto. Their work appears in journals such as European Journal of Human Genetics, The American Journal of Human Genetics, Human Genetics, Scientific Reports and Proceedings of the National Academy of Sciences.
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.