Fabiola Ceroni
Impact in
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- Genetics and Neurodevelopmental Disorders
- Ocular Disorders and Treatments
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Congenital Ear and Nasal Anomalies
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- Language Development and Disorders
Papers in
- Genetics 11
- Genetics and Neurodevelopmental Disorders 5
- Genomic variations and chromosomal abnormalities 5
- Ocular Disorders and Treatments 4
- Genomics and Rare Diseases 1
- Forensic and Genetic Research 1
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- Fibroblast Growth Factor Research 1
- Ion channel regulation and function 1
- Co-authors
- Nicola Ragge (7 shared papers)Richard Holt (4 shared papers)Nicolas Chassaing (3 shared papers)Julie Plaisancié (3 shared papers)Celia Zazo Seco (1 shared paper)Elena Maestrini (6 shared papers)Patrick Calvas (3 shared papers)Dianne F. Newbury (4 shared papers)
- Journals
- European Journal of Human Genetics (5 papers)Scientific Reports (2 papers)Autism Research (1 paper)Journal of Neurodevelopmental Disorders (1 paper)npj Genomic Medicine (1 paper)
- Partner nations
- United KingdomItalyUnited States
In The Last Decade
Fabiola Ceroni
14 papers receiving 247 citations
Peers
Comparison fields: 5 of 50
- Genetics 129
- Developmental and Educational Psychology 26
- Genetics 18
- Cognitive Neuroscience 33
- Molecular Biology 104
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
| # | Work | ||
|---|---|---|---|
| 1 | 2019 | 56 | |
| 2 | 2014 | 38 | |
| 3 | 2015 | 35 | |
| 4 | 2014 | 31 | |
| 5 | 2014 | 18 | |
| 6 | 2020 | 17 | |
| 7 | 2024 | 11 | |
| 8 | 2017 | 11 | |
| 9 | 2022 | 9 | |
| 10 | 2016 | 7 | |
| 11 | 2022 | 7 | |
| 12 | 2023 | 3 | |
| 13 | 2021 | 3 | |
| 14 | 2024 | 2 | |
| 15 | 2026 | 0 |
About Fabiola Ceroni
Fabiola Ceroni is a scholar working on Genetics, Molecular Biology, Cognitive Neuroscience, Cell Biology and Surgery, having authored 15 papers that have together received 248 indexed citations. Recurring topics across this work include Autism Spectrum Disorder Research (5 papers), Genetics and Neurodevelopmental Disorders (5 papers), Genomic variations and chromosomal abnormalities (5 papers), Ocular Disorders and Treatments (4 papers), Genomics and Rare Diseases (1 paper), Forensic and Genetic Research (1 paper), Fibroblast Growth Factor Research (1 paper) and Ion channel regulation and function (1 paper). The work is most often cited by research in Genetics (129 citations), Developmental and Educational Psychology (26 citations), Genetics (18 citations), Cognitive Neuroscience (33 citations) and Molecular Biology (104 citations). Fabiola Ceroni has collaborated with scholars based in United Kingdom, Italy and United States. Frequent co-authors include Nicola Ragge, Richard Holt, Nicolas Chassaing, Julie Plaisancié, Celia Zazo Seco, Elena Maestrini, Patrick Calvas, Dianne F. Newbury, Nuala H. Simpson and Elena Bacchelli. Their work appears in journals such as European Journal of Human Genetics, Scientific Reports, Autism Research, Journal of Neurodevelopmental Disorders and npj Genomic Medicine.
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.