Anna Cereda
Impact in
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genetic Syndromes and Imprinting
- Genomics and Rare Diseases
- Developmental Biology top 10%
Papers in
- Genetics 30
- Genomic variations and chromosomal abnormalities 16
- Genomics and Rare Diseases 9
-
- Genomics and Chromatin Dynamics 26
- RNA modifications and cancer 11
- RNA Research and Splicing 10
- RNA regulation and disease 6
- Cancer-related gene regulation 5
- Co-authors
- John C. Carey (1 shared paper)Angelo Selicorni (36 shared papers)Lidia Larizza (12 shared papers)Cristina Gervasini (18 shared papers)Silvia P. Russo (14 shared papers)Donatella Milani (10 shared papers)Maura Masciadri (8 shared papers)Silvia Beatrice Maitz (12 shared papers)
- Journals
- European Journal of Medical Genetics (4 papers)American Journal of Medical Genetics Part C Seminars in Medical Genetics (3 papers)Epigenetics (3 papers)Clinical Genetics (3 papers)Genetics in Medicine (3 papers)
- Partner nations
- ItalyUnited StatesNetherlands
In The Last Decade
Anna Cereda
60 papers receiving 1.6k citations
Peers
Comparison fields: 5 of 82
- Genetics 656
- Developmental Biology 33
- Molecular Biology 886
- Pediatrics, Perinatology and Child Health 216
- Developmental Neuroscience 39
Countries citing papers authored by Anna Cereda
This map shows the geographic impact of Anna Cereda'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 Anna Cereda with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Anna Cereda more than expected).
Fields of papers citing papers by Anna Cereda
This network shows the impact of papers produced by Anna Cereda. 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 Anna Cereda. The network helps show where Anna Cereda may publish in the future.
Co-authors
The 25 scholars most cited alongside Anna Cereda, 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 61 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2012 | 254 | |
| 2 | 2018 | 236 | |
| 3 | 2017 | 78 | |
| 4 | 2021 | 69 | |
| 5 | 2015 | 65 | |
| 6 | 2009 | 56 | |
| 7 | 2019 | 47 | |
| 8 | 2013 | 46 | |
| 9 | 2010 | 43 | |
| 10 | 2019 | 41 | |
| 11 | 2015 | 38 | |
| 12 | 2009 | 34 | |
| 13 | 2014 | 31 | |
| 14 | 2013 | 30 | |
| 15 | 2018 | 30 | |
| 16 | 2016 | 29 | |
| 17 | 2022 | 29 | |
| 18 | 2018 | 27 | |
| 19 | 2020 | 26 | |
| 20 | 2019 | 26 |
About Anna Cereda
Anna Cereda is a scholar working on Genetics, Molecular Biology, Pathology and Forensic Medicine, Pediatrics, Perinatology and Child Health and Genetics, having authored 61 papers that have together received 1.6k indexed citations. Recurring topics across this work include Genomics and Chromatin Dynamics (26 papers), Genomic variations and chromosomal abnormalities (16 papers), RNA modifications and cancer (11 papers), RNA Research and Splicing (10 papers), Genomics and Rare Diseases (9 papers), RNA regulation and disease (6 papers), Prenatal Screening and Diagnostics (5 papers) and Cancer-related gene regulation (5 papers). The work is most often cited by research in Genetics (656 citations), Developmental Biology (33 citations), Molecular Biology (886 citations), Pediatrics, Perinatology and Child Health (216 citations) and Developmental Neuroscience (39 citations). Anna Cereda has collaborated with scholars based in Italy, United States and Netherlands. Frequent co-authors include John C. Carey, Angelo Selicorni, Lidia Larizza, Cristina Gervasini, Silvia P. Russo, Donatella Milani, Maura Masciadri, Silvia Beatrice Maitz, Maria Rosaria Iascone and Palma Finelli. Their work appears in journals such as European Journal of Medical Genetics, American Journal of Medical Genetics Part C Seminars in Medical Genetics, Epigenetics, Clinical Genetics and Genetics in 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.