Anna Cereda
Impact in
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
- Genetics and Neurodevelopmental Disorders
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- Prenatal Screening and Diagnostics
Papers in
-
- Genomics and Chromatin Dynamics 24
- RNA modifications and cancer 11
- RNA Research and Splicing 9
- RNA regulation and disease 6
- Genetics 20
- Genomic variations and chromosomal abnormalities 13
- Genomics and Rare Diseases 4
- Genetic Syndromes and Imprinting 4
- Co-authors
- John C. Carey (1 shared paper)Angelo Selicorni (35 shared papers)Lidia Larizza (11 shared papers)Cristina Gervasini (17 shared papers)Silvia Russo (13 shared papers)Donatella Milani (10 shared papers)Silvia Maitz (11 shared papers)Maura Masciadri (7 shared papers)
- Journals
- Epigenetics (3 papers)American Journal of Medical Genetics Part C Seminars in Medical Genetics (3 papers)European Journal of Medical Genetics (3 papers)Orphanet Journal of Rare Diseases (2 papers)American Journal of Medical Genetics Part A (17 papers)
- Partner nations
- ItalyUnited StatesGermany
In The Last Decade
Anna Cereda
42 papers receiving 886 citations
Peers
Comparison fields: 5 of 68
- Genetics 369
- Pediatrics, Perinatology and Child Health 178
- Developmental Biology 19
- Developmental Neuroscience 29
- Molecular Biology 452
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 44 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2012 | 236 | |
| 2 | 2009 | 57 | |
| 3 | 2015 | 54 | |
| 4 | 2013 | 45 | |
| 5 | 2010 | 41 | |
| 6 | 2019 | 35 | |
| 7 | 2009 | 33 | |
| 8 | 2014 | 27 | |
| 9 | 2018 | 27 | |
| 10 | 2019 | 25 | |
| 11 | 2018 | 24 | |
| 12 | 2013 | 24 | |
| 13 | 2016 | 22 | |
| 14 | 2011 | 22 | |
| 15 | 2015 | 22 | |
| 16 | 2022 | 19 | |
| 17 | 2013 | 19 | |
| 18 | 2013 | 17 | |
| 19 | 2012 | 16 | |
| 20 | 2010 | 16 |
About Anna Cereda
Anna Cereda is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Surgery and Pathology and Forensic Medicine, having authored 44 papers that have together received 915 indexed citations. Recurring topics across this work include Genomics and Chromatin Dynamics (24 papers), Genomic variations and chromosomal abnormalities (13 papers), RNA modifications and cancer (11 papers), RNA Research and Splicing (9 papers), RNA regulation and disease (6 papers), Genomics and Rare Diseases (4 papers), Genetic Syndromes and Imprinting (4 papers) and Prenatal Screening and Diagnostics (4 papers). The work is most often cited by research in Genetics (369 citations), Pediatrics, Perinatology and Child Health (178 citations), Developmental Biology (19 citations), Developmental Neuroscience (29 citations) and Molecular Biology (452 citations). Anna Cereda has collaborated with scholars based in Italy, United States and Germany. Frequent co-authors include John C. Carey, Angelo Selicorni, Lidia Larizza, Cristina Gervasini, Silvia Russo, Donatella Milani, Silvia Maitz, Maura Masciadri, Maria Iascone and Palma Finelli. Their work appears in journals such as Epigenetics, American Journal of Medical Genetics Part C Seminars in Medical Genetics, European Journal of Medical Genetics, Orphanet Journal of Rare Diseases and American Journal of Medical Genetics Part A.
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.