Anna Capalbo
Impact in
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Developmental Biology top 10%
Papers in
- Genetics 20
- Genomic variations and chromosomal abnormalities 20
- Genomics and Rare Diseases 5
- Congenital Ear and Nasal Anomalies 3
- Genetics and Neurodevelopmental Disorders 3
- Craniofacial Disorders and Treatments 2
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- Congenital heart defects research 9
- Co-authors
- Laura Bernardini (24 shared papers)Antonio Novelli (16 shared papers)Bruno Dallapiccola (13 shared papers)Sara Loddo (2 shared papers)John C. Carey (1 shared paper)Tiziana Filippi (1 shared paper)Agatino Battaglia (1 shared paper)Viola Doccini (1 shared paper)
- Journals
- European Journal of Medical Genetics (3 papers)American Journal of Medical Genetics Part A (10 papers)Scientific Reports (1 paper)Gene (1 paper)Orphanet Journal of Rare Diseases (1 paper)
- Partner nations
- ItalyUnited StatesUnited Kingdom
In The Last Decade
Anna Capalbo
27 papers receiving 530 citations
Peers
Comparison fields: 5 of 60
- Genetics 389
- Developmental Biology 22
- Pediatrics, Perinatology and Child Health 112
- Genetics 41
- Molecular Biology 244
Countries citing papers authored by Anna Capalbo
This map shows the geographic impact of Anna Capalbo'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 Capalbo with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Anna Capalbo more than expected).
Fields of papers citing papers by Anna Capalbo
This network shows the impact of papers produced by Anna Capalbo. 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 Capalbo. The network helps show where Anna Capalbo may publish in the future.
Co-authors
The 25 scholars most cited alongside Anna Capalbo, 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 29 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2013 | 147 | |
| 2 | 2006 | 57 | |
| 3 | 2009 | 40 | |
| 4 | 2008 | 34 | |
| 5 | 2007 | 28 | |
| 6 | 2007 | 27 | |
| 7 | 2011 | 26 | |
| 8 | 2013 | 25 | |
| 9 | 2009 | 24 | |
| 10 | 2015 | 21 | |
| 11 | 2013 | 20 | |
| 12 | 2006 | 19 | |
| 13 | 2009 | 18 | |
| 14 | 2008 | 17 | |
| 15 | 2009 | 16 | |
| 16 | 2021 | 15 | |
| 17 | 2019 | 9 | |
| 18 | 2011 | 6 | |
| 19 | 2018 | 5 | |
| 20 | Prenatal diagnosis and molecular characterization of an interstitial 1q24.3-31.3 deletion: case report and review. | 2011 | 5 |
About Anna Capalbo
Anna Capalbo is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Pathology and Forensic Medicine and Genetics, having authored 29 papers that have together received 579 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (20 papers), Congenital heart defects research (9 papers), Prenatal Screening and Diagnostics (7 papers), Genomics and Rare Diseases (5 papers), Congenital Ear and Nasal Anomalies (3 papers), Lymphoma Diagnosis and Treatment (3 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Craniofacial Disorders and Treatments (2 papers). The work is most often cited by research in Genetics (389 citations), Developmental Biology (22 citations), Pediatrics, Perinatology and Child Health (112 citations), Genetics (41 citations) and Molecular Biology (244 citations). Anna Capalbo has collaborated with scholars based in Italy, United States and United Kingdom. Frequent co-authors include Laura Bernardini, Antonio Novelli, Bruno Dallapiccola, Sara Loddo, John C. Carey, Tiziana Filippi, Agatino Battaglia, Viola Doccini, Rita Mingarelli and Irene Bottillo. Their work appears in journals such as European Journal of Medical Genetics, American Journal of Medical Genetics Part A, Scientific Reports, Gene 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.