Angelo Serra
Impact in
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 28
- Genomic variations and chromosomal abnormalities 13
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 8
- Genetics and Neurodevelopmental Disorders 5
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- Genomics and Chromatin Dynamics 4
- Sexual Differentiation and Disorders 3
- Co-authors
- Giovanni Neri (13 shared papers)James F. Reynolds (2 shared papers)Bruna Tedeschi (5 shared papers)Christina Brahe (10 shared papers)Adelio Rigo (4 shared papers)Giovanni Neri (1 shared paper)Giuseppe Saglio (4 shared papers)W. Schempp (2 shared papers)
- Journals
- Human Genetics (10 papers)Clinical Genetics (4 papers)Blood (2 papers)Journal of Cell Science (2 papers)Neurosurgery (2 papers)
- Partner nations
- ItalyUnited StatesNetherlands
In The Last Decade
Angelo Serra
62 papers receiving 830 citations
Peers
Comparison fields: 5 of 93
- Genetics 349
- Pediatrics, Perinatology and Child Health 199
- Biochemistry 34
- Genetics 48
- Developmental Neuroscience 17
Countries citing papers authored by Angelo Serra
This map shows the geographic impact of Angelo Serra'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 Angelo Serra with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Angelo Serra more than expected).
Fields of papers citing papers by Angelo Serra
This network shows the impact of papers produced by Angelo Serra. 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 Angelo Serra. The network helps show where Angelo Serra may publish in the future.
Co-authors
The 25 scholars most cited alongside Angelo Serra, 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 65 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1986 | 92 | |
| 2 | 1983 | 62 | |
| 3 | 1976 | 58 | |
| 4 | 1994 | 53 | |
| 5 | 1987 | 45 | |
| 6 | 1983 | 43 | |
| 7 | A 45,X male with Y-specific DNA translocated onto chromosome 15. | 1987 | 42 |
| 8 | 1993 | 39 | |
| 9 | A common beta ig-h3 gene mutation (delta f540) in a large cohort of Sardinian Reis Bücklers corneal dystrophy patients. Mutations in brief no. 180. Online. | 1998 | 37 |
| 10 | 1985 | 32 | |
| 11 | 1992 | 31 | |
| 12 | 1989 | 25 | |
| 13 | 1986 | 24 | |
| 14 | 1990 | 24 | |
| 15 | 1983 | 22 | |
| 16 | 2005 | 20 | |
| 17 | 2005 | 18 | |
| 18 | [A 30-year follow-up]. | 1965 | 18 |
| 19 | 1981 | 17 | |
| 20 | 1985 | 13 |
About Angelo Serra
Angelo Serra is a scholar working on Genetics, Molecular Biology, Plant Science, Pediatrics, Perinatology and Child Health and Genetics, having authored 65 papers that have together received 915 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (13 papers), Chromosomal and Genetic Variations (11 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (8 papers), Prenatal Screening and Diagnostics (8 papers), Genetics and Neurodevelopmental Disorders (5 papers), Genomics and Chromatin Dynamics (4 papers), Sexual Differentiation and Disorders (3 papers) and Carcinogens and Genotoxicity Assessment (3 papers). The work is most often cited by research in Genetics (349 citations), Pediatrics, Perinatology and Child Health (199 citations), Biochemistry (34 citations), Genetics (48 citations) and Developmental Neuroscience (17 citations). Angelo Serra has collaborated with scholars based in Italy, United States and Netherlands. Frequent co-authors include Giovanni Neri, James F. Reynolds, Bruna Tedeschi, Christina Brahe, Adelio Rigo, Giovanni Neri, Giuseppe Saglio, W. Schempp, Andreas Gal and Bernhard H. F. Weber. Their work appears in journals such as Human Genetics, Clinical Genetics, Blood, Journal of Cell Science and Neurosurgery.
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.