Antonio Cao
Impact in
- Genetics top 0.05%
- Hemoglobinopathies and Related Disorders
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Hematology top 0.1%
- Iron Metabolism and Disorders
- Blood groups and transfusion
Papers in
- Genetics 173
- Hemoglobinopathies and Related Disorders 162
- Genomic variations and chromosomal abnormalities 22
- Hematology 124
- Iron Metabolism and Disorders 102
- Blood groups and transfusion 29
- Co-authors
- Yuet Wai Kan (12 shared papers)Paolo Moi (27 shared papers)Maria Cristina Rosatelli (74 shared papers)Isadora Asunis (7 shared papers)Anthony Chan (1 shared paper)Renzo Galanello (30 shared papers)R. Galanello (55 shared papers)Mario Pirastu (56 shared papers)
- Journals
- British Journal of Haematology (26 papers)Blood (22 papers)Journal of Medical Genetics (20 papers)Human Mutation (20 papers)Human Genetics (13 papers)
- Partner nations
- ItalyUnited StatesUnited Kingdom
In The Last Decade
Antonio Cao
297 papers receiving 11.6k citations
Antonio Cao's Hit Papers
Peers
Comparison fields: 5 of 145
- Genetics 4.7k
- Hematology 3.4k
- Pediatrics, Perinatology and Child Health 1.8k
- Genetics 2.4k
- Molecular Biology 4.2k
Countries citing papers authored by Antonio Cao
This map shows the geographic impact of Antonio Cao'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 Antonio Cao with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Antonio Cao more than expected).
Fields of papers citing papers by Antonio Cao
This network shows the impact of papers produced by Antonio Cao. 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 Antonio Cao. The network helps show where Antonio Cao may publish in the future.
Co-authors
The 25 scholars most cited alongside Antonio Cao, 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 303 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Isolation of NF-E2-related factor 2 (Nrf2), a NF-E2-like basic leucine zipper transcriptional activator that binds to the tandem NF-E2/AP1 repeat of the beta-globin locus control region. Hit paper breakdown → | 1994 | 1351 |
| 2 | Mutations in GPC3, a glypican gene, cause the Simpson-Golabi-Behmel overgrowth syndrome Hit paper breakdown → | 1996 | 593 |
| 3 | 2008 | 422 | |
| 4 | 2004 | 421 | |
| 5 | 1993 | 300 | |
| 6 | 2007 | 255 | |
| 7 | 2000 | 217 | |
| 8 | 2013 | 199 | |
| 9 | 1980 | 181 | |
| 10 | 1998 | 177 | |
| 11 | 1988 | 168 | |
| 12 | 1983 | 162 | |
| 13 | 1981 | 158 | |
| 14 | 2008 | 139 | |
| 15 | 2011 | 125 | |
| 16 | 1999 | 117 | |
| 17 | 2009 | 115 | |
| 18 | 2002 | 113 | |
| 19 | 2012 | 106 | |
| 20 | 1997 | 104 |
About Antonio Cao
Antonio Cao is a scholar working on Genetics, Hematology, Molecular Biology, Pediatrics, Perinatology and Child Health and Genetics, having authored 303 papers that have together received 12.1k indexed citations. Recurring topics across this work include Hemoglobinopathies and Related Disorders (162 papers), Iron Metabolism and Disorders (102 papers), Prenatal Screening and Diagnostics (39 papers), Blood groups and transfusion (29 papers), Neonatal Health and Biochemistry (24 papers), Genomic variations and chromosomal abnormalities (22 papers), Trace Elements in Health (20 papers) and Heavy Metal Exposure and Toxicity (14 papers). The work is most often cited by research in Genetics (4.7k citations), Hematology (3.4k citations), Pediatrics, Perinatology and Child Health (1.8k citations), Genetics (2.4k citations) and Molecular Biology (4.2k citations). Antonio Cao has collaborated with scholars based in Italy, United States and United Kingdom. Frequent co-authors include Yuet Wai Kan, Paolo Moi, Maria Cristina Rosatelli, Isadora Asunis, Anthony Chan, Renzo Galanello, R. Galanello, Mario Pirastu, M. Furbetta and Antonino Forabosco. Their work appears in journals such as British Journal of Haematology, Blood, Journal of Medical Genetics, Human Mutation and Human Genetics.
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.