M. Furbetta
Impact in
- Genetics top 1%
- Hemoglobinopathies and Related Disorders
- Hematology top 2%
- Iron Metabolism and Disorders
- Blood groups and transfusion
Papers in
- Genetics 33
- Hemoglobinopathies and Related Disorders 33
- Genomic variations and chromosomal abnormalities 6
- Hematology 29
- Iron Metabolism and Disorders 25
- Blood groups and transfusion 7
- Co-authors
- Antonio CaoYuet Wai KanAndrea AngiusR. GalanelloT TuveriM. T. ScalasMaria Cristina RosatelliJudy C. Chang
- Journals
- Journal of Medical Genetics (9 papers)British Journal of Haematology (5 papers)Blood (3 papers)Human Genetics (3 papers)The Lancet (3 papers)
- Partner nations
- ItalyUnited StatesNetherlands
In The Last Decade
M. Furbetta
48 papers receiving 996 citations
Peers
Comparison fields: 5 of 71
- Genetics 802
- Hematology 583
- Pediatrics, Perinatology and Child Health 374
- Genetics 158
- Rheumatology 68
Countries citing papers authored by M. Furbetta
This map shows the geographic impact of M. Furbetta'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 M. Furbetta with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites M. Furbetta more than expected).
Fields of papers citing papers by M. Furbetta
This network shows the impact of papers produced by M. Furbetta. 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 M. Furbetta. The network helps show where M. Furbetta may publish in the future.
Co-authors
The 25 scholars most cited alongside M. Furbetta, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 1996 | 2 | |
| 2 | 1988 | 7 | |
| 3 | 1983 | 60 | |
| 4 | Globin gene mapping studies in Sardinian patients homozygous for beta zero Thalassaemia. | 1983 | 5 |
| 5 | Control of homozygous beta-thalassemia by carrier screening and antenatal diagnosis in Sardinia. | 1982 | 3 |
| 6 | 1982 | 83 | |
| 7 | 1982 | 7 | |
| 8 | Prevention of homozygous beta-thalassemia by carrier screening and prenatal diagnosis in Sardinia. | 1981 | 47 |
| 9 | 1981 | 5 | |
| 10 | Prevention of homozyous /-thalassemia by carrier screening and prenatal diagnosis in Sardinia | 1981 | 1 |
| 11 | 1981 | 157 | |
| 12 | 1981 | 13 | |
| 13 | 1979 | 48 | |
| 14 | [Karyotype 46,XY,22p+ in a male patient (author's transl)]. | 1978 | 2 |
| 15 | 1978 | 48 | |
| 16 | 1977 | 77 | |
| 17 | 1973 | 24 | |
| 18 | 1973 | 12 | |
| 19 | 1972 | 3 | |
| 20 | 1971 | 4 |
About M. Furbetta
M. Furbetta is a scholar working on Genetics, Hematology, Pediatrics, Perinatology and Child Health, Developmental Biology and Rheumatology, having authored 48 papers that have together received 1.1k indexed citations. Recurring topics across this work include Hemoglobinopathies and Related Disorders (33 papers), Iron Metabolism and Disorders (25 papers), Neonatal Health and Biochemistry (9 papers), Blood groups and transfusion (7 papers), Prenatal Screening and Diagnostics (6 papers), Genomic variations and chromosomal abnormalities (6 papers), Folate and B Vitamins Research (4 papers) and Alkaline Phosphatase Research Studies (4 papers). The work is most often cited by research in Genetics (802 citations), Hematology (583 citations), Pediatrics, Perinatology and Child Health (374 citations), Genetics (158 citations) and Rheumatology (68 citations). M. Furbetta has collaborated with scholars based in Italy, United States and Netherlands. Frequent co-authors include Antonio Cao, Yuet Wai Kan, Andrea Angius, R. Galanello, T Tuveri, M. T. Scalas, Maria Cristina Rosatelli, Judy C. Chang, Stephen A. Liebhaber and MA Melis. Their work appears in journals such as Journal of Medical Genetics, British Journal of Haematology, Blood, Human Genetics and The Lancet.
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.