Bruno Masala
Impact in
- Genetics top 2%
- Hemoglobinopathies and Related Disorders
- Genetic and phenotypic traits in livestock
- Genetic diversity and population structure
- Hematology top 5%
- Iron Metabolism and Disorders
- Blood groups and transfusion
Papers in
- Genetics 51
- Hemoglobinopathies and Related Disorders 51
- Hematology 32
- Iron Metabolism and Disorders 24
- Blood groups and transfusion 13
- Co-authors
- Laura Manca (58 shared papers)Eleftherios Hadjisterkotis (8 shared papers)Salvatore Naitana (9 shared papers)Marilena Formato (5 shared papers)Paolo Mereu (13 shared papers)S. Ledda (3 shared papers)Aldo Di Luccia (5 shared papers)Pasquale Ferranti (7 shared papers)
- Journals
- Biochemical Genetics (4 papers)American Journal of Hematology (4 papers)Clinica Chimica Acta (3 papers)Comparative Biochemistry and Physiology Part D Genomics and Proteomics (2 papers)Animal Genetics (2 papers)
- Partner nations
- ItalyUnited StatesFrance
In The Last Decade
Bruno Masala
72 papers receiving 656 citations
Peers
Comparison fields: 5 of 80
- Genetics 352
- Hematology 247
- Cell Biology 175
- Pediatrics, Perinatology and Child Health 124
- Genetics 139
Countries citing papers authored by Bruno Masala
This map shows the geographic impact of Bruno Masala'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 Bruno Masala with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Bruno Masala more than expected).
Fields of papers citing papers by Bruno Masala
This network shows the impact of papers produced by Bruno Masala. 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 Bruno Masala. The network helps show where Bruno Masala may publish in the future.
Co-authors
The 25 scholars most cited alongside Bruno Masala, 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 73 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2008 | 54 | |
| 2 | 1994 | 43 | |
| 3 | 1991 | 41 | |
| 4 | 2000 | 37 | |
| 5 | 2015 | 31 | |
| 6 | 1988 | 22 | |
| 7 | 1991 | 20 | |
| 8 | 1986 | 19 | |
| 9 | 1991 | 18 | |
| 10 | 1990 | 17 | |
| 11 | 1988 | 17 | |
| 12 | 1991 | 16 | |
| 13 | 2008 | 16 | |
| 14 | 1991 | 14 | |
| 15 | 1993 | 14 | |
| 16 | 1992 | 12 | |
| 17 | 1991 | 12 | |
| 18 | 1986 | 12 | |
| 19 | 1996 | 12 | |
| 20 | 1988 | 11 |
About Bruno Masala
Bruno Masala is a scholar working on Genetics, Hematology, Cell Biology, Pediatrics, Perinatology and Child Health and Molecular Biology, having authored 73 papers that have together received 677 indexed citations. Recurring topics across this work include Hemoglobinopathies and Related Disorders (51 papers), Iron Metabolism and Disorders (24 papers), Hemoglobin structure and function (21 papers), Blood groups and transfusion (13 papers), Neonatal Health and Biochemistry (12 papers), Erythrocyte Function and Pathophysiology (9 papers), Prenatal Screening and Diagnostics (4 papers) and Folate and B Vitamins Research (4 papers). The work is most often cited by research in Genetics (352 citations), Hematology (247 citations), Cell Biology (175 citations), Pediatrics, Perinatology and Child Health (124 citations) and Genetics (139 citations). Bruno Masala has collaborated with scholars based in Italy, United States and France. Frequent co-authors include Laura Manca, Eleftherios Hadjisterkotis, Salvatore Naitana, Marilena Formato, Paolo Mereu, S. Ledda, Aldo Di Luccia, Pasquale Ferranti, L. Ferrara and Maurizio Longinotti. Their work appears in journals such as Biochemical Genetics, American Journal of Hematology, Clinica Chimica Acta, Comparative Biochemistry and Physiology Part D Genomics and Proteomics and Animal 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.