M Deminatti
About
In The Last Decade
M Deminatti
43 papers receiving 514 citations
Peers
Comparison fields: 5 of 52
- Hematology 376
- Genetics 224
- Molecular Biology 170
- Public Health, Environmental and Occupational Health 99
- Genetics 81
Countries citing papers authored by M Deminatti
This map shows the geographic impact of M Deminatti'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 Deminatti with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites M Deminatti more than expected).
Fields of papers citing papers by M Deminatti
This network shows the impact of papers produced by M Deminatti. 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 Deminatti. The network helps show where M Deminatti may publish in the future.
Co-authorship network of co-authors of M Deminatti
This figure shows the co-authorship network connecting the top 25 collaborators of M Deminatti. A scholar is included among the top collaborators of M Deminatti based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with M Deminatti. M Deminatti is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 32 | |
| 2 | 3 | |
| 3 | 9 | |
| 4 | 28 | |
| 5 | 2 | |
| 6 | 8 | |
| 7 | 5 | |
| 8 | 33 | |
| 9 | Congenital acute monoblastic leukemia with double translocation (8;16) (p11;p13) and (16;20) (q13;p13). | 10 |
| 10 | 78 | |
| 11 | 21 | |
| 12 | 5 | |
| 13 | 53 | |
| 14 | [Subacute pre-eclampsia and hydramnios as manifestation of fetal triploidy. In utero diagnosis in the 28th week]. | 0 |
| 15 | [Transient leukoblastosis and dysmegakariocytopoiesis with clone 46, XX+21, t(5;7), in a newborn infant with trisomy 21]. | 1 |
| 16 | [Karyotype of peripheral blood lymphocytes in patients treated for Hodgkin disease]. | 1 |
| 17 | [Partial trisomy 12 and 8 with mosaicism, associated with translocation t(8;12) (p21;q13)]. | 6 |
| 18 | A propos d'un cas de chromosome X en anneau. | 1 |
| 19 | [Study of a case of human hermaphroditism with karyotype 46, XY-46, XX]. | 1 |
| 20 | 1 |
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.