graduation at Biomedicina from Universidade Federal de São Paulo (2023). Has experience in Genetics, focusing on Human and Medical Genetics (Source: Lattes Curriculum)
| News published in Agência FAPESP Newsletter about the researcher |
| More itemsLess items |
| TITULO |
| Articles published in other media outlets ( ): |
| More itemsLess items |
| VEICULO: TITULO (DATA) |
| VEICULO: TITULO (DATA) |
Syndromes resulting from copy number variations (CNVs) are characterized by the presence of microdeletions or microduplications of genomic segments. They are detected by cytogenomic techniques, such as MLPA and genomic array, which verify the presence of genomic imbalances, associated with different syndromes. Some individuals, despite having the main clinical signs of syndromes related t…
The investigation of cytogenomic and molecular alterations through refined and powerful research methodologies has been allowing the characterization of genetic variants at a higher resolution, enabling a better understanding of their mechanisms of formation and their impact on the phenotype. The current project proposes the use of innovative approaches, including several types of next-ge…
| 1 / 1 | Ongoing scholarships in Brazil |
| 1 / 1 | Completed scholarships in Brazil |
| 2 / 2 | All Scholarships |
| Associated processes | |
CV Lattes
ORCID