bachelor's at Ciências Biológicas Modalidade Médica from Centro Universitário Herminio Ometto de Araras (2003), master's at Clinical Medicine from Universidade Estadual de Campinas (2007) and doctorate at Clinical Medicine from Universidade Estadual de Campinas (2012). Has experience in Genetics (Source: Lattes Curriculum)
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Genomic imbalances (GIs) are an important class of variation in the human genome. Many of them are related to diseases and responsible for the phenotype in a substantial number (10 - 20%) of individuals with congenital anomalies (CA) and (or) intellectual disability (ID)/ developmental delay (DD). Currently, the chromosomal microarray analysis (CMA) is pointed as a first tier for the mole…
The 22q11.2 deletion syndrome (22q11.2DS) is the most common in humans, with an estimated frequency of 1/4,000 live births. Among the main clinical features, both physical and behavioral characteristics are observed, with a wide clinical heterogeneity. The 22q11.2 region is characterized by the presence of low copy repeats (LCRs) blocks, which can serve as substrate for a mispairing betwe…
| 1 / 1 | Completed research grants |
| 1 / 1 | Completed scholarships in Brazil |
| 2 / 2 | All research grants and scholarships |
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CV Lattes
ORCID