CV Lattes
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Universidade de São Paulo (USP). Instituto de Biociências (IB) (Institutional affiliation from the last research proposal) Birthplace: Brazil
graduation at Ciências Biológicas from Universidade de São Paulo (2011) and doctorate at Genetics from Universidade de São Paulo (2017). Has experience in Genetics, focusing on Human and Medical Genetics, acting on the following subjects: genética de fissuras, fissuras lábio palatinas, síndrome velocardiofacial, síndrome de van der woude and gene expression. (Source: Lattes Curriculum)
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Cleft lip and/or palate (CL/P) is the most common congenital craniofacial malformation and displays a multifactorial pattern of inheritance. Despite of the many at risk loci identified for the CL/P, they do not completely explain the observed high heritability and incomplete penetrance is frequently featured in CL/P familial cases, suggesting the role of additional factors, either genetic…
Within all congenital craniofacial malformation, Non Syndromic Cleft Lip/Palate (NS CL/P) is the most frequent, accounting for 75% of all these malformations. NS CL/Ps are result of craniofacial development errors, which is a multiple signaling molecule involved process, time and spatially dependent. Studies of NS CL/P risk factors suggest the multifactorial inheritance model for this mal…
Non syndromic cleft lip and/or palate (NS CL/P) are the most common craniofacial anomalies, with mundial penetrance estimated in 1 affected for 1000 livebirths. These malformation are caracterized by a large clinical variability and result of genetics and enviromental factors matches. Studies have shown a great number of envolved genes in NS CL/P. The malformation etiology counts a precis…
Oral clefts (OC) are a frequent group of craniofacial malformation caused by a combination of genetic and environmental factors, which may impair craniofacial development by affecting the neural crest (NC). More recently, loss-of-function mutations in genes from the cadherin-catenin complex as CDH1 (E-cadherin) and CTNND1 (p120-catenin) have been found segregating in OC families, however …
Nonsyndromic cleft lip/palate (NSCL/P) is the most common congenital craniofacial malformation, with a prevalence of 1 affected individual to 700 live-births worldwide. NSCL/Ps are clinically variable, ranging from affected lip only to the dental alveolum and palate, uni or bilaterally. Heritability studies show a genetic contribution ranging from 40% to 85% and NSCL/P is classified as a …
| 3 / 3 | Completed scholarships in Brazil |
| 2 / 2 | Completed scholarships abroad |
| 5 / 5 | All Scholarships |
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