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Ágatha Cristhina Oliveira Faria

CV Lattes


Universidade de São Paulo (USP). Instituto de Biociências (IB)  (Institutional affiliation for the last research proposal)
Birthplace: Brazil

Graduated in Pharmacy from the School of Science of Santa Casa de Misericórdia de Vitória (2011). Master in Biotechnology from the Federal University of Espírito Santo (2014). Ph.D. in Genetics from the Biosciences Institute of the University of São Paulo (USP) (2019) and MBA in Business Management from USP/Esalq (2020). She has extensive experience in the field of Genetics, with an emphasis on Human Molecular Genetics, working mainly on the following topics: Genomics, genetic diseases, rare diseases, metagenomics, genetic counseling, congenital malformations, and genetic syndromes. In addition to her academic expertise, she is also an expert in digital marketing and strategic digital communication. She currently acts as a communications analyst at the Mendelics genomics lab, is a career mentor to PhDs, and Co-founder of PhDs EXP Move-first and largest career transition event for graduate students. (Source: Lattes Curriculum)

Scholarships in Brazil
FAPESP support in numbers * Updated June 12, 2021
Total / Available in English
1 / 1   Completed scholarships in Brazil

Associated processes
Most frequent collaborators in research granted by FAPESP
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Keywords used by the researcher
Scientific publications resulting from Research Grants and Scholarships under the grantee's responsibility (1)

(References retrieved automatically from Web of Science and SciELO through information on FAPESP grants and their corresponding numbers as mentioned in the publications by the authors)

SAMOGY-COSTA, CLAUDIA ISMANIA; VARELLA-BRANCO, ELISA; MONFARDINI, FREDERICO; FERRAZ, HELEN; FOCK, RODRIGO AMBROSIO; ALMEIDA BARBOSA, RICARDO HENRIQUE; SANTOS PESSOA, ANDRE LUIZ; ALVAREZ PEREZ, ANA BEATRIZ; LOURENCO, NAILA; VIBRANOVSKI, MARIA; et al. A Brazilian cohort of individuals with Phelan-McDermid syndrome: genotype-phenotype correlation and identification of an atypical case. JOURNAL OF NEURODEVELOPMENTAL DISORDERS, v. 11, . Web of Science Citations: 1. (13/08028-1, 16/17392-7)

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