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Profile Details
Contact
USD 40 /hr
Hire Dr. Thatiana Evilen d.
Brazil
USD 40 /hr
Freelance Scientific Consultant | Expert in Molecular Biology | Geneticist with 10 years of experience
Profile Summary
Subject Matter Expertise
Services
Writing
Clinical Trial Documentation,
Technical Writing,
Copywriting,
Newswriting
Research
Gray Literature Search,
Systematic Literature Review,
Secondary Data Collection
Consulting
Scientific and Technical Consulting
Work Experience
Freelance
PreScouter
August 2020 - Present
Senior Laboratory Analyst
Grupo Fleury SA
October 2018 - August 2019
Research Collaborator
Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo
June 2009 - September 2018
Profissional Experience
Grupo Fleury SA
July 2016 - July 2016
Visiting PhD Student
University of Michigan
April 2016 - June 2016
Education Enhancement Program
Faculdade de Medicina da Universidade de São Paulo
February 2016 - June 2016
Supporting distance learners
Universidade Metodista de São Paulo
September 2009 - December 2009
Education
Speed Woman Mentoring
Sebrae
March 2020 - June 2020
MBA in Health Innovation Management
Instituto Butantan
January 2018 - June 2019
PhD - Science in Molecular Human Genetic
Faculdade de Medicina da Universidade de São Paulo
February 2013 - November 2017
MSc - Science in Molecular Human Genetic
Faculdade de Medicina da Universidade São Paulo
February 2009 - September 2012
Bachelor of Biological Science
University Center of São Camilo
February 2005 - December 2008
Certifications
- Certification details not provided.
Publications
JOURNAL ARTICLE
Thatiana Evilen da Silva, Nathalia Lisboa Gomes, Antonio Marcondes Lerário, Catherine Elizabeth Keegan, Mirian Yumi Nishi, Filomena Marino Carvalho, Eric Vilain, Hayk Barseghyan, Alejandro Martinez-Aguayo, María Verónica Forclaz, et al.(2019). Genetic evidence of the association of {DEAH}-box helicase 37 defects with 46,{XY} gonadal dysgenesis spectrum . The Journal of Clinical Endocrinology {\&} Metabolism. The Endocrine Society
Da Silva, T.E., Gomes, N.L., Lerário, A.M., Keegan, C.E., Nishi, M.Y., Carvalho, F.M., Vilain, E., Barseghyan, H., Martinez-Aguayo, A., Forclaz, M.V., et al.(2019). Genetic Evidence of the Association of DEAH-Box Helicase 37 Defects with 46,XY Gonadal Dysgenesis Spectrum . Journal of Clinical Endocrinology and Metabolism. 104. (12). p. 5923-5934.
Gomes, N.L., de Paula, L.C.P., Silva, J.M., Silva, T.E., Lerário, A.M., Nishi, M.Y., Batista, R.L., Faria Júnior, J.A.D., Moraes, D., Costa, E.M.F., et al.(2019). A 46,XX testicular disorder of sex development caused by a Wilms' tumour Factor-1 (WT1) pathogenic variant . Clinical Genetics. 95. (1). p. 172-176.
Gomes, N.L., Lerário, A.M., Machado, A.Z., de Moraes, D.R., da Silva, T.E., Arnhold, I.J.P., Batista, R.L., Faria Júnior, J.A.D., Costa, E.F., Nishi, M.Y., et al.(2018). Long-term outcomes and molecular analysis of a large cohort of patients with 46,XY disorder of sex development due to partial gonadal dysgenesis . Clinical Endocrinology. 89. (2). p. 164-177.
Machado, A.Z., da Silva, T.E., Frade Costa, E.M., dos Santos, M.G., Nishi, M.Y., Brito, V.N., Mendonca, B.B., Domenice, S.(2012). Absence of inactivating mutations and deletions in the DMRT1 and FGF9 genes in a large cohort of 46,XY patients with gonadal dysgenesis . European Journal of Medical Genetics. 55. (12). p. 690-694.
Da Silva, T.E., Nishi, M.Y., Costa, E.M.F., Martin, R.M., Carvalho, F.M., Mendonca, B.B., Domenice, S.(2011). A novel WT1 heterozygous nonsense mutation (p.K248X) causing a mild and slightly progressive nephropathy in a 46, XY patient with Denys-Drash syndrome . Pediatric Nephrology. 26. (8). p. 1311-1315.