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Hire Dr. Thatiana Evilen d.

Brazil

USD 40 /hr

Freelance Scientific Consultant | Expert in Molecular Biology | Geneticist with 10 years of experience

Profile Summary

Graduated in Biological Sciences (Bachelor's degree) at São Camilo University Center (2008). Science Master’s degree (2012) and Ph.D. (2017) in the program of FMUSP, Discipline of Endocrinology, CAPES, and FAPESP financial supported. She worked with molecular biology and biochemistry at the research about disorders of sex development and testicular development at the Sao Paulo University. In 2019, she worked with a genetic diagnostics services portfolio of hereditary cancer or other diseases (cardiomyopathies, neuropathies, endocrinopathies, and immunodeficiency) using NGS and variant interpreting at the Fleury’s Group. And, she finalized her MBA course of Health innovation Manager in the same year.

Subject Matter Expertise

• ★ Molecular Biology
• ★ Phylogenetics
• ☆ Genetics
• ☆ Epigenetics
• ☆ Biotechnology & Bioengineering
• ☆ Data Science
• ☆ Health Data Analysis
• ☆ Bioinformatics
• ☆ Biogeochemistry
• ☆ Genetic Engineering
• ☆ Behavioral Genetics
• ☆ Preclinical Research
• ☆ Medicine
• ☆ Gene Therapy
• ☆ Medical Sciences
• ☆ Research
• ☆ Research Methodology
• ☆ Regulatory Writing
• ☆ Medical Copywriting
• ☆ Technical & Scientific Writing
• ☆ Manuscript & Journal Article Writing
• ☆ Scientific Proofreading & Editing
• ☆ Language Translation

Services

• Writing
• Research
• Consulting

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.