プロフィール詳細

プロジェクトを作成

★★★★★

☆☆☆☆☆

★★★★★

☆☆☆☆☆

Dr. Thatiana Evilen d.に依頼

Brazil

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

プロフィール概要

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.

専門分野

• ★ Molecular Biology
• ☆ 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

サービス

• 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

職務経験

Freelance

PreScouter

8月 2020 - 現在

Senior Laboratory Analyst

Grupo Fleury SA

10月 2018 - 8月 2019

Research Collaborator

Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo

6月 2009 - 9月 2018

Profissional Experience

Grupo Fleury SA

7月 2016 - 7月 2016

Visiting PhD Student

University of Michigan

4月 2016 - 6月 2016

Education Enhancement Program

Faculdade de Medicina da Universidade de São Paulo

2月 2016 - 6月 2016

Supporting distance learners

Universidade Metodista de São Paulo

9月 2009 - 12月 2009

学歴

Speed Woman Mentoring

Sebrae

3月 2020 - 6月 2020

MBA in Health Innovation Management

Instituto Butantan

1月 2018 - 6月 2019

PhD - Science in Molecular Human Genetic

Faculdade de Medicina da Universidade de São Paulo

2月 2013 - 11月 2017

MSc - Science in Molecular Human Genetic

Faculdade de Medicina da Universidade São Paulo

2月 2009 - 9月 2012

Bachelor of Biological Science

University Center of São Camilo

2月 2005 - 12月 2008

認定資格

• 認定資格の詳細は未入力です。

出版物

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). Microsoft.AspNetCore.Mvc.Localization.LocalizedHtmlString 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). Microsoft.AspNetCore.Mvc.Localization.LocalizedHtmlString 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). Microsoft.AspNetCore.Mvc.Localization.LocalizedHtmlString 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). Microsoft.AspNetCore.Mvc.Localization.LocalizedHtmlString 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). Microsoft.AspNetCore.Mvc.Localization.LocalizedHtmlString 1311-1315.