Fernanda S L Vianna

Investigation of the impact of AXL, TLR3, and STAT2 in congenital Zika syndrome through genetic polymorphisms and protein–protein interaction network analyses

L. Schüler-Faccini, L. R. Fraga, J. A. Gomes, 2023, Birth defects research.

Contribution of miR-124 rs531564 polymorphism to the occurrence of congenital Zika syndrome

L. Schüler-Faccini, J. A. Gomes, Eduarda Sgarioni, 2022, Epigenetics.

Association between Genetic Variants in NOS2 and TNF Genes with Congenital Zika Syndrome and Severe Microcephaly

Juliano André Boquett, L. Schüler-Faccini, J. A. Gomes, 2021, Viruses.

Interaction between TP63 and MDM2 genes and the risk of recurrent pregnancy loss.

P. Ashton-Prolla, L. Schuler‐Faccini, M. Sanseverino, 2014, European journal of obstetrics, gynecology, and reproductive biology.

Molecular Mechanisms of ZIKV-Induced Teratogenesis: A Systematic Review of Studies in Animal Models

L. Schuler‐Faccini, L. R. Fraga, J. A. Gomes, 2022, Molecular neurobiology.

Functional Polymorphisms in the p53 Pathway Genes on the Genetic Susceptibility to Zika Virus Teratogenesis

P. Ashton-Prolla, L. Schuler‐Faccini, L. R. Fraga, 2021, Frontiers in Cellular and Infection Microbiology.

An Efficient Extraction Method Allowing the Genetic Evaluation of Host DNA from Samples Collected for Virus Infection Diagnosis in Viral Transport Medium.

J. Chies, T. S. Gregianini, R. C. Sbruzzi, 2023, Biopreservation and biobanking.

HLA haplotypes and differential regional mortality caused by COVID-19 in Brazil: an ecological study based on a large bone marrow donor bank dataset.

P. Ashton-Prolla, N. Fagundes, J. A. Boquett, 2023, Anais da Academia Brasileira de Ciencias.