B. Ribeiro

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.

A recurrent de novo splice site variant involving DNM1 exon 10a causes developmental and epileptic encephalopathy through a dominant-negative mechanism

I. Helbig, B. Kennedy, A. Gelot, 2022, bioRxiv.

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

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

Long-term impact of early initiation of enzyme replacement therapy in 34 MPS VI patients: A resurvey study.

C. Kim, C. Lourenço, E. Ribeiro, 2021, Molecular genetics and metabolism.

Enzyme replacement therapy with galsulfase in 34 children younger than five years of age with MPS VI.

C. Kim, E. Ribeiro, Dafne D G Horovitz, 2013, Molecular genetics and metabolism.

Comprehensive germline mutation analysis and clinical profile in a large cohort of Brazilian xeroderma pigmentosum patients

L. P. Castro, C. Menck, R. Rocha, 2020, Journal of the European Academy of Dermatology and Venereology : JEADV.

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.

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.