Functional Polymorphisms in the p53 Pathway Genes on the Genetic Susceptibility to Zika Virus Teratogenesis by Gomes, Julia A, Sgarioni, Eduarda, Vieira, Igor A, Fraga, Lucas R, Ashton-Prolla, Patrícia, Terças-Tretell, Ana Cláudia P, da Silva, Juliana H, Ribeiro, Bethânia F R, Galera, Marcial F, de Oliveira, Thalita M, Carvalho de Andrade, Maria Denise F, Carvalho, Isabella F, Schuler-Faccini, Lavínia, Vianna, Fernanda S L

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A recurrent de novo splice site variant involving DNM1 exon 10a causes developmental and epileptic encephalopathy through a dominant-negative mechanism by Parthasarathy, Shridhar, Ruggiero, Sarah McKeown, Gelot, Antoinette, Soardi, Fernanda C, Ribeiro, Bethânia F R, Pires, Douglas E V, Ascher, David B, Schmitt, Alain, Rambaud, Caroline, Represa, Alfonso, Xie, Hongbo M, Lusk, Laina, Wilmarth, Olivia, McDonnell, Pamela Pojomovsky, Juarez, Olivia A, Grace, Alexandra N, Buratti, Julien, Mignot, Cyril, Gras, Domitille, Nava, Caroline, Pierce, Samuel R, Keren, Boris, Kennedy, Benjamin C, Pena, Sergio D J, Helbig, Ingo, Cuddapah, Vishnu Anand

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Contribution of miR-124 rs531564 polymorphism to the occurrence of congenital Zika syndrome by Gomes, Julia A, Vieira, Igor Araujo, Sgarioni, Eduarda, Terças-Tretell, Ana Cláudia P, da Silva, Juliana H, Ribeiro, Bethânia Fr, Galera, Marcial F, de Oliveira, Thalita M, Carvalho de Andrade, Maria Denise F, Carvalho, Isabella F, Schüler-Faccini, Lavínia, Vianna, Fernanda Sl

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23 Evaluation of a functional polymorphism of the P53 gene on ZIKV teratogenesis in humans by Gomes, Julia A., Sgarioni, Eduarda, Silva, Juliana H., Ribeiro, Bethânia F.R., Schüler-Faccini, Lavínia, Vianna, Fernanda S.L.

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Association between Genetic Variants in NOS2 and TNF Genes with Congenital Zika Syndrome and Severe Microcephaly by Gomes, Julia A, Sgarioni, Eduarda, Boquett, Juliano A, Terças-Trettel, Ana Cláudia P, da Silva, Juliana H, Ribeiro, Bethânia F R, Galera, Marcial F, de Oliveira, Thalita M, Carvalho de Andrade, Maria Denise F, Carvalho, Isabella F, Schüler-Faccini, Lavínia, Vianna, Fernanda S L

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Investigation of the impact of AXL, TLR3, and STAT2 in congenital Zika syndrome through genetic polymorphisms and protein-protein interaction network analyses by Gomes, Julia A, Sgarioni, Eduarda, Boquett, Juliano A, Kowalski, Thayne W, Fraga, Lucas R, Terças-Trettel, Ana Cláudia P, da Silva, Juliana H, Ribeiro, Bethânia F R, Galera, Marcial F, de Oliveira, Thalita M, Carvalho de Andrade, Maria Denise F, Carvalho, Isabella F, Schüler-Faccini, Lavínia, Vianna, Fernanda S L

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Long-term impact of early initiation of enzyme replacement therapy in 34 MPS VI patients: A resurvey study by Horovitz, Dafne D.G., Leão, Emília K.E.A., Ribeiro, Erlane M., Martins, Ana M., Barth, Anneliese L., Neri, João I.C.F., Kerstenetzky, Marcelo, Siqueira, Ana C.M., Ribeiro, Bethania F.R., Kim, Chong A., Santos, Francisca C., Franco, José F.S., Lichtvan, Leniza C.L., Giuliani, Liane R., Rodrigues, Maria Do C.S., Bonatti, Renata C.F., Teixeira, Thaís B., Gonçalves, Alexandra, Lourenço, Charles M., Pereira, Ane S.S., Acosta, Angelina X.

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The role of angiogenesis genes in ZIKV teratogenesis: Preliminary findings from a multi-approach study by Gomes, Julia A., Kowalski, Thayne W., Sgarioni, Eduarda, Silva, Juliana H., Ribeiro, Bethania F.R., Schüler-Faccini, Lavínia, Vianna, Fernanda S.L.

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Enzyme replacement therapy with galsulfase in 34 children younger than five years of age with MPS VI by Horovitz, Dafne D.G., Magalhães, Tatiana S.P.C., Acosta, Angelina, Ribeiro, Erlane M., Giuliani, Liane R., Palhares, Durval B., Kim, Chong A., de Paula, Ana Carolina, Kerstenestzy, Marcelo, Pianovski, Mara A.D., Costa, Maria Ione F., Santos, Francisca C., Martins, Ana Maria, Aranda, Carolina S., Neto, Jordão Correa, Holanda, Gervina Brady Moreira, Cardoso, Laércio, da Silva, Carlos A.B., Bonatti, Renata C.F., Ribeiro, Bethania F.R., Rodrigues, Maria do Carmo S., Llerena, Juan C.

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