Author

Elyzabeth Avvad Portari

Instituto Nacional de Saúde da Mulher, da Criança e do Adolescente Fernandes FigueiraORCID 0000-0003-2372-0898Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetics· 1 Systems Biology· 1

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 2 Organism:human· 2 Approach:statistical model· 2 Assay:bulk RNA-seq· 1 Assay:DNA methylation· 1 Research Focus:gene regulatory network inference· 1 Assay:proteomics· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Daniela Prado CunhaiD· 2 shared Leonardo Henrique Ferreira GomesiD· 2 shared Letícia da Cunha GuidaiD· 2 shared Zilton Farias Meira de VasconcelosiD· 2 shared Adriana MeloiD· 1 shared Alessandra Soares SchanoskiiD· 1 shared Alessandro L. Gonçalves· 1 shared Alexandra Lehmkuhl GerberiD· 1 shared

Activity by Year

2019-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 40 mutual co-author links

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2 shared papersGenetics

Daniela Prado CunhaORCID

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2 papers

Recent·Most cited

GeneticsFrontiers in ImmunologyPeer-reviewedNov 25, 2021

Congenital Zika Syndrome is associated with interferon alfa receptor 1

Tamiris Azamor, Daniela Prado Cunha, Andréa Marques Vieira da Silva…·Milton Ozório Moraes

The paper identifies a genetic variant in IFNAR1 associated with increased risk of Congenital Zika Syndrome and shows altered placental gene expression related to type I and III interferon imbalance.

29 citationstop 5%

humanwhole-genome sequencing

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Systems BiologybioRxivPreprintFeb 5, 2019

The potential role of collagens in congenital Zika syndrome: A systems biology approach

Renato Santana Aguiar, Fabio Baldivia Pohl, Guilherme Loss de Morais…·Helder Imoto Nakaya

This study integrates transcriptomic, proteomic, and genomic data from CZS neonates to identify collagen gene reductions and associated polymorphisms, linking them to neuronal migration defects and CZS susceptibility.

DOI 10.1101/541268

humanbulk RNA-seq

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