Author

Jaqueline Yu Ting Wang

Universidade de São Paulo

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetic & Genomic Medicine· 2 Developmental Biology· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Approach:statistical model· 4 Organism:human· 3 Assay:whole-exome sequencing· 2 Research Focus:database / resource· 1 Research Focus:differential expression· 1 Assay:DNA methylation· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1

Frequent Co-Authors

Maria Rita Passos-BuenoiD· 4 shared Andréia S. SouzaiD· 2 shared Camila Ferreira Bannwart CastroiD· 2 shared Celso Teixeira Mendes‐JunioriD· 2 shared Diogo MeyeriD· 2 shared Erick C. CastelliiD· 2 shared Heloisa S. AndradeiD· 2 shared Kelly NunesiD· 2 shared

Activity by Year

2019-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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4 shared papersGenetic & Genomic Medicine

Maria Rita Passos-BuenoORCID

Mutual co-authors in cluster

Author profile →

4 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintDec 27, 2024

Deleterious coding variation associated with autism is consistent across populations, as exemplified by admixed Latin American populations

Marina Natividad Avila, Seulgi Jung, F. Kyle Satterstrom…·Joseph D. Buxbaum

This paper identifies 35 genome-wide significant ASD risk genes in admixed Latin American populations, showing consistency with European cohorts and supporting the universality of ASD biology.

3 citations

humanwhole-exome sequencing

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GenomicsNature CommunicationsPeer-reviewedMar 4, 2022

Whole-genome sequencing of 1,171 elderly admixed individuals from the largest Latin American metropolis (Sao Paulo, Brazil)

Michel Satya Naslavsky, Marília O. Scliar, Guilherme Lopes Yamamoto…·Mayana Zatz

This study presents a high-coverage whole-genome sequencing dataset of 1,171 admixed elderly Brazilians, identifying novel variants and demonstrating the utility of WGS for genomic and clinical research in underrepresented populations.

160 citationstop 1%

humanwhole-genome sequencing

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Genetic & Genomic MedicineFrontiers in ImmunologyPeer-reviewedSep 28, 2021

Immunogenetics of resistance to SARS-CoV-2 infection in discordant couples

Erick C. Castelli, Mateus Vidigal de Castro, Michel Satya Naslavsky…·Mayana Zatz

The paper identifies genetic variants associated with resistance to SARS-CoV-2 infection by analyzing discordant Brazilian couples.

56 citationstop 4%

humanwhole-exome sequencing

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Developmental BiologybioRxivPreprintNov 22, 2019

"mir152 hypomethylation, potentially triggered by embryonic hypoxia, as a mechanism for non-syndromic cleft lip/palate"

Lucas Alvizi, Luciano Abreu Brito, Bárbara Bischain…·Maria Rita Passos‐Bueno

The paper identifies mir152 hypomethylation as a potential mechanism for non-syndromic cleft lip/palate, linked to embryonic hypoxia in zebrafish models.

DOI 10.1101/850016

zebrafishDNA methylation

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