Author

Regina Célia Mingroni‐Netto

Universidade de São PauloORCID 0000-0001-9233-5227Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genetics· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Approach:statistical model· 3 Research Focus:gene regulatory network inference· 2 Organism:human· 2 Research Focus:variant calling· 2 Assay:whole-genome sequencing· 2 Research Focus:database / resource· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1

Frequent Co-Authors

Kelly NunesiD· 2 shared Abdelwahab KawafiiD· 1 shared Alejandro Q. NatoiD· 1 shared Ana Carla BatissocoiD· 1 shared Andréa R. V. R. HorimotoiD· 1 shared Andréia S. SouzaiD· 1 shared Beatriz Cavalcanti de Albuquerque Caiuby NovaesiD· 1 shared Bernardo Lessa HortaiD· 1 shared

Activity by Year

2020-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 16 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Kelly NunesORCID

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3 papers

Recent·Most cited

Genetic & Genomic MedicineJournal of the American Heart AssociationPeer-reviewedMar 21, 2025

Genomic Exploration of Essential Hypertension in African-Brazilian Quilombo Populations: A Comprehensive Approach with Pedigree Analysis and Family-Based Association Studies

Vinícius Magalhães Borges, Andréa R. V. R. Horimoto, Ellen M. Wijsman…·Regina Célia Mingroni‐Netto

This study identifies genetic loci and candidate genes associated with essential hypertension in African-Brazilian Quilombo populations using genome-wide linkage analysis and family-based association studies.

3 citations

humanwhole-genome 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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GeneticsHuman Molecular GeneticsPeer-reviewedOct 23, 2020

NCOA3 identified as a new candidate to explain autosomal dominant progressive hearing loss

Rodrigo Salazar‐Silva, Vitor Lima Goes Dantas, Leandro Ucela Alves…·Regina Célia Mingroni‐Netto

The paper identifies NCOA3 as a candidate gene for autosomal dominant progressive hearing loss through linkage analysis and functional studies in zebrafish.

20 citations

zebrafishstatistical model

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