Author

Renata Moldenhauer Minillo

Hospital Israelita Albert EinsteinORCID 0000-0001-6621-3672Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 3

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 3 Research Focus:variant calling· 3 Assay:whole-genome sequencing· 2 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Antônio Victor Campos CoelhoiD· 3 shared Anne Caroline Barbosa TeixeiraiD· 2 shared Caio Robledo D’Angioli Costa QuaioiD· 2 shared Carolina MorenoiD· 2 shared Eduardo PerroneiD· 2 shared Gabriela Pereira Campilongo· 2 shared Jessica Grasiela Araujo EspolaoriD· 2 shared Joana Rosa Marques ProtaiD· 2 shared

Activity by Year

2022-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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3 shared papersGenetic & Genomic Medicine

Antônio Victor Campos CoelhoORCID

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3 papers

Recent·Most cited

Genetic & Genomic MedicineHuman Genetics and Genomics AdvancesPeer-reviewedMay 4, 2026

Whole Genome Sequencing for the Diagnosis of Rare Disorders

Antônio Victor Campos Coelho, Rafael Sales de Albuquerque, Catarina dos Santos Gomes…·Joao Bosco Oliveira

This study evaluates the diagnostic yield of whole-genome sequencing in 8966 patients with suspected rare diseases, finding a 35.8% diagnostic rate and additional variant detection.

DOI 10.1016/j.xhgg.2026.100624

humanwhole-genome sequencing

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Genetic & Genomic MedicineJournal of Human GeneticsPeer-reviewedMay 18, 2025

ACMG Secondary Findings in the Brazilian Rare Genomes Project: Insights from 5,402 genome sequencing

Eduardo Perrone, Luiza do Amaral Virmond, Antônio Victor Campos Coelho…·Tatiana Ferreira de Almeida

The paper analyzes ACMG secondary findings in 5,402 Brazilian genomes, finding 3.6% had pathogenic variants, mainly in cardiovascular and cancer-related genes.

5 citations

humanwhole-genome sequencing

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Genetic & Genomic MedicineEuropean Journal of Human GeneticsPeer-reviewedMay 9, 2022

The genetics of hereditary cancer risk syndromes in Brazil: a comprehensive analysis of 1682 patients

Jarbas Maciel de Oliveira, Nuria Bengala Zurro, Antônio Victor Campos Coelho…·João Bosco Oliveira

This study analyzes germline variants in 1682 Brazilian patients with cancer histories, identifying 321 pathogenic/likely pathogenic variants across 32 genes and highlighting gaps in current genetic testing guidelines.

21 citations

humanwhole-exome sequencing

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