Darine Villela
11PUBLICATIONS
35CO-AUTHORS
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Publications (11)
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|Mar 08, 2026
VariantMatcher: Phenotypic and Genomic Data Sharing to Facilitate Variant Classification and Disease Gene Discovery.Darine Villela, Marcelo Szeremeta, Joselito Sobreira
|Aug 20, 2025
Assessing the impact of exome sequencing on diagnostic yield in a large cohort of Brazilian patients.Aline Cristiane Planello, Thereza Loureiro, Dayse Alencar-Cupertino
|Jul 24, 2024
MTHFR genetic testing: is there a clinical utility?Aline Cristiane Planello, Darine Villela, Thereza Loureiro
|Jun 26, 2024
Low-pass whole genome sequencing as a cost-effective alternative to chromosomal microarray analysis for low- and middle-income countries.Patricia C Mazzonetto, Darine Villela, Ana C V Krepischi
|Jan 23, 2024
Whole genome sequencing as a first-tier diagnostic test for infants in neonatal intensive care units: A pilot study in Brazil.Michele P Migliavacca, Joselito Sobreira, Diana Bermeo
|Oct 09, 2023
Low-pass whole genome sequencing is a reliable and cost-effective approach for copy number variant analysis in the clinical setting.Patricia C Mazzonetto, Darine Villela, Silvia Souza da Costa
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Frequent Collaborators
4 joint publications
Nara Sobreira
3 joint publications
Thereza Loureiro
2 joint publications
Joselito Sobreira
2 joint publications
Aline Cristiane Planello
2 joint publications
Rodrigo Guarischi-Sousa
1 joint publications
Carlos Augusto Pasqualucci
1 joint publications
Lea T Grinberg
1 joint publications
Jazz Storms
1 joint publications
Koenraad Devriendt
1 joint publications
Alexander A L Jorge
