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American Journal of Medical Genetics. Part A|May 14, 2021
Congenital chromoanagenesis in the routine postnatal chromosomal microarray analysesDarine Villela, Patricia C Mazzonetto, Michele P Migliavacca, et al.Scientific Reports|September 7, 2022
Chromosomal microarray analyses from 5778 patients with neurodevelopmental disorders and congenital anomalies in BrazilAna C V Krepischi, Darine Villela, Silvia Souza da Costa, et al.Diagnostics (Basel, Switzerland)|November 14, 2023
A Benchmark of In-House Homologous Recombination Repair Deficiency Testing Solutions for High-Grade Serous Ovarian Cancer DiagnosisRodrigo Guarischi-Sousa, José Eduardo Kroll, Adriano Bonaldi, et al.Biomedicine Hub|July 3, 2025
Central Diabetes Insipidus in Father and Son Linked to a Rare Variant: A Case ReportPaula Bruna Mattos Coelho Araujo, Luiz Filipe Rocha de Sá, Rafaela Sousa, et al.American Journal of Medical Genetics. Part A|January 23, 2024
Whole genome sequencing as a first-tier diagnostic test for infants in neonatal intensive care units: A pilot study in BrazilMichele P Migliavacca, Joselito Sobreira, Diana Bermeo, et al.American Journal of Medical Genetics. Part A|June 26, 2024
Low-pass whole genome sequencing as a cost-effective alternative to chromosomal microarray analysis for low- and middle-income countriesPatricia C Mazzonetto, Darine Villela, Ana C V Krepischi, et al.Pageof 3