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Author

Darine Villela

Observed names: D Villela, DARINE VILLELA, Darine Christina Maia Villela
Institution: DASA (Brazil)
ORCID: 0000-0002-5930-5269
Observed ORCID: 0000-0002-5930-5269
OpenAlex ID: A5091780257
Differential DNA Methylation of MicroRNA Genes in Temporal Cortex from Alzheimer’s Disease Individuals
2016 · Darine Villela, Rodrigo F. Ramalho, et al. · Neural Plasticity · 55
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Noninvasive prenatal diagnosis by genome-wide haplotyping of cell-free plasma DNA
2020 · Huiwen Che, Darine Villela, et al. · Genetics in Medicine · 37
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Maternal copy-number variations in the DMD gene as secondary findings in noninvasive prenatal screening
2019 · Nathalie Brison, Jazz Storms, et al. · Genetics in Medicine · 29
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Do Copy Number Changes in CACNA2D2, CACNA2D3, and CACNA1D Constitute a Predisposing Risk Factor for Alzheimer’s Disease?
2016 · Darine Villela, Claudia K. Suemoto, et al. · Frontiers in Genetics · 29
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Modulation of Pineal Melatonin Synthesis by Glutamate Involves Paracrine Interactions between Pinealocytes and Astrocytes through NF- κ B Activation
2013 · Darine Villela, Victoria Fairbanks Atherino, et al. · BioMed Research International · 29
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Chromosomal microarray analyses from 5778 patients with neurodevelopmental disorders and congenital anomalies in Brazil
2022 · Ana C. V. Krepischi, Darine Villela, et al. · Scientific Reports · 23
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Breast Cancer Detection and Treatment Monitoring Using a Noninvasive Prenatal Testing Platform: Utility in Pregnant and Nonpregnant Populations
2020 · Liesbeth Lenaerts, Huiwen Che, et al. · Clinical Chemistry · 22
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Norepinephrine activates NF-κB transcription factor in cultured rat pineal gland
2013 · Darine Villela, Larissa de Sá Lima, et al. · Life Sciences · 21
Low‐pass whole genome sequencing is a reliable and cost‐effective approach for copy number variant analysis in the clinical setting
2023 · Patricia C. Mazzonetto, Darine Villela, et al. · Annals of Human Genetics · 20
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Genetic investigation of syndromic forms of obesity
2022 · Laura Machado Lara Carvalho, Carla Sustek D’Angelo, et al. · International Journal of Obesity · 20
BRCA1 and BRCA2 germline mutation analysis from a cohort of 1267 patients at high risk for breast cancer in Brazil
2023 · Patricia Mazzonetto, Fernanda Milanezi, et al. · Breast Cancer Research and Treatment · 15
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Fetal sex determination in twin pregnancies using non-invasive prenatal testing
2019 · Darine Villela, Huiwen Che, et al. · npj Genomic Medicine · 13
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Efficient detection of chromosome imbalances and single nucleotide variants using targeted sequencing in the clinical setting
2017 · Darine Villela, Silvia Souza Costa, et al. · European Journal of Medical Genetics · 13
A Benchmark of In-House Homologous Recombination Repair Deficiency Testing Solutions for High-Grade Serous Ovarian Cancer Diagnosis
2023 · Rodrigo Guarischi-Sousa, José Eduardo Kroll, et al. · Diagnostics · 12
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Increased DNA Copy Number Variation Mosaicism in Elderly Human Brain
2018 · Darine Villela, Claudia K. Suemoto, et al. · Neural Plasticity · 12
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Whole genome sequencing as a first‐tier diagnostic test for infants in neonatal intensive care units: A pilot study in Brazil
2024 · Michele P. Migliavacca, Joselito Sobreira, et al. · American Journal of Medical Genetics Part A · 11
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Germline DNA copy number variation in individuals with Argyrophilic grain disease reveals CTNS as a plausible candidate gene
2013 · Darine Villela, Lilian Kimura, et al. · Genetics and Molecular Biology · 10
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Low‐pass whole genome sequencing as a cost‐effective alternative to chromosomal microarray analysis for low‐ and middle‐income countries
2024 · Patricia C. Mazzonetto, Darine Villela, et al. · American Journal of Medical Genetics Part A · 9
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A microdeletion in Alzheimer’s disease disrupts NAMPT gene
2014 · DARINE VILLELA, DAVID SCHLESINGER, et al. · Journal of Genetics · 8
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Germline variant analysis from a cohort of patients with severe hypertriglyceridemia in Brazil
2024 · Camila Mendes, Thereza Loureiro, et al. · Molecular Genetics and Metabolism Reports · 4
MTHFR genetic testing: is there a clinical utility?
2024 · Aline Cristiane Planello, Darine Villela, et al. · Revista da Associação Médica Brasileira · 4
Detection of mosaicism for segmental and whole chromosome imbalances by targeted sequencing
2020 · Darine Villela, Juliana Sobral de Barros, et al. · Annals of Human Genetics · 4
Mining Novel Candidate Imprinted Genes Using Genome-Wide Methylation Screening and Literature Review
2017 · Adriano Bonaldi, André Kashiwabara, et al. · Epigenomes · 4
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Uniparental disomy (UPD) as the cause of inconsistencies in parentage tests: report of maternal UPD of chromosome 2 and review of the literature
2025 · Cintia Fridman, João Paulo Gervasio Batista, et al. · International Journal of Legal Medicine · 3
HRD-One: CLINICAL VALIDATION AND PERFORMANCE ASSESSMENT. Comparison between Myriad’s myChoice®, SOPHiA GENETICS® SOPHiA Homologous Recombination Solution and AmoyDx® HRD Focus Panel
2023 · Rodrigo Guarischi-Sousa, José Eduardo Kroll, et al. · medRxiv · 3
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Works count: 39
Citation count: 421
H-index: 13
I10-index: 17
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