| Differential DNA methylation of microRNA genes in temporal cortex from Alzheimer’s disease individuals D Villela, RF Ramalho, ART Silva, H Brentani, CK Suemoto, ... Neural plasticity 2016, 2016 | 45 | 2016 |
| Noninvasive prenatal diagnosis by genome-wide haplotyping of cell-free plasma DNA H Che, D Villela, E Dimitriadou, C Melotte, N Brison, M Neofytou, ... Genetics in Medicine 22 (5), 962-973, 2020 | 31 | 2020 |
| Modulation of pineal melatonin synthesis by glutamate involves paracrine interactions between pinealocytes and astrocytes through NF-B activation D Villela, VF Atherino, LS Lima, AA Moutinho, FG Amaral, R Peres, ... BioMed research international 2013, 2013 | 31 | 2013 |
| Norepinephrine activates NF-κB transcription factor in cultured rat pineal gland D Villela, L de Sá Lima, R Peres, RA Peliciari-Garcia, FG do Amaral, ... Life sciences 94 (2), 122-129, 2014 | 24 | 2014 |
| Melatonin and pineal gland SC Afeche, FG Amaral, DCM Villela, MV Abrahão, R Peres, ... New research on neurosecretory systems. Hauppauge: Nova Science Publishers …, 2008 | 22 | 2008 |
| Maternal copy-number variations in the DMD gene as secondary findings in noninvasive prenatal screening N Brison, J Storms, D Villela, KG Claeys, L Dehaspe, T de Ravel, ... Genetics in Medicine 21 (12), 2774-2780, 2019 | 21 | 2019 |
| Do Copy Number Changes in CACNA2D2, CACNA2D3, and CACNA1D Constitute a Predisposing Risk Factor for Alzheimer’s Disease? D Villela, CK Suemoto, CA Pasqualucci, LT Grinberg, C Rosenberg Frontiers in Genetics 7, 107, 2016 | 17 | 2016 |
| Increased DNA copy number variation mosaicism in elderly human brain D Villela, CK Suemoto, R Leite, CA Pasqualucci, LT Grinberg, P Pearson, ... Neural plasticity 2018, 2018 | 13 | 2018 |
| Germline DNA copy number variation in individuals with Argyrophilic grain disease reveals CTNS as a plausible candidate gene D Villela, L Kimura, D Schlesinger, A Gonçalves, PL Pearson, ... Genetics and molecular biology 36, 498-501, 2013 | 13 | 2013 |
| Fetal sex determination in twin pregnancies using non-invasive prenatal testing D Villela, H Che, M Van Ghelue, L Dehaspe, N Brison, ... NPJ Genomic Medicine 4 (1), 15, 2019 | 12 | 2019 |
| Efficient detection of chromosome imbalances and single nucleotide variants using targeted sequencing in the clinical setting D Villela, SS Costa, AM Vianna-Morgante, ACV Krepischi, C Rosenberg European journal of medical genetics 60 (12), 667-674, 2017 | 12 | 2017 |
| Chromosomal microarray analyses from 5778 patients with neurodevelopmental disorders and congenital anomalies in Brazil ACV Krepischi, D Villela, SS da Costa, PC Mazzonetto, J Schauren, ... Scientific Reports 12 (1), 15184, 2022 | 11 | 2022 |
| Breast cancer detection and treatment monitoring using a noninvasive prenatal testing platform: utility in pregnant and nonpregnant populations L Lenaerts, H Che, N Brison, M Neofytou, T Jatsenko, H Lefrere, ... Clinical Chemistry 66 (11), 1414-1423, 2020 | 9 | 2020 |
| Genetic investigation of syndromic forms of obesity LML Carvalho, CS D’Angelo, D Villela, SS da Costa, AA de Lima Jorge, ... International Journal of Obesity 46 (9), 1582-1586, 2022 | 8 | 2022 |
| A microdeletion in Alzheimer’s disease disrupts NAMPT gene D Villela, D Schlesinger, CK Suemoto, LT Grinberg, C Rosenberg Journal of genetics 93, 535-537, 2014 | 8 | 2014 |
| Detection of mosaicism for segmental and whole chromosome imbalances by targeted sequencing D Villela, JS de Barros, SS da Costa, TFM Aguiar, F Campagnari, ... Annals of human genetics 85 (1), 18-26, 2021 | 7 | 2021 |
| New research on neurosecretory systems SC Afeche, FG Amaral, DCM Villela, MV Abrahão, R Peres, ... Nova Science Publishers, New York, NY, 2008 | 6 | 2008 |
| Low‐pass whole genome sequencing is a reliable and cost‐effective approach for copy number variant analysis in the clinical setting PC Mazzonetto, D Villela, SS da Costa, ACV Krepischi, F Milanezi, ... Annals of Human Genetics 88 (2), 113-125, 2024 | 2 | 2024 |
| BRCA1 and BRCA2 germline mutation analysis from a cohort of 1267 patients at high risk for breast cancer in Brazil P Mazzonetto, F Milanezi, M D’Andrea, S Martins, PM Monfredini, ... Breast Cancer Research and Treatment 199 (1), 127-136, 2023 | 2 | 2023 |
| Mining novel candidate imprinted genes using genome-wide methylation screening and literature review A Bonaldi, A Kashiwabara, ÉS de Araújo, LV Pereira, AR Paschoal, ... Epigenomes 1 (2), 13, 2017 | 2 | 2017 |
