Do Copy Number Changes in CACNA2D2, CACNA2D3, and CACNA1D Constitute a Predisposing Risk Factor for Alzheimer’s Disease?

por Villela, Darine, Suemoto, Claudia K., Pasqualucci, Carlos A., Grinberg, Lea T., Rosenberg, Carla
Publicado 2016

Increased DNA Copy Number Variation Mosaicism in Elderly Human Brain

por Villela, Darine, Suemoto, Claudia K., Leite, Renata, Pasqualucci, Carlos Augusto, Grinberg, Lea T., Pearson, Peter, Rosenberg, Carla
Publicado 2018

Germline DNA copy number variation in individuals with Argyrophilic grain disease reveals CTNS as a plausible candidate gene

por Villela, Darine, Kimura, Lilian, Schlesinger, David, Gonçalves, Amanda, Pearson, Peter L., Suemoto, Claudia K., Pasqualucci, Carlos, Krepischi, Ana Cristina, Grinberg, Lea T., Rosenberg, Carla
Publicado 2013

Differential DNA Methylation of MicroRNA Genes in Temporal Cortex from Alzheimer's Disease Individuals

por Villela, Darine, Ramalho, Rodrigo F., Silva, Aderbal R. T., Brentani, Helena, Suemoto, Claudia K., Pasqualucci, Carlos Augusto, Grinberg, Lea T., Krepischi, Ana C. V., Rosenberg, Carla
Publicado 2016

Fetal sex determination in twin pregnancies using non-invasive prenatal testing

por Villela, Darine, Che, Huiwen, Van Ghelue, Marijke, Dehaspe, Luc, Brison, Nathalie, Van Den Bogaert, Kris, Devriendt, Koen, Lewi, Liesbeth, Bayindir, Baran, Vermeesch, Joris Robert
Publicado 2019

A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2

por Migliavacca, Michele Patricia, Fock, Rodrigo Ambrosio, Almeida, Nadia, Cavalcanti, Thereza, Villela, Darine, Perez, Ana Beatriz Alvarez, Valle, David, Wohler, Elizabeth, Sobreira, Nara Lygia de Macena, Raskin, Salmo
Publicado 2023

Modulation of Pineal Melatonin Synthesis by Glutamate Involves Paracrine Interactions between Pinealocytes and Astrocytes through NF-κB Activation

por Villela, Darine, Atherino, Victoria Fairbanks, Lima, Larissa de Sá, Moutinho, Anderson Augusto, do Amaral, Fernanda Gaspar, Peres, Rafael, Martins de Lima, Thais, Torrão, Andréa da Silva, Cipolla-Neto, José, Scavone, Cristóforo, Afeche, Solange Castro
Publicado 2013

A Benchmark of In-House Homologous Recombination Repair Deficiency Testing Solutions for High-Grade Serous Ovarian Cancer Diagnosis

por Guarischi-Sousa, Rodrigo, Kroll, José Eduardo, Bonaldi, Adriano, Pierry, Paulo Marques, Villela, Darine, Souza, Camila Alves, Silva, Juliana Santos, Bürger, Matheus Carvalho, Oliveira, Felipe Azevedo, de Paula, Marcelo Gomes, Meliso, Fabiana Marcelino, de Almeida, Luiz Gustavo, Monfredini, Priscilla Morais, de Oliveira, Ana Gabriela, Milanezi, Fernanda, Scapulatempo-Neto, Cristovam, Yamamoto, Guilherme Lopes
Publicado 2023

Chromosomal microarray analyses from 5778 patients with neurodevelopmental disorders and congenital anomalies in Brazil

por Krepischi, Ana C. V., Villela, Darine, da Costa, Silvia Souza, Mazzonetto, Patricia C., Schauren, Juliana, Migliavacca, Michele P., Milanezi, Fernanda, Santos, Juliana G., Guida, Gustavo, Guarischi-Sousa, Rodrigo, Campana, Gustavo, Kok, Fernando, Schlesinger, David, Kitajima, Joao Paulo, Campagnari, Francine, Bertola, Debora R., Vianna-Morgante, Angela M., Pearson, Peter L., Rosenberg, Carla
Publicado 2022