Found: 4

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  • New insights on familial colorectal cancer type X syndrome.

    Published in:
    Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-06782-8
    By:
    • Garcia, Felipe Antonio de Oliveira;
    • de Andrade, Edilene Santos;
    • de Campos Reis Galvão, Henrique;
    • da Silva Sábato, Cristina;
    • Campacci, Natália;
    • de Paula, Andre Escremin;
    • Evangelista, Adriane Feijó;
    • Santana, Iara Viana Vidigal;
    • Melendez, Matias Eliseo;
    • Reis, Rui Manuel;
    • Palmero, Edenir Inez
    Publication type:
    Article

  • Whole-Exome Sequencing Identifies Pathogenic Germline Variants in Patients with Lynch-Like Syndrome.

    Published in:
    Cancers, 2022, v. 14, n. 17, p. 4233, doi. 10.3390/cancers14174233
    By:
    • dos Santos, Wellington;
    • de Andrade, Edilene Santos;
    • Garcia, Felipe Antonio de Oliveira;
    • Campacci, Natália;
    • Sábato, Cristina da Silva;
    • Melendez, Matias Eliseo;
    • Reis, Rui Manuel;
    • Galvão, Henrique de Campos Reis;
    • Palmero, Edenir Inez
    Publication type:
    Article

  • Detection of NTRK fusions by RNA-based nCounter is a feasible diagnostic methodology in a real-world scenario for non-small cell lung cancer assessment.

    Published in:
    Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-48613-4
    By:
    • de Oliveira Cavagna, Rodrigo;
    • de Andrade, Edilene Santos;
    • Tadin Reis, Monise;
    • de Paula, Flávia Escremim;
    • Noriz Berardinelli, Gustavo;
    • Bonatelli, Murilo;
    • Ramos Teixeira, Gustavo;
    • Garbe Zaniolo, Beatriz;
    • Mourão Dias, Josiane;
    • da Silva, Flávio Augusto Ferreira;
    • Baston Silva, Carlos Eduardo;
    • Xavier Reis, Marina;
    • Lopes Maia, Erika;
    • de Alencar, Thainara Santos;
    • Jacinto, Alexandre Arthur;
    • da Nóbrega Oliveira, Rachid Eduardo Noleto;
    • Molina-Vila, Miguel A.;
    • Ferro Leal, Letícia;
    • Reis, Rui Manuel
    Publication type:
    Article

  • Using Co-segregation and Loss of Heterozygosity Analysis to Define the Pathogenicity of Unclassified Variants in Hereditary Breast Cancer Patients.

    Published in:
    Frontiers in Oncology, 2020, v. 10, p. N.PAG, doi. 10.3389/fonc.2020.571330
    By:
    • Grasel, Rebeca Silveira;
    • Felicio, Paula Silva;
    • de Paula, André Escremim;
    • Campacci, Natalia;
    • Garcia, Felipe Antônio de Oliveira;
    • de Andrade, Edilene Santos;
    • Evangelista, Adriane Feijó;
    • Fernandes, Gabriela Carvalho;
    • Sabato, Cristina da Silva;
    • De Marchi, Pedro;
    • Souza, Cristiano de Pádua;
    • de Paula, Cláudia Alessandra Andrade;
    • Torrezan, Giovana Tardin;
    • Galvão, Henrique de Campos Reis;
    • Carraro, Dirce Maria;
    • Palmero, Edenir Inêz
    Publication type:
    Article