Výsledky vyhledávání - Paula Silva Felicio

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  1. 1
    Differential Profile of BRCA1 vs. BRCA2 Mutated Families: A Characterization of the Main Differences and Similarities in Patients

    Differential Profile of BRCA1 vs. BRCA2 Mutated Families: A Characterization of the Main Differences and Similarities in Patients Autor Gabriela Carvalho Fernandes, Paula Silva Felicio, Rodrigo Augusto Depieri Michelli, Aline Silva Coelho, Cristovam Scapulatempo‐Neto, Edenir Inêz Palmero

    Vydáno 2019
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  2. 2
    Haplotypic characterization of BRCA1 c.5266dupC, the prevailing mutation in Brazilian hereditary breast/ovarian cancer

    Haplotypic characterization of BRCA1 c.5266dupC, the prevailing mutation in Brazilian hereditary breast/ovarian cancer Autor Renan Gomes, Bárbara Luísa Soares, Paula Silva Felicio, Rodrigo Augusto Depieri Michelli, Cristina Brinckmann Oliveira Netto, Bárbara Alemar, Patrícia Ashton‐Prolla, Edenir Inêz Palmero, Miguel Ângelo Martins Moreira

    Vydáno 2020
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  3. 3
    Genetic alterations detected by comparative genomic hybridization in BRCAX breast and ovarian cancers of Brazilian population

    Genetic alterations detected by comparative genomic hybridization in BRCAX breast and ovarian cancers of Brazilian population Autor Paula Silva Felicio, Lucas Tadeu Bidinotto, Matias Eliseo Melendez, Rebeca Silveira Grasel, Natália Campacci, Henrique C.R. Galvão, Cristovam Scapulatempo‐Neto, Rozany Mucha Düfloth, Adriane Feijó Evangelista, Edenir Inêz Palmero

    Vydáno 2018
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  4. 4
    Genetic and epigenetic characterization of the BRCA1 gene in Brazilian women at-risk for hereditary breast cancer

    Genetic and epigenetic characterization of the BRCA1 gene in Brazilian women at-risk for hereditary breast cancer Autor Paula Silva Felicio, Matias Eliseo Melendez, Lídia Maria Rebolho Batista Arantes, Lígia Maria Kerr, Dirce Maria Carraro, Rebeca Silveira Grasel, Natália Campacci, Cristovam Scapulatempo‐Neto, Gabriela Carvalho Fernandes, Ana Carolina de Carvalho, Edenir Inêz Palmero

    Vydáno 2016
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  5. 5
    Using Co-segregation and Loss of Heterozygosity Analysis to Define the Pathogenicity of Unclassified Variants in Hereditary Breast Cancer Patients

    Using Co-segregation and Loss of Heterozygosity Analysis to Define the Pathogenicity of Unclassified Variants in Hereditary Breast Cancer Patients Autor Rebeca Silveira Grasel, Paula Silva Felicio, André Escremim de Paula, Natália Campacci, Felipe Antônio de Oliveira Garcia, Edilene Santos de Andrade, Adriane Feijó Evangelista, Gabriela Carvalho Fernandes, Cristina da Silva Sábato, Pedro De Marchi, Cristiano de Pádua Souza, Cláudia Alessandra Andrade de Paula, Giovana Tardin Torrezan, Henrique de Campos Reis Galvão, Dirce Maria Carraro, Edenir Inêz Palmero

    Vydáno 2020
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  6. 6
    Complex Landscape of Germline Variants in Brazilian Patients With Hereditary and Early Onset Breast Cancer

    Complex Landscape of Germline Variants in Brazilian Patients With Hereditary and Early Onset Breast Cancer Autor Giovana Tardin Torrezan, Fernanda G. dos Santos R. de Almeida, Márcia CP Figueiredo, Bruna Durães de Figueiredo Barros, Cláudia Alessandra Andrade de Paula, Renan Valieris, Jorge Estefano Santana de Souza, Rodrigo Fernandes Ramalho, Felipe Cavalcanti Carneiro da Silva, Elisa Napolitano Ferreira, Amanda França de Nóbrega, Paula Silva Felicio, Maria Isabel Achatz, Sandro J. de Souza, Edenir Inêz Palmero, Dirce Maria Carraro

    Vydáno 2018
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  7. 7
    The Brazilian TP53 mutation (R337H) and sarcomas

    The Brazilian TP53 mutation (R337H) and sarcomas Autor Sáhlua Miguel Volc, Cíntia Regina Niederauer Ramos, Henrique de Campos Reis Galvão, Paula Silva Felicio, Aline Silva Coelho, Gustavo Noriz Berardineli, Natália Campacci, Cristina da Silva Sábato, Lucas Faria Abrahão‐Machado, Iara Viana Vidigal Santana, Nathália C. Campanella, André van Helvoort Lengert, Daniel Onofre Vidal, Rui Manuel Reis, Caio F. Dantas, Robson Coelho, Érica Boldrini, Sérgio Serrano, Edenir Inêz Palmero

    Vydáno 2020
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  8. 8
    Prevalence of <i>BRCA1/BRCA2</i> mutations in a Brazilian population sample at-risk for hereditary breast cancer and characterization of its genetic ancestry

    Prevalence of <i>BRCA1/BRCA2</i> mutations in a Brazilian population sample at-risk for hereditary breast cancer and characterization of its genetic ancestry Autor Gabriela Carvalho Fernandes, Rodrigo Augusto Depieri Michelli, Henrique C.R. Galvão, André Escremim de Paula, Rui Pereira, Carlos Eduardo Mattos Cunha Andrade, Paula Silva Felicio, Cristiano de Pádua Souza, Deise R.P. Mendes, Sáhlua Miguel Volc, Gustavo Nóriz Berardinelli, Rebeca Silveira Grasel, Cristina S. Sabato, Danilo Vilela Viana, José Carlos Machado, José Luís Costa, Edmundo Carvalho Mauad, Cristovam Scapulatempo‐Neto, Banu K. Arun, Rui Manuel Reis, Edenir Inêz Palmero

    Vydáno 2016
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  9. 9
    Whole‐exome sequencing of non‐ <i>BRCA1/BRCA2</i> mutation carrier cases at high‐risk for hereditary breast/ovarian cancer

    Whole‐exome sequencing of non‐ <i>BRCA1/BRCA2</i> mutation carrier cases at high‐risk for hereditary breast/ovarian cancer Autor Paula Silva Felicio, Rebeca Silveira Grasel, Natália Campacci, Andre Escremin de Paula, Henrique C.R. Galvão, Giovana Tardin Torrezan, Cristina S. Sabato, Gabriela Carvalho Fernandes, Cristiano de Pádua Souza, Rodrigo D. Michelli, Carlos Eduardo Mattos Cunha Andrade, Bruna Durães de Figueiredo Barros, Marcus Matsushita, Timothée Revil, Jiannis Ragoussis, Fergus J. Couch, Steven N. Hart, Rui Manuel Reis, Matias Eliseo Melendez, Patricia N. Tonin, Dirce Maria Carraro, Edenir Inêz Palmero

    Vydáno 2020
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