Early-onset breast cancer patients in the South and Southeast of Brazil should be tested for the TP53 p.R337H mutation

por Andrade, Kelvin C., Santiago, Karina M., Fortes, Fernanda P., Mambelli, Lisley I., Nóbrega, Amanda F., Achatz, Maria I.
Publicado 2016

Hereditary breast and ovarian cancer: assessment of point mutations and copy number variations in Brazilian patients

por Silva, Felipe C, Lisboa, Bianca CG, Figueiredo, Marcia CP, Torrezan, Giovana T, Santos, Érika MM, Krepischi, Ana C, Rossi, Benedito M, Achatz, Maria I, Carraro, Dirce M
Publicado 2014

LINE-1 hypermethylation in peripheral blood of cutaneous melanoma patients is associated with metastasis

por De Araújo, Érica S.S., Kashiwabara, André Y., Achatz, Maria I.W., Moredo, Luciana F., De Sá, Bianca C.S., Duprat, João P., Rosenberg, Carla, Carraro, Dirce M., Krepischi, Ana C.V.
Publicado 2015

Analysis of the Li-Fraumeni Spectrum Based on an International Germline TP53 Variant Data Set: An International Agency for Research on Cancer TP53 Database Analysis

por Kratz, Christian P., Freycon, Claire, Maxwell, Kara N., Nichols, Kim E., Schiffman, Joshua D., Evans, D. Gareth, Achatz, Maria I., Savage, Sharon A., Weitzel, Jeffrey N., Garber, Judy E., Hainaut, Pierre, Malkin, David
Publicado 2021

DNA Methylation Levels of Melanoma Risk Genes Are Associated with Clinical Characteristics of Melanoma Patients

por de Araújo, Érica S. S., Pramio, Dimitrius T., Kashiwabara, André Y., Pennacchi, Paula C., Maria-Engler, Silvya S., Achatz, Maria I., Campos, Antonio H. J. F. M., Duprat, João P., Rosenberg, Carla, Carraro, Dirce M., Krepischi, Ana C. V.
Publicado 2015

Complex Landscape of Germline Variants in Brazilian Patients With Hereditary and Early Onset Breast Cancer

por Torrezan, Giovana T., de Almeida, Fernanda G. dos Santos R., Figueiredo, Márcia C. P., Barros, Bruna D. de Figueiredo, de Paula, Cláudia A. A., Valieris, Renan, de Souza, Jorge E. S., Ramalho, Rodrigo F., da Silva, Felipe C. C., Ferreira, Elisa N., de Nóbrega, Amanda F., Felicio, Paula S., Achatz, Maria I., de Souza, Sandro J., Palmero, Edenir I., Carraro, Dirce M.
Publicado 2018

Prevalence of pathogenic/likely pathogenic variants in the 24 cancer genes of the ACMG Secondary Findings v2.0 list in a large cancer cohort and ethnicity-matched controls

por Kim, Jung, Luo, Wen, Wang, Mingyi, Wegman-Ostrosky, Talia, Frone, Megan N., Johnston, Jennifer J., Nickerson, Michael L., Rotunno, Melissa, Li, Shengchao A., Achatz, Maria I., Brodie, Seth A., Dean, Michael, de Andrade, Kelvin C., Fortes, Fernanda P., Gianferante, Matthew, Khincha, Payal, McMaster, Mary L., McReynolds, Lisa J., Pemov, Alexander, Pinheiro, Maisa, Santiago, Karina M., Alter, Blanche P., Caporaso, Neil E., Gadalla, Shahinaz M., Goldin, Lynn R., Greene, Mark H., Loud, Jennifer, Yang, Xiaohong R., Freedman, Neal D., Gapstur, Susan M., Gaudet, Mia M., Calista, Donato, Ghiorzo, Paola, Fargnoli, Maria Concetta, Nagore, Eduardo, Peris, Ketty, Puig, Susana, Landi, Maria Teresa, Hicks, Belynda, Zhu, Bin, Liu, Jia, Sampson, Joshua N., Chanock, Stephen J., Mirabello, Lisa J., Morton, Lindsay M., Biesecker, Leslie G., Tucker, Margaret A., Savage, Sharon A., Goldstein, Alisa M., Stewart, Douglas R.
Publicado 2018