Association of Folate and Vitamins Involved in the 1-Carbon Cycle with Polymorphisms in the Methylenetetrahydrofolate Reductase Gene (MTHFR) and Global DNA Methylation in Patients... von Ferrari, Ariana, Torrezan, Giovana Tardin, Carraro, Dirce Maria, Aguiar Junior, Samuel

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Family-based whole-exome sequencing identifies rare variants potentially related to cutaneous melanoma predisposition in Brazilian melanoma-prone families von Fidalgo, Felipe, Torrezan, Giovana Tardin, Sá, Bianca Costa Soares de, Barros, Bruna Durães de Figueiredo, Moredo, Luciana Facure, Valieris, Renan, de Souza, Sandro J, Duprat, João Pereira, Krepischi, Ana Cristina Victorino, Carraro, Dirce Maria

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A cross-sectional study of clinical, dermoscopic, histopathological, and molecular patterns of scalp melanoma in patients with or without androgenetic alopecia von Porto, Ana Carolina, Pinto Blumetti, Tatiana, Calsavara, Vinícius Fernando, Tardin Torrezan, Giovana, Andrade de Paula, Cláudia Alessandra, Lellis, Rute, Pedreira Duprat Neto, João, Carraro, Dirce Maria, Casagrande Tavoloni Braga, J.

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Recurrent somatic mutation in DROSHA induces microRNA profile changes in Wilms tumour von Torrezan, Giovana T., Ferreira, Elisa N., Nakahata, Adriana M., Barros, Bruna D. F., Castro, Mayra T. M., Correa, Bruna R., Krepischi, Ana C. V., Olivieri, Eloisa H. R., Cunha, Isabela W., Tabori, Uri, Grundy, Paul E., Costa, Cecilia M. L., de Camargo, Beatriz, Galante, Pedro A. F., Carraro, Dirce M.

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Whole‐exome sequencing of non‐BRCA1/BRCA2 mutation carrier cases at high‐risk for hereditary breast/ovarian cancer von Felicio, Paula S., Grasel, Rebeca S., Campacci, Natalia, Paula, Andre E., Galvão, Henrique C. R., Torrezan, Giovana T., Sabato, Cristina S., Fernandes, Gabriela C., Souza, Cristiano P., Michelli, Rodrigo D., Andrade, Carlos E., Barros, Bruna Durães De Figueiredo, Matsushita, Marcus M., Revil, Timothée, Ragoussis, Jiannis, Couch, Fergus J., Hart, Steven N., Reis, Rui M., Melendez, Matias E., Tonin, Patricia N., Carraro, Dirce M., Palmero, Edenir I.

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Li-Fraumeni-associated pancreatic neuroendocrine tumour and XAF1 p.Glu134Ter risk modifier variant von Riechelmann, Rachel P, Soares, Diogo C, Dias, Carla, Carraro, Dirce M, Torrezan, Giovana T

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Does the Addition of Mutations of CTNNB1 S45F to Clinical Factors Allow Prediction of Local Recurrence in Patients With a Desmoid Tumor? A Local Recurrence Risk Model von Pinto, Fabio F. E., Mello, Celso A. L., Nakagawa, Suely A., Chung, Wu Tu, Torrezan, Giovana T., Barros, Bruna D. F., Cunha, Isabela W., Calsavara, Vinícius F., Carraro, Dirce M., Lopes, Ademar

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Hereditary breast and ovarian cancer: assessment of point mutations and copy number variations in Brazilian patients von Silva, Felipe C, Lisboa, Bianca Cg, Figueiredo, Marcia Cp, Torrezan, Giovana T, Santos, Erika Mm, Krepischi, Ana C, Rossi, Benedito M, Achatz, Maria I, Carraro, Dirce M

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Untangling the mechanisms of cancer predisposition von Torrezan, Giovana Tardin

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Clinical and Molecular Characterization of Brazilian Patients Suspected to Have Lynch Syndrome von Carneiro da Silva, Felipe, Ferreira, José Roberto de Oliveira, Torrezan, Giovana Tardin, Figueiredo, Márcia Cristina Pena, Santos, Érika Maria Monteiro, Nakagawa, Wilson Toshihiko, Brianese, Rafael Canfield, Petrolini de Oliveira, Ligia, Begnani, Maria Dirlei, Aguiar-Junior, Samuel, Rossi, Benedito Mauro, Ferreira, Fábio de Oliveira, Carraro, Dirce Maria

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High Prevalence of EGFR Mutations in Lung Adenocarcinomas From Brazilian Patients Harboring the TP53 p.R337H Variant von Barbosa, Malu Viter R., Cordeiro de Lima, Vladmir C., Formiga, Maria Nirvana, Andrade de Paula, Cláudia A., Torrezan, Giovana T., Carraro, Dirce M.

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

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Mutation Detection in Tumor-Derived Cell Free DNA Anticipates Progression in a Patient With Metastatic Colorectal Cancer von de Figueiredo Barros, Bruna D, Kupper, Bruna E C, Aguiar Junior, Samuel, de Mello, Celso A L, Begnami, Maria D, Chojniak, Rubens, de Souza, Sandro J, Torrezan, Giovana T, Carraro, Dirce M

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Characterization of Potential Melanoma Predisposition Genes in High-Risk Brazilian Patients von Soares de Sá, Bianca Costa, Moredo, Luciana Facure, Torrezan, Giovana Tardin, Fidalgo, Felipe, de Araújo, Érica Sara Souza, Formiga, Maria Nirvana, Duprat, João Pereira, Carraro, Dirce Maria

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Characterization of genetic predisposition to molecular subtypes of breast cancer in Brazilian patients von Paixão, Daniele, Torrezan, Giovana Tardin, Santiago, Karina Miranda, Formiga, Maria Nirvana, Ahuno, Samuel Terkper, Dias-Neto, Emmanuel, Tojal da Silva, Israel, Foulkes, William D, Polak, Paz, Carraro, Dirce Maria

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A novel SYBR-based duplex qPCR for the detection of gene dosage: detection of an APC large deletion in a familial adenomatous polyposis patient with an unusual phenotype von Torrezan, Giovana Tardin, da Silva, Felipe Cavalcanti Carneiro, Krepischi, Ana Cristina Victorino, dos Santos, Erika Maria Monteiro, Rossi, Benedito Mauro, Carraro, Dirce Maria

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BAP1 tumor predisposition syndrome case report: pathological and clinical aspects of BAP1-inactivated melanocytic tumors (BIMTs), including dermoscopy and confocal microscopy von Soares de Sá, Bianca Costa, de Macedo, Mariana Petaccia, Torrezan, Giovana Tardin, Braga, Juliana Casagrande Tavoloni, Fidalgo, Felipe, Moredo, Luciana Facure, Lellis, Rute, Duprat, João Pereira, Carraro, Dirce Maria

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Case Report of Small Cell Carcinoma of the Ovary, Hypercalcemic Type (Ovarian Rhabdoid Tumor) with SMARCB1 Mutation: A Literature Review of a Rare and Aggressive Condition von Simões, Maria Fernanda Evangelista, da Costa, Alexandre André Balieiro Anastácio, Silva, Tullio Novaes, Fernandes, Lizieux, Bovolim, Graziele, Torrezan, Giovana Tardin, Carraro, Dirce Maria, Baiocchi, Glauco, Menezes, Ademir Narcizo Oliveira, Santana Dos Santos, Elizabeth, De Brot, Louise

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Prevalence of BRCA1 and BRCA2 pathogenic and likely pathogenic variants in non-selected ovarian carcinoma patients in Brazil von Cotrim, Deborah Porto, Ribeiro, Adriana Regina Gonçalves, Paixão, Daniele, de Queiroz Soares, Diogo Cordeiro, Jbili, Rima, Pandolfi, Natasha Carvalho, Cezana, Camila, de Cássia Mauro, Carine, Mantoan, Henrique, Bovolim, Graziele, de Brot, Louise, Torrezan, Giovana Tardin, Carraro, Dirce Maria, Baiocchi, Glauco, da Cruz Formiga, Maria Nirvana, da Costa, Alexandre A B A

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Breakpoint characterization of a novel large intragenic deletion of MUTYH detected in a MAP patient: case report von Torrezan, Giovana T, da Silva, Felipe C C, Krepischi, Ana C V, Santos, Érika M M, Ferreira, Fábio de O, Rossi, Benedito M, Carraro, Dirce M

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