Neoadjuvant Chemotherapy Followed by Interval Debulking Surgery and the Risk of Platinum Resistance in Epithelial Ovarian Cancer von da Costa, Alexandre A. B. A., Valadares, Camila V., Baiocchi, Glauco, Mantoan, Henrique, Saito, Augusto, Sanches, Solange, Guimarães, Andréia P., Achatz, Maria Isabel W.

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Prevalence of the TP53 p.R337H mutation in breast cancer patients in Brazil von Giacomazzi, Juliana, Graudenz, Marcia S, Osorio, Cynthia A B T, Koehler-Santos, Patricia, Palmero, Edenir I, Zagonel-Oliveira, Marcelo, Michelli, Rodrigo A D, Scapulatempo Neto, Cristovam, Fernandes, Gabriela C, Achatz, Maria Isabel W S, Martel-Planche, Ghyslaine, Soares, Fernando A, Caleffi, Maira, Goldim, José Roberto, Hainaut, Pierre, Camey, Suzi A, Ashton-Prolla, Patricia

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Highly prevalent TP53 mutation predisposing to many cancers in the Brazilian population: a case for newborn screening? von Achatz, Maria Isabel Waddington, MD, Hainaut, Pierre, PhD, Ashton-Prolla, Patricia, Dr

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Germline DNA copy number variation in familial and early-onset breast cancer von Krepischi, Ana Cv, Achatz, Maria Isabel W, Santos, Erika Mm, Costa, Silvia S, Lisboa, Bianca Cg, Brentani, Helena, Santos, Tiago M, Gonçalves, Amanda, Nóbrega, Amanda F, Pearson, Peter L, Vianna-Morgante, Angela M, Carraro, Dirce M, Brentani, Ricardo R, Rosenberg, Carla

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Pheochromocytoma and paraganglioma: implications of germline mutation investigation for treatment, screening, and surveillance von Gómez, Ana Milena, Soares, Diogo Cordeiro, Costa, Alexandre André Balieiro, Pereira, Daniele Paixão, Achatz, Maria Isabel, Formiga, Maria Nirvana

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Number of rare germline CNVs and TP53 mutation types von Silva, Amanda G, Achatz, Isabel Maria W, Krepischi, Ana Cv, Pearson, Peter L, Rosenberg, Carla

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Clinical Management and Tumor Surveillance Recommendations of Inherited Mismatch Repair Deficiency in Childhood von Tabori, Uri, Hansford, Jordan R, Achatz, Maria Isabel, Kratz, Christian P, Plon, Sharon E, Frebourg, Thierry, Brugières, Laurence

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Oral and maxillofacial considerations in Gardner's syndrome: a report of two cases von Pereira, Debora Lima, Carvalho, Paulo Andre, Achatz, Maria Isabel Waddington, Rocha, AndreCaroli, TardinTorrezan, Giovana, Alves, Fabio Abreu

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Monoallelic deleterious MUTYH germline variants as a driver for tumorigenesis von Barreiro, Rodrigo Araujo Sequeira, Sabbaga, Jorge, Rossi, Benedito M, Achatz, Maria Isabel W, Bettoni, Fabiana, Camargo, Anamaria A, Asprino, Paula F, Galante, Pedro

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Cancer Screening Recommendations and Clinical Management of Inherited Gastrointestinal Cancer Syndromes in Childhood von Achatz, Maria Isabel, Porter, Christopher C, Brugières, Laurence, Druker, Harriet, Frebourg, Thierry, Foulkes, William D, Kratz, Christian P, Kuiper, Roland P, Hansford, Jordan R, Hernandez, Hector Salvador, Nathanson, Katherine L, Kohlmann, Wendy K, Doros, Leslie, Onel, Kenan, Schneider, Kami Wolfe, Scollon, Sarah R, Tabori, Uri, Tomlinson, Gail E, Evans, D Gareth R, Plon, Sharon E

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Li-Fraumeni-like syndrome associated with a large BRCA1 intragenic deletion von Silva, Amanda Gonçalves, Ewald, Ingrid Petroni, Sapienza, Marina, Pinheiro, Manuela, Peixoto, Ana, de Nóbrega, Amanda França, Carraro, Dirce M, Teixeira, Manuel R, Ashton-Prolla, Patricia, Achatz, Maria Isabel W, Rosenberg, Carla, Krepischi, Ana C V

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Germline CDKN2A mutations in Brazilian patients of hereditary cutaneous melanoma von de Ávila, Alexandre Leon Ribeiro, Krepischi, Ana Cristina Victorino, Moredo, Luciana Facure, Aguiar, Talita Ferreira Marques, da Silva, Felipe Carneiro, de Sá, Bianca Costa Soares, de Nóbrega, Amanda França, Achatz, Maria Isabel Waddington, Duprat, João Pedreira, Landman, Gilles, Carraro, Dirce Maria

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Germline molecular data in hereditary breast cancer in Brazil: Lessons from a large single-center analysis von Sandoval, Renata Lazari, Leite, Ana Carolina Rathsam, Barbalho, Daniel Meirelles, Assad, Daniele Xavier, Barroso, Romualdo, Polidorio, Natalia, Dos Anjos, Carlos Henrique, de Miranda, Andréa Discaciati, Ferreira, Ana Carolina Salles de Mendonça, Fernandes, Gustavo Dos Santos, Achatz, Maria Isabel

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Testing Positive on a Multigene Panel Does Not Suffice to Determine Disease Risks von Katki, Hormuzd A, Greene, Mark H, Achatz, Maria Isabel

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Germline DNA Damage Repair Gene Alterations in Patients with Metachronous Breast and Colorectal Cancer von Villacis, Rolando André Rios, Côrtes, Luiza, Basso, Tatiane Ramos, do Canto, Luisa Matos, Souza, Jeferson Santos, Aagaard, Mads Malik, da Cruz Formiga, Maria Nirvana, Aguiar, Jr, Samuel, Achatz, Maria Isabel, Rogatto, Silvia Regina

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Double heterozygous pathogenic variants prevalence in a cohort of patients with hereditary breast cancer von Megid, Thais Baccili Cury, Barros-Filho, Mateus C., Pisani, Janina Pontes, Achatz, Maria Isabel

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TP53 mutation p.R337H in gastric cancer tissues of a 12-year-old male child: evidence for chimerism involving a common mutant founder haplotype: case report von da Silva, Edaise M, Achatz, Maria Isabel W, Martel-Planche, Ghyslaine, Montagnini, André L, Olivier, Magali, Prolla, Patricia A, Hainaut, Pierre, Soares, Fernando A

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Early-Onset Colorectal Cancer in Patients with Li Fraumeni Syndrome: Is It Really Enough to Justify Early Colon Cancer Screening? von Nirvana da Cruz Formiga, Maria, Ashton-Prolla, Patrícia, Alves de Souza Waddington Achatz, Maria Isabel

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Molecular analysis of TSC1 and TSC2 genes and phenotypic correlations in Brazilian families with tuberous sclerosis von Rosset, Clévia, Vairo, Filippo, Bandeira, Isabel Cristina, Correia, Rudinei Luis, de Goes, Fernanda Veiga, da Silva, Raquel Tavares Boy, Bueno, Larissa Souza Mario, de Miranda Gomes, Mireille Caroline Silva, Galvão, Henrique de Campos Reis, Neri, João I C F, Achatz, Maria Isabel, Netto, Cristina Brinckmann Oliveira, Ashton-Prolla, Patricia

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The Value of Secondary Cytoreductive Surgery in Recurrent Ovarian Cancer and Application of a Prognostic Score von da Costa, Alexandre Andre Balieiro Anastacio, Valadares, Camila V., Mantoan, Henrique, Saito, Augusto, Salvadori, Marcella Marinelli, Guimarães, Andreia Paiva, Sanches, Solange Moraes, Achatz, Maria Isabel Alves de Souza Wadington, Baiocchi, Glauco

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