publicações selecionadas
- Untangling the mechanisms of cancer predisposition
- 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
- Using Co-segregation and Loss of Heterozygosity Analysis to Define the Pathogenicity of Unclassified Variants in Hereditary Breast Cancer Patients
- Mutational portrait of lung adenocarcinoma in Brazilian patients: past, present, and future of molecular profiling in the clinic
- Tight junction gene expression in salivary gland tumors
- Amplicon-based NGS test for assessing MLH1 promoter methylation and its correlation with BRAF mutation in colorectal cancer patients
- NTRK -rearranged mesenchymal tumour with epithelioid features: expanding the morphological spectrum of NTRK -fused neoplasms
- MLH1 intronic variants mapping to¿+¿5 position of splice donor sites lead to deleterious effects on RNA splicing
- Rhabdomyosarcomatous Transformation as a Mechanism of Resistance to Osimertinib and Savolitinib in EGFR-Mutant Lung Adenocarcinoma With METamp After Osimertinib First-Line Treatment
- A cross-sectional study of clinical, dermoscopic, histopathological, and molecular patterns of scalp melanoma in patients with or without androgenetic alopecia
- Beyond Midline: Diffuse Hemispheric Glioma, H3 K27M-Mutant with Aggressive Behavior'
- Colorectal cancer incidences in Lynch syndrome: a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortium
-
Risk of metastasis in
BRCA2 carriers diagnosed with triple-negative breast cancer - Fibroademoas mamários humanos: epidemiologia e análise da perda de heterozigose na região 3p.
- High Prevalence of EGFR Mutations in Lung Adenocarcinomas From Brazilian Patients Harboring the TP53 p.R337H Variant
- Family-based whole-exome sequencing identifies rare variants potentially related to cutaneous melanoma predisposition in Brazilian melanoma-prone families
- Patient-Derived Renal Cell Carcinoma Xenografts Capture Tumor Genetic Profiles and Aggressive Behaviors
- The mutational repertoire of uterine sarcomas and carcinosarcomas in a Brazilian cohort: A preliminary study
- 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
- Mortality by age, gene and gender in carriers of pathogenic mismatch repair gene variants receiving surveillance for early cancer diagnosis and treatment: a report from the prospective Lynch syndrome database
- Dihydropyrimidine dehydrogenase (DPD) polymorphisms knocking on the door
- Genetic Landscape of Male Breast Cancer
- DNA Mismatch Repair-Deficient Colorectal Carcinoma: Referral Rate for Genetic Cancer Risk Assessment in a Brazilian Cancer Center
- Characterization of genetic predisposition to molecular subtypes of breast cancer in Brazilian patients
- Identificação de mutações nos genes APC e MUTYH em famílias com polipose adenomatosa intestinal.
- Whole¿exome sequencing of non¿ BRCA1/BRCA2 mutation carrier cases at high¿risk for hereditary breast/ovarian cancer
- FIBROADENOMAS MAMÁRIOS HUMANOS: EPIDEMIOLOGIA E ANÁLISE DA PERDA DE HETEROZIGOSE NA REGIÃO 3p
- Desmoplastic Small Round Cell Tumor: A Review of Main Molecular Abnormalities and Emerging Therapy
- Li-Fraumeni-associated pancreatic neuroendocrine tumour and XAF1 p.Glu134Ter risk modifier variant
- Value of the loss of heterozygosity to BRCA1 variant classification
- Impact of BRCA1/2 Mutations on the Efficacy of Secondary Cytoreductive Surgery
- Clinical and Molecular Assessment of Patients with Lynch Syndrome and Sarcomas Underpinning the Association with MSH2 Germline Pathogenic Variants
- Prevalence and clinical implications of germline pathogenic variants in cancer predisposing genes in young patients across sarcoma subtypes
- Germline pathogenic variants in patients with early onset neuroendocrine neoplasms
