| Recurrent somatic mutation in DROSHA induces microRNA profile changes in Wilms tumour GT Torrezan, EN Ferreira, AM Nakahata, BDF Barros, MTM Castro, ... Nature communications 5 (1), 1-10, 2014 | 186 | 2014 |
| Hereditary breast and ovarian cancer: assessment of point mutations and copy number variations in Brazilian patients FC Silva, BCG Lisboa, MCP Figueiredo, GT Torrezan, ÉMM Santos, ... BMC Medical Genetics 15 (1), 55, 2014 | 100 | 2014 |
| Mutational spectrum of the APC and MUTYH genes and genotype–phenotype correlations in Brazilian FAP, AFAP, and MAP patients GT Torrezan, FCC da Silva, ÉÉMM Santos, ACV Krepischi, MIW Achatz, ... Orphanet journal of rare diseases 8 (1), 1-12, 2013 | 58 | 2013 |
| Genetic polymorphisms in oestrogen metabolic pathway and breast cancer: a positive association with combined CYP/GST genotypes C Torresan, MMC Oliveira, GT Torrezan, SFV De Oliveira, CS Abuázar, ... Clinical and experimental medicine 8 (2), 65-71, 2008 | 44 | 2008 |
| Whole‐exome sequencing of non‐BRCA1/BRCA2 mutation carrier cases at high‐risk for hereditary breast/ovarian cancer PS Felicio, RS Grasel, N Campacci, AE de Paula, HCR Galvão, ... Human Mutation, 2020 | 43 | 2020 |
| Enhanced type I interferon gene signature in primary antiphospholipid syndrome: Association with earlier disease onset and preeclampsia MR Ugolini-Lopes, GT Torrezan, APR Gândara, EHR Olivieri, ... Autoimmunity reviews 18 (4), 393-398, 2019 | 41 | 2019 |
| Desmoplastic small round cell tumor: a review of main molecular abnormalities and emerging therapy CA Mello, FAB Campos, TG Santos, MLG Silva, GT Torrezan, FDA Costa, ... Cancers 13 (3), 498, 2021 | 37 | 2021 |
| A genomic case study of desmoplastic small round cell tumor: comprehensive analysis reveals insights into potential therapeutic targets and development of a monitoring tool for … EN Ferreira, BDF Barros, JE de Souza, RV Almeida, GT Torrezan, ... Human Genomics 10 (1), 36, 2016 | 32 | 2016 |
| Genetic Landscape of Male Breast Cancer FAB Campos, E Rouleau, GT Torrezan, DM Carraro, JC Casali da Rocha, ... Cancers 13 (14), 3535, 2021 | 27 | 2021 |
| Clinical and molecular characterization of Brazilian patients suspected to have Lynch syndrome FC da Silva, JR de Oliveira Ferreira, GT Torrezan, MCP Figueiredo, ... PloS one 10 (10), e0139753, 2015 | 26 | 2015 |
| From colorectal cancer pattern to the characterization of individuals at risk: Picture for genetic research in Latin America CA Vaccaro, F López‐Kostner, DV Adriana, EI Palmero, BM Rossi, ... International journal of cancer 145 (2), 318-326, 2019 | 25 | 2019 |
| Breakpoint characterization of a novel large intragenic deletion of MUTYH detected in a MAP patient: Case report G Torrezan, F da Silva, A Krepischi, É Santos, F de O Ferreira, B Rossi, ... BMC medical genetics 12 (1), 128, 2011 | 24 | 2011 |
| Colorectal cancer incidences in Lynch syndrome: a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortium P Møller, T Seppälä, JG Dowty, S Haupt, M Dominguez-Valentin, L Sunde, ... Hereditary cancer in clinical practice 20 (1), 1-11, 2022 | 23 | 2022 |
| Prevalence of BRCA1 and BRCA2 pathogenic and likely pathogenic variants in non-selected ovarian carcinoma patients in Brazil DP Cotrim, ARG Ribeiro, D Paixão, DC de Queiroz Soares, R Jbili, ... BMC cancer 19 (1), 4, 2019 | 23 | 2019 |
| Association of Folate and Vitamins Involved in the 1-Carbon Cycle with Polymorphisms in the Methylenetetrahydrofolate Reductase Gene (MTHFR) and Global DNA Methylation in … A Ferrari, GT Torrezan, DM Carraro, S Aguiar Junior Nutrients 11 (6), 1368, 2019 | 23 | 2019 |
| Complex landscape of germline variants in Brazilian patients with hereditary and early onset breast cancer GT Torrezan, FG de Almeida, MCP Figueiredo, BD Barros, CAA de Paula, ... Frontiers in genetics 9, 161, 2018 | 23 | 2018 |
| 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 GT Torrezan, FCC da Silva, ACV Krepischi, ÉMM dos Santos, BM Rossi, ... BMC medical genetics 13 (1), 1-7, 2012 | 21 | 2012 |
| Use of uracil-DNA glycosylase enzyme to reduce DNA-related artifacts from formalin-fixed and paraffin-embedded tissues in diagnostic routine CM Berra, GT Torrezan, CA de Paula, R Hsieh, SV Lourenço, DM Carraro Applied Cancer Research 39 (1), 7, 2019 | 19 | 2019 |
| Oral and maxillofacial considerations in Gardner's syndrome: a report of two cases. DL Pereira, PA Carvalho, MI Achatz, A Rocha, GT Torrezan, FA Alves Ecancermedicalscience, 2016 | 19 | 2016 |
| High prevalence of EGFR mutations in lung adenocarcinomas from Brazilian patients harboring the TP53 p. R337H variant MVR Barbosa, VCC de Lima, MN Formiga, CAA de Paula, GT Torrezan, ... Clinical Lung Cancer 21 (2), e37-e44, 2020 | 17 | 2020 |
Dirce Maria CarraroHead, Genomics and Molecular Biology Laboratory, AC Camargo Hospitalبريد إلكتروني تم التحقق منه على cipe.accamargo.org.br
