Insights on variant analysis in silico tools for pathogenicity prediction FAO Garcia, ES Andrade, EI Palmero Frontiers in genetics 13, 1010327, 2022 | 43 | 2022 |
New insights on familial colorectal cancer type X syndrome FAO Garcia, ES de Andrade, H de Campos Reis Galvão, ... Scientific Reports 12 (1), 2846, 2022 | 21 | 2022 |
Using co-segregation and loss of heterozygosity analysis to define the pathogenicity of unclassified variants in hereditary breast cancer patients RS Grasel, PS Felicio, AE De Paula, N Campacci, FANDO Garcia, ... Frontiers in Oncology 10, 571330, 2020 | 11 | 2020 |
Whole-exome sequencing identifies pathogenic germline variants in patients with Lynch-Like Syndrome W Dos Santos, ES de Andrade, FAO Garcia, N Campacci, CS Sábato, ... Cancers 14 (17), 4233, 2022 | 9 | 2022 |
High frequency of WNT-activated medulloblastomas with CTNNB1 wild type suggests a higher proportion of hereditary cases in a Latin-Iberian population DA Moreno, M Bonatelli, AP Antoniazzi, FE de Paula, LF Leal, FAO Garcia, ... Frontiers in Oncology 13, 1237170, 2023 | 2 | 2023 |
Functional pri-miR-34b/c rs4938723 and KRAS 3’UTR rs61764370 SNPs: novel phenotype modifiers in Li-Fraumeni syndrome? Gene, 148069, 2023 | 1* | 2023 |
Genomic profile of two Brazilian choroid plexus tumors by whole-exome sequencing FA de Oliveira Garcia, AF Evangelista, BM Mançano, DA Moreno, ... Molecular Case Studies 9 (1), a006245, 2023 | 1 | 2023 |
TMOD-10. ESTABLISHMENT OF ADULT AND PEDIATRIC BRAZILIAN PRE-CLINICAL MODELS FOR HIGH-GRADE GLIOMAS M Baroni, R Megid, L Tshikawa, AC Martin, T Duarte, F Escremim, ... Neuro-Oncology 26 (Supplement_8), viii321-viii321, 2024 | | 2024 |
Anais do VII Curso de Inverno em Oncologia Molecular do Hospital de Câncer de Barretos R de Oliveira Cavagna, FA de Oliveira Garcia, S Calfa, CR Nunes, ... Brazilian Journal of Case Reports 2 (Suppl. 1), 1-13, 2022 | | 2022 |