| Germline variants in DNA repair genes associated with hereditary breast and ovarian cancer syndrome: Analysis of a 21 gene panel in the Brazilian population S da Costa e Silva Carvalho, NM Cury, DB Brotto, LF De Araujo, ... BMC medical genomics 13, 1-24, 2020 | 49 | 2020 |
| Screening of the BRCA1 gene in Brazilian patients with breast and/or ovarian cancer via high-resolution melting reaction analysis ES de Oliveira, BL Soares, S Lemos, RCA Rosa, AN Rodrigues, ... Familial cancer 15, 173-181, 2016 | 17 | 2016 |
| Triagem fitoquímica dos extratos aquosos de Bauhinia candicans, Foeniculum vulgare, Mentha pulegium e Morus nigra RCA Rosa, LR Ribeiro, AMG Souza, TA Fonseca Conexão Ciência (Online) 11 (1), 44-51, 2016 | 11 | 2016 |
| Lynch syndrome identification in a Brazilian cohort of endometrial cancer screened by a universal approach RCA Rosa, JO Santis, LA Teixeira, GA Molfetta, JTT Dos Santos, ... Gynecologic Oncology 159 (1), 229-238, 2020 | 10 | 2020 |
| Overcoming resistance to αPD-1 of MMR-deficient tumors with high tumor-induced neutrophils levels by combination of αCTLA-4 and αPD-1 blockers L Nebot-Bral, A Hollebecque, AA Yurchenko, L de Forceville, M Danjou, ... Journal for Immunotherapy of Cancer 10 (7), 2022 | 6 | 2022 |
| XPC and POLH/XPV genes mutated in a genetic cluster of xeroderma pigmentosum patients in northeast Brazil LP Castro, D Batista-Vieira, TA de Souza, ARS Timoteo, JDL Coutinho, ... Frontiers in Genetics 12, 784963, 2022 | 4 | 2022 |
| First description of ultramutated endometrial cancer caused by germline loss-of-function and somatic exonuclease domain mutations in POLE gene RCA Rosa, AA Yurchenko, F Chahud, A Ribeiro-Silva, MO Brunaldi, ... Genetics and Molecular Biology 43, e20200100, 2020 | 3 | 2020 |
| The Iberian legacy into a young genetic xeroderma pigmentosum cluster in central Brazil LP Castro, M Sahbatou, FSG Kehdy, AA Farias, AA Yurchenko, ... Mutation Research/Genetic Toxicology and Environmental Mutagenesis 852, 503164, 2020 | 3 | 2020 |
| Non-syndromic intellectual disability and its pathways: A long noncoding RNA perspective II Barros, V Leão, JO Santis, RCA Rosa, DB Brotto, CB Storti, ÁDD Siena, ... Non-coding RNA 7 (1), 22, 2021 | 2 | 2021 |
| Caracterização molecular de tumores de endométrio quanto à proficiência do sistema de reparo de pareamento incorreto de DNA RCA Rosa Universidade de São Paulo, 2018 | 1 | 2018 |
| Risk for Hereditary Neoplastic Syndromes in Women with Mismatch Repair-Proficient Endometrial Cancer JTT Dos Santos, RCA Rosa, ALE Pereira, AV Assunção-Luiz, BT Bacalá, ... Genes 14 (11), 1999, 2023 | | 2023 |
| Genetic etiology of DNA-mismatch repair deficiency in cancer RCA Rosa Universidade de São Paulo, 2022 | | 2022 |
| Germline variants in DNA repair genes associated with hereditary breast and ovarian cancer syndrome: analysis of a 21 gene panel in the Brazilian population LF de Araujo, RCA Rosa, LA Texeira, JR Plaça, AA Marques, KC Peronni, ... | | 2020 |
| The loss of a long noncoding RNA can lead to delayed neural development WA Silva Junior, JM Pina Neto, GA Molfetta, SC Carvalho, MF Tellechea, ... Resumos, 2019 | | 2019 |
| Investigation of genetic causes in women with endometrial cancer proficient for the mismatch repair system JO Santis, RCA Rosa, JTT Santos, VEF Ferraz Resumos, 2019 | | 2019 |
| Diagnóstico molecular de síndrome de Lynch em casos de câncer de endométrio deficientes do sistema de reparo de pareamento incorreto de DNA RCA Rosa, F Chahud, A Ribeiro-Silva, MO Brunaldi, WA Silva Junior, ... Anais, 2019 | | 2019 |
| Screening of germline mutations in genes related to DNA repair among lynch-like patients diagnosed with endometrial cancer RCA Rosa, F Chahud, AR Silva, MO Brunaldi, WA Silva Junior, ... Resumos, 2019 | | 2019 |
| In silico characterization of POLE p. Arg446Gln in patients diagnosed with endometrial cancer deficient of the DNA mismatch repair system EJP Naves, AB Sousa, RCA Rosa, VEF Ferraz Resumos, 2019 | | 2019 |
| Analysis of potential disease-causing variants in a patient with intellectual disability via whole-exome sequencing PC Ruy, II Barros, RCA Rosa, JR Plaça, AC Corveloni, C Cardoso, ... Proceedings, 2019 | | 2019 |
| Characterization of missense mutations found on DNA repair genes in hereditary breast and ovarian cancer syndrome patients SC Carvalho, RCA Rosa, DB Brotto, TT Gomes, MA Carvalho, VEF Ferraz, ... Abstracts, 2018 | | 2018 |
Wilson Araujo Silva JrProfessor of Human Genetics, University of São PauloVerified email at usp.br
