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Page 1
Whole-exome sequencing of non-BRCA1/BRCA2 mutation carrier cases at high-risk for hereditary breast/ovarian cancer.
Felicio PS, Grasel RS, Campacci N, de Paula AE, Galvão HCR, Torrezan GT, Sabato CS, Fernandes GC, Souza CP, Michelli RD, Andrade CE, Barros BDF, Matsushita MM, Revil T, Ragoussis J, Couch FJ, Hart SN, Reis RM, Melendez ME, Tonin PN, Carraro DM, Palmero EI. Felicio PS, et al. Among authors: de paula ae. Hum Mutat. 2021 Mar;42(3):290-299. doi: 10.1002/humu.24158. Epub 2020 Dec 28. Hum Mutat. 2021. PMID: 33326660 Free PMC article.
New insights on familial colorectal cancer type X syndrome.
Garcia FAO, de Andrade ES, de Campos Reis Galvão H, da Silva Sábato C, Campacci N, de Paula AE, Evangelista AF, Santana IVV, Melendez ME, Reis RM, Palmero EI. Garcia FAO, et al. Among authors: de paula ae. Sci Rep. 2022 Feb 18;12(1):2846. doi: 10.1038/s41598-022-06782-8. Sci Rep. 2022. PMID: 35181726 Free PMC article.
Optimizing Treatment Outcomes in Crohn's Disease: A Comprehensive Systematic Review and Meta-Analysis of Regenerative Therapies with Emphasis on Platelet-Rich Plasma.
Mazzaro MC, de Paula AEC, Pascoal LB, Genaro LM, Pereira IM, Rodrigues BL, Oliveira PSP, Leal RF. Mazzaro MC, et al. Among authors: de paula aec. Pharmaceuticals (Basel). 2024 Nov 12;17(11):1519. doi: 10.3390/ph17111519. Pharmaceuticals (Basel). 2024. PMID: 39598430 Free PMC article. Review.
High frequency of WNT-activated medulloblastomas with CTNNB1 wild type suggests a higher proportion of hereditary cases in a Latin-Iberian population.
Moreno DA, Bonatelli M, Antoniazzi AP, de Paula FE, Leal LF, Garcia FAO, de Paula AE, Teixeira GR, Santana IVV, Saggioro F, Neder L, Valera ET, Scrideli CA, Stavale J, Malheiros SMF, Lima M, Hajj GNM, Garcia-Rivello H, Christiansen S, Nunes S, Gil-da-Costa MJ, Pinheiro J, Martins FD, Junior CA, Mançano BM, Reis RM. Moreno DA, et al. Among authors: de paula ae. Front Oncol. 2023 Sep 4;13:1237170. doi: 10.3389/fonc.2023.1237170. eCollection 2023. Front Oncol. 2023. PMID: 37746264 Free PMC article.
Using Co-segregation and Loss of Heterozygosity Analysis to Define the Pathogenicity of Unclassified Variants in Hereditary Breast Cancer Patients.
Grasel RS, Felicio PS, de Paula AE, Campacci N, Garcia FAO, de Andrade ES, Evangelista AF, Fernandes GC, Sabato CDS, De Marchi P, Souza CP, de Paula CAA, Torrezan GT, Galvão HCR, Carraro DM, Palmero EI. Grasel RS, et al. Among authors: de paula ae. Front Oncol. 2020 Oct 2;10:571330. doi: 10.3389/fonc.2020.571330. eCollection 2020. Front Oncol. 2020. PMID: 33134171 Free PMC article.