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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: barros bdf. 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.
BRCA1 deficiency is a recurrent event in early-onset triple-negative breast cancer: a comprehensive analysis of germline mutations and somatic promoter methylation.
Brianese RC, Nakamura KDM, Almeida FGDSR, Ramalho RF, Barros BDF, Ferreira ENE, Formiga MNDC, de Andrade VP, de Lima VCC, Carraro DM. Brianese RC, et al. Among authors: barros bdf. Breast Cancer Res Treat. 2018 Feb;167(3):803-814. doi: 10.1007/s10549-017-4552-6. Epub 2017 Nov 7. Breast Cancer Res Treat. 2018. PMID: 29116469
Family-based whole-exome sequencing identifies rare variants potentially related to cutaneous melanoma predisposition in Brazilian melanoma-prone families.
Fidalgo F, Torrezan GT, Sá BCS, Barros BDF, Moredo LF, Valieris R, de Souza SJ, Duprat JP, Krepischi ACV, Carraro DM. Fidalgo F, et al. Among authors: barros bdf. PLoS One. 2022 Jan 27;17(1):e0262419. doi: 10.1371/journal.pone.0262419. eCollection 2022. PLoS One. 2022. PMID: 35085295 Free PMC article.
First Transcriptome Analysis of Hepatoblastoma in Brazil: Unraveling the Pivotal Role of Noncoding RNAs and Metabolic Pathways.
Aguiar TFM, Rivas MP, de Andrade Silva EM, Pires SF, Dangoni GD, Macedo TC, Defelicibus A, Barros BDF, Novak E, Cristofani LM, Odone V, Cypriano M, de Toledo SRC, da Cunha IW, da Costa CML, Carraro DM, Tojal I, de Oliveira Mendes TA, Krepischi ACV. Aguiar TFM, et al. Among authors: barros bdf. Biochem Genet. 2024 Apr 22. doi: 10.1007/s10528-024-10764-y. Online ahead of print. Biochem Genet. 2024. PMID: 38649558
Viral metagenomics in blood donors with post-donation diseases and negative tests for dengue and Zika viruses RNA detection during a major outbreak of arboviruses in Sao Paulo State in 2016.
Bezerra RDS, Peronni KC, Barros BDF, Oliveira LS, Rodrigues ES, Azevedo R, Ubiali EMA, Covas DT, Kashima S, Slavov SN. Bezerra RDS, et al. Among authors: barros bdf. Rev Inst Med Trop Sao Paulo. 2020 Sep 30;62:e70. doi: 10.1590/S1678-9946202062070. eCollection 2020. Rev Inst Med Trop Sao Paulo. 2020. PMID: 33027394 Free PMC article. No abstract available.
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.
Pinto FFE, Mello CAL, Nakagawa SA, Chung WT, Torrezan GT, Barros BDF, Cunha IW, Calsavara VF, Carraro DM, Lopes A. Pinto FFE, et al. Among authors: barros bdf. Clin Orthop Relat Res. 2023 Oct 1;481(10):1978-1989. doi: 10.1097/CORR.0000000000002627. Epub 2023 Apr 27. Clin Orthop Relat Res. 2023. PMID: 37104792
Assessment of somatic mutations in urine and plasma of Wilms tumor patients.
Miguez ACK, Barros BDF, de Souza JES, da Costa CML, Cunha IW, Barbosa PNVP, Apezzato MLP, de Souza SJ, Carraro DM. Miguez ACK, et al. Among authors: barros bdf. Cancer Med. 2020 Aug;9(16):5948-5959. doi: 10.1002/cam4.3236. Epub 2020 Jun 26. Cancer Med. 2020. PMID: 32592321 Free PMC article.
Complex Landscape of Germline Variants in Brazilian Patients With Hereditary and Early Onset Breast Cancer.
Torrezan GT, de Almeida FGDSR, Figueiredo MCP, Barros BDF, de Paula CAA, Valieris R, de Souza JES, Ramalho RF, da Silva FCC, Ferreira EN, de Nóbrega AF, Felicio PS, Achatz MI, de Souza SJ, Palmero EI, Carraro DM. Torrezan GT, et al. Among authors: barros bdf. Front Genet. 2018 May 7;9:161. doi: 10.3389/fgene.2018.00161. eCollection 2018. Front Genet. 2018. PMID: 29868112 Free PMC article.
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 a rare and aggressive disease.
Ferreira EN, Barros BD, de Souza JE, Almeida RV, Torrezan GT, Garcia S, Krepischi AC, Mello CA, Cunha IW, Pinto CA, Soares FA, Dias-Neto E, Lopes A, de Souza SJ, Carraro DM. Ferreira EN, et al. Hum Genomics. 2016 Nov 18;10(1):36. doi: 10.1186/s40246-016-0092-0. Hum Genomics. 2016. PMID: 27863505 Free PMC article.
Genomic imbalances pinpoint potential oncogenes and tumor suppressors in Wilms tumors.
Krepischi ACV, Maschietto M, Ferreira EN, Silva AG, Costa SS, da Cunha IW, Barros BDF, Grundy PE, Rosenberg C, Carraro DM. Krepischi ACV, et al. Among authors: barros bdf. Mol Cytogenet. 2016 Feb 24;9:20. doi: 10.1186/s13039-016-0227-y. eCollection 2016. Mol Cytogenet. 2016. PMID: 26913079 Free PMC article.
11 results