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2021 1
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Page 1
Real-world genomic profiling of acute myeloid leukemia and the impact of European LeukemiaNet risk stratification 2022 update.
da Rosa SEA, de Lima LB, Silveira CN, Cortes LGF, de Oliveira Filho JB, de Souza Reis R, Cervato MC, Rodrigues PHS, de Oliveira Pelegrino K, Petroni RC, da Silva Araujo E, Campregher PV. da Rosa SEA, et al. Among authors: de souza reis r. Clin Transl Oncol. 2023 Dec;25(12):3431-3436. doi: 10.1007/s12094-023-03195-5. Epub 2023 May 11. Clin Transl Oncol. 2023. PMID: 37165281
The Brazilian Rare Genomes Project: Validation of Whole Genome Sequencing for Rare Diseases Diagnosis.
Coelho AVC, Mascaro-Cordeiro B, Lucon DR, Nóbrega MS, Reis RS, de Alexandre RB, Moura LMS, de Oliveira GS, Guedes RLM, Caraciolo MP, Zurro NB, Cervato MC, Oliveira JB. Coelho AVC, et al. Among authors: reis rs. Front Mol Biosci. 2022 May 2;9:821582. doi: 10.3389/fmolb.2022.821582. eCollection 2022. Front Mol Biosci. 2022. PMID: 35586190 Free PMC article.
Mass molecular testing for COVID19 using NGS-based technology and a highly scalable workflow.
de Mello Malta F, Amgarten D, Val FC, Cervato MC, de Azevedo BMC, de Souza Basqueira M, Dos Santos Alves CO, Nobrega MS, de Souza Reis R, Sebe P, Gretschischkin MC, de Oliveira DDC, Nakamura CNI, Chazanas PLN, Pinho JRR. de Mello Malta F, et al. Among authors: de souza reis r. Sci Rep. 2021 Mar 29;11(1):7122. doi: 10.1038/s41598-021-86498-3. Sci Rep. 2021. PMID: 33782491 Free PMC article.
Genomic study of nonsyndromic hearing loss in unaffected individuals: Frequency of pathogenic and likely pathogenic variants in a Brazilian cohort of 2,097 genomes.
Quaio CRAC, Coelho AVC, Moura LMS, Guedes RLM, Chen K, Ceroni JRM, Minillo RM, Caraciolo MP, Reis RS, de Azevedo BMC, Nobrega MS, Teixeira ACB, Martinelli Lima M, da Mota TR, da Matta MC, Colichio GBC, Roncalho AL, Ferreira AFM, Campilongo GP, Perrone E, Virmond LDA, Moreno CA, Prota JRM, de França M, Cervato MC, de Almeida TF, de Oliveira Filho JB. Quaio CRAC, et al. Among authors: reis rs. Front Genet. 2022 Aug 30;13:921324. doi: 10.3389/fgene.2022.921324. eCollection 2022. Front Genet. 2022. PMID: 36147510 Free PMC article.
The hospital Israelita Albert Einstein standards for constitutional sequence variants classification: version 2023.
Quaio CRDC, Ceroni JRM, Pereira MA, Teixeira ACB, Yamada RY, Cintra VP, Perrone E, De França M, Chen K, Minillo RM, Biondo CA, de Mello MRB, Moura LR, do Nascimento ATB, de Oliveira Pelegrino K, de Lima LB, do Amaral Virmond L, Moreno CA, Prota JRM, de Araujo Espolaor JG, Silva TYT, Moraes GHI, de Oliveira GS, Moura LMS, Caraciolo MP, Guedes RLM, Gretschischkin MC, Chazanas PLN, Nakamura CNI, de Souza Reis R, Toledo CM, Lage FSD, de Almeida GB, do Nascimento Júnior JB, Cardoso MA, de Paula Azevedo V, de Almeida TF, Cervato MC, de Oliveira Filho JB. Quaio CRDC, et al. Among authors: de souza reis r. Hum Genomics. 2023 Nov 16;17(1):102. doi: 10.1186/s40246-023-00549-6. Hum Genomics. 2023. PMID: 37968704 Free PMC article.