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Novel mutations in the bone morphogenetic protein 6 gene in patients with iron overload and non-homozygous genotype for the HFE p.Cys282Tyr mutation.
Alvarenga AM, da Silva NK, Fonseca PFS, Oliveira TGM, da Silva Monteiro JB, Cançado RD, Naoum FA, Dinardo CL, Brissot P, Santos PCJL. Alvarenga AM, et al. Among authors: dinardo cl. Blood Cells Mol Dis. 2020 Sep;84:102444. doi: 10.1016/j.bcmd.2020.102444. Epub 2020 May 18. Blood Cells Mol Dis. 2020. PMID: 32464486 Free article.
Non-HFE hemochromatosis.
Santos PC, Dinardo CL, Cançado RD, Schettert IT, Krieger JE, Pereira AC. Santos PC, et al. Among authors: dinardo cl. Rev Bras Hematol Hemoter. 2012;34(4):311-6. doi: 10.5581/1516-8484.20120079. Rev Bras Hematol Hemoter. 2012. PMID: 23049448 Free PMC article.
RHD and RHCE genotyping by next-generation sequencing is an effective strategy to identify molecular variants within sickle cell disease patients.
Dezan MR, Ribeiro IH, Oliveira VB, Vieira JB, Gomes FC, Franco LAM, Varuzza L, Ribeiro R, Chinoca KZ, Levi JE, Krieger JE, Pereira AC, Gualandro SFM, Rocha VG, Mendrone-Junior A, Sabino EC, Dinardo CL. Dezan MR, et al. Among authors: dinardo cl. Blood Cells Mol Dis. 2017 Jun;65:8-15. doi: 10.1016/j.bcmd.2017.03.014. Epub 2017 Mar 31. Blood Cells Mol Dis. 2017. PMID: 28388467
SMIM1 intron 2 gene variations leading to variability in Vel antigen expression among Brazilian blood donors.
Dezan MR, Costa-Neto A, Gomes CN, Ribeiro IH, Oliveira VB, Conrado MCAV, Oliveira TGM, Carvalho MLP, Aranha AF, Bosi SRA, Salles NA, Krieger JE, Pereira AC, Sabino EC, Rocha V, Mendrone-Junior A, Dinardo CL, Levi JE. Dezan MR, et al. Among authors: dinardo cl. Blood Cells Mol Dis. 2019 Jul;77:23-28. doi: 10.1016/j.bcmd.2019.03.006. Epub 2019 Mar 25. Blood Cells Mol Dis. 2019. PMID: 30939337
Diversity of variant alleles encoding Kidd, Duffy, and Kell antigens in individuals with sickle cell disease using whole genome sequencing data from the NHLBI TOPMed Program.
Dinardo CL, Oliveira TGM, Kelly S, Ashley-Koch A, Telen M, Schmidt LC, Castilho S, Melo K, Dezan MR, Wheeler MM, Johnsen JM, Nickerson DA, Jain D, Custer B, Pereira AC, Sabino EC; NHLBI Recipient Epidemiology Donor Evaluation Study (REDS-III) International Component-Brazil, the Outcome Modifying Genes in SCD (OMG) study and the NHLBI Trans-Omics for Precision Medicine (TOPMed) Program Sickle Cell Disease Working Group. Dinardo CL, et al. Transfusion. 2021 Feb;61(2):603-616. doi: 10.1111/trf.16204. Epub 2020 Nov 24. Transfusion. 2021. PMID: 33231305
74 results