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| 36602125 | Genome-wide association study of early ischaemic stroke risk in Brazilian individuals with sickle cell disease implicates ADAMTS2 and CDK18 and uncovers novel loci. | Br J Haematol | 2023 |
| 36114116 | Detection of alloimmunization in Glanzmann Thrombasthenia and Bernard-Soulier Syndrome: Data from a Brazilian Center. | Hematology, Transfusion and Cell Therapy | 2023 |
| 37690979 | Application of Monocyte Monolayer Assay technique to predict hyperhemolysis in patients with sickle cell disease. | | 2023 |
| 36884065 | Estimated glomerular filtration rate in Brazilian adults with sickle cell disease: results from the REDS-III multicenter cohort study. | Ann Hematol | 2023 |
| 36993312 | Genetic regulation of fetal hemoglobin across global populations. | medRxiv | 2023 |
| 35052458 | Quality of Life Scores Remained Different among the Genotypic Groups of Patients with Suspected Hemochromatosis, Even after Treatment Period. | Genes | 2022 |
| 35441384 | The Recipient Epidemiology and Donor Evaluation Study-IV-Pediatric (REDS-IV-P): A research program striving to improve blood donor safety and optimize transfusion outcomes across the lifespan. | Transfusion | 2022 |
| 35873155 | Different Transcriptomic Response to <i>T. cruzi</i> Infection in hiPSC-Derived Cardiomyocytes From Chagas Disease Patients With and Without Chronic Cardiomyopathy. | Front Cell Infect Microbiol | 2022 |
| 35487873 | Impact of HLA-G +3142C>G on the development of antibodies to blood group systems other than the Rh and Kell among sensitized patients with sickle cell disease. | Transfusion and Apheresis Science | 2022 |
| 35368071 | Genetic risk factors and COVID-19 severity in Brazil: results from BRACOVID study. | Human Molecular Genetics | 2022 |
| 35927319 | Rare genetic variants explain missing heritability in smoking. | Nat Hum Behav | 2022 |
| 34990411 | Clonal hematopoiesis in sickle cell disease. | J Clin Invest | 2022 |
| 35023178 | Psychological impact of the COVID-19 pandemic on young professionals in blood banks and transfusion services: A global cross-sectional survey. | Vox Sanguinis | 2022 |
| 35156206 | RHCE null allele causing D-- phenotype in a Latin-American blood donor. | Transfusion | 2022 |
| 35083424 | Association between and the severity of COVID-19: initial observations. | Hematology, Transfusion and Cell Therapy | 2022 |
| 33223472 | Reduced volume of red blood cell priming is safe for pediatric patients undergoing therapeutic plasma exchange. | Transfusion and Apheresis Science | 2021 |
| 33491194 | Correlation between SARS-COV-2 antibody screening by immunoassay and neutralizing antibody testing. | Transfusion | 2021 |
| 33687082 | Variant genotypes associated with reduced expression of RhCE antigens among Brazilian blood donors. | Transfusion | 2021 |
| 33674207 | Changes in blood donation and utilization secondary to Covid-19 outbreak. | Transfusion and Apheresis Science | 2021 |
| 33778377 | Suggested guidelines for convalescent plasma therapy for the treatment of COVID-19. | Hematology, Transfusion and Cell Therapy | 2021 |
| 34309026 | A novel mutation in RHAG causing Rh phenotype in Colombia. | Transfusion | 2021 |
| 33077347 | COVID-19: Further evidence of no transfusion transmission. | Transfusion and Apheresis Science | 2021 |
| 32798060 | Transfusion of ABO non-identical platelets increases the severity of trauma patients at ICU admission. | Hematology, Transfusion and Cell Therapy | 2021 |
| 33231305 | 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. | Transfusion | 2021 |
| 32667816 | Weak D types 38 and 11: determination of frequencies in a Brazilian population and validation of an easy molecular assay for detection. | Immunohematology | 2020 |
| 31980333 | Effectiveness of strategies to screen for blood donors with RH variants in a mixed population. | Transfusion and Apheresis Science | 2020 |
| 32464486 | Novel mutations in the bone morphogenetic protein 6 gene in patients with iron overload and non-homozygous genotype for the HFE p.Cys282Tyr mutation. | Blood Cells, Molecules, and Diseases | 2020 |
| 33240273 | How Ancestry Influences the Chances of Finding Unrelated Donors: An Investigation in Admixed Brazilians. | Front Immunol | 2020 |
| 32579245 | Blood utilization and characteristics of patients treated with chronic transfusion therapy in a large cohort of Brazilian patients with sickle cell disease. | Transfusion | 2020 |
| 32741734 | Using droplet digital PCR to screen for rare blood donors: Proof of principle. | Transfusion and Apheresis Science | 2020 |
| 32681817 | FcγR2B B2.4 haplotype predicts increased risk of red blood cell alloimmunization in sickle cell disease patients. | Transfusion | 2020 |
| 33013863 | Polymorphisms in Inflammatory Genes Modulate Clinical Complications in Patients With Sickle Cell Disease. | Frontiers in Immunology | 2020 |
| 32946153 | Accelerated erythrocyte destruction mimicking post-transfusion hyperhaemolysis in the course of uncomplicated vaso-occlusive crisis associated with sickle cell disease. | Transfusion Medicine | 2020 |
| 31408202 | Diversity of RH and transfusion support in Brazilian sickle cell disease patients with unexplained Rh antibodies. | Transfusion | 2019 |
| 31668730 | Clinical and Genetic Predictors of Priapism in Sickle Cell Disease: Results from the Recipient Epidemiology and Donor Evaluation Study III Brazil Cohort Study. | J Sex Med | 2019 |
| 30615815 | Prevalence of SMIM1 c.64_80del17 homozygotes in southeastern Brazil: the Vel-negative phenotype. | Transfusion | 2019 |
| 31183870 | Prevalence and laboratorial determinants of the clinical relevance of antibodies of undetermined specificity. | Vox Sanguinis | 2019 |
| 30908604 | A Toll-like receptor 2 genetic variant modulates occurrence of bacterial infections in patients with sickle cell disease. | British Journal of Haematology | 2019 |
| 30779172 | A blockage monoclonal antibody protocol as an alternative strategy to avoid anti-CD38 interference in immunohematological testing. | Transfusion | 2019 |
| 30939337 | SMIM1 intron 2 gene variations leading to variability in Vel antigen expression among Brazilian blood donors. | Blood Cells, Molecules, and Diseases | 2019 |
| 29193119 | Evaluation of the applicability and effectiveness of a molecular strategy for identifying weak D and DEL phenotype among D- blood donors of mixed origin exhibiting high frequency of RHD*Ψ. | Transfusion | 2018 |
| 28568311 | Defining the clinical relevance of red blood cell autoantibodies by Monocyte Monolayer Assay. | Journal of Clinical Laboratory Analysis | 2018 |
| 30057979 | Red blood cell alloantibodies and autoantibodies: different presentation, same physiopathology. | Hematology, Transfusion and Cell Therapy | 2018 |
| 30283275 | Optimized Antigen-Matched in Sickle Cell Disease Patients: Chances and Challenges in Molecular Times - the Brazilian Way. | Transfusion Medicine and Hemotherapy | 2018 |
| 30133821 | Massive autoimmune hemolysis documented by monocyte monolayer assay in a multiply transfused patient using reticulocytes isolated by simple centrifugation in microhematocrit tubes. | Transfusion | 2018 |
| 29943480 | High frequency of variant RHD genotypes among donors and patients of mixed origin with serologic weak-D phenotype. | Journal of Clinical Laboratory Analysis | 2018 |
| 29301508 | Quality of life scores differs between genotypic groups of patients with suspected hereditary hemochromatosis. | BMC Medical Genetics | 2018 |
| 27595845 | Determination of Fetal RHD Genotype Including the RHD Pseudogene in Maternal Plasma. | Journal of Clinical Laboratory Analysis | 2017 |
| 28691206 | Duffy null genotype or Fy(a-b-) phenotype are more accurate than self-declared race for diagnosing benign ethnic neutropenia in Brazilian population. | International Journal of Laboratory Hematology | 2017 |
| 28388467 | RHD and RHCE genotyping by next-generation sequencing is an effective strategy to identify molecular variants within sickle cell disease patients. | Blood Cells, Molecules, and Diseases | 2017 |