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| Issue Date | Title | Author(s) |
|---|---|---|
| 2018 | High frequency of variant RHD genotypes among donors and patients of mixed origin with serologic weak-D phenotype | DEZAN, Marcia Regina; OLIVEIRA, Valeria B.; GOMES, Carolina Nunes; LUZ, Fabio; GALLUCCI, Antonio J.; BONIFACIO, Silvia L.; ALENCAR, Cecilia Salete; SABINO, Ester C.; PEREIRA, Alexandre C.; KRIEGER, Jose E.; ROCHA, Vanderson; MENDRONE-JUNIOR, Alfredo; DINARDO, Carla L. |
| 2017 | RHD and RHCE genotyping by next-generation sequencing is an effective strategy to identify molecular variants within sickle cell disease patients | DEZAN, Marcia R.; RIBEIRO, Ingrid Helena; OLIVEIRA, Valeria B.; VIEIRA, Juliana B.; GOMES, Francisco C.; FRANCO, Lucas A. M.; VARUZZA, Leonardo; RIBEIRO, Roberto; CHINOCA, Karen Ziza; LEVI, Jose Eduardo; KRIEGER, Jose Eduardo; PEREIRA, Alexandre Costa; GUALANDRO, Sandra F. M.; ROCHA, Vanderson G.; MENDRONE-JUNIOR, Alfredo; SABINO, Ester Cerdeira; DINARDO, Carla Luana |
| 2018 | Evaluation of the applicability and effectiveness of a molecular strategy for identifying weakD and DEL phenotype among D- blood donors of mixed origin exhibiting high frequency of RHD* | DEZAN, Marcia Regina; GUARDALINI, Luis Giovani O.; PESSOA, Elaine; RIBEIRO, Ingrid Helena; OLIVEIRA, Valeria Brito; LUZ, Fabio; NOVAC, Denise Rossite; GALLUCCI, Antonio; BONIFACIO, Silvia; GOMES, Francisco; LEVI, Jose E.; PEREIRA, Alexandre C.; KRIEGER, Jose E.; MENDRONE-JUNIOR, Alfredo; ROCHA, Vanderson; DINARDO, Carla Luana |
| 2021 | 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, Carla L.; OLIVEIRA, Theo G. M.; KELLY, Shannon; ASHLEY-KOCH, Allison; TELEN, Marilyn; SCHMIDT, Luciana C.; CASTILHO, Shirley; MELO, Karla; DEZAN, Marcia R.; WHEELER, Marsha M.; JOHNSEN, Jill M.; NICKERSON, Deborah A.; JAIN, Deepti; CUSTER, Brian; PEREIRA, Alexandre C.; SABINO, Ester C. |
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