|
| 36349441 | Two new Scianna variants causing loss of high prevalence antigens: ERMAPÂ model and 3D analysis of the antigens. | Transfusion | 2023 |
| 37656962 | Evidence that donors with variant RH genotypes are associated with unexpected Rh antibodies. | Transfusion | 2023 |
| 37970740 | Transfusion management in the era of magrolimab (Hu5F9-G4), an anti-CD47 monoclonal antibody therapy. | Transfusion | 2023 |
| 37921239 | Uncommon S-s-U+ phenotype encoded by two novel GYPB alleles. | Transfusion | 2023 |
| 37002797 | Variant RHD alleles and Rh immunization in patients with sickle cell disease. | Br J Haematol | 2023 |
| 36722377 | Two novel variants that disrupt the RHCE start codon with varying effect on RhCE antigen expression. | Transfusion | 2023 |
| 36738255 | A novel high-prevalence antigen in the Lutheran system, LUGA (LU24), and an updated, full-length 3D BCAM model. | Transfusion | 2023 |
| 36732087 | ABO Genotyping finds more A<sub>2</sub> to B kidney transplant opportunities than lectin-based subtyping. | Am J Transplant | 2023 |
| 35236059 | Intricacies of GATA-ca, continued. | Haematologica | 2022 |
| 35441363 | First report of a null allele on a GYPB*s background: GYPB*s(37â¿¿+â¿¿4_8delAGTGA). | Transfusion | 2022 |
| 35904131 | YTGT: A new high-prevalence antigen in the Yt blood group system in two unrelated Native Americans and transfusion management. | Transfusion | 2022 |
| 36121188 | International Society of Blood Transfusion Working Party on Red Cell Immunogenetics and Blood Group Terminology Report of Basel and three virtual business meetings: Update on blood group systems. | Vox Sang | 2022 |
| 35977098 | The use of pluripotent stem cells to generate diagnostic tools for transfusion medicine. | Blood | 2022 |
| 36317854 | Four novel ABO*AW alleles associated with weak antigen expression. | Transfusion | 2022 |
| 35282947 | Red Cell Antigens and Antibodies. | Hematol Oncol Clin North Am | 2022 |
| 34936100 | An intron c.149-2632T>A change in RHD is associated with aberrant transcription and very weak D phenotype. | Transfusion | 2022 |
| 35175190 | 3D analysis of CROMER (DAF) and a new antigen CRAG. | Blood Transfus | 2022 |
| 34968422 | Accurate long-read sequencing allows assembly of the duplicated RHD and RHCE genes harboring variants relevant to blood transfusion. | Am J Hum Genet | 2022 |
| 32817291 | Severe delayed hemolytic transfusion reaction due to anti-Fy3 in a patient with sickle cell disease undergoing red cell exchange prior to hematopoietic progenitor cell collection for gene therapy. | Haematologica | 2021 |
| 33733475 | A pair of S-silencing single nucleotide variants cis-linked on GYPB. | Transfusion | 2021 |
| 33560383 | Rh alloimmunization in chronically transfused patients with thalassemia receiving RhD, C, E, and K matched transfusions. | Blood Adv | 2021 |
| 33929058 | Screening of blood donors for sickle cell trait using a DNA-based approach: Frequency in a multiethnic donor population. | Transfusion | 2021 |
| 34908758 | Anti-Emm, a rare specificity to the high-incidence antigen Emm in an Indian patient defining the new blood group system EMM (ISBT042). | Asian J Transfus Sci | 2021 |
| 34472116 | Use of an in-house trypsin-based method to resolve the interference of daratumumab. | Transfusion | 2021 |
| 34554576 | Five novel silenced KEL*02 alleles. | Transfusion | 2021 |
| 34487547 | An insertion/deletion polymorphism in the KLF1 gene resulting in an In(Lu) phenotype. | Transfusion | 2021 |
| 34487382 | Three new XK alleles; two associated with a McLeod RBC phenotype. | Transfusion | 2021 |
| 34570912 | Five novel FY null alleles associated with typing discrepancies. | Transfusion | 2021 |
| 34539318 | P-Null Phenotype Due to a Rare Frame-Shift Mutation and with Allo-Anti-PP1Pk Causing a Severe Hemolytic Transfusion Reaction: A Case Report with Clinical Management. | Transfus Med Hemother | 2021 |
| 34480361 | A novel P1PK allele in two Bangladeshi sisters with a history of spontaneous abortion: A4GALT*02N(951C). | Transfusion | 2021 |
| 34535746 | PIGG defines the Emm blood group system. | Sci Rep | 2021 |
| 33475168 | ABO maternal-child discordance: Evidence of variable allelic expression and considerations for investigation. | Transfusion | 2021 |
| 32975828 | Impact of RHD genotyping on transfusion practice in Denmark and the United States and identification of novel RHD alleles. | Transfusion | 2021 |
| 32567058 | Overcoming the challenges of interpreting complex and uncommon RH alleles from whole genomes. | Vox Sang | 2020 |
| 31758587 | How do I incorporate red cell genotyping to improve chronic transfusion therapy? | Transfusion | 2020 |
| 32086951 | Reliability of labeling red cell units with minor antigen historical results and process considerations. | Transfusion | 2020 |
| 31985807 | American Society of Hematology 2020 guidelines for sickle cell disease: transfusion support. | Blood Adv | 2020 |
| 33037611 | A novel RHD*DAU allele with c.1136C>T (p.Thr379Met) and c.17C>T (p. Pro6Leu). | Transfusion | 2020 |
| 32608521 | RHCE*02 (c.148G>A, p.Val50Ile) allele with silenced RHCE*Ce expression. | Transfusion | 2020 |
| 32915977 | A novel algorithm comprehensively characterizes human RH genes using whole-genome sequencing data. | Blood Adv | 2020 |
| 32678083 | Disruption of the tumour-associated EMP3 enhances erythroid proliferation and causes the MAM-negative phenotype. | Nat Commun | 2020 |
| 32750130 | Development and validation of a universal blood donor genotyping platform: a multinational prospective study. | Blood Adv | 2020 |
| 32473076 | Multiple GYPB gene deletions associated with the U- phenotype in those of African ancestry. | Transfusion | 2020 |
| 32163599 | It's time to phase out "serologic weak D phenotype" and resolve D types with RHD genotyping including weak D type 4. | Transfusion | 2020 |
| 30592300 | A whole genome approach for discovering the genetic basis of blood group antigens: independent confirmation for P1 and Xg<sup>a</sup>. | Transfusion | 2019 |
| 30036180 | Experience with RHD*weak D type 4.0 in the USA. | Blood Transfus | 2019 |
| 31408202 | Diversity of RH and transfusion support in Brazilian sickle cell disease patients with unexplained Rh antibodies. | Transfusion | 2019 |
| 31392742 | Automated typing of red blood cell and platelet antigens from whole exome sequences. | Transfusion | 2019 |
| 30808639 | Blood group genotyping. | Blood | 2019 |
| 31021439 | Alloimmunization in patients with sickle cell disease and underrecognition of accompanying delayed hemolytic transfusion reactions. | Transfusion | 2019 |