Associated Papers
Genetic characterization of an ABO*O.01.02-A2.05 hybrid allele associated with the Ael phenotype in a Chinese individual.
Liang S et al.
Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis, 2025
Characterisation of the ABO Blood Group Phenotypes Using Third-Generation Sequencing.
Mobegi FM et al.
International Journal of Molecular Sciences, 2025
Rapid change in red cell blood group systems after the main Out of Africa of Homo sapiens.
Mazières S et al.
Scientific Reports, 2025
Truncated glycosyltransferase coding regions in novel ABO alleles give rise to weak A or B blood group expression and discrepant typing results.
Ricci Hagman J et al.
Transfusion, 2023
Haplotype sequence collection of ABO blood group alleles by long-read sequencing reveals putative A1-diagnostic variants.
Gueuning M et al.
Blood Advances, 2023
RBCeq: A robust and scalable algorithm for accurate genetic blood typing.
Jadhao S et al.
Ebiomedicine, 2022
A 24-base pair deletion in the ABO gene causes a hereditary splice site defect: a novel mechanism underlying ABO blood group O.
Matzhold EM et al.
Transfusion, 2020
Next Generation Sequencing-Based Fetal ABO Blood Group Prediction by Analysis of Cell-Free DNA from Maternal Plasma.
Rieneck K et al.
Transfusion Medicine and Hemotherapy : Offizielles Organ Der Deutschen Gesellschaft Fur Transfusionsmedizin Und Immunhamatologie, 2020
Thorough analysis of unorthodox ABO deletions called by the 1000 Genomes project.
Möller M et al.
Vox Sanguinis, 2018
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