Associated Papers
Novel c.3G>C variant in ABO*B.01 allele associated with an ABweak phenotype.
Wang H et al.
Transfusion, 2025
A novel B group allele with a c.745C>T substitution previously found in ABO*A3.07 subgroup allele.
Liu Y et al.
Transfusion, 2025
Identification and analysis of a novel A allele with a c.565A > G variant on the ABO*A1.02 allele leading to subtype A: A case report.
Lu W et al.
Medicine, 2025
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
Identification of a novel B allele with a c.140_143del on the ABO*B.01 allele.
Liang S et al.
Transfusion, 2025
Identification of a novel ABO allele c.98+1G>A in a Chinese individual using PacBio third-generation sequencing.
Shao LN et al.
Transfusion, 2025
Serological and genetic analysis of a B3 phenotype caused by c.259G > T in the ABO gene.
Zhang M et al.
Transfusion Medicine (oxford, England), 2025
Identification of an AweakB phenotype caused by significant ABO gene deletion in a Chinese woman.
Gao T et al.
Vox Sanguinis, 2025
Identification of a Novel FUT1 Allele with c.425G > A on the FUT1*01 Allele Background.
Shao LN et al.
Indian Journal of Hematology & Blood Transfusion : an Official Journal of Indian Society of Hematology and Blood Transfusion, 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
ABO*cisAB allele with unusual phenotype in a Brazilian family.
Miola MP et al.
Transfusion, 2025
A novel variant c.505C>T based on the ABO*B.01 allele associated with a Bel phenotype.
Wang H et al.
Transfusion, 2024
Identification of a novel c.506A>C variant on the ABO*A1.02 allele in a Chinese individual.
Kong Y et al.
Transfusion, 2024
Genetic and mechanistic evaluation of an individual with para-Bombay phenotype associated with a compound heterozygote comprising two novel FUT1 variants.
Ying Y et al.
Blood Transfusion = Trasfusione Del Sangue, 2024
Four novel ABO*B alleles associated with reduced B antigen expression.
Li Y et al.
Transfusion, 2024
A novel c.29-3C>G variant on the B allele forms the Bel phenotype.
Kong Y et al.
Transfusion, 2024
Identification of a novel A allele with a c.421T>C variant on the ABO*A1.02 allele in a Chinese individual.
Ou G et al.
Transfusion, 2024
Serology and molecular genetic analysis of two unrelated individuals with the same novel CisAB blood type.
Li T et al.
Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis, 2024
Characterization of a novel AEL allele harboring a c.28 + 5G>A mutation on the ABO*A2.01 background: a study utilizing PacBio third-generation sequencing and functional assays.
Shao LN et al.
Frontiers in Immunology, 2024
Identification of a novel B allele with a c.145C>T variant.
Fan C et al.
Transfusion, 2023
Bw phenotype associated with novel start codon variant of ABO gene.
Wu W 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
Identification of a novel A allele with a c.977A>C variation on the ABO*A1.02 allele.
Zhang J et al.
Transfusion, 2022
Molecular basis of weak A subgroups in the Korean population: Identification of three novel subgroup-causing variants in the ABO regulatory regions.
Kim TY et al.
Transfusion, 2022
RBCeq: A robust and scalable algorithm for accurate genetic blood typing.
Jadhao S et al.
Ebiomedicine, 2022
Identification of a novel A allele with a c.36-39delA on the ABO*A1.02 allele.
Liang S et al.
Transfusion, 2021
The novel missense variant c.350G>T on the ABO*B.01 allele associated with a Bel phenotype.
Kim TY et al.
Transfusion, 2020
A novel variant B allele at the ABO gene locus characterized by a duplication-based insertion of 27 nucleotides identified in an Iraqi male with a weak B subgroup phenotype.
Matzhold EM et al.
Transfusion, 2018
Thorough analysis of unorthodox ABO deletions called by the 1000 Genomes project.
Möller M et al.
Vox Sanguinis, 2018