Associated Papers
Distribution characteristics of ABO subgroups and identification of novel alleles among volunteer non-remunerated blood donors in Ningxia, China.
Liu J et al.
Vox Sanguinis, 2026
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 an AweakB phenotype caused by significant ABO gene deletion in a Chinese woman.
Gao T et al.
Vox Sanguinis, 2025
A novel allele of B(A) blood group detected in a donor and a patient during a retrospective review of ABO group anomalies in a tertiary hospital.
Suksard K et al.
Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis, 2025
Identification of five novel ABO blood group alleles.
Kräuchi R et al.
Transfusion, 2025
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
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
Detection and phenotype analysis of a novel Ael blood group allele.
Wang C et al.
Vox Sanguinis, 2024
Identification of a novel B allele with a c.145C>T variant.
Fan C 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
c.586T>C mutation on the ABO*A1.02 allele responsible for Ael phenotype.
Shen Y et al.
Transfusion, 2022
Novel or not? Reference alleles, genes, and genomes to unmask the true nature of the ABO*AW.10 allele associated with weak A phenotype.
Gassner C et al.
Transfusion, 2022
Application of Blood Group Genotyping by Next-Generation Sequencing in Various Immunohaematology Cases.
Kim TY et al.
Transfusion Medicine and Hemotherapy : Offizielles Organ Der Deutschen Gesellschaft Fur Transfusionsmedizin Und Immunhamatologie, 2022
Analysis of the Genomic Sequence of ABO Allele Using Next-Generation Sequencing Method.
He Y et al.
Frontiers in Immunology, 2022
Identification of a novel A allele with a c.36-39delA on the ABO*A1.02 allele.
Liang S et al.
Transfusion, 2021
A novel c.28 + 1G > T mutation in the ABO*A1.02 allele that results in Ael phenotype.
Yu L et al.
Transfusion, 2021
A novel allele arising from c.912C>A mutation in the α-1,3-N-acetylgalactosaminyltransferase gene in a Chinese individual.
Zhang X et al.
Transfusion, 2021
Genomic analysis of blood samples with serologic ABO discrepancy identifies 12 novel alleles in a Chinese Han population.
Zuo Q et al.
Transfusion Medicine (oxford, England), 2020
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
A novel A allele with c.467C > T and c.784G > A nucleotide substitutions in Korean individuals.
Kim HR et al.
Transfusion, 2020
Thorough analysis of unorthodox ABO deletions called by the 1000 Genomes project.
Möller M et al.
Vox Sanguinis, 2018