Associated Papers
[Study on the Production of Anti-D and Anti-E Mixed Antibodies by Alloimmunization in RhD Variant Type33 Recipients].
Liu JC et al.
Zhongguo Shi Yan Xue Ye Xue Za Zhi, 2024
Machine learning to optimize automated RH genotyping using whole-exome sequencing data.
Chang TC et al.
Blood Advances, 2024
Genetic Characterization of Blood Group Antigens for Polynesian Heritage Norfolk Island Residents.
O'Brien S et al.
Genes, 2023
Transfusion management of Africans with RHD variants in China.
Yin Q et al.
Transfusion Clinique Et Biologique : Journal De La Societe Francaise De Transfusion Sanguine, 2023
RHD alleles contributing to serologically weak D phenotypes in China: A single-centre study over 10 years.
Ye L et al.
Vox Sanguinis, 2022
Molecular basis of serological weak D phenotypes and RhD typing discrepancies identified in the Korean population.
Chung YN et al.
Blood Transfusion = Trasfusione Del Sangue, 2021
Insights into anti-D formation in carriers of RhD variants through studies of 3D intraprotein interactions.
Floch A et al.
Transfusion, 2021
Impact of RHD genotyping on transfusion practice in Denmark and the United States and identification of novel RHD alleles.
Vege S et al.
Transfusion, 2021
The Significance of RHD Genotyping and Characteristic Analysis in Chinese RhD Variant Individuals.
Ying Y et al.
Frontiers in Immunology, 2021
A novel algorithm comprehensively characterizes human RH genes using whole-genome sequencing data.
Chang TC et al.
Blood Advances, 2020
Comprehensive Molecular Analysis of Serologically D-Negative and Weak/Partial D Phenotype in Thai Blood Donors.
Thongbut J et al.
Transfusion Medicine and Hemotherapy : Offizielles Organ Der Deutschen Gesellschaft Fur Transfusionsmedizin Und Immunhamatologie, 2020
Genomic characterization of the RH locus detects complex and novel structural variation in multi-ethnic cohorts.
Wheeler MM et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2019
Targeted exome sequencing defines novel and rare variants in complex blood group serology cases for a red blood cell reference laboratory setting.
Schoeman EM et al.
Transfusion, 2018
RHD genotype and zygosity analysis in the Chinese Southern Han D+, D- and D variant donors using the multiplex ligation-dependent probe amplification assay.
Ji YL et al.
Vox Sanguinis, 2017
Prevalence of RHD alleles in Japanese individuals with weak D phenotype: Identification of 20 new RHD alleles.
Isa K et al.
Vox Sanguinis, 2016
Weak D alleles in Japanese: a c.960G>A silent mutation in exon 7 of the RHD gene that affects D expression.
Ogasawara K et al.
Vox Sanguinis, 2016
Molecular basis and zygosity determination of D variants including identification of four novel alleles in Chinese individuals.
He J et al.
Transfusion, 2015
XomAnnotate: Analysis of Heterogeneous and Complex Exome- A Step towards Translational Medicine.
Talukder AK et al.
Plos One, 2015
A comprehensive investigation of RHD polymorphisms in the Chinese Han population in Xi'an.
Ye SH et al.
Blood Transfusion = Trasfusione Del Sangue, 2014
Overcoming methodical limits of standard RHD genotyping by next-generation sequencing.
Stabentheiner S et al.
Vox Sanguinis, 2011
D variants at the RhD vestibule in the weak D type 4 and Eurasian D clusters.
Flegel WA et al.
Transfusion, 2009