Associated Papers
A novel RHCE*02 variant with a recombination of RHD exon 3 in a Chinese D+ voluntary blood donor with weak expression of e antigen.
Yang HM et al.
Transfusion, 2026
Uncommon RHD variants and an unconventional RHCE hybrid allele with D epitope expression in blood donors from northwestern Croatia.
Lilić M et al.
Transfusion, 2025
Assessing reagents and techniques for identifying RhCE variants in routine serological testing.
de Paula Vendrame TA et al.
Vox Sanguinis, 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
Single-exon fetal RHD genotyping: a 31-month follow up in the obstetric population of Western Sweden.
Pardi C et al.
Blood Transfusion = Trasfusione Del Sangue, 2024
Accuracy of RHC/c genotyping in Chinese Han population.
Zhou S et al.
Transfusion Medicine (oxford, England), 2024
D-- phenotype caused by a novel RHCE null allele.
Principi C et al.
Transfusion, 2024
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
Rh Blood Group D Antigen Genotyping Using a Portable Nanopore-based Sequencing Device: Proof of Principle.
Tounsi WA et al.
Clinical Chemistry, 2022
Insights into anti-D formation in carriers of RhD variants through studies of 3D intraprotein interactions.
Floch A et al.
Transfusion, 2021
RHD Genotypes in a Chinese Cohort of Pregnant Women.
Zhang J et al.
Frontiers in Genetics, 2021
Next-generation sequencing of 35 RHD variants in 16 253 serologically D- pregnant women in the Finnish population.
Tammi SM et al.
Blood Advances, 2020
RHD genotyping of serological weak D phenotypes in the Iranian blood donors and patients.
Oodi A et al.
Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis, 2020
A novel algorithm comprehensively characterizes human RH genes using whole-genome sequencing data.
Chang TC et al.
Blood Advances, 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
Alloimmunization risk associated with amino acid 223 substitution in the RhD protein: analysis in the light of molecular modeling.
de Brevern AG et al.
Transfusion, 2018
Whole-exome sequencing for RH genotyping and alloimmunization risk in children with sickle cell anemia.
Chou ST et al.
Blood Advances, 2017
RH diversity in Mali: characterization of a new haplotype RHD*DIVa/RHCE*ceTI(D2).
Ba A et al.
Transfusion, 2015
(C)ce(s) haplotype screening in Tunisian blood donors.
Moussa H et al.
Blood Transfusion = Trasfusione Del Sangue, 2014
A convenient qualitative and quantitative method to investigate RHD-RHCE hybrid genes.
Fichou Y et al.
Transfusion, 2013
RHD*weak partial 4.0 is associated with an altered RHCE*ce(48C, 105T, 733G, 744C, 1025T) allele in the Tunisian population.
Ouchari M et al.
Transfusion Medicine (oxford, England), 2013
On the trail of anti-CDE to unexpected highlights of the RHD*weak 4.3 allele in the Upper Austrian population.
Polin H et al.
Vox Sanguinis, 2012
RHD alleles in Brazilian blood donors with weak D or D-negative phenotypes.
Cruz BR et al.
Transfusion Medicine (oxford, England), 2012
Comprehensive analysis of RHD alleles in Argentineans with variant D phenotypes.
Brajovich ME et al.
Transfusion, 2012
Weak D and DEL alleles detected by routine SNaPshot genotyping: identification of four novel RHD alleles.
Silvy M et al.
Transfusion, 2011
DIIIa and DIII Type 5 are encoded by the same allele and are associated with altered RHCE*ce alleles: clinical implications.
Westhoff CM et al.
Transfusion, 2010
Heterogeneous molecular background of the weak C, VS+, hr B-, Hr B- phenotype in black persons.
Pham BN et al.
Transfusion, 2009
The RHCE allele ceCF: the molecular basis of Crawford (RH43).
Flegel WA et al.
Transfusion, 2006
The RHCE allele ceSL: the second example for D antigen expression without D-specific amino acids.
Chen Q et al.
Transfusion, 2006
RHD(T201R, F223V) cluster analysis in five different ethnic groups and serologic characterization of a new Ethiopian variant DARE, the DIII type 6, and the RHD(F223V).
Grootkerk-Tax MG et al.
Transfusion, 2006
Novel weak D types 31 and 32: adsorption-elution-supported D antigen analysis and comparison to prevalent weak D types.
Körmöczi GF et al.
Transfusion, 2005
Random survey for RHD alleles among D+ European persons.
Chen Q et al.
Transfusion, 2005
Sequence analysis of cDNA derived from reticulocyte mRNAs coding for Rh polypeptides and demonstration of E/e and C/c polymorphisms.
Simsek S et al.
Vox Sanguinis, 1994