Associated Papers
Proof-of-principle: nanopore adaptive sampling enables full blood group genome analysis and resolution of hybrid alleles.
Gueuning M et al.
Blood Advances, 2026
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
First investigation of RH gene polymorphism in patients with sickle cell disease and associated blood donors in Cameroon, Central Africa.
Mbeti JMM et al.
Blood Transfusion = Trasfusione Del Sangue, 2024
Machine learning to optimize automated RH genotyping using whole-exome sequencing data.
Chang TC et al.
Blood Advances, 2024
RHCE null allele causing D-- phenotype in a Latin-American blood donor.
Dezan MR et al.
Transfusion, 2022
A novel algorithm comprehensively characterizes human RH genes using whole-genome sequencing data.
Chang TC et al.
Blood Advances, 2020
New RHCE*ce variant allele in African descent holds 105C>T (silent) in cis to 48C in Exon 1 and 733G in Exon 5.
Sippert E et al.
Transfusion, 2019
RHD and RHCE genotyping by next-generation sequencing is an effective strategy to identify molecular variants within sickle cell disease patients.
Dezan MR et al.
Blood Cells, Molecules & Diseases, 2017
Insights into RHCE Molecular Analysis in Samples with Partial D Variants: the Experience of Western France.
Fichou Y et al.
Transfusion Medicine and Hemotherapy : Offizielles Organ Der Deutschen Gesellschaft Fur Transfusionsmedizin Und Immunhamatologie, 2015
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
The RHCE allele ceSL: the second example for D antigen expression without D-specific amino acids.
Chen Q et al.
Transfusion, 2006
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