Associated Papers
Partial D variant with demonstrated risk of D alloimmunization in the Australian Indigenous population.
Palfreyman E et al.
Vox Sanguinis, 2025
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
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
Machine learning to optimize automated RH genotyping using whole-exome sequencing data.
Chang TC et al.
Blood Advances, 2024
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
Transfusion support during childbirth for a woman with anti-U and the RHD*weak D type 4.0 allele.
Yin Q et al.
Immunohematology, 2021
RHD Genotypes in a Chinese Cohort of Pregnant Women.
Zhang J et al.
Frontiers in Genetics, 2021
RH genotyping by nonspecific quantitative next-generation sequencing.
Stef M et al.
Transfusion, 2020
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
Evaluation of the applicability and effectiveness of a molecular strategy for identifying weak D and DEL phenotype among D- blood donors of mixed origin exhibiting high frequency of RHD*Ψ.
Dezan MR et al.
Transfusion, 2018
Non-invasive fetal RHD genotyping for RhD negative women stratified into RHD gene deletion or variant groups: comparative accuracy using two blood collection tube types.
Hyland CA et al.
Pathology, 2017
Frequency and characterization of known and novel RHD variant alleles in 37 782 Dutch D-negative pregnant women.
Stegmann TC et al.
British Journal of Haematology, 2016
D category IV: a group of clinically relevant and phylogenetically diverse partial D.
von Zabern I 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
Molecular background of D-negative phenotype in the Tunisian population.
Moussa H et al.
Transfusion Medicine (oxford, England), 2012
Variant screening of the RHD gene in a large cohort of subjects with D phenotype ambiguity: report of 17 novel rare alleles.
Fichou Y et al.
Transfusion, 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
RHD allelic identification among D-Brazilian blood donors as a routine test using pools of DNA.
Mota M et al.
Journal of Clinical Laboratory Analysis, 2012
Overcoming methodical limits of standard RHD genotyping by next-generation sequencing.
Stabentheiner S et al.
Vox Sanguinis, 2011
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
Molecular analysis of inactive and active RHD alleles in native Congolese cohorts.
Touinssi M et al.
Transfusion, 2009
D variants at the RhD vestibule in the weak D type 4 and Eurasian D clusters.
Flegel WA et al.
Transfusion, 2009
Heterogeneous molecular background of the weak C, VS+, hr B-, Hr B- phenotype in black persons.
Pham BN et al.
Transfusion, 2009
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
Random survey for RHD alleles among D+ European persons.
Chen Q et al.
Transfusion, 2005
The presence of an RHD pseudogene containing a 37 base pair duplication and a nonsense mutation in africans with the Rh D-negative blood group phenotype.
Singleton BK et al.
Blood, 2000