Associated Papers
Partial D variant with demonstrated risk of D alloimmunization in the Australian Indigenous population.
Palfreyman E 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
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
DNA Reference Reagents for Genotyping RH Variants.
Sippert E et al.
The Journal of Molecular Diagnostics : Jmd, 2024
Characterization of Novel RHD Allele Variants and Their Implications for Routine Blood Group Diagnostics.
Matzhold EM et al.
Biomedicines, 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
Frequency and characterization of RHD and RHCE variants in the Noir Marron population from French Guiana.
Laget L et al.
Transfusion, 2022
A novel complex RHD(L62F,A137V,N152T)-CE(6-7(G336C))-D allele in a patient of African ancestry.
Bénech C et al.
Transfusion, 2022
Insights into anti-D formation in carriers of RhD variants through studies of 3D intraprotein interactions.
Floch A et al.
Transfusion, 2021
A Functional Variant Rs492554 Associated With Congenital Heart Defects Modulates SESN2 Expression Through POU2F1.
Yang W et al.
Frontiers in Cell and Developmental Biology, 2021
RH genotyping by nonspecific quantitative next-generation sequencing.
Stef M et al.
Transfusion, 2020
Classification of major and minor blood group antigens in the Kuwaiti Arab population.
Ameen R et al.
Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis, 2020
Novel RHD alleles in African Brazilians.
de Paula Vendrame TA et al.
Transfusion, 2019
Molecular matching for patients with haematological diseases expressing altered RHD-RHCE genotypes.
Cruz BR et al.
Vox Sanguinis, 2019
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
How do we identify RHD variants using a practical molecular approach?
Arnoni CP et al.
Transfusion, 2014
D category IV: a group of clinically relevant and phylogenetically diverse partial D.
von Zabern I et al.
Transfusion, 2013
A comprehensive survey of both RHD and RHCE allele frequencies in sub-Saharan Africa.
Granier T et al.
Transfusion, 2013
RHCE*ceTI encodes partial c and partial e and is often in cis to RHD*DIVa.
Westhoff CM et al.
Transfusion, 2013
DIII Type 7 is likely the original serologically defined DIIIb.
Lomas-Francis C et al.
Transfusion, 2012
Overcoming methodical limits of standard RHD genotyping by next-generation sequencing.
Stabentheiner S et al.
Vox Sanguinis, 2011
RH genotyping in a sickle cell disease patient contributing to hematopoietic stem cell transplantation donor selection and management.
Fasano RM et al.
Blood, 2010
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 basis of the RHD gene in blood donors with DEL phenotypes in Shanghai.
Li Q et al.
Vox Sanguinis, 2009
Molecular analysis of inactive and active RHD alleles in native Congolese cohorts.
Touinssi M 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
The RHCE allele ceCF: the molecular basis of Crawford (RH43).
Flegel WA 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
Rare RHCE phenotypes in black individuals of Afro-Caribbean origin: identification and transfusion safety.
Noizat-Pirenne F et al.
Blood, 2002