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
Partial D variant with demonstrated risk of D alloimmunization in the Australian Indigenous population.
Palfreyman E et al.
Vox Sanguinis, 2025
A novel RHD allele combining partial D (c.455A>C) and weak D (c.1154G>C) variants.
Ramsey G et al.
Transfusion, 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
A Korean family with RHD*DNT only detectable after anti-D alloimmunization.
Shin DW et al.
American Journal of Clinical Pathology, 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
Sickle cell disease patients in two London trusts: Genotyping including RH variants.
Hui YMT et al.
Transfusion Medicine (oxford, England), 2022
Insights into anti-D formation in carriers of RhD variants through studies of 3D intraprotein interactions.
Floch A et al.
Transfusion, 2021
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
Weak D type 1, 2 and 3 subtype alleles are rare in the Western French population.
Raud L et al.
Transfusion Medicine (oxford, England), 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
Molecular characterization of three novel RHD alleles in Brazilians.
Aparecida de Paula Vendrame T et al.
Transfusion, 2018
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
The DAU Allele and Anti-D Alloimmunization Present With High Frequency in Brazilian Sickle Cell Disease Patients.
de Moura Neto JP et al.
Journal of Hematology, 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
A comparison of methods for the detection of the r'(s) haplotype.
Moulds JM et al.
Transfusion, 2015
How do we identify RHD variants using a practical molecular approach?
Arnoni CP et al.
Transfusion, 2014
Systematic RH genotyping and variant identification in French donors of African origin.
Kappler-Gratias S et al.
Blood Transfusion = Trasfusione Del Sangue, 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
RHD gene polymorphisms in alloimmunized RhD-negative individuals with high rate of racial admixture.
Martin FO et al.
Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis, 2013
Comprehensive analysis of RHD alleles in Argentineans with variant D phenotypes.
Brajovich ME et al.
Transfusion, 2012
DIII Type 7 is likely the original serologically defined DIIIb.
Lomas-Francis C et al.
Transfusion, 2012
Identification of RHCE and KEL alleles in large cohorts of Afro-Caribbean and Comorian donors by multiplex SNaPshot and fragment assays: a transfusion support for sickle cell disease patients.
Silvy M et al.
British Journal of Haematology, 2011
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 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
High frequency of partial DIIIa and DAR alleles found in sickle cell disease patients suggests increased risk of alloimmunization to RhD.
Castilho L et al.
Transfusion Medicine (oxford, England), 2005
Rare RHCE phenotypes in black individuals of Afro-Caribbean origin: identification and transfusion safety.
Noizat-Pirenne F et al.
Blood, 2002
RHD positive haplotypes in D negative Europeans.
Wagner FF et al.
Bmc Genetics, 2001