Associated Papers
Frequency of RHD variants among blood donors in the central region of Iran, Yazd province.
Seddighi N et al.
Transfusion Medicine (oxford, England), 2025
Partial D variant with demonstrated risk of D alloimmunization in the Australian Indigenous population.
Palfreyman E et al.
Vox Sanguinis, 2025
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
Rapid change in red cell blood group systems after the main Out of Africa of Homo sapiens.
Mazières S et al.
Scientific Reports, 2025
A splice site variant defining the novel RHD*01(487-3G) allele in trans to RHD*DAR1.2.
Cezar-Schmidt A et al.
Transfusion, 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
DNA Reference Reagents for Genotyping RH Variants.
Sippert E et al.
The Journal of Molecular Diagnostics : Jmd, 2024
Frequency and characterization of RHD and RHCE variants in the Noir Marron population from French Guiana.
Laget L et al.
Transfusion, 2022
Rh Blood Group D Antigen Genotyping Using a Portable Nanopore-based Sequencing Device: Proof of Principle.
Tounsi WA et al.
Clinical Chemistry, 2022
RHD alleles contributing to serologically weak D phenotypes in China: A single-centre study over 10 years.
Ye L et al.
Vox Sanguinis, 2022
Transfusion support for a woman with RHD*09.01.02 and the novel RHD*01W.161 allele in trans.
Srivastava K et al.
Immunohematology, 2022
High prevalence of weak D type 42 in a large-scale RHD genotyping program in the province of Quebec (Canada).
Leiva-Torres GA et al.
Transfusion, 2021
Insights into anti-D formation in carriers of RhD variants through studies of 3D intraprotein interactions.
Floch A et al.
Transfusion, 2021
A Review of the Literature Organized Into a New Database: RHeference.
Floch A et al.
Transfusion Medicine Reviews, 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
Impact of RHD genotyping on transfusion practice in Denmark and the United States and identification of novel RHD alleles.
Vege S 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
Characterising Indian RhD variants by serological and molecular methods.
Mishra G et al.
Transfusion Medicine (oxford, England), 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
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
Molecular basis of weak D expression in the Indian population and report of a novel, predominant variant RHD allele.
Fichou Y et al.
Transfusion, 2018
Transfusion strategy for weak D Type 4.0 based on RHD alleles and RH haplotypes in Tunisia.
Ouchari M 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
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
Whole-exome sequencing for RH genotyping and alloimmunization risk in children with sickle cell anemia.
Chou ST et al.
Blood Advances, 2017
Diverse and novel RHD variants in Australian blood donors with a weak D phenotype: implication for transfusion management.
McGowan EC et al.
Vox Sanguinis, 2017
Identification of four novel RHD alleles with altered expression of D in Brazilians.
Arnoni CP et al.
Transfusion, 2016
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
RHD genotyping and its implication in transfusion practice.
Sassi A et al.
Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis, 2014
A comprehensive investigation of RHD polymorphisms in the Chinese Han population in Xi'an.
Ye SH et al.
Blood Transfusion = Trasfusione Del Sangue, 2014
The RHD*weak D type 4.0 allele is predominantly but not exclusively cis-associated with the altered RHCE*ce(c.48C, c.105T, c.733G, c.744C, c.1025T) allele in the French population.
Fichou Y et al.
Transfusion Medicine (oxford, England), 2014
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
Serologic and molecular investigations of DAR1 (weak D Type 4.2), DAR1.2, DAR1.3, DAR2 (DARE), and DARA.
Lejon Crottet S 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*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
RHD alleles in the Tunisian population.
Ouchari M et al.
Asian Journal of Transfusion Science, 2013
[System RH: screening of partials D with RHD/RHCE hybrid gene].
Ouchari M et al.
Transfusion Clinique Et Biologique : Journal De La Societe Francaise De Transfusion Sanguine, 2013