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
Alloanti-D induction in a rare RhD variant (DBT-2) case: Insights from serological and molecular biological testing.
Xu Z et al.
Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis, 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
Characterization of Novel RHD Allele Variants and Their Implications for Routine Blood Group Diagnostics.
Matzhold EM et al.
Biomedicines, 2024
RHD Positive Haplotype in D Negative Omani Blood Donor.
Al Lawati M et al.
Oman Medical Journal, 2023
Transfusion support for a patient with alloanti-D and the RHD*DV.1 allele.
Jiang L et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry, 2023
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
Sickle cell disease patients in two London trusts: Genotyping including RH variants.
Hui YMT et al.
Transfusion Medicine (oxford, England), 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
Optimization of diagnostic strategy for non-invasive cell-free foetal RHD determination from maternal plasma.
Pazourkova E et al.
Vox Sanguinis, 2021
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
Nation-wide investigation of RHD variants in Thai blood donors: Impact for molecular diagnostics.
Thongbut J 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
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
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
Comprehensive Molecular Analysis of Serologically D-Negative and Weak/Partial D Phenotype in Thai Blood Donors.
Thongbut J et al.
Transfusion Medicine and Hemotherapy : Offizielles Organ Der Deutschen Gesellschaft Fur Transfusionsmedizin Und Immunhamatologie, 2020
Characterization of RHD alleles present in serologically RHD-negative donors determined by a sensitive microplate technique.
de Paula Vendrame TA et al.
Vox Sanguinis, 2019
Amplicon Sequencing-Based Noninvasive Fetal Genotyping for RHD-Positive D Antigen-Negative Alleles.
Takahashi K et al.
Clinical Chemistry, 2019
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
Validated Reference Panel from Renewable Source of Genomic DNA Available for Standardization of Blood Group Genotyping.
Volkova E et al.
The Journal of Molecular Diagnostics : Jmd, 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 characterization of three novel RHD alleles in Brazilians.
Aparecida de Paula Vendrame T et al.
Transfusion, 2018
A recurrent point mutation in PRKCA is a hallmark of chordoid gliomas.
Rosenberg S et al.
Nature Communications, 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
Serologic and molecular characterization of weak D type 29.
Ouchari M et al.
Transfusion, 2017
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
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
The DAU cluster: a comparative analysis of 18 RHD alleles, some forming partial D antigens.
Srivastava K et al.
Transfusion, 2016
A D+ blood donor with a novel RHD*D-CE(5-6)-D gene variant exhibits the low-frequency antigen RH23 (D(W) ) characteristic of the partial DVa phenotype.
Lopez GH et al.
Transfusion, 2016
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