Associated Papers
Introduction of an Optimized Protocol for Long-Read Nanopore Sequencing of Blood Group Genes in Immunohematology Case Studies.
Wörner L et al.
Transfusion Medicine and Hemotherapy : Offizielles Organ Der Deutschen Gesellschaft Fur Transfusionsmedizin Und Immunhamatologie, 2026
Frequency of RHD variants among blood donors in the central region of Iran, Yazd province.
Seddighi N et al.
Transfusion Medicine (oxford, England), 2025
A novel RHD allele combining partial D (c.455A>C) and weak D (c.1154G>C) variants.
Ramsey G et al.
Transfusion, 2025
Weak D phenotype in transfusion medicine and obstetrics: Challenges and opportunities.
Sainath PB et al.
World Journal of Experimental Medicine, 2025
Prediction of immunogenicity of Rh antigens using in silico analysis of binding to human leukocyte antigen peptide, Basic/Translational Research.
Youk HJ et al.
Plos One, 2025
Evaluation of the LightCycler® PRO Instrument as a Platform for Rhesus D Typing.
Polin H et al.
Biomedicines, 2024
Machine learning to optimize automated RH genotyping using whole-exome sequencing data.
Chang TC et al.
Blood Advances, 2024
Estimating the serological underrecognition of patients with weak or partial RHD variants.
Ramsey G et al.
Transfusion, 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
RHD alleles contributing to serologically weak D phenotypes in China: A single-centre study over 10 years.
Ye L et al.
Vox Sanguinis, 2022
[Identification of Weak D Type 1 in Rh Blood Group System and Discussion of Transfusion Strategy].
Zhang RY et al.
Zhongguo Shi Yan Xue Ye Xue Za Zhi, 2022
Optimization of diagnostic strategy for non-invasive cell-free foetal RHD determination from maternal plasma.
Pazourkova E et al.
Vox Sanguinis, 2021
Molecular characterization of RhD variant phenotypes among blood donors: A study from the coastal region of India.
Polavarapu I et al.
Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis, 2021
A Review of the Literature Organized Into a New Database: RHeference.
Floch A et al.
Transfusion Medicine Reviews, 2021
RHD Genotypes in a Chinese Cohort of Pregnant Women.
Zhang J et al.
Frontiers in Genetics, 2021
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 multi-centre study on the performance of the molecular genotyping platform ID RHD XT for resolving serological weak RhD phenotype in routine clinical practice.
Londero D et al.
Vox Sanguinis, 2020
Reinterpretation of common pathogenic variants in ClinVar revealed a high proportion of downgrades.
Xiang J et al.
Scientific Reports, 2020
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
Complete RHD next-generation sequencing: establishment of reference RHD alleles.
Tounsi WA et al.
Blood Advances, 2018
Performance evaluation study of ID RHD XT, a new genotyping assay for the detection of high-prevalence RhD negative and weak D types.
Molano A et al.
Vox Sanguinis, 2018
Evaluation of targeted exome sequencing for 28 protein-based blood group systems, including the homologous gene systems, for blood group genotyping.
Schoeman EM et al.
Transfusion, 2017
RHCE variants inherited with altered RHD alleles in Brazilian blood donors.
Prisco Arnoni C et al.
Transfusion Medicine (oxford, England), 2016
Prevalence of RhD status and clinical application of non-invasive prenatal determination of fetal RHD in maternal plasma: a 5 year experience in Cyprus.
Papasavva T et al.
Bmc Research Notes, 2016
A comprehensive investigation of RHD polymorphisms in the Chinese Han population in Xi'an.
Ye SH et al.
Blood Transfusion = Trasfusione Del Sangue, 2014
How do we identify RHD variants using a practical molecular approach?
Arnoni CP et al.
Transfusion, 2014
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
Anti-D investigations in individuals expressing weak D Type 1 or weak D Type 2: allo- or autoantibodies?
Pham BN et al.
Transfusion, 2011
Weak D and DEL alleles detected by routine SNaPshot genotyping: identification of four novel RHD alleles.
Silvy M et al.
Transfusion, 2011
RHD positive among C/E+ and D- blood donors in Denmark.
Christiansen M et al.
Transfusion, 2010
The structure and function of the Rh antigen complex.
Westhoff CM
Seminars in Hematology, 2007
[Molecular approaches to the Rh blood group system].
Kajii E
Nihon Hoigaku Zasshi = the Japanese Journal of Legal Medicine, 2006
Weak D type 1.1 exemplifies another complexity in weak D genotyping.
Doescher A et al.
Transfusion, 2005
Novel weak D types 31 and 32: adsorption-elution-supported D antigen analysis and comparison to prevalent weak D types.
Körmöczi GF et al.
Transfusion, 2005
Random survey for RHD alleles among D+ European persons.
Chen Q et al.
Transfusion, 2005
RhD variants in Caucasians: consequences for checking clinically relevant alleles.
Ansart-Pirenne H et al.
Transfusion, 2004
The evolution and formation of RH genes.
Okuda H et al.
Legal Medicine (tokyo, Japan), 2002
Molecular characterization of weak D phenotypes by site-directed mutagenesis and expression of mutant Rh-green fluorescence protein fusions in K562 cells.
Kamesaki T et al.
Vox Sanguinis, 2001
PCR screening for common weak D types shows different distributions in three Central European populations.
Müller TH et al.
Transfusion, 2001
RHD gene mutations and the weak D phenotype: an Australian blood donor study.
Cowley NM et al.
Vox Sanguinis, 2000
Advance in the Rh blood group system.
Kajii E
Nihon Hoigaku Zasshi = the Japanese Journal of Legal Medicine, 1998
Molecular genetics of RH and its clinical application.
Flegel WA
Transfusion Clinique Et Biologique : Journal De La Societe Francaise De Transfusion Sanguine, 0