Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Evaluating RhD assessment by automated methodology: A potential "blind spot" for RhD variant identification.

Transfusion - 1 Sept 2025

Yurtsever Nalan, Tormey Christopher A, Bizzario Laurie, Lee Edward S

Abstract excerpt

BACKGROUND: The Rh blood group is highly polymorphic, and individuals with RHD variant alleles can form antibodies against antigens found in the conventional RhD protein. To prevent transfusion of D+ blood to groups at risk of forming anti-D antibodies, such as women of childbearing age and newborns, our transfusion service has established protocols to accurately identify D variants that can be missed by...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Alleles
Share to Blood Grouping and Crossmatching
Share to ABO gene

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to RHD gene

Share to Genotype

Share to Genotyping Techniques

Share to Rh-Hr Blood-Group System

Source

Identifiers

PMID: 40944507
DOI: 10.1111/trf.18343

Genes

RHD
ABO

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Evaluating RhD assessment by automated methodology: A potential "blind spot" for RhD variant identification.PMID 40944507Read ↗

Molecular Characterization of RhD Variants in the Turkish Population: A Multicenter Study for Population-Specific Diagnostic Strategy DevelopmentSemantic proximity Read ↗

Identifying D-positive donors using a second automated testing platform.Semantic proximity Read ↗

RhDnostics: A Machine Learning-Based Predictive Algorithm Model for RhD-Negative and DEL Blood Group Screening.Semantic proximity Read ↗

Identification and pedigree analysis of a hidden partial D antigen with rare RHD*DV.1 allele.Semantic proximity Read ↗

Clinical performance of cell free DNA for fetal RhD detection in RhD-negative pregnant individuals in the USSemantic proximity Read ↗

Recommendation for validation and quality assurance of non-invasive prenatal testing for foetal blood groups and implications for IVD risk classification according to EU regulations.Semantic proximity Read ↗

Performance evaluation study of ID RHD XT, a new genotyping assay for the detection of high-prevalence RhD negative and weak D types.Semantic proximity Read ↗

Evaluation of an automated platform for non-invasive single-exon fetal RHD genotyping early in pregnancy.Semantic proximity Read ↗

Clinical Performance of Cell-Free DNA for Fetal RhD Detection in RhD-Negative Pregnant Individuals in the United StatesSemantic proximity Read ↗

Determining the accuracy of a rapid point-of-care test for determining Rh(D) phenotype.Semantic proximity Read ↗

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.Semantic proximity Read ↗

Rh flow cytometry: An updated methodology for D antigen density applied to weak D types 164 and 165.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.