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

A Review of the Literature Organized Into a New Database: RHeference.

Transfusion medicine reviews - 1 Apr 2021

Floch Aline, Téletchéa Stéphane, Tournamille Christophe, de Brevern Alexandre G, Pirenne France

Abstract excerpt

Hundreds of articles containing heterogeneous data describe D variants or add to the knowledge of known alleles. Data can be difficult to find despite existing online blood group resources and genetic and literature databases. We have developed a modern, elaborate database for D variants, thanks to an extensive literature search with meticulous curation of 387 peer-reviewed articles and 80 abstracts from major...

Read the complete abstract on PubMed

Topics

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

Share to Blood Group Antigens
Share to Alleles
Share to Databases, Factual

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Phenotype

Share to Rh-Hr Blood-Group System

Source

Identifiers

PMID: 33994075
DOI: 10.1016/j.tmrv.2021.04.002

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A Review of the Literature Organized Into a New Database: RHeference.PMID 33994075Read ↗

Overview of the serologic and molecular basis of D variants with a focus on D variants in the Indian population.Semantic proximity Read ↗

Characterization of novel RHD alleles: relationship between phenotype, genotype, and trimeric architecture.Semantic proximity Read ↗

Five-Years Review of RHCE Alleles Detected after Weak and/or Discrepant C Results in Southern France.Semantic proximity Read ↗

Systematic RH genotyping and variant identification in French donors of African origin.Semantic proximity Read ↗

RHCE variants inherited with altered RHD alleles in Brazilian blood donors.Semantic proximity Read ↗

Serologic and molecular characterization of D variants in Brazilians: impact for typing and transfusion strategy.Semantic proximity Read ↗

Genetic diversity in RHD and RHCE genes among a selected Kenyan blood donor population.Semantic proximity Read ↗

Molecular characterization of D variants in Brazilian blood donors and their association with RhCE and Duffy phenotypes.Semantic proximity Read ↗

RHD variants in Flanders, Belgium.Semantic proximity Read ↗

New RHD variant alleles.Semantic proximity Read ↗

Molecular characterization of 13 new RHD alleles.Semantic proximity Read ↗

BGvar - a comprehensive resource for blood group immunogeneticsSemantic proximity Read ↗

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