Associated Papers
Machine learning to optimize automated RH genotyping using whole-exome sequencing data.
Chang TC et al.
Blood Advances, 2024
The Crawford variant as a cause of RhD typing discrepancies in blood banks: A case report.
Barrera S et al.
Transfusion Clinique Et Biologique : Journal De La Societe Francaise De Transfusion Sanguine, 2022
Molecular Blood Group Screening in Donors from Arabian Countries and Iran Using High-Throughput MALDI-TOF Mass Spectrometry and PCR-SSP.
Flesch BK et al.
Transfusion Medicine and Hemotherapy : Offizielles Organ Der Deutschen Gesellschaft Fur Transfusionsmedizin Und Immunhamatologie, 2020
A novel algorithm comprehensively characterizes human RH genes using whole-genome sequencing data.
Chang TC et al.
Blood Advances, 2020
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
Genotyping of 28 blood group alleles in blood donors from Mali: Prediction of rare phenotypes.
Ba A et al.
Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis, 2016
Identification of six new RHCE variant alleles in individuals of diverse racial origin.
Goldman M et al.
Transfusion, 2016
A Molecular Evolutionary Reference for the Human Variome.
Liu L et al.
Molecular Biology and Evolution, 2016
RHCE*ceAG (254C>G, Ala85Gly) is prevalent in blacks, encodes a partial ce-phenotype, and is associated with discordant RHD zygosity.
Westhoff CM et al.
Transfusion, 2015
Molecular structures identified in serologically D- samples of an admixed population.
Trucco Boggione C et al.
Transfusion, 2014
Report of the fourth International Workshop on molecular blood group genotyping.
Daniels G et al.
Vox Sanguinis, 2011
Analysis of RhCE variants among 806 individuals in France: considerations for transfusion safety, with emphasis on patients with sickle cell disease.
Pham BN et al.
Transfusion, 2011
RHCE*ceCF encodes partial c and partial e but not CELO, an antigen antithetical to Crawford.
Hipsky CH et al.
Transfusion, 2011
DIIIa and DIII Type 5 are encoded by the same allele and are associated with altered RHCE*ce alleles: clinical implications.
Westhoff CM et al.
Transfusion, 2010
RHCE alleles detected after weak and/or discrepant results in automated Rh blood grouping of blood donors in Northern Germany.
Döscher A et al.
Transfusion, 2009
RhCE protein variants in Southwestern Germany detected by serologic routine testing.
Bugert P et al.
Transfusion, 2009
The RHCE allele ceCF: the molecular basis of Crawford (RH43).
Flegel WA et al.
Transfusion, 2006
Serological studies of monoclonal RH antibodies with RH1 (D), RH2 (C), RH3 (E) and RH5 (e) variant RBCs.
Noizat-Pirenne F et al.
Transfusion Clinique Et Biologique : Journal De La Societe Francaise De Transfusion Sanguine, 2003
E variants found in Japanese and c antigenicity alteration without substitution in the second extracellular loop.
Kashiwase K et al.
Transfusion, 2001
Molecular biology and genetics of the Rh blood group system.
Huang CH et al.
Seminars in Hematology, 2000
Heterogeneity of blood group RhE variants revealed by serological analysis and molecular alteration of the RHCE gene and transcript.
Noizat-Pirenne F et al.
British Journal of Haematology, 1998
Molecular analysis of selected Rh variants.
Noizat-Pirenne F et al.
Transfusion Clinique Et Biologique : Journal De La Societe Francaise De Transfusion Sanguine, 1996
Blood group immunochemistry and genetics.
Unknown Author
Seminars in Hematology, 1981