Associated Papers
Assessing reagents and techniques for identifying RhCE variants in routine serological testing.
de Paula Vendrame TA et al.
Vox Sanguinis, 2025
RHCE genotyping using next generation sequencing: Allele specific reference sequences.
Tounsi WA et al.
Transfusion, 2025
Ethnic diversity in Chilean blood groups: A comprehensive analysis of genotypes, phenotypes, alleles and the immunogenic potential of antigens in northern, southern and central regions.
Núñez Ahumada MA et al.
Vox Sanguinis, 2024
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
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
Transfusing children with sickle cell disease using blood group genotyping when the pool of Black donors is limited.
Leiva-Torres GA et al.
Transfusion, 2024
Antigen matching for transfusion support in Brazilian female patients with sickle cell disease to reduce RBC alloimmunization.
Muniz JG et al.
Transfusion, 2021
RH genotyping by nonspecific quantitative next-generation sequencing.
Stef M et al.
Transfusion, 2020
A novel algorithm comprehensively characterizes human RH genes using whole-genome sequencing data.
Chang TC et al.
Blood Advances, 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
A Tutsi family harbouring two new RHCE variant alleles and a new haplotype in the Rh blood group system.
Deleers M et al.
Vox Sanguinis, 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
A comparison of methods for the detection of the r'(s) haplotype.
Moulds JM et al.
Transfusion, 2015
Erythrocyte genotyping for transfusion-dependent patients at the Azienda Universitaria Policlinico of Naples.
Belsito A et al.
Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis, 2015
RHD genotyping and its implication in transfusion practice.
Sassi A et al.
Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis, 2014
RHD positive among C/E+ and D-negative blood donors in Tunisia.
Moussa H et al.
Transfusion Clinique Et Biologique : Journal De La Societe Francaise De Transfusion Sanguine, 2014
(C)ce(s) haplotype screening in Tunisian blood donors.
Moussa H et al.
Blood Transfusion = Trasfusione Del Sangue, 2014
Systematic RH genotyping and variant identification in French donors of African origin.
Kappler-Gratias S et al.
Blood Transfusion = Trasfusione Del Sangue, 2014
RHD alleles in the Tunisian population.
Ouchari M et al.
Asian Journal of Transfusion Science, 2013
Investigation of pseudogenes RHDΨ and RHD-CE-D hybrid gene in D-negative blood donors by the real time PCR method.
Szulman A et al.
Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis, 2012
Molecular background of D-negative phenotype in the Tunisian population.
Moussa H et al.
Transfusion Medicine (oxford, England), 2012
DIII Type 7 is likely the original serologically defined DIIIb.
Lomas-Francis C et al.
Transfusion, 2012
Identification of RHCE and KEL alleles in large cohorts of Afro-Caribbean and Comorian donors by multiplex SNaPshot and fragment assays: a transfusion support for sickle cell disease patients.
Silvy M et al.
British Journal of Haematology, 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
Molecular basis of blood group expression.
Denomme GA
Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis, 2011
A novel RHCE*ce 48C, 733G allele with Nucleotide 941C in Exon 7 encodes an altered red blood cell e antigen.
Hue-Roye K 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
Partial C antigen in sickle cell disease patients: clinical relevance and prevention of alloimmunization.
Tournamille C et al.
Transfusion, 2010
Alloanti-c/ce in a c+ceAR/Ce patient suggests that the rare RHCE ceAR allele (ceAR) encodes a partial c antigen.
Peyrard T et al.
Transfusion, 2009
Alloanti-c (RH4) revealing that the (C)ce s haplotype encodes a partial c antigen.
Pham BN et al.
Transfusion, 2009
Molecular analysis of inactive and active RHD alleles in native Congolese cohorts.
Touinssi M et al.
Transfusion, 2009
The JAL antigen (RH48) is the result of a change in RHCE that encodes Arg114Trp.
Westhoff CM et al.
Transfusion, 2009
Heterogeneous molecular background of the weak C, VS+, hr B-, Hr B- phenotype in black persons.
Pham BN et al.
Transfusion, 2009
The RHCE allele ceCF: the molecular basis of Crawford (RH43).
Flegel WA et al.
Transfusion, 2006
Rare RHCE phenotypes in black individuals of Afro-Caribbean origin: identification and transfusion safety.
Noizat-Pirenne F et al.
Blood, 2002
The VS and V blood group polymorphisms in Africans: a serologic and molecular analysis.
Daniels GL et al.
Transfusion, 1998
[The molecular basis of RH system and its applications in obstetrics and transfusion medicine].
Nardozza LM et al.
Revista Da Associacao Medica Brasileira (1992), 0