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A novel nonsense variant in RHAG underlies a Nordic Rhnull phenotype
Vox sanguinis, 2023-08, Vol.118 (8), p.690-694
2023
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Association of Maternal Regulatory Single Nucleotide Polymorphic CD99 Genotype with Preeclampsia in Pregnancies Carrying Male Fetuses in Ethiopian Women
International journal of molecular sciences, 2020-08, Vol.21 (16), p.5837
2020
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Disruption of a GATA1-binding motif upstream of XG / PBDX abolishes Xg a expression and resolves the Xg blood group system
Blood, 2018-07, Vol.132 (3), p.334
2018
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A new missense variant in exon 7 of the ABO gene, c.662G>A, in a family with B w phenotype
Transfusion (Philadelphia, Pa.), 2022-10, Vol.62 (10), p.E55
2022
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Characterization of GYPMur and novel GYPBun‐like hybrids in Thai blood donors reveals a qualitatively altered s antigen
Vox sanguinis, 2020-07, Vol.115 (5), p.472-477
2020
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Homozygosity for a null allele of SMIM1 defines the Vel-negative blood group phenotype
Nature genetics, 2013-05, Vol.45 (5), p.537-541
2013
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Identification of six new alleles at the FUT1 and FUT2 loci in ethnically diverse individuals with Bombay and Para-Bombay phenotypes
Transfusion (Philadelphia, Pa.), 2006-12, Vol.46 (12), p.2149-2155
2006
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Nomenclature for red blood cell blood group alleles
Transfusion (Philadelphia, Pa.), 2013-11, Vol.53 (11pt2), p.2844-2846
2013
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International Society of Blood Transfusion Working Party on Red Cell Immunogenetics and Blood Group Terminology Report of Basel and three virtual business meetings: Update on blood group systems
Vox sanguinis, 2022-11, Vol.117 (11), p.1332-1344
2022
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Matrix‐assisted laser desorption/ionization time‐of‐flight mass spectrometry analysis of 36 blood group alleles among 396 Thai samples reveals region‐specific variants
Transfusion (Philadelphia, Pa.), 2018-07, Vol.58 (7), p.1752-1762
2018
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ABO transcript levels in peripheral blood and erythropoietic culture show different allele‐related patterns independent of the CBF/NF‐Y enhancer motif and multiple novel allele‐specific variations in the 5′‐ and 3′‐noncoding regions
Transfusion (Philadelphia, Pa.), 2008-03, Vol.48 (3), p.493-504
2008
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A novel RHCE02 allele, containing the single-nucleotide change c.460A>G, encodes weakened expression of C and e antigens
Transfusion (Philadelphia, Pa.), 2016-09, Vol.56 (9), p.2391-2392
2016
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SMIM1 variants rs1175550 and rs143702418 independently modulate Vel blood group antigen expression
Scientific reports, 2017-01, Vol.7 (1), p.40451-40451, Article 40451
2017
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An age-dependent ABO discrepancy between mother and baby reveals a novel A(weak) allele
Transfusion (Philadelphia, Pa.), 2015-02, Vol.55 (2), p.422-426
2015
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Characterization of Jk(a+weak): a new blood group phenotype associated with an altered JK01 allele
Transfusion (Philadelphia, Pa.), 2011-02, Vol.51 (2), p.380-392
2011
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FUT1 mutations responsible for the H-deficient phenotype in the Polish population, including the first example of an abolished start codon
Blood transfusion = Trasfusione del sangue, 2018-01, Vol.16 (1), p.101-104
2018
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Mutations in GYPB exon 5 drive the S-s-U+(var) phenotype in persons of African descent: implications for transfusion
Transfusion (Philadelphia, Pa.), 2003-12, Vol.43 (12), p.1738-1747
2003
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Erythroid urea transporter deficiency due to novel JKnull alleles
Transfusion (Philadelphia, Pa.), 2008-02, Vol.48 (2), p.365-372
2008
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A new missense variant in exon 7 of the ABO gene, c.662G>A, in a family with B w phenotype
Transfusion (Philadelphia, Pa.), 2022, Vol.62 (10), p.55
2022
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Genetic basis of the K(0) phenotype in the Swedish population
Transfusion (Philadelphia, Pa.), 2005-04, Vol.45 (4), p.545-549
2005
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KEL02 alleles with alterations in and around exon 8 in individuals with apparent KEL:1,−2 phenotypes
Vox sanguinis, 2010-08, Vol.99 (2), p.150-157
2010
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