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The need for rare blood programs is real

Transfusion (Philadelphia, Pa.), 2023-04, Vol.63 (4), p.659-664

2023

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Monoclonal anti‐CD47 interference in red cell and platelet testing

Transfusion (Philadelphia, Pa.), 2019-02, Vol.59 (2), p.730-737

2019

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Three new XK alleles; two associated with a McLeod RBC phenotype

Transfusion (Philadelphia, Pa.), 2021-10, Vol.61 (10), p.E69-E70

2021

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Uncommon S–s–U+ phenotype encoded by two novel GYPB alleles

Transfusion (Philadelphia, Pa.), 2023-12, Vol.63 (12), p.E59-E61

2023

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A novel RHDDAU allele with c.1136C>T (p.Thr379Met) and c.17C>T (p. Pro6Leu)

Transfusion (Philadelphia, Pa.), 2020-12, Vol.60 (12), p.E51-E52

2020

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Two new Scianna variants causing loss of high prevalence antigens: ERMAP model and 3D analysis of the antigens

Transfusion (Philadelphia, Pa.), 2023-01, Vol.63 (1), p.230-238

2023

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A novel high‐prevalence antigen in the Lutheran system, LUGA (LU24), and an updated, full‐length 3D BCAM model

Transfusion (Philadelphia, Pa.), 2023-04, Vol.63 (4), p.798-807

2023

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An insertion/deletion polymorphism in the KLF1 gene resulting in an In(Lu) phenotype

Transfusion (Philadelphia, Pa.), 2021-10, Vol.61 (10), p.E73-E74

2021

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A novel P1PK allele in two Bangladeshi sisters with a history of spontaneous abortion: A4GALT02N(951C)

Transfusion (Philadelphia, Pa.), 2021-10, Vol.61 (10), p.E71-E72

2021

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Two novel variants that disrupt the RHCE start codon with varying effect on RhCE antigen expression

Transfusion (Philadelphia, Pa.), 2023-04, Vol.63 (4), p.E12-E14

2023

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Impact of RHD genotyping on transfusion practice in Denmark and the United States and identification of novel RHD alleles

Transfusion (Philadelphia, Pa.), 2021-01, Vol.61 (1), p.256-265

2021

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Four novel ABOAW alleles associated with weak antigen expression

Transfusion (Philadelphia, Pa.), 2022-12, Vol.62 (12), p.E76-E78

2022

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An intron c.149‐2632T>A change in RHD is associated with aberrant transcription and very weak D phenotype

Transfusion (Philadelphia, Pa.), 2022-02, Vol.62 (2), p.E14-E16

2022

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Five novel silenced KEL02 alleles

Transfusion (Philadelphia, Pa.), 2021-11, Vol.61 (11), p.E77-E79

2021

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Automated typing of red blood cell and platelet antigens from whole exome sequences

Transfusion (Philadelphia, Pa.), 2019-10, Vol.59 (10), p.3253-3263

2019

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YTGT: A new high‐prevalence antigen in the Yt blood group system in two unrelated Native Americans and transfusion management

Transfusion (Philadelphia, Pa.), 2022-09, Vol.62 (9), p.1917-1922

2022

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Use of an in‐house trypsin‐based method to resolve the interference of daratumumab

Transfusion (Philadelphia, Pa.), 2021-10, Vol.61 (10), p.3000-3007

2021

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Reliability of labeling red cell units with minor antigen historical results and process considerations

Transfusion (Philadelphia, Pa.), 2020-04, Vol.60 (4), p.822-830

2020

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A pair of S‐silencing single nucleotide variants cis‐linked on GYPB

Transfusion (Philadelphia, Pa.), 2021-04, Vol.61 (4), p.E34-E36

2021

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Novel JK allele background associated with production of anti‐JK3 during pregnancy

Transfusion (Philadelphia, Pa.), 2018-04, Vol.58 (4), p.1078-1079

2018

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Fatal hemolytic disease of the newborn caused by an antibody to KEAL, a new low‐prevalence Kell blood group antigen

Transfusion (Philadelphia, Pa.), 2017-01, Vol.57 (1), p.217-218

2017

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Determination of 24 minor red blood cell antigens for more than 2000 blood donors by high-throughput DNA analysis

Transfusion (Philadelphia, Pa.), 2007-04, Vol.47 (4), p.736-747

2007

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The Blood Group Antigen FactsBook

3, 2012

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The need for rare blood programs is real

Monoclonal anti‐CD47 interference in red cell and platelet testing

Three new XK alleles; two associated with a McLeod RBC phenotype

Uncommon S–s–U+ phenotype encoded by two novel GYPB alleles

A novel RHDDAU allele with c.1136C>T (p.Thr379Met) and c.17C>T (p. Pro6Leu)

Two new Scianna variants causing loss of high prevalence antigens: ERMAP model and 3D analysis of the antigens

A novel high‐prevalence antigen in the Lutheran system, LUGA (LU24), and an updated, full‐length 3D BCAM model

An insertion/deletion polymorphism in the KLF1 gene resulting in an In(Lu) phenotype

A novel P1PK allele in two Bangladeshi sisters with a history of spontaneous abortion: A4GALT02N(951C)

Two novel variants that disrupt the RHCE start codon with varying effect on RhCE antigen expression

Impact of RHD genotyping on transfusion practice in Denmark and the United States and identification of novel RHD alleles

Four novel ABOAW alleles associated with weak antigen expression

An intron c.149‐2632T>A change in RHD is associated with aberrant transcription and very weak D phenotype

Five novel silenced KEL02 alleles

International Society of Blood Transfusion Working Party on Red Cell Immunogenetics and Blood Group Terminology: Report of the Dubai, Copenhagen and Toronto meetings

Automated typing of red blood cell and platelet antigens from whole exome sequences

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

YTGT: A new high‐prevalence antigen in the Yt blood group system in two unrelated Native Americans and transfusion management

Use of an in‐house trypsin‐based method to resolve the interference of daratumumab

Reliability of labeling red cell units with minor antigen historical results and process considerations

A pair of S‐silencing single nucleotide variants cis‐linked on GYPB

Novel JK allele background associated with production of anti‐JK3 during pregnancy

Fatal hemolytic disease of the newborn caused by an antibody to KEAL, a new low‐prevalence Kell blood group antigen

Determination of 24 minor red blood cell antigens for more than 2000 blood donors by high-throughput DNA analysis

The Blood Group Antigen FactsBook

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